rac-Eth­yl(phen­yl)phosphinic acid

Abstract

The crystal structure of the title compound, C₈H₁₁O₂P, features O—H⋯O hydrogen bonds, which link mol­ecules related by the b-glide plane into chains along [010].

Related literature  

For background to metal-organic frameworks involving phospho­nate ligands, see: Gagnon et al. (2012 ▶). For details of coordination polymers constructed using phosphinic acids as the spacer ligand, see: Siqueira et al. (2006 ▶); Beckmann et al. (2009 ▶). For further details of phosphinic acids and the crystal structures of similar compounds, see: Burrow et al. (2000 ▶); Burrow & Siqueira da Silva (2011a ▶,b ▶). For a description of the Cambridge Structural Database, see: Allen (2002 ▶). For geometry analysis using Mogul, see: Bruno et al. (2004 ▶).

Experimental  

Crystal data  

• C₈H₁₁O₂P

• M _r = 170.14

• Orthorhombic,

• a = 13.5314 (16) Å

• b = 8.0328 (9) Å

• c = 15.922 (2) Å

• V = 1730.6 (4) ų

• Z = 8

• Mo Kα radiation

• μ = 0.27 mm⁻¹

• T = 296 K

• 0.41 × 0.12 × 0.11 mm

Data collection  

• Bruker X8 Kappa APEXII diffractometer

• Absorption correction: multi-scan (SADABS; Bruker, 2012 ▶) T _min = 0.906, T _max = 0.971

• 14069 measured reflections

• 2650 independent reflections

• 1499 reflections with I > 2σ(I)

• R _int = 0.054

Refinement  

• R[F ² > 2σ(F ²)] = 0.045

• wR(F ²) = 0.128

• S = 1.09

• 2650 reflections

• 104 parameters

• H atoms treated by a mixture of independent and constrained refinement

• Δρ_max = 0.24 e Å⁻³

• Δρ_min = −0.34 e Å⁻³

Data collection: APEX2 (Bruker, 2012 ▶); cell refinement: SAINT (Bruker, 2012 ▶); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: DIAMOND (Brandenburg, 2012 ▶); software used to prepare material for publication: SHELXL97 and publCIF (Westrip, 2010 ▶).

Supplementary Material

Additional supplementary materials: crystallographic information; 3D view; checkCIF report

Table 1. Hydrogen-bond geometry (Å, °).

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
O1—H1⋯O2i	0.87 (2)	1.64 (2)	2.4931 (19)	168 (2)

Symmetry code: (i) .

supplementary crystallographic information

Comment

Coordination polymers are the basis of metal-organic frameworks usually based on carboxylate ligands or phosphonate ligands (Gagnon et al., 2012). Coordination polymers have also been constructed using phosphinic acids as the spacer ligand (Siqueira et al., 2006; Beckmann et al., 2009). Continuing our research on phosphinic acids (Burrow et al., 2000; Burrow & Siqueira da Silva, 2011a,b), we report herein on the synthesis and crystal structure of the title compound.

The title compound, Fig. 1, is found to crystallize as a racemic mixture of enantiomers in the centrosymmetric space group Pbcn. An analysis of the geometry with Mogul [Bruno et al., 2004] using the Cambridge Structural Database [CSD; Allen, 2002] showed a slightly wider C—P—C angle [110.87 (9) °] than average [mean = 106.0(2.2)° of 15 observations] with |z-score| = 2.178. The P—O distance, though not unusual at 1.5529 (14) Å, is slightly longer than average value [mean 1.542 (22) Å of 17 observations] and is similar to that in methyl(phenyl)phosphinic acid [1.5526 (16) Å; Burrow & Siqueira da Silva, 2011b].

In the crystal, hydrogen bonding interactions (Table 1 and Fig. 2) of the type OH···O=P—OH···O=P join molecules related by the b glide plane into continuous chains along [010]. The short P—O···O=P distance of 2.4931 (19) Å indicates a strong hydrogen bond. This is slightly shorter than the average O···O interaction distance in the CSD [2.51 (5) Å of 60 observations] for other phosphinic acids, but is equal that for methyl(phenyl)phosphinic acid, 2.4838 (18) Å [Burrow & Siqueira da Silva, 2011b].

The crystal packing diagram, Fig. 2, shows that the hydrogen bonded chains of the title compound form columns in the crystallographic b direction, with the chains alternating direction in the other two dimensions. There are no phenyl-phenyl interactions.

Experimental

To a solution of phenylphosphinic acid (2.0 g, 14.1 mmol) in dichloromethane, diisopropylethylamine (5.16 ml, 29.6 mmol) and trimethylsilyl chloride (3.74 ml, 29.6 mmol) were separately added at 273 K under argon. The reaction mixture was stirred at room temperature for 2–3 h, cooled to 273 K and ethyliodide (1.25 ml, 19.6 mmol) was added. After further stirring at room temperature for 48 h, the solvent was removed under vacuum. The residue was suspended in hydrochloric acid (2 M, 20 ml) and filtered on a glass frit. The white solid was washed with acetone and dried giving a yield of 0.84 g (35%) of pure product. Crystals suitable for single-crystal X-ray analysis were grown from an acetone solution in a desiccator with silica gel. Spectroscopic and TGA data for the title compound are available in the archived CIF.

