Citation: LI Shang-Jun, TAN Ning-Xin, YAO Qian, LI Ze-Rong, LI Xiang-Yuan. Calculation of Rate Constants for Intramolecular Hydrogen Migration Reactions of Alkylperoxy Radicals[J]. Acta Physico-Chimica Sinica, ;2015, 31(5): 859-865. doi: 10.3866/PKU.WHXB201503131 shu

Calculation of Rate Constants for Intramolecular Hydrogen Migration Reactions of Alkylperoxy Radicals

1.
1 College of Chemistry, Sichuan University, Chengdu 610064, P. R. China;
2 College of Chemical Engineering, Sichuan University, Chengdu 610065, P. R. China

Received Date: 27 November 2014
Available Online: 13 March 2015
Fund Project: 国家自然科学基金(91441114)资助项目 (91441114)

Intramolecular hydrogen migration in alkylperoxy reactions is one of the most important reaction classes in hydrocarbon combustion at low temperatures. In this study, the kinetic parameters for reactions in this class were calculated using the isodesmic reaction method. The geometries for all the reactants, transition states, and products were optimized at the B3LYP/6-311+G(d,p) level. A criterion based on conservation of the reaction-center geometry of the transition state was proposed for the reaction class, and the intramolecular hydrogen migration reactions studied were divided into four classes, i.e., (1,3), (1,4), (1,5), and (1,n) (n=6, 7, 8) hydrogen migration. The simplest reaction system for each reaction class was defined as the principal reaction; the approximate single-point energies were obtained at the low level of B3LYP/6-311+G(d,p) and accurate single-point energies were obtained at the high level of CBS-QB3. The other reactions in this class were chosen as the target reactions and the approximate single-point energies were obtained at the B3LYP/6- 311+G(d,p) level. The energy barriers and rate constants of these target reactions were corrected using the isodesmic reaction method. The results showed that accurate energy barriers and rate constants for the reactions of large molecules can be obtained by a relatively low level method using the isodesmic reaction method. In this study, classification of the basic isodesmic reaction showed the essential features of the reaction classes. The present work provides accurate kinetic parameters for modeling intramolecular hydrogen migration reactions of hydrocarbons at low temperatures.
1. [1]
  
