Weakly bonded Lewis base adducts of plumbocene and stannocene: A synthetic and calculational study

被引:19
作者
Armstrong, DR
Beswick, MA
Cromhout, NL
Harmer, CN
Moncrieff, D
Russell, CA
Raithby, PR
Steiner, A
Wheatley, AEH
Wright, DS
机构
[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
[2] Univ Strathclyde, Dept Pure & Appl Chem, Glasgow G1 1XL, Lanark, Scotland
[3] Florida State Univ, Supercomp Computat Res Inst, Tallahassee, FL 32306 USA
关键词
D O I
10.1021/om980077k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The coordination of [(eta-Cp)(2)Pb] and [(eta-Cp)(2)Sn] by bidentate Lewis-base ligands gives the first examples of adducts of neutral p-block metallocenes. Ab initio MO calculations of [(eta-Cp)(2)Pb . TMEDA] (1) (TMEDA = (Me2NCH2)(2)), [Cp2Pb . 4,4'-Me(2)bipy] (2) (4,4'-Me(2)bipy = 4,4'-dimethylbipyridine), and the new complex [(eta-Cp)(2)Sn . TMEDA] (3) confirm that despite the presence of longer Pb-N and Sn-N bonds in the solid-state structures of the TMEDA adducts, the association of TMEDA with the metallocenes is more favorable than with 4,4'-Me(2)bipy. This finding is a consequence of the greater reorganization energy of 4,4'-Me(2)bipy compared to TMEDA. The low association energies of these species can be rationalized in terms of metal lone pair/ligand lone pair repulsion.
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页码:3176 / 3181
页数:6
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