Synthesis of carbazole-based BODIPY dimers showing red fluorescence in the solid state

Chihiro Maeda, Takumi Todaka, Tomomi Ueda, Tadashi Ema

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Carbazole-based BODIPY dimers 2a-g were synthesized via direct arylation. They showed red-shifted solid-state fluorescence spectra as compared with the corresponding monomer. In addition, unsymmetrical dimers 2d, 2f, and 2g with two different substituents showed red fluorescence with improved quantum yields in the solid state.

Original languageEnglish
Pages (from-to)9283-9287
Number of pages5
JournalOrganic and Biomolecular Chemistry
Volume15
Issue number44
DOIs
Publication statusPublished - Jan 1 2017

Fingerprint

carbazoles
Dimers
Fluorescence
dimers
solid state
fluorescence
Quantum yield
synthesis
monomers
Monomers
4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
carbazole

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

Synthesis of carbazole-based BODIPY dimers showing red fluorescence in the solid state. / Maeda, Chihiro; Todaka, Takumi; Ueda, Tomomi; Ema, Tadashi.

In: Organic and Biomolecular Chemistry, Vol. 15, No. 44, 01.01.2017, p. 9283-9287.

Research output: Contribution to journalArticle

@article{acc13897d1f344a38f568d67751ae317,
title = "Synthesis of carbazole-based BODIPY dimers showing red fluorescence in the solid state",
abstract = "Carbazole-based BODIPY dimers 2a-g were synthesized via direct arylation. They showed red-shifted solid-state fluorescence spectra as compared with the corresponding monomer. In addition, unsymmetrical dimers 2d, 2f, and 2g with two different substituents showed red fluorescence with improved quantum yields in the solid state.",
author = "Chihiro Maeda and Takumi Todaka and Tomomi Ueda and Tadashi Ema",
year = "2017",
month = "1",
day = "1",
doi = "10.1039/c7ob02419c",
language = "English",
volume = "15",
pages = "9283--9287",
journal = "Organic and Biomolecular Chemistry",
issn = "1477-0520",
publisher = "Royal Society of Chemistry",
number = "44",

}

TY - JOUR

T1 - Synthesis of carbazole-based BODIPY dimers showing red fluorescence in the solid state

AU - Maeda, Chihiro

AU - Todaka, Takumi

AU - Ueda, Tomomi

AU - Ema, Tadashi

PY - 2017/1/1

Y1 - 2017/1/1

N2 - Carbazole-based BODIPY dimers 2a-g were synthesized via direct arylation. They showed red-shifted solid-state fluorescence spectra as compared with the corresponding monomer. In addition, unsymmetrical dimers 2d, 2f, and 2g with two different substituents showed red fluorescence with improved quantum yields in the solid state.

AB - Carbazole-based BODIPY dimers 2a-g were synthesized via direct arylation. They showed red-shifted solid-state fluorescence spectra as compared with the corresponding monomer. In addition, unsymmetrical dimers 2d, 2f, and 2g with two different substituents showed red fluorescence with improved quantum yields in the solid state.

UR - http://www.scopus.com/inward/record.url?scp=85034419517&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85034419517&partnerID=8YFLogxK

U2 - 10.1039/c7ob02419c

DO - 10.1039/c7ob02419c

M3 - Article

VL - 15

SP - 9283

EP - 9287

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

SN - 1477-0520

IS - 44

ER -