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  • Wiley-Blackwell  (16,132)
  • 1995-1999  (1,566)
  • 1990-1994  (14,566)
  • 1999  (1,566)
  • 1994  (14,566)
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  • 1995-1999  (1,566)
  • 1990-1994  (14,566)
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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2147-2156 
    ISSN: 1434-1948
    Keywords: Tetrapodal pentadentate ligand ; Ligand periphery ; Polydentate amine complex ; Nickel ; Podand ; Schiff base ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The tetrapodal pentaamine ligand 2,6-bis(1′,3′-diamino-2′-methylprop-2′-yl)pyridine (1), which contains four equivalent primary amino groups, can be derivatised partly or completely by Schiff base condensation with suitable carbonyl compounds. The new ligands thus obtained are mononucleating, as shown by the X-ray crystal structures of their respective nickel(II) complexes. Reaction of 1 with 1 equiv. of salicylaldehyde and subsequent reduction allows the selective modification of one of the four sidearms. The resulting ligand 2 is hexadentate and uninegative in its nickel(II) complex {[(2)Ni]PF6} (3) with both the secondary amine and the phenoxide functionalities coordinated to the metal centre. The unreduced Schiff base form of the ligand, 4, does not form a complex with nickel(II) as readily, and only a small quantity of the mixed salt {[(4)Ni][(1)Ni(H2O)](Br)2(PF6)} (5)has been obtained. While the overall coordination of 4 resembles that of 2, there is considerably more strain in the appended chelate ring, due to the presence of the C=N double bond. Modification of one arm in 1 can also be achieved by condensation with 1 equiv. of acetylacetone, to give the new ligand 6 which, likewise, is hexadentate in its NiII complex {[(6)Ni](PF6)2} (7). In this case, however, the N/O-functional sidearm is not deprotonated. Rather, it is coordinated as the keto-imine tautomer, making 7 a rare example of a metal complex containing this structural fragment. Two-fold functionalisation of 1 is observed upon reaction with acetone, regardless of whether the ketone is present in stoichiometric amounts or in excess, to give the pentadentate ligand 8with two diagonally juxtaposed isopropylidene-imine units. The complex isolated with this ligand {[(8)Ni](PF6)2} (9) contains pentacoordinate NiII, the sixth coordination site being blocked by the rigidly positioned isopropylidene groups. When reacted with 4 equiv. of trans-cinnamaldehyde, all the primary amino groups in 1 condense to give the four-fold Schiff base 10, which acts as a pentadentate podand towards nickel(II). In this complex, {[(10)Ni(OH2)]Br2} (11), an aqua ligand completes the coordination octahedron. All ligands are stable towards hydrolysis when coordinated to the metal, despite the presence of alkyl-imine groups in some cases.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2157-2166 
    ISSN: 1434-1948
    Keywords: Septadentate N5S2-ligand ; Dinuclear complexes ; Nickel ; Reactivity ; Redox chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The coordination chemistry of a series of dinickel complexes of the new septadentate amine-thiolate ligand N,N′-bis[2-thio-3-aminomethyl-5-tert-butylbenzyl]diethylenetriamine, H29, has been investigated in the context of ligand binding and oxidation state changes. The complexes [Ni2(9)(L)][ClO4]2 (10), [Ni2(9)(Cl)][Cl] (11), [Ni2(9)(L)][BPh4]2 (12), and [Ni2(9)(NCS)][OH·OH2] (13) have central N2Ni(μ-SR)2NiN′3L cores [L = labile solvent molecule (10, 12), Cl- (11), and NCS- (13)] composed of dithiolate bridged planar NiN2S2 and six-coordinate NiN′3S2L units. This is demonstrated for 11 and 13 by crystal structure determinations and for 10 and 12 by UV/Vis spectroscopy and room temperature magnetic susceptibility measurements. Complexes 10, 11, or 12 readily add other co-ligands at the NiN′3S2L fragment by substitution of the solvent molecule L (10, 12) or the chloride substituent (11). The overall structure of the parent complexes is not affected by the substitution reactions. An electrochemical study has shown that complex 10 undergoes two successive one-electron oxidations at +0.88 and +0.41 V vs SCE. The oxidized species are not thermally stable, but electronic absorption spectra and EPR spectra are indicative of the presence of NiIII species.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2167-2172 
    ISSN: 1434-1948
    Keywords: Macrocyclic compounds ; Amine-Thiolate Donors ; Polynuclear Complexes ; Nickel ; Condensation reactions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A novel route to macrocyclic amine-thiophenolate ligands is described. The new, air-stable thiophenolate precursor 1,2-bis(4-tert-butyl-2,6-diformyl-phenylsulfanyl)ethane (4) is readily condensed with two equivalents of 1,2-ethanediamine or 1,3-propanediamine under medium to high dilution conditions to give 2 × 4 condensation products. The smaller 1 × 2 macrocyclic compounds are not produced under these conditions. Subsequent reduction with NaBH4 (reduction of imine groups) and Na/NH3 (reductive cleavage of aryl-alkylsulfides) provides the 36- and 40-membered amine-thiophenolate ligands H46a and H46b. The macrocyclic compounds are versatile ligands for the preparation of polynuclear transition metal complexes. With divalent nickel H46a forms the di- and tetranuclear complexes [Ni2(6a)] (7) and [Ni4(6a)][ClO4]4 (8). Reaction of 8 with four equivalents of NH4SCN yields the novel isothiocyanate complex [Ni4II(6a)(NCS)4]·10MeCN (9). The structure consists of well-separated molecules of the tetranuclear complex [NiII4(6a)(NCS)4] (Ci symmetry). Two symmetry-related binuclear [N2Ni(μ2-SR)2NiN4] fragments composed of thiolate-bridged distorted planar {N2S2Ni}- and distorted cis-octahedral {(SCN)2N2S2Ni} units reside within the cavity of the macrocycle. The intramolecular distance between the two binuclear units is 6.144(1) Å.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2173-2185 
    ISSN: 1434-1948
    Keywords: EPR spectroscopy ; Metallocenylboranes ; Organovanadium radicals ; Redox chemistry (CV) ; X-ray diffraction ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The paramagnetic complexes di(mesityl)([5]trovacenyl)borane (5·), (mesityl)di([5]trovacenyl)borane (6··), and tri([5]trovacenyl)borane (7···) were prepared from [5]trovacenyllithium, (η5-C7H7)V(η5-C5H4Li), and (Mes)2BF, (Mes)BF2, and BF3, respectively. The propeller-shaped species 5·, 6··, and 7··· were subjected to X-ray diffraction with the aim of possibly correlating the twist angles with intramolecular intermetallic communication. Cyclic voltammetry points to successive vanadium-centered oxidation processes and boron-centered reduction, a small redox splitting δE1/2[(2+/+), (+/0)] being observed for 6··. According to EPR spectroscopy, performed in fluid solution, the exchange interaction J in the diradical 6·· approaches the fast-exchange region and is attenuated significantly by quaternization at boron in [6··-nBu]-. Although EPR spectroscopy of the triradical 7··· also indicates an extensive exchange interaction, the exchange parameters, derived from spectral simulation, follow the gradation J(7···) ≈ 1/3 J(6··). The magnetic susceptibility of 6·· and 7··· follows the same trend. As expected, compound 7··· exhibits spin frustration because it contains three antiferromagnetically coupled S = 1/2 systems that are arranged in an equilateral triangle.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2187-2199 
    ISSN: 1434-1948
    Keywords: Ansa compounds ; Cp-derived chelate ligands ; Neopentane chemistry ; Spiro compounds ; Tripodal ligands ; Cyclopentadienyl compounds ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The neopentane-derived functionalized oxetane O(CH2)2C(CH3)(CH2OMs), 1, reacts with indenyllithium (LiInd) or fluorenyllithium (LiFlu) to produce the derivatives O(CH2)2C(CH3)(CH2R) (R = indenyl, fluorenyl), 2. The oxetane ring of 2 undergoes nucleophilic ring-opening by reaction with LiPR′2 to give the chiral chelate ligands (HOCH2)(CH3)C(CH2R)(CH2PR′2) (R = indenyl, fluorenyl), 5. Nucleophilic ring-opening by LiInd or LiFlu is possible too, resulting in the functionalized ansa-Cp ligands (HOCH2)(CH3)C(CH2R)(CH2R′) (R, R′ = indenyl, fluorenyl), 12. Electrophilic ring-opening of 2 with HBr to give (HOCH2)(CH3)C(CH2R)(CH2Br) (R = indenyl, fluorenyl), 3, is also possible. The alcohol function of 3 may be activated directly, whereas activation of this group in 5 is only possible after BH3 protection of the phosphane function. The mesylates (MsOCH2)(CH3)C(CH2R)(CH2Br) (R = indenyl, fluorenyl), 4, undergo, under basic conditions, spiro cyclization to produce spirocyclobutane derivatives 9 with the α-carbons of the five-membered cycles acting as the spiro centres. Substitution of the mesylate group of 4 by PR2 nucleophiles is therefore not possible. Ansa-Cp derivative (MsOCH2)(CH3)C(CH2Ind)(CH2Flu), 12c also reacts with LiPPh2 with spiro cyclization to produce 9d, instead of giving the substitution product. Tripodal ligands (CH3)C(CH2R)(CHPPh2)2 (R = indenyl, fluorenyl), 11, are accessible by the reaction of (MsOCH2)(CH3)C(CH2PPh2)2 with LiInd or LiFlu. All compounds are fully characterized by the usual spectroscopic and analytical techniques including single-crystal X-ray analyses in several cases.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2201-2207 
    ISSN: 1434-1948
    Keywords: Carboxylate syn-anti ; N-centered tripodal ligand ; Manganese ; Imidazole ; Helicoïdal inorganic chiral chain ; Magnetism ; π-π interaction ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The crystal structure of an infinite inorganic chain consisting of MnII and an N-centered tripodal ligand N,N-(2-pyridylmethyl)[(1-methylimidazol-2-yl)-methyl]glycinate is presented. It exhibits a chiral helical structure with a pitch of two monomeric units (each monomeric unit containing one Mn atom). Each manganese is connected to its neighbor through a carboxylate bridge in a syn-anti geometry. Around each manganese center, two carboxylates bind in a cis geometry. This peculiar bridging geometry (syn-anticis) provides a broken-line chain, running in a zig-zag manner along the b axis of the P21 space group. The magnetic properties have been investigated. They show a pseudo-2D magnetic structure, with one major pathway along the chain and an inter-chain minor one. The intrachain coupling is a weak antiferromagnetic interaction (J/k = -0.25). This low value is entirely consistent with the geometry of the bridge. The interchain coupling is a weaker antiferromagnetic coupling (J′/k = -0.11) and could be mediated through π-π interactions between pyridine and imidazole from two adjacent helixes.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2221-2231 
    ISSN: 1434-1948
    Keywords: Calixarenes ; Inclusion compounds ; Imido Complexes ; Molybdenum ; Tungsten ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Syntheses, spectroscopic properties, molecular structures, and bonding of novel calix[4]arene imido compounds are described. Treatment of M(NtBu)2(NHtBu)2Ia (M = Mo), Ib (M = W) or M(NMes)2Cl2(dme) IIa (M = Mo), IIb (M = W) (Mes = 2,4,6-Me3-C6H2) with p-tBu-calix[4]arene LH4 affords calix[4]arene metal complexes LM(NR) 1a, b (M = Mo, W; R = tBu) and 2a, b (M = Mo, W; R = Mes). Analytical and spectroscopic data are consistent with monomeric structures for 1 and 2, retaining a local C4v symmetry for the calix[4]arene metal fragment. These complexes are well-suited to bind small molecules like acetonitrile, tBu-isonitrile, or water within their macrocyclic pockets. The spectroscopic data of some inclusion compounds and the crystal structures of LMo(NtBu)(NCMe) 1a(NCMe), LW(NtBu)(OH2) 1b(OH2), LW(NtBu)(CNtBu) 1b(CNt Bu), LMo(NMes)(NCMe) 2a(NCMe), and LW(NMes)(NCMe) 2b(NCMe) are reported. All complexes contain a group VI metal imido [M=NR] moiety mounted on the phenoxide rim of the calix[4]arene ligand as well as an incorporated guest molecule within the cavity. Some insights into the structures of complexes of the type L′W(NR′) (L′ = p-H-calix[4]arene; R′ = H, Me) and into bonding in these compounds are provided by density functional theory, applying the B-P86 density functional and an all SVP basis set within the RI-J-DFT approximation. At least one π bond is of importance for calix[4]arene-metal bonding in these compounds. The metal-imido bond can be described as a triple bond. A geometrically optimized minimum structure of L′W(NMe) 4 shows a calix[4]arene ligand only slightly distorted from a local C4v symmetry and an almost linear tungsten-imido moiety.
