Stepwise double excited-state proton transfer is not possible in 7-azaindole dimer-Reference-Cited by-同舟云学术

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Stepwise double excited-state proton transfer is not possible in 7-azaindole dimer

Published:2015 Issue:10 Volume:6 Page:5762-5767
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Crespo-Otero Rachel¹²³⁴,Kungwan Nawee⁵⁶⁷⁸⁹,Barbatti Mario¹⁰¹¹¹²^ORCID

Affiliation:

1. School of Biological and Chemical Sciences

2. Queen Mary University of London

3. London E1 4NS

4. UK

5. Department of Chemistry

6. Faculty of Science

7. Chiang Mai University

8. Chiang Mai 50200

9. Thailand

10. Max-Planck-Institut für Kohlenforschung

11. Mülheim an der Ruhr

12. Germany

Abstract

Topographical analysis of the dimer's excited state shows that internal conversion after first proton transfer blocks the stepwise process.

Funder

German Academic Exchange Service

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/SC/C5SC01902H

Reference44 articles.

1. EXCITED-STATE TWO-PROTON TAUTOMERISM IN HYDROGEN-BONDED N-HETEROCYCLIC BASE PAIRS

2. Femtosecond molecular dynamics of tautomerization in model base pairs

3. H-bonded N-heterocyclic base-pair phototautomerizational potential barrier and mechanism: The 7-azaindole dimer

4. The answer to concerted versus step-wise controversy for the double proton transfer mechanism of 7-azaindole dimer in solution

5. Resolution of concerted versus sequential mechanisms in photo-induced double-proton transfer reaction in 7-azaindole H-bonded dimer

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