RT Journal Article
T1 Peculiarities of the spatial and electronic structure of 2-Aryl-1,2,3-triazol-5-carboxylic acids and their salts on the basis of spectral studies and DFT calculations
A1 Alcolea Palafox, Mauricio
A1 Belskaya, Nataliya
A1 Kostova, Irena
AB The molecular structure and vibrational spectra of six 1,2,3-triazoles-containing molecules with possible anticancer activity were investigated. For two of them, the optimized geometry was determined in the monomer, cyclic dimer and stacking forms using the B3LYP, M06-2X and MP2 methods implemented in the GAUSSIAN-16 program package. The effect of the para-substitution on the aryl ring was evaluated based on changes in the molecular structure and atomic charge distribution of the triazole ring. An increment in the positive N4 charge was linearly related to a decrease in both the aryl ring and the carboxylic group rotation, with respect to the triazole ring, and by contrast, to an increment in the pyrrolidine ring rotation. Anionic formation had a larger effect on the triazole ring structure than the electronic nature of the different substituents on the aryl ring. Several relationships were obtained that could facilitate the selection of substituents on the triazole ring for their further synthesis. The observed IR and Raman bands in the solid state of two of these compounds were accurately assigned according to monomer and dimer form calculations, together with the polynomic scaling equation procedure (PSE). The large red-shift of the C=O stretching mode indicates that strong H-bonds in the dimer form appear in the solid state through this group.
PB MDPI
SN 1422-0067
YR 2023
FD 2023
LK https://hdl.handle.net/20.500.14352/109132
UL https://hdl.handle.net/20.500.14352/109132
LA eng
NO Alcolea Palafox, M.; Belskaya, N.P.; Kostova, I.P. Peculiarities of the Spatial and Electronic Structure of 2-Aryl-1,2,3-Triazol-5-Carboxylic Acids and Their Salts on the Basis of Spectral Studies and DFT Calculations. Int. J. Mol. Sci. 2023, 24, 14001. https://doi.org/10.3390/ ijms241814001
DS Docta Complutense
RD 30 dic 2025