Development of BODIPY dyes with versatile functional groups at 3,5-positions from diacyl peroxides via Cu(ii)-catalyzed radical alkylation-Reference-Cited by-同舟云学术

Development of BODIPY dyes with versatile functional groups at 3,5-positions from diacyl peroxides via Cu(ii)-catalyzed radical alkylation

Published:2019 Issue:32 Volume:55 Page:4691-4694
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Tang Bing¹²³⁴⁵,Lv Fan¹²³⁴⁵,Chen Kangkang¹²³⁴⁵,Jiao Lijuan¹²³⁴⁵^ORCID,Liu Qingyun⁶⁷⁸⁵^ORCID,Wang Hua¹²³⁴⁵,Hao Erhong¹²³⁴⁵^ORCID

Affiliation:

1. The Key Laboratory of Functional Molecular Solids, Ministry of Education

2. School of Chemistry and Materials Science

3. Anhui Normal University

4. Wuhu

5. China

6. College of Chemistry and Environmental Engineering

7. Shandong University of Science and Technology

8. Qingdao

Abstract

A Cu(ii)-catalyzed, α-regioselective C–H alkylation of BODIPY with alkyl diacyl peroxides provides structurally diverse alkylated BODIPYs via a radical pathway.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/CC/C9CC01602C

Reference49 articles.

1. BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic Properties

2. The Chemistry of Fluorescent Bodipy Dyes: Versatility Unsurpassed

3. Structural modification strategies for the rational design of red/NIR region BODIPYs

4. Far-red and near infrared BODIPY dyes: synthesis and applications for fluorescent pH probes and bio-imaging

5. Azadipyrromethenes: from traditional dye chemistry to leading edge applications

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