Dysprosium acetylacetonate

Last updated
Dysprosium acetylacetonate [1]
Dy(acac)3(H2O)2.svg
Names
IUPAC name
dysprosium(3+); (''Z'')-4-oxopent-2-en-2-olate
Other names
Dysprosium(III) 2,4-pentanedionate
Identifiers
3D model (JSmol)
ChemSpider
PubChem CID
  • InChI=1S/3C5H7O2.Dy/c3*1-4(6)3-5(2)7;/h3*3H,1-2H3;/q3*-1;+3
    Key: VABPDCUJKLETFM-UHFFFAOYSA-N
  • CC(=O)[CH-]C(=O)C.CC(=O)[CH-]C(=O)C.CC(=O)[CH-]C(=O)C.[Dy+3]
Properties
C15H21DyO6
Molar mass 459.827 g·mol−1
AppearanceYellow powder
Hazards
GHS labelling:
GHS-pictogram-exclam.svg
Warning
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Dysprosium acetylacetonate is a chemical compound of dysprosium with formula Dy(C5H7O2)3(H2O)n.

Contents

Preparation and properties

Dysprosium acetylacetonate can be prepared by reacting dysprosium [2] or dysprosium hydride [3] with acetylacetone. Dy(acac)3·EtOH·0.5Hacac (where Hacac represents acetylacetone) can be obtained by electrolysis of dysprosium cathode in ethanol solution of acetylacetone, which can be heated to generate Dy(acac)3 through Dy(acac)3·EtOH. [4] It is a colorless solid. Its anhydrous form is stable in dry atmosphere and it forms a hydrate in humid air. [5] It can form Dy(acac)3·2CH3OH and Dy(acac)3·CH3OH·CH3CN in a methanol solution of acetonitrile. [6]

Applications

Dysprosium acetylacetonate can be used to catalyze the addition reaction of norbornene and carbon tetrachloride. [7] The dihydrate has been characterized by X-ray crystallography. [8]

References

  1. ↑ Dysprosium acetylacetonate at American Elements
  2. ↑ J.R. Blackborow, C.R. Eady, E.A.Koerner Von Gustorf, A. Scrivanti, O. Wolfbeis (March 1976). "Chemical syntheses with metal atoms". Journal of Organometallic Chemistry. 108 (3): C32 –C34. doi:10.1016/S0022-328X(00)92025-4. Archived from the original on 2018-06-26. Retrieved 2021-09-20.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. ↑ Janice M. Koehler, William G. Bos (December 1967). "A novel synthesis of some anhydrous rare earth acetylacetonates" . Inorganic and Nuclear Chemistry Letters. 3 (12): 545–548. doi:10.1016/0020-1650(67)80023-0 . Retrieved 2021-09-20.
  4. ↑ Kostyuk, N. N.; Shirokii, V. L.; Vinokurov, I. I.; Maier, N. A. Electrochemical synthesis of dysprosium(III) acetylacetonate complex and its thermolysis. Zhurnal Obshchei Khimii, 1994. 64 (9): 1432-1434. ISSN   0044-460X. (in Russian)
  5. ↑ Trembovetskii, G. V.; Martynenko, L. I.; Murav'eva, I. A.; Spitsyn, V. Synthesis and study of volatile rare earth acetylacetonates. Doklady Akademii Nauk SSSR, 1984. 277 (6): 1411-1414. ISSN: 0002-3264. (in Russian)
  6. ↑ Pod'yachev, S. N.; Mustafina, A. R.; Vul'fson, S. G. Structure of tris(acetylacetonato)dysprosium and its monoadduct with acetonitrile in a methanol solution. Zhurnal Neorganicheskoi Khimii, 1994. 39 (1): 67-70. ISSN   0044-457X. (in Russian)
  7. ↑ R. I. Khusnutdinov, T. M. Oshnyakova (February 2014). "Tetrachloromethane addition to norbornene catalyzed by lanthanide(III) compounds" . Russian Journal of Organic Chemistry. 50 (2): 303–305. doi:10.1134/S1070428014020304. ISSN   1070-4280. S2CID   98681877 . Retrieved 2021-09-20.
  8. ↑ Ilyukhin, A. B.; Gavrikov, A. V.; Dobrokhotova, Zh. V.; Novotortsev, V. M. (2018). "New Solvate Polymorphs of Lanthanide Trisacetylacetonates: Crystal Structures of [Ln(acac)3(H2O)2] · Solv (Ln = Eu, Dy; Solv = THF, H2O + EtOH, MeOH)". Russian Journal of Inorganic Chemistry. 63 (9): 1186–1191. doi:10.1134/S003602361809005X. S2CID   106025242.
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