Open Access
Open access
volume 12 issue 19 pages 6607-6628

Design of BODIPY dyes as triplet photosensitizers: electronic properties tailored for solar energy conversion, photoredox catalysis and photodynamic therapy

Elena Bassan 1, 2, 3, 4
Andrea Gualandi 1, 2, 3, 4
Pier Giorgio Cozzi 1, 2, 3, 4
Paola Ceroni 1, 2, 3, 4
Publication typeJournal Article
Publication date2021-04-15
scimago Q1
wos Q1
SJR2.138
CiteScore12.6
Impact factor7.4
ISSN20416520, 20416539
PubMed ID:  34040736
General Chemistry
Abstract
BODIPYs are renowned fluorescent dyes with strong and tunable absorption in the visible region, high thermal and photo-stability and exceptional fluorescence quantum yields. Transition metal complexes are the most commonly used triplet photosensitisers, but, recently, the use of organic dyes has emerged as a viable and more sustainable alternative. By proper design, BODIPY dyes have been turned from highly fluorescent labels into efficient triplet photosensitizers with strong absorption in the visible region (from green to orange). In this perspective, we report three design strategies: (i) halogenation of the dye skeleton, (ii) donor–acceptor dyads and (iii) BODIPY dimers. We compare pros and cons of these approaches in terms of optical and electrochemical properties and synthetic viability. The potential applications of these systems span from energy conversion to medicine and key examples are presented.
Found 
Found 

Top-30

Journals

2
4
6
8
10
12
14
16
Dyes and Pigments
16 publications, 6.04%
Chemistry - A European Journal
12 publications, 4.53%
Physical Chemistry Chemical Physics
10 publications, 3.77%
Coordination Chemistry Reviews
10 publications, 3.77%
Chemical Science
10 publications, 3.77%
Journal of Organic Chemistry
7 publications, 2.64%
New Journal of Chemistry
7 publications, 2.64%
Organic Letters
6 publications, 2.26%
Chemical Communications
6 publications, 2.26%
Journal of Materials Chemistry C
6 publications, 2.26%
Molecules
5 publications, 1.89%
Journal of Fluorescence
5 publications, 1.89%
ChemPhotoChem
5 publications, 1.89%
Angewandte Chemie
5 publications, 1.89%
Angewandte Chemie - International Edition
5 publications, 1.89%
Journal of Chemical Physics
5 publications, 1.89%
Journal of the American Chemical Society
5 publications, 1.89%
Journal of Molecular Structure
5 publications, 1.89%
Journal of Medicinal Chemistry
4 publications, 1.51%
Journal of Photochemistry and Photobiology A: Chemistry
4 publications, 1.51%
Photochemistry and Photobiology
4 publications, 1.51%
Journal of Physical Chemistry Letters
4 publications, 1.51%
Journal of Materials Chemistry B
4 publications, 1.51%
Journal of Physical Chemistry B
4 publications, 1.51%
Tetrahedron
4 publications, 1.51%
International Journal of Molecular Sciences
3 publications, 1.13%
Photochemical and Photobiological Sciences
3 publications, 1.13%
Bioorganic Chemistry
3 publications, 1.13%
Journal of Porphyrins and Phthalocyanines
3 publications, 1.13%
Dalton Transactions
3 publications, 1.13%
2
4
6
8
10
12
14
16

Publishers

10
20
30
40
50
60
70
Elsevier
61 publications, 23.02%
Royal Society of Chemistry (RSC)
60 publications, 22.64%
American Chemical Society (ACS)
51 publications, 19.25%
Wiley
51 publications, 19.25%
MDPI
13 publications, 4.91%
Springer Nature
11 publications, 4.15%
AIP Publishing
6 publications, 2.26%
World Scientific
3 publications, 1.13%
Beilstein-Institut
2 publications, 0.75%
Shanghai Institute of Organic Chemistry
2 publications, 0.75%
Japan Society of Applied Physics
1 publication, 0.38%
Lviv Polytechnic National University
1 publication, 0.38%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 0.38%
Georg Thieme Verlag KG
1 publication, 0.38%
Walter de Gruyter
1 publication, 0.38%
10
20
30
40
50
60
70
  • We do not take into account publications without a DOI.
  • Statistics recalculated weekly.

Are you a researcher?

Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
265
Share
Cite this
GOST |
Cite this
GOST Copy
Bassan E. et al. Design of BODIPY dyes as triplet photosensitizers: electronic properties tailored for solar energy conversion, photoredox catalysis and photodynamic therapy // Chemical Science. 2021. Vol. 12. No. 19. pp. 6607-6628.
GOST all authors (up to 50) Copy
Bassan E., Gualandi A., Cozzi P. G., Ceroni P. Design of BODIPY dyes as triplet photosensitizers: electronic properties tailored for solar energy conversion, photoredox catalysis and photodynamic therapy // Chemical Science. 2021. Vol. 12. No. 19. pp. 6607-6628.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1039/d1sc00732g
UR - https://xlink.rsc.org/?DOI=D1SC00732G
TI - Design of BODIPY dyes as triplet photosensitizers: electronic properties tailored for solar energy conversion, photoredox catalysis and photodynamic therapy
T2 - Chemical Science
AU - Bassan, Elena
AU - Gualandi, Andrea
AU - Cozzi, Pier Giorgio
AU - Ceroni, Paola
PY - 2021
DA - 2021/04/15
PB - Royal Society of Chemistry (RSC)
SP - 6607-6628
IS - 19
VL - 12
PMID - 34040736
SN - 2041-6520
SN - 2041-6539
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2021_Bassan,
author = {Elena Bassan and Andrea Gualandi and Pier Giorgio Cozzi and Paola Ceroni},
title = {Design of BODIPY dyes as triplet photosensitizers: electronic properties tailored for solar energy conversion, photoredox catalysis and photodynamic therapy},
journal = {Chemical Science},
year = {2021},
volume = {12},
publisher = {Royal Society of Chemistry (RSC)},
month = {apr},
url = {https://xlink.rsc.org/?DOI=D1SC00732G},
number = {19},
pages = {6607--6628},
doi = {10.1039/d1sc00732g}
}
MLA
Cite this
MLA Copy
Bassan, Elena, et al. “Design of BODIPY dyes as triplet photosensitizers: electronic properties tailored for solar energy conversion, photoredox catalysis and photodynamic therapy.” Chemical Science, vol. 12, no. 19, Apr. 2021, pp. 6607-6628. https://xlink.rsc.org/?DOI=D1SC00732G.