MD Study of S(N)1 Reactivity of 2-Chloro-2-methylpropane in the Room-Temperature Ionic Liquid 1-Ethyl-3-methylimidazolium Hexafluorophosphate.

MD Study of S(N)1 Reactivity of 2-Chloro-2-methylpropane in the Room-Temperature Ionic Liquid 1-Ethyl-3-methylimidazolium Hexafluorophosphate. Research Abstract Details 

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MD Study of S(N)1 Reactivity of 2-Chloro-2-methylpropane in the Room-Temperature Ionic Liquid 1-Ethyl-3-methylimidazolium Hexafluorophosphate. Abstract Text:

Youngseon Shim,Hyung J Kim,

The SN1 ionization reaction RX --> R+ + X- for 2-chloro-2-methylpropane in ionic liquid 1-ethyl-3-methylimidazolium hexafluorophosphate ([emim]+P%@mt;sys@%F%@sx@%6%@be@%-%@sxx@%%@mx@% ) is studied via molecular dynamics computer simulations. By employing a two-state valence-bond description for electronic structure variations of the reaction complex, the free energy curve relevant to its SN1 ionization in [emim]+P%@mt;sys@%F%@sx@%6%@be@%-%@sxx@%%@mx@% is computed via the thermodynamic integration method and compared with those in water and in acetonitrile. It is found that the detailed reaction mechanism differs among the three solvents. To be specific, the dissociation of 2-chloro-2-methylpropane in [emim]+P%@mt;sys@%F%@sx@%6%@be@%-%@sxx@%%@mx@% is a stepwise process consisting of the formation of a solvent-separated ion pair and ensuing dissociation, while that in acetonitrile appears to proceed without any stable reaction intermediates. The SN1 pathway in water on the other hand is characterized by the formation of a contact ion pair, followed by dissociation to free ions. The activation free energy in water is much lower than those in [emim]+P%@mt;sys@%F%@sx@%6%@be@%-%@sxx@%%@mx@% and acetonitrile. Between the two latter solvents, the barrier height is lower in [emim]+P%@mt;sys@%F%@sx@%6%@be@%-%@sxx@%%@mx@% than in acetonitrile, indicating that the SN1 reactivity of 2-chloro-2-methylpropane would be higher in %@mt;sys@%[S_EL2;quad]\ %@fn;[vis;full;auto@%emim%@fnx;]vis;full@%%@ex@%+%@exx@%PF%@sx@%6%@be@%-%@sxx@%%@mx@% than in acetonitrile. Its implication for solvolysis in these solvents is briefly discussed.

MD Study of S(N)1 Reactivity of 2-Chloro-2-methylpropane in the Room-Temperature Ionic Liquid 1-Ethyl-3-methylimidazolium Hexafluorophosphate. Publishing Authors By Initials

Y Shim,HJ Kim,

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MD Study of S(N)1 Reactivity of 2-Chloro-2-methylpropane in the Room-Temperature Ionic Liquid 1-Ethyl-3-methylimidazolium Hexafluorophosphate. Journal Published:

PUBLICATION TYPE: Journal Article

Journal: The journal of physical chemistry. B

VOLUME: 112

Page Numbers: 2637-43

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ISSN: 1520-6106

DAY: 13

MONTH: 02

YEAR: 2008

MD Study of S(N)1 Reactivity of 2-Chloro-2-methylpropane in the Room-Temperature Ionic Liquid 1-Ethyl-3-methylimidazolium Hexafluorophosphate. Information

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LANGUAGE: eng

NlmUniqueID: 101157530

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AFFILIATION: Department of Chemistry, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, and Department of Physics, Korea University, Seoul 136-701, Korea.

Country: United States

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MEDLINETA: J Phys Chem B

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