1,1′-Bis(diphenylphosphino)­ferrocene
Names
Preferred IUPAC name
(Ferrocene-1,1′-diyl)bis(diphenylphosphane)
Other names
1,1′-Bis(diphenylphosphino)ferrocene, 1,1′-ferrocenediylbis(diphenylphosphine), Dppf, 1,1′-ferrocenebis(diphenylphosphine), 1,1′-bis(diphenylphosphanyl)ferrocene
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.167.773
EC Number
  • 640-119-0
24075
UNII
  • InChI=1S/2C17H14P.Fe/c2*1-3-9-15(10-4-1)18(17-13-7-8-14-17)16-11-5-2-6-12-16;/h2*1-14H; checkY
    Key: HPXNTHKXCYMIJL-UHFFFAOYSA-N checkY
  • InChI=1/2C17H14P.Fe/c2*1-3-9-15(10-4-1)18(17- -13-7-8-14-17)16-11-5-2-6-12-16;/h2*1-14H;/q2*-1;+2
    Key: HPXNTHKXCYMIJL-UHFFFAOYSA-N
  • InChI=1/2C17H14P.Fe/c2*1-3-9-15(10-4-1)18(17-13-7-8-14-17)16-11-5-2-6-12-16;/h2*1-14H;/rC34H28FeP2/c1-5-13-21(14-6-1)36(22-15-7-2-8-16-22)33-29-25-26-30(33)35(25,26,29,33)27-28(35)32(35)34(35,31(27)35)37(23-17-9-3-10-18-23)24-19-11-4-12-20-24/h1-20,25-32H
    Key: HPXNTHKXCYMIJL-KDKHWAOJAX
  • c1ccc(cc1)P(c2ccccc2)C34C5[Fe]3678912(C5C6C74)C3C8C9C1(C23)P(c1ccccc1)c1ccccc1
  • C1=CC=C(C=C1)P([C-]2C=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P([C-]2C=CC=C2)C3=CC=CC=C3.[Fe+2]
Properties
C34H28FeP2
Molar mass 554.391
Melting point 181 to 183 °C (358 to 361 °F; 454 to 456 K)
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 Toxic
GHS labelling:
GHS07: Exclamation markGHS08: Health hazard
Warning
H302, H312, H315, H319, H332
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

1,1′-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(C5H4Li)2 + 2 ClPPh2 → Fe(C5H4PPh2)2 + 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, (dppf)PdCl2, 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 + PdCl2(RCN)2 → (dppf)PdCl2 + 2 RCN (RCN = acetonitrile or benzonitrile)
Structure of the complex PtCl2(dppf)

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]

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]

Synthesis of (dppf)Ni(o-tolyl)Cl

See also

References

  1. ↑ Ian R. Butler (2010). "3.15 The Use of Organolithium Reagents in the Preparation of Ferrocene Derivatives" (Google Books excerpt). In J. Derek Woollins (ed.). Inorganic Experiments. John Wiley & Sons. pp. 175–179. ISBN 978-3-527-32472-9.
  2. 1 2 Nataro, Chip; Fosbenner, Stephanie M. (2009). "Synthesis and Characterization of Transition-Metal Complexes Containing 1,1′-Bis(diphenylphosphino)ferrocene". J. Chem. Educ. 86 (12): 1412. Bibcode:2009JChEd..86.1412N. doi:10.1021/ed086p1412.
  3. ↑ Dey, Subhayan; Pietschnig, Rudolf (2021). "Chemistry of sterically demanding dppf-analogs". Coord. Chem. Rev. 437: 213850. doi:10.1016/j.ccr.2021.213850.
  4. ↑ Ge, Shaozhong; Hartwig, John F. (2012-12-14). "Highly Reactive, Single-Component Nickel Catalyst Precursor for Suzuki–Miyuara Cross-Coupling of Heteroaryl Boronic Acids with Heteroaryl Halides". Angewandte Chemie International Edition. 51 (51): 12837–12841. doi:10.1002/anie.201207428. PMC 3613336. PMID 23136047.
  5. ↑ Park, Nathaniel H.; Teverovskiy, Georgiy; Buchwald, Stephen L. (2014-01-03). "Development of an Air-Stable Nickel Precatalyst for the Amination of Aryl Chlorides, Sulfamates, Mesylates, and Triflates". Organic Letters. 16 (1): 220–223. doi:10.1021/ol403209k. PMC 3926134. PMID 24283652.
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