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首页> 外文期刊>The Journal of Chemical Physics >Crossed beam reaction of cyano radicals with hydrocarbon molecules. II. Chemical dynamics of 1-cyano-1-methylallene (CNCH_3CCCH_2; X~1A') formation from reaction of CN(X~2#SIGMA#~+) with dimethylacetylene CH_3CCCH_3(X~1A_1')
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Crossed beam reaction of cyano radicals with hydrocarbon molecules. II. Chemical dynamics of 1-cyano-1-methylallene (CNCH_3CCCH_2; X~1A') formation from reaction of CN(X~2#SIGMA#~+) with dimethylacetylene CH_3CCCH_3(X~1A_1')

机译:氰基自由基与烃分子的交叉束反应。二。 CN(X〜2#SIGMA#〜+)与二甲基乙炔CH_3CCCH_3(X〜1A_1')反应生成1-氰基-1-甲基烯丙基(CNCH_3CCCH_2; X〜1A')的化学动力学

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摘要

The reaction dynamics to form the 1-cyano-1-methylallene isomer CNCH_3CCCH_2 in its ~1A' ground state via the radical-closed shell reaction of the cyano radical CN(X ~2 #SIGMA#~+) with dimethylacetylene CH_3CCCH_3(X ~1A_1') are unraveled in a crossed molecular beam experiment at a collision energy of 20.8 kJ mol~(-1) together with state-of-the-art electronic structure and Rice-Ramsperger-Kassel-Marcus (RRKM) calculations. Forward convolution fitting of the laboratory angular distribution together with the time-of-flight spectra verify that the reaction is indirect and proceeds by addition of the CN radical to the #pi# orbital to form a cis/trans CH_3CNC=CCH_3 radical intermediate. This decomposes via a rather lose exit transition state located only 6-7 kJ mol~(-1) above the products to CNCH_3CCCH_2 and atomic hydrogen. The best fit of the center-of-mass angular distribution is forward-backward symmetric and peaks at #pi#/2 documenting that the fragmenting intermediate holds a lifetime longer than its rotational period. Further, the hydrogen atom leaves almost perpendicular to the C_5H_5N plane resulting in sideways scattering. This finding, together with low frequency bending and wagging modes, strongly support our electronic structure calculations showing a H-C-C angle of about 106.5 deg in the exit transition state. The experimentally determined reaction exothermicity of 90 +- 20 kJ mol~(-1) is consistent with the theoretical value, 80.4 kJ mol~(-1). Unfavorable kinematics prevent us from observing the CN versus CH_3 exchange channel, even though our RRKM calculations suggest that this pathway is more important. Since the title reaction is barrierless and exothermic, and the exit transition state is well below the energy of the reactants, this process might be involved in the formation of unsaturated nitriles even in the coldest interstellar environments such as dark, molecular clouds and the saturnian satellite Titan.
机译:通过氰基CN(X〜2#SIGMA#〜+)与二甲基乙炔CH_3CCCH_3(X〜)的自由基闭壳反应,反应动力学形成〜1A'基态的1-氰基-1-甲基丙二烯异构体CNCH_3CCCH_2 1A_1')在交叉分子束实验中以20.8 kJ mol〜(-1)的碰撞能量进行了解离,并结合了最新的电子结构和Rice-Ramsperger-Kassel-Marcus(RRKM)计算。实验室角度分布的正向卷积拟合与飞行时间光谱一起证明了该反应是间接的,并且是通过将CN自由基加到#pi#轨道上而形成顺/反CH_3CNC = CCH_3自由基中间体而进行的。这通过相当失活的出口过渡态分解,该过渡态仅位于产物上方至CNCH_3CCCH_2和原子氢之上6-7 kJ mol〜(-1)。质量中心角分布的最佳拟合是前后对称,并且在#pi#/ 2处出现峰,这表明碎片中间体的寿命比其旋转周期更长。此外,氢原子几乎垂直于C_5H_5N平面离开,导致侧向散射。这一发现与低频弯曲和摆动模式一起,强烈支持了我们的电子结构计算,在出口过渡状态下,H-C-C角约为106.5度。实验确定的90±20 kJ mol〜(-1)的反应放热与理论值80.4 kJ mol〜(-1)一致。运动学方面的不利因素使我们无法观察CN与CH_3的交换通道,即使我们的RRKM计算表明该途径更为重要。由于标题反应是无障碍且放热的,并且出口跃迁状态远低于反应物的能量,因此即使在最冷的星际环境(例如黑暗,分子云和土星卫星)中,该过程也可能涉及不饱和腈的形成。泰坦

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