Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S160053680301393X/bt6291sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S160053680301393X/bt6291IIsup2.hkl |
CCDC reference: 217617
A solution of compound (I) and P[OCH(CH3)2]3 was heated to reflux in toluene for 4 h. The resulting solution was evaporated and acetonitrile was added. After 24 h, compound (II) crystallized with a yield 75%. The determined melting point is 398–399 K.
Data collection: CrysAlis CCD (Oxford Diffraction, 2002); cell refinement: CrysAlis RED (Oxford Diffraction, 2002); data reduction: CrysAlis RED; program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: SHELXTL (Sheldrick, 1990); software used to prepare material for publication: SHELXL9.
C17H23PO4 | F(000) = 688 |
Mr = 322.32 | Dx = 1.231 Mg m−3 |
Monoclinic, P21 | Mo Kα radiation, λ = 0.71073 Å |
Hall symbol: P 2yb | Cell parameters from 6056 reflections |
a = 9.166 (1) Å | θ = 3.6–25.0° |
b = 22.484 (2) Å | µ = 0.17 mm−1 |
c = 9.579 (1) Å | T = 293 K |
β = 118.21 (1)° | Irregular, colourless |
V = 1739.7 (3) Å3 | 0.2 × 0.15 × 0.1 mm |
Z = 4 |
Xcalibur diffractometer | 6056 independent reflections |
Radiation source: fine-focus sealed tube | 4614 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.029 |
Detector resolution: 1024 x 1024 with blocks 2 x 2 pixels mm-1 | θmax = 25.0°, θmin = 3.6° |
ω–scan | h = −10→10 |
Absorption correction: multi-scan (SADABS; Sheldrick, 1996) | k = −26→26 |
Tmin = 0.966, Tmax = 0.979 | l = −11→6 |
10929 measured reflections |
Refinement on F2 | Secondary atom site location: difference Fourier map |
Least-squares matrix: full | Hydrogen site location: inferred from neighbouring sites |
R[F2 > 2σ(F2)] = 0.043 | H atoms treated by a mixture of independent and constrained refinement |
wR(F2) = 0.084 | w = 1/[σ2(Fo2) + (0.0387P)2] where P = (Fo2 + 2Fc2)/3 |
S = 1.00 | (Δ/σ)max < 0.001 |
6056 reflections | Δρmax = 0.15 e Å−3 |
463 parameters | Δρmin = −0.21 e Å−3 |
1 restraint | Absolute structure: Flack H D (1983), Acta Cryst. A39, 876-881 |
Primary atom site location: structure-invariant direct methods | Absolute structure parameter: 0.00 (8) |
C17H23PO4 | V = 1739.7 (3) Å3 |
Mr = 322.32 | Z = 4 |
Monoclinic, P21 | Mo Kα radiation |
a = 9.166 (1) Å | µ = 0.17 mm−1 |
b = 22.484 (2) Å | T = 293 K |
c = 9.579 (1) Å | 0.2 × 0.15 × 0.1 mm |
β = 118.21 (1)° |
Xcalibur diffractometer | 6056 independent reflections |
Absorption correction: multi-scan (SADABS; Sheldrick, 1996) | 4614 reflections with I > 2σ(I) |
Tmin = 0.966, Tmax = 0.979 | Rint = 0.029 |
10929 measured reflections |
R[F2 > 2σ(F2)] = 0.043 | H atoms treated by a mixture of independent and constrained refinement |
wR(F2) = 0.084 | Δρmax = 0.15 e Å−3 |
S = 1.00 | Δρmin = −0.21 e Å−3 |
6056 reflections | Absolute structure: Flack H D (1983), Acta Cryst. A39, 876-881 |
463 parameters | Absolute structure parameter: 0.00 (8) |
1 restraint |
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 > σ(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. |
x | y | z | Uiso*/Ueq | ||
