| dc.contributor.author | Glukhovtsev, M. N. | en |
| dc.contributor.author | Pross, A. | en |
| dc.contributor.author | Nicolaïdes, Andrew N. | en |
| dc.contributor.author | Radom, L. | en |
| dc.creator | Glukhovtsev, M. N. | en |
| dc.creator | Pross, A. | en |
| dc.creator | Nicolaïdes, Andrew N. | en |
| dc.creator | Radom, L. | en |
| dc.date.accessioned | 2019-11-21T06:19:12Z | |
| dc.date.available | 2019-11-21T06:19:12Z | |
| dc.date.issued | 1995 | |
| dc.identifier.uri | http://gnosis.library.ucy.ac.cy/handle/7/55515 | |
| dc.description.abstract | The 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.source | Journal of the Chemical Society, Chemical Communications | en |
| dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-0002512437&doi=10.1039%2fC39950002347&partnerID=40&md5=114b5780f0e83caa20a9a771004d1a2c | |
| dc.title | Is the most stable gas-phase isomer of the benzenium cation a face-protonated π-complex? | en |
| dc.type | info:eu-repo/semantics/article | |
| dc.identifier.doi | 10.1039/C39950002347 | |
| dc.description.issue | 22 | |
| dc.description.startingpage | 2347 | |
| dc.description.endingpage | 2348 | |
| dc.author.faculty | 002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences | |
| dc.author.department | Τμήμα Χημείας / Department of Chemistry | |
| dc.type.uhtype | Article | en |
| dc.description.notes | <p>Cited By :52</p> | en |
