Electronic structure of planar-quasicycled organic molecules with intramolecular hydrogen bond

By means of the HF/6-311G(d,p) method, the electronic structure of the series of organic molecules, among which are malonaldehyde, acetylacetone, thiomalonaldehyde,’the derivatives of aniline 2-XC6H4NH2, phenol 2-XC6H4OH, benzenethiol 2-XC6H4SH (X = CHO, COOH, COO-, NO, NO2, OH, OCH3, SH, SCH3, F, C...

Celý popis

Podrobná bibliografie
Hlavní autoři: ALEXEI N. PANKRATOV, ALEXEI V. SHALABAY
Médium: Článek
Jazyk:English
Vydáno: Serbian Chemical Society 2007-03-01
Edice:Journal of the Serbian Chemical Society
Témata:
On-line přístup:http://www.shd.org.yu/JSCS/Vol72/No3/JSCS_V72_No03-07.pdf
Popis
Shrnutí:By means of the HF/6-311G(d,p) method, the electronic structure of the series of organic molecules, among which are malonaldehyde, acetylacetone, thiomalonaldehyde,’the derivatives of aniline 2-XC6H4NH2, phenol 2-XC6H4OH, benzenethiol 2-XC6H4SH (X = CHO, COOH, COO-, NO, NO2, OH, OCH3, SH, SCH3, F, Cl, Br), 8-hydroxyquinoline, 8-mercaptoquinoline, tropolone, has been studied. The intramolecular hydrogen bond (IHB) has been established to lead to a local electron redistribution in quasicycle, and primarily to the electron density transfer between the direct IHB participants – from the hydrogen atom toward the proton-aceptor atom. On forming the IHB of the S–H···O type, the electron density in general decreases on the sulphohydryl hydrogen atom and increases on the sulphur atom.
ISSN:0352-5139