Evidence that steric factors modulate reactivity of tautomeric iron–oxo species in stereospecific alkane C–H hydroxylation
| dc.contributor.author | Mitra, Mainak | |
| dc.contributor.author | Lloret-Fillol, Julio | |
| dc.contributor.author | Haukka, Matti | |
| dc.contributor.author | Costas, Miquel | |
| dc.contributor.author | Nordlander, Ebbe | |
| dc.date.accessioned | 2016-02-05T11:20:30Z | |
| dc.date.available | 2016-02-05T11:20:30Z | |
| dc.date.issued | 2014 | |
| dc.identifier.citation | Mitra, M., Lloret-Fillol, J., Haukka, M., Costas, M., & Nordlander, E. (2014). Evidence that steric factors modulate reactivity of tautomeric iron–oxo species in stereospecific alkane C–H hydroxylation. <i>Chemical Communications</i>, <i>50</i>(12), 1408-1410. <a href="https://doi.org/10.1039/C3CC47830K" target="_blank">https://doi.org/10.1039/C3CC47830K</a> | |
| dc.identifier.other | CONVID_23543225 | |
| dc.identifier.other | TUTKAID_60949 | |
| dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/48651 | |
| dc.description.abstract | MnI carbonyl terpyridyl complexes have been synthesized and characterized. The tricarbonyl derivative exhibits interesting behaviors for controlled CO-release by both thermal and photosynthetic pathways. | |
| dc.language.iso | eng | |
| dc.publisher | RSC Publications | |
| dc.relation.ispartofseries | Chemical Communications | |
| dc.relation.uri | http://pubs.rsc.org/EN/content/articlepdf/2014/cc/c3cc47830k | |
| dc.subject.other | koordinaatioyhdisteet | |
| dc.subject.other | coordination compunds | |
| dc.title | Evidence that steric factors modulate reactivity of tautomeric iron–oxo species in stereospecific alkane C–H hydroxylation | |
| dc.type | article | |
| dc.identifier.urn | URN:NBN:fi:jyu-201602041449 | |
| dc.contributor.laitos | Kemian laitos | fi |
| dc.contributor.laitos | Department of Chemistry | en |
| dc.contributor.oppiaine | Epäorgaaninen ja analyyttinen kemia | fi |
| dc.contributor.oppiaine | Inorganic and Analytical Chemistry | en |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
| dc.date.updated | 2016-02-04T13:15:08Z | |
| dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
| dc.description.reviewstatus | peerReviewed | |
| dc.format.pagerange | 1408-1410 | |
| dc.relation.issn | 1359-7345 | |
| dc.relation.numberinseries | 12 | |
| dc.relation.volume | 50 | |
| dc.type.version | publishedVersion | |
| dc.rights.copyright | © The Royal Society of Chemistry 2014. This is an open access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. | |
| dc.rights.accesslevel | openAccess | fi |
| dc.subject.yso | rauta | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p11738 | |
| dc.rights.url | http://creativecommons.org/licenses/by-nc/3.0/ | |
| dc.relation.doi | 10.1039/C3CC47830K | |
| dc.type.okm | A1 |
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