A computational study of the structure, aromaticity and enthalpy of formation of UVA filter 4-tert-butyl-4 '-methoxydibenzoylmethane

• Type: Article in International Scientific Journal
• Date: 2014

Authors

Paulo J O Ferreira (Author) Other; Luis Pinto da Silva (Author) Other; Dario J R Duarte (Author) Other; Margarida S Miranda (Author) Other; Joaquim C G E Esteves da Silva (Author) FCUP

Journal

Title: Computational and Theoretical Chemistry

Vol. 1038

Pages: 6-16

ISSN: 2210-271X

Publisher: Elsevier

Indexing

ISI Web of Knowledge - 1 Citation

Scopus - 2 Citations

Scientific classification

FOS: Natural sciences > Chemical sciences

Other information

Authenticus ID: P-009-S9B

DOI: 10.1016/j.comptc.2014.03.037

Abstract (EN): In this study we have performed a density functional theory (DFT) study of the molecular structure and energetics of the enol and keto tautomers of UVA filter 4-tert-butyl-4'-methoxydibenzoylmethane (BMDBM) and for comparison and validation purposes a similar study has been carried out for the parent molecule: dibenzoylmethane (DBM). The molecular structure of the enol and keto tautomers were obtained at the B3LYP/6-311++G(d,p) level. The enol forms were found to have a strong intramolecular resonance assisted hydrogen bond that accounts for the greater energetic stability of the enol relative to the keto form. The aromatic character of the six-membered enol rings has been analyzed by calculation of Nucleus Independent Chemical Shifts (NICS). The standard molar enthalpy of formation in the gas phase of BMDBM was derived from appropriately chosen reactions.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 11