Literature DB >> 22091072

rac-Dimethyl [(9-anthr-yl)(4-methyl-anilino)meth-yl]phospho-nate.

Ivanka Kraicheva1, Ivelina Tsacheva, Elitsa Vodenicharova, Emil Tashev, Kolio Troev.   

Abstract

The title compound, C(24)H(24)NO(3)P, crystallizes as a racemate with two mol-ecules in the asymmetric unit. The structural features (bond lengths and angles) of the two mol-ecules are almost identical. The dihedral angle between the anthracene and toluidine rings is similar in the two mol-ecules, with values of 48.36 (9) and 51.15 (9)°. The methyl groups of one of the meth-oxy groups in one mol-ecule is disordered over two sets of sites, the major component having a site occupancy of 0.636 (3). In the crystal, both molecules are linked into inversion dimers by pairs of N-H⋯O hydrogen bonds.

Entities:  

Year:  2011        PMID: 22091072      PMCID: PMC3213493          DOI: 10.1107/S1600536811027711

Source DB:  PubMed          Journal:  Acta Crystallogr Sect E Struct Rep Online        ISSN: 1600-5368


Related literature

For general background to the use of amino­phospho­nic acid derivatives in organic synthesis and as biologically active compounds, see: Cherkasov & Galkin (1998 ▶); Orsini et al. (2010 ▶); Green (2000 ▶); Rassukana et al. (2009 ▶); Kraicheva et al. (2011 ▶) and references therein.

Experimental

Crystal data

C24H24NO3P M = 405.41 Triclinic, a = 7.944 (3) Å b = 11.389 (4) Å c = 24.007 (4) Å α = 100.92 (4)° β = 91.63 (3)° γ = 95.17 (4)° V = 2121.5 (11) Å3 Z = 4 Mo Kα radiation μ = 0.15 mm−1 T = 290 K 0.24 × 0.22 × 0.20 mm

Data collection

Enraf–Nonius CAD-4 diffractometer 8902 measured reflections 8275 independent reflections 2944 reflections with I > 2σ(I) R int = 0.085 3 standard reflections every 120 min intensity decay: 1%

