Holmium acetylacetonate
Names | |
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Other names
Holmium(III) acetylacetonate
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Identifiers | |
3D model (JSmol)
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Properties | |
C15H21HoO6 | |
Molar mass | 462.257 g·mol−1 |
Appearance | yellow-pink[1] |
Insoluble | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Holmium acetylacetonate is a coordination compound with the formula Ho(C5H7O2)3. This anhydrous acetylacetonate complex is often discussed but unlikely to exist per se. The 8-coordinated dihydrate Ho(C5H7O2)3(H2O)2 is a more plausible formula based on the behavior of other lanthanide acetylacetonates. The dihydrate has been characterized by X-ray crystallography.[1]
Attempts to dehydrate other lanthanide acetylacetonates results in decomposition.[2]
Further reading
- R. G. Bulgakov, S. P. Kuleshov, R. R. Vafin, A. G. Ibragimov, U. M. Dzhemilev (2008-03-01). "Reactions of lanthanide acetylacetonates with triethylaluminum". Kinetics and Catalysis. 49 (2): 299–304. doi:10.1134/S0023158408020195. ISSN 0023-1584. S2CID 97171472. Retrieved 2021-09-20.
{{cite journal}}
: CS1 maint: multiple names: authors list (link) - Kent J. Eisentraut, Robert E. Sievers (1967-08-01). "Thermogravimetric studies of metal β-diketonates". Journal of Inorganic and Nuclear Chemistry. 29 (8): 1931–1936. doi:10.1016/0022-1902(67)80452-4. Archived from the original on 2018-06-12. Retrieved 2021-09-20.
References
- ^ a b Kooijman, Huub; Nijsen, Frank; Spek, Anthony L.; Schip, Fred van het (2000). "Diaquatris(pentane-2,4-dionato-O,O′)holmium(III) monohydrate and diaquatris(pentane-2,4-dionato-O,O′)holmium(III) 4-hydroxypentan-2-one solvate dihydrate". Acta Crystallographica Section C Crystal Structure Communications. 56 (2): 156–158. doi:10.1107/S0108270199013566. PMID 10777870.
- ^ Tamang, Sem Raj; Singh, Arpita; Bedi, Deepika; Bazkiaei, Adineh Rezaei; Warner, Audrey A.; Glogau, Keeley; McDonald, Corey; Unruh, Daniel K.; Findlater, Michael (2020). "Polynuclear Lanthanide–Diketonato Clusters for the Catalytic Hydroboration of Carboxamides and Esters". Nat. Catal. 3 (2): 154–162. doi:10.1038/s41929-019-0405-5. S2CID 209897045.
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