Investigation of side chain liquid crystal polymers bearing cholesterol and bile acid derivatives

作     者：Stephen Freiberg Franεois Brisse C. Géraldine Bazuin 

作者机构：Département de chimie Université de Montréal C. P. 6128 succursale Centre-ville Montreal (QC) CanadaH3C 3J7. Département de chimie Université de Montréal C. P. 6128 succursale Centre-ville Montreal (QC) CanadaH3C 3J7. Département de chimie Université de Montréal C. P. 6128 succursale Centre-ville Montreal (QC) CanadaH3C 3J7. 

出 版 物：《合成化学》 (Chinese Journal of Synthetic Chemistry)

年 卷 期：2004年第12卷第Z1期

页      面：79-79页

学科分类：07[理学] 0703[理学-化学] 

基　　金：Financially supported by the Natural Sciences and Engineering Research Council (NSERC) ofCanada Canada Research Chair Program and the Fond québécois de recherche et nature en technologie (FQRNT) ofQuebec 

主　　题：bile acids, liquid-crystalline polymers, X-ray 

摘      要：Cholic acid (or 3a,7a,12a-trihydoxyl-5a-cholan-24-oic acid) and lithocholic acid (or 3a-hydroxyl-5a-cholanic-24-oic acid) are commonly occurring bile acids synthesized from cholesterol in the liver in mammals. They all possess a steroid skeleton containing four rings, three with six carbons and one with five carbons. The transformation of cholesterol to cholic acid results in two major structural changes that affect the steroid skeleton. The first is the hydrogenation of the double bond between C5 and C6 and the second is a conformational flip of ring A from the 5a-position to the 5a-position. In addition, one or more hydroxyl groups are added to the steroid skeleton. Outside of the ring system, C24 is converted from a saturated alkyl to a carboxylic acid *** chain polymers based on cholesterol moiety have been made as reported in the *** bile acids and cholesterol are all in the family of steroid molecules, it is of interest to investigate whether bile acids may also act as mesogenic ***, flexible spacer groups with 10 carbons are introduced between bile acid skeleton and the poymerizable double bonds. The monomers and polymers are compared with cholesterol and dihydrocholesterol monomers and polymers with the same spacers. Dihydrocholesterol is chosen to investigate the influence of the double bond in the formation of LC, given that both cholesterol and dihydrocholesterol have a planar structure but there is no double bond in the latter. These monomers and their corresponding polymers were characterized for their liquid crystalline (LC) properties by differential scanning calorimetry (DSC), polarizing optical microscopy (POM) and X-ray *** was found that only the compounds bearing the planar cholesterol moieties possess LC phases. It is concluded that the 5a-configuration between the first and second cycles on the steroid skeleton of bile acids does not favor proper alignment of the rigid part of the bile acid moieties.