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  • 8
    ISSN: 1434-1948
    Keywords: Arsonium salts ; Superacidic systems ; Structure elicidation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of trimethylarsane in the superacidic systems hydrogen/fluoride antimony pentafluoride and hydrogen fluoride/arsenic pentafluoride leads to trimethylarsonium fluorometallates. These salts are stable up to 60 °C and 5 °C, respectively. Structures were successfully elucidated in the cases of trimethylarsonium undecafluorodiarsenate and trimethylarsonium hexafluoroantimonate. (CH3)3AsH+As2F11- crystallizes in the monoclinic space group P21/n with four formula units per unit cell with the dimensions a = 7.362(1), b = 12.589(1), c = 13.598(1) Å and β = 95.37(1)°. (CH3)3AsH+SbF6- crystallizes in the monoclinic space group P21/m with four formula units per unit cell with the dimensions a = 8.313(1), b = 8.855(1), c = 13.285(1) Å and β = 94.358(1)°.
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  • 9
    ISSN: 1434-1948
    Keywords: Molybdenum ; μ-Oxo ; Conformational equilibrium ; X-ray diffraction ; NMR spectroscopy ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new thiocyanatomolybdenum(VI) dioxo-μ-oxo complex dimer bearing a 4,4′-di-tert-butyl-2,2′-bipyridine ligand (2) is shown to exist in the crystal cell unit as a meso (Mo-O-Mo angle of 180°) and d,l, pair (Mo-O-Mo angle of 155.7°). These conformers are in equilibrium in solution and have been observed clearly by 1H NMR spectroscopy.
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  • 10
    ISSN: 1434-1948
    Keywords: Macrocycles ; Lithium ; Fluorescence ; Cryptands ; Coordination ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three aza-cages with the anthracene-containing photoactive groups L1, L2, and L3 have been synthesized. All compounds are able to selectively encapsulate a lithium ion and solid complexes have been isolated. The formation equilibria have been investigated by UV/Vis and 1H, 13C and 7Li NMR spectroscopic techniques. The fluorescence emission of both free ligands and lithium complexes have been investigated. Results indicate that the CHEF (chelation enhancement of the fluorescence) effect obtained by lithium coordination exits although lower than that occurring upon full protonation.
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  • 11
    ISSN: 1434-1948
    Keywords: Copper ; Trinuclear complexes ; Formamidines ; Magnetism ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three new copper(II) linear trinuclear compounds are reported, all of which were synthesized in-situ, with the general formula [Cu3(L)4](CF3SO3)2(Y)x, where L is the dehydronated ligand: N,N′-bis(pyridine-2-yl)formamidine (abbreviated as Hpdf), N,N′-bis(pyrimidine-2-yl)formamidine (abbreviated as Hpmf) and N,N′-bis(5-methylpyridine-2-yl)formamidine (abbreviated as Hmpdf), Y = EtOH or H2O and x = 0.5-1.5. The compounds were characterized by X-ray diffraction, IR, LF, and EPR spectroscopy and by magnetic susceptibility down to 4 K. The structure of the compound [Cu3(pmf)4](CF3SO3)2(H2O)1/2 was determined by X-ray crystallography; it was found to crystallise in the triclinic space group P-1 with a = 8.529(5), b = 15.760(5), c = 19.639(5) Å, α = 101.793(5), β = 101.263(5), γ = 102.389(5)°, Z = 2. The structure [Cu-Cu-Cu angle 174.96(11)°] consists of four nearly flat molecules of the ligand, which contribute to the propeller-type structure around the Cu-Cu-Cu axis. A strong antiferromagnetic interaction between the CuII ions is observed with calculated J values, based on the Hamiltonian H = -2J(S1·S2 + S2·S3) - 2J′·S1·S3, of -174(1) cm-1, -120(1) cm-1, and -167(1) cm-1 for the compounds studied with L = pdf, pmf, and mpdf, respectively. These values are in agreement with an S = 1/2 ground state below temperatures of 120-160 K.
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  • 12
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2277-2281 
    ISSN: 1434-1948
    Keywords: Boron ; Iron ; Nickel ; Carbyne complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The μ3-boryloxycarbyne complexes [{Fe(CO)3}3{μ3-COBCl{NtBu(SiMe3)}}2] (1) and [{(η5-C5H5)Ni}3{μ3-COBX(NR2)}μ3-CO] (2a: NR2 = NtBu(SiMe3), × = Cl; 2b: NR2 = N(SiMe3)2, × = Cl; 2c: NR2 = NMe2, × = BNMe2Cl) were obtained by reaction of the anionic complexes K2[{Fe(CO)3}3{μ3-CO}2] and K[{(η5-C5H5)Ni(CO)] with the corresponding chloroboranes Cl2BNR2 {NR2 = NtBu(SiMe3), N(SiMe3)2}, or 1,2-dichlorodiboranes(4) B2(NMe2)2Cl2, respectively. The products are formed by a nucleophilic attack of the CO oxygen atom at the boron centres with subsequent salt elimination. All compounds were characterized by IR and multinuclear NMR spectroscopy, and the structures of 1 and 2c in the solid state were determined by single-crystal X-ray diffraction studies.
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  • 13
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1271-1279 
    ISSN: 1434-1948
    Keywords: Chirality ; Dinuclear complexes ; Rhodium ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dinuclear and polynuclear metal complexes with octahedral centers coordinated to di- or polydentate ligands are often obtained as complicated mixtures of various stereoisomers. Stereospecific synthesis of such species is therefore of high current interest. Chiral derivatives of pyridine can be used for this purpose. Dinuclear μ-chloro-bridged RhIII complexes with two didentate, cyclometalated thienylpyridine-type ligands at each metal center are formed stereoselectively when pinene groups are fused to the pyridine rings. The two octahedral RhIII centers have homochiral configurations, ΔΔ and ΛΛ. The heterochiral diastereomer ΔΛ is not observed. With (8R,10R)-2-(2′-thienyl)-4,5-pinenopyridine [Hth4,5-(R,R)ppy] the ΔΔ to ΛΛ ratio is 9:1 when the separation eluent contains NaCl. Modeling the ΛΛ and the ΔΛ isomers of the dinuclear species shows crowding of the pinene groups in both cases; however, the strain can be released by relatively small distortions only in the case of the ΛΛ isomer. NO3- cleaves the dichloro bridge, yielding the mononuclear species Δ[Rh(L2)2(NO3)] (2) in a completely stereoselective manner when NaCl is replaced by KNO3 in the eluent mixture. The molecular structure has been determined by X-ray structure analysis for both the ΔΔ and the mononuclear complex Δ[Rh(L2)2(NO3)] (2) in order to confirm the configuration at the metal center. 1H-NMR, 13C-NMR and CD spectra were measured and the latter shows that the CD activity is solely due to the chirality at the metal center.
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  • 14
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1281-1289 
    ISSN: 1434-1948
    Keywords: Phosphaalkynes ; Dimerization mechanism ; Diphosphacyclobutenes ; Density functional theory ; Ab initio calculations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dimerization of phosphaalkynes (R-C≡P, R = H, Me, tBu) without and with the presence of transition metal fragments, including CpCo (Cp = cyclopentadienyl) and COT-Ti (COT = cyclooctatetraene), has been probed using density functional theory calculations (B3LYP with different basis sets). MP2 and CCSD(T) calculations were also performed for the [H2C2P2] systems. In an attempt to address the exciting controversy and uncertainty about phosphaalkyne dimerization, a number of dimer formation mechanisms proposed in the literature have been examined. Some new and plausible intermediates have also been identified.
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  • 15
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1315-1324 
    ISSN: 1434-1948
    Keywords: Ab initio calculations ; EHMO ; Vinylidene complexes ; Cobalt ; Rhodium ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The transformation of acetylene into vinylidene, as promoted by the metal fragment [(pp3)Co]+ [pp3 = P(CH2CH2PPh2)3], is unimolecular and features the hydride-acetylide species as an intermediate. The paper describes a detailed ab initio study of the reaction, in particular with regard to the step involving 1,3-H shift. The best computational results are obtained by mimicking the pp3 ligand with actual ethylenic chains rather than with single PH3 molecules. The keypoints along the two-step reaction path (π-acetylene, hydride-acetylide, and vinylidene complexes, as well as intermediate transition states) have been optimized for CoI and RhI derivatives at the MP2 level. For the fragment [(pp3)Co]+, the barrier associated with transformation of the hydride-acetylide intermediate to vinylidene (20.6 kcal/mol) is easier to surmount compared to that for reversion to the reactants (28.6 kcal/mol). The situation is reversed for the analogous RhI system, with the initial π-acetylene adduct being slightly more stable. Although higher in energy, the hydride-acetylide species is the experimentally detected product of the reaction of acetylene with the fragment [(pp3)Rh]+. The salient chemical aspects of the 1,3-H shift are discussed in terms of perturbation theory arguments. Parallel EHMO calculations, which have provided a relatively good consistency with the ab initio results, allow the proposal of an orbital rationale for the mode of migration of the hydride ligand along the substantially linear Co-Cα-Cβ grouping.
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  • 16
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1335-1342 
    ISSN: 1434-1948
    Keywords: Photolysis ; Alkynes ; Matrix isolation ; DFT ; Oxygenations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photolytically-induced reactions of chromyl chloride with acetylene and but-2-yne (dimethylacetylene) in low-temperature argon matrices yield end-on ketene and dimethylketene complexes of O=CrCl2, respectively. The product formation probably results from an electrophilic attack of a Cr=O linkage on the C≡C triple bonds, leading to radical-like transition states or intermediates, which subsequently rearrange through 1,2-H or 1,2-methyl shifts. Consequently, allene is attacked at its central carbon and the allyl radical thus generated undergoes subsequent ring-closure to give a cyclopropanone complex of O=CrCl2.
