Department of Chemistry, University of Hawai'i at Manoa, Honolulu, Hawaii 96822, USA.
J Phys Chem A. 2010 Apr 29;114(16):5256-62. doi: 10.1021/jp912054p.
The crossed molecular beam experiment of the deuterated ethynyl radical (C(2)D; X(2)Sigma(+)) with benzene [C(6)H(6)(X(1)A(1g))] and its fully deuterated analog [C(6)D(6)(X(1)A(1g))] was conducted at a collision energy of 58.1 kJ mol(-1). Our experimental data suggest the formation of the phenylacetylene-d(6) via indirect reactive scattering dynamics through a long-lived reaction intermediate; the reaction is initiated by a barrierless addition of the ethynyl-d(1) radical to benzene-d(6). This initial collision complex was found to decompose via a tight exit transition state located about 42 kJ mol(-1) above the separated products; here, the deuterium atom is ejected almost perpendicularly to the rotational plane of the decomposing intermediate and almost parallel to the total angular momentum vector. The overall experimental exoergicity of the reaction is shown to be 121 +/- 10 kJ mol(-1); this compares nicely with the computed reaction energy of -111 kJ mol(-1). Even though the experiment was conducted at a collisional energy higher than equivalent temperatures typically found in the atmosphere of Titan (94 K and higher), the reaction may proceed in Titan's atmosphere as it involves no entrance barrier, all transition states involved are below the energy of the separated reactants, and the reaction is exoergic. Further, the phenylacetylene was found to be the sole reaction product.
氘代乙炔基自由基(C(2)D;X(2)Σ(+))与苯[C(6)H(6)(X(1)A(1g))]及其全氘代类似物[C(6)D(6)(X(1)A(1g))]的交叉分子束实验在碰撞能为 58.1 kJ mol(-1)的条件下进行。我们的实验数据表明,通过长寿命反应中间体的间接反应散射动力学形成了苯乙炔-d(6);反应是由乙炔-d(1)自由基无势垒地加成到苯-d(6)引发的。该初始碰撞复合物被发现通过位于分离产物上方约 42 kJ mol(-1)的紧密出口过渡态分解;在这里,氘原子几乎垂直于分解中间体的旋转平面且几乎平行于总角动量矢量被逐出。反应的总实验放能被证明为 121 +/- 10 kJ mol(-1);这与计算的反应能-111 kJ mol(-1)非常吻合。尽管实验是在高于通常在泰坦大气中发现的等效温度(94 K 及更高)的碰撞能下进行的,但由于反应没有入口势垒,所有涉及的过渡态都低于分离反应物的能量,并且反应是放能的,因此反应可能在泰坦的大气中进行。此外,发现苯乙炔是唯一的反应产物。