| Revision as of 15:05, 5 July 2009 editRifleman 82 (talk | contribs)Extended confirmed users32,435 edits start | Revision as of 15:08, 5 July 2009 edit undoRifleman 82 (talk | contribs)Extended confirmed users32,435 edits exotic ligands and chiral catalystsNext edit → | ||
| Line 3: | Line 3: | ||
| * ] between ]s and aryl halides | * ] between ]s and aryl halides | ||
| * ] between aryl halides and ] | * ] between aryl halides and ] | ||
| * ] between an ]s and ]s | * ] between an ]s and ]s | ||
| * ] between aryl halides and ]s, with ] as a co-catalyst | * ] between aryl halides and ]s, with ] as a co-catalyst | ||
| * ] between an organohalide and an ] | * ] between an organohalide and an ] | ||
| Line 13: | Line 13: | ||
| * ] | * ] | ||
| Unoptimized reactions typically use 10-15 mol% of palladium; where optimized, catalyst loadings can be on the order of 0.1 mol % or below. | Unoptimized reactions typically use 10-15 mol% of palladium; where optimized, catalyst loadings can be on the order of 0.1 mol % or below. Many exotic ligands and chiral catalysts have been reported, but they are largely not available commercially, and do not find widespread use. Much work is being done on replacing the phosphine ligands with other classes, such as Arduengo-type ] complexes, as the phosphine ligands are typically oxygen sensitive (easily oxidized), and are labile (requiring additional free ligands). | ||
| With these reactions becoming ubiquitous, there has been interest in better techniques for removing the palladium catalyst. Metal scavenger columns such as QuadruPure<ref>http://www.sigmaaldrich.com/chemistry/drug-discovery/medicinal-chemistry/quadrapure.html</ref> and ISOLUTE<ref>http://www.biotage.com/DynPage.aspx?id=36161</ref> promise more efficient separation than ordinary ]. | With these reactions becoming ubiquitous, there has been interest in better techniques for removing the palladium catalyst. Metal scavenger columns such as QuadruPure<ref>http://www.sigmaaldrich.com/chemistry/drug-discovery/medicinal-chemistry/quadrapure.html</ref> and ISOLUTE<ref>http://www.biotage.com/DynPage.aspx?id=36161</ref> promise more efficient separation than ordinary ]. | ||
Revision as of 15:08, 5 July 2009
Palladium compounds are used as a catalyst in many coupling reactions, usually as a homogenous catalyst. Examples include:
- Heck reaction between alkenes and aryl halides
- Suzuki reaction between aryl halides and boronic acids
- Stille reaction between an organohalides and organotin compounds
- Sonogashira coupling between aryl halides and alkynes, with copper(I) iodide as a co-catalyst
- Negishi coupling between an organohalide and an organozinc compound
Typical palladium catalysts used include the following compounds:
- palladium acetate
- tetrakis(triphenylphosphine)palladium(0)
- bis(triphenylphosphine)palladium(II) dichloride
- 1,1'-Bis(diphenylphosphino)ferrocene-palladium(II) dichloride
Unoptimized reactions typically use 10-15 mol% of palladium; where optimized, catalyst loadings can be on the order of 0.1 mol % or below. Many exotic ligands and chiral catalysts have been reported, but they are largely not available commercially, and do not find widespread use. Much work is being done on replacing the phosphine ligands with other classes, such as Arduengo-type carbene complexes, as the phosphine ligands are typically oxygen sensitive (easily oxidized), and are labile (requiring additional free ligands).
With these reactions becoming ubiquitous, there has been interest in better techniques for removing the palladium catalyst. Metal scavenger columns such as QuadruPure and ISOLUTE promise more efficient separation than ordinary column chromatography.
References
- http://www.sigmaaldrich.com/chemistry/drug-discovery/medicinal-chemistry/quadrapure.html
- http://www.biotage.com/DynPage.aspx?id=36161