Tautomerism in an NH- and CH- acid: A theoretical approach
محل انتشار: نخستین همایش ملی توسعه در علوم و صنایع شیمیایی
سال انتشار: 1395
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 500
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شناسه ملی سند علمی:
SCIC01_043
تاریخ نمایه سازی: 10 تیر 1396
چکیده مقاله:
Intermolecular proton transfer in barbituric acid (BA) both in gas phase and in the presence the water molecule was investigated using B3LYP method with aug-cc-pVDZ basis set. The overall process involves keto-enol and lactam-lactim tautomerism that occurs. The most stable form of barbituric acid turns into the intermediates with three steps proton transfer at three different positions of the structure of this compound. Then, these intermediates becomes to the final products passing from two competing processes. In order to determine of the preference of each competitive process, energy changes of all possible tautomerism forms was investigated along with the role of solvent molecules in multiple routes. Also, transposition in the proton transfer process makes changes in the electron transfer energy which was investigated both in gas phase and in the presence of water molecule. Frequency calculations performed in order to determination of ground and transition states and also evaluation of zero point energies at B3LYP/aug-cc-pVDZ level of theory. Natural bond orbital analysis and topological property were investigated using natural bond orbital (NBO) and atom in molecule (AIM) analysis
کلیدواژه ها:
نویسندگان
Mohammad Zakarianezhad
Department of Chemistry, Payam Noor University, P. O. Box: ۷۸۱۵۷۵۳۶۱۳, Tehran, Iran
Batoul Makiabadi
Department of Chemical Engineering, Sirjan University of Technology, Sirjan, Iran