Refinement

R[F 2 > 2σ(F 2)] = 0.090 wR(F 2) = 0.278 S = 1.00 8275 reflections 539 parameters H-atom parameters constrained Δρmax = 0.29 e Å−3 Δρmin = −0.32 e Å−3 Data collection: CAD-4 EXPRESS (Enraf–Nonius, 1994 ▶); cell refinement: CAD-4 EXPRESS; data reduction: XCAD4 (Harms & Wocadlo, 1995) ▶; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); 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 ▶). Crystal structure: contains datablock(s) I, global. DOI: 10.1107/S1600536811027711/kp2342sup1.cif Structure factors: contains datablock(s) I. DOI: 10.1107/S1600536811027711/kp2342Isup2.hkl Supplementary material file. DOI: 10.1107/S1600536811027711/kp2342Isup3.cml Additional supplementary materials: crystallographic information; 3D view; checkCIF report
C24H24NO3PZ = 4
Mr = 405.41F(000) = 856
Triclinic, P1Dx = 1.269 Mg m3
Hall symbol: -P 1Melting point = 452–453 K
a = 7.944 (3) ÅMo Kα radiation, λ = 0.71073 Å
b = 11.389 (4) ÅCell parameters from 22 reflections
c = 24.007 (4) Åθ = 16.0–17.8°
α = 100.92 (4)°µ = 0.15 mm1
β = 91.63 (3)°T = 290 K
γ = 95.17 (4)°Prism, colourless
V = 2121.5 (11) Å30.24 × 0.22 × 0.20 mm
Enraf–Nonius CAD-4 diffractometerRint = 0.085
Radiation source: Enraf Nonius FR590θmax = 26.0°, θmin = 0.9°
graphiteh = 0→9
non–profiled ω/2τ scansk = −14→13
8902 measured reflectionsl = −29→29
8275 independent reflections3 standard reflections every 120 min
2944 reflections with I > 2σ(I) intensity decay: 1%
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.090Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.278H-atom parameters constrained
S = 1.00w = 1/[σ2(Fo2) + (0.0998P)2] where P = (Fo2 + 2Fc2)/3
8275 reflections(Δ/σ)max = 0.003
539 parametersΔρmax = 0.29 e Å3
0 restraintsΔρmin = −0.32 e Å3
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.
xyzUiso*/UeqOcc. (<1)
C1010.5221 (8)0.7612 (5)0.5699 (2)0.0376 (16)
H1010.50810.84070.56150.045*
C1020.5951 (7)0.7858 (5)0.6315 (3)0.0388 (16)
C1030.6205 (8)0.9055 (6)0.6617 (3)0.0436 (17)
C1040.5628 (9)1.0076 (6)0.6425 (3)0.0520 (18)
H1040.50310.9960.60770.062*
C1050.5929 (10)1.1198 (6)0.6735 (3)0.070 (2)
H1050.55061.18340.66020.084*
C1060.6869 (11)1.1428 (7)0.7256 (4)0.078 (3)
H1060.71041.22110.74560.094*
C1070.7426 (10)1.0506 (7)0.7462 (3)0.069 (2)
H1070.80491.06630.78060.083*
C1080.7086 (8)0.9296 (7)0.7165 (3)0.0500 (18)
C1090.7569 (9)0.8358 (7)0.7409 (3)0.060 (2)
H1090.81580.85240.77590.073*
C1100.7177 (8)0.7162 (7)0.7130 (3)0.0500 (18)
C1110.7586 (11)0.6232 (8)0.7402 (3)0.075 (2)
H1110.81120.64180.77630.09*
C1120.7228 (11)0.5074 (8)0.7147 (4)0.082 (3)
H1120.75110.44620.73290.098*
C1130.6424 (11)0.4802 (7)0.6604 (4)0.071 (2)
H1130.61450.40010.64350.085*
C1140.6037 (9)0.5671 (6)0.6315 (3)0.058 (2)
H1140.55620.54550.59470.069*
C1150.6357 (8)0.6912 (6)0.6574 (3)0.0428 (16)
C16A0.217 (8)0.722 (3)0.4555 (8)0.108 (13)0.64 (7)
