Citation: CAO Chen-Zhong, WU Ya-Xin. An Extended Istomin-Palm Model for Estimating the Enthalpies of Formation of the Two-Direction Extending Compounds R1-Y-R2[J]. Acta Physico-Chimica Sinica, ;2013, 29(01): 35-42. doi: 10.3866/PKU.WHXB201210261 shu

An Extended Istomin-Palm Model for Estimating the Enthalpies of Formation of the Two-Direction Extending Compounds R1-Y-R2

  • Received Date: 3 July 2012
    Available Online: 26 October 2012

    Fund Project: 国家自然科学基金(21072053) (21072053)湖南省教育厅科研基金(10K025)资助项目 (10K025)

  • Istomin and Palm proposed a model, ΔfH0(RX)=h[R]+h[X]+φ[R]φ[X], (the h[R] and h[X] are the contributions of alkyl R and substituent X to the ΔfH0(RX), respectively. φ[R]φ[X] represents the interaction of alkyl R and substituent X), to express the enthalpies of formation of monoderivatives of hydrocarbons ΔfH0(RX). However, in two-direction extending compounds R1-Y-R2, the Y substituent is attached to two alkyl groups (R1 and R2), and the intramolecular interactions are more complicated than that in monosubstituted alkanes. Thus, the Istomin-Palm model must be modified. In this work, the interactions among Y, R1, and R2 contributing to the enthalpy of formation, ΔfH0(R1-Y-R2), are divided into three parts: the interaction between R1Y and R2(φ[R2]φ[R1Y]), the interaction between YR2 and R1 (φ[R1]φ[YR2]), and the interaction between R1 and R2 (ψ[R1]ψ[R2]). These three interactions replace the φ[R]φ[X] term, and a new extended Istomin-Palm model, ΔfH0(R1-Y-R2)=h[R1]+h[R2]+h[Y] +φ[R1]φ[YR2]+φ[R2]φ[R1Y]+ψ[R1]ψ[R2], is proposed. In this model, h[Y] is the contribution of substituent Y to ΔfH0(R1-Y-R2). The h[R1] and h[R2] terms are the contributions of alkyls R1 and R2 to ΔfH0(R1-Y-R2). The last three terms are the total contribution of interactions among Y, R1, and R2. Furthermore, the interaction potential index IPI(X) reported in our recent work (Wu, Y. X.; Cao, C. Z.; Yuan, H. Chin. J. Chem. Phys. 2012, 25 (2), 153.) was employed to express the intrinsic interaction of Y with alkyl groups (φ[Y]), and two general expressions were established to estimate ΔfH0, in which one is for thioethers, secondary amines, ethers, and ketones, and the other is for esters. These two estimating equations give results, which are as accurate as G3 and G3MP2 models in calculating ΔfH0 for R1-Y-R2 compounds. Moreover, our method avoids time consuming calculations.

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    1. [1]

      (1) Wiberg, K. B.;Waldron, R. F. J. Am. Chem. Soc. 1991, 113,7 697. doi: 10.1021/ja00020a036

    2. [2]

      (2) Laurencelle, N.; Pacey, P. D. J. Am. Chem. Soc. 1993, 115, 625.doi: 10.1021/ja00055a035

    3. [3]

      (3) Milburn, R. K.; Rodriquez, C. F.; Hopkinson, A. C. J. Phys.Chem. B 1997, 101, 1837. doi: 10.1021/jp962303e

    4. [4]

      (4) Herndon,W. C.; Biedermann, P. U.; Agranat, I. J. Org. Chem.1998, 63, 7445. doi: 10.1021/jo981280s

    5. [5]

      (5) Zheng, K. C.; Kuang, D. B.; Yun, F. C.; He, F. ActaPhys. -Chim. Sin. 2000, 16, 133. [郑康成, 匡代彬, 云逢存,何峰. 物理化学学报, 2000, 16, 133.] doi: 10.3866/PKU.W HXB20000208

    6. [6]

      (6) Zheng, K. C.; Zhang, Z. Q.; Shen, Y.; Yun, F. C. ActaPhys. -Chim. Sin. 2001, 17, 448. [郑康成, 张仲钦, 沈勇,云逢存. 物理化学学报, 2001, 17, 448.] doi: 10.3866/PKU.W HXB20010514

    7. [7]

      (7) Sorkhabi, O.; Qi, F.; Rizvi, A. H.; Suits, A. G. J. Am. Chem. Soc.2001, 123, 671. doi: 10.1021/ja0017312

    8. [8]

      (8) Yang, F.;Wang, Z.; Huang, Y.; Ding, X. J. Chem. Inf. Comput.Sci. 2003, 43, 753. doi: 10.1021/ci025663+

