ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

X
feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Wiley-Blackwell  (20)
  • Wiley  (19)
  • 1985-1989  (22)
  • 1975-1979  (17)
  • 1
    Electronic Resource
    Electronic Resource
    High-pressure particulate expansion and minimum bubbling of fine carbon powders (1987)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 33 (1987), S. 1698-1706 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Particulate expansion and minimum bubbling parameters (n, u′t, umB, εmB) are measured for fine carbon powders (dp = 44 and 112 μm) fluidized with synthesis gas (H2/CO = 0.8) at pressures within the range 2,070 〈 P 〈 12,420 kPa in an industrial, pilot-scale fluidized bed. Deviations between minimum bubbling (umB and εmB) and minimum fluidization (umf and εmf) conditions increase with increasing pressure, P. The expansion index, n, decreases with increasing P and always exceeds values recommended by Richardson and Zaki for solid/liquid systems. Particulate bed expansion for the fine powders is well characterized by the equations of Foscolo et al. and Abrahamsen and Geldart. The theory of Foscolo and Gibilaro adequately estimates the onset of bubbling for both powders at all P, provided that experimentally determined values of n and u′t, are applied. For the dp = 112 μm powder, the theory of Foscolo and Gibilaro is applicable with calculated values of ut and experimental values of n.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690331013
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Mass spectrometry of dimethylthiophosphinates of aromatic hydroxy compounds (1978)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 5 (1978), S. 302-311 
    Details
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of 20 differently substituted dimethylthiophosphinic esters of aromatic hydroxy compounds are presented. Fragmentation routes were investigated using high resolution mass measurements, decoupled metastable determinations and deuterium labelling. All compounds exhibited abundant molecular ions and typical phosphorus-containing ions. Characteristic elimination processes strongly dependent upon the respective type of substitution were observed. Due to their high stability, their great ease of formation and their good gas chromatographic properties these new types of derivatives are of special interest for establishing gas chromatography mass spectrometry profiles of acidic catecholamine metabolites.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200050406
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Beiträge zur Chemie der Alkylverbindungen von Übergangsmetallen. XX. [1]. Zur Reaktion von NiCl2 · 2PR3 und CoCl2 · 2PR3 mit LiSn(CH2C6H5)3 (1976)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 425 (1976), S. 151-154 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Transition Metal Alkyl Compounds. XX. On the Reaction of NiCl2 · 2 PR3 and CoCl2 · 2 PR3 with LiSn(CH2C6H5)3LiSn(CH2C6H5)3 reacts with NiCl2 · 2 P(n-C4H9)3 in tetrahydrofuran forming benzyl nickel chloride, which could be isolated in form of the bipyridyl complex C6H5CH2-NiCl · dipy. NiCl2 · 2 P(C6H5)3 and CoCl2 · 2 P(C6H5)3 are reduced to complexes of the formula MCl · 2 P(C6H5)3 · 3 THF (M = Ni, Co).
    Notes: LiSn(CH2C6H5)3 reagiert mit NiCl2 · 2 P(n-C4H9)3 in Tetrahydrofuran zu Benzylnickelchlorid, das als Dipyridylkomplex isoliert werden konnte. Bei Einsatz von NiCl2 · 2 P(C6H5)3 und CoCl2 · 2 P(C6H5)3 erfolgt dagegen eine Reduktion zu Komplexen der Zusammensetzung MCl · 2 P(C6H5)3 · 3 THF (M = Ni, Co).
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19764250209
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    Beiträge zur Chemie der Alkylverbindugen von Übergangsmetallen. XXIX. Dibenzylmangan - Darstellung und Reaktionen (1979)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 455 (1979), S. 3-12 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Transition Metal Alkyl Compounds. XXIX. Dibenzyl Manganese - Preparation and ReactionsManganese(II) acetylacetonate reacts with tribenzyl aluminium and dibenzyl magnesium forming the yellow complexes 3(C6H5CH2)2Mn · Al(acac)3 and (C6H5CH2)2Mn · Mg(acac)2 Dibenzyl manganese is also formed at the reaction of dibenzyl magnesium or benzyl magnesium chloride with MnCl2 · 1.5 THF and was separated as the dioxan complex (C6H5CH2)2Mn · 2C4H8O2, the ligands of which can be removed to a great extent in vacuum.Dibenzyl manganese reacts with CO2, CS2 and SO2 with insertion into the Mn-C-bonds. The corresponding manganese compounds were isolated and furtherly characterized.