H16A0.15010.77810.44240.163*0.64 (7)
H16B0.16610.64170.44180.163*0.64 (7)
H16C0.32910.73020.44170.163*0.64 (7)
C16B0.120 (7)0.695 (4)0.467 (3)0.092 (15)0.36 (7)
H16D0.07770.75790.45040.138*0.36 (7)
H16E0.0270.6470.47840.138*0.36 (7)
H16F0.18080.64540.43890.138*0.36 (7)
C1170.0511 (11)0.6710 (9)0.6141 (4)0.111 (3)
H17A−0.00630.66090.57760.167*
H17B0.00020.72980.64080.167*
H17C0.04220.59580.62680.167*
C1180.7049 (8)0.7741 (5)0.4881 (3)0.0402 (16)
C1190.7440 (9)0.8952 (6)0.5003 (3)0.060 (2)
H1190.72540.93740.53630.072*
C1200.8111 (10)0.9574 (6)0.4600 (3)0.065 (2)
H1200.83421.04050.46940.078*
C1210.8434 (10)0.8983 (7)0.4070 (3)0.061 (2)
C1220.8069 (10)0.7770 (7)0.3948 (3)0.073 (2)
H1220.83030.73480.35920.087*
C1230.7351 (9)0.7143 (6)0.4344 (3)0.0528 (19)
H1230.70750.63170.42440.063*
C1240.9191 (11)0.9658 (7)0.3632 (3)0.084 (3)
H24A0.93431.05020.37890.127*
H24B0.84420.95170.330.127*
H24C1.02660.93780.3530.127*
C2010.0364 (8)0.7345 (5)0.9271 (2)0.0399 (16)
H2010.01580.65630.93830.048*
C2020.0977 (8)0.7055 (6)0.8668 (3)0.0409 (16)
C2030.0967 (8)0.5839 (6)0.8392 (3)0.0457 (17)
C2040.0218 (9)0.4839 (6)0.8613 (3)0.060 (2)
H204−0.03070.49780.89570.072*
C2050.0264 (11)0.3685 (7)0.8325 (4)0.077 (2)
H205−0.02410.30540.84770.092*
C2060.1059 (12)0.3430 (9)0.7805 (4)0.087 (3)
H2060.10960.26390.76190.105*
C2070.1757 (11)0.4331 (8)0.7581 (3)0.081 (3)
H2070.22930.41540.7240.097*
C2080.1710 (9)0.5562 (7)0.7847 (3)0.060 (2)
C2090.2349 (9)0.6472 (8)0.7585 (3)0.062 (2)
H2090.28470.62840.72380.074*
C2100.2256 (9)0.7655 (8)0.7832 (3)0.059 (2)
C2110.2790 (11)0.8597 (9)0.7548 (3)0.076 (3)
H2110.31850.83960.71840.092*
C2120.2756 (12)0.9752 (9)0.7773 (4)0.087 (3)
H2120.31721.03440.7580.104*
C2130.2078 (10)1.0066 (7)0.8312 (3)0.073 (2)
H2130.20191.08730.84660.087*
C2140.1508 (9)0.9223 (6)0.8612 (3)0.059 (2)
H2140.10770.94620.89670.071*
C2150.1562 (8)0.7976 (6)0.8386 (3)0.0460 (17)
C216−0.2316 (14)0.7801 (11)1.0400 (4)0.139 (5)
H16G−0.16750.85731.0460.208*
H16H−0.17350.72711.05880.208*
H16I−0.34130.78861.05530.208*
C217−0.4401 (10)0.7696 (9)0.8752 (4)0.101 (3)
H17D−0.49730.71030.84530.151*
H17E−0.44060.84760.86560.151*
H17F−0.4970.76870.90990.151*
C2180.2376 (8)0.7492 (6)1.0106 (3)0.0442 (17)
C2190.2670 (8)0.6297 (6)1.0007 (3)0.0491 (18)
H2190.23730.58190.96530.059*
C2200.3395 (9)0.5800 (6)1.0424 (3)0.060 (2)
H2200.35620.49891.03440.072*
C2210.3879 (9)0.6457 (7)1.0953 (3)0.059 (2)
C2220.3618 (10)0.7680 (7)1.1050 (3)0.065 (2)
H2220.39340.81621.14020.079*
C2230.2902 (9)0.8174 (6)1.0631 (3)0.0533 (19)
H2230.27670.89911.07030.064*
C2240.4689 (12)0.5892 (8)1.1404 (3)0.094 (3)
H24D0.38280.54521.15760.141*
H24E0.52760.6511.16890.141*
H24F0.54750.53551.12330.141*
N10.6388 (7)0.7089 (4)0.5283 (2)0.0470 (15)
H10.66730.63790.52830.056*
N20.1617 (7)0.8036 (4)0.9698 (2)0.0470 (14)
H20.18890.87840.96990.056*
