Unprecedented phthalocyanine–porphyrin-fused oligomers with induced chirality nature

August 13, 2018

Title

Unprecedented phthalocyanine–porphyrin-fused oligomers with induced chirality nature

Author

Yuehong Zhang , Luyang Zhao , Kang Wang, Jianzhuang Jiang

Year

2017

Journal

Inorganic Chemistry Frontiers

Abstract

Optically active binaphthyl units have been introduced onto the periphery of the phthalocyanine chromophores in phthalocyanine–porphyrin-fused oligomers, resulting in the first (R)- and (S)-enantiomers of Pc–Por-fused dimer 1 and trimer 2 with induced chirality nature. This represents the largest chiral tetrapyrrole-based conjugated system, to the best of our knowledge. Electronic absorption, MCD, and CD spectroscopic results in combination with theoretical calculations disclose the effective transfer of the chiral information from the binaphthyl groups to both the central tetrapyrrole-fused chromophores, indicating the effective delocalization of the π-electron density over the fused systems due to the effective electronic communication between/among the tetrapyrrole chromophores.

Instrument

J-1500

Keywords

Circular dichroism, Magnetic circular dichroism, Stereochemistry, Inorganic chemistry