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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 719-724 
    ISSN: 0044-2313
    Keywords: Undecahydroaza-nido-undecaborate(2-) ; azametalla-closo-dodecaboranes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Azametalla-closo-dodecaboraneAus nido-NB10H13 erhält man mit der doppelten Menge an K[BHEt3] das Azaborat K2[nido-NB10H11]. Das Anion [NB10H112-] ist isoelektronisch mit [C2B9H11]2-. Es reagiert mit [{η6-(C6R6)RuCl2}2] (R = H, Me), [{η5-(C5Me5)RhCl2}2] oder [Ni(PPh3)2Cl2] zu den Azametalla-closo-dodecaboranen MNB10H11 mit M = (C6Me6)Ru (2), (C6H6)Ru (3), (C5Me5)Rh (4) bzw. (Ph3P)2Ni (5). Aus K2[NB10H11] und CoCl2 läßt sich das Azametallaboran K[Co(NB10H11)2] (6) gewinnen, in welchem das Co-Atom sandwichartig von zwei [NB10H11]2--Ionen koordiniert wird. Vom Produkt 2 · CH2Cl2 liegt eine Röntgenstrukturanalyse vor. Die Produkte 2-6 lassen sich vom ikosaedrisch gebauten Anion [B12H12]2- dadurch ableiten, daß eine BH2--Einheit durch das isoelektronische Nitren NH und eine BH-Einheit durch das isolobale Metallkomplex-Fragment M ersetzt werden. Das N-Atom ist in den Clustergerüsten 2-6 jeweils sechsfach koordiniert.
    Notes: The azaborate K2[nido-NB10H11] is gained from nido-NB10H13 and K[BHEt3] in a 1:2 ratio. The anion [NB10H11]2-, which is isoelectronic with [C2B9H11]2-, reacts with [{η6-(C6R6) · RuCl2}2] (R = H, Me), [{η5-(C5Me5)RhCl2}2], or [Ni(PPh3)2Cl2] to give the azametalla-closo-dodecaboranes MNB10H11 with M = (C6Me6)Ru (2), (C6H6)Ru (3), (C5Me5)Rh (4), and (Ph3P)2Ni (5), respectively. The azametallaborane K[Co(NB10H11)2] (6), which contains a sandwich-type coordinated Co atom, is formed from K2[NB10H11] and CoCl2. The structure of 2 · CH2Cl2 was determined by X-ray diffraction. The products 2-6 can be derived from the icosahedral anion [B12H12]2- on replacing a BH2- moiety by the isoelectronic nitrene NH and a BH moiety by the isolobal metal-complex fragment M. The N atom is six-coordinated in the cluster skeletons 2-6.
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  • 2
    ISSN: 0044-2313
    Keywords: (Borylorganyl)phosphanes ; (Borylorganyl)phosphoniumsalt ; X-ray structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthese und Reaktionen von {o-{[Bis(dimethylamino)boryl]methyl}phenyl}diphenyl-phosphanDas neue α,ω-[Boryl(organyl)]phosphan o-Ph2PC6H4CH2 (NMe2)2 (10) wurde synthetisiert und spektroskopisch charakterisiert. Die Reaktivität dieser Verbindung, vor allem gegenüber Substitutionsreaktionen am Boratom war der Gegenstand unserer Untersuchungen. Verbindung 10 reagiert mit MeOH, BCl3 bzw. HCl zu den Verbindungen o-Ph2PC6H4CH2B(OMe)2 (10 a), o-Ph2PC6H4CH2BCl2 (10 c), o-Ph2PC6H4CH2BCl2 (HNMe2) (10 d) und o-Ph2P(HCl)C6H4CH2 BCl2(HNMe2) (10 e). Die Umsetzung von 10 a mit LiAlH4 führt zu o-Ph2PC6H4CH2BH2 (10 b). Verbindung 10 e wurde zusätzlich durch eine Röntgenstrukturanalyse charakterisiert.
    Notes: The new α,ω-[boryl(organyl)]phosphane o-Ph2PC6H4CH2B (NMe2)2 (10) was obtained in good yields from the reaction of CIB(NMe2)2 with o-Ph2PC6H4CH2Li(tmeda). Five derivatives of 10 were obtained by substituting the boron-bound amino groups by reactions with MeOH, BCl3, HCl, and LiAlH4, respectively, in particular, o-Ph2(HCl)PC6H4CH2BCl2 (HNMe2) (10 e) which shows a unique P—H—Cl—H—N unit. Compound 10 and its derivatives were characterized by multinuclear NMR methods, mass spectra, and elemental analyses. In addition, the structure of 10 e · 1.5 C6H6 was determined by single crystal X-ray diffraction.
