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Phase/current information descriptors and equilibrium states in molecules

机译:相/电流信息描述符和分子中的平衡状态

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Quantum-generalized entropic descriptors of the complex electronic states and their information distances are reexamined and applied to the phase-equilibria in molecules. The relation between densities of the ordinary Fisher and Shannon measures of information content is used in determining their supplements due to phases/currents. These nonclassical terms complement the familiar classical (probability) functionals of information theory in the resultant information descriptors. The nonclassical Shannon entropy measures the average magnitude of the system phase distribution, while the current term in the related Fisher measure accounts for the gradient content of the state phase. The density constrained (vertical) and unconstrained (horizontal) equilibria in molecules are distinguished. The consistency requirement that the extreme entropic principles in terms of both these resultant measures have common solutions calls for the modified, negative sign of the nonclassical Fisher indeterminicity term. The equilibrium criteria are shown to give rise to the unitary phase-transformation of molecular states in a thermodynamic representation of quantum-mechanical description. Possible applications of this generalized description are discussed and thermodynamical analogies are commented upon. A separation of the density (modulus) and current (phase) factors of general many-electron states is effected using the Harriman-Zumbach-Maschke construction of antisymmetric states yielding the specified electron density. A phenomenological description of molecular subsystems is outlined, which accounts for both the density and phase degrees-of-freedom of electronic states, and the current promotion of molecular fragments is explored. (c) 2014 Wiley Periodicals, Inc.
机译:重新审查了复杂电子态的量子广义熵描述符及其信息距离,并将其应用于分子中的相平衡。信息内容的常规Fisher和Shannon度量的密度之间的关系用于确定由于相位/电流而导致的补充。这些非经典术语补充了所得信息描述符中熟悉的信息论经典(概率)功能。非经典香农熵度量的是系统相位分布的平均幅度,而相关Fisher度量中的当前项则说明了状态相位的梯度含量。区分了分子中的密度约束(垂直)平衡和非约束(水平)平衡。极端熵原则在这两种结果度量方面都具有通用解决方案的一致性要求,要求对非经典费舍尔不确定性术语进行修改后的负号。在量子力学描述的热力学表示中,平衡标准显示出引起分子态的单相转变。讨论了这种广义描述的可能应用,并对热力学类比进行了评论。一般多电子态的密度(模量)和电流(相位)因数的分离是使用产生指定电子密度的反对称态的Harriman-Zumbach-Maschke构造实现的。概述了分子子系统的现象学描述,它解释了电子态的密度和相自由度,并探讨了分子碎片的当前发展。 (c)2014年威利期刊有限公司

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