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Acta Crystallogr Sect E Struct Rep Online. 2009 January 1; 65(Pt 1): o78.
Published online 2008 December 10. doi:  10.1107/S1600536808040737
PMCID: PMC2967987

Cyclo­hexyl­methyl­ammonium N,N′-dicyclo­hexyl-N,N′-dimethyl-N′′-(2,2,2-trifluoro­acet­yl)phospho­nic triamide)

Abstract

In the salt, C7H16N+·C16H28F3N3O2P, the P atom shows tetra­hedral coordination. Two ion pairs are linked by N—H(...)O hydrogen bonds across a center of inversion. The phosphoryl and carbonyl groups are staggered [O—P—N—C = 64.8 (3)°].

Related literature

For alkali metal salts of dimethyl-N-trichlor­acetyl­amido­phosphate, see: Trush et al. (2005 [triangle]). For a related structure, see: Yazdanbakhsh & Sabbaghi (2007 [triangle]). For bond-length data, see: Corbridge (1995 [triangle]). For synthetic details, see: Shokol et al. (1969 [triangle]).

An external file that holds a picture, illustration, etc.
Object name is e-65-00o78-scheme1.jpg

Experimental

Crystal data

  • C7H16N+·C16H28F3N3O2P
  • M r = 496.59
  • Monoclinic, An external file that holds a picture, illustration, etc.
Object name is e-65-00o78-efi1.jpg
  • a = 9.183 (3) Å
  • b = 30.893 (7) Å
  • c = 9.241 (2) Å
  • β = 93.039 (7)°
  • V = 2617.9 (12) Å3
  • Z = 4
  • Mo Kα radiation
  • μ = 0.15 mm−1
  • T = 120 (2) K
  • 0.40 × 0.30 × 0.25 mm

Data collection

  • Bruker SMART 1000 CCD area-detector diffractometer
  • Absorption correction: multi-scan (SADABS; Sheldrick, 1996 [triangle]) T min = 0.947, T max = 0.969
  • 23153 measured reflections
  • 5148 independent reflections
  • 2673 reflections with I > 2σ(I)
  • R int = 0.064

Refinement

  • R[F 2 > 2σ(F 2)] = 0.060
  • wR(F 2) = 0.113
  • S = 1.08
  • 5148 reflections
  • 304 parameters
  • H-atom parameters constrained
  • Δρmax = 0.33 e Å−3
  • Δρmin = −0.32 e Å−3

Data collection: SMART (Bruker, 1998 [triangle]); cell refinement: SAINT-Plus (Bruker, 1998 [triangle]); data reduction: SAINT-Plus; program(s) used to solve structure: SHELXTL (Sheldrick, 2008 [triangle]); program(s) used to refine structure: SHELXTL; molecular graphics: DIAMOND (Brandenburg, 2001 [triangle]); software used to prepare material for publication: SHELXTL.

Table 1
Hydrogen-bond geometry (Å, °)

Supplementary Material

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536808040737/ng2519sup1.cif

Structure factors: contains datablocks I. DOI: 10.1107/S1600536808040737/ng2519Isup2.hkl

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

Acknowledgments

Support of this investigation by Ferdowsi University is gratefully acknowledged.

