Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807032527/bh2120sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536807032527/bh2120Isup2.hkl |
CCDC reference: 657721
The compound was prepared according to the procedure described by Pisareva et al. (2005) and recrystallized from dichloroethane.
The H atoms of the organic molecule were refined in idealized geometrical positions with displacement parameters being equal to 1.2 (CH2 groups and phenyl rings) or 1.5 (CH3 groups) times Ueq of the attached C atoms. The H atoms of the water molecule were located in a difference map and refined with individual isotropic displacement parameters and free coordinates.
Organophosphorus ligands with three phosphoryl groups are considered as promising agents to ensure selectivity of separation of metal mixtures by extraction (Pisareva et al., 2005).
The arrangement of phosphoryl groups and phenyl rings in the title compound, (I, Fig. 1), is far from a threefold symmetry. Selected bond lengths and angles in (I) are given in Table 1. The P═O distances range from 1.4899 (12) to 1.4927 (12) Å. The O═P—C angles with C atoms of CH2 groups differ significantly from ideal tetrahedral values, the maximum value being 117.08 (7)° (Table 1). The C—C—C angles around the central atom C1 vary from 107.92 (12) to 111.91 (12)°.
The same behaviour of the O═P—C angles can be found in Ln nitrate complexes with CH3C[CH2P(O)Ph2] (Lees & Platt, 2005). The P═O distances in these complexes are slightly longer due to coordination of phosphoryl groups to Ln atoms [from 1.499 (3) to 1.510 (3) Å]. Apparent P═ O distances in partially oxygenated C2H5C(CH2PPh2)3 (Chekhlov, 2000) are significantly shorter, due to a statistical character of the structure.
In (I), the hydrogen bonds in which water molecules act as proton donors (Table 2, Fig. 2) link organic molecules into chains along the [100] direction.
The synthesis of the title compound was described by Pisareva et al. (2005). A structure of a solid solution of C2H5C(CH2PPh2)3 and its partially oxygenated derivatives was described by Chekhlov (2000). Lees & Platt (2005) describe the structure of La and Pr nitrate complexes with CH3C[CH2P(O)Ph2], in which tridentate organic ligands are linked by phosphoryl O atoms to two Ln atoms, to one atom in a bidentate-chelating way and to the other in a monodentate way.
Data collection: SMART (Bruker, 1998); cell refinement: SAINT-Plus (Bruker, 1998); data reduction: SAINT-Plus; program(s) used to solve structure: SHELXS97 (Sheldrick, 1997a); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997a); molecular graphics: SHELXTL (Sheldrick, 1997b); software used to prepare material for publication: SHELXTL.
C42H41O3P3·H2O | F(000) = 744 |
Mr = 704.67 | Dx = 1.305 Mg m−3 |
Monoclinic, Pc | Mo Kα radiation, λ = 0.71073 Å |
Hall symbol: P -2yc | Cell parameters from 5344 reflections |
a = 9.5303 (2) Å | θ = 2.1–30.0° |
b = 10.4028 (2) Å | µ = 0.21 mm−1 |
c = 18.0951 (4) Å | T = 100 K |
β = 90.1433 (14)° | Fragment, colourless |
V = 1793.98 (6) Å3 | 0.18 × 0.16 × 0.10 mm |
Z = 2 |
Bruker Kappa APEX II area-detector diffractometer | 8909 reflections with I > 2σ(I) |
Radiation source: fine-focus sealed tube | Rint = 0.059 |
Graphite monochromator | θmax = 30.0°, θmin = 2.1° |
ω and φ scans | h = −13→13 |
