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Local hardness equalization: Exploiting the ambiguity
被引:78
作者:
Ayers, Paul W.
[1
]
Parr, Robert G.
[2
]
机构:
[1] McMaster Univ, Dept Chem, Hamilton, ON L8S 4M1, Canada
[2] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
基金:
加拿大自然科学与工程研究理事会;
关键词:
D O I:
10.1063/1.2918731
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 the density-functional theory of chemical reactivity, the local hardness is known to be an ambiguous concept. The mathematical structure associated with this problematic situation is elaborated and three common definitions for the local hardness are critically examined: the frontier local hardness [S. K. Ghosh, Chem. Phys. Lett. 172, 77 (1990)], the total local hardness [S. K. Ghosh and M. Berkowitz, J. Chem. Phys. 83, 2976 (1985)], and the unconstrained local hardness [P. W. Ayers and R. G. Parr, J. Am. Chem. Soc. 122, 2010 (2000)]. The frontier local hardness has particularly nice properties: (a) it has smaller norm than most, if not all, other choices of the local hardness and (b) it is "unbiased" in an information-theoretic sense. For the ground electronic state of a molecular system, the frontier local hardness is equal to the global hardness. For an electronic system in its ground state, both the chemical potential and the frontier local hardness are equalized. The frontier local hardness equalization principle provides a computational approach for designing reagents with desirable chemical reactivity profiles. (C) 2008 American Institute of Physics.
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