Conformational behaviour of organic carbonyl compounds. Part 2. Aldehydes and acetyl derivatives of condensed aromatic hydrocarbons
- 1 January 1981
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 2
- No. 2,p. 228-232
- https://doi.org/10.1039/p29810000228
Abstract
The relative conformer stability in a number of acetyl and formyl derivatives of condensed hydrocarbons has been determined by the lanthanide induced shift (LIS) method and by simulating the experimental chemical shifts. For the aldehydes of naphthalene the conformational results were confirmed by examining the n.m.r. spectra of model compounds with known probable conformation. In condensed hydrocarbons containing carbonyl substituents the behaviour found may be substantially related to three distinct situations, those comparable to the α- and β-positions of naphthalene and overcrowded positions comparable to position 4 in phenanthrene. Calculation of the conformation behaviour by the semi-empirical methods provide qualitative correct results only for systems where steric interactions are small.Keywords
This publication has 0 references indexed in Scilit: