期刊
CHEMICAL COMMUNICATIONS
卷 -, 期 12, 页码 1362-1363出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/b405331a
关键词
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The reversible switching from the C-4v-symmetric vase to the C-2v-symmetric kite conformation of an amphiphilic resorcin[4]arene cavitand was induced by Zn-II ion coordination. Langmuir monolayers were obtained of both conformers. with the area per molecule increasing dramatically from 120 Angstrom(2) for the vase to 270 Angstrom(2) for the kite form. H-1 NMR spectroscopy in chloroform solution supports the formation of a stoichiometric kite-cavitand(.)(ZnII)(2) complex, with the metal ions coordinating to pairs of neighbouring quinoxaline N-atoms.
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