Potassium tri­fluoro­[(Z)-3-(oxan-2-yl­­oxy)prop-1-en-1-yl]borate monohydrate

The title compound, K⁺·C₈H₁₃BF₃O₂⁻·H₂O, which was obtained from the reaction of a modified form of Z-vinylic telluride via a transmetalation reaction with n-BuLi, crystallizes as K⁺ and C₈H₁₃BF₃O₂⁻ ions along with a water mol­ecule. The K⁺ cation is surrounded by four anions, making close contacts with six F atoms at 2.659 (3)–2.906 (3) Å and with two O atoms at 2.806 (3) and 2.921 (3) Å in a distorted bicapped trigonal-prismatic geometry.

Related literature

For related structures, see: Stefani et al. (2006); Caracelli et al. (2007); Zukerman-Schpector et al. (2008). For related literature, see: Vieira et al. (2008). For the synthesis, see: Bernady et al. (1979). For ring puckering analysis, see: Cremer & Pople (1975).

Experimental

Crystal data

• K⁺·C₈H₁₃BF₃O₂⁻·H₂O

• M_r = 266.11

• Orthorhombic, P c a 2₁

• a = 8.5210 (7) Å

• b = 17.056 (1) Å

• c = 8.6318 (7) Å

• V = 1254.50 (16) ų

• Z = 4

• Mo Kα radiation

• μ = 0.45 mm⁻¹

• T = 291 (2) K

• 0.27 × 0.10 × 0.04 mm

Data collection

• Nonius KappaCCD diffractometer

• Absorption correction: multi-scan (SADABS; Bruker, 2006) T_min = 0.888, T_max = 0.982

• 11914 measured reflections

• 2324 independent reflections

• 1604 reflections with I > 2σ(I)

• R_int = 0.074

Refinement

• R[F² > 2σ(F²)] = 0.041

• wR(F²) = 0.096

• S = 1.03

• 2324 reflections

• 145 parameters

• 1 restraint

• H-atom parameters constrained

• Δρ_max = 0.23 e Å⁻³

• Δρ_min = −0.19 e Å⁻³

• Absolute structure: Flack (Flack, 1983), 1064 Friedel pairs

• Flack parameter: 0.07 (9)

Data collection: COLLECT (Nonius, 1998); cell refinement: PHICHI (Duisenberg et al., 2000); data reduction: EVAL-14 (CCD) (Duisenberg et al., 2003); program(s) used to solve structure: SIR97 (Altomare et al., 1999); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997); software used to prepare material for publication: WinGX (Farrugia, 1999).

Supporting information

S1. Comment

Organic compounds of tellurium, such as Z-vinylic tellurides, are important synthetic precursors of organometallic molecules and organic salts and can be useful in the synthesis of new potassium vinyl trifluoroborate salts. Organotrifluoroborates represent an alternative to boronic acids, boronate esters, and organoboranes for use in the Suzuki-Miyaura reaction and other transition-metal-catalyzed cross-coupling reactions (Vieira et al. 2008). The title compound (I), Fig. 1, was studied as part of an ongoing systematic synthesis of trifluoroborate compounds (Stefani et al.(2006), Caracelli et al. (2007); Zukerman-Schpector et al. (2008)). The oxane ring is in a slightly distorted chair conformation, the ring-puckering parameters (Cremer & Pople, 1975) are q₂ = 0.033 (6) Å, q₃ = 0.555 (6) Å, Q = 0.556 (7)°, θ = 3.4 (6)° and ϕ₂ = 156 (11)°. The geometry around the K⁺ ion can be described as a distorted bicaped trigonal prism as shown in Figure 2. Besides the K⁺ interactions,the molecules are connected via C3···O2ⁱ = 3.600 (6) Å, C3—H3A···O2ⁱ = 132° (i = -x + 3/2, y, z + 1/2) contact.

Related literature

For related structures, see: Stefani et al. (2006); Caracelli et al. (2007); Zukerman-Schpector et al. (2008). For related literature, see: Vieira et al. (2008). For the synthesis, see: Bernady et al. (1979). For ring puckering analysis, see: Cremer & Pople (1975).

