Zhang Fangtong, Gu Xibin, Kaiser Ralf I
Department of Chemistry, University of Hawai'i at Manoa, Honolulu, Hawaii 96822, USA.
J Chem Phys. 2008 Feb 28;128(8):084315. doi: 10.1063/1.2834221.
The chemical dynamics to form the D5-diphenyl molecule, C6H5C6D5, via the neutral-neutral reaction of phenyl radicals (C6H5) with D6-benzene (C6D6), was investigated in a crossed molecular beams experiment at a collision energy of 185 kJ mol(-1). The laboratory angular distribution and time-of-flight spectra of the C6H5C6D5 product were recorded at mass to charge mz of 159. Forward-convolution fitting of our data reveals that the reaction dynamics are governed by an initial addition of the phenyl radical to the pi electron density of the D6-benzene molecule yielding a short-lived C6H5C6D6 collision complex. The latter undergoes atomic deuterium elimination via a tight exit transition state located about 30 kJ mol(-1) above the separated reactants; the overall reaction to form D5-diphenyl from phenyl and D6-benzene was found to be weakly exoergic. The explicit identification of the D5-biphenyl molecules suggests that in high temperature combustion flames, a diphenyl molecule can be formed via a single collision event between a phenyl radical and a benzene molecule.
通过交叉分子束实验,在185 kJ mol⁻¹的碰撞能量下,研究了苯基自由基(C₆H₅)与D₆-苯(C₆D₆)发生中性-中性反应形成D₅-二苯基分子(C₆H₅C₆D₅)的化学动力学。在质荷比m/z为159时记录了C₆H₅C₆D₅产物的实验室角分布和飞行时间光谱。对我们的数据进行正向卷积拟合表明,反应动力学由苯基自由基最初加成到D₆-苯分子的π电子密度上控制,产生一个短寿命的C₆H₅C₆D₆碰撞复合物。后者通过位于分离反应物上方约30 kJ mol⁻¹处的紧密出口过渡态进行原子氘消除;发现由苯基和D₆-苯形成D₅-二苯基的整体反应是弱放热的。D₅-联苯分子的明确鉴定表明,在高温燃烧火焰中,二苯基分子可以通过苯基自由基与苯分子之间的单次碰撞事件形成。