2-(Phenyltelluromethyl)tetrahydrofuran (L1) and 2-(2-{4-methoxyphenyl}telluroethyl)-1,3- dioxolane (L2) and their palladium(II) and platinum(II) complexes
作者:Raman Batheja、Ajai K. Singh
DOI:10.1016/s0277-5387(97)00203-9
日期:1997.10
The nucleophile [ArTe-] generated ill situ borohydride solution of Ar2Te2, reacts with 2-(chloromethyl) tetrahydrofuran and 2-(2-bromoethyl)-1,3-dioxolane resulting in L-1 and L-2, respectively. The complexes of palladium(II) and platinum(II) with L-1/L-2 having stoichiometries [MCl2 . L-2], [ML2](ClO4)(2), [(DPPE)ML2](ClO4)(2), [(PPh3)(2)ML2](ClO4)(2) and [(phen)ML2](ClO4)(2) (where L = L-1/L-2 DPPE = Ph2PCH2CH2PPh2, phen = 1,10-phenanthroline and M = Pd/Pt) have been synthesized. IR, H-1, Te-125H-1} and P-31H-1} NMR and UV-vis spectral data of these species in conjunction with their molar conductance and molecular weight data have been used to authenticate the new species. In all complexes (1-20) the ligands L-1 and L? are coordinated through tellurium and in the complexes of formula [ML2](ClO4)(2) (M = Pd, Pt) the ligand is bidentate with the oxygen atom used in complexation. In solution, complexes PtCl2L2 exist as a mixture of cis and trans isomers whereas only the trans isomer was observed for the palladium analogues. The [(phen)PdL2](ClO4)(2)(Q) quenches O-1(2) readily. The plot of log [Q] vs time is linear. Mechanism compatible with the experimental observations is proposed. (C) 1997 Elsevier Science Ltd.