The First Five‐Membered‐Heterocycle‐Fused Subphthalocyanine Analogues: Chiral Tri(benzo[b]thiopheno)subporphyrazines

August 13, 2018

Title

The First Five‐Membered‐Heterocycle‐Fused Subphthalocyanine Analogues: Chiral Tri(benzo[b]thiopheno)subporphyrazines

Author

Hong Shang, Luyang Zhao, Dongdong Qi, Chao Chen, Jianzhuang Jiang

Year

2014

Journal

Chemistry A European Journal

Abstract

Two tri(benzo[b]thiopheno)subporphyrazine regioisomers with C3 and C1 molecular symmetry have been isolated from the cyclotrimerization of benzo[b]thiophene‐2,3‐dicarbonitrile as the first five‐membered‐heterocycle‐fused subphthalocyanine analogues. Optical resolution of both regioisomers was achieved by using a chiral HPLC technique, affording the first chiral subphthalocyanine analogues.

Instrument

J-1500

Keywords

Circular dichroism, Magnetic circular dichroism, Stereochemistry, Soret band, Chemical stability, Organic chemistry, Materials