Refinement

The H atom on O1 was located in a difference Fourier map and its position was allowed to refine freely with U_iso(H) = 1.5 U_eq(O). The C-bound H atoms were positioned geometrically and allowed to ride on their parent atoms: C—H = 0.93, 0.97 and 0.97 Å for CH, CH₂ and CH₃ H atoms, respectively, with = k × U_eq(C), where k = 1.5 for CH₃ H atoms and = 1.2 for other H atoms.

Figures

Fig. 1.

The molecular structure of the title molecule, with the atom numbering. The displacement ellipsoids are drawn at the 50% probability level.

Fig. 2.

A perspective view along the a axis of the crystal packing of the title compound. The O-H···O hydrogen bonds are shown as dashed lines.

Crystal data

C8H11O2P	Dx = 1.306 Mg m−3
Mr = 170.14	Melting point = 336–341 K
Orthorhombic, Pbcn	Mo Kα radiation, λ = 0.71073 Å
a = 13.5314 (16) Å	Cell parameters from 2263 reflections
b = 8.0328 (9) Å	θ = 2.6–26.5°
c = 15.922 (2) Å	µ = 0.27 mm−1
V = 1730.6 (4) Å3	T = 296 K
Z = 8	Block, colourless
F(000) = 720	0.41 × 0.12 × 0.11 mm

Data collection

Bruker X8 Kappa APEXII diffractometer	2650 independent reflections
Radiation source: sealed ceramic X ray tube, Siemens KFF	1499 reflections with I > 2σ(I)
Graphite crystal monochromator	Rint = 0.054
Detector resolution: 8.3333 pixels mm-1	θmax = 30.5°, θmin = 3.2°
0.5 ° ω & φ scans	h = −19→19
Absorption correction: multi-scan (SADABS; Bruker, 2012)	k = −9→11
Tmin = 0.906, Tmax = 0.971	l = −18→22
14069 measured reflections

Refinement

Refinement on F2	Primary atom site location: structure-invariant direct methods
Least-squares matrix: full	Secondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.045	Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.128	H atoms treated by a mixture of independent and constrained refinement
S = 1.09	w = 1/[σ2(Fo2) + (0.0525P)2 + 0.0622P] where P = (Fo2 + 2Fc2)/3
2650 reflections	(Δ/σ)max < 0.001
104 parameters	Δρmax = 0.24 e Å−3
0 restraints	Δρmin = −0.34 e Å−3

Special details

Experimental. Spectroscopic and TGA data for the title compound:IR: 1438 (m), 1177 (versus), 1137 (s), 998 (versus), 935 (versus), 745 (m), 718 (s), 692 (versus), 565 (m), 537 (m), 495 (m) cm-1. TGA: 483 - 603 K; 88% loss.

Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes.

Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > 2σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R-factors based on ALL data will be even larger.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Ų)

	x	y	z	Uiso*/Ueq
P1	0.31872 (4)	0.19541 (6)	0.40958 (3)	0.03859 (18)
O1	0.34640 (11)	0.35269 (17)	0.35798 (8)	0.0468 (4)
H1	0.3212 (16)	0.444 (3)	0.3780 (15)	0.07*
O2	0.21554 (10)	0.13429 (17)	0.39751 (8)	0.0496 (4)
C11	0.40682 (16)	0.0441 (3)	0.37446 (13)	0.0539 (5)
H11A	0.4004	−0.0541	0.4095	0.065*
H11B	0.3897	0.012	0.3176	0.065*
C12	0.51433 (18)	0.0978 (3)	0.37521 (16)	0.0740 (7)
H12C	0.5222	0.1953	0.341	0.111*
H12A	0.5547	0.0096	0.3533	0.111*
H12B	0.5341	0.1224	0.4318	0.111*
C21	0.33743 (13)	0.2444 (2)	0.51841 (11)	0.0368 (4)
C22	0.41968 (14)	0.3314 (2)	0.54585 (13)	0.0474 (5)
H22	0.4675	0.3645	0.5073	0.057*
C23	0.43146 (16)	0.3697 (3)	0.62986 (14)	0.0584 (6)
H23	0.4868	0.4286	0.6476	0.07*
C24	0.36130 (17)	0.3207 (3)	0.68740 (14)	0.0579 (6)
H24	0.3694	0.3464	0.7439	0.069*
C25	0.28001 (17)	0.2344 (3)	0.66167 (13)	0.0576 (6)
H25	0.2329	0.2012	0.7008	0.069*
C26	0.26725 (15)	0.1960 (2)	0.57756 (12)	0.0466 (5)
H26	0.2115	0.1374	0.5605	0.056*

Atomic displacement parameters (Ų)

