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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 955-958 
    ISSN: 0044-2313
    Keywords: Template Reactions ; Benzoylhydrazine ; Hydrazide Ligands ; Molybdenum Complexes ; Crystal Structure ; Triphenylphosphane ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Template Reactions of Bis(acetylacetonato)-dioxo-molybdenum(VI) with Benzoylhydrazine and TriphenylphosphaneBy reaction of MoO2(acac)2 with C6H5—CO—NH—NH2 in the presence of P(C6H5)3 Mo(NNCOC6H5)((CH3)2CNNCOC6H5)(P(C6H5)) was obtained besides MoO(acac-NNHCOC6H5)(NNHCOC6H5). The earlier compound was characterized by X-ray structural analysis. Crystallographic data see „Inhaltsübersicht“.
    Notes: Bei der Umsetzung von MoO2(acac)2 mit C6H5—CONH—NH2 in Gegenwart von P(C6H5)3 wurde neben MoO(acac-NNHCOC6H5)(NNHCOC6H5) als weitere Substanz Mo(NNCOC6H5)(NNHCOC6H5)((CH3)2CNNCOC6H5) · (P(C6H5)3) erhalten, welche Benzoylhydrazidoliganden in verschiedenen Bindungsformen aufweist. Die Verbindung wurde durch Röntgenkristallstrukturanalyse charakterisiert.Raumgruppe P 21/c, Z = 4, 2 632 beobachtete unabhängige Reflexe, R = 5,9%, Gitterabmessungen bei 19°C: a = 1 583,6(2) pm, b = 1 485,0(2) pm, c = 1 656,1(2) pm, β = 100,79(1)°C.
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  • 2
    ISSN: 0044-2313
    Keywords: Phosphoraneiminato ; Complexes of Titanium ; Synthesis ; IR Spectra ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Phosphoraneiminato Complexes of Titanium. Synthesis and Crystal Structures of CpTiCl2(NPMe3), [TiCl3(NPMe3)]2, [Ti2Cl5(NPMe2Ph)3], and [Ti3Cl6(NPMe3)5][BPh4]The title compounds are formed from Cp2TiCl2 and titanium tetrachloride, respectively, and the corresponding phosphane imino compounds Me3SiNPMe3 and Me3SiNPMe2Ph. The tetraphenyl borate salt yielded from the reaction of [Ti3Cl6(NPMe3)5]Cl with NaBPh4. All compounds form yellow crystals which are sensitive to moisture. They were characterized by IR-spectroscopy and crystal structure analyses.CpTiCl2(NPMe3) (1): Space group Pbca, Z = 8, solution of the structure with 1632 observed independent reflections, R = 0.037. Lattice dimensions at 19°C: a = 1202.6, b = 1224.2, c = 1766.7 pm. The molecules of the compound are monomeric with the (NPMe3)- ligand in almost linear array (bond angle Ti—N—P 170.7°).[TiCl3(NPMe3)]2 (2): Space group Pbca, Z = 8, structure solution with 698 observed independent reflections, R = 0.030. Lattice dimensions at -60°C: a = 1140.5, b = 1112.2, c = 1589.4 pm. In 2 the titanium atoms, which occur in trigonal bipyramidal coordination, are linked by the N atoms of the (NPMe3)- groups to form a centrosymmetric dimer with Ti—N bond lengths of 184.3 and 208.2 pm.[Ti2Cl5(NPMe2Ph)3] · CH2Cl2 (3): Space group Pca21, Z = 4, structure solution with 8477 observed independent reflections, R = 0.051. The lattice dimensions at 20°C are: a = 1221.0; b = 1407.5, c = 2139.3 pm. 3 can be understood as a reaction product of TiCl2(NPMe2Ph)2 and TiCl3(NPMe2Ph). In the resulting, heavily distorted Ti2N2-four-membered ring the Ti—N bond lenghts are 1804., 194.4, 199.2, and 234.6 pm. The longest Ti—N bond is in trans-position to the N atom of the terminal (NPMe2Ph)- ligand, in which the Ti—N distance is 175.6 pm. .[Ti3CL6(NPMe3)5][BPh4] (4): Space group P21/n, structure solution with 2846 observed independent reflections, R = 0.062. The lattice dimensions at 20°C are: a = 1495.2, b = 2335.4, c = 155,8 pm, β = 93.28°. In the cation of 4 the three titanium atoms along with three (NPMe3)- groups with μ2- N functions and two (NPMe3)- groups with μ3- N functions form a nation number 6 with two terminal chlorine atoms.
