Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/70251
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dc.contributor.authorSu, C.C.en_US
dc.contributor.authorLin, C.K.en_US
dc.contributor.authorWu, C.C.en_US
dc.contributor.authorLien, M.H.en_US
dc.date1999zh_TW
dc.date.accessioned2014-06-11T05:59:34Z-
dc.date.available2014-06-11T05:59:34Z-
dc.identifier.issn1089-5639zh_TW
dc.identifier.urihttp://hdl.handle.net/11455/70251-
dc.description.abstractAb initio molecular orbital calculations have been performed on the alpha-substituted acetaldehydes XH(2)CCH=O (X=H, BH(2), CH(3), NH(2), OH, F, CN, NC, and Cl) to investigate the substituent effects on the keto-enol tautomerisms. Structures for all stationary point (ketones, enols, and transition states) were optimized and characterized at the MP2(full)/6-31G* and MP2(full)/6-31G** levels of theory. intrinsic reaction coordinates (IRC) calculations were performed in order to connect transition structures with the appropriate tautomeric pairs. Results from various levels of calculations all show that the keto forms are thermodynamically more stable than the enol forms. At the G2 level, the former tautomers are energetically favored over the latter forms by 2.9, 5.6, 7.8, 9.6, 9.7, 10.2, 10.4, 11.8, and 12.1 kcal/mol for X = BH(2), CN, NC, NH(2), CH(3), OH, Cl, H, and F, respectively. All substituents except F stabilize the enol form relative to its keto counterpart as shown by the reduction of the energy gaps between the former and the latter forms. At the same G2 level, the respective activation energies of enolizations relative to the keto form were found to be 42.2, 58.0, 60.8, 61.8, 62.4, 63.3, 63.8, 64.5, and 65.3 kcal/mol for X = BH(2), CN, NC, NH(2), Cl, OH, CH(3), H, and F. Except for X = F, the alpha-substituted aldehydes all lower the barrier to the tautomeric interconversions. The substituent effects on the energetics in this study were compared with the results obtained from our previous theoretical investigations on the tautomeric interconversion of CH(3)COX and XCH(2)CHNH where X = BH(2), CH(3), NH(2), OH, F, CN, H, and Cl.en_US
dc.language.isoen_USzh_TW
dc.relationJournal of Physical Chemistry Aen_US
dc.relation.ispartofseriesJournal of Physical Chemistry A, Volume 103, Issue 17, Page(s) 3289-3293.en_US
dc.relation.urihttp://dx.doi.org/10.1021/jp9839910en_US
dc.subjectvinyl alcoholen_US
dc.subjectvibrational frequenciesen_US
dc.subjectenamine tautomerismen_US
dc.subjectenergiesen_US
dc.subjectcomplexesen_US
dc.subjecthydrogenationen_US
dc.subjectequilibriaen_US
dc.subjectsystemsen_US
dc.subjectiminesen_US
dc.subjectstateen_US
dc.titleAb initio study on the keto-enol tautomerism of the alpha-substituted acetaldehydes XH(2)CCH=O (X = H, BH(2), CH(3), NH(2), OH, F, CN, NC, and Cl): Comparison with the tautomerism in alpha-substituted acetaldimines and acetyl derivativesen_US
dc.typeJournal Articlezh_TW
dc.identifier.doi10.1021/jp9839910zh_TW
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