期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 123, 期 38, 页码 9264-9267出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja010443i
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Ab initio calculations at the MP2/6-311++G** level on model systems (N-methylpyridinium complexes of dimethyl ether and dimethyl phosphate anion) provide quantitative measures of the large stabilization energies that arise from [C-H . . .O] contacts in charged systems. These attractive interactions control (i) the self-assembly of bipyridinium-based catenanes and rotaxanes in solution, (ii) the self-organization of left-handed Z-DNA with alternating [dC-dG] sequences in the solid state, and (iii) the binding of pyridinium derivatives with single- and double-stranded DNA. Slightly attractive interactions occur between the donor ether and phosphate moieties and a neutral pyridine molecule in the gas phase. Electrostatic potential and solvation calculations demonstrate that [C-H . . .O] interactions which involve a cationic [C-H] donor are dominated by electrostatic terms.
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