Synthesis, electrochemical, spectral and DFT study of novel thiazole-annelated subphthalocyanines with inherent chirality
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文摘

Subphthalocyanines (SubPcs) with annelated thiazole rings were synthesized.

SubPcs with C3-symmetry were resolved to enantiomers.

Electrochemical and spectral experiments correlate well with DFT calculations.

All novel SubPcs exhibit high quantum yields of singlet oxygen production.

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