Unexpected differences in reactivity between tin and lead organyl chlorides - crystal structures of their organylphosphonium salts

摘要

Pentacoordinated tin is known since the late 1950s but little is known about the ability of lead to form similar structures. Originally we investigated the reaction between a number of tetraorganylphosphonium chlorides [PR4]Cl-+(-) (R = Me, Bu-n, and Ph) and several diorganyltin dichlorides SnR'Cl-2(2) (R= Me, Et, Pr-n, Bu-n, Ph, o-, m-, p-Tol) between 100 and 240 degreesC. Novel pentacoordinated tin complexes, tetraorganylphosphonium diorganyltrichlorostannates [PR4][SnR'Cl-2(3)] (1-19), were formed in good to excellent yields. In a second step, this synthetic approach was extended to include the reaction of diphenyllead dichloride Ph2PbCl2 with [PR4]C-divided by(l)- (R=Bu-n, Ph). Surprisingly, a two chloride transfer was observed to form the hexacoordinated lead species [PBu4n](2)[PbPh2Cl4] (20). Under similar conditions, the pentacoordinated [PPh4][PbPh3Cl2] (21) was obtained by a phenyl transfer. Complexes 20 and 21 were characterised by NMR (H-1, C-13, P-31, and Pb-207), IR, MS, and X-ray crystallography. The anion of 20 assumes a lightly distorted octahedral geometry with the phenyl substituents in trans-positions. In the anion of 21 the phenyl substituents occupy the equatorial positions of a lightly distorted trigonal bipyramid. A thorough spectroscopical investigation of the tin complexes 1-19, including X-ray structural studies, which were possible for complexes with R' = aryl, revealed that these complexes are monomeric with a distorted trigonal bipyramidal [SnR'Cl-2(3)](-) anion. Both aryl groups occupy equatorial positions. (C) 2003 Elsevier B.V. All rights reserved. [References: 47]