Controlling the fluorescence quantum yields of benzothiazole-difluoroborates by optimal substitution-Reference-Cited by-同舟云学术

Controlling the fluorescence quantum yields of benzothiazole-difluoroborates by optimal substitution

Published:2022 Issue:45 Volume:13 Page:13347-13360
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Rybczyński Patryk¹,Bousquet Manon H. E.²,Kaczmarek-Kędziera Anna¹,Jędrzejewska Beata³^ORCID,Jacquemin Denis²⁴^ORCID,Ośmiałowski Borys¹^ORCID

Affiliation:

1. Faculty of Chemistry, Nicolaus Copernicus University in Toruń, Gagarina Street 7, 87-100 Toruń, Poland

2. Nantes Université, CNRS, CEISAM UMR 6230, F-44000 Nantes, France

3. Bydgoszcz University of Science and Technology, Faculty of Chemical Technology and Engineering, Seminaryjna 3, 85-326 Bydgoszcz, Poland

4. Institut Universitaire de France (IUF), Paris, FR-75005, France

Abstract

A full palette of FQY (form ca. 0 to 98%) was covered by exchanging two groups in a series of nine compounds. The darkest (OMe/CF3) and brightest (CF3/OMe) are isomers. All experimental data are supported by TD-DFT calculations.

Funder

Narodowe Centrum Nauki

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/SC/D2SC05044G

Reference67 articles.

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2. Twisted Intramolecular Charge Transfer and Aggregation-Induced Emission of BODIPY Derivatives

3. An Electron‐Accepting aza‐BODIPY‐Based Donor–Acceptor–Donor Architecture for Bright NIR Emission

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