41040 measured reflections | k = −14→14 |
10441 independent reflections | l = −25→25 |
Refinement on F2 | Secondary atom site location: difference Fourier map |
Least-squares matrix: full | Hydrogen site location: mixed |
R[F2 > 2σ(F2)] = 0.035 | H atoms treated by a mixture of independent and constrained refinement |
wR(F2) = 0.068 | w = 1/[σ2(Fo2) + (0.0298P)2] where P = (Fo2 + 2Fc2)/3 |
S = 0.95 | (Δ/σ)max = 0.001 |
10441 reflections | Δρmax = 0.29 e Å−3 |
450 parameters | Δρmin = −0.26 e Å−3 |
2 restraints | Absolute structure: Flack (1983), 5207 Friedel pairs |
Primary atom site location: structure-invariant direct methods | Absolute structure parameter: −0.04 (4) |
C42H41O3P3·H2O | V = 1793.98 (6) Å3 |
Mr = 704.67 | Z = 2 |
Monoclinic, Pc | Mo Kα radiation |
a = 9.5303 (2) Å | µ = 0.21 mm−1 |
b = 10.4028 (2) Å | T = 100 K |
c = 18.0951 (4) Å | 0.18 × 0.16 × 0.10 mm |
β = 90.1433 (14)° |
Bruker Kappa APEX II area-detector diffractometer | 8909 reflections with I > 2σ(I) |
41040 measured reflections | Rint = 0.059 |
10441 independent reflections |
R[F2 > 2σ(F2)] = 0.035 | H atoms treated by a mixture of independent and constrained refinement |
wR(F2) = 0.068 | Δρmax = 0.29 e Å−3 |
S = 0.95 | Δρmin = −0.26 e Å−3 |
10441 reflections | Absolute structure: Flack (1983), 5207 Friedel pairs |
450 parameters | Absolute structure parameter: −0.04 (4) |
2 restraints |
x | y | z | Uiso*/Ueq | ||
P1 | 0.36674 (4) | 0.40193 (4) | 0.75195 (2) | 0.01293 (9) | |
P2 | 0.62248 (4) | 0.41286 (4) | 0.92906 (2) | 0.01280 (8) | |
P3 | 0.76944 (4) | 0.11940 (4) | 0.72480 (2) | 0.01326 (8) | |
O1 | 0.33318 (11) | 0.30643 (11) | 0.81087 (6) | 0.0176 (2) | |
O2 | 0.53020 (11) | 0.52545 (11) | 0.91384 (6) | 0.0173 (2) | |
O3 | 0.90964 (12) | 0.12698 (12) | 0.76149 (6) | 0.0211 (3) | |
O4 | 0.11458 (18) | 0.14636 (18) | 0.87526 (9) | 0.0428 (4) | |
H4C | 0.172 (3) | 0.187 (2) | 0.8590 (13) | 0.040 (7)* | |
H4D | 0.049 (3) | 0.140 (2) | 0.8426 (15) | 0.059 (8)* | |
C1 | 0.66847 (15) | 0.37270 (15) | 0.77288 (8) | 0.0128 (3) | |
C2 | 0.54549 (15) | 0.46501 (15) | 0.75384 (8) | 0.0127 (3) | |
H2A | 0.5649 | 0.5027 | 0.7047 | 0.015* | |
H2B | 0.5478 | 0.5364 | 0.7900 | 0.015* | |
C3 | 0.64933 (16) | 0.30879 (15) | 0.84973 (8) | 0.0127 (3) | |
H3A | 0.7333 | 0.2555 | 0.8597 | 0.015* | |
H3B | 0.5681 | 0.2497 | 0.8465 | 0.015* | |
C4 | 0.67527 (16) | 0.26866 (15) | 0.71198 (8) | 0.0138 (3) | |
H4A | 0.7151 | 0.3103 | 0.6675 | 0.017* | |
H4B | 0.5772 | 0.2456 | 0.6996 | 0.017* | |
C5 | 0.80796 (16) | 0.44960 (16) | 0.77433 (9) | 0.0152 (3) | |
H5A | 0.8074 | 0.5055 | 0.8186 | 0.018* | |
H5B | 0.8860 | 0.3877 | 0.7804 | 0.018* | |
C6 | 0.83946 (18) | 0.53319 (17) | 0.70727 (9) | 0.0214 (4) | |
H6A | 0.9297 | 0.5768 | 0.7144 | 0.032* | |
H6B | 0.7651 | 0.5974 | 0.7013 | 0.032* | |
H6C | 0.8439 | 0.4792 | 0.6630 | 0.032* | |
C11 | 0.33661 (16) | 0.33075 (16) | 0.66157 (8) | 0.0137 (3) | |
C12 | 0.40089 (16) | 0.37265 (16) | 0.59636 (9) | 0.0169 (3) | |
H12 | 0.4595 | 0.4465 | 0.5971 | 0.020* | |
C13 | 0.37941 (17) | 0.30679 (17) | 0.53082 (9) | 0.0195 (3) | |
H13 | 0.4229 | 0.3359 | 0.4867 | 0.023* | |
C14 | 0.29503 (17) | 0.19891 (17) | 0.52929 (9) | 0.0202 (4) | |
H14 | 0.2823 | 0.1528 | 0.4845 | 0.024* | |
C15 | 0.22902 (18) | 0.15812 (17) | 0.59328 (9) | 0.0216 (4) | |
