Chemistry:Bis(triphenylphosphineoxide) manganese(III) chloride
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| Names | |
|---|---|
| Systematic IUPAC name
trichloridobis(triphenylphopshineoxide)manganese(III) | |
| Other names
MnCl
3(OPPh 3) 2 | |
| Identifiers | |
3D model (JSmol)
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| Properties | |
| C36H30Cl3MnO2P2 | |
| Molar mass | 717.87 g·mol−1 |
| Appearance | blue solid |
| Melting point | 140 °C (284 °F; 413 K) (with decomposition) |
| μeff = 4.96 μB.H. (solid-state), 4.83 μB.H. (DCM) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Bis(triphenylphosphineoxide) manganese(III) chloride is a coordination complex of manganese(III) chloride. Unlike most compounds containing "Mn(III)Cl3", [MnCl3(OPPh3)2] can be stored under normal laboratory conditions.[1] It is a blue, paramagnetic solid.
Synthesis and reactions
Treatment of meta-stable solutions of Mn(III)Cl3 with triphenylphosphine oxide results in precipitation of solid [MnCl3(OPPh3)2]. This compound was first prepared using the thermally unstable ethereal adduct (dioxane)Mn(III)Cl3.[2] A convenient synthesis starts from Mn(OAc)2, trimethylsilylchloride, and potassium permanganate.[3]
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[MnCl3(OPPh3)2] can be used as a starting material in coordination chemistry.[3]
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[MnCl3(OPPh3)2] can also be used as a stoichiometric reagent in alkene dihalogenation reactions.[3]
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References
- ↑ Goedecke, Catharina (2022-09-08). "Bench-Stable Manganese(III) Chloride Source" (in en-US). https://www.chemistryviews.org/bench-stable-manganeseiii-chloride-source/.
- ↑ Uson, R. (1976). "Pentacoordinate Neutral Manganese(III) Complexes". Transition. Met. Chem 1 (3): 122–126.
- ↑ 3.0 3.1 3.2 Saju, Ananya; Griffiths, Justin R.; MacMillan, Samantha N.; Lacy, David C. (2022-09-06). "Synthesis of a Bench-Stable Manganese(III) Chloride Compound: Coordination Chemistry and Alkene Dichlorination" (in en). Journal of the American Chemical Society 144 (37): 16761–16766. doi:10.1021/jacs.2c08509. ISSN 0002-7863. PMID 36067378. https://pubs.acs.org/doi/10.1021/jacs.2c08509.
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