	U11	U22	U33	U12	U13	U23
P1	0.0484 (3)	0.0289 (3)	0.0386 (3)	0.0015 (2)	−0.0015 (2)	0.0000 (2)
O1	0.0652 (9)	0.0336 (8)	0.0416 (8)	0.0046 (7)	0.0087 (6)	0.0029 (6)
O2	0.0536 (8)	0.0376 (8)	0.0576 (9)	−0.0038 (7)	−0.0134 (7)	−0.0018 (6)
C11	0.0701 (13)	0.0399 (12)	0.0516 (12)	0.0116 (11)	0.0031 (10)	−0.0035 (9)
C12	0.0666 (15)	0.0666 (17)	0.0887 (19)	0.0219 (13)	0.0124 (13)	−0.0028 (14)
C21	0.0423 (10)	0.0295 (9)	0.0386 (9)	0.0002 (8)	0.0005 (7)	0.0011 (8)
C22	0.0479 (11)	0.0445 (12)	0.0498 (12)	−0.0086 (9)	−0.0002 (9)	−0.0006 (9)
C23	0.0613 (14)	0.0576 (14)	0.0563 (13)	−0.0077 (11)	−0.0151 (11)	−0.0097 (11)
C24	0.0732 (16)	0.0599 (15)	0.0405 (11)	0.0076 (12)	−0.0076 (11)	−0.0081 (10)
C25	0.0620 (14)	0.0667 (15)	0.0442 (12)	0.0032 (11)	0.0132 (10)	0.0001 (11)
C26	0.0444 (11)	0.0458 (12)	0.0496 (12)	−0.0047 (9)	0.0028 (8)	−0.0014 (9)

Geometric parameters (Å, º)

P1—O2	1.4925 (14)	C21—C22	1.385 (2)
P1—O1	1.5529 (14)	C21—C26	1.393 (3)
P1—C11	1.792 (2)	C22—C23	1.382 (3)
P1—C21	1.7950 (19)	C22—H22	0.93
O1—H1	0.87 (2)	C23—C24	1.377 (3)
C11—C12	1.517 (3)	C23—H23	0.93
C11—H11A	0.97	C24—C25	1.363 (3)
C11—H11B	0.97	C24—H24	0.93
C12—H12C	0.96	C25—C26	1.385 (3)
C12—H12A	0.96	C25—H25	0.93
C12—H12B	0.96	C26—H26	0.93
O2—P1—O1	115.16 (8)	C22—C21—C26	118.40 (18)
O2—P1—C11	111.05 (10)	C22—C21—P1	121.91 (14)
O1—P1—C11	103.08 (9)	C26—C21—P1	119.69 (14)
O2—P1—C21	109.17 (8)	C23—C22—C21	120.68 (19)
O1—P1—C21	107.36 (8)	C23—C22—H22	119.7
C11—P1—C21	110.87 (9)	C21—C22—H22	119.7
P1—O1—H1	113.5 (16)	C24—C23—C22	120.06 (19)
C12—C11—P1	116.28 (16)	C24—C23—H23	120.0
C12—C11—H11A	108.2	C22—C23—H23	120.0
P1—C11—H11A	108.2	C25—C24—C23	120.1 (2)
C12—C11—H11B	108.2	C25—C24—H24	119.9
P1—C11—H11B	108.2	C23—C24—H24	119.9
H11A—C11—H11B	107.4	C24—C25—C26	120.3 (2)
C11—C12—H12C	109.5	C24—C25—H25	119.8
C11—C12—H12A	109.5	C26—C25—H25	119.8
H12C—C12—H12A	109.5	C25—C26—C21	120.43 (19)
C11—C12—H12B	109.5	C25—C26—H26	119.8
H12C—C12—H12B	109.5	C21—C26—H26	119.8
H12A—C12—H12B	109.5
O2—P1—C11—C12	174.11 (16)	C26—C21—C22—C23	−0.3 (3)
O1—P1—C11—C12	50.26 (18)	P1—C21—C22—C23	179.01 (16)
C21—P1—C11—C12	−64.34 (19)	C21—C22—C23—C24	0.3 (3)
O2—P1—C21—C22	−168.19 (15)	C22—C23—C24—C25	−0.1 (3)
O1—P1—C21—C22	−42.73 (17)	C23—C24—C25—C26	−0.2 (3)
C11—P1—C21—C22	69.16 (18)	C24—C25—C26—C21	0.2 (3)
O2—P1—C21—C26	11.07 (18)	C22—C21—C26—C25	0.0 (3)
O1—P1—C21—C26	136.53 (16)	P1—C21—C26—C25	−179.28 (15)
C11—P1—C21—C26	−111.58 (17)

Hydrogen-bond geometry (Å, º)

D—H···A	D—H	H···A	D···A	D—H···A
O1—H1···O2i	0.87 (2)	1.64 (2)	2.4931 (19)	168 (2)

Symmetry code: (i) −x+1/2, y+1/2, z.