P1 | 0.80393 (9) | 0.27391 (3) | 0.14087 (8) | 0.0365 (2) | |
O1 | 0.9884 (2) | 0.25154 (8) | 0.2243 (2) | 0.0418 (5) | |
O2 | 0.7106 (3) | 0.23366 (10) | −0.0097 (2) | 0.0470 (6) | |
O3 | 0.7897 (3) | 0.33771 (9) | 0.1070 (2) | 0.0484 (6) | |
O4 | 0.5684 (3) | 0.34736 (10) | 0.2986 (3) | 0.0542 (6) | |
H4A | 0.536 (5) | 0.3790 (18) | 0.310 (4) | 0.081* | |
C1 | 0.7926 (4) | 0.28200 (14) | 0.4204 (3) | 0.0388 (8) | |
C2 | 0.7139 (4) | 0.33292 (14) | 0.4252 (4) | 0.0437 (8) | |
C3 | 0.7848 (6) | 0.36989 (16) | 0.5611 (5) | 0.0603 (11) | |
H3A | 0.725 (5) | 0.4000 (17) | 0.560 (4) | 0.072* | |
C4 | 0.9293 (6) | 0.35468 (17) | 0.6876 (5) | 0.0637 (11) | |
H4B | 0.979 (4) | 0.3796 (16) | 0.773 (4) | 0.076* | |
C5 | 1.1619 (6) | 0.2850 (2) | 0.8213 (5) | 0.0690 (13) | |
H5A | 1.193 (5) | 0.3134 (17) | 0.898 (4) | 0.083* | |
C6 | 1.2397 (6) | 0.2341 (2) | 0.8239 (5) | 0.0782 (13) | |
H6A | 1.345 (5) | 0.2200 (18) | 0.908 (5) | 0.094* | |
C7 | 1.1688 (5) | 0.1961 (2) | 0.6913 (5) | 0.0659 (11) | |
H7A | 1.225 (5) | 0.1610 (17) | 0.691 (4) | 0.079* | |
C8 | 1.0269 (5) | 0.21071 (16) | 0.5624 (4) | 0.0501 (9) | |
H8A | 0.979 (4) | 0.1866 (15) | 0.478 (4) | 0.060* | |
C9 | 0.9425 (4) | 0.26435 (13) | 0.5546 (3) | 0.0393 (8) | |
C10 | 1.0125 (4) | 0.30172 (16) | 0.6900 (4) | 0.0495 (9) | |
C11 | 0.7212 (4) | 0.24748 (15) | 0.2663 (4) | 0.0383 (8) | |
H11A | 0.753 (3) | 0.2025 (14) | 0.286 (3) | 0.046* | |
H11B | 0.608 (4) | 0.2560 (13) | 0.209 (3) | 0.046* | |
C12 | 1.1294 (4) | 0.28735 (16) | 0.2418 (4) | 0.0478 (9) | |
H12A | 1.096 (4) | 0.3118 (14) | 0.146 (4) | 0.057* | |
C13 | 1.1815 (5) | 0.32914 (17) | 0.3803 (4) | 0.0665 (11) | |
H13A | 1.0909 | 0.3550 | 0.3626 | 0.100* | |
H13B | 1.2740 | 0.3525 | 0.3913 | 0.100* | |
H13C | 1.2128 | 0.3066 | 0.4754 | 0.100* | |
C14 | 1.2607 (4) | 0.24318 (18) | 0.2635 (5) | 0.0728 (12) | |
H14A | 1.2321 | 0.2241 | 0.1642 | 0.109* | |
H14B | 1.2694 | 0.2138 | 0.3398 | 0.109* | |
H14C | 1.3649 | 0.2633 | 0.3004 | 0.109* | |
C15 | 0.7457 (4) | 0.24166 (17) | −0.1441 (4) | 0.0492 (9) | |
H15A | 0.825 (4) | 0.2787 (15) | −0.125 (3) | 0.059* | |
C16 | 0.8368 (6) | 0.18832 (18) | −0.1534 (5) | 0.0763 (13) | |
H16A | 0.9331 | 0.1821 | −0.0529 | 0.114* | |
H16B | 0.8701 | 0.1943 | −0.2335 | 0.114* | |
H16C | 0.7660 | 0.1541 | −0.1797 | 0.114* | |
C17 | 0.5847 (5) | 0.2523 (3) | −0.2885 (4) | 0.0993 (18) | |
H17A | 0.5304 | 0.2858 | −0.2714 | 0.149* | |
H17B | 0.5159 | 0.2177 | −0.3104 | 0.149* | |
H17C | 0.6041 | 0.2601 | −0.3769 | 0.149* | |
P1' | 0.56977 (10) | 0.01555 (4) | 0.70498 (9) | 0.0395 (2) | |
O1' | 0.7551 (2) | 0.03493 (8) | 0.7918 (2) | 0.0422 (5) | |
O2' | 0.4823 (3) | 0.05866 (10) | 0.5598 (2) | 0.0509 (6) | |
O3' | 0.5477 (3) | −0.04770 (9) | 0.6633 (3) | 0.0532 (6) | |
O4' | 0.3312 (3) | −0.05856 (10) | 0.8586 (3) | 0.0516 (6) | |
H4C | 0.303 (4) | −0.0958 (17) | 0.866 (4) | 0.077* | |
C1' | 0.5581 (4) | 0.00600 (13) | 0.9840 (3) | 0.0367 (7) | |
C2' | 0.4760 (4) | −0.04524 (14) | 0.9877 (4) | 0.0416 (8) | |
C3' | 0.5416 (5) | −0.08186 (15) | 1.1223 (4) | 0.0539 (9) | |
