Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution
Publication type: Journal Article
Publication date: 2006-01-01
scimago Q1
wos Q2
SJR: 1.037
CiteScore: 7.4
Impact factor: 4.2
ISSN: 13597345, 1364548X
DOI:
10.1039/B512756D
PubMed ID:
16391729
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Abstract
The BODIPY chromophore can be easily modified by nucleophilic mono- or disubstitution of 3,5-dichloroBODIPY with O-, N-, S- and C-nucleophiles. Absorption and fluorescence spectral data of the new BODIPY derivatives are also reported.
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Metrics
264
Total citations:
264
Citations from 2024:
17
(6.44%)
Cite this
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RIS |
BibTex
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GOST
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Rohand T. et al. Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution // Chemical Communications. 2006. Vol. 3. pp. 266-268.
GOST all authors (up to 50)
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Rohand T., Baruah M., Qin W., Boens N., Dehaen W. Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution // Chemical Communications. 2006. Vol. 3. pp. 266-268.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1039/B512756D
UR - https://doi.org/10.1039/B512756D
TI - Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution
T2 - Chemical Communications
AU - Rohand, Taoufik
AU - Baruah, Mukulesh
AU - Qin, Wenwu
AU - Boens, Noël
AU - Dehaen, Wim
PY - 2006
DA - 2006/01/01
PB - Royal Society of Chemistry (RSC)
SP - 266-268
IS - 3
PMID - 16391729
SN - 1359-7345
SN - 1364-548X
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2006_Rohand,
author = {Taoufik Rohand and Mukulesh Baruah and Wenwu Qin and Noël Boens and Wim Dehaen},
title = {Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution},
journal = {Chemical Communications},
year = {2006},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/B512756D},
number = {3},
pages = {266--268},
doi = {10.1039/B512756D}
}
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