Unravelling the early photochemical behavior of (8-substituted-7-hydroxyquinolinyl)methyl acetates through electronic structure theory and ultrafast transient absorption spectroscopy-Reference-Cited by-同舟云学术

Unravelling the early photochemical behavior of (8-substituted-7-hydroxyquinolinyl)methyl acetates through electronic structure theory and ultrafast transient absorption spectroscopy

Published:2017 Issue:2 Volume:19 Page:1089-1096
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Ma Jiani¹²³⁴⁵,Mewes Jan-Michael⁶⁷⁸⁹,Harris Kyle T.¹⁰¹¹¹²¹³,Dore Timothy M.¹⁰¹¹¹²¹³¹⁴^ORCID,Phillips David Lee¹⁰¹⁵⁵,Dreuw Andreas⁶⁷⁸⁹

Affiliation:

1. Key Laboratory of Synthetic and Natural Functional Molecular Chemistry of Ministry of Education

2. College of Chemistry and Materials Science

3. Northwest University

4. Xi'an

5. P. R. China

6. Interdisciplinary Center for Scientific Computing

7. University of Heidelberg

8. 69120 Heidelberg

9. Germany

10. Department of Chemistry

11. University of Georgia

12. Athens

13. USA

14. New York University Abu Dhabi

15. The University of Hong Kong

Abstract

Role of solvent, prototropic states, excited state proton transfers, and excited states on biological effector release from quinoline-based phototriggers.

Funder

Division of Chemistry

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2017/CP/C6CP05499D

Reference57 articles.

1. Photosensitive Protecting Groups

2. Photosensitive protection of functional groups

3. 654. Photochemical transformations. Part XIX. Some photosensitive protecting groups