O110.3150 (6)0.5491 (4)0.5302 (2)0.0685 (15)
O120.2263 (8)0.7445 (4)0.5129 (2)0.0842 (18)
O130.2235 (6)0.7100 (5)0.6101 (2)0.0815 (17)
O21−0.1452 (6)0.9311 (4)0.9540 (2)0.0797 (17)
O22−0.2498 (7)0.7329 (5)0.9825 (2)0.0760 (16)
O23−0.2654 (6)0.7425 (5)0.8827 (2)0.0772 (16)
P10.3154 (2)0.67682 (16)0.55329 (8)0.0498 (6)
P2−0.1609 (2)0.80141 (17)0.93785 (8)0.0507 (6)
U11U22U33U12U13U23
C1010.044 (4)0.032 (3)0.039 (4)0.008 (3)0.007 (3)0.009 (3)
C1020.032 (4)0.047 (4)0.038 (4)−0.001 (3)0.011 (3)0.010 (3)
C1030.046 (4)0.047 (4)0.038 (4)0.000 (3)0.010 (3)0.010 (3)
C1040.066 (5)0.043 (4)0.044 (4)−0.003 (4)0.001 (4)0.006 (3)
C1050.094 (7)0.047 (5)0.064 (5)−0.003 (4)0.009 (5)0.005 (4)
C1060.090 (7)0.052 (5)0.082 (7)0.003 (5)−0.003 (5)−0.011 (5)
C1070.066 (6)0.081 (6)0.049 (5)−0.001 (5)−0.005 (4)−0.015 (5)
C1080.036 (4)0.065 (5)0.045 (4)0.001 (4)0.008 (3)0.004 (4)
C1090.050 (5)0.082 (6)0.048 (5)0.000 (4)−0.004 (4)0.014 (4)
C1100.040 (4)0.068 (5)0.050 (4)0.018 (4)0.009 (4)0.024 (4)
C1110.091 (7)0.082 (6)0.056 (5)0.022 (5)0.006 (5)0.017 (5)
C1120.097 (7)0.083 (7)0.078 (6)0.037 (6)0.000 (5)0.039 (5)
C1130.091 (7)0.054 (5)0.076 (6)0.018 (4)0.008 (5)0.025 (4)
C1140.068 (5)0.051 (5)0.059 (5)0.013 (4)0.008 (4)0.021 (4)
C1150.045 (4)0.048 (4)0.038 (4)0.006 (3)0.004 (3)0.013 (3)
C16A0.11 (3)0.18 (2)0.050 (11)0.06 (2)0.016 (13)0.020 (11)
C16B0.03 (2)0.17 (3)0.07 (3)0.02 (2)−0.011 (17)−0.01 (2)
C1170.058 (7)0.151 (9)0.121 (9)−0.012 (6)0.021 (6)0.026 (7)
C1180.052 (4)0.033 (4)0.036 (4)0.008 (3)−0.004 (3)0.006 (3)
C1190.078 (6)0.053 (5)0.047 (4)0.001 (4)0.028 (4)0.005 (4)
C1200.078 (6)0.046 (4)0.071 (6)0.001 (4)0.021 (5)0.012 (4)
C1210.071 (6)0.067 (5)0.052 (5)0.012 (4)0.010 (4)0.023 (4)
C1220.094 (7)0.073 (6)0.047 (5)0.002 (5)0.019 (5)0.000 (4)
C1230.067 (5)0.047 (4)0.040 (4)−0.007 (4)0.012 (4)0.001 (3)
C1240.098 (7)0.091 (6)0.075 (6)0.007 (5)0.026 (5)0.041 (5)
C2010.044 (4)0.041 (4)0.036 (4)0.006 (3)−0.003 (3)0.012 (3)
C2020.032 (4)0.052 (4)0.040 (4)0.006 (3)−0.001 (3)0.011 (3)
C2030.036 (4)0.055 (5)0.042 (4)0.006 (3)−0.006 (3)0.000 (3)
C2040.062 (5)0.052 (5)0.060 (5)−0.002 (4)0.004 (4)−0.001 (4)
C2050.073 (6)0.065 (6)0.086 (7)0.003 (5)−0.012 (5)0.002 (5)
C2060.076 (7)0.078 (7)0.091 (8)0.017 (6)−0.017 (6)−0.026 (6)
C2070.076 (7)0.092 (7)0.059 (6)0.013 (6)0.008 (5)−0.026 (5)
C2080.056 (5)0.079 (6)0.040 (4)0.009 (4)0.001 (4)−0.004 (4)
C2090.042 (5)0.099 (7)0.042 (4)0.011 (4)0.005 (4)0.002 (5)
C2100.054 (5)0.088 (6)0.036 (4)−0.003 (4)0.001 (4)0.018 (4)
C2110.072 (6)0.106 (7)0.052 (5)0.007 (6)0.009 (4)0.016 (5)
C2120.102 (8)0.111 (8)0.055 (6)−0.018 (6)−0.002 (5)0.050 (6)
C2130.088 (7)0.067 (5)0.064 (6)−0.007 (5)−0.004 (5)0.024 (5)
C2140.077 (6)0.059 (5)0.043 (4)−0.010 (4)−0.003 (4)0.019 (4)
C2150.039 (4)0.054 (5)0.043 (4)−0.003 (3)−0.004 (3)0.008 (3)
C2160.128 (10)0.198 (13)0.083 (8)−0.021 (9)0.039 (7)0.024 (8)