H15 | 0.1695 | 0.0849 | 0.5919 | 0.026* | |
C16 | 0.24919 (17) | 0.22344 (17) | 0.65929 (9) | 0.0179 (3) | |
H16 | 0.2034 | 0.1950 | 0.7029 | 0.021* | |
C21 | 0.25877 (16) | 0.54402 (16) | 0.75900 (9) | 0.0169 (3) | |
C22 | 0.19743 (17) | 0.57038 (19) | 0.82698 (10) | 0.0232 (4) | |
H22 | 0.2074 | 0.5112 | 0.8666 | 0.028* | |
C23 | 0.12141 (18) | 0.6833 (2) | 0.83705 (11) | 0.0307 (5) | |
H23 | 0.0801 | 0.7014 | 0.8836 | 0.037* | |
C24 | 0.10612 (18) | 0.76866 (19) | 0.77967 (12) | 0.0297 (4) | |
H24 | 0.0555 | 0.8463 | 0.7868 | 0.036* | |
C25 | 0.16454 (18) | 0.74143 (19) | 0.71131 (11) | 0.0270 (4) | |
H25 | 0.1523 | 0.7999 | 0.6715 | 0.032* | |
C26 | 0.24067 (17) | 0.62945 (17) | 0.70078 (10) | 0.0211 (4) | |
H26 | 0.2804 | 0.6112 | 0.6538 | 0.025* | |
C31 | 0.55012 (16) | 0.30556 (16) | 0.99754 (8) | 0.0154 (3) | |
C32 | 0.42571 (17) | 0.24121 (17) | 0.98061 (9) | 0.0192 (3) | |
H32 | 0.3829 | 0.2532 | 0.9336 | 0.023* | |
C33 | 0.36416 (18) | 0.16000 (17) | 1.03175 (9) | 0.0218 (4) | |
H33 | 0.2799 | 0.1158 | 1.0197 | 0.026* | |
C34 | 0.42611 (18) | 0.14341 (17) | 1.10081 (9) | 0.0206 (4) | |
H34 | 0.3849 | 0.0866 | 1.1356 | 0.025* | |
C35 | 0.54691 (17) | 0.20900 (17) | 1.11887 (9) | 0.0190 (3) | |
H35 | 0.5871 | 0.1993 | 1.1667 | 0.023* | |
C36 | 0.61033 (17) | 0.28930 (17) | 1.06753 (9) | 0.0179 (3) | |
H36 | 0.6946 | 0.3332 | 1.0799 | 0.022* | |
C41 | 0.79016 (16) | 0.46439 (16) | 0.96587 (8) | 0.0159 (3) | |
C42 | 0.79740 (17) | 0.58912 (17) | 0.99403 (9) | 0.0189 (3) | |
H42 | 0.7180 | 0.6441 | 0.9909 | 0.023* | |
C43 | 0.92054 (19) | 0.63294 (18) | 1.02658 (10) | 0.0241 (4) | |
H43 | 0.9257 | 0.7178 | 1.0458 | 0.029* | |
C44 | 1.03596 (19) | 0.55195 (19) | 1.03080 (10) | 0.0258 (4) | |
H44 | 1.1198 | 0.5814 | 1.0538 | 0.031* | |
C45 | 1.03050 (18) | 0.42938 (19) | 1.00206 (10) | 0.0253 (4) | |
H45 | 1.1105 | 0.3750 | 1.0048 | 0.030* | |
C46 | 0.90713 (17) | 0.38523 (17) | 0.96887 (9) | 0.0210 (4) | |
H46 | 0.9033 | 0.3012 | 0.9484 | 0.025* | |
C51 | 0.78361 (16) | 0.05900 (15) | 0.63142 (9) | 0.0146 (3) | |
C52 | 0.90304 (17) | −0.01057 (17) | 0.61250 (10) | 0.0215 (4) | |
H52 | 0.9718 | −0.0288 | 0.6491 | 0.026* | |
C53 | 0.92244 (19) | −0.05350 (19) | 0.54055 (11) | 0.0275 (4) | |
H53 | 1.0043 | −0.1009 | 0.5281 | 0.033* | |
C54 | 0.82304 (19) | −0.02736 (18) | 0.48714 (10) | 0.0249 (4) | |
H54 | 0.8379 | −0.0545 | 0.4376 | 0.030* | |
C55 | 0.70208 (19) | 0.03810 (17) | 0.50538 (10) | 0.0225 (4) | |
H55 | 0.6325 | 0.0538 | 0.4688 | 0.027* | |
C56 | 0.68198 (17) | 0.08104 (16) | 0.57717 (9) | 0.0188 (3) | |
H56 | 0.5984 | 0.1258 | 0.5895 | 0.023* | |
C61 | 0.65514 (16) | 0.00712 (15) | 0.77204 (8) | 0.0137 (3) | |
C62 | 0.71799 (17) | −0.10455 (16) | 0.79916 (9) | 0.0181 (3) | |
H62 | 0.8166 | −0.1155 | 0.7952 | 0.022* | |
C63 | 0.63681 (19) | −0.19994 (17) | 0.83196 (9) | 0.0213 (4) | |
H63 | 0.6800 | −0.2764 | 0.8496 | 0.026* | |
C64 | 0.4936 (2) | −0.18373 (15) | 0.83895 (10) | 0.0213 (3) | |
H64 | 0.4383 | −0.2491 | 0.8612 | 0.026* | |
C65 | 0.43039 (18) | −0.07184 (17) | 0.81350 (9) | 0.0212 (4) | |
H65 | 0.3322 | −0.0598 | 0.8193 | 0.025* | |
C66 | 0.51071 (16) | 0.02237 (16) | 0.77960 (9) | 0.0168 (3) | |
H66 | 0.4668 | 0.0980 | 0.7614 | 0.020* |
U11 | U22 | U33 | U12 | U13 | U23 | |
P1 | 0.01193 (19) | 0.0149 (2) | 0.01195 (19) | −0.00107 (16) | −0.00066 (14) | 0.00143 (16) |
