DFT (BLYP) calculations with full geometry optimization on the PH3 addition to CpMCl(2)(PH3) show very different results for M = Cr and Mo, in accord with the experimentally established stability of 15-electron CpCrX(2)L and 17-electron CpMoX(2)L(2) (X = 1-electron ligand; L = 2-electron ligand). The calculations point to the paramount importance of electron pairing energy: 22.53 kcal/mol must be spent to promote the ground state (4)A '' CpCrCl(2)(PH3) to the (2)A' excited state, and only 16.51 kcal/mol are regained upon formation of the second Cr-PH, bond. The cost of pairing the electrons in CpMoCl(2)(PH3), on the other hand, is much less (3.95 kcal/mol) and the bond formation energy along the spin doublet surface is 12.26 kcal/mol. The relevance of electron pairing energy as a stabilizing factor for the general class of open-shell organometallics is pointed out.

Electron pairing as a stabilizing factor in open-shell organometallics. The case of 15-electron CpMCl(2)(PH3) (M=Cr and Mo)

CACELLI, IVO;
1997-01-01

Abstract

DFT (BLYP) calculations with full geometry optimization on the PH3 addition to CpMCl(2)(PH3) show very different results for M = Cr and Mo, in accord with the experimentally established stability of 15-electron CpCrX(2)L and 17-electron CpMoX(2)L(2) (X = 1-electron ligand; L = 2-electron ligand). The calculations point to the paramount importance of electron pairing energy: 22.53 kcal/mol must be spent to promote the ground state (4)A '' CpCrCl(2)(PH3) to the (2)A' excited state, and only 16.51 kcal/mol are regained upon formation of the second Cr-PH, bond. The cost of pairing the electrons in CpMoCl(2)(PH3), on the other hand, is much less (3.95 kcal/mol) and the bond formation energy along the spin doublet surface is 12.26 kcal/mol. The relevance of electron pairing energy as a stabilizing factor for the general class of open-shell organometallics is pointed out.
1997
Cacelli, Ivo; Keogh, Dw; Poli, R; Rizzo, A.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/46027
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