Abstract
AbstractDecarboxylation reactions between the complexes cis–[PtCl2L] (L = 1, n–bis(diphenylphosphino)–ethane (n = 2, dppe), –propane (n = 3, dppp) or –butane (n = 4, dppb)) and thallium(I) pentafluorobenzoate in pyridine give cis–[PtCl(C6F5)L] and cis–[Pt(C6F5)2L] complexes in high yields with short reaction times. X–ray crystal structures of cis–[PtCl(C6F5)(dppe)] · 0.5 C5H5N, cis–[PtCl(C6F5)(dppp)], cis–[PtCl(C6F5)(dppb)] · C3H6O, cis–[Pt(C6F5)2L] (L = dppe, dppp and dppb) and the reactants cis–[PtCl2(dppp)] (as a CH2Cl2 solvate) and cis–[PtCl2(dppb)] show monomeric structures with chelating diphosphine ligands in all cases rather than dimers with bridging diphosphines. 31P NMR data are consistent with these structures in solution.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Zeitschrift für anorganische und allgemeine Chemie
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
