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Multiple noncovalent interaction constructed polymeric supramolecular crystals: recognition of butyl viologen by para-dicyclohexanocucurbit[6]uril and alpha,alpha ',delta,delta '-tetramethylcucurbit[6]uril  ( SCI-EXPANDED收录)   被引量:8

文献类型:期刊文献

英文题名:Multiple noncovalent interaction constructed polymeric supramolecular crystals: recognition of butyl viologen by para-dicyclohexanocucurbit[6]uril and alpha,alpha ',delta,delta '-tetramethylcucurbit[6]uril

作者:Xiao, Zhi-You Lin, Rui-Lian Tao, Zhu Liu, Qing-Yun Liu, Jing-Xin Xiao, Xin

第一作者:肖志友

通信作者:Liu, JX[1];Xiao, X[2]

机构:[1]Guizhou Inst Technol, Sch Chem Engn, Guiyang 550003, Guizhou, Peoples R China;[2]Anhui Univ Technol, Coll Chem & Chem Engn, Maanshan 243002, Peoples R China;[3]Shandong Univ Sci & Technol, Coll Chem & Environm Engn, Qingdao, Peoples R China;[4]Guizhou Univ, Key Lab Macrocycl & Supramol Chem Guizhou Prov, Guiyang 550025, Guizhou, Peoples R China

第一机构:贵州理工学院化学工程学院

通信机构:corresponding author), Anhui Univ Technol, Coll Chem & Chem Engn, Maanshan 243002, Peoples R China;corresponding author), Shandong Univ Sci & Technol, Coll Chem & Environm Engn, Qingdao, Peoples R China.

年份:2017

卷号:4

期号:12

起止页码:2422-2427

外文期刊名:ORGANIC CHEMISTRY FRONTIERS

收录:;WOS:【SCI-EXPANDED(收录号:WOS:000416065700022)】;

基金:This work was financially supported by the National Natural Science Foundation of China (No. 21561007, 21371004), the Innovation Program for High-level Talents of Guizhou Province (No. 2016-5657), and the Science and Technology Fund of Guizhou Province (No. 2016-1030, 2013-2263).

语种:英文

摘要:Binding interactions of butyl viologen (BV+) with para-dicyclohexanocucurbit[6]uril (Cy2Q[6]) and alpha,alpha',delta,delta'-tetramethyl cucurbit[6]uril (TMeQ[6]) were investigated by H-1 NMR spectroscopy, isothermal titration calorimetry (ITC) and X-ray crystallography. In the solid state, the BV+ guest and both hosts form polymeric supramolecular crystals through multiple noncovalent interactions, including host-guest interaction, pi-pi stacking interaction, and metal-host coordination. In the aqueous solution, the butyl chain of BV+ was selectively encapsulated into the hosts Cy2Q[6] and TMeQ[6], while the bipyridinium group resides outside of the host portals, forming [2]pseudorotaxane. The ITC experiment indicates that the host-guest binding processes are exclusively enthalpy driven.

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