S2. Experimental

The starting propargylic alcohol was protected with dihydropyran (Bernady et al. 1979) and via hydrotelluration of the alkyne transformed in the correspondent Z-vinylic telluride. Next, nBuLi (0.8 mmol) was added dropwise at 203 K to a solution of the Z-vinylic telluride (1 mmol) in Et₂O (6 ml). The bath temperature was raised to 253 K. After 20 minutes B(OiPr)₃ (1.0 mmol) was added at 233 K. After 1 h, an aqueous solution of KHF₂ (4 mmol in 10 ml of water) was added to the reaction mixture. Then, the solvent and water were eliminated by evaporation. To the obtained solid hot acetone was added and the bulk reactional was filtered and dried, yielding 24% of (Z)-potassium vinyltrifluoroborate salt. Single crystals were obtained by slow evaporation from Et₂O.

S3. Refinement

The H atoms were refined in the riding-model approximation with U_iso(H) = 1.2U_eq, and with C—H = 0.93 - 0.97 Å. The water molecule H atoms were refined riding in the position found in a difference map.

Computing details

Data collection: COLLECT (Nonius, 1998); cell refinement: PHICHI (Duisenberg et al., 2000); data reduction: EVAL14 (CCD) (Duisenberg et al., 2003); program(s) used to solve structure: SIR97 (Altomare et al., 1999); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997); software used to prepare material for publication: WinGX (Farrugia, 1999).

Figures

	Fig. 1. The molecular structure of the title compound showing atom labelling scheme and displacement ellipsoids at the 50% probability level (arbitrary spheres for the H atoms).
	Fig. 2. The bicapped trigonal prism around the K^+ ion. Symmetry operations: a = 1 - x, -y, z - 1/2; b = 1/2 - x, y, z - 1/2; c = x - 1/2, -y, z.

Potassium trifluoro[(Z)-3-(oxan-2-yloxy)prop-1-en-1-yl]borate monohydrate

Crystal data

K^+·C8H13BF3O2^−·H2O	F(000) = 552
Mr = 266.11	Dx = 1.409 Mg m^−3
Orthorhombic, Pca21	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: P 2c -2ac	Cell parameters from 9536 reflections
a = 8.5210 (7) Å	θ = 2.3–21.8°
b = 17.056 (1) Å	µ = 0.45 mm^−1
c = 8.6318 (7) Å	T = 291 K
V = 1254.50 (16) Å^3	Plate, colourless
Z = 4	0.27 × 0.10 × 0.04 mm

Data collection

Nonius KappaCCD diffractometer	2324 independent reflections
Radiation source: fine-focus sealed tube	1604 reflections with I > 2σ(I)
Graphite monochromator	Rint = 0.074
ϕ and ω scans	θmax = 25.5°, θmin = 3.4°
Absorption correction: multi-scan (SADABS; Bruker, 2006)	h = −10→10
Tmin = 0.888, Tmax = 0.982	k = −20→20
11914 measured reflections	l = −10→10

Refinement

Refinement on F^2	Secondary atom site location: difference Fourier map
Least-squares matrix: full	Hydrogen site location: inferred from neighbouring sites
R[F^2 > 2σ(F^2)] = 0.041	H-atom parameters constrained
wR(F^2) = 0.096	w = 1/[σ^2(Fo^2) + (0.0438P)^2] where P = (Fo^2 + 2Fc^2)/3
S = 1.03	(Δ/σ)max < 0.001
2324 reflections	Δρmax = 0.23 e Å^−3
145 parameters	Δρmin = −0.19 e Å^−3
1 restraint	Absolute structure: Flack (Flack, 1983), 1064 Friedel pairs
Primary atom site location: structure-invariant direct methods	Absolute structure parameter: 0.07 (9)

Special details

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.

