New subsidiary interaction mode of counteranions with the periphery cavity of cailpyrroles binding with the anion subunits
Department甘肃省天然药物重点实验室
Liu K(刘凯); Guo Y(郭勇); Xu J(徐健); Shao SJ(邵士俊); Jiang SX(蒋生祥)
2006
Source PublicationChinese Chemical Letters
ISSN1001-8417
Volume17Issue:3Pages:387-390
AbstractThe solution binding properties of calix[4]pyrroles with anion (as tetraalkylammonium salts) were investigated using UV-Vis spectroscopic techniques. The obvious red-shift of absorption maximum band of calix[4]pyrrole in EtOH in the presence of the tetramethylammonium (TMA+) salts or tetraethylammonium (TEA+) salts were observed, due to the charge-transfer interactions between the electron-rich pyrrole rings of calix[4]pyrroles and TMA+ or TEA+ cation subunit. The results indicated that calix[4]pyrrole receptors, which link the anionic species through multiple hydrogen bonding interactions, can use the periphery cavity for selectively binding cation subunits by cation-π charge-transfer interaction. The subsidiary interaction mode helps to further stabilize the calix[4]pyrrole-anion complex.
KeywordAnion Recognition Calix[4]Pyrrole Charge-transfer Interactions Tetraalkylammonium Salts
Subject Area分析化学与药物化学
Funding Organizationthe National Natural Science Foundation of China (No.20372067)
Indexed BySCI
Language英语
Funding Project药物分子识别研究组 ; 药物分离材料研究组
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/1456
Collection中科院西北特色植物资源化学重点实验室/甘肃省天然药物重点实验室
Corresponding AuthorShao SJ(邵士俊)
Recommended Citation
GB/T 7714
Liu K,Guo Y,Xu J,et al. New subsidiary interaction mode of counteranions with the periphery cavity of cailpyrroles binding with the anion subunits[J]. Chinese Chemical Letters,2006,17(3):387-390.
APA 刘凯,郭勇,徐健,邵士俊,&蒋生祥.(2006).New subsidiary interaction mode of counteranions with the periphery cavity of cailpyrroles binding with the anion subunits.Chinese Chemical Letters,17(3),387-390.
MLA 刘凯,et al."New subsidiary interaction mode of counteranions with the periphery cavity of cailpyrroles binding with the anion subunits".Chinese Chemical Letters 17.3(2006):387-390.
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