Different Mechanisms of Photochemical Re−Me and Re−Et Bond Homolysis in [Re(R)(CO)3(4,4‘-dimethyl-2,2‘-bipyridine)]. A Time-Resolved IR Spectroscopic Study Ranging from Picoseconds to Microseconds-Reference-Cited by-同舟云学术

Different Mechanisms of Photochemical Re−Me and Re−Et Bond Homolysis in [Re(R)(CO)3(4,4‘-dimethyl-2,2‘-bipyridine)]. A Time-Resolved IR Spectroscopic Study Ranging from Picoseconds to Microseconds

Published:2006-03-21 Issue:9 Volume:25 Page:2148-2156
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Gabrielsson Anders¹,Blanco-Rodríguez Ana María¹,Matousek Pavel¹,Towrie Mike¹,Vlček Antonín¹

Affiliation:

1. School of Biological and Chemical Sciences, Queen Mary, University of London, Mile End Road, London E1 4NS, United Kingdom, and Central Laser Facility, CCLRC Rutherford Appleton Laboratory, Chilton, Didcot, Oxfordshire OX11 0QX, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om0508886

Reference64 articles.

1. Light Sensitive Organometallic Compounds in Photopolymerization

2. Syntheses, spectroscopic properties and photochemistry of [Re(R)(CO)3(4,4′-Me2-bpy)] (R=alkyl) complexes

3. Metal to ligand charge transfer photochemistry of Re(I)-alkyl complexes

4. Photoinduced Radical Formation from the Complexes [Re(R)(CO)3(4,4‘-Me2-bpy)] (R = CH3, CD3, Et, iPr, Bz): A Nanosecond Time-Resolved Emission, UV−Vis and IR Absorption, and FT-EPR Study

5. Ultrafast Dynamics of Photochemical Radical Formation from [Re(R)(CO)3(dmb)] (R=Me, Et; dmb=4,4′-dimethyl-2,2′-bipyridine): A Femtosecond Time-Resolved Visible Absorption Study

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