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  • 17
    ISSN: 1434-1948
    Keywords: Copper chelates ; EPR spectroscopy ; Electronic structure ; Schiff base ligands ; Structure elucidation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of tetrahedrally distorted copper(II) complexes with thiolate and imine coordination were synthesized. Schiff bases derived from 4-benzoyl-3-methyl-1-phenyl-2-pyrazoline-5-thione and various diamines were used as tetradentate ligands to obtain tetrahedrally distorted metal chelates with [CuN2S2] complex units. Crystal structures of the complexes 1, 2, 5 and 6 and of ligand H25 have been determined by means of single-crystal X-ray structure analysis. The structure data show a strong influence of the diamine building blocks on the tetrahedral distortion of the copper(II) complexes. Results of Extended Hückel LCAO calculations correlate strongly with structural, electrochemical, UV/Vis- and EPR-spectroscopic features obtained experimentally. The calculations confirm for the whole complex series a strong delocalization of the frontier orbitals. The highest fully occupied molecular orbital shows a weak contribution, resulting from thiolate donor atoms, whereas the antibonding singly occupied molecular orbitals (SOMOs) are distributed between the copper(II) centre (ca. 35-40%) and the N2S2 donor set. The SOMO energy significantly lowers with increasing tetrahedral distortion of the coordination sphere. The influence of the tetrahedral distortion of copper(II) complexes on redox potentials, UV/Vis and EPR spectra is discussed.
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  • 18
    ISSN: 1434-1948
    Keywords: Half-sandwich complexes ; Molybdenum ; Optically active complexes ; Rhenium ; Tungsten ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of (η5-PinCp*)Re(CO)3 [PinCp* = tetramethyl(pinanyl)cyclopentadienyl] is described. Successive substitution of two CO ligands by NO+ and PPh3 generates a 1:1 diastereomeric mixture of chiral-at-metal [(SRe)/(RRe)-(PinCp*)Re(CO)(NO)(PPh3)]BF4. The diastereomers are converted with sodium methoxide into the derivative “esters” (SRe)/(RRe)-(PinCp*)Re(COOCH3)(NO)(PPh3), and then with (+)-(R)-(1-naphthylethyl)amine to the “amides” (SRe)/(RRe)-(PinCp*)Re(NO)(PPh3)[CONHCH(CH3)C10H7] [(SRe)/(RRe) = 1:1]. Fractional crystallisation separates the (SRe) isomer with an optical purity of 〉 98%. The latter compound has been characterized by X-ray structure analysis. By treating the (SRe)-amide with CF3CO2H and NaBF4, (SRe)-(PinCp*)Re(CH3)(NO)(PPh3) can be generated. Protolysis of this compound with HBF4/Et2O in CD2Cl2 at -78 °C leads to the solvent-stabilized complex (SRe)-[(PinCp*)Re(NO)(PPh3)(ClCD2Cl)]+BF4-. The thermal and configurational stability of this chiral Lewis acid is investigated at various temperatures. The syntheses of [PinCp*RhCl2]2, PinCp*TiCl3 and PinCp*M(CO)2(NO) (M = Mo, W) are also described. Starting with PinCp*M(CO)2(NO), the relatively stable 16-VE complexes PinCp*MCl2(NO) and PinCp*W(CH2SiMe3)2(NO) are synthesized.
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  • 19
    ISSN: 1434-1948
    Keywords: 2,2′-Bipyridines ; Chelate complexes ; Hydrogen bonding ; π-π stacking ; Crystal structure ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new synthetic route for the synthesis of 5,5′-diamino-2,2-bipyridine (5) based on the coupling of 2-chloro-5-aminopyridine in the presence of NiCl2 × 6 H2O/PPh3/Zn in dimethylformamide is described. The reactions of the potentially ambidentate ligand 5 with salts of the transition metals Mn, Fe, Ni, Cu, Zn, Ag, and Cd gave a variety of 13 metal-ligand complexes depending on the anion, the crystallization conditions and the metal-to-ligand ratio. The complexes obtained were characterized by thermal analyses, NMR including 113Cd-NMR, IR, and for the iron complex 57Fe-Mößbauer spectroscopy. The structure of eight of the compounds was elucidated by X-ray crystallography. All of these metal complexes show a bipyridine-metal coordination. The amino functionality was never involved in metal coordination. The intermolecular arrangement is dictated by hydrogen bonding from the amino functionality and by π-π stacking of the bipyridine rings.Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2005/1999/99078_s.pdf or from the author.
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  • 20
    ISSN: 1434-1948
    Keywords: Iron(III) ; Peroxo Complexes ; Kinetics ; Hydrogen Peroxide ; Catalase ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The new diiron complex [Fe2(tbpo){O2As(CH3)2}(CH3O)(CH3OH)](ClO4)3 · 5 CH3OH · 2 H2O (1) containing a (μ-alkoxo)(μ-dimethylarsinato)diiron(III) core was synthesized using the heptadentate ligand N,N,N′,N′-Tetrakis(2-benzimidazolylmethyl)-1,3-diamino-2-propanol (Htbpo). The complex was characterized structurally by X-ray crystallography. 1reproduces the coordination mode and the stoichiometry of the proposed purple acid phosphatase-arsenate inhibitor complex. More importantly, 1 is a good functional model for the activation of small molecules, since the solvent molecule in the coordination sphere of each iron ion can be substituted very easily by a small substrate molecule. This is confirmed by the comparatively high pH-dependent catalase-like activity of 1. In order to study the influence of the cacodylate bridge on the formation of the metastable adduct with hydrogen peroxide, the analogous hydroxo-bridged complex [Fe2(tbpo)(OH)(NO3)2](NO3)2 · CH3OH · 2 H2O (2) was employed. The reactions of 1and 2 with H2O2 were studied as a function of [H2O2], pH, temperature, and pressure, and the kinetic results including the activation parameters are reported. In the case of compound 2 the reaction proceeds in one step, and the observed first order rate constant, kobs, shows a linear dependence on the hydrogen peroxide concentration with a zero intercept. For complex 1 the kinetic traces could be fitted to two exponential functions. One of the observed pseudo-first-order rate constants, kobs1, exhibits a linear dependence on the hydrogen peroxide concentration with a zero intercept, whereas the other rate constant, kobs2, was independent of the hydrogen peroxide concentration. A mechanistic interpretation is presented.Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2005/1999/99068_s.pdf or from the author.
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  • 21
    ISSN: 1434-1948
    Keywords: Ruthenium ; Coordination chemistry ; Paramagnetic complexes ; Magnetic properties ; Ion exchange ; Antitumor agents ; Colon tumors ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Indazolium trans-tetrachlorobis(indazole)ruthenate(III) exhibits excellent results against different tumor models in vitro and in vivo. To improve the water solubility necessary for the introduction of this tumor-inhibiting compound into clinical trials, we synthesized the corresponding sodium salt in a two-step ion exchange via the tetramethylammonium salt. The sodium salt shows a 35-fold higher solubility in water relative to the indazolium salt. We also synthesized the n-butylammonium, n-octylammonium, and tetraphenylphosphonium salts, all of which showed improved solubility in organic solvents. The X-ray crystal structure of the latter could be solved, proving the trans configuration of the complex anion. In spite of the paramagnetic RuIII center an assignement of the coordinated indazole protons could be made with the help of a COSY experiment.
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  • 22
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2355-2368 
    ISSN: 1434-1948
    Keywords: Phosphane complexes ; Lithium ; Aminophosphanes ; Hydrazides ; (N-lithioamino)diorganophosphanes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Butyllithium (nBuLi) deprotonates Ph2P-NHtBu in ether to give (Ph2P-NLitBu)2·OEt2. There is no Li···P interaction in this molecule. Three compounds of the type R′P(NLiR)2 have been obtained by lithiation of R′P(NHR)2, isolated as [BuP(NLitBu)2·OEt2]2, [PhP(NLiPh)2·OEt2]2 and [PhP(NLiPh)2]2. Reaction of nBuLi with MeP(NHiPr)2 in hexane/THF leads to [MeP{N(Li)iPr]2·THF}4 with an asymmetric cluster structure comprising one LiP3, three LiPN2, three LiP2N and one LiN3 cluster units. The molecular structures of these compounds as determined by X-ray structure analysis show that they are best depicted as N-lithioaminophosphanes and not as the isomeric P-lithioiminophosphoranes.
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  • 23
    ISSN: 1434-1948
    Keywords: Alkylation ; Carbonyl complexes ; Lewis acids ; Phosphaalkenes ; Protonation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of the carbonyl-functionalized phosphaalkenes RC(O)P=C(NMe2)2 [R = tBu (2a), Ph (2b)] with protic acids and alkylating reagents occurred at the two-coordinate phosphorus atom to give the phosphanyl-substituted carbocations 3a,b and 4a,b. In contrast, treatment with Me3SiOSO2CF3 resulted in attack at the oxygen atom by the silyl group, and the formation of [RC(OSiMe3)=PC(NMe2)2]SO3CF3 (5a,b). Similarly, the Lewis acids B(C6F5)3, Al(tBu)2Cl and AlMe3 were ligated to the oxygen atom of the carbonyl group. Two equivalents of GaMe3 were added to the oxygen and phosphorus atom of the phosphaalkene to yield the thermolabile complexes [RC(OGaMe3)=P(GaMe3)C(NMe2)2] (10a,b). In contrast, one molecule of InMe3 was bound to the phosphorus center of the phosphorus compound. Reaction of the phosphaalkenes with [Ni(CO)4], [Fe2(CO)9] or [{(Z)-cyclooctene}Cr(CO)5] also took place at the pnictogen atom, resulting in complexes of the type [RC(O)P{M(CO)n}C(NMe2)2] (R = tBu, Ph; M = Ni, n = 3; Fe, n = 4; Cr, n = 5). The chemical transformations reported here underline the versatile chemistry of phosphaalkenes and emphasize a relationship between carbonyl-functionalized phosphaalkenes and the well-investigated class of phosphorus ylides. X-ray structures of compounds 6b, 7b*, 10a, 11a and 12a are reported.
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  • 24
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    AIChE Journal 40 (1994), S. 1-1 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 25
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    AIChE Journal 40 (1994), S. 11-18 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The dynamic evolution of the cluster-size distribution (CSD) in the precoalescence stages of nucleation and growth for sizes within and beyond the nucleation barrier layer (NBL) has been obtained. The existence of several universal kinetic laws of nucleation is predicted. In the precoalescence stages of nucleation, the CSD for sizes within and beyond the NBL obeys dynamic scaling relations. In a range of sizes beyond the NBL, the CSD exhibits a universal power law behavior, the exponent of which depends only on the interphase monomer transfer mechanism. Based on the results for the CSD, a general foundation is developed for nucleation kinetic measurements including the determination of the nucleation barrier and the inter-facial monomer transport rate by measuring the CSD. A preliminary comparison with an experimental study confirms the predicted dynamic scaling and the power law behavior of the CSD in the early stages of nucleation and growth.
