Abstract

Information channels from SCF MO calculations using different basis sets and their entropic bond descriptors are compared within the orbital communication theory. In this information-theoretic (IT) treatment of communications between basis functions the overall covalency and ionicity bond components reflect the average communication noise and information flow, respectively, in the resolution level specified by the adopted set of basis functions. The basis-set dependence of the orbital conditional probabilities and their entropic descriptors of the information covalency/ionicity content is explored. Compared to the minimum set \({{\bf \chi}}\) of the occupied atomic orbitals of the separated constituent atoms, the extended basis sets of Gaussian orbitals and/or their formal contractions generally give rise to a higher IT-covalency and lower IT-ionicity descriptors of the system chemical bonds. In the augmented set case, \({{\bf \chi}^{aug.} = ({\bf \chi},{\bf \psi})}\) , containing the polarization function complement \({{\bf \psi}}\) of \({{\bf \chi}}\) , the use of only \({{\bf \chi} \rightarrow {\bf \chi}}\) communications is advocated in a semi-quantitative chemical interpretation of the IT bond indices. The maximum-overlap criterion is used to transform the general (orthonormal) extended basis \({{\bf \xi}}\) to its semi-augmented form \({\widetilde{\bf \chi}^{aug.} = \widetilde{\bf \xi}=(\widetilde{\bf \chi}, \widetilde{\bf \psi}),}\) in which \({\widetilde {\bf \chi} \approx {\bf \chi}}\) and \({\widetilde {\bf \psi} \approx{\bf \psi}}\), which facilitates the near minimum basis set interpretation of bond descriptors and extraction of communications involving the polarization functions \({{\widetilde {\mathbf \psi}}}\) . A similar transformation using the minimum information distance criterion can be also envisaged. The effect of the atomic reduction of the molecular channels, which misses the effect of the “internal” communications (bonds) on constituent atoms, is also examined. As intuitively expected, the IT descriptors of such reduced channels are found to be less sensitive to the basis set enlargement.

Highlights

  • The information theory (IT) [1,2,3,4,5,6,7] has recently been effectively used as a unifying concept in physics [8] and in an exploration of the electronic structure of molecules [9,10,11]

  • P(i → j |k); i ∈ χ, j ∈ χ, k ∈ χaug. . (21). This information channel involves the extended-set of basis functions as intermediates in the effective communications between the minimum-set atomic orbitals (AO) in the cascade input and output, which are occupied in the promolecule combining the free atoms placed in their molecular positions

  • SAξ B(i nt.) SAχB(i nt.) SAχB(i nt.) SAξ B(ext.) SAχB(ext.) SAχB(ext.). It was the main goal of the present analysis to find satisfactory tools for interpreting the entropic descriptors of the molecular information channels in orbital resolution, which are known to be strongly basis-set dependent

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Summary

Introduction

The information theory (IT) [1,2,3,4,5,6,7] has recently been effectively used as a unifying concept in physics [8] and in an exploration of the electronic structure of molecules [9,10,11]. It generates the communication noise in the ground-state propagation of signals of the electron allocations to basis functions of SCF MO calculations, e.g., the (orthogonalized) atomic orbitals (AO), and gives rise to an effective flow of information contained in the electron probability distributions The former has been linked to the molecular overall bond-covalency, while the latter reflects the associated bond-ionicity. The non-additive part of the Fisher information in MO resolution [25] has been shown to generate the familiar electron localization function (ELF) [39,40,41], while the associated AO-resolved measure provides the basis of the Contra-gradience (CG) probe [10,11,26] of the chemical bond localization in molecular systems [10,11,26,27,28,29] These novel IT criteria complement the familiar density-difference analysis reflecting the reconstruction of the initial densities of free atoms of the promolecule through the polarization (promotion) of the constituent atoms and the charge-transfer (CT) between them. The entropic descriptors are measured in bits, the unit corresponding to the basis 2 of the logarithmic measure of information

Molecular conditional probabilities and their information descriptors
Molecular communications in the minimum and augmented bases
Use of the maximum overlap criterion
Atomic reductions and diatomic subchannels
Maximum information-similarity criterion
Numerical calculations
HF F2 NaCl H2 O CO2 NH3 CH4 C2 H6 C2 H2 C6H6
HF F2 NaCl H2 O CO2 NH3 CH4 C2 H6
Conclusions
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