P2 | 0.01457 (19) | 0.0123 (2) | 0.01157 (19) | 0.00009 (16) | −0.00123 (14) | −0.00020 (16) |
P3 | 0.01216 (18) | 0.0129 (2) | 0.01469 (19) | −0.00004 (15) | −0.00148 (14) | −0.00014 (16) |
O1 | 0.0176 (6) | 0.0211 (7) | 0.0140 (5) | −0.0026 (5) | −0.0015 (4) | 0.0043 (5) |
O2 | 0.0202 (6) | 0.0154 (6) | 0.0164 (6) | 0.0038 (5) | −0.0008 (4) | 0.0006 (4) |
O3 | 0.0153 (5) | 0.0230 (7) | 0.0251 (6) | −0.0006 (5) | −0.0064 (5) | −0.0005 (5) |
O4 | 0.0309 (8) | 0.0641 (12) | 0.0334 (9) | −0.0231 (8) | −0.0093 (7) | 0.0192 (8) |
C1 | 0.0133 (7) | 0.0118 (8) | 0.0133 (7) | −0.0010 (6) | −0.0012 (5) | 0.0013 (6) |
C2 | 0.0129 (7) | 0.0130 (8) | 0.0121 (7) | −0.0026 (6) | −0.0013 (5) | 0.0011 (6) |
C3 | 0.0136 (7) | 0.0121 (8) | 0.0125 (7) | −0.0006 (6) | −0.0020 (5) | 0.0000 (6) |
C4 | 0.0139 (7) | 0.0141 (8) | 0.0135 (7) | −0.0015 (6) | −0.0002 (6) | 0.0003 (6) |
C5 | 0.0142 (7) | 0.0143 (8) | 0.0170 (8) | −0.0022 (6) | −0.0004 (6) | 0.0005 (6) |
C6 | 0.0200 (8) | 0.0240 (9) | 0.0203 (8) | −0.0091 (7) | 0.0018 (6) | 0.0010 (7) |
C11 | 0.0121 (7) | 0.0160 (8) | 0.0130 (7) | 0.0023 (6) | −0.0015 (5) | 0.0007 (6) |
C12 | 0.0147 (7) | 0.0167 (9) | 0.0194 (8) | −0.0008 (6) | −0.0026 (6) | 0.0032 (7) |
C13 | 0.0189 (8) | 0.0239 (9) | 0.0155 (8) | 0.0004 (7) | 0.0016 (6) | 0.0006 (7) |
C14 | 0.0213 (8) | 0.0234 (9) | 0.0159 (8) | 0.0010 (7) | −0.0034 (6) | −0.0029 (7) |
C15 | 0.0227 (9) | 0.0188 (9) | 0.0232 (9) | −0.0069 (7) | −0.0022 (7) | 0.0002 (7) |
C16 | 0.0172 (8) | 0.0189 (9) | 0.0176 (8) | −0.0031 (7) | −0.0008 (6) | 0.0032 (6) |
C21 | 0.0118 (7) | 0.0166 (8) | 0.0224 (8) | −0.0008 (6) | −0.0026 (6) | −0.0008 (7) |
C22 | 0.0184 (8) | 0.0286 (10) | 0.0227 (9) | 0.0035 (7) | 0.0008 (7) | −0.0013 (7) |
C23 | 0.0200 (9) | 0.0376 (12) | 0.0344 (11) | 0.0041 (8) | 0.0027 (8) | −0.0157 (9) |
C24 | 0.0133 (8) | 0.0234 (10) | 0.0523 (13) | 0.0019 (7) | 0.0007 (8) | −0.0078 (9) |
C25 | 0.0173 (8) | 0.0216 (10) | 0.0420 (11) | 0.0020 (7) | 0.0023 (8) | 0.0046 (8) |
C26 | 0.0151 (8) | 0.0224 (9) | 0.0258 (9) | 0.0008 (7) | 0.0022 (6) | 0.0030 (7) |
C31 | 0.0174 (8) | 0.0151 (8) | 0.0138 (8) | 0.0022 (6) | 0.0002 (6) | 0.0005 (6) |
C32 | 0.0180 (8) | 0.0259 (10) | 0.0137 (8) | 0.0004 (7) | −0.0014 (6) | 0.0025 (7) |
C33 | 0.0184 (8) | 0.0250 (10) | 0.0221 (9) | −0.0032 (7) | 0.0020 (7) | 0.0042 (7) |
C34 | 0.0232 (9) | 0.0207 (9) | 0.0180 (8) | 0.0023 (7) | 0.0054 (7) | 0.0047 (7) |
C35 | 0.0274 (9) | 0.0179 (9) | 0.0119 (7) | 0.0045 (7) | −0.0013 (6) | 0.0016 (6) |
C36 | 0.0226 (8) | 0.0165 (9) | 0.0147 (8) | 0.0014 (7) | −0.0024 (6) | −0.0022 (6) |
C41 | 0.0180 (8) | 0.0183 (9) | 0.0115 (7) | −0.0042 (6) | −0.0018 (6) | 0.0017 (6) |
C42 | 0.0212 (8) | 0.0194 (9) | 0.0161 (8) | −0.0035 (7) | −0.0012 (6) | −0.0010 (7) |
C43 | 0.0265 (9) | 0.0232 (10) | 0.0227 (9) | −0.0104 (7) | −0.0010 (7) | −0.0047 (7) |
C44 | 0.0230 (9) | 0.0327 (11) | 0.0216 (9) | −0.0121 (8) | −0.0053 (7) | 0.0020 (8) |
C45 | 0.0188 (8) | 0.0296 (11) | 0.0275 (10) | 0.0002 (7) | −0.0038 (7) | 0.0047 (8) |
C46 | 0.0228 (8) | 0.0185 (9) | 0.0217 (9) | −0.0016 (7) | −0.0044 (7) | 0.0005 (7) |
C51 | 0.0157 (7) | 0.0120 (8) | 0.0162 (8) | −0.0014 (6) | 0.0025 (6) | 0.0000 (6) |
C52 | 0.0145 (8) | 0.0217 (9) | 0.0282 (10) | −0.0007 (7) | −0.0013 (7) | −0.0047 (7) |