C2170.060 (6)0.146 (9)0.096 (7)0.028 (6)−0.014 (5)0.018 (6)
C2180.042 (4)0.057 (5)0.035 (4)0.007 (3)0.003 (3)0.010 (3)
C2190.060 (5)0.041 (4)0.044 (4)0.014 (3)−0.008 (4)−0.001 (3)
C2200.064 (5)0.051 (5)0.068 (5)0.014 (4)0.001 (4)0.019 (4)
C2210.049 (5)0.084 (6)0.050 (5)0.019 (4)0.001 (4)0.026 (4)
C2220.073 (6)0.083 (6)0.045 (5)0.017 (5)0.004 (4)0.018 (4)
C2230.062 (5)0.052 (4)0.044 (4)0.013 (4)−0.003 (4)0.003 (4)
C2240.103 (8)0.118 (8)0.072 (6)0.023 (6)−0.008 (5)0.042 (6)
N10.067 (4)0.031 (3)0.047 (3)0.012 (3)0.017 (3)0.010 (3)
N20.052 (4)0.044 (3)0.046 (3)−0.001 (3)−0.002 (3)0.014 (3)
O110.061 (4)0.039 (3)0.100 (4)0.002 (2)−0.011 (3)0.001 (3)
O120.107 (5)0.066 (4)0.076 (4)0.014 (3)−0.046 (4)0.012 (3)
O130.044 (3)0.117 (5)0.071 (4)−0.006 (3)0.015 (3)−0.010 (3)
O210.064 (4)0.054 (3)0.121 (5)0.020 (3)0.010 (3)0.010 (3)
O220.079 (4)0.078 (4)0.068 (4)−0.001 (3)0.032 (3)0.007 (3)
O230.044 (3)0.113 (4)0.069 (4)0.020 (3)−0.012 (3)0.000 (3)
P10.0489 (12)0.0455 (11)0.0529 (12)0.0063 (9)−0.0024 (10)0.0041 (9)
P20.0466 (13)0.0537 (13)0.0515 (12)0.0109 (10)0.0074 (10)0.0058 (10)
C101—N11.463 (7)C201—P21.808 (6)
C101—C1021.538 (8)C201—H2010.98
C101—P11.820 (6)C202—C2151.404 (8)
C101—H1010.98C202—C2031.416 (8)
C102—C1151.398 (8)C203—C2041.434 (9)
C102—C1031.412 (8)C203—C2081.442 (9)
C103—C1041.435 (8)C204—C2051.369 (9)
C103—C1081.440 (9)C204—H2040.93
C104—C1051.349 (9)C205—C2061.409 (12)
C104—H1040.93C205—H2050.93
C105—C1061.405 (10)C206—C2071.331 (11)
C105—H1050.93C206—H2060.93
C106—C1071.345 (10)C207—C2081.431 (10)
C106—H1060.93C207—H2070.93
C107—C1081.425 (9)C208—C2091.377 (10)
C107—H1070.93C209—C2101.375 (10)
C108—C1091.389 (9)C209—H2090.93
C109—C1101.402 (9)C210—C2111.418 (10)
C109—H1090.93C210—C2151.449 (9)
C110—C1111.401 (9)C211—C2121.327 (11)
C110—C1151.437 (9)C211—H2110.93
C111—C1121.346 (10)C212—C2131.410 (11)
C111—H1110.93C212—H2120.93
C112—C1131.403 (10)C213—C2141.359 (9)
C112—H1120.93C213—H2130.93
C113—C1141.364 (9)C214—C2151.426 (9)
C113—H1130.93C214—H2140.93
C114—C1151.429 (9)C216—O221.383 (10)
C114—H1140.93C216—H16G0.96
C16A—O121.350 (18)C216—H16H0.96
C16A—H16A0.96C216—H16I0.96
C16A—H16B0.96C217—O231.462 (9)
C16A—H16C0.96C217—H17D0.96
C16B—O121.37 (3)C217—H17E0.96
C16B—H16D0.96C217—H17F0.96
C16B—H16E0.96C218—C2191.379 (8)
C16B—H16F0.96C218—C2231.381 (8)
C117—O131.413 (9)C218—N21.402 (7)
C117—H17A0.96C219—C2201.377 (9)
C117—H17B0.96C219—H2190.93
C117—H17C0.96C220—C2211.370 (9)
C118—C1191.360 (8)C220—H2200.93
C118—C1231.378 (8)C221—C2221.403 (10)
C118—N11.409 (8)C221—C2241.517 (9)
C119—C1201.393 (9)C222—C2231.375 (9)
C119—H1190.93C222—H2220.93
C120—C1211.366 (10)C223—H2230.93
C120—H1200.93C224—H24D0.96
C121—C1221.359 (10)C224—H24E0.96
C121—C1241.522 (9)C224—H24F0.96
C122—C1231.398 (10)N1—H10.86
C122—H1220.93N2—H20.86
C123—H1230.93O11—P11.455 (5)
C124—H24A0.96O12—P11.542 (5)
C124—H24B0.96O13—P11.563 (5)
