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  • General Chemistry  (2)
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  • 1
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 2000 (2000), S. 59-63 
    ISSN: 1434-1948
    Schlagwort(e): Phosphorane imine ; Sulfur ligands ; Nickel ; Palladium ; Platinum ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Reaction of the trinuclear [M(′S3′)]3 complexes {M = Ni (4), Pd (5), Pt (6); ′S3′2- = bis(2-mercaptophenyl)sulfide (2-)} with HNPnPr3 yielded the new phosphorane imine complexes [M(NHPnPr3)(′S3′)] {M = Ni (1), Pd (2), Pt (3)}. The complexes 1-3 have been completely characterized and are rare examples of mononuclear phosphorane imine complexes with late transition metals. Spectroscopic and structural results indicate that the HNPnPr3 ligands favor the ylidic structure when binding to [M(′S3′)] fragments. X-ray structure determinations showed that [M(NHPnPr3)(′S3′)] complexes associate through N-H···S(thiolate) bridges to give centrosymmetric dimers.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 2000 (2000), S. 271-279 
    ISSN: 1434-1948
    Schlagwort(e): Nickel complexes ; Palladium complexes ; S ligands ; Exchange reactions ; Azide ; Sulfinylimide ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: In order to obtain suitable precursors for nickel and palladium complexes that model the reactivity of the active sites of hydrogenases and CO dehydrogenases, a series of [M(L)(‘S3’)] complexes has been synthesized [M = NiII, PdII; ‘S3’2- = bis(2-mercaptophenyl)sulfide(2-)]. X-ray structure determinations of [Ni(‘S3’)]3 (1) and [Pd(‘S3’)]3 (2) have revealed that the [M(‘S3’)] fragments trimerize to give six-membered [MS]3 rings, which exhibit chair conformations with alternating MII centers and thiolate bridging atoms. Reactions of the parent complex [Ni(‘S3’)]3 (1) with nucleophiles L, such as thiolates SR- (R = tBu, Cy, Me, Ph), phosphanes PR3 (R = Cy, Ph), chloride, or azide, have been found to yield the corresponding anionic or neutral [Ni(L)(‘S3’)] complexes, which were isolated as (NBu4)[Ni(SR)(‘S3’)] [R = tBu (3), Cy (4), Me (5), Ph (6)], [Ni(PR3)(‘S3’)] [R = Cy (7), Ph (8)], (NBu4)[Ni(Cl)(‘S3’)] (9), and (NBu4)[Ni(N3)(‘S3’)] (10). When treated with Me3SiX, the StBu- ligand in (NBu4)[Ni(StBu)(‘S3’)] (3) was exchanged to give (NBu4)[Ni(X)(‘S3’)] [X = Cl- (9), N3- (10), NCS- (11), NSO- (12)]. The palladium complex [Pd(‘S3’)]3 (2) could also be cleaved with StBu-, but the resulting (NBu4)[Pd(StBu)(‘S3’)] (13) proved inert towards exchange reactions with Me3SiX. All the mononuclear complexes have been characterized by standard spectroscopic techniques and by elemental analysis. The molecular structures of 3, 4, 6, 7, 8, 9, and 13 have been determined by X-ray crystallography. The [MS3L] core geometries of all the complexes are non-planar, exhibiting a considerable tetrahedral distortion.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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