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NH_2(~2B_1)与CH_4反应机理的理论研究
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作者 孙仁安 靳菲 +2 位作者 孙延波 陶占良 韩克利 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2002年第12期2344-2347,共4页
在密度泛函理论 B3LYP/6 -31 1 G*水平下 ,研究了 NH2 与 CH4的反应机理 .通过振动频率和内禀反应坐标 ( IRC)分析 ,对反应过渡态进行了确认 .在 QCISD( T) /6 -31 1 G*水平下进行了单点能计算 ,并进行了零点能校正 ,结果表明 ,反应 NH2... 在密度泛函理论 B3LYP/6 -31 1 G*水平下 ,研究了 NH2 与 CH4的反应机理 .通过振动频率和内禀反应坐标 ( IRC)分析 ,对反应过渡态进行了确认 .在 QCISD( T) /6 -31 1 G*水平下进行了单点能计算 ,并进行了零点能校正 ,结果表明 ,反应 NH2 + CH4NH3 + CH3 是主要的反应通道 . 展开更多
关键词 理论研究 密度泛函理论 反应机理 CH4 反应通道 NH2 氮氢自由基 甲烷 动力学
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NH_2(~2A_1,090,4_(23))的电子猝灭和转动态-态传能
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作者 沈关林 张敏 +2 位作者 董峰 李学初 王秀岩 《物理化学学报》 SCIE CAS CSCD 北大核心 2001年第9期840-844,共5页
在束-气和束-束实验条件下,详细研究了NH_2(~2A_1,090,4_(23))自由基分别与 Ar,N2,O2和 NH3碰撞引起的电子态猝灭和转动态-态传能,获得了总的猝灭截面σQ (分别为≤ 0.17、 0.26、 0.30和 0.48 nm^2),以及相对转动态-态传能截面 .... 在束-气和束-束实验条件下,详细研究了NH_2(~2A_1,090,4_(23))自由基分别与 Ar,N2,O2和 NH3碰撞引起的电子态猝灭和转动态-态传能,获得了总的猝灭截面σQ (分别为≤ 0.17、 0.26、 0.30和 0.48 nm^2),以及相对转动态-态传能截面 .利用碰撞络合物模型计算的电子猝灭截面与实验测得的截面具有基本相同的趋势,表明长程吸引势在猝灭过程中起着重要的作用 .同时还发现,转动态-态传能中相对截面随着碰撞对的折合质量的减小而下降 .由于 NH_3具有较大的偶极矩以及 O_2的开壳层电子结构使得猝灭截面增大,而转动态-态传能截面减小 . 展开更多
关键词 电子激发态传能 单次碰撞 碰撞络合物模型 NH2自由 电子猝灭 氮氢自由基
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Halogen Bonding or Hydrogen Bonding between 2,2,6,6-Tetramethyl- piperidine-noxyl Radical and Trihalomethanes CHX3 (X=CI, Br, I)
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作者 赵晓冉 庞雪 +1 位作者 阎晓青 晋卫军 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2013年第2期172-180,I0003,共10页
The halogen and hydrogen bonding complexes and trihalomethanes (CHX3, X=C1, Br, I) are between 2,2,6,6-tetramethylpiperidine-noxyl simulated by computational quantum chem- istry. The molecular electrostatic potentia... The halogen and hydrogen bonding complexes and trihalomethanes (CHX3, X=C1, Br, I) are between 2,2,6,6-tetramethylpiperidine-noxyl simulated by computational quantum chem- istry. The molecular electrostatic potentials, geometrical parameters and interaction energy of halogen and hydrogen bonding complexes combined with natural bond orbital analysis are obtained. The results indicate that both halogen and hydrogen bonding interactions obey the order CI〈Br〈I, and hydrogen bonding is stronger than the corresponding halogen bond- ing. So, hydrogen bonding complexes should be dominant in trihalomethanes. However, it is possible that halogen bonding complex is competitive, even preponderant, in triiodomethane due to the similar interaction energy. This work might provide useful information on specific solvent effects as well as for understanding the mechanism of nitroxide radicals as a bioprobe to interact with the halogenated compounds in biological and biochemical fields. 展开更多
关键词 Halogen bonding Hydrogen bonding Theoretical study Nitroxide radical Natural bond orbital
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Oxidative co-dehydrogenation of ethane and propane over h-BN as an effective means for C-H bond activation and mechanistic investigations 被引量:4
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作者 Hao Tian Bingjun Xu 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 2022年第8期2173-2182,共10页
Hexagonal boron nitride(h-BN)is a highly selective catalyst for oxidative dehydrogenation of light alkanes to produce the corresponding alkenes.Despite intense recent research effort,many aspects of the reaction mecha... Hexagonal boron nitride(h-BN)is a highly selective catalyst for oxidative dehydrogenation of light alkanes to produce the corresponding alkenes.Despite intense recent research effort,many aspects of the reaction mechanism,such as the observed supra-linear reaction order of alkanes,remain unresolved.In this work,we show that the introduction of a low concentration of propane in the feed of ethane oxidative dehydrogenation is able to enhance the C_(2)H_(6) conversion by 47%,indicating a shared reaction intermediate in the activation of ethane and propane.The higher activity of propane makes it the dominant radical generator in the oxidative co-dehydrogenation of ethane and propane(ODEP).This unique feature of the ODEP renders propane an effective probe molecule to deconvolute the two roles of alkanes in the dehydrogenation chemistry,i.e.,radical generator and substrate.Kinetic studies indicate that both the radical generation and the dehydrogenation pathways exhibit a first order kinetics toward the alkane partial pressure,leading to the observed second order kinetics of the overall oxidative dehydrogenation rate.With the steady-state approximation,a radical chain reaction mechanism capable of rationalizing observed reaction behaviors is proposed based on these insights.This work demonstrates the potential of ODEP as a strategy of both activating light alkanes in oxidative dehydrogenation on BN and mechanistic investigations. 展开更多
关键词 Hexagonal boron nitride Oxidative dehydrogenation Radical chain reaction Reaction order C-H activation
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High Nitrogen Pressure Solution (HNPS) growth of GaN on 2 inch free standing GaN substrates 被引量:2
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作者 M.BOKOWSKI I.GRZEGORY +4 位作者 B.LUCZNIK T.SOCHACKI M.KRYKO G.KAMLER S.POROWSKI 《Science China(Technological Sciences)》 SCIE EI CAS 2011年第1期42-46,共5页
Recent results of High Nitrogen Pressure Solution (HNPS) growth of GaN crystals deposited on and separated from 2 inch,and smaller,GaN substrates grown by Hydride Vapor Phase Epitaxy (HVPE) have been presented. The in... Recent results of High Nitrogen Pressure Solution (HNPS) growth of GaN crystals deposited on and separated from 2 inch,and smaller,GaN substrates grown by Hydride Vapor Phase Epitaxy (HVPE) have been presented. The influence of the c-plane bowing in the initial substrate on quality,rate and mode of growth by HNPS method has been analyzed in details. 展开更多
关键词 High Nitrogen Pressure Solution (HNPS) growth seeded growth Hydride Vapor Phase Epitaxy (HVPE) growth
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