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  • 3
    ISSN: 0044-2313
    Keywords: Methylboratabenzene indium ; conformational variability ; automerization ; crystal packing effects ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Borabenzene Derivatives. 25 [1]. Methylbis(1-methylboratabenzene)indium: Synthesis and Structure. An Example for the Variability of Soft Structural Parameters in the Crystalline EnvironmentThe new boratabenzene derivative InMe(C5H5BMe)2 has been synthesized from 2-(Me3Sn)C5H5BMe and InMe3. The compound proves fluxional on the nmr time scale with average C2v symmetry in solution. An x-ray structure determination shows the existence of four molecules in the asymmetric unit differing mainly in the bonding geometry of the metal atoms with respect to the eight symmetrically independent boratabenzene ligands. Thus the dynamical behaviour in solution is reflected in the solid state by the soft structural parameters of the indium-ring coordination, with their variability exceeding the standard deviations of the corresponding individual observations by an order of magnitude.
    Notes: Ausgehend von 2-(Me3Sn)C5H5BMe und InMe3 wurde der neue Boratabenzol-Komplex InMe(C5H5BMe)2 erhalten. Die Verbindung zeigt in Lösung auf der NMR-Zeitskala eine fluktuierende Struktur mit effektiver C2v-Symmetrie. Die Kristallstrukturanalyse zeigt, daß im Festkörper vier Moleküle in der asymmetrischen Einheit vorliegen, die sich vorwiegend in der Bindung des Metallatoms an die insgesamt acht symmetrieunabhängigen Boratabenzol-Liganden unterscheiden. Das in Lösung dynamische Verhalten findet im Kristall seine Entsprechung in weichen Strukturparametern bezüglich der Indium-Ring-ligand-Koordination, deren Variabilität die Standardabweichungen der Einzelbeobachtung um eine Größenordnung übersteigt.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 614 (1992), S. 131-141 
    ISSN: 0044-2313
    Keywords: Rhenium complexes ; oxygen ligands ; tripod ligands ; 31P-NMR ; radionuclides ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Rhenium Complexes Stabilized by Tris-chelating Oxygen Ligands: Potential New Radiopharmaca?Ris-chelating oxygen ligands of the general formula L- = [(C5H4R)Co{P(O)R′R″}3]- (R = COOCH3, COOH and R′ = OCH3; R = H and R′ = O(CH2)5COOCH3, O(CH2)5COOH; R″ = OCH3) have been synthesized. These ligands L- and others of the same type have been used to prepare the rhenium oxo complexes [LReO3] and [LReOX2] (X = Cl, Br, I). In order to judge their use in radioimmunotherapy the corresponding complexes containing radioactive rhenium isotopes have also been synthesized. The rhenium(VII) as well as the diamagnetic rhenium(V) complexes are stable in air in the solid state as well as in organic solvents. They hydrolyze slowly in water to yield perrhenic acid. The X-ray structures of the sodium salt Na[(C5H4COOCH3)Co{P(O)(OCH3)2}3] and of the rhenium complex [LReOBr2] (R = H, R′ = R″ = OCH3) have been determined. The sodium salt crystallizes in trimeric units with the composition [(NaL)3 · 3 H2O]. Each sodium has a distorted octahedral oxygen coordination. In [LReOBr2] the ReO4Br2 octahedron is only slightly distorted.
    Notes: Vier neue Sauerstoffchelatliganden L- der allgemeinen Formel [(C5H4R)Co{P(O)R′R″}3]- (R = COOCH3, COOH und R′ = OCH3; R = H und R′ = O(CH2)5COOCH3, O(CH2)5COOH; R″ = OCH3) wurden synthetisiert. Diese neuen Liganden L- und andere Liganden des gleichen Typs wurden für die Darstellung von Rhenium(VII)-Komplexen [LReO3] und Rhenium(V)-Komplexen [LReOX2] (X = Cl, Br, I) eingesetzt. Im Hinblick auf deren mögliche Verwendbarkeit in der Radioimmunotherapie wurden die Synthesen auch auf radioaktive Rheniumisotope übertragen. Sowohl die Rhenium(VII)- als auch die diamagnetischen Rhenium(V)-Komplexe sind in fester Form und in organischen Lösungsmitteln an Luft beständig; sie zersetzen sich in Wasser langsam unter Bildung von Perrheniumsäure. Das Natriumsalz Na[(C5H4COOCH3)Co{P(O)(OCH3)2}3] kristallisiert als dreikernige Einheit der Zusammensetzung [(NaL)3 · 3 H2O]. Jedes Natrium ist verzerrt oktaedrisch von Sauerstoff umgeben. Die Kristallstrukturbestimmung der Verbindung [LReOBr2] (R = H, R′ = R″ = OCH3) zeigt die erwartete schwach verzerrte oktaedrische Koordination des Rheniums.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 2209-2216 
    ISSN: 0009-2940