C124—H24C0.96O21—P21.447 (5)
C201—N21.469 (7)O22—P21.586 (5)
C201—C2021.526 (8)O23—P21.546 (5)
N1—C101—C102113.6 (5)C202—C203—C204124.2 (6)
N1—C101—P1108.0 (4)C202—C203—C208119.3 (7)
C102—C101—P1118.9 (4)C204—C203—C208116.5 (6)
N1—C101—H101105C205—C204—C203121.1 (7)
C102—C101—H101105C205—C204—H204119.4
P1—C101—H101105C203—C204—H204119.4
C115—C102—C103120.3 (6)C204—C205—C206121.5 (9)
C115—C102—C101120.6 (5)C204—C205—H205119.3
C103—C102—C101119.0 (5)C206—C205—H205119.3
C102—C103—C104125.1 (6)C207—C206—C205119.5 (8)
C102—C103—C108118.8 (6)C207—C206—H206120.3
C104—C103—C108116.1 (6)C205—C206—H206120.3
C105—C104—C103121.8 (7)C206—C207—C208122.2 (8)
C105—C104—H104119.1C206—C207—H207118.9
C103—C104—H104119.1C208—C207—H207118.9
C104—C105—C106121.4 (8)C209—C208—C207120.5 (7)
C104—C105—H105119.3C209—C208—C203120.4 (7)
C106—C105—H105119.3C207—C208—C203119.1 (8)
C107—C106—C105119.5 (7)C210—C209—C208120.6 (7)
C107—C106—H106120.2C210—C209—H209119.7
C105—C106—H106120.2C208—C209—H209119.7
C106—C107—C108121.6 (7)C209—C210—C211121.2 (8)
C106—C107—H107119.2C209—C210—C215120.9 (7)
C108—C107—H107119.2C211—C210—C215117.9 (7)
C109—C108—C107120.2 (7)C212—C211—C210123.4 (8)
C109—C108—C103120.4 (7)C212—C211—H211118.3
C107—C108—C103119.3 (7)C210—C211—H211118.3
C108—C109—C110120.6 (7)C211—C212—C213118.7 (8)
C108—C109—H109119.7C211—C212—H212120.6
C110—C109—H109119.7C213—C212—H212120.6
C111—C110—C109119.4 (7)C214—C213—C212122.0 (8)
C111—C110—C115121.2 (7)C214—C213—H213119
C109—C110—C115119.4 (6)C212—C213—H213119
C112—C111—C110120.9 (8)C213—C214—C215120.6 (7)
C112—C111—H111119.5C213—C214—H214119.7
C110—C111—H111119.5C215—C214—H214119.7
C111—C112—C113119.1 (7)C202—C215—C214123.8 (6)
C111—C112—H112120.4C202—C215—C210118.8 (6)
C113—C112—H112120.4C214—C215—C210117.4 (7)
C114—C113—C112122.4 (8)O22—C216—H16G109.5
C114—C113—H113118.8O22—C216—H16H109.5
C112—C113—H113118.8H16G—C216—H16H109.5
C113—C114—C115120.4 (7)O22—C216—H16I109.5
C113—C114—H114119.8H16G—C216—H16I109.5
C115—C114—H114119.8H16H—C216—H16I109.5
C102—C115—C114124.1 (6)O23—C217—H17D109.5
C102—C115—C110120.0 (6)O23—C217—H17E109.5
C114—C115—C110115.9 (6)H17D—C217—H17E109.5
O12—C16A—H16A109.5O23—C217—H17F109.5
O12—C16A—H16B109.5H17D—C217—H17F109.5
H16A—C16A—H16B109.5H17E—C217—H17F109.5
O12—C16A—H16C109.5C219—C218—C223117.1 (6)
H16A—C16A—H16C109.5C219—C218—N2123.2 (6)
H16B—C16A—H16C109.5C223—C218—N2119.6 (6)
O12—C16B—H16D109.5C220—C219—C218121.1 (6)
O12—C16B—H16E109.5C220—C219—H219119.5
H16D—C16B—H16E109.5C218—C219—H219119.5
O12—C16B—H16F109.5C221—C220—C219122.4 (7)
H16D—C16B—H16F109.5C221—C220—H220118.8
H16E—C16B—H16F109.5C219—C220—H220118.8
O13—C117—H17A109.5C220—C221—C222116.6 (6)
O13—C117—H17B109.5C220—C221—C224121.5 (7)
H17A—C117—H17B109.5C222—C221—C224121.9 (7)
O13—C117—H17C109.5C223—C222—C221120.8 (7)
H17A—C117—H17C109.5C223—C222—H222119.6
H17B—C117—H17C109.5C221—C222—H222119.6
