完整後設資料紀錄
DC 欄位語言
dc.contributor.authorMendez-Vega, Enriqueen_US
dc.contributor.authorMaehara, Mikaen_US
dc.contributor.authorRaut, Akshay Hemanten_US
dc.contributor.authorMieres-Perez, Joelen_US
dc.contributor.authorTsuge, Masashien_US
dc.contributor.authorLee, Yuan-Pernen_US
dc.contributor.authorSander, Wolframen_US
dc.date.accessioned2019-04-02T05:58:26Z-
dc.date.available2019-04-02T05:58:26Z-
dc.date.issued2018-12-12en_US
dc.identifier.issn0947-6539en_US
dc.identifier.urihttp://dx.doi.org/10.1002/chem.201804657en_US
dc.identifier.urihttp://hdl.handle.net/11536/148594-
dc.description.abstractThe hydrogenation reactions of diphenylcarbene 1, fluorenylidene 2, and dibenzocycloheptadienylidene 3 were investigated in solid H-2 and D-2 matrices and in H-2- and D-2-doped argon matrices at cryogenic temperatures. The reactivity of the carbenes towards H-2 increases in the order 1<3<2. Whereas 1 is stable in solid H-2, 2 and 3 react fast under the same conditions via quantum chemical tunneling. In D-2 both 1 and 3 are stable, whereas 2 slowly reacts. The different reactivity of the three carbenes is rationalized in terms of differing carbene stabilization energies.en_US
dc.language.isoen_USen_US
dc.subjectcarbenesen_US
dc.subjecthydrogen activationen_US
dc.subjectIR spectroscopyen_US
dc.subjectmatrix isolationen_US
dc.subjecttunnelingen_US
dc.titleActivation of Molecular Hydrogen by Arylcarbenesen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/chem.201804657en_US
dc.identifier.journalCHEMISTRY-A EUROPEAN JOURNALen_US
dc.citation.volume24en_US
dc.citation.spage18801en_US
dc.citation.epage18808en_US
dc.contributor.department交大名義發表zh_TW
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.departmentNational Chiao Tung Universityen_US
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000453065900031en_US
dc.citation.woscount0en_US
顯示於類別:期刊論文