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A crossed molecular beams study of the reaction of dicarbon molecules with benzene

机译:交叉分子束研究二碳分子与苯的反应

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We conducted the reaction of dicarbon molecules in their electronic ground, C-2 (X-I Sigma(+)(g)), and first excited state, C-2(a(3)Pi(u)), with benzene, C6H6(X(1)A(1g)). The phenylethynyl radical (C6H5CC; X(2)A') and atomic hydrogen were inferred to be the reaction products under single collision conditions. The reactions were indirect via short-lived C8H6 intermediates which decomposed via atomic hydrogen elimination without exit barrier (singlet surface) and via a tight exit transition state (triplet surface). Our experiments suggest that the phenylethynyl radical can be likely formed via bimolecular reactions involving dicarbon molecules with benzene in extreme environments such as circumstellar envelopes of carbon stars, planetary nebulae, and combustion flames. Published by Elsevier B.V.
机译:我们进行了电子碳C-2(XI Sigma(+)(g))和第一激发态C-2(a(3)Pi(u))与苯C6H6( X(1)A(1g))。苯乙炔基(C6H5CC; X(2)A')和氢原子被认为是在单次碰撞条件下的反应产物。反应是通过短寿命的C8H6中间体间接进行的,该中间体通过消除氢原子而没有出口壁垒(单一表面)和紧密的出口过渡态(三重态表面)分解。我们的实验表明,在诸如碳星,行星状星云和燃烧火焰等极端环境中,涉及二碳分子与苯的双分子反应很可能形成苯乙炔基。由Elsevier B.V.发布

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