    Notes: Mangan(II)-acetylacetonat reagiert mit Tribenzylaluminium bzw. Dibenzylmagnesium zu den gelben Komplexen 3(C6H5CH2)2Mn · Al(acac)3 bzw. (C6H5CH2)2Mn Mg(acac)2. Dibenzylmangan entsteht auch bei Einwirkung von Dibenzylmagnesium oder Benzyl magnesiumchlorid auf MnCl2 · 1,5 THF; eine Abtrennung von den Magnesiumsalzen gelingt in Form des 1,4-Dioxankomplexes (C6H5CH2)2Mn · 2C4H8O2, dessen Ligandenmoleküle im Vakuum weit gehend entfernt werden können.Dibenzylmangan reagiert mit CO2, CS2 und SO2 unter Insertion in die Mn-C-Bindungen. Die entsprechenden Mangansalze wurden isoliert und näher charakterisiert.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19794550101
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 5
    Electronic Resource
    Electronic Resource
    Beiträge zur Chemie der Alkylverbindungen von Übergangsmetallen. XXXIX. Über 3(N, N-Dimethylamino)propyllanthanoid-Verbindungen (1985)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 521 (1985), S. 57-60 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Transition Metal alkyl Compounds. XXXIX. About 3(N,N-Dimethylamino) propyl Lanthanide CompoundsLaCl3, PrCl3, and ErCl3 react with dimethylaminopropyl lithium (RLi) in tetrahydro-furan as a solvent with formation of complexes of the type Li3[LnR3Cl3]. In a similar way the Li3[CeR6] derivative is formed from CeCl3.The organolanthanide complexes were characterized by elementary analysis, hydrolysis and thermolysis products, the effective magnetic moments and the i.r. spectra.
    Notes: LaCl3, PrCl3, und ErCl3 reagieren mit Dimethylaminopropyllithium (RLi) in Tetrahydrofuran als Lösungsmittel zu Komplexen des Typs Li3[LnR3Cl3]. Die entsprechende Reaktion mit CeCl3 führt dagegen zum Li3[CeR6]-Derivat.Eine nähere Charakterisierung der Verbindungen erfolgte durch Elementaranalysen, ihre Hydrolyse- und Thermolyseprodukte, die effektiven magnetischen Momente und ihre IR-Spektren.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19855210208
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 6
    Electronic Resource
    Electronic Resource
    Beiträge zur Chemie der Alkylverbindungen von Übergangsmetallen. XLIX. Reaktionen von Cerium(IV)-acetylacetonat mit Lithium- und Magnesiumorganylen (1986)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 543 (1986), S. 192-198 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Organo Transition Metal Compounds. XLIX. Reactions of Cerium(IV) Acetylacetonate with Organolithium and Organomagnesium CompoundsReacting Ce(acac)4 with lithium organyls RLi (R = CH3 1-Nor1), ((CH3)2NCH2CH2CH2) in the molar ratio 1:1 the cerium compound is reduced with formation of Li[Ce(acac)4]. Using a molar ratio of Ce:Li = 1:4 organocerium complexes of the composition R3Ce · 3 Li(acac) or Li3[R3Ce(acac)3] are formed. From reactions with excess CH3Li (Ce: Li = 1:7) Li3[Ce(CH3)6] · 3 Li(acac) could be isolated.All cerium complexes are characterized by elementary analysis, hydrolysis products, i.r. spectra, and molecular weight determination.
    Notes: Ce(acac)4 reagiert mit Lithiumorganylen RLi (R = CH3, 1-Nor1), ((CH3)2NCH2CH2CH2) im Molverhältnis 1:1 unter Reduktion zum Cerium(III)-Komplex Li[Ce(acac)4]. Wählt man ein Molverhältnis von 1:4, so entstehen Organocerium(III)-Komplexe der Zusammensetzung R3Ce · 3 Li(acac) bzw. Li3[R3Ce(acac)3]. Donormoleküle bewirken keine Abspaltung des Li(acac), sondern werden zusätzlich addiert unter Bildung von Komplexen des Typs Li3[R3Ce(acac)3] · n D (D = THF, n = 2; D = DME, TMED2), n = 1. Bei Reaktionen mit überschüssigem CH3Li (Ce:Li = 1:7) wurde Li3[Ce(CH3)6] · 3 Li(acac) isoliert.Bei Umsetzungen von Ce(acac)4 mit Dibenzyl- und Bis(1-naphthylmethyl)magnesium wurden Cerium(III)-Komplexe der Zusammensetzung Ce(acac)3 · RMg(acac) gebildet.Alle erhaltenen Verbindungen wurden durch ihre Elementaranalysen, Hydrolyseprodukte, IR-Spektren und durch Molmassebestimmungen charakterisiert.Ce(acac)4 reacts with dibenzyl and bis (1-naphthylmethyl) magnesium with formation of complexes of the type Ce(acac)3 · RMg(acac).