H3B | 0.479 (4) | −0.1194 (16) | 1.122 (4) | 0.065* | |
C4' | 0.6855 (5) | −0.06769 (15) | 1.2494 (5) | 0.0580 (10) | |
H4D | 0.714 (4) | −0.0938 (16) | 1.333 (4) | 0.070* | |
C5' | 0.9258 (5) | −0.00020 (18) | 1.3880 (4) | 0.0625 (11) | |
H5B | 0.970 (4) | −0.0336 (17) | 1.480 (4) | 0.075* | |
C6' | 1.0070 (5) | 0.0504 (2) | 1.3888 (5) | 0.0683 (12) | |
H6B | 1.114 (5) | 0.0600 (16) | 1.483 (4) | 0.082* | |
C7' | 0.9401 (5) | 0.08862 (19) | 1.2575 (5) | 0.0601 (10) | |
H7B | 1.003 (4) | 0.1274 (17) | 1.273 (4) | 0.072* | |
C8' | 0.7954 (5) | 0.07504 (16) | 1.1284 (4) | 0.0480 (9) | |
H8B | 0.753 (4) | 0.1001 (14) | 1.038 (4) | 0.058* | |
C9' | 0.7066 (4) | 0.02249 (13) | 1.1199 (3) | 0.0401 (7) | |
C10' | 0.7731 (4) | −0.01565 (15) | 1.2538 (4) | 0.0501 (9) | |
C11' | 0.4885 (4) | 0.04128 (15) | 0.8316 (4) | 0.0428 (8) | |
H11C | 0.369 (4) | 0.0387 (13) | 0.769 (3) | 0.051* | |
H11D | 0.514 (4) | 0.0833 (14) | 0.846 (3) | 0.051* | |
C12' | 0.8955 (4) | −0.00166 (15) | 0.8077 (4) | 0.0472 (9) | |
H12B | 0.851 (4) | −0.0226 (15) | 0.703 (4) | 0.057* | |
C13' | 0.9469 (5) | −0.04302 (17) | 0.9461 (4) | 0.0683 (11) | |
H13D | 0.8546 | −0.0675 | 0.9307 | 0.102* | |
H13E | 0.9830 | −0.0202 | 1.0415 | 0.102* | |
H13F | 1.0360 | −0.0678 | 0.9545 | 0.102* | |
C14' | 1.0271 (4) | 0.04136 (19) | 0.8246 (5) | 0.0753 (13) | |
H14D | 0.9811 | 0.0702 | 0.7410 | 0.113* | |
H14E | 1.1152 | 0.0203 | 0.8187 | 0.113* | |
H14F | 1.0696 | 0.0612 | 0.9251 | 0.113* | |
C15' | 0.5190 (4) | 0.05305 (17) | 0.4257 (4) | 0.0504 (9) | |
H15B | 0.591 (4) | 0.0156 (16) | 0.450 (3) | 0.061* | |
C16' | 0.5995 (6) | 0.10896 (19) | 0.4154 (5) | 0.0832 (13) | |
H16D | 0.7065 | 0.1124 | 0.5067 | 0.125* | |
H16E | 0.5322 | 0.1423 | 0.4116 | 0.125* | |
H16F | 0.6117 | 0.1084 | 0.3213 | 0.125* | |
C17' | 0.3609 (5) | 0.0393 (3) | 0.2821 (4) | 0.1032 (19) | |
H17D | 0.3190 | 0.0019 | 0.2960 | 0.155* | |
H17E | 0.3797 | 0.0371 | 0.1918 | 0.155* | |
H17F | 0.2817 | 0.0700 | 0.2656 | 0.155* |
U11 | U22 | U33 | U12 | U13 | U23 | |
P1 | 0.0398 (5) | 0.0371 (5) | 0.0376 (4) | 0.0010 (4) | 0.0225 (4) | −0.0007 (4) |
O1 | 0.0382 (13) | 0.0395 (12) | 0.0507 (12) | −0.0007 (10) | 0.0236 (11) | 0.0036 (10) |
O2 | 0.0520 (15) | 0.0602 (15) | 0.0349 (11) | −0.0159 (11) | 0.0256 (11) | −0.0099 (11) |
O3 | 0.0590 (15) | 0.0397 (13) | 0.0590 (13) | 0.0098 (11) | 0.0383 (12) | 0.0087 (11) |
O4 | 0.0582 (16) | 0.0465 (15) | 0.0632 (15) | 0.0094 (13) | 0.0331 (14) | 0.0029 (13) |
C1 | 0.048 (2) | 0.0382 (19) | 0.0422 (17) | −0.0066 (16) | 0.0315 (17) | −0.0040 (15) |
C2 | 0.057 (2) | 0.0370 (19) | 0.051 (2) | −0.0039 (17) | 0.0374 (19) | −0.0023 (17) |
C3 | 0.080 (3) | 0.045 (2) | 0.074 (3) | −0.002 (2) | 0.052 (3) | −0.008 (2) |
C4 | 0.092 (3) | 0.053 (2) | 0.054 (2) | −0.017 (2) | 0.041 (3) | −0.0183 (19) |
C5 | 0.076 (3) | 0.080 (4) | 0.051 (2) | −0.015 (3) | 0.030 (2) | −0.006 (2) |
C6 | 0.065 (3) | 0.102 (4) | 0.057 (3) | −0.002 (3) | 0.020 (2) | 0.010 (3) |
C7 | 0.065 (3) | 0.074 (3) | 0.060 (3) | 0.010 (2) | 0.031 (2) | 0.010 (2) |
C8 | 0.063 (3) | 0.048 (2) | 0.045 (2) | 0.0014 (19) | 0.030 (2) | 0.0043 (17) |
