• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

关于氢原子与灭火剂2-H七氟丙烷和CF3Br之间两个反应的密度泛函理论(DFT)和从头算计算。

DFT and ab initio calculations on two reactions between hydrogen atoms and the fire suppressants 2-H heptafluoropropane and CF3Br.

作者信息

Lee Edmond P F, Dyke John M, Chow Wan-Ki, Chau Foo-Tim, Mok Daniel K W

机构信息

Department of Building Services Engineering, The Hong Kong Polytechnic University, Hung Hom, Hong Kong.

Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Hong Kong.

出版信息

J Comput Chem. 2007 Jul 15;28(9):1582-1592. doi: 10.1002/jcc.20695.

DOI:10.1002/jcc.20695
PMID:17340604
Abstract

Reaction enthalpies and barrier heights of the reactions CF3Br+H-->CF3+HBr {reaction (1)} and CF3CHFCF3+H-->CF3CFCF3+H2 {reaction (2)} have been calculated at the near state-of-the-art ab initio level, and also by employing the B3LYP, BH&HLYP, BB1K, MPW1K, MPWB1K and TPSS1KCIS functionals. In addition, the integrated molecular orbital+molecular orbital (IMOMO) method has been used to study reaction (2). The ab initio benchmark values of the reaction enthalpy (298 K) and barrier height (0 K) of reaction (2) are reported for the first time {-(0.7+/-0.7) and 13.3+/-0.5 kcal/mole respectively}. When density functional theory (DFT) results are compared with ab initio benchmarks for both reactions (1) and (2), the MPWB1K functional is found to have the best performance of the six functionals used. The IMOMO method with the RCCSD/aug-cc-pVTZ and/or RCCSD(T)/aug-cc-pVTZ levels, as the high levels of calculation on the model system, gives reaction enthalpies and barrier heights of reaction (2), which agree with ab initio benchmark values to within 1 kcal/mole. Computed key geometrical parameters and imaginary vibrational frequencies of the transition state structures of reactions (1) and (2) obtained at different levels of calculation are compared. The magnitudes of the computed imaginary vibrational frequencies of the transition states of both reactions considered are found to be very sensitive to the levels of calculation used to obtain them. The heat of formation (298 K) of CF3CFCF3 calculated at the near state-of-the-art level has a value of -(318+/-3) kcal/mole.

摘要

在接近最新的从头算水平下,以及通过使用B3LYP、BH&HLYP、BB1K、MPW1K、MPWB1K和TPSS1KCIS泛函,计算了反应CF3Br + H→CF3 + HBr{反应(1)}和CF3CHFCF3 + H→CF3CFCF3 + H2{反应(2)}的反应焓和势垒高度。此外,采用集成分子轨道+分子轨道(IMOMO)方法研究反应(2)。首次报道了反应(2)的反应焓(298 K)和势垒高度(0 K)的从头算基准值{分别为-(0.7±0.7)和13.3±0.5 kcal/mol}。当将密度泛函理论(DFT)结果与反应(1)和(2)的从头算基准进行比较时,发现MPWB1K泛函在所使用的六种泛函中具有最佳性能。以RCCSD/aug-cc-pVTZ和/或RCCSD(T)/aug-cc-pVTZ水平作为模型体系的高水平计算方法的IMOMO方法,给出了反应(2)的反应焓和势垒高度,其与从头算基准值的偏差在1 kcal/mol以内。比较了在不同计算水平下得到的反应(1)和(2)过渡态结构的计算关键几何参数和虚振动频率。发现所考虑的两个反应过渡态的计算虚振动频率大小对用于获得它们的计算水平非常敏感。在接近最新水平下计算得到的CF3CFCF3的生成热(298 K)值为-(318±3) kcal/mol。

相似文献

1
DFT and ab initio calculations on two reactions between hydrogen atoms and the fire suppressants 2-H heptafluoropropane and CF3Br.关于氢原子与灭火剂2-H七氟丙烷和CF3Br之间两个反应的密度泛函理论(DFT)和从头算计算。
J Comput Chem. 2007 Jul 15;28(9):1582-1592. doi: 10.1002/jcc.20695.
2
Rate coefficients of the CF3CHFCF3 + H → CF3CFCF3 + H2 reaction at different temperatures calculated by transition state theory with ab initio and DFT reaction paths.用从头计算和密度泛函理论反应路径的过渡态理论计算不同温度下 CF3CHFCF3 + H → CF3CFCF3 + H2 反应的速率系数。
J Comput Chem. 2013 Mar 15;34(7):545-57. doi: 10.1002/jcc.23163. Epub 2012 Nov 1.
3
Oxidative addition of the fluoromethane C-F bond to Pd. An ab initio benchmark and DFT validation study.氟甲烷C-F键向钯的氧化加成。一项从头算基准和密度泛函理论验证研究。
J Phys Chem A. 2005 Oct 27;109(42):9685-99. doi: 10.1021/jp053587i.
4
Benchmark database of barrier heights for heavy atom transfer, nucleophilic substitution, association, and unimolecular reactions and its use to test theoretical methods.重原子转移、亲核取代、缔合及单分子反应能垒的基准数据库及其在理论方法测试中的应用
J Phys Chem A. 2005 Mar 10;109(9):2012-8. doi: 10.1021/jp045141s.
5
An assessment of theoretical procedures for predicting the thermochemistry and kinetics of hydrogen abstraction by methyl radical from benzene.关于预测甲基自由基从苯中夺取氢的热化学和动力学的理论程序的评估。
J Phys Chem A. 2006 Jul 20;110(28):8942-51. doi: 10.1021/jp061823z.
6
Toward a physical interpretation of substituent effects: the case of fluorine and trifluoromethyl groups.走向取代基效应的物理解释:氟和三氟甲基的例子。
J Org Chem. 2014 Aug 15;79(16):7321-31. doi: 10.1021/jo501013p. Epub 2014 Jul 29.
7
Kinetic isotope effects for Cl + CH4 ⇌ HCl + CH3 calculated using ab initio semiclassical transition state theory.利用从头算半经典过渡态理论计算的 Cl + CH4 ⇌ HCl + CH3 的动力学同位素效应。
J Phys Chem A. 2012 Jun 21;116(24):6408-19. doi: 10.1021/jp212383u. Epub 2012 Feb 22.
8
Anharmonic force field and vibrational dynamics of CH2F2 up to 5000 cm(-1) studied by Fourier transform infrared spectroscopy and state-of-the-art ab initio calculations.通过傅里叶变换红外光谱和最先进的从头算计算研究了 CH2F2 的非谐力场和振动动力学,直至 5000 cm(-1)。
J Chem Phys. 2012 Jun 7;136(21):214302. doi: 10.1063/1.4720502.
9
Benchmark study of DFT functionals for late-transition-metal reactions.用于后过渡金属反应的密度泛函理论(DFT)泛函的基准研究。
J Phys Chem A. 2006 Jan 19;110(2):709-16. doi: 10.1021/jp054449w.
10
Ab Initio Chemical Kinetics for the CH3 + O((3)P) Reaction and Related Isomerization-Decomposition of CH3O and CH2OH Radicals.CH3 + O((3)P)反应及CH3O和CH2OH自由基相关异构化-分解反应的从头算化学动力学
J Phys Chem A. 2015 Jul 16;119(28):7404-17. doi: 10.1021/acs.jpca.5b00553. Epub 2015 Mar 24.