Schwartz's reagent
 | This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
 | This article or section is in a state of significant expansion or restructuring. You are welcome to assist in its construction by editing it as well. If this article or section has not been edited in several days, please remove this template. If you are the editor who added this template and you are actively editing, please be sure to replace this template with {{in use}} during the active editing session. Click on the link for template parameters to use.
This article was last edited by Haligonian1 (talk | contribs) 19 years ago. (Update timer) |
| Schwartz's reagent | |
|---|---|
| |
| General | |
| Systematic name | Bis(η5-cyclopentadienyl)- zirconium(IV) chloride hydride |
| Other names | Cp2ZrClH |
| Molecular formula | [Zr(η5C5H5)2] |
| Molar mass | 257.87 g/mol |
| Appearance | ? |
| CAS number | 37342-97-5 |
| EINECS number | ???-???-? |
| Related compounds | |
| Related metallocenes | Ferrocene Cobaltocene Nickelocene |
Schwartz's Reagent is the common name for bis(cyclopentadienyl)zirconium(IV) chloride hydride). This metallocene is used in organometallic chemistry for the hydrozirconation of alkenes and alkynes.[1]
Reference
- [1] D. W. Hart and J. Schwartz (1974). "Hydrozirconation. Organic Synthesis via Organozirconium Intermediates. Synthesis and Rearrangement of Alkylzirconium(IV) Complexes and Their Reaction with Electrophiles". Journal of the American Chemical Society. 96.: 8815–8116.