Extended conjugation in enynones, dienones and related species: A theoretical and experimental study. the molecular structures of 3-ethynyl-2-methylcyclopent-2-enone, 3-ethenyl-2-methylcyclopent-2-enone and 3-ethyl-2-methylcyclopent-2-enone, as studied by gas electron diffraction

Marit Trætteberg, Joel F. Liebman, Martin Hulce, Anthony A. Bonn, Donald W. Rogers

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Abstract

The molecular structures of three 3-R substituted conjugated enones have been determined by the gas electron difraction method. Depending on the nature of the substituents the molecules represent examples of molecules with no additional conjugation, relative to that of the enone system (R = CH3CH2-), or those with extended conjugation involving different π systems (R = CH2=CH-; R = HC≡C-). The molecular structures of the three enones have also been calculated by ab initio MP2/6-31G* optomizations. In order to better understand the conjugative effects of ethynyl and ethynyl substituents on a conjugated enone system, a large number of hydrogenation reactions and substituent exchange reactions have been studied, based on the energies of the various molecules involved in the reactions, as calculated by MP2/6-31G* optimizationS. The studies indicate that the conjugative effect of an ethynyl substituent on a conjugated enone system is approximately 4.2 kcal mol-1, while that of an ethynyl substituent is considerably lower and more variable; on average ca. 2.3 kcal mol-1.

Original languageEnglish
Pages (from-to)1925-1932
Number of pages8
JournalJournal of the Chemical Society. Perkin Transactions 2
Issue number10
StatePublished - Oct 1997

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Electron diffraction
Molecular structure
Molecules
Electron gas
Hydrogenation
Ion exchange

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

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title = "Extended conjugation in enynones, dienones and related species: A theoretical and experimental study. the molecular structures of 3-ethynyl-2-methylcyclopent-2-enone, 3-ethenyl-2-methylcyclopent-2-enone and 3-ethyl-2-methylcyclopent-2-enone, as studied by gas electron diffraction",
abstract = "The molecular structures of three 3-R substituted conjugated enones have been determined by the gas electron difraction method. Depending on the nature of the substituents the molecules represent examples of molecules with no additional conjugation, relative to that of the enone system (R = CH3CH2-), or those with extended conjugation involving different π systems (R = CH2=CH-; R = HC≡C-). The molecular structures of the three enones have also been calculated by ab initio MP2/6-31G* optomizations. In order to better understand the conjugative effects of ethynyl and ethynyl substituents on a conjugated enone system, a large number of hydrogenation reactions and substituent exchange reactions have been studied, based on the energies of the various molecules involved in the reactions, as calculated by MP2/6-31G* optimizationS. The studies indicate that the conjugative effect of an ethynyl substituent on a conjugated enone system is approximately 4.2 kcal mol-1, while that of an ethynyl substituent is considerably lower and more variable; on average ca. 2.3 kcal mol-1.",
author = "Marit Tr{\ae}tteberg and Liebman, {Joel F.} and Martin Hulce and Bonn, {Anthony A.} and Rogers, {Donald W.}",
year = "1997",
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language = "English",
pages = "1925--1932",
journal = "Journal of the Chemical Society, Perkin Transactions 2",
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TY - JOUR

T1 - Extended conjugation in enynones, dienones and related species

T2 - A theoretical and experimental study. the molecular structures of 3-ethynyl-2-methylcyclopent-2-enone, 3-ethenyl-2-methylcyclopent-2-enone and 3-ethyl-2-methylcyclopent-2-enone, as studied by gas electron diffraction

AU - Trætteberg, Marit

AU - Liebman, Joel F.

AU - Hulce, Martin

AU - Bonn, Anthony A.

AU - Rogers, Donald W.

PY - 1997/10

Y1 - 1997/10

N2 - The molecular structures of three 3-R substituted conjugated enones have been determined by the gas electron difraction method. Depending on the nature of the substituents the molecules represent examples of molecules with no additional conjugation, relative to that of the enone system (R = CH3CH2-), or those with extended conjugation involving different π systems (R = CH2=CH-; R = HC≡C-). The molecular structures of the three enones have also been calculated by ab initio MP2/6-31G* optomizations. In order to better understand the conjugative effects of ethynyl and ethynyl substituents on a conjugated enone system, a large number of hydrogenation reactions and substituent exchange reactions have been studied, based on the energies of the various molecules involved in the reactions, as calculated by MP2/6-31G* optimizationS. The studies indicate that the conjugative effect of an ethynyl substituent on a conjugated enone system is approximately 4.2 kcal mol-1, while that of an ethynyl substituent is considerably lower and more variable; on average ca. 2.3 kcal mol-1.

AB - The molecular structures of three 3-R substituted conjugated enones have been determined by the gas electron difraction method. Depending on the nature of the substituents the molecules represent examples of molecules with no additional conjugation, relative to that of the enone system (R = CH3CH2-), or those with extended conjugation involving different π systems (R = CH2=CH-; R = HC≡C-). The molecular structures of the three enones have also been calculated by ab initio MP2/6-31G* optomizations. In order to better understand the conjugative effects of ethynyl and ethynyl substituents on a conjugated enone system, a large number of hydrogenation reactions and substituent exchange reactions have been studied, based on the energies of the various molecules involved in the reactions, as calculated by MP2/6-31G* optimizationS. The studies indicate that the conjugative effect of an ethynyl substituent on a conjugated enone system is approximately 4.2 kcal mol-1, while that of an ethynyl substituent is considerably lower and more variable; on average ca. 2.3 kcal mol-1.

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