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  • 1
    ISSN: 1434-4475
    Keywords: Keywords. Silsesquioxanes; Organotin(IV) compounds; Mößbauer spectroscopy; Organohafnium(IV) compounds; X-Ray crystallography.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung.  Vier Komplexe von Silsesquioxanen mit Di- und Triorganozinn(IV)-Kationen wurden hergestellt; ihre Zusammensetzung wurde mit analytischen und spektroskopischen Standardmethoden bestimmt. Die Ergebnisse zeigen, daß in den gebildeten Komplexen Organozinneinheit und Ligand im Verhältnis von 1:1 vorhanden sind. FTIR-Spektren stehen im Einklang mit dem Auftreten von Sn*O-Schwingungen in den Verbindungen. Die Struktur der Komplexe wird auf der Grundlage von Mößbauer-Spektren und multinuklearen NMR-Experimenten (1H, 13C, 119Sn, 29Si) diskutiert. Ein Vergleich der experimentell beobachteten Quadrupolaufspaltung (QS) mit nach dem Konzept der partiellen Quadrupolaufspaltung (PQS) berechneten Werten ergab sowohl für die mit dem Dialkyzinn(IV)-Kation gebildeten Komplexe als auch für die Trialkylderivate eine regelmäßige tetraedrische Struktur. Ein neues Organohafniumsilsesquioxanderivat ([Cy 7Si7O12Hf(C5Me5)], Cy=Cyclohexyl, 5) wurde durch Umsetzung von [Cy 7Si7O9(OH)3] mit (C5Me5)HfMe3 unter Abspaltung von Methan hergestellt; seine Molekülstruktur wurde mittels Röntgenstrukturanalyse bestimmt.
    Notes: Summary.  Four complexes of silsesquioxanes with di- and triorganotin(IV) cations have been prepared; their composition was determined by standard analytical and spectroscopic methods. The results show that complexes containing an organotin(IV) moiety and the ligand in a 1:1 ratio are formed. FTIR spectra are consistent with the presence of Sn*O vibrations in the compounds. The structure of the complexes is discussed on the basis of Mößbauer and multinuclear (1H, 13C, 119Sn, and 29Si) NMR spectroscopic measurements. Comparison of the experimental quadrupole splitting (QS) with that calculated on the basis of the partial quadrupole splitting (PQS) concept revealed that the complexes formed with dialkyltin(IV) cations as well as the trialkyl derivatives have a regular tetrahedral structure. A new organohafnium silsesquioxane derivative ([Cy 7Si7O12Hf(C5Me5)], Cy=cyclohexyl, 5), was prepared by treatment of [Cy 7Si7O9(OH)3] with (C5Me5)HfMe3 under elimination of methane. The molecular structure of 5 was determined by X-ray crystallography.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 87-91 
    ISSN: 1434-1948
    Keywords: Imido complexes ; Titanium ; Heteroallylic ligands ; Benzamidinate ligands ; Diiminophosphinate ligands ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Treatment of Ti(NtBu)Cl2(py)2 (1, py = pyridine) with bulky heteroallylic ligands in a 1:1 molar ratio affords the monosubstituted derivatives [PhC(NSiMe3)2]Ti(NtBu)Cl(py)2 (2), [MeOC6H4C(NSiMe3)2]Ti(NtBu)Cl(py) (3), and [Ph2P(NSiMe3)2]Ti(NtBu)Cl(py) (4). Similarly, 2:1 reactions afforded the disubstitution products [PhC(NiPr)2]2Ti(NtBu)(py) (6) and [Ph2P(NSiMe3)2]2Ti(NtBu) (7). The bis(pyridine) adduct Ph2P(NSiMe3)2Li(py)2 (5) was isolated as a by-product during the preparation of 4. The molecular structures of 7 has been established by X-ray crystallography.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 340 (1998), S. 393-407 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Heterobimetallic Complexes Containing 2-(Dimethylaminomethyl)ferrocenyl LigandsThe chemistry of heterobimetallic complexes containing the 2-(dimethylaminomethyl)ferrocenyl ligand is reviewed, including main group element, transition metal, and f-element derivatives. An overview on synthetic methods and molecular structures is given.
