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 language | English |
|---|---|
| Pages (from-to) | 1925-1932 |
| Number of pages | 8 |
| Journal | Journal of the Chemical Society. Perkin Transactions 2 |
| Issue number | 10 |
| State | Published - Oct 1997 |
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All Science Journal Classification (ASJC) codes
- Chemistry(all)
Cite this
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. / Trætteberg, Marit; Liebman, Joel F.; Hulce, Martin; Bonn, Anthony A.; Rogers, Donald W.
In: Journal of the Chemical Society. Perkin Transactions 2, No. 10, 10.1997, p. 1925-1932.Research output: Contribution to journal › Article
}
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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M3 - Article
AN - SCOPUS:0345911388
SP - 1925
EP - 1932
JO - Journal of the Chemical Society, Perkin Transactions 2
JF - Journal of the Chemical Society, Perkin Transactions 2
SN - 1470-1820
IS - 10
ER -