Concurrent Phenomena at the Transition Region of Selected Elementary Chemical Reactions: An Information-Theoretical Complexity Analysis

被引:17
作者
Esquivel, Rodolfo O. [1 ,2 ,3 ]
Molina-Espiritu, Moyocoyani [1 ]
Dehesa, Jesus S. [2 ,3 ]
Carlos Angulo, Juan [2 ,3 ]
Antolin, Juan [3 ,4 ]
机构
[1] Univ Autonoma Metropolitana Iztapalapa, Dept Quim, Mexico City 09340, DF, Mexico
[2] Univ Granada, Dept Fis Atom Mol & Nucl, E-18071 Granada, Spain
[3] Univ Granada, Inst Carlos Fis Teor & Computac 1, E-18071 Granada, Spain
[4] Univ Zaragoza, EINA, Dept Fis Aplicada, Zaragoza 50018, Spain
关键词
statistical complexity; Fisher information; Shannon entropy; disequilibrium; chemical reactions; FISHER-INFORMATION; STATISTICAL COMPLEXITY; DENSITY; ENTROPY; STATE; REACTIVITY; POSITION; ENERGY; PLANE;
D O I
10.1002/qua.24219
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, we have investigated in position (r) and momentum (p) spaces the concurrent phenomena occurring at the vicinity of the transition state (TS) (the so-called transition region) of selected chemical reactions (such as the hydrogenic abstraction and the exchange hydrogenic reactions) by means of a broad set of single information-theoretic functionals of the one-particle density (such as the disequilibrium (D), exponential entropy (L), Fisher information (I) and the power entropy (J)) and composite information-theoretic measures which includes various information planes (such as the I-D, D-L, and I-J planes) and complexities of the Fisher-Shannon and Lopez-Mancini-Calbet (LMC) types. The analysis of the single functionals and the information planes revealed that these information-theoretical elements can identify all the chemically significant regions, not only the reactant/product regions (R/P) and the TS but also those that are not present in the energy profile, such as the bond cleavage energy region (BCER), the bond breaking/forming regions (B-B/F) and the charge transfer complex. Moreover, the analysis of the complexities shows that in position as well as in the joint (r-p) spaces, the energy profile of the abstraction reaction bears the same information-theoretical features of the LMC and FS measures. Finally, it is shown why most of the chemical features of interest (such as e. g., BCER and B-B/F) are lost in the energy profile, being only revealed when particular information-theoretical aspects of localizability (L or J), uniformity (D) and disorder (I) are considered. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:3578 / 3586
页数:9
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