    9. [9]

      (9) Yang, F.;Wang, Z.; Huang, Y.; Zhou, P. J. Chem. Inf. Comput.Sci. 2003, 43, 1337. doi: 10.1021/ci0340512

    10. [10]

      (10) Exner, O.; Böhm, S. J. Comput. Chem. 2004, 25, 1979. doi: 1 0.1002/jcc.v25:16

    11. [11]

      (11) Emel'yanenko, V. N.; Kabo, G. J.; Verevkin, S. P. J. Chem. Eng.Data 2006, 51, 79. doi: 10.1021/je050230z

    12. [12]

      (12) Cao, C. Z.; Liu, J. L. Acta Phys. -Chim. Sin. 2007, 23, 955.[ 曹晨忠, 刘金玲. 物理化学学报, 2007, 23, 955.] doi: 10.3866/P KU.WHXB20070632

    13. [13]

      (13) Bond, D. J. Org. Chem. 2007, 72, 7313. doi: 10.1021/jo071213a

    14. [14]

      (14) Thalladi, V. R.;Weiss, H. C.; Blalser, D.; Boese, R.; Nangia, A.;D esiraju, G. R. J. Am. Chem. Soc. 1998, 120, 8702. doi: 1 0.1021/ja981198e

    15. [15]

      (15) Glaser, R. J. Org. Chem. 2001, 66, 771. doi: 10.1021/jo001241s

    16. [16]

      (16) Ju, X. H.; Li, Y. M.; Xiao, H. M. J. Phys. Chem. A 2005, 109,9 34. doi: 10.1021/jp045071p

    17. [17]

      (17) Gung, B.W.; Zou, Y.; Xu, Z.; Amicangelo, J. C.; Irwin, D. G.;M a, S.; Zhou, H. C. J. Org. Chem. 2008, 73, 689. doi: 10.1021/j o702170j

    18. [18]

      (18) Mathieu, D. J. Chem. Theory Comput. 2012, 8, 1295. doi: 1 0.1021/ct2006083

    19. [19]

      (19) Jabloński, M. J. Phys. Chem. A 2012, 116, 3753. doi: 10.1021/j p300993b

    20. [20]

      (20) (a) Istomin, B. I.; Palm, V. A. Reakts. Sposobnost Organ.Soedin. (Tartu) 1971, 8, 845.

    21. [21]

      (b) Istomin, B. I.; Palm, V. A. Reakts. Sposobnost Organ.Soedin. (Tartu) 1972, 9, 433.

    22. [22]

      (c) Istomin, B. I.; Palm, V. A. Reakts. Sposobnost Organ.Soedin. (Tartu) 1972, 9, 469.

    23. [23]

      (d) Istomin, B. I.; Palm, V. A. Reakts. Sposobnost Organ.Soedin. (Tartu) 1972, 9, 847.

    24. [24]

      (21) Cao, C. Z.; Gao, S. Acta Phys. -Chim. Sin. 2005, 21, 1028.[ 曹晨忠, 高硕. 物理化学学报, 2005, 21, 1028.] doi: 10.3866/P KU.WHXB20050917

    25. [25]

      (22) Cao, C. Z.; Gao, S.; Zeng, R. J. J. Mol. Struct. -Theochem 2005,728, 85. doi: 10.1016/j.theochem.2005.05.008

    26. [26]

      (23) Cao, C. Z. QSAR Comb. Sci. 2008, 27, 555.

    27. [27]

      (24) Wu, Y. X.; Cao, C. Z.; Yuan, H. Chin. J. Chem. Phys. 2012, 25 (2), 153. doi: 10.1088/1674-0068/25/02/153-160

    28. [28]

      (25) Cao, C. Z.; Li, Z. L. J. Chem. Inf. Comput. Sci. 1998, 38, 1. doi: 1 0.1021/ci9601729

    29. [29]

      (26) Cao, C. Z. Substituent Effects in Organic Chemistry; ScienceP ress: Beijing, 2003. [曹晨忠. 有机化学中的取代基效应. 北京 : 科学出版社, 2003.]

    30. [30]

      (27) Cao, C. Z.; Liu, L. J. Chem. Inf. Comput. Sci. 2004, 44, 678.d oi: 10.1021/ci034266b

    31. [31]

      (28) Haynes,W. M. CRC Handbook of Chemistry and Physics, 91ste d.; CRC Press: Boca Raton, FL, 2010-2011.

    32. [32]

      (29) Domalski, E. S.; Hearing, E. D. J. Phys. Chem. Ref. Data 1993,22, 805. doi: 10.1063/1.555927


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