Integration of inherent and induced chirality into subphthalocyanine analogue

July 28, 2017

Title

Integration of inherent and induced chirality into subphthalocyanine analogue

Author

Luyang Zhao, Dongdong Qi, Kang Wang, Tianyu Wang, Bing Han, Zhiyong Tang, Jianzhuang Jiang

Year

2016

Journal

Scientific Reports

Abstract

Conventional conjugated systems are characteristic of only either inherent or induced chirality because of synthetic challenge in combination of chiral segment into the main chromophore. In this work, chiral binaphthyl segment is directly fused into the central chromophore of a subphthalocyanine skeleton, resulting in a novel type of chiral subphthalocyanine analogue (R/S)-1 of integrated inherent and induced chirality. Impressively, an obviously enhanced optical activity is discerned for (R/S)-1 molecules, and corresponding enhancement mechanism is elucidated in detail. The synthesis strategy based on rational molecular design will open the door towards fabrication of chiral materials with giant optical activity, which will have great potential in chiroptical devices.

Instrument

J-1500

Keywords

Circular dichroism, Magnetic circular dichroism, Stereochemistry, Materials