Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 남원우 | * |
dc.date.accessioned | 2016-08-27T04:08:44Z | - |
dc.date.available | 2016-08-27T04:08:44Z | - |
dc.date.issued | 2016 | * |
dc.identifier.issn | 1359-7345 | * |
dc.identifier.issn | 1364-548X | * |
dc.identifier.other | OAK-16251 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/217947 | - |
dc.description.abstract | Previous experimental results revealed that the C-H bond activation reaction by a synthetic trans-dioxo Mn-V porphyrin complex, [(TF(4)TMAP)(OMnO)-O-V](3+), does not occur via the well-known oxygen rebound mechanism, which has been well demonstrated in (FeO)-O-IV porphyrin pi-cation radical reactions. In the present study, theoretical calculations offer an explanation through the energetics involved in the C-H bond activation reaction, where a multi-spin state scenario cannot be excluded. | * |
dc.language | English | * |
dc.publisher | ROYAL SOC CHEMISTRY | * |
dc.title | A theoretical study into a trans-dioxo Mn-V porphyrin complex that does not follow the oxygen rebound mechanism in C-H bond activation reactions | * |
dc.type | Article | * |
dc.relation.issue | 5 | * |
dc.relation.volume | 52 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 904 | * |
dc.relation.lastpage | 907 | * |
dc.relation.journaltitle | CHEMICAL COMMUNICATIONS | * |
dc.identifier.doi | 10.1039/c5cc08734a | * |
dc.identifier.wosid | WOS:000367614000009 | * |
dc.identifier.scopusid | 2-s2.0-84954063317 | * |
dc.author.google | Cho, Kyung-Bin | * |
dc.author.google | Nam, Wonwoo | * |
dc.contributor.scopusid | 남원우(7006569723) | * |
dc.date.modifydate | 20240116111857 | * |