C9 | 0.053 (2) | 0.0389 (19) | 0.0372 (17) | −0.0082 (16) | 0.0308 (16) | −0.0022 (14) |
C10 | 0.061 (2) | 0.053 (2) | 0.0414 (19) | −0.0158 (18) | 0.0296 (19) | −0.0045 (17) |
C11 | 0.042 (2) | 0.0419 (19) | 0.0392 (18) | −0.0036 (16) | 0.0263 (17) | −0.0010 (15) |
C12 | 0.0376 (19) | 0.062 (3) | 0.0469 (19) | −0.0060 (16) | 0.0226 (16) | 0.0022 (17) |
C13 | 0.062 (3) | 0.064 (3) | 0.068 (2) | −0.018 (2) | 0.026 (2) | −0.015 (2) |
C14 | 0.049 (2) | 0.082 (3) | 0.095 (3) | 0.004 (2) | 0.039 (2) | −0.005 (2) |
C15 | 0.061 (2) | 0.059 (2) | 0.0376 (18) | −0.0126 (19) | 0.0316 (19) | −0.0053 (17) |
C16 | 0.119 (4) | 0.066 (3) | 0.075 (3) | −0.008 (3) | 0.072 (3) | −0.011 (2) |
C17 | 0.085 (4) | 0.165 (6) | 0.044 (2) | 0.007 (3) | 0.027 (3) | 0.012 (3) |
P1' | 0.0437 (5) | 0.0398 (5) | 0.0415 (4) | −0.0010 (4) | 0.0255 (4) | 0.0017 (4) |
O1' | 0.0352 (12) | 0.0419 (12) | 0.0526 (12) | 0.0021 (9) | 0.0233 (10) | −0.0016 (10) |
O2' | 0.0556 (15) | 0.0656 (15) | 0.0410 (12) | 0.0111 (12) | 0.0306 (12) | 0.0136 (11) |
O3' | 0.0686 (16) | 0.0409 (14) | 0.0655 (14) | −0.0110 (11) | 0.0444 (13) | −0.0085 (11) |
O4' | 0.0523 (15) | 0.0434 (14) | 0.0657 (15) | −0.0048 (12) | 0.0333 (13) | 0.0009 (12) |
C1' | 0.0452 (19) | 0.0345 (18) | 0.0428 (17) | 0.0045 (15) | 0.0311 (16) | 0.0001 (15) |
C2' | 0.050 (2) | 0.0414 (19) | 0.0447 (19) | 0.0017 (16) | 0.0311 (18) | −0.0013 (16) |
C3' | 0.075 (3) | 0.038 (2) | 0.058 (2) | −0.0026 (19) | 0.039 (2) | 0.0072 (18) |
C4' | 0.084 (3) | 0.041 (2) | 0.053 (2) | 0.006 (2) | 0.036 (2) | 0.0122 (18) |
C5' | 0.074 (3) | 0.067 (3) | 0.043 (2) | 0.011 (2) | 0.025 (2) | −0.0022 (19) |
C6' | 0.060 (3) | 0.086 (3) | 0.055 (3) | −0.007 (2) | 0.023 (2) | −0.024 (3) |
C7' | 0.069 (3) | 0.064 (3) | 0.059 (3) | −0.014 (2) | 0.039 (2) | −0.015 (2) |
C8' | 0.062 (3) | 0.047 (2) | 0.045 (2) | −0.0064 (19) | 0.033 (2) | −0.0046 (17) |
C9' | 0.054 (2) | 0.0360 (18) | 0.0415 (17) | 0.0021 (17) | 0.0322 (16) | −0.0039 (15) |
C10' | 0.064 (2) | 0.050 (2) | 0.0435 (19) | 0.0081 (19) | 0.0314 (19) | 0.0021 (17) |
C11' | 0.048 (2) | 0.0406 (19) | 0.046 (2) | 0.0042 (16) | 0.0274 (18) | 0.0064 (16) |
C12' | 0.053 (2) | 0.047 (2) | 0.050 (2) | 0.0112 (16) | 0.0307 (18) | −0.0005 (16) |
C13' | 0.071 (3) | 0.061 (3) | 0.072 (3) | 0.021 (2) | 0.034 (2) | 0.015 (2) |
C14' | 0.045 (2) | 0.092 (3) | 0.097 (3) | 0.011 (2) | 0.040 (2) | 0.017 (3) |
C15' | 0.056 (2) | 0.063 (2) | 0.0446 (19) | 0.0057 (19) | 0.0336 (19) | 0.0044 (17) |
C16' | 0.113 (4) | 0.079 (3) | 0.087 (3) | −0.011 (3) | 0.072 (3) | 0.006 (2) |
C17' | 0.079 (3) | 0.181 (6) | 0.046 (2) | −0.018 (3) | 0.026 (2) | −0.013 (3) |
P1—O3 | 1.463 (2) | P1'—O3' | 1.465 (2) |
P1—O2 | 1.570 (2) | P1'—O1' | 1.559 (2) |
P1—O1 | 1.573 (2) | P1'—O2' | 1.569 (2) |
P1—C11 | 1.798 (3) | P1'—C11' | 1.793 (3) |
O1—C12 | 1.463 (4) | O1'—C12' | 1.474 (4) |
O2—C15 | 1.479 (3) | O2'—C15' | 1.480 (3) |
O4—C2 | 1.351 (4) | O4'—C2' | 1.352 (4) |
O4—H4A | 0.80 (4) | O4'—H4C | 0.89 (4) |
C1—C2 | 1.366 (4) | C1'—C2' | 1.385 (4) |
C1—C9 | 1.424 (4) | C1'—C9' | 1.418 (4) |
