Library

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
  • Benzamidinate ligands  (4)
  • Heterocycles with As, N, P, S  (1)
  • Homogeneous catalysis  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Imidotitanium Complexes with Heteroallylic Ligands: Synthesis and Solid-State Structure (1998)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 87-91 
    Details
    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
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
  • 2
    Electronic Resource
    Electronic Resource
    Stabilisierung von Uran(IV)-Alkylen durch raumerfüllende Chelatliganden: Molekülstruktur von [PhC(NSiMe3)2]3UMe (1992)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1313-1318 
    Details
    ISSN: 0009-2940
    Keywords: Actinides, organo- ; Uranium complexes ; σ-Alkyl complexes ; Chelating ligands ; Benzamidinate ligands ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Stabilization of Uranium(IV) Alkyls by Bulky Chelating Ligands: Molecular Structure of [PhC(NSiMe3)2]3UMeChelate ligand-stabilized uranium σ-methyl complexes are obtained in good yields by treatment of [RC6H4C-(NSiMe3)2]3UCl (1) with methyllithium. The molecular structure of [PhC(NSiMe3)2]3UMe (3a) has been determined by X-ray crystallography. A long uranium - carbon bond [249.8(5) pm] indicates steric crowding in the molecule. Analogously the dimethyluranium complex [(CF3)3C6H2C(NSiMe3)2]2UMe2 (4b) is prepared from [(CF3)3C6H2C(NSiMe3)2]2UCl2 and two equivalents of methyllithium. Reaction of 1 with NaBH4 yields the tetrahydroborates [RC6H4C(NSiMe3)2]3UBH4 (5). The strongly temperature-dependent 1H-NMR spectra of the complexes 1 and 3 have been studied in detail.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19921250603
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Sterische Cyclopentadienyl-Äquivalente in der Chemie der f-Elemente: Monomere, homoleptische Lanthanid(III)-tris[N,N′-bis(trimethylsilyl)-benzamidinate] (1992)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 2171-2181 
    Details
    ISSN: 0009-2940
    Keywords: Lanthanides ; Benzamidinate ligands ; Steric cyclopentadienyl equivalents ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Steric Cyclopentadienyl Equivalents in f-Element Chemistry: Monomeric, Homoleptic Lanthanide(III) Tris[N,N′-bis(trimethylsilyl)benzamidinates]Anhydrous lanthanide trichlorides react with N-silylated sodium benzamidinates, Na[4-RC6H4C(NSiMe3)2], (1a-d), to give the monomeric, homoleptic lanthanide(III) benzamidinates [4-RC6H4C(NSiMe3)2]3Ln (2-23, R = H, MeO, CF3, Ph). The molecular structure of [4-MeOC6H4C(NSiMe3)2]3Pr (11) has been determined by X-ray diffraction. Absorption and emission measurements reveal that the three benzamidinate ligands produce an unusually large crystal field which is comparable with that of cyclopentadienyl.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19921251003
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    Metallorganische Verbindungen der Lanthanoide, 89. Cyclooctatetraenyl-Komplexe der frühen Übergangsmetalle und Lanthanoide, 6. (Cyclooctatetraenyl)[N,N′-bis(trimethylsilyl)benzamidinato]-und -[diphenylbis(trimethylsilylimido)phosphinato]-Komplexe der Seltenen Erden; Röntgenstrukturanalyse von (C8H8)Tm[PhC(NSiMe3)2](THF), (C8H8)Lu[4-MeOC6H4C(NSiMe3)2](THF) und (C8H8)Nd[Ph2P(NSiMe3)2](THF) (1995)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 128 (1995), S. 395-404 
