高等学校化学学报 ›› 1998, Vol. 19 ›› Issue (S1): 310.
• Organic Synthesis Chemistry • 上一篇 下一篇
Xiao-Qi Zheng1, Qing-Xiang Guo2, Li Yang1, You-Cheng Liu1,2
Xiao-Qi Zheng1, Qing-Xiang Guo2, Li Yang1, You-Cheng Liu1,2
摘要: Cyclodextrins (CD) have been found wide applications in the artificial enzymes[1] due to their ability of recognizing and binding a variety of organic and inorganic substrates in aqueous solution. In some cases, however, their binding capacity and selectivity are not good enough to make them useful (Ka~102-104L/mol). Breslow et.al[2,3] have reported that the bridged cyclodextrin dimers can complex some kinds of substrates strongly (Ka~106-1011L/mol) because of their more recognition sites. Recently, we synthesized a series of bridged β-CD dimers. It has been observed that the conformation of the dimers changed markedly upon the solvents.
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