    Additional Material: 23 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0009-2940
    Keywords: Lanthanides, organo-, complexes ; Cyclooctatetraenyl complexes ; Benzamidinate ligands ; Diimidophosphinate ligands ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organometallic Compounds of the Lanthanoids, 89. - Cyclooctatetraenyl Complexes of the Early Transition Metals and Lanthanoids, 6. - (Cyclooctatetraenyl)[N,N′-bis(trimethylsilyl)benzamidinato]- and -[diphenylbis(trimethylsilylimido)-phosphinato] Complexes of the Rare Earths; X-Ray Structural Analyses of (C8H8)Tm[PhC(NSiMe3)2](THF), (C8H8)Lu[4-MeOC6H4C(NSiMe3)2](THF), and (C8H8)Nd[Ph2P(NSiMe3)2](THF)[(C8H8)Ln(μ-Cl)(THF)2]2 or [(C8H8)Ln(μ-O3SCF3)(THF)2]2 (Ln = Y, Ce, Pr, Nd, Sm, Tm, Lu) react with Na[4-RC6H4C(NSiMe3)2] (R = H, OMe, CF3) or Li[PhC(NSiMe3)2] to give the monomeric (cyclooctatetraenyl)lanthanide benzamidinates (C8H8)Ln[4-RC6H4C(NSiMe3)2](THF) [R = H, Ln = Y (1), Ce (4), Pr (6), Nd (8), Sm (10), Tm (12), Lu (15); R = OMe, Ln = Y (2), Ce (5), Pr (7), Nd (9), Sm (11), Tm (13), Lu (16); R = CF3, Ln = Y (3), Tm (14), Lu (17)]. The reaction of [(C8H8)Ln(μ-Cl)(THF)2]2 (Ln = Ce, Pr, Nd, Sm) with Li[Ph2P(NSiMe3)2] in THF leads directly to the monomeric compounds (C8H8)Ln[Ph2P(NSiMe3)2](THF) [Ln = Ce (18), Pr (19), Nd (20), Sm (21)] in good yields. The 1H-, 13C-, 31P- and 29Si-NMR and mass spectra of the new compounds as well as the molecular structures of 12, 16, and 20 are discussed. The Raman spectra of the complexes 1-3, 12, and 14-17 have been studied in detail.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 107 (1995), S. 2647-2669 
    ISSN: 0044-8249
    Keywords: Cyclooctatetraenkomplexe ; Homogenkatalyse ; Lanthanoide ; Organolanthanoidverbindungen ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Organometallchemie der Lanthanoide hat in den letzten zehn Jahren einen ungeheuren Aufschwung erlebt. Grund dafür ist nicht zuletzt die Erkenntnis, daß Lanthanoidmetallocene katalytisch ungewöhnlich aktiv sind. Bedeutende Fortschritte gibt es aber auch bei der Erforschung von Organolanthanoidverbindungen, die nicht durch Cyclopentadienylliganden stabilisiert werden. So gelang kürzlich die Synthese der ersten homoleptischen Trialkyllanthanoide, [Ln{CH(SiMe3)2}3]. Anionische Allylkomplexe der Lanthanoide weisen vielversprechende Katalysatoreigenschaften auf, und auch Cyclooctatetraenkomplexe dieser Elemente werden zur Zeit intensiv untersucht. Der vorliegende Beitrag bietet einen Überblick über dieses in rascher Entwicklung begriffene Forschungsgebiet.
    Additional Material: 36 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 107 (1995), S. 1071-1075 
    ISSN: 0044-8249
    Keywords: Fullerene ; Lanthanoidverbindungen ; Metallofullerene ; Nanoröhren ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0044-2313
    Keywords: Tetramethyltitanium ; transition metal alkyls ; benzamidinate complexes ; X-ray structure ; 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. 64 [1] Preparation and Crystal Structure of Bis[N,N′ -bis(trimethylsilyl)-benzamidinato]dimethyltitaniumTetramethyltitanium reacts with excess N,N′-bis(trimethylsilyl)-benzamidine (1) to give bis[N,N′-bis(trimethylsilyl)benzamidinato]dimethyl-titanium (2) via protolysis. This compound was isolated and characterized by X-ray crystal structure analysis. In the crystal, 2 adopts an octahedral coordination with the methyl groups in cis-positions. The monomethyl complexes [PhC(NSiMe3)2]2M(Me)Cl (3: M = Ti, 4: M = Zr) have been prepared by treatment of the dichloro precursors with one equivalent of methyllithium.
    Notes: Tetramethyltitan wird von einem Überschuß an N,N′-Bis(trimethylsilyl)benzamidin (1) zum Bis[N,N′-bis(trimethylsilyl)benzamidinato]dimethyltitan (2) protolysiert. Diese Verbindung konnte isoliert und ihre Kristallstruktur ermittelt werden. Danach liegt 2 im Kristall in oktaedrischer Koordination vor, wobei die beiden Methylgruppen in cis-Position zueinander stehen. Die Monomethylkomplexe [PhC(NSiMe3)2]2M(Me)Cl (3: M = Ti, 4: M = Zr) wurden durch Umsetzung der Dichlorovorstufen mit einem Äquivalent Methyllithium dargestellt.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 34 (1995), S. 981-985 
    ISSN: 0570-0833
    Keywords: fullerenes ; lanthanide compounds ; metallofullerenes ; nanotubes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 34 (1995), S. 2466-2488 
    ISSN: 0570-0833
    Keywords: cyclooctatetraene complexes ; homogeneous catalysis ; lanthanides organolanthanide compounds ; Cyclooctatetraenes ; Homogeneous catalysis ; Lanthanides ; Organolanthanides ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: During the past ten years the organometallic chemistry of the lanthanides has witnessed enormous growth. One of the main reasons for this development was the finding that lanthanide metallocenes can exhibit an unusually high catalytic activity. Considerable advances have also been achieved in the chemistry of organolanthanide complexes that are not stabilized by cyclopentadienyl ligands. For example, the successful synthesis of the first unsolvated homoleptic trialkyllanthanides, [Ln{CH(SiMe3)2}3], has recently been reported. Anionic allyl complexes of the lanthanides show promising catalytic properties and cyclooctatetraene complexes of these elements are also under active investigation. This review is intended to provide an overview of this rapidly developing area of research.
    Additional Material: 37 Ill.
    Type of Medium: Electronic Resource
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