    Details
    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
    URL: http://dx.doi.org/10.1002/cber.19951280411
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 5
    Electronic Resource
    Electronic Resource
    Anorganische Ringsysteme mit Ferrocenyl-Substituenten (1989)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 1247-1254 
    Details
    ISSN: 0009-2940
    Keywords: Ferrocenyl-substituted heterocycles ; Heterocycles with As, N, P, S ; Metallaheterocycles ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Inorganic Ring System Containing Ferrocenyl SubstituentsThree-, four-, five-, and eight-membered heterocycles are synthesized starting from FcPCl2 (1), FcPH2 (2), FcAsCl2 (3) and Fe(C5H4AsCl2)2 (4) (Fc = Ferrocenyl). Treatment of 1 with 2 in the presence of DBU yields (FcP)n, which reacts with (Ph3P)2Pt(C2H4) to give (7). The corresponding As2Pt ring system 9 is available in high yield via (FcAs)3 (8). The reduction of 1 with LiAlH4 yields (FcP)4 (10). A five-membered arsenic sulfur heterocycle, Fc2As2S3 (12), is formed in the reaction of FcAs=P(2,4,6-tBu3C6H2) (11) with sulfur. FcAsCl2 (3) reacts with Me3SiNSNSiMe3 to give FcAs(NSN)2AsFc (13), which contains an eight-membered As2S2N4 ring. Its complexation with (norbornadiene)M(CO)4 leads to the tetracarbonyl complexes [FcAs(NSN)2AsFc]M(CO)4 (14, 15; M = Cr, Mo). An arsenic-bridged ferrocenophane 16 can be isolated from the reaction of Fe(C5H4Li)2 x TMEDA with AsCl3. The reaction of 4 with Me3SiNSNSiMe3 also produces a condensed ferrocenophane derivative, (C5H4)2FeAs2N6S4 (17). The molecular structures of 13 and 17 have been determined by X-ray diffraction.
    Notes: Ausgehend von FcPCl2 (1), FcPH2 (2), FcAsCl2 (3) und Fe(C5H4AsCl2)2 (4) werden drei-, vier-, fünf- und achtgliedrige Heterocyclen mit Ferrocenyl-Substitutenten synthetisiert (Fc = Ferrocenyl). Durch Umsetzung von 1 mit 2 in Gegenwart von DBU entsteht (FcP)n, das mit (Ph3P)2Pt(C2H4) zu (7) reagiert. Der analoge As2Pt-Ring 9 ist über (FcAs)3 (8) in guter Ausbeute zugänglich. Die Reduktion von 1 mit LiAlH4 liefert (FcP)4 (10). Ein fünfgliedriger Arsen-Schwefel-Heterocyclus, Fc2As2S3 (12), entsteht durch Umsetzung von FcAs=P(2,4,6-tBu3C6H2) (11) mit Schwefel. FcAsCl2 (3) reagiert mit Me3SiNSNSiMe3 zu FcAs(NSN)2AsFc (13), das einen achtgliedrigen As2S2N4-Ring enthält. Dessen Komplexierung mit (Norbornadien)M(CO)4 führt zu den Tetracarbonyl-Komplexen [FcAs(NSN)2AsFc]M(CO)4 (14, 15; M = Cr, Mo). Ein Arsenüberbrücktes Ferrocenophan 16 kann bei der Reaktion von Fe(C5H4Li)2 × TMEDA mit AsCl3 isoliert werden. Auch die Umsetzung von 4 mit Me3SiNSNSiMe3 liefert ein kondensiertes Ferrocenophan-Derivat der Zusammensetzung (C5H4)2FeAs2N6S4 (17). Die Molekülstrukturen von 13 und 17 wurden röntgenographisch bestimmt.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19891220706
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 6
    Electronic Resource
    Electronic Resource
    Cyclopentadienyl-Free Organolanthanide ChemistryDedicated to Professor Herbert W. Roesky on the occasion of his 60th birthday (1995)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 34 (1995), S. 2466-2488 
    Details
    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
    URL: http://dx.doi.org/10.1002/anie.199524661
    Library Location Call Number Volume/Issue/Year 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...