Bulletin of the Chemical Society of Japan

Introduction of a Disulfide Bond as a Key Element of Acyclic Bis-Thiourea-Type Anion Receptors

K Tomita, T Ishioka, A Harata

Index: Tomita, Kentaro; Ishioka, Toshio; Harata, Akira Bulletin of the Chemical Society of Japan, 2014 , vol. 87, # 3 p. 425 - 434

Full Text: HTML

Citation Number: 0

Abstract

This article shows that a difference in the building blocks of the molecular framework, C–C to S–S, results in a significant influence on its optical properties. Acyclic anion receptors, bis {2- [3-(substituted) thioureido] ethyl} disulfides were newly synthesized, and their optical properties in response to complex formation with an acetate ion were compared with those of a hexamethylene framework between two thioureido groups. Quantum chemical ...

Related Articles:

Selective colorimetric sensing of geometrical isomers of dicarboxylates in water by using functionalized gold nanoparticles

[Liu, Yanyun; Liu, Yun; Liang, Zhongshi; Li, Xiangyang; Liu, Shunying; Yu, Jiahui Chinese Journal of Chemistry, 2011 , vol. 29, # 3 p. 531 - 538]

2-Amino-2-thiazoline. IV. Ring-opening of 2-amino-2-thiazolines and 2-amino-2-selenazoline with hydrogen sulfide to form thiourea derivatives

[Klayman,D.L.; McIntyre,P.T. Journal of Organic Chemistry, 1968 , vol. 33, # 2 p. 884 - 887]

More Articles...