C53 | 0.0207 (9) | 0.0272 (11) | 0.0345 (10) | 0.0012 (8) | 0.0074 (7) | −0.0107 (8) |
C54 | 0.0314 (10) | 0.0235 (10) | 0.0198 (9) | −0.0066 (8) | 0.0079 (7) | −0.0066 (7) |
C55 | 0.0307 (10) | 0.0175 (9) | 0.0193 (9) | −0.0016 (7) | −0.0027 (7) | 0.0019 (7) |
C56 | 0.0211 (8) | 0.0177 (9) | 0.0178 (8) | 0.0036 (7) | 0.0000 (6) | 0.0005 (7) |
C61 | 0.0194 (8) | 0.0117 (8) | 0.0098 (7) | −0.0026 (6) | −0.0019 (6) | −0.0024 (6) |
C62 | 0.0208 (8) | 0.0180 (9) | 0.0156 (8) | 0.0021 (7) | −0.0023 (6) | −0.0010 (6) |
C63 | 0.0358 (10) | 0.0137 (8) | 0.0142 (8) | 0.0023 (7) | −0.0027 (7) | 0.0003 (6) |
C64 | 0.0332 (9) | 0.0159 (8) | 0.0148 (7) | −0.0083 (8) | 0.0016 (6) | 0.0006 (8) |
C65 | 0.0198 (8) | 0.0222 (9) | 0.0216 (9) | −0.0063 (7) | 0.0013 (6) | −0.0011 (7) |
C66 | 0.0178 (8) | 0.0143 (8) | 0.0183 (8) | 0.0000 (6) | −0.0033 (6) | 0.0000 (6) |
P1—O1 | 1.4927 (12) | C24—H24 | 0.9500 |
P1—C21 | 1.8057 (17) | C25—C26 | 1.386 (2) |
P1—C11 | 1.8175 (16) | C25—H25 | 0.9500 |
P1—C2 | 1.8257 (15) | C26—H26 | 0.9500 |
P2—O2 | 1.4899 (12) | C31—C32 | 1.395 (2) |
P2—C31 | 1.8060 (16) | C31—C36 | 1.399 (2) |
P2—C41 | 1.8109 (16) | C32—C33 | 1.385 (2) |
P2—C3 | 1.8165 (16) | C32—H32 | 0.9500 |
P3—O3 | 1.4926 (12) | C33—C34 | 1.392 (2) |
P3—C4 | 1.8081 (16) | C33—H33 | 0.9500 |
P3—C51 | 1.8081 (16) | C34—C35 | 1.377 (2) |
P3—C61 | 1.8128 (16) | C34—H34 | 0.9500 |
O4—H4C | 0.75 (3) | C35—C36 | 1.389 (2) |
O4—H4D | 0.86 (3) | C35—H35 | 0.9500 |
C1—C2 | 1.553 (2) | C36—H36 | 0.9500 |
C1—C3 | 1.553 (2) | C41—C46 | 1.387 (2) |
C1—C4 | 1.546 (2) | C41—C42 | 1.396 (2) |
C1—C5 | 1.552 (2) | C42—C43 | 1.389 (2) |
C2—H2A | 0.9900 | C42—H42 | 0.9500 |
C2—H2B | 0.9900 | C43—C44 | 1.388 (3) |
C3—H3A | 0.9900 | C43—H43 | 0.9500 |
C3—H3B | 0.9900 | C44—C45 | 1.378 (3) |
C4—H4A | 0.9900 | C44—H44 | 0.9500 |
C4—H4B | 0.9900 | C45—C46 | 1.397 (2) |
C5—C6 | 1.523 (2) | C45—H45 | 0.9500 |
C5—H5A | 0.9900 | C46—H46 | 0.9500 |
C5—H5B | 0.9900 | C51—C52 | 1.392 (2) |
C6—H6A | 0.9800 | C51—C56 | 1.396 (2) |
C6—H6B | 0.9800 | C52—C53 | 1.389 (2) |
C6—H6C | 0.9800 | C52—H52 | 0.9500 |
C11—C16 | 1.393 (2) | C53—C54 | 1.379 (3) |
C11—C12 | 1.400 (2) | C53—H53 | 0.9500 |
C12—C13 | 1.384 (2) | C54—C55 | 1.380 (3) |
C12—H12 | 0.9500 | C54—H54 | 0.9500 |
C13—C14 | 1.381 (2) | C55—C56 | 1.387 (2) |
C13—H13 | 0.9500 | C55—H55 | 0.9500 |
C14—C15 | 1.386 (2) | C56—H56 | 0.9500 |
C14—H14 | 0.9500 | C61—C66 | 1.393 (2) |
C15—C16 | 1.387 (2) | C61—C62 | 1.396 (2) |
C15—H15 | 0.9500 | C62—C63 | 1.392 (2) |
C16—H16 | 0.9500 | C62—H62 | 0.9500 |
C21—C26 | 1.389 (2) | C63—C64 | 1.382 (3) |
C21—C22 | 1.391 (2) | C63—H63 | 0.9500 |
C22—C23 | 1.393 (3) | C64—C65 | 1.389 (2) |
C22—H22 | 0.9500 | C64—H64 | 0.9500 |
C23—C24 | 1.373 (3) | C65—C66 | 1.387 (2) |
C23—H23 | 0.9500 | C65—H65 | 0.9500 |
C24—C25 | 1.387 (3) | C66—H66 | 0.9500 |
O1—P1—C2 | 115.31 (7) | C23—C24—C25 | 120.02 (18) |
O1—P1—C11 | 109.75 (7) | C23—C24—H24 | 120.0 |
O1—P1—C21 | 111.79 (7) | C25—C24—H24 | 120.0 |
C2—P1—C11 | 107.97 (7) | C26—C25—C24 | 120.38 (18) |
C2—P1—C21 | 103.67 (7) | C26—C25—H25 | 119.8 |
C11—P1—C21 | 107.96 (7) | C24—C25—H25 | 119.8 |
O2—P2—C3 | 114.00 (7) | C25—C26—C21 | 119.85 (16) |
O2—P2—C31 | 112.73 (7) | C25—C26—H26 | 120.1 |
O2—P2—C41 | 110.81 (7) | C21—C26—H26 | 120.1 |
C3—P2—C31 | 103.21 (7) | C32—C31—C36 | 119.16 (15) |
