Intramolecular RET enhanced visible light-absorbing bodipy organic triplet photosensitizers and application in photooxidation and triplet-triplet annihilation upconversion.
Publication type: Journal Article
Publication date: 2013-07-08
scimago Q1
wos Q1
SJR: 5.554
CiteScore: 22.5
Impact factor: 15.6
ISSN: 00027863, 15205126
PubMed ID:
23790008
General Chemistry
Catalysis
Biochemistry
Colloid and Surface Chemistry
Abstract
Resonance energy transfer (RET) was used for the first time to enhance the visible light absorption of triplet photosensitizers. The intramolecular energy donor (boron-dipyrromethene, Bodipy) and acceptor (iodo-Bodipy) show different absorption bands in visible region, thus the visible absorption was enhanced as compared to the monochromophore triplet photosensitizers (e.g., iodo-Bodipy). Fluorescence quenching and excitation spectra indicate that the singlet energy transfer is efficient for the dyad triplet photosensitizers. Nanosecond time-resolved transient absorption spectroscopy has confirmed that the triplet excited states of the dyads are distributed on both the energy donor and acceptor, which is the result of forward singlet energy transfer from the energy donor to the energy acceptor and in turn the backward triplet energy transfer. This 'ping-pong' energy transfer was never reported for organic molecular arrays, and so it is useful to study the energy level of organic chromophores. The triplet photosensitizers were used for singlet oxygen ((1)O2) mediated photooxidation of 1,5-dihydroxylnaphthalene to produce juglone. The visible light absorption of the new visible light-absorbing triplet photosensitizers are higher than the conventional monochromophore based triplet photosensitizers, as a result, the (1)O2 photosensitizing ability is improved with the new triplet photosensitizers. Triplet-triplet annihilation upconversion with these triplet photosensitizers was also studied. Our results are useful to design the triplet photosensitizers showing strong visible light absorbance and for their applications in photocatalysis and photodynamic therapy.
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Zhang C. et al. Intramolecular RET enhanced visible light-absorbing bodipy organic triplet photosensitizers and application in photooxidation and triplet-triplet annihilation upconversion. // Journal of the American Chemical Society. 2013. Vol. 135. No. 28. pp. 10566-10578.
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Zhang C., Zhao J., Wu S., Wang Z., Wu W., Ma J., Guo S., Huang L. Intramolecular RET enhanced visible light-absorbing bodipy organic triplet photosensitizers and application in photooxidation and triplet-triplet annihilation upconversion. // Journal of the American Chemical Society. 2013. Vol. 135. No. 28. pp. 10566-10578.
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TY - JOUR
DO - 10.1021/ja405170j
UR - https://doi.org/10.1021/ja405170j
TI - Intramolecular RET enhanced visible light-absorbing bodipy organic triplet photosensitizers and application in photooxidation and triplet-triplet annihilation upconversion.
T2 - Journal of the American Chemical Society
AU - Zhang, Caishun
AU - Zhao, Jianzhang
AU - Wu, Shuo
AU - Wang, Zilong
AU - Wu, Wanhua
AU - Ma, Jie
AU - Guo, Song
AU - Huang, Ling
PY - 2013
DA - 2013/07/08
PB - American Chemical Society (ACS)
SP - 10566-10578
IS - 28
VL - 135
PMID - 23790008
SN - 0002-7863
SN - 1520-5126
ER -
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@article{2013_Zhang,
author = {Caishun Zhang and Jianzhang Zhao and Shuo Wu and Zilong Wang and Wanhua Wu and Jie Ma and Song Guo and Ling Huang},
title = {Intramolecular RET enhanced visible light-absorbing bodipy organic triplet photosensitizers and application in photooxidation and triplet-triplet annihilation upconversion.},
journal = {Journal of the American Chemical Society},
year = {2013},
volume = {135},
publisher = {American Chemical Society (ACS)},
month = {jul},
url = {https://doi.org/10.1021/ja405170j},
number = {28},
pages = {10566--10578},
doi = {10.1021/ja405170j}
}
Cite this
MLA
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Zhang, Caishun, et al. “Intramolecular RET enhanced visible light-absorbing bodipy organic triplet photosensitizers and application in photooxidation and triplet-triplet annihilation upconversion..” Journal of the American Chemical Society, vol. 135, no. 28, Jul. 2013, pp. 10566-10578. https://doi.org/10.1021/ja405170j.