Zhang Fangtong, Sun Hui Lun, Chang Agnes H H, Gu Xibin, Kaiser Ralf I
Department of Chemistry, University of Hawaii, Honolulu, Hawaii 96822, USA.
J Phys Chem A. 2007 Dec 27;111(51):13305-10. doi: 10.1021/jp076341h. Epub 2007 Dec 4.
The reaction of ground state boron atoms, 11B(2Pj), with allene, H2CCCH2(X1A1), was studied under single collision conditions at a collision energy of 21.5 kJ mol(-1) utilizing the crossed molecular beam technique; the experimental data were combined with electronic structure calculations on the 11BC3H4 potential energy surface. The chemical dynamics were found to be indirect and initiated by an addition of the boron atom to the pi-electron density of the allene molecule leading ultimately to a cyclic reaction intermediate. The latter underwent ring-opening to yield an acyclic intermediate H2CCBCH2. As derived from the center-of-mass functions, this structure was long-lived with respect to its rotational period and decomposed via an atomic hydrogen loss through a tight exit transition state to form the closed shell, C2v symmetric H-C is equivalent C-B=CH2 molecule. A brief comparison of the product isomers formed in the reaction of boron atoms with methylacetylene is also presented.
利用交叉分子束技术,在21.5 kJ mol⁻¹ 的碰撞能量下,在单次碰撞条件下研究了基态硼原子¹¹B(²Pj) 与丙二烯H₂CCCH₂(X¹A₁) 的反应;实验数据与¹¹BC₃H₄势能面上的电子结构计算相结合。发现化学动力学是间接的,由硼原子加成到丙二烯分子的π电子密度引发,最终产生环状反应中间体。后者发生开环反应生成无环中间体H₂CCBCH₂。从质心函数推导可知,该结构相对于其旋转周期寿命较长,并通过紧密的出口过渡态经由原子氢损失分解,形成闭壳层、C₂v对称的H-C≡C-B=CH₂分子。还简要比较了硼原子与甲基乙炔反应中形成的产物异构体。