Abstract
AbstractThe N‐heterocyclic carbene–phosphinidene adduct IPrPSiMe3 is introduced as a synthon for the preparation of terminal carbene–phosphinidyne transition metal complexes of the type [(IPrP)MLn] (MLn=(η6‐p‐cymene)RuCl) and (η5‐C5Me5)RhCl). Their spectroscopic and structural characteristics, namely low‐field 31P NMR chemical shifts and short metal–phosphorus bonds, show their similarity with arylphosphinidene complexes. The formally mononegative IPrP ligand is also capable of bridging two or three metal atoms as demonstrated by the preparation of bi‐ and trimetallic RuAu, RhAu, Rh2, and Rh2Au complexes.
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Dates
Type | When |
---|---|
Created | 10 years, 10 months ago (Oct. 6, 2014, 4:31 p.m.) |
Deposited | 1 year, 10 months ago (Oct. 17, 2023, 6:31 p.m.) |
Indexed | 1 year, 1 month ago (July 24, 2024, 5:07 a.m.) |
Issued | 10 years, 10 months ago (Oct. 6, 2014) |
Published | 10 years, 10 months ago (Oct. 6, 2014) |
Published Online | 10 years, 10 months ago (Oct. 6, 2014) |
Published Print | 10 years, 8 months ago (Dec. 1, 2014) |
@article{Doddi_2014, title={N‐Heterocyclic Carbene–Phosphinidyne Transition Metal Complexes}, volume={126}, ISSN={1521-3757}, url={http://dx.doi.org/10.1002/ange.201408354}, DOI={10.1002/ange.201408354}, number={49}, journal={Angewandte Chemie}, publisher={Wiley}, author={Doddi, Adinarayana and Bockfeld, Dirk and Bannenberg, Thomas and Jones, Peter G. and Tamm, Matthias}, year={2014}, month=oct, pages={13786–13790} }