C1—C11 | 1.515 (4) | C1'—C11' | 1.512 (4) |
C2—C3 | 1.418 (5) | C2'—C3' | 1.403 (4) |
C3—C4 | 1.350 (6) | C3'—C4' | 1.344 (5) |
C3—H3A | 0.87 (4) | C3'—H3B | 1.02 (3) |
C4—C10 | 1.409 (5) | C4'—C10' | 1.409 (5) |
C4—H4B | 0.91 (4) | C4'—H4D | 0.92 (4) |
C5—C6 | 1.342 (6) | C5'—C6' | 1.358 (5) |
C5—C10 | 1.403 (5) | C5'—C10' | 1.425 (5) |
C5—H5A | 0.91 (4) | C5'—H5B | 1.08 (4) |
C6—C7 | 1.409 (6) | C6'—C7' | 1.402 (5) |
C6—H6A | 0.97 (4) | C6'—H6B | 0.99 (4) |
C7—C8 | 1.344 (5) | C7'—C8' | 1.353 (5) |
C7—H7A | 0.94 (4) | C7'—H7B | 1.02 (4) |
C8—C9 | 1.416 (5) | C8'—C9' | 1.415 (5) |
C8—H8A | 0.90 (3) | C8'—H8B | 0.95 (3) |
C9—C10 | 1.419 (4) | C9'—C10' | 1.419 (4) |
C11—H11A | 1.04 (3) | C11'—H11C | 0.97 (3) |
C11—H11B | 0.93 (3) | C11'—H11D | 0.97 (3) |
C12—C14 | 1.498 (5) | C12'—C14' | 1.493 (5) |
C12—C13 | 1.507 (4) | C12'—C13' | 1.501 (5) |
C12—H12A | 0.98 (3) | C12'—H12B | 1.01 (3) |
C13—H13A | 0.9600 | C13'—H13D | 0.9600 |
C13—H13B | 0.9600 | C13'—H13E | 0.9600 |
C13—H13C | 0.9600 | C13'—H13F | 0.9600 |
C14—H14A | 0.9600 | C14'—H14D | 0.9600 |
C14—H14B | 0.9600 | C14'—H14E | 0.9600 |
C14—H14C | 0.9600 | C14'—H14F | 0.9600 |
C15—C16 | 1.488 (5) | C15'—C17' | 1.484 (5) |
C15—C17 | 1.489 (5) | C15'—C16' | 1.484 (5) |
C15—H15A | 1.07 (3) | C15'—H15B | 1.03 (3) |
C16—H16A | 0.9600 | C16'—H16D | 0.9600 |
C16—H16B | 0.9600 | C16'—H16E | 0.9600 |
C16—H16C | 0.9600 | C16'—H16F | 0.9600 |
C17—H17A | 0.9600 | C17'—H17D | 0.9600 |
C17—H17B | 0.9600 | C17'—H17E | 0.9600 |
C17—H17C | 0.9600 | C17'—H17F | 0.9600 |
O3—P1—O2 | 114.13 (12) | O3'—P1'—O1' | 113.07 (13) |
O3—P1—O1 | 112.83 (12) | O3'—P1'—O2' | 114.29 (13) |
O2—P1—O1 | 105.69 (12) | O1'—P1'—O2' | 105.75 (12) |
O3—P1—C11 | 116.80 (14) | O3'—P1'—C11' | 116.71 (15) |
O2—P1—C11 | 101.78 (13) | O1'—P1'—C11' | 104.21 (14) |
O1—P1—C11 | 104.28 (14) | O2'—P1'—C11' | 101.44 (14) |
C12—O1—P1 | 124.15 (19) | C12'—O1'—P1' | 125.27 (19) |
C15—O2—P1 | 118.8 (2) | C15'—O2'—P1' | 119.1 (2) |
C2—O4—H4A | 111 (3) | C2'—O4'—H4C | 109 (2) |
C2—C1—C9 | 120.2 (3) | C2'—C1'—C9' | 119.4 (3) |
C2—C1—C11 | 118.1 (3) | C2'—C1'—C11' | 118.3 (3) |
C9—C1—C11 | 121.7 (3) | C9'—C1'—C11' | 122.2 (3) |
O4—C2—C1 | 119.0 (3) | O4'—C2'—C1' | 118.1 (3) |
O4—C2—C3 | 120.8 (3) | O4'—C2'—C3' | 121.3 (3) |
C1—C2—C3 | 120.2 (3) | C1'—C2'—C3' | 120.6 (3) |
C4—C3—C2 | 120.3 (4) | C4'—C3'—C2' | 120.3 (3) |
C4—C3—H3A | 124 (3) | C4'—C3'—H3B | 120.7 (19) |
C2—C3—H3A | 115 (3) | C2'—C3'—H3B | 119.0 (19) |
C3—C4—C10 | 121.5 (4) | C3'—C4'—C10' | 121.7 (3) |
C3—C4—H4B | 120 (2) | C3'—C4'—H4D | 113 (2) |
C10—C4—H4B | 118 (2) | C10'—C4'—H4D | 125 (2) |
C6—C5—C10 | 122.0 (4) | C6'—C5'—C10' | 120.8 (4) |
C6—C5—H5A | 128 (3) | C6'—C5'—H5B | 125.9 (19) |
C10—C5—H5A | 110 (2) | C10'—C5'—H5B | 113.2 (19) |
C5—C6—C7 | 119.1 (4) | C5'—C6'—C7' | 120.1 (4) |
C5—C6—H6A | 127 (2) | C5'—C6'—H6B | 119 (2) |
C7—C6—H6A | 114 (2) | C7'—C6'—H6B | 120 (2) |
C8—C7—C6 | 120.8 (4) | C8'—C7'—C6' | 120.4 (4) |
C8—C7—H7A | 120 (2) | C8'—C7'—H7B | 125 (2) |
C6—C7—H7A | 119 (2) | C6'—C7'—H7B | 115 (2) |
