Cho, Seung Joo Mohamed, Adel A. Elroby, Shaaban A. K. 2024-01-21T01:35:41Z 2024-01-21T01:35:41Z 2021-09-05 2007-01 0020-7608 https://pubs.kist.re.kr/handle/201004/134778 In the present investigation, the tautomeric and conformational equilibrium of isoorotic acid have been studied using Moller-Plesset second-order (MP2) and density functional theory (DFT) methods in the gas phase and aqueous solution (epsilon = 78.5) using the IPCM model. The relative energies of these tautomers have been calculated at the two levels of theory using 6-311++G** basis set. Energetics and relative stabilities of the tautomers; were compared and analyzed in both the gaseous and aqueous phases. The results indicate that the diketo tautomer (iso) is the most stable form in the gas phase and water. The carboxylic substitution in the uracil ring does not alter its relative stability order of the tautomers. The proton affinity of the oxygen atoms and the deprotonation enthalpy of the NH bonds of isoorotic acid have been compared with recent data of uracil. The relative stability of both syn- and anti-conformations was investigated and the syn form was found to be more stable by 17.65 kcal/mol. It was determined in ab initio calculations that an electron can attach to isoorotic acid, forming a stable anion better than uracil. (C) 2006 Wiley Periodicals, Inc. English WILEY INITIO QUANTUM-MECHANICS GAS-PHASE ELECTRON CORRELATION EQUILIBRIA URACIL THYMINE 3-HYDROXYPYRAZOLE STABILITIES PROTONATION AFFINITIES Theoretical investigation of the tautomerism of isoorotic acid in gaseous and aqueous phases Article 10.1002/qua.21013 1 INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, v.107, no.1, pp.63 - 71 INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY 107 1 63 71 scie scopus 000242000300008 2-s2.0-33751533021 Chemistry, Physical Mathematics, Interdisciplinary Applications Quantum Science & Technology Physics, Atomic, Molecular & Chemical Chemistry Mathematics Physics Article INITIO QUANTUM-MECHANICS GAS-PHASE ELECTRON CORRELATION EQUILIBRIA URACIL THYMINE 3-HYDROXYPYRAZOLE STABILITIES PROTONATION AFFINITIES MP2 DFT calculations tautomerism isoorotic acid IPCM