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  • 26
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    AIChE Journal 40 (1994), S. 50-64 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Monitoring and control of batch pulp digesters, which convert wood chips to pulp by Kraft process are discussed. The Kappa number, which represents the extent of delignification, is the key controlled variable, which cannot be measured on-line and must be estimated through secondary liquor measurements. Given a fixed batch time, the final Kappa number should be as close to the target Kappa number as possible, despite errors in the initial state estimates and input disturbances. To fulfill this objective, a state-observer-based model-predictive controller is designed using a detailed nonlinear dynamic model of the digester. The extended Kalman filter (EKF) using on-line measurements of various liquor characteristics is capable of recovering from significant errors in the initial state estimates. In addition, the EKF is shown to be robust to the errors in the covariance matrices and most model parameters, but quite sensitive to some model parameter errors. Coupled with the EKF, a finite-horizon model predictive controller (MFC) based on successive linearization of the nonlinear pulping model, is found to work efficiently for controlling the Kappa number and batch time.
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  • 27
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    AIChE Journal 40 (1994), S. 88-96 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A dynamic model for emulsion polymerization in a tubular reactor has been developed and compared with experimental data. The model uses an axial dispersion coefficient to fit experimentally measured residence time distributions and to represent axial mixing during reaction. Very general emulsion polymerization kinetics are assumed so that a wide range of monomers and operating conditions can be handled. Orthogonal collocation on finite elements was chosen as the numerical solution technique. Comparisons show good agreement between model and experiments for two different monomers.
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    AIChE Journal 40 (1994), S. 120-130 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Spatiotemporal patterns existing in a one-dimensional fixed-bed reactor with oscillatory or excitable kinetics are analyzed to develop the methodology of motion identification and classification. The reactor model accounts for a local (solid-phase) oscillator and a global (gas-phase) convective interaction. The local oscillator incorporates a fast and diffusing surface temperature and a localized activity as its dynamic variables. Such kinetics admit a traveling pulse solution or homogeneous oscillations in a uniform medium. In a fixed-bed reactor, the local conditions in the bed (the phase plane character) vary along the system. The response of an excitable bed to local perturbations depends on its location (at inlet or outlet) and the nature of the initial steady state ( ignite or extinguished). The main spatiotemporal-sustained patterns in the bed are: almost homogeneous oscillations that appear as parallel bands in the time-space contour map; oscillatory fronts that emerge from the reactor exit, and aperiodic motion that appears as split-bands. Pattern selection is determined by the phase planes spanned by the reactor and the ratio of the two slowest time scales: front residence time and period of oscillations.
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  • 29
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    AIChE Journal 40 (1994), S. 152-159 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A generalized quartic equation of state has been developed for pure nonpolar fluids. The equation of state contains four parameters which depend on three properties of the fluid - critical temperature, critical volume, and acentric factor. A mathematical approximation based on previously reported hard-sphere molecular dynamics simulations has been used to model repulsive contributions to the pressure. Attractive forces were modeled using an empirical term. While the quartic equation yields four roots, one root is always negative and hence physically meaningless, and three roots behave like three roots of a cubic equation. Thus, the new equation of state has the advantages of a cubic, simplicity and unequivocal identification of the roots, while correctly modeling the attractive and repulsive contributions to the pressure. The new equation of state is more accurate than either the Peng-Robinson or a previously proposed quartic equation of state. Accuracy in the supercritical and compressed liquid regions is improved substantially.
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  • 30
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    AIChE Journal 40 (1994), S. 187-192 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 40 (1994), S. 178-181 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 40 (1994), S. 536-542 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Increasing and constant temperature gravimetric methods were used to measure the thermal decomposition rates of Mg(OH)2 particles. An Arrhenius-type kinetic equation was proposed and tested. Temperature, exposure time on surface area of the calcined particles and other effects of variables were explored. A fractional-order sintering rate expression was developed on the basis of collected experimental data. An integrated model is also presented that considers the surface area generation by calcination and the simultaneous surface reduction caused by sintering of the nascent oxide. Obtained results enable specifying the operating conditions needed for the production of the high surface, reactive magnesium oxide.
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    AIChE Journal 40 (1994), S. 570-575 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 34
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    AIChE Journal 40 (1994), S. 207-214 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The interactive effects of heat and mass transfer in evaporation of binary mixtures flowing as falling films on vertical surfaces was investigated. Evaporative heat-transfer coefficients were measured for aqueous mixtures of ethylene and propylene glycol, with boiling ranges up to 55°C. Tests were carried out at atmospheric pressure with heat fluxes ranging from 3,000 to 25,000 W/m2, and film Reynolds numbers ranging from 300 to 3,000. Results indicated that the heat-transfer coefficient for mixtures depends weakly on wall superheat and film Reynolds number, but strongly depends on mixture composition. Analysis of the results indicates that mass-transfer resistance in the liquid film causes significant elevation of the interface temperature, causing a reduction of the effective temperature driving force. A semiempirical model for correlation of the interactive heat-and mass-transfer phenomena is proposed.
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  • 35
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    AIChE Journal 40 (1994), S. 627-646 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The Åström-Hägglund autotuner is extended to multivariable systems. The proposed multivariable automatic tuning performs the identification-design procedure in a sequential manner. Its advantages are discussed, as well as the process characteristics resulted from sequential design. One important feature is that the sequential design often leads to underdamped process characteristics. Given these characteristics, potential problems in the Ziegler-Nichols tuning are discussed and a modification is made. The sequential identification and the modified Ziegler-Nichols controller design method form the basic structure for the multivariable autotuner. The properties of convergence, the implications of tuning sequence, and the indications of undesirable pairing for the autotuner are explored. Consequently, a multivariable autotuning procedure is proposed. Two nonlinear distillation examples and a 3 × 3 linear system are used to illustrate the effectiveness of the autotuner. Simulation results show that good performance can be obtained with minimal engineering effort and the autotuner works well for very difficult processes in a very simple way.
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    AIChE Journal 40 (1994), S. 312-320 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A statistical thermodynamics model based on the original work of van der Waals and Platteeuw is presented for structure-H hydrates. The model is an extension of the hydrate prediction method generalized by Parrish and Prausnitz for structure-I and-II hydrates. Four structure-H-forming systems, methane+ adamantane, methane+ neohexane, methane+isopentane, and methane+methylcyclohexane, were considered. Optimized Kihara core parameters are presented for each of the large hydrocarbon guest molecules. The optimized reference chemical potential difference and reference enthalpy difference for structure-H hydrates are also presented. The results show good agreement with the experimentally determined phase-equilibria conditions. A sensitivity analysis is presented for the parameters in the model, and their relative order of influence on the accurate evaluation of the quilibrium pressure is determined.
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    AIChE Journal 40 (1994), S. 381-381 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
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    AIChE Journal 40 (1994), S. 381-382 
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    Keywords: Chemistry ; Chemical Engineering
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  • 39
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    AIChE Journal 40 (1994), S. 385-394 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Two methods are presented for calculating the interfacial tension between two immiscible Newtonian fluids. The procedures require only two measurements of the approximate interface shape during the low-Reynold-number interfacial-tension-driven transient motion of (i) the relaxation of a modestly elongated drop back to a spherical shape or (ii) the growth of capillary wave instabilities along the surface of a thread. The interfacial tension can be estimated by comparing the time differences between the two experimental measurements with tabulated and numerically generated results for the approximate shape evolution. The numerical results are generated using boundary integral method for similar model free-boundary problems at low Reynolds numbers. The tabulated results are presented for drop to suspending fluid viscosity ratios 0.01 to 10.
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  • 40
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    AIChE Journal 40 (1994), S. 424-432 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Mixing effects are evaluated for double jet semibatch and continuous stirred precipitators by a model which gives the variation of the primary nucleation flux from the mixing conditions. The predicted trends are compared with results of various authors, including those from a new study of calcium oxalate semibatch double-jet precipitation. Satisfactory qualitative agreement is found for the different chemical systems as a function of feed rate, stirring speed and feed locations for calcium oxalate precipitation. Two types of precipitation systems are demonstrated, depending on the ratio added/tank volume, the initial supersaturations and the intrinsic stiffness factor of a given precipitation. The difference between the two types depends on the increase or reduction of the primary nucleation flux by imperfect mixing with respect to the reference primary nucleation flux obtained with perfect mixing.
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    AIChE Journal 40 (1994), S. 473-495 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: This work concerns the synthesis of discrete-time feedforward/feedback control systems for general nonlinear processes with stable zero dynamics. Depending on the process under consideration, the derived feedforward/feedback controllers can completely eliminate the effect of measurable disturbances and produce a prespecified linear response with respect to a reference input, or provide integral-square error optimal response to step changes in the disturbances and a prespecified linear response with respect to a reference input. In either case, the developed feedforward/feedback controllers allow for the asymptotic rejection of unmeasurable disturbances. These controllers are derived within the globally linearizing control frame-work, first under full state information and then in the absence of state measurements. The internal stability of the closed-loop system is addressed. The derived controllers are interpreted from a model-predictive point of view, and their connections with the feedforward internal model control and the model algorithmic control are established. The theoretical results are illustrated through a continuous stirred-tank reactor example.
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    AIChE Journal 40 (1994), S. 521-535 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The oxidative coupling of methane was carried out in the absence of catalyst in a continuous flow setup at total pressures up to 1,000 kPa, temperatures from 950 to 1,230 K, and inlet molar ratios of CH4/O2 down to 2.5. At constant temperature and residence time, the conversions of methane and oxygen increase drastically with increasing pressure. At oxygen conversions higher than 80%, product selectivities are comparable at different pressures. The space-time yield of the C2 products reaches a level comparable to that required for industrial operations from 400 kPa on. A radical-reaction network consisting of 38 elementary reactions allows to describe the experimental data. To describe adequately the effect of total pressure, the pressure fall-off behavior of the rate coefficients for the unimolecular reactions in the network has to be taken into account explicitly.General features of the reaction mechanism do not depend on the total pressure. Methyl and hydrogen peroxy radicals are the most abundant radicals. The total pressure increase results in a drastic increase of the concentrations of the chain carriers, particularly the hydrogen peroxy radical. Higher pressure favor the oxidative route from ethane to ethylene compared to the pyrolytic route. Increasing the total pressure leads to an increase of the primary and a decrease of the consecutive CO formation relative to the coupling. The balance between these nonselective routes determines the effect of the total pressure on the integral selectivity to C2 products at different conversions. The major contribution to the integral CO selectivity comes from the oxidation of methyl radicals.
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    AIChE Journal 40 (1994) 
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    Keywords: Chemistry ; Chemical Engineering
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    AIChE Journal 40 (1994), S. 606-612 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Influence of local voids on flow maldistribution in randomly packed fiber bundles is examined by Voronoi tessellation. A theoretical expression for the local void distribution caused by random placement of fibers is developed by using a randomcell model. Simulations and packing experiments have been conducted to assess the accuracy of the theoretical distribution of cell sizes. In the case of shell side, laminar flow parallel to the fibers, the theoretical distribution is used to estimate fRe (friction factor times Reynolds number) and volumetric flows, and to compare results with ordered arrays and experimental data from literature. The results are used to assess the contributions of local voidage variation to flow bypass. This has implications for the prediction of pressure drop and heat and mass transfer in hollow-fiber module applications where transport is dominated by flow on the shell side.
