Reactions of di- or trialkynylphosphine and di- or trialkynylarsine oxides with a cationic platinum-hydride complex: mechanistic features
摘要:
The reaction between a cationic Pt-H complex and O=P(=CMe3)3 was followed by P-31 NMR at three temperatures. Addition of the Pt-H bond to an alkynyl substituent to give a PtP-mu-alkenylidene complex is observed with subsequent formation of the expected 1,2-dihydrophosphete product. A similar reaction with O=AsPh(C=CCMe3)2 occurs with unexpected overall transfer of both alkynyl substituents from the As atom to the Pt ion, giving eventually a cationic Pt(II)(eta1-alkynyl)(eta1-alkenyl) product. The X-ray structure of this latter complex has been determined: P1BAR; Z = 2; a = 11.391 (4) angstrom, b = 16.040 (4) angstrom, c = 10.801 (1) angstrom; alpha = 100.13 (1)-degrees, beta = 100.71 (2)-degrees, gamma = 80.23 (2)0. A mechanism of formation of 1,2-dihydrophosphete or -arsete complexes involving Pt-H addition and subsequent alkynyl transmetalation is postulated.