Hafnium acetylacetonate

Hafnium acetylacetonate^[1]
Names
	IUPAC name hafnium(4+); (Z)-4-oxopent-2-en-2-olate
	Other names tetrakis(acetylacetonato)hafnium, hafnium tetrakis(acetylacetonate)
Identifiers
CAS Number	17475-67-1;
3D model (JSmol)	Interactive image;
PubChem CID	21953595;
	InChI InChI=1S/4C5H8O2.Hf/c41-4(6)3-5(2)7;/h43,6H,1-2H3;/q;;;;+4/p-4/b4*4-3-; Key: MCFIMQJAFAOJPD-MTOQALJVSA-J;
	SMILES [Hf+4].O=C(C)\C=C(/[O-])C.[O-]\C(C)=C/C(C)=O.[O-]\C(C)=C/C(C)=O.[O-]\C(C)=C/C(C)=O;
Properties
Chemical formula	C20H28HfO8
Molar mass	574.93 g·mol−1
Appearance	White to off-white powder
Density	1.42 g/cm3
Melting point	193 °C (379 °F; 466 K) (decomposes)
Solubility in benzene	good
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Hafnium acetylacetonate, also known as Hf(acac)₄, is a coordination compound with formula Hf(C₅H₇O₂)₄. This white solid is the main hafnium complex of acetylacetonate. The complex has a square antiprismatic geometry with eight nearly equivalent Hf-O bonds. The molecular symmetry is D₂, i.e., the complex is chiral. It is prepared from hafnium tetrachloride and acetylacetone, and base. Zr(acac)₄ is very similar in structure and properties.^[2]

Uses[edit]

Along with titanium tetrabutoxide (TBT), hafnium acetylacetonate serves as a catalyst for the production of poly(butylene terephthalate).^[3]

Related compounds[edit]

Tetrakis(1,1,1-trifluoro-2,4-pentanedionato)hafnium^[4]

References[edit]

^ "Hafnium Acetylacetonate". American Elements. Retrieved 2015-04-05.
^ Zherikova, K. V.; Morozova, N. B.; Kuratieva, N. V.; Baidina, I. A.; Igumenov, I. K. (November 2005). "Synthesis and structural investigation of hafnium(IV) complexes with acetylacetone and trifluoroacetylacetone". Journal of Structural Chemistry. 46 (6): 1039–1046. doi:10.1007/s10947-006-0239-2. S2CID 95300586.
^ Banach, T.E; Berti, C; Colonna, M; Fiorini, M; Marianucci, E; Messori, M; Pilati, F; Toselli, M (August 2001). "New catalysts for poly(butylene terephthalate) synthesis". Polymer. 42 (18): 7511–7516. doi:10.1016/S0032-3861(01)00219-1.
^ Morris, Melvin L.; Moshier, Ross W.; Sievers, Robert E. (1967). "Tetrakis(1,1,1-trifluoro-2,4-pentanedionato)zirconium (and Hafnium)". Inorganic Syntheses. 9: 50–52. doi:10.1002/9780470132401.ch15.

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[americanelements-1] "Hafnium Acetylacetonate". American Elements. Retrieved 2015-04-05.

[2] Zherikova, K. V.; Morozova, N. B.; Kuratieva, N. V.; Baidina, I. A.; Igumenov, I. K. (November 2005). "Synthesis and structural investigation of hafnium(IV) complexes with acetylacetone and trifluoroacetylacetone". Journal of Structural Chemistry. 46 (6): 1039–1046. doi:10.1007/s10947-006-0239-2. S2CID 95300586.

[TBT-3] Banach, T.E; Berti, C; Colonna, M; Fiorini, M; Marianucci, E; Messori, M; Pilati, F; Toselli, M (August 2001). "New catalysts for poly(butylene terephthalate) synthesis". Polymer. 42 (18): 7511–7516. doi:10.1016/S0032-3861(01)00219-1.

[4] Morris, Melvin L.; Moshier, Ross W.; Sievers, Robert E. (1967). "Tetrakis(1,1,1-trifluoro-2,4-pentanedionato)zirconium (and Hafnium)". Inorganic Syntheses. 9: 50–52. doi:10.1002/9780470132401.ch15.

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v t e Hafnium compounds
Hf(II)	HfB₂
Hf(IV)	HfC HfBr₄ HfCl₄ HfF₄ HfI₄ Hf(C₅H₇O₂)₄ Hf(OSO₂CF₃)₄ HfO₂ Hf(NO₃)₄ HfSiO₄ HfS₂ La₂Hf₂O₇ Ta₄HfC₅