C119—C118—C123117.6 (6)C222—C223—C218121.9 (7)
C119—C118—N1122.6 (6)C222—C223—H223119
C123—C118—N1119.8 (6)C218—C223—H223119
C118—C119—C120121.6 (6)C221—C224—H24D109.5
C118—C119—H119119.2C221—C224—H24E109.5
C120—C119—H119119.2H24D—C224—H24E109.5
C121—C120—C119121.0 (7)C221—C224—H24F109.5
C121—C120—H120119.5H24D—C224—H24F109.5
C119—C120—H120119.5H24E—C224—H24F109.5
C122—C121—C120117.7 (7)C118—N1—C101120.5 (5)
C122—C121—C124121.1 (7)C118—N1—H1119.7
C120—C121—C124121.2 (7)C101—N1—H1119.7
C121—C122—C123121.6 (7)C218—N2—C201121.0 (5)
C121—C122—H122119.2C218—N2—H2119.5
C123—C122—H122119.2C201—N2—H2119.5
C118—C123—C122120.4 (7)C16A—O12—P1128.7 (11)
C118—C123—H123119.8C16B—O12—P1127 (2)
C122—C123—H123119.8C117—O13—P1121.2 (5)
C121—C124—H24A109.5C216—O22—P2120.8 (6)
C121—C124—H24B109.5C217—O23—P2119.7 (5)
H24A—C124—H24B109.5O11—P1—O12112.9 (3)
C121—C124—H24C109.5O11—P1—O13115.9 (3)
H24A—C124—H24C109.5O12—P1—O13103.5 (3)
H24B—C124—H24C109.5O11—P1—C101116.3 (3)
N2—C201—C202115.3 (5)O12—P1—C101104.2 (3)
N2—C201—P2107.6 (4)O13—P1—C101102.5 (3)
C202—C201—P2118.4 (4)O21—P2—O23118.1 (3)
N2—C201—H201104.7O21—P2—O22114.8 (3)
C202—C201—H201104.7O23—P2—O22101.1 (3)
P2—C201—H201104.7O21—P2—C201115.3 (3)
C215—C202—C203119.7 (6)O23—P2—C201102.0 (3)
C215—C202—C201120.9 (6)O22—P2—C201103.4 (3)
C203—C202—C201119.4 (6)
N1—C101—C102—C115−64.1 (7)C204—C203—C208—C207−4.0 (10)
P1—C101—C102—C11564.7 (7)C207—C208—C209—C210177.9 (7)
N1—C101—C102—C103116.0 (6)C203—C208—C209—C210−1.4 (11)
P1—C101—C102—C103−115.2 (6)C208—C209—C210—C211−175.1 (7)
C115—C102—C103—C104−171.1 (6)C208—C209—C210—C2153.0 (11)
C101—C102—C103—C1048.8 (9)C209—C210—C211—C212−178.6 (8)
C115—C102—C103—C1088.0 (9)C215—C210—C211—C2123.1 (12)
C101—C102—C103—C108−172.1 (6)C210—C211—C212—C213−3.3 (14)
C102—C103—C104—C105−179.5 (7)C211—C212—C213—C2142.0 (13)
C108—C103—C104—C1051.4 (10)C212—C213—C214—C215−0.6 (12)
C103—C104—C105—C1061.9 (12)C203—C202—C215—C214175.3 (6)
C104—C105—C106—C107−2.7 (13)C201—C202—C215—C214−5.2 (10)
C105—C106—C107—C108−0.1 (13)C203—C202—C215—C210−4.4 (9)
C106—C107—C108—C109−175.2 (8)C201—C202—C215—C210175.2 (6)
C106—C107—C108—C1033.5 (11)C213—C214—C215—C202−179.2 (7)
C102—C103—C108—C109−4.5 (10)C213—C214—C215—C2100.5 (10)
C104—C103—C108—C109174.7 (6)C209—C210—C215—C202−0.2 (10)
C102—C103—C108—C107176.8 (6)C211—C210—C215—C202178.1 (6)
C104—C103—C108—C107−4.0 (9)C209—C210—C215—C214−179.8 (7)
C107—C108—C109—C110177.3 (7)C211—C210—C215—C214−1.6 (10)
C103—C108—C109—C110−1.3 (10)C223—C218—C219—C2202.5 (10)
C108—C109—C110—C111−176.0 (7)N2—C218—C219—C220−178.9 (6)
C108—C109—C110—C1153.7 (10)C218—C219—C220—C221−0.8 (11)
C109—C110—C111—C112−180.0 (8)C219—C220—C221—C222−0.7 (11)
C115—C110—C111—C1120.3 (12)C219—C220—C221—C224−179.5 (7)
C110—C111—C112—C113−0.4 (13)C220—C221—C222—C2230.4 (11)
C111—C112—C113—C1142.2 (13)C224—C221—C222—C223179.2 (7)