  (1) Battin-Leclerc, F. Prog. Energy Combust. Sci. 2008, 34, 440. doi: 10.1016/j.pecs.2007.10.002
2. [2]
  (2) Pousse, E.; Glaude, P. A.; Fournet, R.; Battin-Leclerc, F. Combust. Flame 2009, 156, 954. doi: 10.1016/j.combustflame.2008.09.012
3. [3]
  (3) Taatjes, C. A. J. Phys. Chem. A 2006, 110, 4299. doi: 10.1021/jp056997f
4. [4]
  (4) Walker, R.W.; Morley, C. Basic Chemistry of Combustion. In Low-Temperature Combustion and Autoignition; Pilling, M. J. Ed.; Elsevier: Amsterdam, The Netherlands, 1997; pp 1-124.
5. [5]
  (5) Zádor, J.; Taatjes, C. A.; Fernandes, R. X. Prog. Energy Combust. Sci. 2011, 37, 371. doi: 10.1016/j.pecs.2010.06.006
6. [6]
  (6) Miller, J. A.; Klippenstein, S. J.; Robertson, H. Proc. Combust. Inst. 2000, 28, 1479. doi: 10.1016/S0082-0784(00)80544-5
7. [7]
  (7) Villano, S. M.; Huynh, L. K.; Carstensen, H. H.; Dean, A. M. J. Phys. Chem. A 2012, 116, 5068. doi: 10.1021/jp3023887
8. [8]
  (8) Villano, S. M.; Huynh, L. K.; Carstensen, H. H.; Dean, A. M. J. Phys. Chem. A 2011, 115, 13425. doi: 10.1021/jp2079204
9. [9]
  (9) Zhang, F.; Dibble, T. S. J. Phys. Chem. A 2011, 115, 655. doi:10.1021/jp1111839
10. [10]
  (10) Sharma, S.; Raman, S.; Green, W. H. J. Phys. Chem. A 2010, 114, 5689. doi: 10.1021/jp9098792
11. [11]
  (11) Miyoshi, A. J. Phys. Chem. A 2011, 115, 3301. doi: 10.1021/jp112152n
12. [12]
  (12) Truong, T. N. J. Chem. Phys. 2000, 113, 4957. doi: 10.1063/1.1287839
13. [13]
  (13) Huynh, L. K.; Ratkiewicz, A.; Truong, T. N. J. Phys. Chem. A 2006, 110, 473. doi: 10.1021/jp051280d
14. [14]
  (14) Muszynska, M.; Ratkiewicz, A.; Huynh, L. K.; Truong, T. N. J. Phys. Chem. A 2009, 113, 8327. doi: 10.1021/jp903762x
15. [15]
  (15) Bankiewicz, B; Huynh, L. K.; Ratkiewicz, A.; Truong, T. N. J. Phys. Chem. A 2009, 113, 1564. doi: 10.1021/jp808874j
16. [16]
  (16) Zhang, S.W.; Truong, T. N. J. Phys. Chem. A 2003, 107, 1138. doi: 10.1021/jp021265y
17. [17]
  (17) Kungwan, N.; Truong, T. N. J. Phys. Chem. A 2005, 109, 7742. doi: 10.1021/jp051799+
18. [18]
  (18) Huynh, L. K.; Truong, T. N. Theor. Chem. Account 2008, 120, 107. doi: 10.1007/s00214-007-0311-9
19. [19]
  (19) Wang, B. Y.; Li, Z. R.; Tan, N. X.; Yao, Q.; Li, X. Y. J. Phys. Chem. A 2013, 117, 3279. doi: 10.1021/jp400924w
20. [20]
  (20) Wang, B. Y.; Tan, L. X.; Yao, Q.; Li, Z. R.; Li, X. Y. Acta Phys. -Chim. Sin. 2012, 28, 2824. [汪必耀, 谈宁馨, 姚倩, 李泽荣, 李象远. 物理化学学报, 2012, 28, 2824.] doi: 10.3866/PKU.WHXB201209053
21. [21]
  (21) Frisch, M. J.; Trucks, G.W.; Schlegel, H. B.; et al. Gaussian 03, Revision B.01; Gaussian Inc.: Pittsburgh, PA, 2003.
22. [22]
  (22) Scott, A. P.; Radom, L. J. Phys. Chem. 1996, 100, 16502. doi: 10.1021/jp960976r
23. [23]
  (23) NIST. Computational Chemistry Comparison and Benchmark Database. NIST Standard Reference Database Number 101. 2013, available at http://webbook.nist. v/
24. [24]
  (24) Mont mery, J. A.; Frisch, M. J.; Ochterski, J.W.; Petersson, G. A. J. Chem. Phys. 1999, 110, 2822. doi: 10.1063/1.477924
25. [25]
  (25) Zhu, L.; Bozzelli, J.W.; Kardos, L. M. J. Phys. Chem. A 2007, 111, 6361. doi: 10.1021/jp070342s
26. [26]
  (26) Mokrushin, V.; Tsang, W. Chemrate v.1.5.8; National Institute of Standards and Technology: Gaithersburg, MD, 2009.
27. [27]
  (27) Sheng, C. Y.; Bozzelli, J.W.; Dean, A. M.; Chang, A. Y. J. Phys. Chem. A 2002, 106, 7276. doi: 10.1021/jp014540+
28. [28]
  (28) Huynh, L. K.; Carstensen, H. H.; Dean, A. M. J. Phys. Chem. A 2010, 114, 6594.
29. [29]
  (29) Baldwin, R. R.; Hisham, M.W. M.; Walker, R.W. J. Chem. Soc. Faraday Trans. 1 1982, 78, 1615. doi: 10.1039/f19827801615
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