متن کامل ترجمه مقاله ISI در Elsevier در فایل word به فروش می رسد که ترجمه چکیده آن را به عنوان نمونه می توانید ملاحظه فرمایید. 14 صفحه ورد و6صفحه PDF به زبان اصلی Correlation of aqueous pKa values of carbon acids with theoretical descriptors: A DFT study Abstract Theoretical calculations are carried out to predict gas- and aqueous-phase acidities of a series of 21 carbon acids with pKa values varying from 6.20 to 50. Acceptable linear correlations (R2> 0.93, SD < 4) are obtained between calculated deprotonation Gibbs free energy changes and experimental pKa values (measured in water). Solvent effects are taken into account by means of the polarizable continuum model (PCM). Our calculations also show that the high acidity of a-proton carbonyl compounds and electron-withdrawing substituted methanes can be related to the strong increase in the vicinal charge interactions nc fi p* in anion species. Calculations are performed at the B3LYP/6-311++G(d,p) level of theory. ارتباط مقادی ...
دریافت فایل