C112—C113—C114—C115−3.7 (12)C221—C222—C223—C2181.5 (12)
C103—C102—C115—C114175.6 (6)C219—C218—C223—C222−2.9 (11)
C101—C102—C115—C114−4.3 (10)N2—C218—C223—C222178.5 (7)
C103—C102—C115—C110−5.7 (9)C119—C118—N1—C10135.5 (9)
C101—C102—C115—C110174.4 (6)C123—C118—N1—C101−145.7 (6)
C113—C114—C115—C102−177.9 (7)C102—C101—N1—C118−113.7 (6)
C113—C114—C115—C1103.3 (10)P1—C101—N1—C118112.1 (5)
C111—C110—C115—C102179.5 (7)C219—C218—N2—C20130.8 (9)
C109—C110—C115—C102−0.2 (10)C223—C218—N2—C201−150.7 (6)
C111—C110—C115—C114−1.7 (10)C202—C201—N2—C218−107.5 (6)
C109—C110—C115—C114178.6 (6)P2—C201—N2—C218117.9 (5)
C123—C118—C119—C1200.4 (11)C16A—O12—P1—O11−32 (4)
N1—C118—C119—C120179.2 (7)C16B—O12—P1—O1116 (4)
C118—C119—C120—C121−1.4 (12)C16A—O12—P1—O13−158 (4)
C119—C120—C121—C1220.4 (12)C16B—O12—P1—O13−110 (4)
C119—C120—C121—C124−179.1 (7)C16A—O12—P1—C10195 (4)
C120—C121—C122—C1231.5 (12)C16B—O12—P1—C101143 (4)
C124—C121—C122—C123−179.1 (7)C117—O13—P1—O11−57.8 (7)
C119—C118—C123—C1221.4 (11)C117—O13—P1—O1266.3 (7)
N1—C118—C123—C122−177.4 (7)C117—O13—P1—C101174.4 (7)
C121—C122—C123—C118−2.4 (12)N1—C101—P1—O1134.0 (5)
N2—C201—C202—C215−59.1 (8)C102—C101—P1—O11−97.4 (5)
P2—C201—C202—C21570.3 (7)N1—C101—P1—O12−90.9 (4)
N2—C201—C202—C203120.4 (6)C102—C101—P1—O12137.7 (5)
P2—C201—C202—C203−110.2 (6)N1—C101—P1—O13161.5 (4)
C215—C202—C203—C204−172.4 (6)C102—C101—P1—O1330.1 (5)
C201—C202—C203—C2048.1 (9)C217—O23—P2—O21−54.9 (7)
C215—C202—C203—C2086.0 (9)C217—O23—P2—O2271.2 (6)
C201—C202—C203—C208−173.5 (6)C217—O23—P2—C201177.6 (6)
C202—C203—C204—C205−179.5 (7)C216—O22—P2—O21−32.4 (8)
C208—C203—C204—C2052.0 (10)C216—O22—P2—O23−160.7 (7)
C203—C204—C205—C2060.6 (12)C216—O22—P2—C20194.0 (8)
C204—C205—C206—C207−1.2 (13)N2—C201—P2—O2137.4 (5)
C205—C206—C207—C208−0.9 (14)C202—C201—P2—O21−95.6 (5)
C206—C207—C208—C209−175.8 (8)N2—C201—P2—O23166.7 (4)
C206—C207—C208—C2033.6 (12)C202—C201—P2—O2333.7 (6)
C202—C203—C208—C209−3.2 (10)N2—C201—P2—O22−88.7 (4)
C204—C203—C208—C209175.4 (6)C202—C201—P2—O22138.4 (5)
C202—C203—C208—C207177.5 (6)
D—H···AD—HH···AD···AD—H···A
N1—H1···O11i0.862.343.066 (6)143.
N2—H2···O21ii0.862.623.239 (7)130.
Table 1

Hydrogen-bond geometry (Å, °)

D—H⋯AD—HH⋯ADAD—H⋯A
N1—H1⋯O11i0.862.343.066 (6)143
N2—H2⋯O21ii0.862.623.239 (7)130

Symmetry codes: (i) ; (ii) .

  3 in total

Review 1.  Anti-tumor potential of bisphosphonates.

Authors:  J R Green
Journal:  Med Klin (Munich)       Date:  2000-10-15

2.  A short history of SHELX.

Authors:  George M Sheldrick
Journal:  Acta Crystallogr A       Date:  2007-12-21       Impact factor: 2.290

Review 3.  Aminophosphonic acids and derivatives. Synthesis and biological applications.

Authors:  F Orsini; G Sello; M Sisti
Journal:  Curr Med Chem       Date:  2010       Impact factor: 4.530

  3 in total

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