C7—C8—C9 | 121.6 (4) | C7'—C8'—C9' | 122.0 (4) |
C7—C8—H8A | 122 (2) | C7'—C8'—H8B | 120 (2) |
C9—C8—H8A | 116 (2) | C9'—C8'—H8B | 118 (2) |
C8—C9—C10 | 117.2 (3) | C8'—C9'—C10' | 117.6 (3) |
C8—C9—C1 | 123.7 (3) | C8'—C9'—C1' | 123.2 (3) |
C10—C9—C1 | 119.1 (3) | C10'—C9'—C1' | 119.2 (3) |
C4—C10—C5 | 122.2 (4) | C4'—C10'—C9' | 118.7 (3) |
C4—C10—C9 | 118.6 (3) | C4'—C10'—C5' | 122.2 (3) |
C5—C10—C9 | 119.2 (3) | C9'—C10'—C5' | 119.2 (3) |
C1—C11—P1 | 110.9 (2) | C1'—C11'—P1' | 111.3 (2) |
C1—C11—H11A | 111.5 (16) | C1'—C11'—H11C | 113.8 (18) |
P1—C11—H11A | 105.6 (16) | P1'—C11'—H11C | 105.6 (18) |
C1—C11—H11B | 108.4 (18) | C1'—C11'—H11D | 114.3 (18) |
P1—C11—H11B | 103.9 (17) | P1'—C11'—H11D | 104.9 (18) |
H11A—C11—H11B | 116 (2) | H11C—C11'—H11D | 106 (3) |
O1—C12—C14 | 105.0 (3) | O1'—C12'—C14' | 105.7 (3) |
O1—C12—C13 | 109.8 (3) | O1'—C12'—C13' | 109.3 (3) |
C14—C12—C13 | 113.1 (3) | C14'—C12'—C13' | 113.9 (3) |
O1—C12—H12A | 109.6 (18) | O1'—C12'—H12B | 103.6 (18) |
C14—C12—H12A | 111.9 (18) | C14'—C12'—H12B | 109.8 (18) |
C13—C12—H12A | 107.4 (19) | C13'—C12'—H12B | 113.7 (19) |
C12—C13—H13A | 109.5 | C12'—C13'—H13D | 109.5 |
C12—C13—H13B | 109.5 | C12'—C13'—H13E | 109.5 |
H13A—C13—H13B | 109.5 | H13D—C13'—H13E | 109.5 |
C12—C13—H13C | 109.5 | C12'—C13'—H13F | 109.5 |
H13A—C13—H13C | 109.5 | H13D—C13'—H13F | 109.5 |
H13B—C13—H13C | 109.5 | H13E—C13'—H13F | 109.5 |
C12—C14—H14A | 109.5 | C12'—C14'—H14D | 109.5 |
C12—C14—H14B | 109.5 | C12'—C14'—H14E | 109.5 |
H14A—C14—H14B | 109.5 | H14D—C14'—H14E | 109.5 |
C12—C14—H14C | 109.5 | C12'—C14'—H14F | 109.5 |
H14A—C14—H14C | 109.5 | H14D—C14'—H14F | 109.5 |
H14B—C14—H14C | 109.5 | H14E—C14'—H14F | 109.5 |
O2—C15—C16 | 108.3 (3) | O2'—C15'—C17' | 107.4 (3) |
O2—C15—C17 | 107.5 (3) | O2'—C15'—C16' | 108.0 (3) |
C16—C15—C17 | 114.3 (3) | C17'—C15'—C16' | 114.4 (4) |
O2—C15—H15A | 111.0 (16) | O2'—C15'—H15B | 105.1 (18) |
C16—C15—H15A | 106.4 (17) | C17'—C15'—H15B | 106.1 (17) |
C17—C15—H15A | 109.5 (17) | C16'—C15'—H15B | 115.1 (18) |
C15—C16—H16A | 109.5 | C15'—C16'—H16D | 109.5 |
C15—C16—H16B | 109.5 | C15'—C16'—H16E | 109.5 |
H16A—C16—H16B | 109.5 | H16D—C16'—H16E | 109.5 |
C15—C16—H16C | 109.5 | C15'—C16'—H16F | 109.5 |
H16A—C16—H16C | 109.5 | H16D—C16'—H16F | 109.5 |
H16B—C16—H16C | 109.5 | H16E—C16'—H16F | 109.5 |
C15—C17—H17A | 109.5 | C15'—C17'—H17D | 109.5 |
C15—C17—H17B | 109.5 | C15'—C17'—H17E | 109.5 |
H17A—C17—H17B | 109.5 | H17D—C17'—H17E | 109.5 |
C15—C17—H17C | 109.5 | C15'—C17'—H17F | 109.5 |
H17A—C17—H17C | 109.5 | H17D—C17'—H17F | 109.5 |
H17B—C17—H17C | 109.5 | H17E—C17'—H17F | 109.5 |
O3—P1—O1—C12 | −10.2 (3) | O3'—P1'—O1'—C12' | 10.5 (3) |
O2—P1—O1—C12 | 115.2 (2) | O2'—P1'—O1'—C12' | −115.2 (2) |
C11—P1—O1—C12 | −137.9 (2) | C11'—P1'—O1'—C12' | 138.3 (2) |
O3—P1—O2—C15 | 53.5 (3) | O3'—P1'—O2'—C15' | −54.7 (3) |
O1—P1—O2—C15 | −71.1 (2) | O1'—P1'—O2'—C15' | 70.4 (2) |
C11—P1—O2—C15 | −179.8 (2) | C11'—P1'—O2'—C15' | 178.9 (2) |
C9—C1—C2—O4 | −177.3 (3) | C9'—C1'—C2'—O4' | 177.3 (2) |
C11—C1—C2—O4 | 6.2 (4) | C11'—C1'—C2'—O4' | −4.9 (4) |
