Английская Википедия:1,1'-Bis(diphenylphosphino)ferrocene

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Шаблон:Chembox

1,1Шаблон:Prime-Bis(diphenylphosphino)ferrocene, commonly abbreviated dppf, is an organophosphorus compound commonly used as a ligand in homogeneous catalysis. It contains a ferrocene moiety in its backbone, and is related to other bridged diphosphines such as 1,2-bis(diphenylphosphino)ethane (dppe).

Preparation

This compound is commercially available. It may be prepared by treating dilithioferrocene with chlorodiphenylphosphine:[1]

Fe(CШаблон:SubHШаблон:SubLi)Шаблон:Sub + 2 ClPPhШаблон:Sub → Fe(CШаблон:SubHШаблон:SubPPhШаблон:Sub)Шаблон:Sub + 2 LiCl

The dilithiation of ferrocene is easily achieved with n-butyllithium in the presence of TMEDA. Many related ligands can be made in this way. The Fe center is typically not involved in the behavior of the ligand.

Reactions

Dppf readily forms metal complexes.[2] The palladium derivative, [[(1,1'-Bis(diphenylphosphino)ferrocene)palladium(II) dichloride|(dppf)PdClШаблон:Sub]], which is popular for palladium-catalyzed coupling reactions, is prepared by treating dppf with the acetonitrile or benzonitrile adducts of palladium dichloride:[2] Substitution of the phenyl substituents in dppf leads to derivatives with modified donor-acceptor properties at the phosphorus atoms.[3]

dppf + PdClШаблон:Sub(RCN)Шаблон:Sub → (dppf)PdClШаблон:Sub + 2 RCN (RCN = acetonitrile or benzonitrile)
Файл:Dppf-PtCl2-from-xtal-3D-balls-B.png
Structure of the complex PtClШаблон:Sub(dppf)

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Another example of dppf in homogeneous catalysis is provided by the air- and moisture-stable Ni(II) precatalyst [(dppf)Ni(cinnamyl)Cl. It promotes Suzuki-Miyuara cross-coupling of heteroaryl boronic acids with nitrogen- and sulfur-containing heteroaryl halides.[4]

Файл:Hartwig synthesis.tif
Synthesis of [(dppf)Ni(cinnamyl)Cl)]

Another dppf-based catalyst is (dppf)Ni(o-tolyl)Cl, can be prepared from ligand exchange with (PPh3)2Ni(o-tolyl)Cl. It promotes the amination of aryl chlorides, sulfamates, mesylates, and triflates.[5]

Файл:Buchwald Synthesis.tif
Synthesis of (dppf)Ni(o-tolyl)Cl

See also

References

Шаблон:Reflist