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Updated: Mar 6, 2026
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Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions
Published on: July 17, 2020
Pyridinium-Substituted TetraphenylethyleneEntailing Alkyne Moiety: Enhancement of Photosensitizing Efficiency and
Xue You1,2, Huili Ma3, Yuancheng Wang1,2
1CAS Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, P.R. China.
Abstract:
Apart from sensing and imaging, luminogens with aggregation-induced emission (AIE) are also interesting for photosensitizing. The photosensitizing behavior and bacteria-killing performance of a pyridinium-substituted tetraphenylethylene with an alkyne group (TPE-A-Py+ ) is reported herein. Interestingly, TPE-A-Py+ exhibits higher photosensitizing efficiency than TPE-Py+ (without alkyne group) when I- was used as a counteranion. This is well explained by the fact that the ΔΕST between the excited singlet state (S1 ) and triplet state (T1 ) was lower for TPE-A-Py+ than for TPE-Py+ , according to theoretical calculations. Moreover, replacement of I- with other anions (PF6- , N(SO2 CF3 )2- and BPh4- ) led to a decrease of photosensitizing efficiency for TPE-A-Py+ . Notably, TPE-A-Py+ could be used as an efficient photosensitizer to photo-inactivate ampicillin-resistant (ampr ) E. coli at low concentration under white-light irradiation very quickly.
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