2014
DOI: 10.1016/j.jphotochem.2014.04.009
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Phosphorescence of BODIPY dyes

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Cited by 45 publications
(31 citation statements)
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“…[46][47][48][49] However, reports of phosphorescence emission of metal-free Bodipy derivatives are still rare and are restricted to low temperature or deoxidized conditions. [50][51][52][53] Herein, two pure organic NIR RTP emitting materials in the amorphous state are facilely prepared by radical binary copolymerization of acrylamide and iodine-substituted Bodipy dyes (Scheme 1). The heavy atom effect of iodine can enhance the spin-orbital coupling and facilitate the ISC process.…”
Section: Introductionmentioning
confidence: 99%
“…[46][47][48][49] However, reports of phosphorescence emission of metal-free Bodipy derivatives are still rare and are restricted to low temperature or deoxidized conditions. [50][51][52][53] Herein, two pure organic NIR RTP emitting materials in the amorphous state are facilely prepared by radical binary copolymerization of acrylamide and iodine-substituted Bodipy dyes (Scheme 1). The heavy atom effect of iodine can enhance the spin-orbital coupling and facilitate the ISC process.…”
Section: Introductionmentioning
confidence: 99%
“…Additionally, the electron-rich BODIPY core also allows facile synthetic modification to tune the absorption, emission properties. In recent years halogenation of BODIPY core has been used to increase the efficiency of intersystem crossing and formation of triplet state by enhancing spin-orbit coupling [35,36]. Photosensitisers derived from BODIPY have been widely studied over the last decade for their potential applications in photodynamic therapy [37], however, phosphorescence of halogenated BODIPY dyes and their quenching by molecular oxygen has not been thoroughly explored.…”
Section: Introductionmentioning
confidence: 99%
“…10). 104,120 The Ί T increased to 0.66 for the hexa bromoBodipy. The 60 corresponding Ί Δ is up to 0.64.…”
mentioning
confidence: 96%