Construction of diene-extended meso-CF3-BODIPY for spectroscopic study and photothermal exploration
The thermogenesis process is enhanced by the accelerated non-radiative transition energy dissipation induced by the free rotation of the –CF3 group at meso-site in BODIPY system, which is a valuable strategy for tumor photothermal therapy. In this work, we first introduced the diene bonds to meso-CF...
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Published in | Dyes and pigments Vol. 218; p. 111500 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
01.10.2023
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Subjects | |
Online Access | Get full text |
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Summary: | The thermogenesis process is enhanced by the accelerated non-radiative transition energy dissipation induced by the free rotation of the –CF3 group at meso-site in BODIPY system, which is a valuable strategy for tumor photothermal therapy. In this work, we first introduced the diene bonds to meso-CF3-BODIPY at 3,5-sites. This diene-extended meso-CF3-BODIPY possessed remarkable photostability with a near-infrared absorption (λabs = 836 nm), and the fluorescence emission and triplet transition are both inhibited. meso-CF3-BODIPY-NPs by self-assembly has a photothermal conversion efficiency (PCE: 44.4%) and good promotion of cancer cell apoptosis upon irradiation. Therefore, this molecular design performed as a critical reference for the construction of forthcoming photothermal reagents.
•The diene bonds were introduced to meso-CF3-BODIPY at 3,5-sites.•This diene-extended meso-CF3-BODIPY possessed near-infrared absorption (λabs = 836 nm).•meso-CF3-BODIPY-NPs by self-assembly had a photothermal conversion efficiency (PCE: 44.4%) and could kill cancer cells via apoptosis upon irradiation. |
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ISSN: | 0143-7208 1873-3743 |
DOI: | 10.1016/j.dyepig.2023.111500 |