Polyphosphinoylmethanide complexes of tin(II). Crystal and molecular structure of {[(C6H5)2PO]3C}2Sn
摘要:
The reaction of SnCl2 and two equiv. of Na{[(C6H5)2PO]3C} yields {[(C6H5)2PO]3C}2Sn (1). The solid state structure of 1 has been determined by X-ray crystallography: trigonal, space group R3BARc, with a = 29.216(3), c = 42.120(5) angstrom, V = 31.136 angstrom-3 and Z = 18. Both potentially tridentate [(C6H5)2PO]3C-ligands are coordinated to the tin atom in a bidentate manner. The coordination geometry about tin is a pseudo trigonal bipyramid. Each phosphinoylmethanide ligand occupies an axial and equatorial site with the remaining equatorial site filled by the lone pair on tin. The reaction of Na{[(C6H5)2PO]2CH} and SnCl2 yields the analogous complex {[(C6H5)2PO]2CH}2Sn (2).
Iridium(I), -(III), and -(V) complexes of an O-donor ligand in alkyne hydrosilylation
作者:Robin S. Tanke、Robert H. Crabtree
DOI:10.1039/c39900001056
日期:——
The O-donor ligand C(Ph2PO)3–(triso) stabilises iridium-(I), -(III), and -(V) species such as [(triso)IrH2(SiMePh2)2]; the complexes catalyse the net anti-addition of silanes to alkynes.