    Keywords: Tetrazatetraborocanes ; Boron-nitrogen ring compounds ; [2 + 3] Cycloadditions ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Eight-Membered BN Rings (RBNR')4 from Four-Membered BN Rings (RBNtBu)2 by an Exchange NtBu/NR'Reactions of the four-membered BN ring compounds (RBNtBu)2 (1a - e: R = Me, Et, iPr, iBu, Pr) with azides R'N3 (R' = PhCH2, Pr, iBu, Ph) and with the nitrone PhHC=N(Me)=O are studied. The five-membered ring [=(Me)B=N(tBu)-N=N-(PhCH2)N=] (2a) is formed from the four-membered ring 1a and PhCH2N3 in the ratio 1:2. An exchange of NtBu for NR' with elimination of tBuN3 is observed, however, in the reaction of the ring compounds 1b -d with R'N3. Instead of four-membered BN rings, the six-membered BN ring (RBNR')3 (3a: R/R' = Et/PhCH2) and the eight-membered BN rings (RBNR')4 (4a -h: R/R' = iPr/PhCH2, iBu/PhCH2, iPr/Pr, iBu/Pr, iPr/iBu, iBu/iBu, Et/Ph, iBu/Ph) are formed, respectively. The NMR spectra reveal diastereotopic methylene protons (Et, Pr, iBu, PhCH2) and methyl groups (iPr, iBu) and thus elucidate the tub-like structure of the eight-membered rings. 3a and 4a crystallize in the space group P2,/c. The reaction of the four-membered rings 1c - e with the nitrone gives five-membered rings [=(R)B=N(tBu)=B(R)=N(Me) - O=] (5c - e). Both of the reactions of the four-membered rings with azides and with the nitrone can be rationalized in terms of a similar sequence of reaction steps.
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  • 6
    ISSN: 0009-2940
    Keywords: Rhodium(I) phosphane complexes ; 14-Electron intermediates ; MO theory, applied ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bis(di-tert-butylphosphanyl)methane Complexes of Rhodium: Geometry, Electronic Structure, and Derivatives of the 14-Electron Fragment [Rh(dtbpm)Cl]. Molecular Structure of Rh(dtbpm)Cl(PMe3)14-Electron fragments [M(PR3)2X] (M = Rh, Ir, X = halogen etc.) are considered to be an important class of highly reactive, coordinatively unsaturated intermediates in many metal-induced stoichiometric or catalytic transformations of organic substrates. As available theoretical data suggest a slightly preferred T-shaped groundstate geometry with a less symmetric cis rather than the usually implied trans phosphane arrangement for such tricoordinate d8-ML3-type systems with monodentate phosphanes PR3, the chemistry of η2-diphosphanylmethane complexes of rhodium with four-membered RhPCP-chelate rings and thus with enforced cis phosphane coordination and anomalously small cis P - Rh - P angles has been studied by theory and by experiment. MO calculations (EH) have been performed both for the model 14-electron system [Rh(dhpm)Cl] (dhpm = diphosphanylmethane, H2P - CH2 - PH2) and for the experimentally accessible fragment [Rh(dhbpm)Cl], where dtbpm is bis(di-tert-butylphosphanyl)-methane, (tBu)2P - CH2 - P(tBu)2. The electronic and geometric structure of these species is described. Employing the unusual ligand dtbpm, tailor-made for stabilizing mononuclear η2- and destabilizing dinuclear μ-diphosphanylmethane coordination, the chloro-bridged dimer [Rh(dtbpm)Cl]2, has been synthesized. In agreement with steric and electronic considerations, its chemistry is dominated by a facile dissociation to monomeric (presumably solvent coordinated) fragments [Rh(dtbpm)Cl], even in benzene, as suggested by molecular mass determinations. Accordingly, by using [Rh(dtbpm)Cl]2 as a starting material, a series of sterically very congested but nevertheless mononuclear, square-planar complexes Rh(dtbpm)Cl(L) (L = CO, PMe3, PPh3, PCy3, pyridine, acrylonitrile) with chelating dtbpm could be readily prepared and fully characterized. The relative stability of these potential alternative precursors of a [Rh(dtbpm)Cl] intermediate towards dissociation of ligands L is reported. The molecular structure of Rh(dtbpm)Cl(PMe3) as the first representative of this class of compounds has been determined by X-ray crystallography.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 97-102 
    ISSN: 0009-2940
    Keywords: Aza-nido-decaborane(12) ; Aza-arachno-undecaborate(1  - ) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Novel Syntheses of the Aza-nido-decaborane SkeletonThe known nido-NB9H12 (3) can be synthesized by thermolysis of either arachno-B9H13(NH3) (4) in xylene (11%) or arachno-B10H12(N3)(NH2) (5) in diglyme (100%). The deprotonation of 5 yields the anion arachno-[NB10H13(N3)]- (6), whose skeleton is derived from the closed 13-vertex deltahedron. On protonation, a degradation of 6 is observed to give nido-NB9H11(N3) (7), which crystallizes in the monoclinic space group P21/c. The borane 3 is attacked by Et3N · BH3 with evolution of H2 and formation of the 6-BH2  -  NEt3 derivative of 3 (8). Both nido-species 8 and 7 add the isonitrile CNtBu at the position 9 to yield the arachno-products 9 and 10, respectively. The adduct 11 is formed from 7 and the azadiboriridine (- tBuB  -  BtBu  -  NtBu  - ).
