Structural, spectroscopic (FT-IR, FT-Raman) and theoretical studies of the 1:1 cocrystal of isoniazid with p-coumaric acid

2013 ◽  
Vol 1033 ◽  
pp. 272-279 ◽  
Author(s):  
N. Ravikumar ◽  
Gopikrishna Gaddamanugu ◽  
K. Anand Solomon
2007 ◽  
Vol 834-836 ◽  
pp. 572-580 ◽  
Author(s):  
Monika Kalinowska ◽  
Renata Świsłocka ◽  
Włodzimierz Lewandowski

Molecules ◽  
2015 ◽  
Vol 20 (2) ◽  
pp. 3146-3169 ◽  
Author(s):  
Małgorzata Kowczyk-Sadowy ◽  
Renata Świsłocka ◽  
Hanna Lewandowska ◽  
Jolanta Piekut ◽  
Włodzimierz Lewandowski

2012 ◽  
Vol 27 (1) ◽  
pp. 35-48 ◽  
Author(s):  
Renata Swislocka ◽  
Malgorzata Kowczyk-Sadowy ◽  
Monika Kalinowska ◽  
Wlodzimierz Lewandowski

The evaluation of the electronic charge distribution in metal complexes enables more precise interpretation of mechanism by which particular metal ions affect biochemical properties of ligands [J. Inorg. Biochem. 99 (2005), 1407–1423, J. Mol. Struct. 919 (2009), 284–289]. In this paper we investigated the influence of alkali metal cations (lithium, sodium, potassium, rubidium and cesium) on the electronic structure ofp-coumaric acid (p-CA). It allowed to observe the systematic changes in the spectra of investigated complexes depending on the position of the element in the periodic table.p-Coumaric acid is a derivative of cinnamic acid that occurs in several plant species. Li, Na, K, Rb and Csp-coumarates were synthesized and the experimental and theoretical FT-IR, FT-Raman,1H and13C NMR spectra ofp-coumaric acid and its salts were registered and analyzed. The structures, atomic charges, infrared and NMR spectra ofp-coumaric acid and Li, Na, K salts were calculated by B3LYP/6-311++G**method.


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