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

	x	y	z	Uiso*/Ueq
K	0.24966 (12)	−0.03852 (4)	0.49817 (17)	0.04270 (18)
B	0.3952 (4)	0.1021 (2)	0.7488 (8)	0.0421 (8)
F1	0.2390 (2)	0.07214 (10)	0.7452 (5)	0.0524 (4)
F2	0.4623 (4)	0.08281 (14)	0.6069 (3)	0.0627 (8)
F3	0.4710 (3)	0.05485 (16)	0.8649 (3)	0.0714 (9)
O1	0.5509 (3)	0.32819 (14)	0.5091 (4)	0.0665 (8)
O2	0.5808 (3)	0.28932 (14)	0.2496 (5)	0.0675 (7)
O3	0.3979 (3)	−0.12040 (12)	0.7392 (4)	0.0516 (6)
H1O3	0.4374	−0.1060	0.8252	0.062*
H2O3	0.4006	−0.1711	0.7375	0.062*
C1	0.4036 (5)	0.1914 (2)	0.7978 (4)	0.0585 (12)
H1	0.3581	0.2026	0.8932	0.070*
C2	0.4642 (5)	0.2527 (2)	0.7267 (6)	0.0614 (11)
H2	0.4563	0.3010	0.7758	0.074*
C3	0.5447 (6)	0.2502 (3)	0.5726 (5)	0.0673 (12)
H3A	0.6502	0.2297	0.5846	0.081*
H3B	0.4877	0.2159	0.5028	0.081*
C4	0.6461 (6)	0.3325 (2)	0.3741 (6)	0.0677 (12)
H4	0.7499	0.3110	0.3982	0.081*
C6	0.4336 (7)	0.3192 (3)	0.1981 (7)	0.101 (2)
H6A	0.3585	0.3169	0.2824	0.121*
H6B	0.3944	0.2868	0.1143	0.121*
C7	0.4488 (8)	0.4031 (4)	0.1427 (8)	0.114 (2)
H7A	0.3468	0.4229	0.1115	0.137*
H7B	0.5183	0.4054	0.0538	0.137*
C8	0.5146 (8)	0.4530 (3)	0.2740 (10)	0.100 (2)
H8A	0.5340	0.5059	0.2372	0.120*
H8B	0.4392	0.4558	0.3580	0.120*
C9	0.6638 (8)	0.4176 (3)	0.3308 (7)	0.0904 (17)
H9A	0.6999	0.4467	0.4205	0.108*
H9B	0.7431	0.4223	0.2507	0.108*

Atomic displacement parameters (Ų)

	U^11	U^22	U^33	U^12	U^13	U^23
K	0.0363 (3)	0.0543 (4)	0.0374 (3)	−0.0017 (5)	0.0004 (3)	0.0036 (7)
B	0.0300 (17)	0.053 (2)	0.0437 (18)	−0.0018 (16)	0.007 (3)	−0.001 (3)
F1	0.0330 (9)	0.0674 (10)	0.0569 (10)	−0.0045 (9)	0.0018 (15)	−0.005 (2)
F2	0.0665 (17)	0.0580 (15)	0.0635 (15)	−0.0067 (13)	0.0313 (13)	−0.0131 (13)
F3	0.0493 (17)	0.0804 (18)	0.085 (2)	−0.0009 (15)	−0.0228 (15)	0.0288 (16)
O1	0.080 (2)	0.0450 (14)	0.0746 (19)	0.0016 (14)	0.010 (2)	0.0035 (17)
O2	0.0800 (18)	0.0491 (14)	0.0735 (16)	−0.0009 (14)	0.004 (2)	−0.002 (2)
O3	0.0605 (14)	0.0446 (13)	0.0497 (13)	0.0003 (11)	0.0093 (17)	−0.0057 (18)
C1	0.073 (3)	0.056 (3)	0.046 (2)	−0.007 (2)	0.0120 (19)	−0.0077 (17)
C2	0.066 (2)	0.049 (2)	0.069 (3)	−0.0020 (19)	0.008 (3)	−0.019 (2)
C3	0.079 (3)	0.053 (3)	0.070 (3)	0.003 (2)	0.015 (2)	0.003 (2)
C4	0.060 (3)	0.057 (3)	0.086 (3)	−0.008 (2)	0.014 (2)	0.005 (3)
C6	0.093 (4)	0.108 (4)	0.101 (5)	−0.014 (3)	−0.016 (3)	−0.008 (3)
C7	0.115 (6)	0.105 (5)	0.123 (6)	0.024 (4)	−0.017 (4)	0.034 (5)
C8	0.133 (5)	0.053 (3)	0.113 (6)	0.023 (3)	0.015 (4)	0.012 (3)
C9	0.106 (5)	0.067 (3)	0.098 (4)	−0.022 (3)	0.021 (3)	0.004 (3)