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19865431223
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 7
    Electronic Resource
    Electronic Resource
    An experimental-numerical hybrid technique for three dimensional stress analysis (1977)
    Chichester [u.a.] : Wiley-Blackwell
    International Journal for Numerical Methods in Engineering 11 (1977), S. 1845-1863 
    Details
    ISSN: 0029-5981
    Keywords: Engineering ; Engineering General
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mathematics , Technology
    Notes: The paper describes a numerical method for determining the stress distribution in the interior of a three-dimensional body using experimentally determined surface stresses, and the interior displacements from surface displacements. The normal and shear stresses inside the body are obtained by solving Laplace's equation in terms of sum of normal stresses together with the three-dimensional compatibility equations in terms of stresses, using the finite difference technique, when the stresses on the surface of the body are known. On the other hand if surface displacements are known (from which strain components could be determined) then displacement components in the interior of a body can be determined by solving Laplace's equation in terms of sum of normal strains together with the three-dimensional equilibrium equations in terms of displacements. It is shown that axi-symmetric problems can also be solved in an identical way by transforming the equations into cylindrical co-ordinates. The application of the method has been illustrated through several examples.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/nme.1620111208
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 8
    Electronic Resource
    Electronic Resource
    Steroid phosphorus compounds. V - mass spectrometry of phosphinic esters of monohydroxy steroidsAbbreviations: E1 = estrone; A = androsterone; 3αEt = 3α-etiocholanolone; 3βEt = 3β-etiocholanolone; DHEA = dehydroepiandrosterone; DHT = 5α-dihydrotestosterone: T = testosterone: PO, PS and P = the dimethylphosphinic, dimethylthiophosphinic and dimethylphosphinous ester groups of the corresponding hydroxy steroid, respectively. (1976)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1976), S. 64-70 
    Details
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of the dimethylphosphinic, dimethylthiophosphinic and dimethylphosphinous ester derivatives of several monohydroxy steroids are reported. The fragmentations of the derivatized steroids largely depend on the nature of the the phosphorus-containing ester group. Phenolic ester derivatives exhibit the base peak at the molecular ion, whereas the spectra of the secondary phosphinic esters are dominated by very intense protonated phosphinic acid ions [Me2 P(XH)(OH)]+ at m/e 95 (X = O) or at m/e 111 (X = S). The present results also indicate the low ionization potential for the phosphinic ester group. Due to their good gas chromatographic properties, these steroid derivatives appear to be particularly suitable for gas chromatographic mass spectrometric analysis of biochemical materials.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200030205
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 9
    Electronic Resource
    Electronic Resource
    Beiträge zur Chemie der Alkylverbindungen von Übergangsmetallen. XXIII. Phosphinstabilisierte Benzylverbindungen des Nickels, Kobalts und Eisens (1977)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 432 (1977), S. 187-192 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Transition Metal Alkyl Compounds. XXIII. Phosphine Complexes of Benzyl Compounds of Nickel, Cobalt, and IronThe benzyl compound BzNi(acac) · PPh3 · 2 O(C2H5)2 could be obtained from Ni(acac)2, Bz3Al, and PPh3 in diethyl ether as a solvent. Using PBz3 and P(C6H11)3 complexes of the type BzNi(acac) · PR3 are formed. In a similar way Co(acac)3 and Fe(acac)3 react to BzCo(acac)2 · 2 PPh3, BzCo · 2 PPh3 · 2 O(C2H5)2 and BzFe · 3 PPh3 · 2 O(C2H5)2 (acacH = acetylacetone; Bz = C6H5CH2).
    Notes: Aus Ni(acac)2, Bz3Al und PPh3 konnte in Diäthyläther als Lösungsmittel die Benzylverbindung BzNi(acac) · PPh3 · 2 O(C2H5)2 gewonnen werden. Bei Verwendung von PBz3 und P(C6H11)3 entstehen Komplexe des Typs BzNi(acac) · PR3. Auf ähnliche Weise wurden aus Co(acac)3 und Fe(acac)3 die Komplexe BzCo(acac)2 · 2 PPh3, BzCo · 2 PPh3 · 2 O(C2H5)2 und BzFe · 3 PPh3 · 2 O(C2H5)2 erhalten (acacH = Acetylaceton; Bz = C6H5CH2).
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19774320126
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 10
    Electronic Resource
    Electronic Resource
    Beiträge zur Chemie der Alkylverbindungen von Übergangsmetallen. XXVIII. Zur Benzylierung der Acetylacetonate des dreiwertigen Titans, Vanadiums und Chroms (1978)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 447 (1978), S. 136-142 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contribution to the Chemistry of Transition Metal Alkyl Compounds. XXVIII. Benzylation of the Trivalent Titanium, Vanadium, and Chromium AcetylacetonatesBzCr(acac)2, 2Bz(Vacac)2 · Mg(acac)2 and 3BzV(acac)2 · Al(acac)3 were obtained in definite form by reaction of Cr(acac)3 and V(acac)3 with Bz3Al, Bz2Mg, and BzMgCl. Ti(acac)3, reacts with Bz2Mg and BzLi forming deep green Bz3Ti, which could'nt be isolated free of impurities (Bz = C6H5CH2, acacH = acetylacetone).
    Notes: Bei Reaktionen von Cr (acac)3 und V(acac)3 mit Bz3Al, Bz2Mg und BzMgCl wurden als definierte Verbindungen BzCr(acac)2, 2BzV(acac)2 · Mg(acac)2 und 3BzV(acac)2, Al(acac)3 erhalten. Aus Ti(acac)3 und Bz2Mg bzw. BzLi entsteht tiefgrünes Bz3Ti, das jedoch nicht frei von Verunreinigungen erhalten werden konnte. (Bz = C6H5CH2, acacH = Acetylaceton).
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19784470114
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...