Photoinduced electron transfer in covalent ruthenium–anthraquinone dyads: relative importance of driving-force, solvent polarity, and donor–bridge energy gap-Reference-Cited by-同舟云学术

Photoinduced electron transfer in covalent ruthenium–anthraquinone dyads: relative importance of driving-force, solvent polarity, and donor–bridge energy gap

Published:2012 Issue:8 Volume:14 Page:2685
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Hankache Jihane,Wenger Oliver S.

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2012/CP/C2CP23240E

Reference72 articles.

1. Ru(II) polypyridine complexes: photophysics, photochemistry, eletrochemistry, and chemiluminescence

2. Long-range electron transfer in artificial systems with d6 and d8 metal photosensitizers

3. Bis(2,2‘-bipyridine)(1,2-diimino-9,10-anthraquinone)ruthenium(II) Derivatives: A ZINDO Analysis of a Redox Series Involving Coupled Proton and Electron Transfers

4. Photoinduced electron transfer from excited [tris(2,2′-bipyridine)ruthenium(II)]2+ to a series of anthraquinones with small positive or negative Gibbs energy of reaction. Marcus behavior and negative activation enthalpies

5. Photo-Induced Electron Transfer from Excited Tris[2,2′-bipyridine-κN1,κN1′]ruthenium(2+) Ions to Dyadic Electron Acceptors That Can Be Protected by Host-Guest Interaction against Fast Back Electron Transfer, Characterization of the Guest Molecules

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