Intramolecular hydrogen bonding in α-phenylcinnamic acids and their heteroatom-containing derivatives studied by ab initio quantum chemical methods
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry
Reference17 articles.
1. Hydrogen bonding interactions of α-phenylcinnamic acid isomers in the liquid phase studied by IR and NMR spectroscopies and computational methods
2. Multimerization of Z-α-phenylcinnamic acid in solution: analysis via deconvoluted FTIR spectra
3. Calculated vs. measured IR characteristics of α-phenylcinnamic acid stereoisomers – structural consequences
4. Hydrogen-bonding interactions in the crystalline-phase structures of cinnamic acid derivatives
Cited by 5 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. Conformations of E-2-phenyl-3(2′-furyl)propenoic acid and its methyl ester in various solvents—an NMR study;Journal of Molecular Structure;2005-06
2. Conformations of stereoisomer furyl- and/or phenyl-substituted propenoic acid methyl esters—a computational study;Journal of Molecular Structure: THEOCHEM;2005-02
3. Hydrogen bonding interactions in E - or Z -2-phenyl-3-( X ?-pyridyl)propenoic acid ( X =2, 3 or 4) assemblies?a molecular modeling study;Journal of Molecular Modeling;2004-04-01
4. Hydrogen bonding networks in E- or Z-2-(3'-pyridyl)-3-phenylpropenoic (α-pyridylcinnamic) acid assemblies – a molecular modeling study;Journal of Molecular Modeling;2001-11
5. Structural motifs in α-pyridyl- and α-furylcinnamic acid assemblies- A molecular modeling study;International Journal of Quantum Chemistry;2001
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