Geometric parameters (Å, º)

B—F1	1.426 (4)	C3—H3B	0.9700
B—F2	1.392 (6)	C4—C9	1.507 (6)
B—F3	1.439 (6)	C4—H4	0.9800
B—C1	1.582 (5)	C6—C7	1.514 (8)
O1—C4	1.422 (5)	C6—H6A	0.9700
O1—C3	1.439 (5)	C6—H6B	0.9700
O2—C4	1.417 (6)	C7—C8	1.525 (10)
O2—C6	1.425 (6)	C7—H7A	0.9700
O3—H1O3	0.8518	C7—H7B	0.9700
O3—H2O3	0.8651	C8—C9	1.490 (8)
C1—C2	1.317 (6)	C8—H8A	0.9700
C1—H1	0.9300	C8—H8B	0.9700
C2—C3	1.497 (7)	C9—H9A	0.9700
C2—H2	0.9300	C9—H9B	0.9700
C3—H3A	0.9700
F2—B—F1	106.2 (4)	C9—C4—H4	108.8
F2—B—F3	107.2 (3)	O2—C6—C7	111.2 (4)
F1—B—F3	103.5 (3)	O2—C6—H6A	109.4
F2—B—C1	116.4 (3)	C7—C6—H6A	109.4
F1—B—C1	113.2 (3)	O2—C6—H6B	109.4
F3—B—C1	109.4 (4)	C7—C6—H6B	109.4
C4—O1—C3	112.3 (3)	H6A—C6—H6B	108.0
C4—O2—C6	113.4 (4)	C6—C7—C8	108.9 (5)
H1O3—O3—H2O3	107.0	C6—C7—H7A	109.9
C2—C1—B	131.1 (4)	C8—C7—H7A	109.9
C2—C1—H1	114.5	C6—C7—H7B	109.9
B—C1—H1	114.5	C8—C7—H7B	109.9
C1—C2—C3	124.8 (4)	H7A—C7—H7B	108.3
C1—C2—H2	117.6	C9—C8—C7	109.4 (5)
C3—C2—H2	117.6	C9—C8—H8A	109.8
O1—C3—C2	109.2 (3)	C7—C8—H8A	109.8
O1—C3—H3A	109.8	C9—C8—H8B	109.8
C2—C3—H3A	109.8	C7—C8—H8B	109.8
O1—C3—H3B	109.8	H8A—C8—H8B	108.2
C2—C3—H3B	109.8	C8—C9—C4	112.7 (5)
H3A—C3—H3B	108.3	C8—C9—H9A	109.0
O2—C4—O1	111.8 (3)	C4—C9—H9A	109.0
O2—C4—C9	110.6 (4)	C8—C9—H9B	109.0
O1—C4—C9	108.1 (4)	C4—C9—H9B	109.0
O2—C4—H4	108.8	H9A—C9—H9B	107.8
O1—C4—H4	108.8
F2—B—C1—C2	0.1 (7)	C3—O1—C4—O2	66.2 (5)
F1—B—C1—C2	−123.4 (6)	C3—O1—C4—C9	−171.9 (4)
F3—B—C1—C2	121.8 (5)	C4—O2—C6—C7	60.0 (6)
B—C1—C2—C3	−0.3 (8)	O2—C6—C7—C8	−57.6 (7)
C4—O1—C3—C2	171.2 (4)	C6—C7—C8—C9	54.2 (7)
C1—C2—C3—O1	161.9 (4)	C7—C8—C9—C4	−53.4 (7)
C6—O2—C4—O1	63.8 (5)	O2—C4—C9—C8	53.8 (6)
C6—O2—C4—C9	−56.6 (5)	O1—C4—C9—C8	−68.9 (6)