M−P versus MM Bonds as Protonation Sites in the Organophosphide-Bridged Complexes [M2Cp2(μ-PR2)(μ-PR‘2)(CO)2], (M = Mo, W; R, R‘ = Ph, Et, Cy)-Reference-Cited by-同舟云学术

M−P versus MM Bonds as Protonation Sites in the Organophosphide-Bridged Complexes [M2Cp2(μ-PR2)(μ-PR‘2)(CO)2], (M = Mo, W; R, R‘ = Ph, Et, Cy)

Published:2006-07-27 Issue:17 Volume:45 Page:6965-6978
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Alvarez M. Angeles¹,García M. Esther¹,Martínez M. Eugenia¹,Ramos Alberto¹,Ruiz Miguel A.¹,Sáez David¹,Vaissermann Jacqueline¹

Affiliation:

1. Departamento de Química Orgánica e Inorgánica/IUQOEM, Universidad de Oviedo, E-33071 Oviedo, Spain, and Laboratoire de Chimie Inorganique et Matériaux Moléculaires, Université P. et M. Curie, 4 Place Jussieu, 75252 Paris, Cedex 05, France

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ic060544n

Reference64 articles.

1. Reactions of the metal-metal triple bond in Cp2Mo2(CO)4 and related complexes

2. Unsaturated Dimetal Cyclopentadienyl Carbonyl Complexes

3. A Highly Electrophilic Unsaturated Ditungsten Dication

4. Chemistry of Highly Electrophilic Binuclear Cations. 1. Oxidation Reactions of [M2(η5-C5H5)2(CO)4(μ-Ph2PCH2PPh2)] (M = Mo, W) with [FeCp2]X (X = BF4, PF6)

5. Chemistry of Highly Electrophilic Binuclear Cations. 2. Oxidation Reactions of [W2(η5-C5H5)2(CO)4(μ-Ph2PCH2PPh2)] with [FeCp2][B{3,5-C6H3(CF3)2}4]

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