Aromaticity versus regioisomeric effect of β-substituents in porphyrinoids-Reference-Cited by-同舟云学术

Aromaticity versus regioisomeric effect of β-substituents in porphyrinoids

Published:2019 Issue:19 Volume:21 Page:10152-10162
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Yao Yuhang¹²³⁴⁵,Rao Yu¹²³⁴⁵,Liu Yiwei¹²³⁴⁵,Jiang Liang⁶⁷⁸⁹¹⁰,Xiong Jin¹²³⁴⁵,Fan Ying-Jie¹²³⁴⁵,Shen Zhen⁶⁷⁸⁹¹⁰^ORCID,Sessler Jonathan L.¹¹¹²¹³¹⁰¹⁴^ORCID,Zhang Jun-Long¹²³⁴⁵^ORCID

Affiliation:

1. Beijing National Laboratory for Molecular Sciences

2. State Key Laboratory of Rare Earth Materials Chemistry and Applications

3. College of Chemistry and Molecular Engineering

4. Peking University

5. Beijing 100871

6. State Key Laboratory of Coordination Chemistry

7. School of Chemistry and Chemical Engineering

8. Nanjing University

9. Nanjing 210093

10. P. R. China

11. Institute for Supramolecular Chemistry and Catalysis

12. Shanghai University

13. Shanghai

14. Department of Chemistry

Abstract

Maximizing the regioisomeric effect of β-substituents on photophysical properties of porphyrinoids through disruption of TT-conjugation and reducing the aromaticity.

Funder

National Natural Science Foundation of China

Welch Foundation

National Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2019/CP/C9CP01177C

Reference76 articles.

1. Formyl group modification of chlorophylla: a major evolutionary mechanism in oxygenic photosynthesis