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dc.contributor.authorNishimura, Yoshifumien_US
dc.contributor.authorYokogawa, Daisukeen_US
dc.contributor.authorIrle, Stephanen_US
dc.date.accessioned2014-12-08T15:36:04Z-
dc.date.available2014-12-08T15:36:04Z-
dc.date.issued2014-05-30en_US
dc.identifier.issn0009-2614en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.cplett.2014.04.014en_US
dc.identifier.urihttp://hdl.handle.net/11536/24416-
dc.description.abstractThe S(N)1-type hydrolysis reaction of cellobiose in ionic liquids (ILs) was theoretically investigated. First principles and ab initio quantum chemical methods were used in conjunction with the \'reference interaction site model self-consistent field with spatial electron density distribution\' (RISM-SCF-SEDD) method. Reaction mechanism pathways are discussed and compared to calculations in gas phase and in aqueous solution. Analysis of solvation effects indicates strong interaction between hydrogen atoms of glucose hydroxyl groups and the anions in ILs, contributing to large stabilization of the reaction product. The calculated activation energy in ILs (24.5 kcal/mol) agrees quantitatively with the experimental value (26.5 kcal/mol). (C) 2014 Elsevier B. V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleTheoretical study of cellobiose hydrolysis to glucose in ionic liquidsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.cplett.2014.04.014en_US
dc.identifier.journalCHEMICAL PHYSICS LETTERSen_US
dc.citation.volume603en_US
dc.citation.issueen_US
dc.citation.spage7en_US
dc.citation.epage12en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000336485400002-
dc.citation.woscount3-
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