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Dual Functioning Thieno-Pyrrole Fused BODIPY Dyes for NIR Optical Imaging and Photodynamic Therapy: Singlet Oxygen Generation without Heavy Halogen Atom Assistance.


ABSTRACT: We discovered a rare phenomenon wherein a thieno-pyrrole fused BODIPY dye (SBDPiR690) generates singlet oxygen without heavy halogen atom substituents. SBDPiR690 generates both singlet oxygen and fluorescence. To our knowledge, this is the first example of such a finding. To establish a structure-photophysical property relationship, we prepared SBDPiR analogs with electron-withdrawing groups at the para-position of the phenyl groups. The electron-withdrawing groups increased the HOMO-LUMO energy gap and singlet oxygen generation. Among the analogs, SBDPiR688, a CF3 analog, had an excellent dual functionality of brightness (82290?m(-1) ?cm(-1) ) and phototoxic power (99170?m(-1) ?cm(-1) ) comparable to those of Pc 4, due to a high extinction coefficient (211?000?m(-1) ?cm(-1) ) and balanced decay (?flu =0.39 and ?? =0.47). The dual functionality of the lead compound SBDPiR690 was successfully applied to preclinical optical imaging and for PDT to effectively control a subcutaneous tumor.

SUBMITTER: Watley RL 

PROVIDER: S-EPMC7297209 | biostudies-literature | 2015 Jun

REPOSITORIES: biostudies-literature

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Dual Functioning Thieno-Pyrrole Fused BODIPY Dyes for NIR Optical Imaging and Photodynamic Therapy: Singlet Oxygen Generation without Heavy Halogen Atom Assistance.

Watley Ryan L RL   Awuah Samuel G SG   Bio Moses M   Cantu Robert R   Gobeze Habtom B HB   Nesterov Vladimir N VN   Das Sushanta K SK   D'Souza Francis F   You Youngjae Y  

Chemistry, an Asian journal 20150423 6


We discovered a rare phenomenon wherein a thieno-pyrrole fused BODIPY dye (SBDPiR690) generates singlet oxygen without heavy halogen atom substituents. SBDPiR690 generates both singlet oxygen and fluorescence. To our knowledge, this is the first example of such a finding. To establish a structure-photophysical property relationship, we prepared SBDPiR analogs with electron-withdrawing groups at the para-position of the phenyl groups. The electron-withdrawing groups increased the HOMO-LUMO energy  ...[more]

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