Citation: Zhao Qing, Qi Boyu, Wang Baojin, Chen Feiwu. Theoretical Investigation on Weak Interactions of HXeBr with Benzene and Its Derivatives[J]. Acta Chimica Sinica, ;2015, 74(3): 285-292. doi: 10.6023/A15100641 shu

Theoretical Investigation on Weak Interactions of HXeBr with Benzene and Its Derivatives

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Department of Chemistry and Chemical Engineering, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing Key Laboratory for Science and Application of Functional Molecular and Crystalline Materials, Beijing 100083

Corresponding author: Chen Feiwu, chenfeiwu@ustb.edu.cn
Received Date: 3 October 2015

Fund Project: the National Natural Science Foundation of China 21173020, 21473008

Figures(7)

Geometries of complexes HXeBr…C₆H₅X (X=H, CH₃, NH₂, N(CH₃)₂, NHCH₃, OH, OCH₃, CN, F, Cl, Br, I, COOH, SO₃H, CF₃) and its monomers are optimized with MP2/aug-cc-pVDZ (aug-cc-pVDZ-PP for Xe and I). The aug-cc-pVDZ-PP is a small core pseudopotential basis set. It ignores 28 electrons for Xe and I atoms. Two types of weak interactions, π…H bond and bifurcated hydrogen bonds, are analyzed in detail. The effects of substituting group of the benzene ring on the weak interaction energies are investigated. Their effects on π…H bond are different from that on bifurcated hydrogen bonds. As for the complexes with π…H bond, electron withdrawing groups reduce the interaction energies while electron donating groups increase the interaction energies. However, for the complexes with bifurcated hydrogen bonds, electron withdrawing groups increase the interaction energies while electron-donating groups decrease the interaction energies. The effects of substituting groups on geometrical parameters of HXeBr are also analyzed. As for 14 complexes of HXeBr…C₆H₅X with bifurcated hydrogen bonds, it is found that their weak interaction energies have very good linear relationships with dipole moments of C₆H₅X, bond length changes of Xe—Br and H—Xe bonds, vibrational frequency changes of H—Xe bonds, and the sum of two interpenetration distances of Van der Waals surfaces of bromine and two hydrogen atoms which are connected to the bromine atom by hydrogen bonds. It is also found that the weak interaction energies of 14 complexes above have very good linear relationships with the sum of electron densities (ρ), the sum of ∇²ρ and the sum of electrostatic potentials at two critical points of bifurcated hydrogen bonds, and with the electron density, ∇²ρ and the electrostatic potential at the ring critical point which is inside a ring formed by the bifurcated hydrogen bonds and two carbon atoms of the benzene ring. As for the complexes with bifurcated hydrogen bonds, the weak interaction energies between the monomers can be understood approximately as dipole-dipole interaction.
- rare gas,
- HXeBr,
- benzene,
- π…H bond,
- bifurcated hydrogen bonds
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