C3—P2—C41 | 109.94 (7) | C32—C31—P2 | 118.14 (12) |
C31—P2—C41 | 105.59 (7) | C36—C31—P2 | 122.64 (13) |
O3—P3—C4 | 117.08 (7) | C33—C32—C31 | 120.48 (15) |
O3—P3—C51 | 111.42 (7) | C33—C32—H32 | 119.8 |
O3—P3—C61 | 111.26 (7) | C31—C32—H32 | 119.8 |
C4—P3—C51 | 102.51 (7) | C32—C33—C34 | 119.76 (16) |
C4—P3—C61 | 108.37 (7) | C32—C33—H33 | 120.1 |
C51—P3—C61 | 105.26 (7) | C34—C33—H33 | 120.1 |
H4C—O4—H4D | 107 (3) | C35—C34—C33 | 120.29 (15) |
C2—C1—C3 | 111.91 (12) | C35—C34—H34 | 119.9 |
C2—C1—C4 | 107.92 (12) | C33—C34—H34 | 119.9 |
C2—C1—C5 | 109.33 (12) | C34—C35—C36 | 120.28 (15) |
C3—C1—C4 | 110.11 (12) | C34—C35—H35 | 119.9 |
C3—C1—C5 | 107.95 (12) | C36—C35—H35 | 119.9 |
C4—C1—C5 | 109.60 (12) | C35—C36—C31 | 119.99 (15) |
C1—C2—P1 | 119.05 (11) | C35—C36—H36 | 120.0 |
C1—C2—H2A | 107.6 | C31—C36—H36 | 120.0 |
P1—C2—H2A | 107.6 | C46—C41—C42 | 119.91 (15) |
C1—C2—H2B | 107.6 | C46—C41—P2 | 123.17 (13) |
P1—C2—H2B | 107.6 | C42—C41—P2 | 116.89 (13) |
H2A—C2—H2B | 107.0 | C43—C42—C41 | 120.06 (16) |
C1—C3—P2 | 118.01 (11) | C43—C42—H42 | 120.0 |
C1—C3—H3A | 107.8 | C41—C42—H42 | 120.0 |
P2—C3—H3A | 107.8 | C44—C43—C42 | 119.54 (17) |
C1—C3—H3B | 107.8 | C44—C43—H43 | 120.2 |
P2—C3—H3B | 107.8 | C42—C43—H43 | 120.2 |
H3A—C3—H3B | 107.1 | C45—C44—C43 | 120.79 (17) |
C1—C4—P3 | 122.10 (11) | C45—C44—H44 | 119.6 |
C1—C4—H4A | 106.8 | C43—C44—H44 | 119.6 |
P3—C4—H4A | 106.8 | C44—C45—C46 | 119.84 (17) |
C1—C4—H4B | 106.8 | C44—C45—H45 | 120.1 |
P3—C4—H4B | 106.8 | C46—C45—H45 | 120.1 |
H4A—C4—H4B | 106.7 | C41—C46—C45 | 119.82 (17) |
C6—C5—C1 | 116.83 (13) | C41—C46—H46 | 120.1 |
C6—C5—H5A | 108.1 | C45—C46—H46 | 120.1 |
C1—C5—H5A | 108.1 | C52—C51—C56 | 118.58 (15) |
C6—C5—H5B | 108.1 | C52—C51—P3 | 118.26 (12) |
C1—C5—H5B | 108.1 | C56—C51—P3 | 123.14 (12) |
H5A—C5—H5B | 107.3 | C53—C52—C51 | 120.56 (16) |
C5—C6—H6A | 109.5 | C53—C52—H52 | 119.7 |
C5—C6—H6B | 109.5 | C51—C52—H52 | 119.7 |
H6A—C6—H6B | 109.5 | C54—C53—C52 | 120.05 (16) |
C5—C6—H6C | 109.5 | C54—C53—H53 | 120.0 |
H6A—C6—H6C | 109.5 | C52—C53—H53 | 120.0 |
H6B—C6—H6C | 109.5 | C53—C54—C55 | 120.18 (17) |
C16—C11—C12 | 119.16 (15) | C53—C54—H54 | 119.9 |
C16—C11—P1 | 116.50 (12) | C55—C54—H54 | 119.9 |
C12—C11—P1 | 124.26 (12) | C54—C55—C56 | 120.02 (17) |
C13—C12—C11 | 120.24 (15) | C54—C55—H55 | 120.0 |
C13—C12—H12 | 119.9 | C56—C55—H55 | 120.0 |
C11—C12—H12 | 119.9 | C55—C56—C51 | 120.55 (16) |
C14—C13—C12 | 120.28 (15) | C55—C56—H56 | 119.7 |
C14—C13—H13 | 119.9 | C51—C56—H56 | 119.7 |
C12—C13—H13 | 119.9 | C66—C61—C62 | 118.93 (15) |
C13—C14—C15 | 119.85 (16) | C66—C61—P3 | 124.63 (12) |
C13—C14—H14 | 120.1 | C62—C61—P3 | 116.37 (12) |
C15—C14—H14 | 120.1 | C63—C62—C61 | 120.32 (15) |
C14—C15—C16 | 120.48 (16) | C63—C62—H62 | 119.8 |
C14—C15—H15 | 119.8 | C61—C62—H62 | 119.8 |
C16—C15—H15 | 119.8 | C64—C63—C62 | 120.15 (16) |
C15—C16—C11 | 119.97 (15) | C64—C63—H63 | 119.9 |
C15—C16—H16 | 120.0 | C62—C63—H63 | 119.9 |
C11—C16—H16 | 120.0 | C63—C64—C65 | 119.98 (16) |
C26—C21—C22 | 119.55 (16) | C63—C64—H64 | 120.0 |
C26—C21—P1 | 122.68 (13) | C65—C64—H64 | 120.0 |
C22—C21—P1 | 117.70 (13) | C66—C65—C64 | 119.96 (16) |
C21—C22—C23 | 120.14 (18) | C66—C65—H65 | 120.0 |
C21—C22—H22 | 119.9 | C64—C65—H65 | 120.0 |
C23—C22—H22 | 119.9 | C65—C66—C61 | 120.63 (15) |
C24—C23—C22 | 120.03 (17) | C65—C66—H66 | 119.7 |
