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Origin of attraction, magnitude, and directionality of interactions in benzene complexes with pyridinium cations
被引:140
作者:
Tsuzuki, Seiji
[1
]
Mikami, Masuhiro
Yamada, Shinji
机构:
[1] Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki 3058568, Japan
[2] Ochanomizu Univ, Fac Sci, Dept Chem, Bunkyo Ku, Tokyo 1128610, Japan
关键词:
CORRELATED MOLECULAR CALCULATIONS;
MODEL CHEMISTRY CALCULATIONS;
GAUSSIAN-BASIS SETS;
PI INTERACTIONS;
IONIC LIQUIDS;
AROMATIC INTERACTIONS;
CH/PI-INTERACTION;
GAS-PHASE;
ENERGY;
DIMER;
D O I:
10.1021/ja071372b
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Geometries and interaction energies of benzene complexes with pyridine, pyridinium, N-methylpyridinium were studied by ab initio molecular orbital calculations. Estimated CCSD(T) interaction energies of the complexes at the basis set limit were -3.04, -14.77, and -9.36 kcal/mol, respectively. The interactions in the pyridinium and N-methylpyridinium complexes should be categorized into a cation/pi interaction, because the electrostatic and induction interactions greatly contribute to the attraction. On the other hand, the interaction in the pyridine complex is a pi/pi interaction. The dispersion interaction is mainly responsible for the attraction in the benzene-pyridine complex. Short-range interactions including charge-transfer interactions are not important for the attraction in the three complexes. The most stable pyridinium complex has a T-shaped structure, in which the N-H bond points toward the benzene, while the N-methylpyridinium complex prefers a slipped-parallel structure. The benzene-pyridine complex has two nearly isoenergetic (Slipped-parallel and T-shaped) structures.
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页码:8656 / 8662
页数:7
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