    Notes: Die Titelverbindungen entstehen aus Cp2TiCl2 bzw. Titantetrachlorid und den entsprechenden silylierten Phosphaniminen Me3SiNPMe3 bzw. Me3SiNPMe2Ph. Das Tetraphenyloborat-Derivat erhielten wir durch Umsetzung von [Ti3Cl6(NPMe3)5]Cl mit NaBPh4. Alle Verbindungen bilden gelbe, feuchtigkeitsempfindliche Kristalle, die durch IR-Spektroskopie und durch Kristallstrukturanalysen charakterisiert wurden.CpTiCl2(NPMe3) (1): Raumgruppe Pbca, Z = 8, Strukturlösung mit 1632 beobachteten unabhängigen Reflexen, R = 0,037. Gitterabmessungen bei 19°C: a = 1202,6; b = 1224,2; c = 1766,7 pm. Die Verbindung bildet monomere Moleküle mit dem (NPMe3)--Liganden in nahezu gestreckter Anordnung TiNP (Bindungswinkel 170,7°).[TiCl3(NPMe3)]2 (2): Raumgruppe Pbca, Z = 8, Strukturlösung mit 698 beobachteten unabhängigen Reflexen, R = 0,030. Gitterabmessungen bei -60°C: a = 1140,5; b = 1112,2; c = 1589,4 pm. In 2 sind die trigonal-bipyramidal koordinierten Titanatome über die N-Atome der (NPMe3)- - Gruppen zu einem zentrosymmetrischen Dimer mit TiN-Abständen von 184,3 und 208,2 pm verknüpft.[Ti2Cl5(NPMe2Ph)3] · CH2Cl2 (3): Raumgruppe Pca21, Z = 4, Strukturlösung mit 8477 beobachteten unabhängigen Reflexen, R = 0,051. Gitterabmessungen bei 20°C: a = 1221,0; b = 1407,5; c = 2139,3 pm. 3 läßt sich als Dimerisierungsprodukt aus TiCl2(NPMe2Ph)2 und TiCl3(NPMe2Ph) auffassen, wobei ein stark verzerrter ebener Ti2N2-Vierring mit TiN-Abständen von 180,4, 194,4, 199,2, und 234,6 pm entsteht. Die längste TiN-Bindung befindet sich in trans-Stellung zu dem N-Atom des terminal gebundenen (NPMe2Ph)--Liganden, der eine TiN-Bindungslänge von 175,6 pm aufweist.[Ti3Cl6(NPMe3)5][BPh4] (4): Raumgruppe P21/n, Z = 4, Strukturlösung mit 2846 beobachteten unabhängigen Reflexen, R = 0,062. Gitterabmessungen bei 20°C: a = 1495,2; b = 2335,4; c = 1555,8 pm, β = 93,28°. In dem Kation von 4 bilden die drei Titanatome zusammen mit drei (NPMe3)--Gruppen mit μ2-N-Funktion und zwei (NPMe3)--Gruppen mit μ3-N-Funktion eine trigonale Bipyramide. Zusammen mit den terminal gebundenen Chloratomen erreichen die Titanatome die Koordinationszahl sechs.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 343-345 
    ISSN: 0044-2313
    Keywords: Hexamethyl guanidinium cation ; tetrachloro iron(II) anion ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Concerning the Reaction of Cp2TiCl2 with [C(NMe2)3][(CO)4FeC(O)NMe2] - Crystal Structure of [C(NMe2)3]2[FeCl4]The title compound forms by the reaction of Cp2TiCl2 with [C(NMe2)3][(CO)4FeC(O)NMe2] in THF solution. It crystallizes in the space group Pbcn with a = 1 566.6(3); b = 976.4(2); c = 1 580.4(4) pm; Z = 4; R = 3.8%. Each [FeCl4]2- in is surrounded by eight cations. Two cations each are connected with one Cl atom by relatively short H … Cl contacts leading to a distortion of the tetrahedral geometry of the anion.
