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Conformations of some αβ-unsaturated carbonyl compounds. Part I. Infrared spectra of acraldehyde, crotonaldehyde, methyl vinyl ketone, and ethylideneacetone

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TLDR
In this article, the infrared spectra of acraldehyde, crotonaldehyde, methyl vinyl ketone, and ethylideneacetone in solution and vapour states are reported, and band intensity measurements at temperatures between -110° and 200° are interpreted in terms of conformational equilibrium between the s-trans and non-trans forms of the ketones.
Abstract
Infrared spectra of acraldehyde, crotonaldehyde, methyl vinyl ketone, and ethylideneacetone in solution and vapour states are reported. Band intensity measurements at temperatures between –110° and 200° are interpreted in terms of conformational equilibrium between the s-trans and non-trans forms of the ketones. The additional enthalpy (ΔH) of the non-trans forms are: [graphic omitted] No evidence is found for more than one form of the aldehydes and the rotational structure of vibrational bands of both acraldehyde and crotonaldehyde suggest these exist in the s-trans conformation. Vibrational assignments are provided for the various conformations detected in these compounds.

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Improved chemoselective hydrogenation of crotonaldehyde over bimetallic AuAg/SBA-15 catalyst

TL;DR: In this article, bimetallic AuAg/SBA-15 catalysts were disclosed to efficiently catalyze vapor-phase chemoselective hydrogenation of crotonaldehyde (CRAL) with improved hydrogenation rate and selectivity to crotonyl alcohol (CROL).
Journal ArticleDOI

Matrix isolation study of the early intermediates in the ozonolysis of cyclopentene and cyclopentadiene: observation of two Criegee intermediates.

TL;DR: Evidence is presented for the formation, identification, and characterization of the long sought-after Criegee intermediate for each system, as well as the primary and secondary ozonides.
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Étude par spectrométrie photoélectronique d'aldéhydes et de cétones éthyléniques conjugués

TL;DR: In this paper, the methode MINDO/3 was used for the analysis of photo-electrons (SPE-UV) in terms of their geometries optimisees des molecules, l'ordre des orbitales moleculaires and les energies des molecules peu substituees en revanche.
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