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  • 45
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    AIChE Journal 40 (1994), S. 1055-1066 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The conversion of radiant light energy into chemical affinity by microorganisms in photobioreactors is examined. The kinetics of entropy production in the system is theoretically established from entropy and energy balances for the material and photonic phases in the reactor. A negative chemical affinity term compensated for by a radiant energy term at a higher level of energy characterizes photosynthetic organisms. The local volumetric rate of radiant light energy absorbed, which appears in the dissipation function as an irreversible term, is calculated for monodimensional approximations providing analytical solutions and for general tridimensional equations requiring the solution of a new numerical algorithm. Solutions for the bluegreen alga Spirulina platensis cultivated in photoreactors with different geometries and light energy inputs are compared. Thermodynambic efficiency of the photosynthesis is calculated. The highest value of 15% found for low radiant energy absorption rates corresponds to a maximum quantum yield in the reactor.
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    AIChE Journal 40 (1994), S. 1089-1089 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
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    AIChE Journal 40 (1994) 
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    Keywords: Chemistry ; Chemical Engineering
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    AIChE Journal 40 (1994), S. 1105-1117 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Pressure drops, gas holdup, and mass-transfer coefficients were measured in two concentric-tube airlift reactors of 30 and 300 L (nominal volume). The aspect ratio and the ratio of riser to downcomer cross section were the same for both reactors, but the geometry of the gas separation section was different. The influence of the bottom and top clearances was studied using water and carboxymethyl cellulose solutions and covering a range of effective viscosity from 10-3 to 25 × 10-3 Pa·s. The pressure drop results expressed as a Euler number were satisfactorily correlated with Fr, Ga, and a bubble disengagement group M. Correlations are presented also for the gas holdup in the riser, downcomer, and gas separator. The last-mentioned coincides with the correlation for the total holdup in the reactor. The gas-liquid mass-transfer coefficients for all the liquids and geometric variables in both reactors were successfully correlated as Sherwood numbers.
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    AIChE Journal 40 (1994), S. 911-911 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
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    AIChE Journal 40 (1994) 
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    AIChE Journal 40 (1994), S. 935-943 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Equilibrium and kinetic data for adsorption of trace CF2Cl2 (Freon-12) from various carrier gases on BPL activated carbon are reported. Coadsorption of the bulk carrier gas can severely reduce the equilibrium adsorption capacity and adsorptive mass-transfer coefficient of strongly adsorbed CF2Cl2. The difference in size between CF2Cl2 and the bulk carrier gas molecules plays a major role in establishing the binary or multicomponent equilibrium adsorption properties. The multisite (single and multicomponent) Langmuir model, which accounts for differences in adsorbate sizes, provides a reasonable framework for describing the size effects. The adsorptive mass transfer of CF2Cl2 under the experimental conditions investigated is dominated by surface diffusion into the pores of the activated carbon. The surface diffusivity is a strong function of the extent of coverage and strength of adsorption of the bulk components.
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    AIChE Journal 40 (1994), S. 980-990 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: This experimental work concerns the multivariable nonlinear control of a pilotsize continuous polymerization reactor with generically singular characteristic matrix. The control problem is to control conversion and temperature in a continuous stirred tank reactor by manipulating two coordinated flow rates (reactor residence time) and two coordinated heat inputs. A nonlinear controller is synthesized within the framework of the globally linearizing control (GLC) method and is implemented on a microcomputer. Conversion is inferred from on-line measurements of density and temperature. A key feature of the control problem is that its characteristic matrix is generically singular. Singularity of the characteristic matrix is handled by using a dynamic input/output linearizing state feedback rather than a static feedback. A reduced-order observer is used to calculate the monomer, initiator, and solvent concentration estimates, which are needed for the calculation of controller action. In the presence of active state and input constraints, the reactor-startup and setpointtracking performance of the controller is evaluated through experimental runs.
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    Notes: The mechanism of alginate droplet formation and experimental parameters for producing very small polymer microbeads (less than 100 μm dia.) using an electrostatic droplet generator studied showed that the microbead size was a function of needle diameter, charge arrangement (electrode geometry and spacing) and strength of electric field. Perfectly spherical and uniform polymer beads, 170 μm dia., for example, were obtained at a potential difference of 6 kV with a 26-gauge needle and an electrode distance of 2.5 cm. Increasing the electric field, and thus the surface charge in the vicinity of the needle, by increasing the applied potential, resulted in needle oscillation, giving a bimodal bead size distribution with a large fraction (30-40%) of microbeads with a mean diameter of 50 μm. The process of alginate droplet formation under the influence of electrostatic forces assessed with an image analysis/video system revealed distinct stages. After a voltage was applied, the liquid meniscus at the needle tip was distorted from a spherical shape into an inverted cone-like shape. Consequently, alginate solution flowed into this cone at an increasing rate causing formation of a neck-like filament. When this filament broke away, producing small droplets, the meniscus relaxed back to a spherical shape until flow of the polymer caused the process to start again. A large-scale multineedle device with a processing capacity of 0.7 L/h was also designed and produced uniform 400 ± 150 μm microbeads.
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    AIChE Journal 40 (1994), S. 1067-1081 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Protein denaturation, common in hydrophobic adsorption systems, causes misinterpretation of adsorption mechanisms, interferes with analysis in analytical chromatography, and complicates the design of large-scale adsorption processes. A detailed adsorption model isolates the effects due to denaturation from those due to mass transfer and intrinsic adsorption kinetics. The model is verified using protein gradient elution data. Simulations establish that typical symptoms of denaturation in frontal and elution chromatogrrams include sensitivity to changes in feed composition, column length, particle size, and operating conditions (feed size, flow rate, and column history). When a denatured species adsorbs irreversibly, the elution chromatogram shows decreasing peak area with increasing incubation time and apparent adsorption hysteresis over repeated cycles. In gradient elution, the peak elution order, resolution, and relative peak height depend highly on modulator properties and operating conditions. Interfering species limit solid-phase induced denaturation by competing for binding sites. Strategies for detecting and minimizing denaturation are proposed.
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    AIChE Journal 40 (1994), S. 1087-1087 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
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    AIChE Journal 40 (1994), S. 1312-1327 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The open-loop optimal control strategy to regulate the crystal-size distribution of batch cooling crystallizers handles input, output, and final-time constraints, and is applicable to crystallization with size-dependent growth rate, growth dispersion, and fines dissolution. The objective function can be formulated to consider solid-liquid separation in subsequent processing steps.A model-based control algorithm requires a model that accurately predicts system behavior. Uncertainty bounds on model parameter estimates are not reported in most crystallization model identification studies. This obscures the fact that resulting models are often based on experiments that do not provide sufficient information and are therefore unreliable. A method for assessing parameter uncertainty and its use in experimental design are presented. Measurements of solute concentration in the continuous phase and the transmittance of light through a slurry sample allow reliable parameter estimation. Uncertainty in the parameter estimates is decreased by data from experiments that achieve a wide range of supersaturation. The sensitivity of the control policy to parameter uncertainty, which connects the model identification and control problems, is assessed. The model identification and control strategies were experimentally verified on a bench-scale KNO3-H2O system. Compared to natural cooling, increases in the weight mean size of up to 48% were achieved through implementation of optimal cooling policies.
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    AIChE Journal 40 (1994), S. 1287-1296 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A mean free path gas kinetic theory is used to model the conductive heat transport of a gas within a void volume enclosed in a Fourier solid. A variational upper bound principle is derived for a void of arbitrary shape and applied to obtain a rigorous upper bound equation for the void gas conductivity in a spherical void. The variational void gas conductivity equation is exact in both the large and small Knudsen number (Kn) limits and provides a means to determine the accuracy of the reciprocal additivity interpolation formula as applied to thermal conductivity rather than diffusive mass transfer (maximum error 6% at Kn = 0.5 and α = 1). Temperature jump will occur even at atmospheric pressures and higher for sufficiently small thermal accommodation coefficients (α 〈 0.1). Experimental void gas heat conductivities vs. pressure data for H2, He, Ne, N2, CO2, and F12 in a polyurethane foam are compared with theoretical mean free path void gas conductivity vs. inverse Knudsen number curves drawn for various α. Estimates of the thermal accommodation coefficients for the gas- polyurethane surface exhibit a maximum with increasing molecular mass of the gas molecules, which qualitatively agrees with the predictions of Baule's classical theory. Results also point to a rather sharp shift of the S curve to higher pressures with decreasing thermal accommodation.
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    AIChE Journal 40 (1994), S. 1223-1237 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
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    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Heavy metals like Cu2+, Cr6+, and Hg2+ were removed successfully from wastewater and concentrated in a strip aqueous solution for recycle using the hollowfiber-contained liquid membrane (HFCLM) technique. Using cotransport, Cr6+ and Hg2+ present as anions in the feed solution were transferred individually through a liquid membrane containing tri-n-octylamine in xylene and concentrated in an alkaline solution on the strip side. The removal efficiency of each heavy metal was studied as a function of the aqueous feed flow rate in an HFCLM permeator. Copper present as cation Cu2+ was removed and concentrated by countertransport using LIX84 in n-heptane as the liquid membrane. The efficiency of copper removal was studied as a function of feed copper concentration, feed flow rate, strip flow rate, and area ratio between the feed fiber set and strip fiber set. The strip side flow rate did not affect the Cu2+ transfer rate. A theoretical model presented predicts the copper transport rate from the feed solution to the strip solution in an HFCLM permeator with a variable feed to strip-side membrane area. Both feed aqueous boundary layer and interfacial complexation reaction on the feed side dominate the observed Cu2+ removal process through LIX 84 in n-heptane for feed concentration levels used 90-500 mg/L. It was verified by providing two times larger liquid-liquid interfacial area in the feed aqueous side or in the strip aqueous side. The model can be used to design the membrane area required on the feed and strip fiber sides to remove essentially all of the copper from a given wastewater stream.
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    AIChE Journal 40 (1994), S. 1262-1267 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Magnetic resonance imaging is used to make nondestructive experimental measurements of fluid flow velocity and rock porosity inside a brine-filled Casper sand-stone sample during brine injection. Two-dimensional images of these values are obtained in arbitrary cross sections, with pixel sizes on the order of 1 mm2. The data are then statistically analyzed to find the variation of the average interstitial velocity as a function of porosity, as well as frequency distributions for both the velocity and porosity. The results show that as local porosity increases, the local flow velocity increases, according to the empirical relationship, V = 0.0669 φ + 0.0055. Thus, higher porosity regions of the core are better contacted by the displacement fluid. Results also imply bypassing of fluid around the perimeter of the core, indicating the need for a coreholder capable of sustaining higher overburden pressures on the order of 225 psi (1.55 MPa).
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    AIChE Journal 40 (1994), S. 1549-1557 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A “capillary condensation” in liquid phase was analyzed theoretically and experimentally, in which a solute in solvent could be separated out as a liquid into small pores by capillary effect. The “liquid-phase capillary condensation” is defined as capillary phase separation. The separated phase is counted as “adsorbed” amount on porous materials. The relation between the concentration and a critical radius of the phase separation was derived. A new method to estimate liquid-phase adsorption isotherms of adsorbates with limited solubility from pore-size distribution of solids is based on this concept. The amount absorbed consists of the separated phase and adsorption on surface expressed with a single parameter. While the surface adsorption alone could not explain measured isotherms, this model showed good agreements between experimental and estimated isotherms for adsorption of four kinds of aromatic compounds from aqueous solution onto three categories of porous solids to demonstrate the significance of the capillary phase separation. The applicability of the method to solid solutes is also discussed.
