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Synthesis and reactivity of mixed pentafluorophenyl platinum(I)-palladium(I) derivatives
Affiliation:1. Department of Chemistry, College of Science, University of Tikrit, Tikrit, Iraq;2. Department of Chemistry, University College London, 20 Gordon Street, London WC1H OAJ, UK;3. Institut für Chemie, Martin-Luther-Universität, Halle-Wittenberg, Kurt-Mothes-Str. 2, D-06120 Halle, Germany;4. Instituto de Sintesis Quimica y Catalisis Homogenea (ISQCH), Facultad de Ciencias, Universidad de Zaragoza, Plaza S. Francisco s/n, 50009, Spain;5. Applied Chemistry Department, Public University of Navarra, Campus Arrosadía, 31006 Pamplona, Spain;6. Department of Chemistry, King’s College London, Britannia House, 7 Trinity Street, London SE1 IDB, UK
Abstract:XPd(μ-dppm)2Pt(C6F5) (X = Cl (I), Br (II)) have been prepared by reacting Pd2(dba)3·CHCl3 and PtX- (C6F5)(η1-dppm)2. Reaction of complex I with SnCl2 gives the SnCl3 derivative, whilst ligands L (PPh3, P(OPh)3, SbPh3) render the cationic complexes. The species R2N+, SO2 or MeOOC)CCCOOMe insert into the PdPt bond of I to give A-frame Pd(II)- Pt(II) complexes. The reactions of CIPd(μ-dppm)2- Pt(C6F5) with isonitriles CNR (R = p-Tol, Cy) lead to products containing either terminal or inserted isocyanide or both.
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