New molecular design for blue BODIPYs-Reference-Cited by-同舟云学术

New molecular design for blue BODIPYs

Published:2019 Issue:19 Volume:43 Page:7233-7242
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Wu Zhiyuan¹²³⁴^ORCID,Fujita Hikaru¹²³⁴^ORCID,Magdaong Nikki Cecil M.¹⁵⁶⁴^ORCID,Diers James R.¹⁷⁸⁴^ORCID,Hood Don¹⁵⁶⁴^ORCID,Allu Srinivasarao¹²³⁴^ORCID,Niedzwiedzki Dariusz M.⁹¹⁰⁵⁶⁴^ORCID,Kirmaier Christine¹⁵⁶⁴^ORCID,Bocian David F.¹⁷⁸⁴^ORCID,Holten Dewey¹⁵⁶⁴^ORCID,Lindsey Jonathan S.¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. North Carolina State University

3. Raleigh

4. USA

5. Washington University

6. St. Louis

7. University of California

8. Riverside

9. Department of Energy

10. Environmental & Chemical Engineering, and Center for Solar Energy and Energy Storage

Abstract

Dihydro analogues of BODIPYs exhibit spectral features (Φ_f ∼ 0.4–0.9) resembling aminocoumarins and suggest applications for broad-band photosensitization or where large Stokes shifts are desired.

Funder

Basic Energy Sciences

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/NJ/C9NJ01114E

Reference35 articles.

1. Difluorboryl-Komplexe von Di- und Tripyrrylmethenen

2. Boron-dipyrromethene dyes for incorporation in synthetic multi-pigment light-harvesting arrays

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

4. The chemistry of Bodipy: A new El Dorado for fluorescence tools

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