NMR evidence for protonated tetraethyl p-tert-butylcalix[4]arene tetraacetate

被引:0
作者
Kriz, J.
Dybal, J.
Makrlik, E.
Vanura, P.
机构
[1] Univ W Bohemia, Fac Sci Appl, Plzen 30614, Czech Republic
[2] Acad Sci Czech Republic, Inst Macromol Chem, CR-16206 Prague, Czech Republic
[3] Inst Chem Technol, CR-16628 Prague, Czech Republic
关键词
calix[4]arene; protonation; NMR; acetonitrile;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In addition to well-known complexes of tetraethyl p-tert-butylcalix[4]arene tetraacetate (abbrev. 1) with alkali metal cations, an equimolar complex of this compound with H3O+, i.e. 1 center dot H3O+, was found to be formed slowly in acetonitrile, however, with a very high equilibrium constant, the value of which is beyond the possibilities of exact determination by NMR. Hydrogen bis(1,2-dicarbollyl) cobaltate (HDCC) was used as a proton source. Further, by a combination of 1D and 2D H-1 NMR with C-13 NMR spectra, it was proved that the ester carbonyls of 1 are not strongly involved in coordination of H3O+. It means that the most probable structure of the 1 center dot H3O+ complex is obviously that with H3O+ bound by strong hydrogen bonds to the phenoxy oxygen atoms of 1.
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页码:1321 / 1326
页数:6
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