Evidence that steric factors modulate reactivity of tautomeric iron–oxo species in stereospecific alkane C–H hydroxylation

Mitra, Mainak; Lloret-Fillol, Julio; Haukka, Matti; Costas, Miquel; Nordlander, Ebbe

doi:10.1039/C3CC47830K

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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. Chemical Communications, 50(12), 1408-1410. https://doi.org/10.1039/C3CC47830K

Julkaistu sarjassa

Chemical Communications

Tekijät

Mitra, Mainak |

Lloret-Fillol, Julio |

Haukka, Matti |

Costas, Miquel |

Nordlander, Ebbe

Päivämäärä

2014

Oppiaine

Epäorgaaninen ja analyyttinen kemia Inorganic and Analytical Chemistry

Tekijänoikeudet

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.

Julkaisija

RSC Publications

ISSN Hae Julkaisufoorumista

1359-7345

Lisenssi

© The Royal Society of Chemistry 2014. This is an open access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.

Ellei muuten mainita, aineiston lisenssi on © The Royal Society of Chemistry 2014. This is an open access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.

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