C24—C23—H23 | 120.0 | C61—C66—H66 | 119.7 |
C22—C23—H23 | 120.0 | ||
C4—C1—C2—P1 | 63.32 (15) | C41—P2—C31—C36 | 8.84 (16) |
C5—C1—C2—P1 | −177.53 (10) | C3—P2—C31—C36 | 124.26 (14) |
C3—C1—C2—P1 | −57.98 (15) | C36—C31—C32—C33 | −1.4 (2) |
O1—P1—C2—C1 | 38.96 (14) | P2—C31—C32—C33 | −178.59 (13) |
C21—P1—C2—C1 | 161.48 (11) | C31—C32—C33—C34 | 0.6 (3) |
C11—P1—C2—C1 | −84.16 (12) | C32—C33—C34—C35 | 1.1 (3) |
C4—C1—C3—P2 | −174.49 (10) | C33—C34—C35—C36 | −2.0 (3) |
C5—C1—C3—P2 | 65.90 (15) | C34—C35—C36—C31 | 1.1 (2) |
C2—C1—C3—P2 | −54.46 (16) | C32—C31—C36—C35 | 0.6 (2) |
O2—P2—C3—C1 | 39.48 (14) | P2—C31—C36—C35 | 177.59 (12) |
C31—P2—C3—C1 | 162.10 (11) | O2—P2—C41—C46 | −164.41 (13) |
C41—P2—C3—C1 | −85.64 (13) | C31—P2—C41—C46 | 73.23 (15) |
C5—C1—C4—P3 | 78.24 (15) | C3—P2—C41—C46 | −37.48 (16) |
C3—C1—C4—P3 | −40.37 (17) | O2—P2—C41—C42 | 17.44 (15) |
C2—C1—C4—P3 | −162.79 (11) | C31—P2—C41—C42 | −104.92 (13) |
O3—P3—C4—C1 | −42.42 (14) | C3—P2—C41—C42 | 144.37 (12) |
C51—P3—C4—C1 | −164.67 (12) | C46—C41—C42—C43 | −1.5 (2) |
C61—P3—C4—C1 | 84.37 (13) | P2—C41—C42—C43 | 176.71 (13) |
C4—C1—C5—C6 | 67.01 (17) | C41—C42—C43—C44 | 0.1 (3) |
C3—C1—C5—C6 | −173.05 (13) | C42—C43—C44—C45 | 1.0 (3) |
C2—C1—C5—C6 | −51.09 (17) | C43—C44—C45—C46 | −0.6 (3) |
O1—P1—C11—C16 | 19.90 (15) | C42—C41—C46—C45 | 1.9 (2) |
C21—P1—C11—C16 | −102.17 (13) | P2—C41—C46—C45 | −176.20 (13) |
C2—P1—C11—C16 | 146.34 (12) | C44—C45—C46—C41 | −0.8 (3) |
O1—P1—C11—C12 | −156.57 (13) | O3—P3—C51—C52 | 20.61 (15) |
C21—P1—C11—C12 | 81.36 (15) | C4—P3—C51—C52 | 146.62 (13) |
C2—P1—C11—C12 | −30.13 (16) | C61—P3—C51—C52 | −100.10 (14) |
C16—C11—C12—C13 | −1.0 (2) | O3—P3—C51—C56 | −158.05 (13) |
P1—C11—C12—C13 | 175.35 (12) | C4—P3—C51—C56 | −32.04 (15) |
C11—C12—C13—C14 | −0.3 (2) | C61—P3—C51—C56 | 81.23 (15) |
C12—C13—C14—C15 | 1.5 (3) | C56—C51—C52—C53 | 2.0 (3) |
C13—C14—C15—C16 | −1.3 (3) | P3—C51—C52—C53 | −176.72 (14) |
C14—C15—C16—C11 | −0.1 (3) | C51—C52—C53—C54 | 0.0 (3) |
C12—C11—C16—C15 | 1.3 (2) | C52—C53—C54—C55 | −2.0 (3) |
P1—C11—C16—C15 | −175.39 (13) | C53—C54—C55—C56 | 1.8 (3) |
O1—P1—C21—C26 | −161.46 (13) | C54—C55—C56—C51 | 0.2 (3) |
C11—P1—C21—C26 | −40.65 (16) | C52—C51—C56—C55 | −2.1 (2) |
C2—P1—C21—C26 | 73.72 (15) | P3—C51—C56—C55 | 176.55 (13) |
O1—P1—C21—C22 | 21.58 (15) | O3—P3—C61—C66 | 144.99 (13) |
C11—P1—C21—C22 | 142.39 (13) | C4—P3—C61—C66 | 14.91 (15) |
C2—P1—C21—C22 | −103.24 (14) | C51—P3—C61—C66 | −94.19 (14) |
C26—C21—C22—C23 | −1.6 (3) | O3—P3—C61—C62 | −38.16 (14) |
P1—C21—C22—C23 | 175.42 (13) | C4—P3—C61—C62 | −168.25 (12) |
C21—C22—C23—C24 | 0.4 (3) | C51—P3—C61—C62 | 82.65 (13) |
C22—C23—C24—C25 | 1.0 (3) | C66—C61—C62—C63 | 1.2 (2) |
C23—C24—C25—C26 | −1.2 (3) | P3—C61—C62—C63 | −175.86 (12) |
C24—C25—C26—C21 | −0.1 (3) | C61—C62—C63—C64 | −1.0 (2) |
C22—C21—C26—C25 | 1.5 (2) | C62—C63—C64—C65 | −0.3 (2) |
P1—C21—C26—C25 | −175.43 (13) | C63—C64—C65—C66 | 1.4 (3) |
O2—P2—C31—C32 | 64.77 (15) | C64—C65—C66—C61 | −1.3 (2) |
C41—P2—C31—C32 | −174.11 (13) | C62—C61—C66—C65 | 0.0 (2) |
C3—P2—C31—C32 | −58.69 (14) | P3—C61—C66—C65 | 176.74 (13) |
O2—P2—C31—C36 | −112.27 (14) |
D—H···A | D—H | H···A | D···A | D—H···A |
O4—H4C···O1 | 0.75 (3) | 2.16 (3) | 2.912 (2) | 179 (3) |
O4—H4D···O3i | 0.86 (3) | 1.98 (3) | 2.8413 (19) | 176 (3) |
