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Hydrophobic terminal group of surfactant initiating micellization as revealed by^1H NMR spectroscopy
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作者 Gang-Jin Yu Xiao-Ying Chen +2 位作者 Shi-Zhen Mao Mai-Li Liu You-Ru Du 《Chinese Chemical Letters》 SCIE CAS CSCD 2017年第7期1413-1416,共4页
The critical aggregation concentration(CAC) of four with three kinds of conventional surfactants, namely,two cationic surfactants [hexadecyltrimethyl ammonium bromide(CTAB) and tetradecyltrimethyl ammonium bromide... The critical aggregation concentration(CAC) of four with three kinds of conventional surfactants, namely,two cationic surfactants [hexadecyltrimethyl ammonium bromide(CTAB) and tetradecyltrimethyl ammonium bromide(TTAB)], one anionic surfactant [sodium dodecyl sulfate(SDS)], and a nonionic surfactant [Triton X-100(TX-100)], were determined by variation of ^1H chemical shifts with surfactant concentrations. Results show that the CAC values of protons at different positions of the same molecule are different, and those of the terminal methyl protons are the lowest, respectively, which suggests that the terminal groups of the alkyl chains aggregates first during micellization. Measurement of the transverse relaxation time(T2) of different protons in SDS also show that the terminal methyl protons start to decrease with the increase in concentration first, which supports the above mentioned tendency. 展开更多
关键词 1H NMR Surfactants Critical aggregation concentration hydrophobic terminal group Micellization
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Design of Multivalent Galactoside Ligands and Their Binding to Hepatic Asialoglycoprotein Receptor
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作者 张晓茹 贾继龙 +2 位作者 张荣军 许敏华 张书圣 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2006年第8期1058-1061,共4页
In an effort to find highly efficient ligands for hepatic asialoglycoprotein receptor (ASGPR), four cluster galactosides with different scaffolds were synthesized in this paper. The affinity of these compounds for A... In an effort to find highly efficient ligands for hepatic asialoglycoprotein receptor (ASGPR), four cluster galactosides with different scaffolds were synthesized in this paper. The affinity of these compounds for ASGPR was analyzed by binding study in vitro. The results showed that trivalent cluster galactosides behaved better than divalent analogues and the cluster galactosides with aryl groups on their scaffolds presented better binding affinity than those with aliphatic chain scaffolds. 展开更多
关键词 cluster galactoside aryl group cluster effect binding affinity hydrophobic group
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