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9篇 您的检索式:作者名="Geerlings De Proft"
    题名 作者 年代 出处 被引量
1Conceptual density functional theory显示文摘Geerlings De Proft Langenaeke 2003Chem Rev2003,103,:1
2Density functional theory study of the conformation and energetics of silanol and disiloxane显示文摘Tielens F De proft F Geerlings P 2001Journal of MolecularStructure: THEOCHEM2001,542,13:1
3显示文摘GEERLINGS P DE PROFT F LANGENAEKER W 2003Chem Rev2003,103,:1
4Conceptual density functional theory 显示文摘GEERLINGS P de PROFT F LANGENAEKER W 2003Chem Rev2003,103,:1
5Conceptual Density Functional Theory显示文摘Geerlings P De Proft F Langenaeker W 1971Chem Rev1971,103,5:1
6Acidity of alkyl substituted alcohols are alkyl-groups electron-donating or eectron-withdrawing显示文摘De Proft F Langenaeker W Geerlings P 1995Tetrahedron1995,51,:1
7Conceptual density functional theory显示文摘GEERLINGS P DE PROFT F LANGENAEKER W 2003Chem Rev2003,103,:1
8Analogies between Density Functional Theory Response Kernels and Derivatives of Thermodynamic State Functions显示文摘In view of its use as reactivity theory,Conceptual Density Functional Theory(DFT),introduced by Parr et al.,has mainly concentrated up to now on the E = E[N,v] functional.However,different ensemble representations can be used involving other variables also,such as ρ and μ.In this study,these different ensemble representations(E,?,F,and R) are briefly reviewed.Particular attention is then given to the corresponding second-order(functional) derivatives,and their analogieswith the second-order derivatives of thermodynamic state functions U,F,H,and G,which are related to each other via Legendre transformations,just as the DFT functionals(Nalewajski and Parr,1982).Starting from an analysis of the convexity/concavity of the DFT functionals,for which explicit proofs are discussed for some cases,the positive/negative definiteness of the associated kernels is derived and a detailed comparison is made with the thermodynamic derivatives.The stability conditions in thermodynamics are similar in structure to the convexity/concavity conditions for the DFT functionals.Thus,the DFT functionals are scrutinized based on the convexity/concavity of their two variables,to yield the possibility of establishing a relationship between the three second-order reactivity descriptors derived from the considered functional.Considering two ensemble representations,F and ?,F is eliminated as it has two dependent(extensive)variables,N and ρ.For ?,on the other hand,which is concave for both of its intensive variables(μ and υ),an inequality is derived from its three second-order(functional) derivatives:the global softness,the local softness,and the softness kernel.Combined with the negative value of the diagonal element of the linear response function,this inequality is shown to be compatible with the Berkowitz-Parr relationship,which relates the functional derivatives of ρ with υ,at constant N and μ.This was recently at stake upon quantifying Kohn's Nearsightedness of Electronic Matter.The analogy of the resulting inequality and the thermodynamic inequality for the G derivatives is highlighted.Potential research paths for this study are briefly addressed;the analogies between finite-temperature DFT response functions and their thermodynamic counterparts and the quest for analogous relationships,as derived in this paper,for DFT functionals that are analogues of entropy-dimensioned thermodynamic functions such as the Massieu function.GEERLINGS Paul DE PROFT Frank FIAS Stijn 2018物理化学学报2018,34,6:1
9Conceptualdensity functional theory显示文摘P Geerlings F De Proft W Langenaeker 2003Chemical Reviews2003,103,5:1
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