Configuration-controllable synthesis of Z/E isomers based on o-carborane-functionalized tetraphenylethene-Reference-Cited by-同舟云学术

Configuration-controllable synthesis of Z/E isomers based on o-carborane-functionalized tetraphenylethene

Published:2021 Issue:29 Volume:45 Page:12830-12837
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Zhou Qin¹²³⁴⁵,Zhu Miao¹²³⁴⁵,Chen Wei¹²³⁴⁵,Qin Na¹²³⁴⁵,Liu Yujie¹²³⁴⁵,Zhang Weihua¹²³⁴⁵,Li Xiang¹²³⁴⁵^ORCID,Sha Ye⁶⁷⁸⁹⁵^ORCID,Yan Hong¹⁰¹¹¹²¹³⁵^ORCID

Affiliation:

1. Jiangsu Key Laboratory of Pesticide Science and Department of Chemistry

2. College of Sciences

3. Nanjing Agricultural University

4. Nanjing 210095

5. China

6. Department of Chemistry and Material Science

7. College of Science

8. Nanjing Forestry University

9. Nanjing 210037

10. State Key Laboratory of Coordination Chemistry

11. School of Chemistry and Chemical Engineering

12. Nanjing University

13. Nanjing

Abstract

Two Z/E isomers, namely, Z-TPE-2Car and E-TPE-2Car, with clear configuration were synthesized using an effective route and have high solid-state fluorescence quantum yields, reaching 99% and 90%, respectively.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2021/NJ/D1NJ02029C

Reference59 articles.

1. High-Contrast On/Off Fluorescence Switching via Reversible E–Z Isomerization of Diphenylstilbene Containing the α-Cyanostilbenic Moiety

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5. Interindividual variation in the isomerization of 4- hydroxytamoxifen by human liver microsomes: involvement of cytochromes P450

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