|
Type |
Poster Presentation |
Area |
Organic Chemistry |
Room No. |
Event Hall |
Time |
4월 19일 (목요일) 11:00~12:30 |
Code |
ORGN.P-350 |
Subject |
Preparation of dial for synthesis of 9,9’,13,13’-tetra-Pheyl-substituted-carotenoids |
Authors |
Hyebin Yoo, Sangho KOO1,* Department of Energy Science and Technology, Myungji University, Korea 1Department of Chemistry, Myungji University, Korea |
Abstract |
Phenyl substituents attached to the polyene chain provide not only improved stability, but also diverse physicochemical characteristics, depending on the electronic nature of the substituent. Carotene with tetra-Phenyl substituents has better electrical conductivity than carotene with di-Phenyl substituents. Carotenoid molecular wires containing tetra-Phenyl substituents can be assembled by the Wittig reaction between tetra-Phenyl-substituted-dial and 4-thiomethylbenzyl phosphonium bromide(Wittig salt). tetra-Phenyl-substitued-dial can be effectively synthesized by the Julia-Kocienski olefination of the Phenyl-substituted-C5-BT(benzothiazole)-sulfone with C10 2,7-diphenyl-2,4,6-octatrienedial. |
E-mail |
qlsl94@hanmail.net |
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