The proton affinity of a series of substituted acetophenones in their low-lying excited triplet state: A DFT study
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry
Reference22 articles.
1. The ground state basicities of a series of substituted crotonaldehyde
2. The basicities of a series of substituted crotonaldehyde in their low-lying excited triplet state
3. Thiocarbonyl versus carbonyl compounds: A comparison of intrinsic reactivities
4. Background of the Hammett Equation As Observed for Isolated Molecules: Meta- and Para-Substituted Benzoic Acids
5. Quest for the Origin of Basicity: Initial vs Final State Effect in Neutral Nitrogen Bases
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Proton affinity and molecular basicity of m - and p -substituted benzamides in gas phase and in solution: A theoretical study;Chemical Physics Letters;2014-08
2. Proton affinity of para-substituted acetophenones in gas phase and in solution: a theoretical study;Journal of Molecular Modeling;2012-09-21
3. Complete gas-phase proton microaffinity analysis of five linear tetraamines containing two ethylenediamine residues;Journal of Molecular Structure: THEOCHEM;2010-07
4. The Li+ affinities of a series of substituted acetophenones in their low-lying excited triplet state: A DFT study;Journal of Molecular Structure: THEOCHEM;2009-01
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