DFT Study of the Role of Bridging Diphosphine Ligands in the Structure and the Internal Rotation in Quadruply Bonded Metal Dimers of the Mo2Cl4(P−P)2 Type-Reference-Cited by-同舟云学术

DFT Study of the Role of Bridging Diphosphine Ligands in the Structure and the Internal Rotation in Quadruply Bonded Metal Dimers of the Mo2Cl4(P−P)2 Type

Published:1999-10-29 Issue:23 Volume:38 Page:5443-5448
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Demachy Isabelle¹,Lledos Agusti¹,Jean Yves¹

Affiliation:

1. Laboratoire de Chimie Théorique, ESA Q8077, Bât. 490, Université de Paris-Sud, 91405 Orsay Cedex, France, and Departament de Quimica, Universitat Autonoma de Barcelona, 08193 Bellaterra, Catalonia, Spain

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ic990541t

Reference41 articles.

1. Structures of the bridged and chelated isomers of tetrachlorobis[1,2-bis(diphenylphosphino)ethane]ditungsten(II)

2. Molecular and electronic structures of two quadruply bonded ditungsten compounds and a dimolybdenum homolog

3. The synthesis and characterization of α-Re2Cl4(depe)2 and α-W2Cl4(depe)2

4. Solid-state structure of .alpha.-bis[bis(diphenylphosphino)ethane]tetrachlorodimolybdenum and its transformation to .beta.-bis[bis(diphenylphosphino)ethane]tetrachlorodimolybdenum. Evidence for the internal flip mechanism

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