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231224s2014 xx |||||o 00| ||eng c |
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|a 10.1002/jcc.23599
|2 doi
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|a pubmed24n0791.xml
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|a (NLM)24740548
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|a DE-627
|b ger
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|e rakwb
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|a eng
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| 100 |
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|a Tsuneda, Takao
|e verfasserin
|4 aut
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|a Reactivity index based on orbital energies
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|c 2014
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Completed 13.04.2015
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|a Date Revised 22.04.2014
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a Copyright © 2014 Wiley Periodicals, Inc.
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|a This study shows that the chemical reactivities depend on the orbital energy gaps contributing to the reactions. In the process where a reaction only makes progress through charge transfer with the minimal structural transformation of the reactant, the orbital energy gap gradient (OEGG) between the electron-donating and electron-accepting orbitals is proven to be very low. Using this relation, a normalized reaction diagram is constructed by plotting the normalized orbital energy gap with respect to the normalized intrinsic reaction coordinate. Application of this reaction diagram to 43 fundamental reactions showed that the majority of the forward reactions provide small OEGGs in the initial stages, and therefore, the initial processes of the forward reactions are supposed to proceed only through charge transfer. Conversely, more than 60% of the backward reactions are found to give large OEGGs implying very slow reactions associated with considerable structural transformations. Focusing on the anti-activation-energy reactions, in which the forward reactions have higher barriers than those of the backward ones, most of these reactions are shown to give large OEGGs for the backward reactions. It is also found that the reactions providing large OEGGs in the forward directions inconsistent with the reaction rate constants are classified into SN 2, symmetric, and methyl radical reactions. Interestingly, several large-OEGG reactions are experimentally established to get around the optimum pathways. This indicates that the reactions can take significantly different pathways from the optimum ones provided no charge transfer proceeds spontaneously without the structural transformations of the reactants
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|a Journal Article
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|a SN2 reactions
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|a charge transfer
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|a chemical reactivity
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|a long-range correction
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| 650 |
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|a orbital energy gap
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| 650 |
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|a reaction pathway
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|a Singh, Raman K
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Journal of computational chemistry
|d 1984
|g 35(2014), 14 vom: 30. Mai, Seite 1093-100
|w (DE-627)NLM098138448
|x 1096-987X
|7 nnns
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| 773 |
1 |
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|g volume:35
|g year:2014
|g number:14
|g day:30
|g month:05
|g pages:1093-100
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| 856 |
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|u http://dx.doi.org/10.1002/jcc.23599
|3 Volltext
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