C9—C1—C2—C3 | 2.9 (4) | C9'—C1'—C2'—C3' | −2.3 (4) |
C11—C1—C2—C3 | −173.7 (3) | C11'—C1'—C2'—C3' | 175.4 (3) |
O4—C2—C3—C4 | 179.2 (3) | O4'—C2'—C3'—C4' | −179.8 (3) |
C1—C2—C3—C4 | −0.9 (5) | C1'—C2'—C3'—C4' | −0.2 (5) |
C2—C3—C4—C10 | −1.0 (6) | C2'—C3'—C4'—C10' | 1.3 (5) |
C10—C5—C6—C7 | −0.5 (7) | C10'—C5'—C6'—C7' | 0.8 (6) |
C5—C6—C7—C8 | 1.2 (7) | C5'—C6'—C7'—C8' | −0.9 (6) |
C6—C7—C8—C9 | −0.4 (6) | C6'—C7'—C8'—C9' | −0.1 (6) |
C7—C8—C9—C10 | −1.0 (5) | C7'—C8'—C9'—C10' | 1.0 (5) |
C7—C8—C9—C1 | 179.5 (3) | C7'—C8'—C9'—C1' | −177.6 (3) |
C2—C1—C9—C8 | 176.5 (3) | C2'—C1'—C9'—C8' | −177.9 (3) |
C11—C1—C9—C8 | −7.1 (4) | C11'—C1'—C9'—C8' | 4.5 (4) |
C2—C1—C9—C10 | −2.9 (4) | C2'—C1'—C9'—C10' | 3.6 (4) |
C11—C1—C9—C10 | 173.5 (3) | C11'—C1'—C9'—C10' | −174.0 (3) |
C3—C4—C10—C5 | −179.3 (3) | C3'—C4'—C10'—C9' | 0.1 (5) |
C3—C4—C10—C9 | 0.9 (5) | C3'—C4'—C10'—C5' | 180.0 (3) |
C6—C5—C10—C4 | 179.1 (4) | C8'—C9'—C10'—C4' | 178.9 (3) |
C6—C5—C10—C9 | −1.0 (6) | C1'—C9'—C10'—C4' | −2.5 (4) |
C8—C9—C10—C4 | −178.4 (3) | C8'—C9'—C10'—C5' | −1.1 (4) |
C1—C9—C10—C4 | 1.1 (4) | C1'—C9'—C10'—C5' | 177.6 (3) |
C8—C9—C10—C5 | 1.7 (4) | C6'—C5'—C10'—C4' | −179.7 (4) |
C1—C9—C10—C5 | −178.8 (3) | C6'—C5'—C10'—C9' | 0.2 (5) |
C2—C1—C11—P1 | 88.2 (3) | C2'—C1'—C11'—P1' | −88.6 (3) |
C9—C1—C11—P1 | −88.3 (3) | C9'—C1'—C11'—P1' | 89.0 (3) |
O3—P1—C11—C1 | −53.6 (3) | O3'—P1'—C11'—C1' | 55.7 (3) |
O2—P1—C11—C1 | −178.6 (2) | O1'—P1'—C11'—C1' | −69.7 (3) |
O1—P1—C11—C1 | 71.7 (3) | O2'—P1'—C11'—C1' | −179.4 (2) |
P1—O1—C12—C14 | −157.4 (2) | P1'—O1'—C12'—C14' | 153.4 (2) |
P1—O1—C12—C13 | 80.7 (3) | P1'—O1'—C12'—C13' | −83.6 (3) |
P1—O2—C15—C16 | 110.5 (3) | P1'—O2'—C15'—C17' | 119.7 (3) |
P1—O2—C15—C17 | −125.6 (3) | P1'—O2'—C15'—C16' | −116.4 (3) |
D—H···A | D—H | H···A | D···A | D—H···A |
O4—H4A···O3′i | 0.80 (4) | 1.88 (4) | 2.683 (3) | 178 (4) |
O4′—H4C···O3ii | 0.89 (4) | 1.80 (4) | 2.669 (3) | 166 (3) |
C3′—H3B···O3ii | 1.02 (3) | 2.59 (3) | 3.318 (5) | 128 (2) |
Symmetry codes: (i) −x+1, y+1/2, −z+1; (ii) −x+1, y−1/2, −z+1. |
Experimental details
Crystal data | |
Chemical formula | C17H23PO4 |
Mr | 322.32 |
Crystal system, space group | Monoclinic, P21 |
Temperature (K) | 293 |
a, b, c (Å) | 9.166 (1), 22.484 (2), 9.579 (1) |
β (°) | 118.21 (1) |
V (Å3) | 1739.7 (3) |
Z | 4 |
Radiation type | Mo Kα |
µ (mm−1) | 0.17 |
Crystal size (mm) | 0.2 × 0.15 × 0.1 |
Data collection | |
Diffractometer | Xcalibur diffractometer |
Absorption correction | Multi-scan (SADABS; Sheldrick, 1996) |
Tmin, Tmax | 0.966, 0.979 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 10929, 6056, 4614 |
Rint | 0.029 |
(sin θ/λ)max (Å−1) | 0.594 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.043, 0.084, 1.00 |
No. of reflections | 6056 |
No. of parameters | 463 |
No. of restraints | 1 |
H-atom treatment | H atoms treated by a mixture of independent and constrained refinement |
Δρmax, Δρmin (e Å−3) | 0.15, −0.21 |
Absolute structure | Flack H D (1983), Acta Cryst. A39, 876-881 |
Absolute structure parameter | 0.00 (8) |
