Ren Fu-de, Cao Duan-Lin, Wang Wen-Liang, Ren Jun, Hou Su-Qing, Chen Shu-Sen
College of Chemical Engineering and environment, North University of China, Taiyuan 030051, China.
J Mol Model. 2009 May;15(5):515-23. doi: 10.1007/s00894-008-0415-8. Epub 2008 Dec 17.
The unusual T-shaped X-H...pi hydrogen bonds are found between the B=B double bond of the singlet state HB=BH and the acid hydrogen of HF, HCl, HCN and H2C2 using MP2 and B3LYP methods at 6-311++G(2df,2p) and aug-cc-pVTZ levels. The binding energies follow the order of HB=BH...HF>HB=BH...HCl>HB=BH...HCN>HB=BH...H2C2. The hydrogen-bonded interactions in HB=BH...HX are found to be stronger than those in H2C=CH2...HX and OCB identical withBCO...HX. The analyses of natural bond orbital (NBO) and the electron density shifts reveal that the nature of the T-shaped X-H...pi hydrogen-bonded interaction is that much of the lost density from the pi-orbital of B=B bond is shifted toward the hydrogen atom of the proton donor, leading to the electron density accumulation and the formation of the hydrogen bond. The atoms in molecules (AIM) theory have also been applied to characterize bond critical points and confirm that the B=B double bond can be a potential proton acceptor.
利用MP2和B3LYP方法,在6 - 311++G(2df,2p)和aug-cc-pVTZ水平下,发现单重态HB=BH的B=B双键与HF、HCl、HCN和H₂C₂的酸性氢之间存在不寻常的T形X-H...π氢键。结合能顺序为HB=BH...HF>HB=BH...HCl>HB=BH...HCN>HB=BH...H₂C₂。发现HB=BH...HX中的氢键相互作用比H₂C=CH₂...HX和OCB≡BCO...HX中的更强。自然键轨道(NBO)分析和电子密度转移表明,T形X-H...π氢键相互作用的本质是B=B键π轨道损失的大部分密度向质子供体的氢原子转移,导致电子密度积累并形成氢键。分子中的原子(AIM)理论也已用于表征键临界点,并证实B=B双键可以是潜在的质子受体。