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 2681-2686 
    ISSN: 0009-2940
    Keywords: 1,2,3,4-Diazadiboretidines ; Oxadiazadiborolidines ; Triazadiborolidines ; Diazadiboracyclohexanes ; Tetraazadiboracyclohexanes ; 1,2,5,6,3,4,7,8-Tetraazatetraborocane ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,2,3,4-Diazadiboretidines: Reactions of a Novel Class of Unsaturated Boron-Nitrogen Four-Membered Rings1,2,3,4-Diazadiboretidines [=B(tBu)-B(tBu)=NR-NR=] (R=Et, iPr: 2a, b) belong to the hitherto unknown class of head-head isomers of the known 1,3,2,4-diazadiboretidines (1). They are formed from the diborane(4) Cl-B(tBu)-B(tBu)-Cl and the hydrazines RHN-NHR in the presence of NEt3 via the partially unsaturated four-membered rings [-B(tBu)Cl-B(tBu)=NR-NHR-] (4a, b), which are transformed into 2a, b by the abstraction of HCl by means of the base LiNC9H18. Whereas the pure products 2a, b are instable, solutions of 2a, b in alkanes can be handled at 0°C without considerable decomposition. Reaction of 2a, b with the amine oxide Me3NO leads to insertion of an O atom, reaction with diazoalkane tBuCR′N2 (R′ = H, Me) to insertion of its β-N atom, and reaction with the azide PhCH2N3 to insertion of a nitrene N atom into the B-B bond of 2a, b with formation of five-membered rings 5a, b or 6a, b or 7a, b, respectively. Six-membered rings 8a, 9a, 10a, respectively, are the products of the insertion of the C≡C unit of 3-hexyne, the N=N unit of EtO2C-N=N-CO2Et, or the unsaturated C atoms of two molecules of C≡NtBu into the B-B bond of 2a. The condensation of the diaminodiborane(4) Cl-B(NMe2)-B(NMe2)-Cl with the hydrazine EtHN-NHEt in the presence of NEt3 yields the corresponding eight-membered ring [-B(NMe2)-B(NMe2)-NEt-NEt-]2 (11), which crystallizes in a twist conformation with symmetry group D2.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 853-855 
    ISSN: 0009-2940
    Keywords: Diethylamine - arachno-nonaborane ; Diethylamine - octadecaborane ; conjuncto-Bis[6′5′:5,6]decaborane ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Thermolysis of Amine-arachno-NonaboraneTwo molecules of diethylamine-arachno-nonaborane, B9H13-(NHEt2), undergo a condensation at 140°C to give diethylamine-conjuncto-bis[6′,5′:5,6]decaborane, B18H20(NHEt2) (4). The deprotonation of 4 yields the anion [B18H19(NHEt2)]-which can be crystallized with the cation [NEt3(CH2Ph)]+ (space group P1).
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 129 (1996), S. 1227-1231 
    ISSN: 0009-2940
    Keywords: Aza-closo-decaboranes, halogenation of, methylation of ; Aza-closo-dodecaboranes, halogenation of, methylation of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The aza-closo-boranes ArNB9H9 (1, Ar = p-ClC6H4) and MeNB11H11 (2) were brominated, iodinated, or methylated under Friedel-Crafts conditions to give ArNB9H4Br5 (3), ArNB9H7I2 (4), ArNB9H4Me5 (7), MeNB11H10Br (5), MeNB11H10I (6), and MeNB11H5Me6 (9), respectively. The upper boron belt adjacent to nitrogen is not involved in the substitution reactions with 1 and 2. The antipodal position and the lower belt are attacked by electrophiles in the case of 1; the antipodal position is the preferred one in the case of 2. By prolongated action of triflic acid on the methylated species 7 and 9, one methyl group is replaced by the triflate group to give ArNB9H4Me4(OTrf) (8) and MeNB11H5Me5-(OTrf) (10) with this group in the positions 6 and 12, respectively. The NMR data indicate the cluster symmetries Cs (4, 8), C4v (3, 7), and C5v (5, 6, 9, 10). Crystal structure investigations of 5 (space group Cc) and 10 (space group C2/c) showed that the molecular dimensions of the NB11 skeleton are comparable to those of closo, -(PhCH2)NB11H11.
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