Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 남원우 | * |
dc.date.accessioned | 2017-01-05T02:01:24Z | - |
dc.date.available | 2017-01-05T02:01:24Z | - |
dc.date.issued | 2003 | * |
dc.identifier.issn | 0036-8075 | * |
dc.identifier.other | OAK-1341 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/233746 | - |
dc.description.abstract | Following the heme paradigm, it is often proposed that dioxygen activation by nonheme monoiron enzymes involves an iron(IV)=oxo intermediate that is responsible for the substrate oxidation step. Such a transient species has now been obtained from a synthetic complex with a nonheme macrocyclic ligand and characterized spectroscopically. Its high-resolution crystal structure reveals an iron-oxygen bond length of 1.646(3) angstroms, demonstrating that a terminal iron(IV)=oxo unit can exist in a nonporphyrin ligand environment and lending credence to proposed mechanisms of nonheme iron catalysis. | * |
dc.language | English | * |
dc.title | Crystallographic and spectroscopic characterization of a Nonheme Fe(IV)=O complex | * |
dc.type | Article | * |
dc.relation.issue | 5609 | * |
dc.relation.volume | 299 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 1037 | * |
dc.relation.lastpage | 1039 | * |
dc.relation.journaltitle | Science | * |
dc.identifier.doi | 10.1126/science.299.5609.1037 | * |
dc.identifier.wosid | WOS:000180960000038 | * |
dc.identifier.scopusid | 2-s2.0-0037436143 | * |
dc.author.google | Rohde J.-U. | * |
dc.author.google | In J.-H. | * |
dc.author.google | Lim M.H. | * |
dc.author.google | Brennessel W.W. | * |
dc.author.google | Bukowski M.R. | * |
dc.author.google | Stubna A. | * |
dc.author.google | Munck E. | * |
dc.author.google | Nam W. | * |
dc.author.google | Que Jr. L. | * |
dc.contributor.scopusid | 남원우(7006569723) | * |
dc.date.modifydate | 20240116111857 | * |