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dc.contributor.authorGlukhovtsev, M. N.en
dc.contributor.authorPross, A.en
dc.contributor.authorNicolaïdes, Andrew N.en
dc.contributor.authorRadom, L.en
dc.creatorGlukhovtsev, M. N.en
dc.creatorPross, A.en
dc.creatorNicolaïdes, Andrew N.en
dc.creatorRadom, L.en
dc.date.accessioned2019-11-21T06:19:12Z
dc.date.available2019-11-21T06:19:12Z
dc.date.issued1995
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55515
dc.description.abstractThe recent suggestion, based on gas-phase experimental data, that the most stable isomer of protonated benzene has a face-protonated π-complex structure is not supported by our detailed computations which indicate that the π-complex is a second-order saddle point on the potential energy surface, lying 199 kJ mol-1 higher in energy than the well-established C 2v σ-protonated structure.en
dc.sourceJournal of the Chemical Society, Chemical Communicationsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0002512437&doi=10.1039%2fC39950002347&partnerID=40&md5=114b5780f0e83caa20a9a771004d1a2c
dc.titleIs the most stable gas-phase isomer of the benzenium cation a face-protonated π-complex?en
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1039/C39950002347
dc.description.issue22
dc.description.startingpage2347
dc.description.endingpage2348
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :52</p>en


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