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首页> 外文期刊>The Journal of Chemical Physics >Infrared spectra of the 1,1-dimethylallyl and 1,2-dimethylallyl radicals isolated in solid para-hydrogen
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Infrared spectra of the 1,1-dimethylallyl and 1,2-dimethylallyl radicals isolated in solid para-hydrogen

机译:1,1-二甲基ally1的红外光谱和固体对氢气中分离的1,2-二甲基allyl基团

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The reaction of hydrogen atoms (H) with isoprene (C5H8) in solid para-hydrogen (p-H2) matrices at 3.2 K has been studied using infrared (IR) spectroscopy. Mixtures of C5H8 and Cl-2 were co-deposited in p-H2 at 3.2 K, followed by irradiation with ultraviolet light at 365 nm to produce Cl atoms from the Cl-2, and subsequent irradiation with IR light to produce H atoms from the reaction of the Cl atoms with p-H-2. The H atoms then react with the C5H8 to form H atom addition radicals (C5H9 center dot). Upon 365-nm/IR photolysis, a multitude of new lines appeared in the IR spectrum and, based on the secondary photolysis behavior, it was determined that the majority of the new lines belong to two distinct chemical species, denoted as setX(an intense line at 776.0 cm 1 and 12 other weaker lines) and set Y (an intense line at 766.7 cm(-1) and 12 other weaker lines). Quantum-chemical calculations were performed at the B3PW91/6-311++ G(2d, 2p) level to determine the relative energetics and predict the IR spectra for the four possible isomers of C5H9 center dot that can be produced from the addition of the H atom to the four distinct carbon atoms in C5H8. The newly observed lines of set X and Y are assigned to the 1,2-dimethylallyl (addition to carbon 4) and the 1,1-dimethylallyl (addition to carbon 1) radicals according to comparison with the predicted IR spectra of the possible products. The 1,2-dimethylallyl radical and the 1,1-dimethylallyl radical were predicted to be the most stable isomers, with the latter similar to 8 kJ mol(-1) lower in energy than the former and to have significantly lower barriers than the addition pathways for the two central carbons. The ratio of the 1,1-dimethylallyl to the 1,2-dimethylallyl radicals is estimated to be (1.0 +/- 0.5): 1.0, indicating that the two radicals are produced in similar amounts, which is consistent with the theoretical predictions that the barrier heights are very similar for the H atom addition to the two terminal carbon
机译:使用红外(IR)光谱研究了3.2K的固体对氢(P-H2)基质中与异戊二烯(C5H8)的氢原子(H)的反应已经研究。 C5H8和Cl-2的混合物在3.2K的p-H 2中共沉积,然后用365nm的紫外线照射,从Cl-2产生Cl原子,随后用红外光照射,从而产生H原子Cl原子与pH-2的反应。然后H原子与C5H8反应以形成H原子添加自由基(C5H9中心点)。在365纳米/红外光解中,在IR光谱中出现多种新的线,并基于二次光解作用,确定大部分新线属于两个不同的化学物质,表示为setx(强烈的线在776.0cm 1和12其他较弱的线条上),并设定Y(处于766.7厘米(-1)和12条其他较弱的线条)。量子化学计算在B3PW91 / 6-311 ++ G(2D,2P)水平上进行以确定相对能量,并预测C5H9中心点的四种可能的异构体的IR光谱,可以从添加H原子在C5H8中的四个不同碳原子。新观察到的集合X和Y的线被分配给1,2-二甲基(除碳4),并根据与所述可能的产品的预测IR光谱比较1,1-二甲基(除碳1)的基团。预测1,2-二甲基allyL基团和1,1-二甲基ally1自由基是最稳定的异构体,后者类似于能量低于8kJ摩尔(-1)的能量,并且具有比前者显着降低的障碍两个中央碳的附加途径。估计1,1-二甲基alally1的1,1-二甲基ally1的比例估计为(1.0 +/- 0.5):1.0,表明两种基团以类似的量产生,这与理论预测一致对于两个终端碳的H原子,屏障高度非常相似

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