Dimethylphenylphosphine

Dimethylphenylphosphine
Names
IUPAC name
Dimethylphenylphosphane
Other names
Dimethylphenylphosphine
Identifiers
672-66-2 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:30671 YesY
ChemSpider 62800 YesY
ECHA InfoCard 100.010.543
EC Number 211-595-3
PubChem 69597
Properties
C8H11P
Molar mass 138.14 g/mol
Appearance transparent light pale yellow liquid
Density 0.971 g/cm3
Melting point N/A
Boiling point 74 to 75 °C (165 to 167 °F; 347 to 348 K) at 12 mmHg
Insoluble
Structure
Pyramidal
Hazards
Safety data sheet
R-phrases R10 R36 R37 R38
S-phrases S26 S36
Flash point 49 °C (120 °F; 322 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Dimethylphenylphosphine is an organophosphorus compound with a formula P(C6H5)(CH3)2. The phosphorus is connected to a phenyl group and two methyl groups, making it the simplest aromatic alkylphosphine. This colorless air sensitive liquid is commonly used as a ligand in transition metal complexes. These complexes are often soluble in organic solvents.

Preparation

Dimethylphenylphosphine is prepared by the reaction of methylmagnesium halide with dichlorophenylphosphine.

(C6H5)Cl2P + 2CH3MgBr → (C6H5)(CH3)2P + 2MgBrCl

The phosphine is purified by distillation under reduced pressure.[1] A solution of (C6H5)(CH3)2P in CDCl3 shows proton NMR signals at δ 7.0-7.5 and a doublet at δ 1.2. The phosphorus-31 NMR spectrum shows a singlet at -45.89 ppm in CDCl3.[2]

Structure and properties

Dimethylphenylphosphine is a pyramidal molecule where the phenyl group and two methyl groups are connected to the phosphorus. The bond length and angles are the following: P-CMe: 1.844, P-CPh: 1.845 Å, C-C: 1.401 Å, C-HMe: 1.090 Å, C-HPh: 1.067 Å, C-P-C: 96.9°, C-P-C (ring): 103.4°, P-C-H: 115.2°.[3]

When attached to chiral metal centers, the P-methyl groups are diastereotopic, appearing as separate doublets in the 1H NMR spectrum.

The nνCO of IrCl(CO)(PPh3)2 and IrCl(CO)(PMe2Ph)2 are both at 1960 cm−1, whereas nCO for Ir-Cl(CO)(PMe3)2 is at 1938 cm−1.[4][5]

The acidity of various protonated phosphine ligands gives insights into their basicity as ligands:[6][7]

Thus PMe2Ph is intermediate in basicity relative to PPh3 and PEt3.

The ligand cone angle (θ) is the apex angle of a cylindrical cone, which is centered 2.28 Å from the center of the P atom. However, the cone angle of an unsymmetrical ligand cannot be determined in the same. In order to determine an effective cone angle for an unsymmetrical ligand PX1X2X3, the following equation is used:

Where θi represent the half angle.

The resulting angles for -PMe3, PMe2Ph, PPh3 are the following: PMe3= 118°, PMe2Ph= 122°, PPh3= 145°. Thus PMe2Ph is intermediate in size relative to PMe3 and PPh3.[8]

References

  1. ↑ C. Frajerman; B. Meunier; M. E. Strem., Inorganic Syntheses, Preparation of Dimethylphenylphosphine, 2007, volume 22, 133-135, doi:10.1002/9780470132531. ch29
  2. ↑ Laszlo T. Mika, Laszlo Orha, Norbert Farkas and Istvan T. Horvath, Organometallics, 2009, vol. 28, 1593
  3. ↑ Novikov, V. P.; Kolomeets, V. I., Syshchikov, Yu. N.; Vilkov, L. V.; Yarkov, A. V.; Tsvetkov, E. N.; Raevskii, O.A. "Investigation of structure of dimethylphenylphosphine by means of gas-phase electron diffraction and vibrational spectroscopy" Zh. Strukt. Khim. (J. Struc. Chem.) 1984, volume 25, No. 5, 688. doi:10.1007/BF00747909
  4. ↑ S.A. Cotton, Chemistry of Precious Metals., 1997, 152-157, ISBN 0-7514-0413-6, ISBN 978-0-7514-0413-5
  5. ↑ A. R. Norrris ; J. A. V. Kessel, Oxidative addition of 3,5-Dinitrobenzoyl Chloride to trans-Chlorocarbonylbis(dimethylphenylphosphine)iridium(I) Canadian Journal of Chemistry, 1973, volume 51, 4145-4151, doi:10.1139/CJC-51-24-4145.
  6. ↑ Russell C; Bush and Robert J. Angelici. Inorg. Chem, Phosphine Basicities As Determined by Enthalpies of Protonation 1988, 27, 681-686. doi:10.1021/ic00277a022
  7. ↑ Tianshu Li ; Alan J.; Robert H., Chemistry- A European Journal, An Acidity scale of Tetrafluoroborate Salts of Phosphonium and Iron Hydride compounds in [D2]Dichloromethane, 2007, volume 13, 3796-3803, doi: 10.1002/chem..200601484.
  8. ↑ C.A.Tolman, Chem.Rev., Steric effects of phosphorus ligands in organometallic chemistry and homogeneous catalysis., 1977, 313-348, doi:10.1021/cr60307a002
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