Symmetry code: (i) x−1, y, z. |
Experimental details
Crystal data | |
Chemical formula | C42H41O3P3·H2O |
Mr | 704.67 |
Crystal system, space group | Monoclinic, Pc |
Temperature (K) | 100 |
a, b, c (Å) | 9.5303 (2), 10.4028 (2), 18.0951 (4) |
β (°) | 90.1433 (14) |
V (Å3) | 1793.98 (6) |
Z | 2 |
Radiation type | Mo Kα |
µ (mm−1) | 0.21 |
Crystal size (mm) | 0.18 × 0.16 × 0.10 |
Data collection | |
Diffractometer | Bruker Kappa APEX II area-detector |
Absorption correction | – |
No. of measured, independent and observed [I > 2σ(I)] reflections | 41040, 10441, 8909 |
Rint | 0.059 |
(sin θ/λ)max (Å−1) | 0.703 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.035, 0.068, 0.95 |
No. of reflections | 10441 |
No. of parameters | 450 |
No. of restraints | 2 |
H-atom treatment | H atoms treated by a mixture of independent and constrained refinement |
Δρmax, Δρmin (e Å−3) | 0.29, −0.26 |
Absolute structure | Flack (1983), 5207 Friedel pairs |
Absolute structure parameter | −0.04 (4) |
Computer programs: SMART (Bruker, 1998), SAINT-Plus (Bruker, 1998), SAINT-Plus, SHELXS97 (Sheldrick, 1997a), SHELXL97 (Sheldrick, 1997a), SHELXTL (Sheldrick, 1997b), SHELXTL.
P1—O1 | 1.4927 (12) | P2—C41 | 1.8109 (16) |
P1—C21 | 1.8057 (17) | P2—C3 | 1.8165 (16) |
P1—C11 | 1.8175 (16) | P3—O3 | 1.4926 (12) |
P1—C2 | 1.8257 (15) | P3—C4 | 1.8081 (16) |
P2—O2 | 1.4899 (12) | P3—C51 | 1.8081 (16) |
P2—C31 | 1.8060 (16) | P3—C61 | 1.8128 (16) |
O1—P1—C2 | 115.31 (7) | C3—P2—C31 | 103.21 (7) |
O1—P1—C11 | 109.75 (7) | C3—P2—C41 | 109.94 (7) |
O1—P1—C21 | 111.79 (7) | C31—P2—C41 | 105.59 (7) |
C2—P1—C11 | 107.97 (7) | O3—P3—C4 | 117.08 (7) |
C2—P1—C21 | 103.67 (7) | O3—P3—C51 | 111.42 (7) |
C11—P1—C21 | 107.96 (7) | O3—P3—C61 | 111.26 (7) |
O2—P2—C3 | 114.00 (7) | C4—P3—C51 | 102.51 (7) |
O2—P2—C31 | 112.73 (7) | C4—P3—C61 | 108.37 (7) |
O2—P2—C41 | 110.81 (7) | C51—P3—C61 | 105.26 (7) |
D—H···A | D—H | H···A | D···A | D—H···A |
O4—H4C···O1 | 0.75 (3) | 2.16 (3) | 2.912 (2) | 179 (3) |
O4—H4D···O3i | 0.86 (3) | 1.98 (3) | 2.8413 (19) | 176 (3) |
Symmetry code: (i) x−1, y, z. |
Organophosphorus ligands with three phosphoryl groups are considered as promising agents to ensure selectivity of separation of metal mixtures by extraction (Pisareva et al., 2005).
The arrangement of phosphoryl groups and phenyl rings in the title compound, (I, Fig. 1), is far from a threefold symmetry. Selected bond lengths and angles in (I) are given in Table 1. The P═O distances range from 1.4899 (12) to 1.4927 (12) Å. The O═P—C angles with C atoms of CH2 groups differ significantly from ideal tetrahedral values, the maximum value being 117.08 (7)° (Table 1). The C—C—C angles around the central atom C1 vary from 107.92 (12) to 111.91 (12)°.
The same behaviour of the O═P—C angles can be found in Ln nitrate complexes with CH3C[CH2P(O)Ph2] (Lees & Platt, 2005). The P═O distances in these complexes are slightly longer due to coordination of phosphoryl groups to Ln atoms [from 1.499 (3) to 1.510 (3) Å]. Apparent P═ O distances in partially oxygenated C2H5C(CH2PPh2)3 (Chekhlov, 2000) are significantly shorter, due to a statistical character of the structure.
In (I), the hydrogen bonds in which water molecules act as proton donors (Table 2, Fig. 2) link organic molecules into chains along the [100] direction.