Does 2-Methylacetophenone Comply with Steric Inhibition of Resonance? A Direct Experimental Proof of Its Nonplanar Conformation from a Joint Ab Initio/Electron Diffraction Analysis-Reference-Cited by-同舟云学术

Does 2-Methylacetophenone Comply with Steric Inhibition of Resonance? A Direct Experimental Proof of Its Nonplanar Conformation from a Joint Ab Initio/Electron Diffraction Analysis

Published:2010-07-15 Issue:15 Volume:75 Page:4939-4943
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hnyk Drahomír¹,Samdal Svein²,Exner Otto³,Wann Derek A.⁴,Rankin David W. H.⁴

Affiliation:

1. Institute of Inorganic Chemistry of the ASCR, v.v.i., No. 1001, CZ-250 68 Husinec-Řež, Czech Republic

2. Centre for Theoretical and Computational Chemistry (CTCC), Department of Chemistry, University of Oslo, P.O. Box 1033 Blindern, NO-0315 Oslo, Norway

3. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, CZ-166 10 Praha 6, Czech Republic

4. School of Chemistry, University of Edinburgh, West Mains Road, Edinburgh EH9 3JJ, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo100291r

Reference44 articles.

1. Chemical constitution and the dissociation constants of monocarboxylic acids. Part XIII. Some alkylbenzoic acids exhibiting steric effects

2. Acid–base equilibria of substituted benzoic acids. Part I

3. Methyl group effect on the proton affinity of methylated acetophenones studied by two mass spectrometric techniques

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