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    AIChE Journal 40 (1994), S. 1601-1610 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
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    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The effect of imposed large-amplitude oscillations on turbulent drag is studied. The system consists of water flow through a straight 5.08-cm pipe. The velocity gradient at the wall is measured with flush-mounted electrochemical mass-transfer probes. Newly developed numerical algorithms are used to analyze the probe performance in the presence of unsteady flows. Sinusoidal oscillations are at large enough frequencies, ω+ = 0.0138-0.0506, that a pseudo-steady-state approximation cannot be made. The ratio of the time-averaged velocity gradient at the wall, with and without oscillations, S̄, varies between 1.00 and 1.03, provided flow reversal does not occur. However, two experiments in which reversed flows existed at the wall for an appreciable period of time show drag reductions of 7 and 13%.Imposed nonsinusoidal oscillations are also studied for a period of favorable pressure gradient, about twice longer than that of unfavorable, and two sudden changes in the pressure gradient. Experiments at Re = 9,700 with T0 of 2.00, 2.45, and 3.46 s, and at Re = 19,200 with T0 = 3.46 give values of S̄ = 1.04-1.08. At Re = 19,200 and T0 = 2.00, 1.50, 1.00 s, drag reductions are 10-15%. This phenomenon could be associated with the speed with which a flow adjusts to sudden changes in the pressure gradient.
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    AIChE Journal 40 (1994), S. 1639-1649 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
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    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Elliptical basis function (EBF) networks are introduced as a new nonparametric method of estimating probability density functions for process data. Unlike Parzen window density estimators that use identical hyperspherical basis functions, the EBF method uses elliptical basis functions adapted to the local character of the data. This technique overcomes the spikiness problem associated with Parzen windows, where in high dimension, they can fail to produce smooth probability density estimates. The EBF estimator produces valid density functions that converage to the underlying distribution of the data in the limit of an infinite number of training examples. A technique based on statistical cross validation is introduced for evaluating different density estimators. The criterion is a measure of how well the density estimator estimates the density of data not used in the training. The EBF density estimation method and the evaluation technique are demonstrated using several examples of fault diagnosis.
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    AIChE Journal 40 (1994), S. 1459-1465 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Experimental studies were performed to assess the effect of salt addition on the extraction of 1-butanol, ethanol and acetone from dilute aqueous solutions using cyclopentanol, n-valeraldehyde, tert-amyl alcohol, and Adol 85NF as extractants. The liquid-liquid partitioning was examined for a few strong electrolytes in a broad range of concentrations. Results demonstrate that the distribution coefficient and selectivity in systems with reduced water activity resulting from salt addition were markedly increased. These observations can be qualitatively explained on the basis of the hydration theory. It was also determined that strong electrolytes added to the aqueous feed reduced extractant solubility in the aqueous phase, thus contributing to lower solvent losses. The results showed that the extraction efficiency was not significantly affected by increasing salt content beyond a level that reduces the water activity to a value of 0.92.
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    AIChE Journal 40 (1994), S. 1669-1684 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: In heterogenous olefin polymerization with Ziegler catalysts, the influence of monomer mass transport in the growing granule on polymer properties has been extensively modeled, but it has not been possible to clearly establish the importance of diffusion experimentally since the multisited nature of most Ziegler catalysts can produce similar effects. In this study, ethylene-propylene copolymers were made with single-sited metallocene catalysts by slurry polymerization in liquid monomers. These copolymers had a relatively narrow molecular weight distribution with a composition distribution (CD) broader than expected for a single-site catalyst. Data analysis indicates that mass-transfer limitations in the polymer particles are the most likely explanation for the observed results. For amorphous copolymers, a diffusion/reaction model could predict CD breadth in good agreement with experimental data, but for semicrystalline polymers the model was inaccurate. We postulate that model inadequacies are due to radial gradients in monomer diffusivity during polymerization which the model does not account for.
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    AIChE Journal 40 (1994), S. 1524-1534 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Isobutene is the only product of the uncatalyzed and acid-catalyzed dehydration of tert-butanol in compressed liquid water at 250°C. The uncatalyzed dehydration reaction is fast: equilibrium is established after about 30 s. Only one of many chemically-motivated kinetic models is able to fit all the experimental data. This model presumes a heterolytic dehydration mechanism that involves protonated alcohol, carbocation, di-tert-butyl ether, and protonated ether as intermediates. The model permits tert-butanol to dissociate as both an Arrhenius acid and a Bronsted acid while catalyzing its dehydration to isobutene. The pKa of tert-butanol at 250°C is predicted to be about 9, whereas its value at normal temperature and pressure is 18. This 109 increase in the Ka value of tert-butanol hints of the promising new world of reaction chemistry in near- and supercritical water.
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    AIChE Journal 40 (1994), S. 1574-1579 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A relatively simple continuous dilution method with on-line spectrophotometric measurement has been used to determine the phase transition boundaries of aqueous two-phase polymer systems. The observed range of compositions over which the phase transition occurs is dominated by the polydispersity of the polymers, but also is a function of the dilution path followed. The binodal curve obtained by the continuous dilution method agrees well with the results obtained by the traditional method of phase equilibration, separation and analysis of liquid chromatography, which is slower and requires more expensive equipment.
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    AIChE Journal 40 (1994), S. 1558-1573 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A general molecular-based formalism developed rigorously establishes microscopic bases of the supercritical solubility enhancement in terms of well-defined molecular correlation function integrals by unambiguously splitting the mixture's properties into short-(finite) and long-range (diverging) contributions. Consequently, the short-range nature of the solute's and solvent's residual chemical potentials is proved and the change of the solvent's local environment around an infinitely dilute solute and its finite contribution to solute mechanical partial molar properties are interpreted in terms of the short-range solute-solvent and solvent-solvent direct correlation function integrals. The solute-induced effect on the system's microstructure and thermodynamics approaches zero as the mixture approaches ideality or the solute becomes an ideal gas particle. At the solvent's critical conditions, the solute-induced effect on the solute's partial molar properties shows no compressibility-driven singularity, though along the critical isotherm it can exhibit a finite extremum or a change of curvature near critical density, depending on the type and strength of solute-solvent interactions. The utility of the proposed solvation formalism is illustrated using statistical mechanical integral equation calculations for three simple models of infinitely dilute near-critical mixtures: pyrene-CO2, diterbutyl nitroxide-ethane, and Ne-Xe.
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    AIChE Journal 40 (1994), S. 1594-1598 
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    Keywords: Chemistry ; Chemical Engineering
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    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 40 (1994), S. 1925-1926 
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    Keywords: Chemistry ; Chemical Engineering
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    AIChE Journal 40 (1994), S. 1927-1927 
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    AIChE Journal 40 (1994), S. 1940-1949 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Studies on the dynamics of phase inversion available offer limited information due to the difficulty of following the transient mean and drop-size distribution. A new technique developed provides such data. A stereo microscope with a very shallow depth of field attached to a video camera gives sharp images of droplets in intensely-agitated, immiscible liquid dispersions by using a Strobotach pulsing at the camera framing rate. Droplets from 40 μm upward at concentrations up to 70% by volume dispersed phase can be measured accurately. Droplets of continuous organic phase in aqueous drops can be seen. The pictures can be analyzed semiautomatically using a computer and in-house software to give, using a variety of discretizations, cumulative and frequency distributions to any base and any mean size. Means and distributions are a function of time for phase inversions generated in three ways. The technique gives a powerful tool for understanding fast, complex dispersion processes.
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    AIChE Journal 40 (1994), S. 1983-1992 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A novel device for gas-liquid contact operations is proposed to feed a liquid onto wires (or threads) hanging down in a gas stream is proposed. The liquid disintegrates into beads strung on each wire at regular intervals; if the wire is moderately wettable, a thin film forms to sheathe the wire, thereby interconnecting the beads. Since the beads fall down slowly, which possibly renews the film flowing down even more slowly a sufficient gas-liquid contact time is available even in a contactor with considerably limited height. An approximate calculation method is developed for predicting the variation in the temperature effectiveness for the liquid (the fractional approach of the liquid exit temperature to the gas inlet temperature) with the falling distance, assuming an applicability of strings-of-beads contactors to thermal energy recovery from hot gas streams.
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  • 77
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    AIChE Journal 40 (1994), S. 2055-2059 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 78
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    AIChE Journal 40 (1994), S. 2060-2064 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 79
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    AIChE Journal 40 (1994), S. 2034-2044 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The parallel transport of a protein by surface and pore diffusion within a highly porous ion exchanger is studied by measuring equilibria and uptake curves for adsorption of bovine serum albumin (BSA) on two different strongly basic chitosan ion exchangers (hard gels): Ch-2503 and Ch-2507 at pH 6.9 and 298 K. Experimental equilibrium isotherms are correlated by the Langmuir equation. Intraparticle effective diffusivities of BSA (Deff) are determined from the homogeneous Fickian diffusion model, increasing with the bulk phase concentration increase of BSA (C0). It suggests the existence of parallel diffusion. The surface diffusivity DS for the parallel diffusion model is determined from the Deff, and DS = 0.47 × 10-13 m2 · s-1 (Ch-2507) and 2.4 × 10-13 m2 · s-1 (Ch-2503) were obtained. Pore diffusivities based on the pore diffusion control (D′P) are obtained by matching the shrinking core model with the experimental uptake curves. D′P decreases with increasing C0. Since D′P in Ch-2507 is constant when C0 ≥ 1 kg·m-3, the constant value 2.7 × 10-11 m2 · s-1 is taken as the accurate pore diffusivity (DP). As D′P in Ch-2503 does not approach a constant value, DP = 1.0 × 10-11 m2 · s-1 is determined by matching the parallel diffusion model with the uptake data, and the model calculated using experimental values of DS and DP agrees reasonably well with the uptake data for Ch-2507 and Ch-2503. This theoretical approach may be applied not only for intraparticle diffusion of proteins but any adsorbates in porous materials.
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  • 80
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    AIChE Journal 40 (1994), S. 888-898 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The design of efficient continuous sterilization equipment for flowing solid-liquid food mixtures requires that temperature and velocity distributions within the fluid are known. In electrical (ohmic) heating, electric current is passed through a two-sterilize it. This allows rapid sterilization of solid-liquid mixtures which minimizes quality loss. A computational process model simulates the effect of realistic physical property changes. The effect of variations in physical properties can have a significant effect on the temperature of the product and thus on its sterility. Realistic designs will have to cope with temperature differences between phases. Experimental data for velocities in a food flow have been incorporated into an enthalpy balance model for heat transfer in solid-liquid mixtures. The effect of inlet temperature on the length of hold tube required to give the necessary process sterility calculated shows the variation in output conditions that might results in real systems.
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  • 81
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    AIChE Journal 40 (1994), S. 957-965 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A study of flash equations associated with multicomponent systems that can form three phases at a given temperature and pressure indicated that different equations are needed at different boundaries of the solution space. This problem dictates that one- and two-phase trial solutions be obtained first on the boundaries prior to a search in the three-phase interior region. Two new formulations of the flash equations have been developed to avoid this problem. Solutions at boundaries as well as those in the three-phase region can now be obtained with a single search procedure. The new formulations are made using functions that are monotonic in the selected coordinates. These properties facilitate the use of nested, single-variable search methods. Interpolating with second-order functions, when applicable, nested search methods are often faster than two-dimensional simultaneous search methods. Tests of these formulations have demonstrated the advantages of these characteristics.
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  • 82
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    AIChE Journal 40 (1994), S. 966-979 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The dynamic behavior of processing systems exhibits both continuous and significant discrete aspects. Process simulation is therefore a combined discrete/continuous simulation problem. In addition, there is a critical need for a declarative process modeling environment to encompass the entire range of processing system operation, from purely continuous to batch. These issues are addressed by this article.A new formal mathematical description of the combined discrete/continuous simulation problem is introduced to enhance the understanding of the fundamental discrete changes required to model processing systems. The modeling task is decomposed into two distinct activities: modeling fundamental physical behavior, and modeling the external actions imposed on this physical system. Both require significant discrete components. Important contributions include a powerful representation for discontinuities in physical behavior, and the first detailed consideration of how complex sequences of control actions may be modeled in a general manner.
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  • 83
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    AIChE Journal 40 (1994), S. 1005-1017 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Ignition and extinction characteristics of homogeneous combustion of methane in air near inert surfaces are studied by numerical bifurcation theory for premixed methane/air gases impinging on planar surfaces with detailed chemistry involving 46 reversible reactions and 16 species. One-parameter bifuraction diagrams as functions of surface temperature and two-parameter bifurcation diagrams as functions of equivalence ratio and strain rate are constructed for both isothermal and adiabatic walls. Lean and rich composition limits for ignition and extinction, and energy production are determined from two parameter bifurcation diagrams. For a strain rate of 500 s-1, CH4/air mixtures exhibit hysteresis from ∼ 0.5% up to ∼ 12.5% and from ∼ 5.5% up to ∼ 13.5% near isothermal surfaces and adiabatic walls, respectively. Ignition temperature rises with composition from 1,700 to 1,950 K, without a maximum around the stoichiometric ratio. Under some conditions multiple ignitions and extinctions can occur with up to five multiple solutions, and wall quenching, kinetic limitations, and transport can strongly affect flame stability. Flames near the stoichiometric ratio cannot be extinguished by room temperature surfaces for sufficiently low strain rates. The role of intermediates in enhancing or retarding ignition and extinction is studied, and implications of the effect of catalytic surfaces on homogeneous ignition and extinction are discussed. Removal of H atoms and CH3 radicals by wall adsorption can increase extinction and ignition temperature of 6% CH4 in air by up to 300 K for a strain rate of 500 s-1.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2127-2134 
    ISSN: 1434-1948
    Keywords: Gallium ; Azides ; Chemical vapour deposition ; Gallium nitride ; Single source precursors ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis, properties and X-ray single crystal structure analysis of the intramolecularly adduct-stabilised organogallium bisazide (N3)2Ga[(CH2)3NMe2] (1), the mono azide (N3)Ga[(CH2)3NMe2]2 (2) and the trialkylamine adducts of triazidogallium of the type (N3)3Ga(NR3) (3a-d; R = alkyl) are reported. An unusual isomer 1b of compound 1 is described, which was obtained by slow cooling of the analytically pure neat liquid compound 1 to 0 °C. The new and unusual structure 1b can be regarded as a weak associate of dimers linked together by head-to-tail azide bridges. In contrast, compounds 2 and 3a-b (R = CH3, C2H5) are monomeric in the solid state. The suitability of the volatile compounds 1 and 2 as single source precursors to grow GaN thin films by chemical vapour deposition is compared, showing that preferentially oriented crystalline films can be obtained from compound 2 on sapphire substrates at 600-700 °C in vacuo (0.1 Pa). However the films have a grey rather than a transparent appearance, which is presumably due to N-deficiency owing to the lower N-content of the single molecule precursor 2 relative to 1.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2135-2145 
    ISSN: 1434-1948
    Keywords: Density functional calculations ; Epoxidation ; Peroxo complexes ; Titanium ; Transition states ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Epoxidation of olefins by TiIV peroxo and hydroperoxo (alkylperoxo) complexes was investigated using a hybrid DFT method (B3LYP). Reaction energies and activation barriers for direct oxygen transfer to ethylene as a model olefin were computed for various model complexes to compare the epoxidation activity of Ti(η2-O2) and TiOOR (R = H, CH3) moieties. The activity of complexes with a Ti(O2) peroxo group is shown to be essentially quenched when the coordination sphere of the complex is saturated by strongly basic (σ-donor) ligands. In contrast, the activity of a TiOOH functional group depends only weakly on the saturation of the coordination sphere of the Ti center. Substitution of methyl for hydrogen in a TiOOH group is found to slightly increase the activation barrier of epoxidation. The computational results give preference to reaction paths that involve TiOOR species. The factors governing the activity of Ti(O2) and TiOOR groups, in particular the effects of donor ligands, are discussed on the basis of a molecular orbital analysis.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2289-2294 
    ISSN: 1434-1948
    Keywords: Intercalations ; Vanadyl phosphate ; Ethanol ; Hydration ; Kinetics ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The course of the replacement of ethanol by water molecules in the VOPO4·2C2H5OH intercalate, and of water by ethanol in VOPO4·2H2O has been studied by X-ray diffraction and infrared and Raman spectroscopy. Formation of mixed phase VOPO4·C2H5OH·H2O was not observed. The shape of the kinetics curves indicates a transition of at least one reaction zone through the crystal. A delay in formation of the product in comparison with the decrease in the amount of starting material can be explained by the existence of non-diffracting advancing phase boundary. In a VOPO4/ethanol/water system, VOPO4·2C2H5OH is formed as the only product when the system contained more than 96 vol% of ethanol, whereas in the system with less than 94 vol% of ethanol only VOPO4·2H2O is present.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2295-2299 
    ISSN: 1434-1948
    Keywords: Lewis acids ; Bismuth ; Aluminum ; Phosphorus ; Tin ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dilithium salts of N-methyl-N′,N′′-bis(diisopropyl)- and -(trimethylsilyl)-diethylenetriamine 1a,b react with SnCl2 affording the corresponding stannylenes 2a,b in 60 and 80% yield, respectively. Compound 1b also reacts with BiCl3 to give the bismuth chloride 5 (90% yield). Derivatives 2b and 5 have a symmetrical bicyclic structure and are monomeric both in solution and in the solid state. When 2b is treated with BiCl3 or PCl3, an oxidation reaction leads to the hypercoordinated tin(IV) dichloride 3 (58% yield), or a transmetallation gives rise to the oniophosphane 4 (95% yield), respectively. Transmetalation reactions also occurred when 5 was treated with AlCl3, GaCl3 or SnCl2 affording the corresponding aluminum chloride 6 (81% yield), gallium chloride 7 (38% yield) or tin dichloride 3 (38% yield). The observed reactivity for 2 and 5 is compared to that reported for Veith's stannylene or bismuth chloride.
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  • 88
    ISSN: 1434-1948
    Keywords: Ruthenium ; Triazole ; Titanium ; Electron Transfer ; Sensitizers ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complexes [Ru(dcb)2(L)] {L = 3-(2-hydroxyphenyl)-5-(pyridin-2-yl)-1,2,4-triazole (2-ppt), 3-(4-hydroxyphenyl)-5-(pyridin-2-yl)-1,2,4-triazole (4-ppt), 3,5-bis(pyrazin-2-yl)-1,2,4-triazole (bpzt), 3-(2-hydroxyphenyl)-5-(pyrazin-2-yl)-1,2,4-triazole (2-ppzt) and dcb = 4,4′-(CO2H)2-2,2′-bipyridine} have been synthesized, spectroscopically characterized and anchored to nanocrystalline TiO2 electrodes for the conversion of light into electricity in regenerative solar cells. The different efficiencies observed have been rationalized on the basis of an analytical expression relating the incident photon-to-current conversion efficiency (IPCE) to the kinetic parameters of the relevant electron transfer processes involved in the solar cell.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1295-1299 
    ISSN: 1434-1948
    Keywords: Solid-state chemistry ; Structure elucidation ; Reactive flux syntheses ; Oxysulfides ; Niobium chalcogenides ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The new compounds K4Nb2S10O and Rb4Nb2S10O have been synthesized by the reaction of potassium or rubidium alkaline polychalcogenides with NbO2, Nb2O5, or mixtures of Nb and NbO. Their structures consist of discrete [Nb2Q11]4- anions (Q = O, S) built up of two face-sharing pentagonal bipyramids, which are connected via the alkali metal cations.
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  • 90
    ISSN: 1434-1948
    Keywords: Pyrazolato ligands ; Rhenium ; Group-11 metals ; Heterometallic complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: By treating [(CO)3Re(Hpz)2(pz)] (Hpz = pyrazole) with [Cu(CH3CN)4]BF4, AgNO3, or [Au(tht)Cl] (tht = tetrahydrothiophene) in acetonitrile in the presence of Et3N, the corresponding trinuclear complexes {(CO)3Re(pz)3[M(CH3CN)]2} (1a-c) have been obtained. Treatment of complexes 1a-c with cyclohexyl isocyanide (c-C6H11NC) afforded the derivatives {(CO)3Re(pz)3[M(c-C6H11NC)]2} (2a-c). Complexes 2a-c have been characterized in solution by 1H-NMR spectroscopy and in the solid state by single-crystal X-ray diffraction analysis.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1309-1313 
    ISSN: 1434-1948
    Keywords: Phthalocyanines ; Rhenium ; Nitrido(octa-n-alkylphthalocyaninato)rhenium compounds ; Nucleophilic additions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of nitrido(tetra-tert-butylphthalocyaninato)rhenium (1) with boron tribromide leading to (tBu4Pc)ReNBBr3 (4) and with acetone to give the imido complex (tBu4Pc)Re[NC(CH3)2CH2C(O)CH3]OH (2b) and its μ-oxo dimer 3 are reported. Starting from the corresponding 4,5-di-n-alkylphthalonitriles and ammonium perrhenate four soluble nitrido(octa-n-alkylphthalocyaninato)rhenium complexes 5-8 were synthesized. Nitrido(octa-n-pentylphthalocyaninato)rhenium (6) was treated with boron tribromide to afford [(C5H11)8Pc]ReNBBr3 (9).
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1325-1333 
    ISSN: 1434-1948
    Keywords: Platinum ; Palladium ; Platinum blues ; Naphthyridine complexes ; Trinuclear complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: All three dinuclear complexes [Pd2(donp)2(bpy)2] (1) (H2donp = 1,8-naphthyridin-2,7-dione), [Pd2(H2nonp)2(bpy)2](ClO4)2 (2), and [Pt2(H2nonp)2(bpy)2](PF6)2 (3) (H3nonp = 7-amino-1,8-naphthyridin-2-one) exhibit the μ-1ĸN1:2ĸN8 bridging mode for their head/tail orientated naphthyridine ligands. Whereas 1 and 3 may be prepared by direct reaction of the dinucleating ligand with [MCl2(bpy)], formation of competing tripalladium(II) complexes must be avoided for 2 by employment of the precursor H2acnonp (7-acetamido-1,8-naphthyridin-2-one), which affords [H2nonp]- on cleavage of its original acetyl group. A mixture of the head/tail (4a) and head/head (4b) isomers of [Pd3(Hnonp)2(bpy)3](ClO4)2 is obtained when H3nonp is treated with [PdCl2(bpy)] and LiOH at room temperature for 2 d, followed by precipitation with LiClO4. Contrastingly exclusive formation of 4a is observed upon refluxing this reaction mixture for 3 d in aqueous solution. The [Hnonp]2- ligands exhibit a μ3-1ĸN1:2ĸN8:3ĸN7 bridging mode that leads to short Pd···Pd interactions of 2.781(2) and 2.775(2) Å. Similar metal-metal distances of 2.771(3) and 2.816(3) Å are observed in head/head-[Pt3(acnonp)(Hnonp)(bpy)3]Cl2 (5). An in situ 2e--oxidation (Ag+/Ag) of the [Pt3]6+ core in triplatinum(II) species such as 5 formed by the reaction of [PtCl2(bpy)] with H2acnonp allows the isolation of diamagnetic dark-brown head/head-[Pt3(Hnonp)2(NO3)(bpy)3](ClO4)2(NO3) (6) with an average oxidation state of Pt (2.67+). The Pt-Pt distances of 2.723(2) and 2.670(2) Å are markedly shorter than in 5.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1343-1350 
    ISSN: 1434-1948
    Keywords: Indium ; O ligands ; N ligands ; C ligands ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New heteroleptic indium compounds have been synthesized starting from indium(III) halides and hexamethyldisilazyllithium to form MeXInN(SiMe3)2 [X = Cl (1), Br (2)], and then subsequent alcoholysis to afford the molecules [ClMeIn(OtBu)]2 (3), [BrMeIn(OtBu)]2 (4), {ClMeIn[O(C6H4)OMe]}2 (5), {[(SiMe3)2N]MeIn(OtBu)}2 (6) and [MeIn(OtBu)2]2 (7). The molecular structures of molecules 3-7 have been obtained by single crystal X-ray diffraction studies. The structures of the compounds 3-7 are almost identical: 3-5 crystallize in the monoclinic crystal system with two dimeric molecules per unit cell in the space group P21/c, 6 crystallizes in the monoclinic space group C2/c with four molecules per unit cell, and compound 7 crystallizes in the triclinic crystal system with one dimeric molecule per unit cell in the space group P-1. The central centrosymmetric In2O2 ring, common to all the compounds, is achieved by two bridging oxygen atoms. Due to the additional coordination by an oxygen atom of the methoxy group, the coordination number of the metal center rises from 4 to “4+1” if the OtBu ligand (compounds 3, 4, 6, and 7) is exchanged for a methoxyphenol ligand (compound 5). In addition to the In2O2 ring the compound 5 possesses two annealed five-membered InO2C2 rings. The common indium methyl group of all compounds, which is transfered by an original route from the silicon to the indium atom, is used to compare structural and spectroscopic properties of the molecules, as there is a correlation between the In-C bond length and the chemical shift of the methyl group which depends on the ligand system used.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1359-1366 
    ISSN: 1434-1948
    Keywords: Selenium ; Fluorine ; Multinuclear NMR ; Raman spectroscopy ; X-ray crystallography ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of perfluoroaryllithium RC6F4Li, where R = F or 4-CF3C6F4O, respectively, with selenium gives the known diselanes (RC6F4Se)2 (1a, 1b). Redox reactions of 1 with hydrogen peroxide result in the formation of the seleninic acids RC6F4SeOOH which crystallize as hydrates (2a, 2b); with mercury give the bis(arylseleno)mercuries (RC6F4Se)2Hg (3a, 3b); with sulfuryl chloride or bromine give the selenenyl chlorides (4a, 4b) or selenenyl bromides (5a, 5b). Selenenyl chlorides (4a, 4b) react with a variety of trimethylsilyl reagents Me3SiX (X = Br, CN, NMe2, NEt2) to form 5a, 5b; selenocyanates RC6F4SeCN (6a, 6b); selenenyl amides RC6F4SeNMe2 (7a, 7b) and RC6F4SeNEt2 (8a, 8b). A new synthetic route to diorgano selanes is developed by reaction of 4a, 4b with perfluoroaryllithium to give the symmetric (RC6F4)2Se (9a, 9b). All derivatives are thoroughly characterized and in addition the molecular structures of 2a, 6a, and 9a are established by X-ray crystallography.
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  • 95
    ISSN: 1434-1948
    Keywords: Metallomesogens ; Nickel ; Salicylidenediamines ; Azo compounds ; (E)/(Z) photoisomerization ; Isomerizations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The bis[4-(n-CmH2m+1O)-5-(p-C14H29C6H4N=N)]-substituted N,N′-salicylidenediamines H2[LN(m,14)] (N = 1: 1,2-diaminoethane; N = 2: 1,3-diaminopropane; N = 3: 1,3-diamino-2,2-dimethylpropane; m = 6 or 18) have been synthesized. Both the N = 2 and 3 series of compounds display a smectic C (SmC) mesophase, with clearing points well below 100 °C. By treating the H2[LN(m,14)] ligands with an NiII salt, liquid crystalline mononuclear complexes with “unconventional” (lateral-tailed) molecular shape form. These Ni[LN(m,14)] complexes, showing nematic and smectic disordered phases, are stable over a quite large temperature range and have been characterized by different spectroscopic techniques. The newly synthesized mesogens exhibit lower transition temperatures and higher thermal stability than homologous complexes Ni[LN(14)] with a “conventional” rod-like molecular geometry.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1467-1477 
    ISSN: 1434-1948
    Keywords: Oxidations ; Tertiary alcohol ; Porphyrins ; Neophyl rearrangement ; Cleavage reactions ; β-Scission ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidation of 4-(1-hydroxy-1-phenylethyl)benzoic acid HPEBA with a water-soluble metalloporphyrin as catalyst and KHSO5 as oxygen atom donor gives the major products, acetophenone AC and acetylbenzoic acid ABA, by a Caliph-CAr bond cleavage, but a minor product, benzoyloxybenzoic acid BOBA, requires the insertion of an oxygen atom to form the ester. This compound becomes the main oxidation product on increasing the amount of acetonitrile in the reaction medium, and its formation is oxygen-dependent. The conversion is drastically lowered by using D2O instead of H2O, suggesting that an alkoxyl radical is formed in the rate-determining step. Labeling experiments using 18O2 or H218O under different reaction conditions show that the carbonyl oxygen atoms of AC and ABA originate either from substrate, water or dioxygen. However, the carbonyl oxygen atom in the ester group of BOBA originates from dioxygen while the other oxygen atom of the ester remains unlabeled. These results can be explained by an O-neophyl rearrangement of the initial alkoxyl radical to afford a carbon-based radical which then reacts with dioxygen or MnIV-OH/water. In a competitive reaction pathway, direct β-scission of the alkoxyl radical leads to unlabeled products. The oxidation of other tertiary diaryl alcohols is also discussed.
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  • 97
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1489-1495 
    ISSN: 1434-1948
    Keywords: Peroxo complexes ; Vanadium ; Mass spectrometry ; 51V-NMR spectroscopy ; Vanadium dependent bromoperoxidases ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ESI mass spectrometry and 51V-NMR spectroscopy have been used to study the reactions occurring between bisperoxo vanadates and a number of histidine and histidine-like ligands, in aqueous alcoholic solutions. Coordination of one and two molecules of ligand is observed with all the compounds investigated affording [VO5L]- and [VO52L]-, respectively. Characterization of these species has been achieved by MSn experiments, which have allowed specific fragmentations of the peroxidic moiety to be distinguished. In particular, with [VO52L]-, two distinct modes of decomposition were observed, depending on the presence in the ligand of a free carboxylic function. - Possible biochemical implications related to vanadium haloperoxidase enzymes are discussed.
    Additional Material: 6 Ill.
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  • 98
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1479-1488 
    ISSN: 1434-1948
    Keywords: Phosphorus heterocycles ; Cations ; Tungsten complexes ; Coordination modes ; Phosphaalkenes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1,1,3-tris(diisopropylamino)diphosphirenium salt 1 reacts with lithium aluminium hydride leading to the P-hydrogeno-C-phosphinophosphaalkenes 2, which on treatment with a catalytic amount of BF3·OEt2 afford the 1,3-bis(diisopropylamino)-1H-diphosphirene 3. The corresponding η1-coordinated 1H-diphosphirene 6 can be prepared by treatment of 2 or 3 with one equivalent of [W(CO)5(thf)]. Alternatively, the diphosphirenium salt 1 reacts with an excess of [W(CO)5(thf)], affording the corresponding η1-coordinated diphosphirenium salt complex 4, which is converted into the P-hydrogenophosphaalkene complex 5 with lithium aluminium hydride. The dinuclear tungsten complexes 7 and 8 are obtained by treatment of the free 1H-diphosphirene 3 with two equivalents of [W(CO)5(thf)] or one equivalent of [W(CO)4(thf)2], respectively. Compound 6 reacts with two equivalents of hydrogen chloride, giving the 1-chloro-3-diisopropylamino-1H-diphosphirene 9, which can be subsequently converted into the 1-diisopropylamino-, 1-azido, or 1-phenyl-3-diisopropylamino-1H-diphosphirenes 6, 10 and 11 by nucleophilic substitution with diisopropylamine, azidotrimethylsilane or sodium tetraphenylborate, respectively. The [η2-(3-diisopropylaminodiphosphirenylium salt)·W(CO)5] complexes 12a-c can be prepared by reaction of 9 with silver trifluoromethanesulfonate, aluminium or gallium trichloride or, alternatively, by treatment of 6 with two equivalents of trifluoromethanesulfonic acid. Reaction of 12a with diisopropylamine, water, bis(triphenylphosphoranylidene)ammonium chloride or tetrabutylammonium fluoride gives the corresponding 1H-diphosphirene complexes 6, 13, 9, or 14, respectively. Compound 12a also reacts with one or two equivalents of [W(CO)5(thf)], leading to the di- and tri-nuclear complexes 15and 16, respectively.
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  • 99
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 40 (1994), S. 73-87 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Experimental results using a pulsed tubular reactor are presented. The use of a pulsation source eliminates the reactor fouling and plugging issue that has occurred in previous investigations. Startup data and steady-state profiles are presented. Comparisons in monomer conversion and particle-size distribution for batch, CSTR and tubular reactor are made. The influence of pulsation on the particle-size dis-tribution is discussed. It is shown that high-conversion latex with a narrow particle size distribution can be produced continuously in the pulsed tubular reactor.
    Additional Material: 26 Ill.
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  • 100
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 40 (1994), S. 19-28 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A theoretical model for the process of bubble and drop formation in flowing liquids, applicable for both terrestrial and microgravity environments, has been developed by using a force balance. The contact angle variation at the nozzle due to the bubble motion and the added mass coefficient of the bubble moving through a pipe have been theoretically analyzed, considering bubble motions during its expansion and detachment stages. Predictions of bubble size of the model show satisfactory agreement with available experimental results in the case of normal gravity. The effects of the nondimensional variables on bubble and drop size are evaluated in microgravity conditions. In microgravity, the bubble is detached from the nozzle only by the liquid flow drag, and in the region of low liquid velocity the bubble size becomes much larger than that in normal gravity.
    Additional Material: 9 Ill.
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