Computer programs: CrysAlis CCD (Oxford Diffraction, 2002), CrysAlis RED (Oxford Diffraction, 2002), CrysAlis RED, SHELXS97 (Sheldrick, 1997), SHELXL97 (Sheldrick, 1997), SHELXTL (Sheldrick, 1990), SHELXL9.
C1—C2 | 1.366 (4) | C1'—C2' | 1.385 (4) |
C2—C3 | 1.418 (5) | C2'—C3' | 1.403 (4) |
C14—C12—C13 | 113.1 (3) | C14'—C12'—C13' | 113.9 (3) |
C9—C1—C2—O4 | −177.3 (3) | C9'—C1'—C2'—O4' | 177.3 (2) |
C2—C1—C11—P1 | 88.2 (3) | C2'—C1'—C11'—P1' | −88.6 (3) |
O2—P1—C11—C1 | −178.6 (2) | O2'—P1'—C11'—C1' | −179.4 (2) |
D—H···A | D—H | H···A | D···A | D—H···A |
O4—H4A···O3'i | 0.80 (4) | 1.88 (4) | 2.683 (3) | 178 (4) |
O4'—H4C···O3ii | 0.89 (4) | 1.80 (4) | 2.669 (3) | 166 (3) |
C3'—H3B···O3ii | 1.02 (3) | 2.59 (3) | 3.318 (5) | 128 (2) |
Symmetry codes: (i) −x+1, y+1/2, −z+1; (ii) −x+1, y−1/2, −z+1. |
Phosphorus derivatives are an important class of biologically active compounds (Kabacnik, 1987). The reaction of the phenolic Mannich base with trialcoxyphosphites leads to methylen-phosphorous derivatives of phenols (Ivanov & Valitova, 1967; Hahn & Weglewski, 1968; Rupp & Heiner, 1982). In our investigations, we used a β-naphthol derivative of L-proline, (I), and triisopropyl phosphite. In this paper, we present X-ray crystallographic analysis of the title compound, (II).
The presence of a stereogenic centre in derivative (I) creates the possibility of stereoselective synthesis of chiral phosphorous derivatives; this is still under the investigation.
The title compound crystallizes in the space group P21, with two nearly centrosymmetrically related molecules. The two independent conformers, A and B, are shown in Fig. 1. In conformer A, the dihedral angle between planes C2–C1–C11 and C1–C11–P1 is 88.2 (3)°, while in the conformer B it is −88.6 (3)°. This corresponds with the twist of the —CPO(OC3H7)2 and hydroxynaphthyl groups of 176.8 (3)° between the two conformers. Analysis of the structure does not reveal significant differences in the bond distances and angles of the two molecules in the asymmetric unit. The most significant deviations in bond lengths between the two conformers are 0.026 (4) and 0.023 (5) Å for C1–C2 and C2–C3, respectively. The 2-hydroxynaphthyl group is nearly planar. The torsion angles which most deviate from 0° or 180° are C9—C1—C2—O4 [−177.3 (3)°] and C9'-C1'-C2'-O4' [177.3 (2)°] (Table 1.). The bond lengths and angles in the structure are in accordance with anticipated values (Tahar et al., 1996; Langley et al. 1996). In these compounds, there is a characteristic pattern of torsion angles and of the orientation of the C and P tetrahedra (Ružić-Toroš & Kojić-Prodić, 1978). The aromatic system and O2(') are anti to each other [O2–P1–C11–C1 = 178.6 (2) and O2'–P1'–C11'–C1' = 179.4 (2)°], while the P—C bond is perpendicular to the plane of hydroxynaphthyl group in both conformers (Benedetto et al., 1997). No H atoms were located in the region of O3 or O3'. In the crystal structure, conformers A and B are linked by O–H···O=P hydrogen bonds, leading to dimerization (Figure 2.). Those dimers are joined by weak C—H···O hydrogen bonds (Table 2.).