    Notes: Die Titelverbindung entsteht bei der Umsetzung von Cp2TiCl2 mit [C(NMe2)3][(CO)4FeC(O)NMe2] in THF-Lösung. Sie kristallisiert in der Raumgruppe Pbcn mit a = 1 566,6(3); b = 976,4(2); c = 1 580,4(4) pm; Z = 4; R = 3,8%. Jedes [FeCl4]2- Ion ist von acht Kationen umgeben. Je zwei Kationen sind über relativ kurze H … Cl Kontakte mit einem Cl-Atom verbunden, was zu einer Verzerrung der Tetraedergeometrie des Anions führt.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 357-360 
    ISSN: 0044-2313
    Keywords: Template Reaction ; Benzolhydrazido(2-)-acetylacetonebenzoylhydrazonato(2-)-oxomolybdenum(VI) ; Acetylacetonebenzoylhydrazone ; Mass Spectra ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Template Reaction of Bis(acetylacetonato)-dioxo-molybdenum(VI) with BenzoylhydrazoneBy reaction of bis(acetylacetonato)-dioxo-molybdenum(VI) with benzoylhydrazine benzoylhydrazido(2-)-acetylacetonebenzoylhydrazonato(2-)-oxo-molybdenum(VI) was formed beside another species. The compound was characterized by mass spectrometry and X-ray structural analysis. Crystallographic data see „Inhaltsübersicht“.
    Notes: Als Reaktionsprodukt der Umsetzung von Bis(acetylacetonato)-dioxo-molybdän(VI) mit Benzoylhydrazin in Gegenwart von Triphenylphosphan wurde Benzoylhydrazido-(2-)-acetylacetonbenzoylhydrazonato(2-)-oxo-molybdän(VI) neben einem weiteren Molybdänkomplex erhalten und massenspektrometrisch sowie röntgenkristallstrukturanalytisch charakterisiert. (Raumgruppe Cc, Z = 4, 2 020 beobachtete Reflexe, R = 3,7%. Gitterabmessungen bei 19°C: a = 1 188,5(2) pm, b = 2 110,2(2) pm, c = 813,2(2) pm, β = 105,77(2)°).
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 67-72 
    ISSN: 0044-2313
    Keywords: Phosphoraneiminato complex of antimony ; Synthesis ; IR-spectra ; 121Sb-Mössbauer spectra ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: [Sb(NPPh3)4]+SbF6-: Synthesis, Crystal Structure, and 121Sb Mössbauer SpectrumThe title compound as well as the hexachloro antimonate [Sb(NPPh3)4]+SbCl6- have been prepared by the reaction of Me3SiNPPh3 with SbF5 and SbCl5, respectively, in acetonitrile solutions. The compounds form colourless, moisture sensitive crystals, which were characterized by IR spectroscopy, by 121Sb Mössbauer spectroscopy, and by crystal structure analyses. A complete crystal structure analysis, however, could be carried out with [Sb(NPPh3)4]+SbF6- only. The compound crystallizes orthorhombically in the space group Pccn with four formula units per unit cell. The structure determination was done with 3 972 observed unique reflections, R = 0.053. Lattice dimensions at 19°C: a = 1 658,6; b = 1 698.9, c = 2 361.9 pm. In the cation [Sb(NPPh3)4]+ the antimony atom is tetrahedrally coordinated by the four nitrogen atoms of the phosphoraneiminato ligands with extremely short Sb—N bond lengths of 193 pm.
    Notes: Die Titelverbindung entsteht ebenso wie das Hexachloroantimonat [Sb(NPPh3)4]+SbCl6- durch Reaktion von Me3SiNPPh3 auf SbF5 bzw. SbCl5 in Acetonitrillösung. Die Verbindungen bilden farblose, feuchtigkeitsempfindliche Kristalle, die wir durch ihre IR-Spektren, durch 121Sb-Mößbauer-Spektren und durch Kristallstrukturanalysen charakterisiert haben. Eine vollständige Strukturanalyse gelang jedoch nur an [Sb(NPPh3)4]+SbF6-. Die Verbindung kristallisiert orthorhombisch in der Raumgruppe Pccn mit vier Formeleinheiten pro Elementarzelle. Strukturlösung mit 3 972 beobachteten unabhängigen Reflexen, R = 0,053. Die Gitterkonstanten sind bei 19°C: a = 1 658,6; b = 1 698,9; c = 2 361,9 pm. In dem Kation [Sb(NPPh3)4]+ ist das Antimonatom tetraedrisch von den vier Stickstoffatomen der Triphenylphosphaniminatoliganden umgeben. Die Sb—N-Bindungslängen sind mit 193 pm extrem kurz.
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  • 6
    Publication Date: 1994-01-01
    Print ISSN: 2194-4946
    Electronic ISSN: 2196-7105
    Topics: Geosciences , Physics
    Published by De Gruyter
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  • 7
    Publication Date: 1994-01-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
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  • 8
    Publication Date: 1994-05-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
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  • 9
  • 10
    Publication Date: 1994-02-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
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