Chemistry:Hafnocene dichloride
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| Names | |
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| Other names
bis(cyclopentadienyl)hafnium dichloride
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
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PubChem CID
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| Properties | |
| C10H10Cl2Hf | |
| Molar mass | 379.58 g·mol−1 |
| Appearance | white solid |
| Melting point | 230–233 °C (446–451 °F; 503–506 K) |
| Hazards | |
| GHS pictograms |  
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| GHS Signal word | Danger |
| H314, H315, H319, H335 | |
| P260, P261, P264, P264+265Script error: No such module "Preview warning".Category:GHS errors, P271, P280, P301+330+331, P302+352, P302+361+354Script error: No such module "Preview warning".Category:GHS errors, P304+340, P305+351+338, P305+354+338Script error: No such module "Preview warning".Category:GHS errors, P316Script error: No such module "Preview warning".Category:GHS errors, P319Script error: No such module "Preview warning".Category:GHS errors, P321, P332+317Script error: No such module "Preview warning".Category:GHS errors, P337+317Script error: No such module "Preview warning".Category:GHS errors, P362+364Script error: No such module "Preview warning".Category:GHS errors, P363, P403+233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Hafnocene dichloride is the organohafnium compound with the formula (C
5H
5)
2HfCl
2. It is a white solid that is sparingly soluble in some organic solvents. The lighter homologues zirconacene dichloride and titanocene dichloride have received much more attention. While hafnocene is only of academic interest, some more soluble derivatives are precatalysts for olefin polymerization. Moreso than the Zr analogue, this compound is highly resistant to reduction.
It is prepared by a salt metathesis reaction from hafnium tetrachloride by salt metathesis:
- 2 NaC
5H
5 + HfCl
4 → (C
5H
5)
2HfCl
2 + 2 NaCl
Derivatives
Hydrolysis gives the trimer [(C
5H
5)
2HfO]
3.[2]
The chloride ligands can be replaced by other halides.[3]
The bis(phosphide) (C
5H
5)
2Hf(PR
2)
2 can be prepared by salt metathesis from hafnocene dichloride.[4]
References
- ↑ "Hafnocene dichloride" (in en). https://pubchem.ncbi.nlm.nih.gov/compound/24942143#section=Safety-and-Hazards.
- ↑ Rogers, Robin D.; Vann Bynum, R.; Atwood, Jerry L. (1982). "Synthesis and Crystal Structure of [(η5-C5H5)2HfO]3C6H5Me". Journal of Crystallographic and Spectroscopic Research 12 (3): 239–244. doi:10.1007/BF01195715.
- ↑ Druce, P. M.; Kingston, B. M.; Lappert, M. F.; Spalding, T. R.; Srivastava, R. C. (1969). "Metallocene Halides. Part I. Synthesis, Spectra, and Redistribution Equilibria of di-π-Cyclopentadienyldihalogeno-Titanium(IV),-Zirconium-(IV), and -Hafnium(IV)". J. Chem. Soc. A: 2106–2110. doi:10.1039/J19690002106.
- ↑ Baker, R. T.; Whitney, J. F.; Wreford, S. S. (1983). "Characterization and Interconversion of Metal-Phosphorus Single and Double bonds: Bis(cyclopentadienyl)zirconium and -Hafnium Bis(diorganophosphide) Complexes". Organometallics 2 (8): 1049–1051. doi:10.1021/om50002a022.
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