supplementary crystallographic information

Comment

Alkali onic-salts (Na+, Rb+) of dimethyl-N-trichloracetylamidophosphate [HL] were synthesized from aqueous-alcoholic solutions (Trush et al., 2005). Furthermore synthesis and investigation of onic-salts SbPh4+ allowed the determination of the preferable donor center of the deprotonated ligand (the oxygen atom of the phosphoryl group). Using non-coordinating ions PPh4+ permits to synthesize and characterize structurally of the "free" non-solvated [HL] anion. This information could be used for the molecular design of coordination systems based on carbacylamidophosphates. Here, we report on a new onic-salt (NH2CH3C6H11+) of [CF3CONPO(NCH3C6H11)2]- obtained from a reaction between LiOH and ligand. Single crystal of the product [NH2CH3C6H11][CF3CONPO(NCH3C6H11)2] was obtained from a solution of CH3OH—H2O (3:1) after a slow evaporation at room temperature. The proton transfer compound contains N-methyl cyclohexyl ammonium cation and deprotonated N'-2,2,2,-tri-flouroacetyl bis N"-methyl cyclohexyl phosphortriamide (Fig. 1). The structure of the title compound is composed of centrosymmetric dimmers (of two bridged cations between two anions) forming by intermolecular N+—H···OP hydrogen bonds (N···O = 2.771 (3) Å & 2.804 (3) Å), Fig. 2. The phosphoryl and the carbonyl groups in the structure are not in anti position (O(1)—P(1)—N(1)—C(1) = 64.8 (3)°) against the previous reported carbacylamidophosphates (Yazdanbakhsh & Sabbaghi, 2007). The phosphorus atom has slightly distorted tetrahedral configuration. The bond angles around P(1) atom is in the range of 100.79 (12)°-115.26 (13)° that the highest and the lowest values were obtained for the angles OPN(1)amide and N(2)aminePN(1)amide. The P(1)—N(1), P(1)—N(2) and P(1)—N(3) bond lengths are 1.629 (3) Å, 1.651 (2) Å and 1.643 (2) Å. They are significantly shorter than the typical P—N single bond length (1.77 Å) (Corbridge, 1995). Sum of the surrounding angles around N(2) and N(3) atoms are 353.5° and 356.0° that indicate some deviation from planarity. Furthermore the angle C(1)—N(1)—P(1) (123.4 (2)°) confirm the sp2 hybridization for the nitrogen atom. The PO bond length (1.511 (2) Å) is larger than the normal P?O bond length (1.45 Å). The CO group cooperates in weak C—H···O hydrogen bonds forming four hydrogen bonds with two neighboring cations (C(17)—H(17 C)···O(2)—C(1), C(17)···O(2) = 3.320 Å; C(18)—H(18 A)···O(2)—C(1), C(18)···O(2) = 3.214 Å; C(17)—H(17B)···O(2)—C(1), C(17)···O(2) = 3.365 Å; C(23)—H(23 A)···O(2)—C(1), C(23)···O(2) = 3.562 Å) (Fig. 3). Moreover, the C—H···F hydrogen bonds exist in the crystal network (C(5)—H(5 A)···F(3), C(5)···F(3) = 3.593 Å) (Fig. 4).

Experimental

CF3C(O)N(H)P(O)Cl2 was prepared similar to the literature method (Shokol et al., 1969) from the reaction of phosphorus pentachloride and 2,2,2-triflouoroacetamide in CCl4 and then the treatment of formic acid. Synthesis of CF3C(O)N(H)P(O)[N(CH3)(C6H11)]2 To a solution of (1.15 g, 5 mmol) triflouroacetyl phosphoramidic dichloride in CCl4 (20 ml), a solution of N-methylcyclohexylamine (2.26 g, 20 mmol) in CCl4 (10 ml) was added dropwise at 0°C. After 24 h stirring, the solvent was removed in vacuum and the solid product was washed with distilled water. The residue recrystallized in CH3CN. Anal. Calc. for C16H29F3N3O2P: C, 50.10; H, 7.56; N, 10.95. Found: C, 49.72; H, 7.84; N, 10.74%. 31P NMR ([D6]DMSO): 12.22. 13C NMR ([D6]DMSO): 54.35 (d, 2J(P,C) = 4.2 Hz 2 C, CH3), 30.22 (d, 2J(P,C) = 2.7 Hz, 2 C, CH), 27.30 (d, 3J(P,C) = 4.4 Hz, 4 C, CH2), 25.60 (s), 25.00 (s). 1H NMR ([D6]DMSO): 1.02 (m, 2 H), 1.17 (m, 4 H), 1.48 (m, 8 H), 1.73 (m, 4 H), 2.49 (s, 6 H), 3.27 (m, 2 H), 10.23 (b, 1 H, NH). IR (KBr, cm-1): 3067, 2925, 2802, 1735 (C?O), 1498, 1271, 1236, 1202, 1158, 1005, 980, 893, 851. Raman (cm-1): 2929, 2858, 1736, 1446, 1341, 1259, 1188, 1151, 1025, 857, 808, 742, 533, 493, 442, 308. MS (70 ev) m/z (%): 383 (20, [M]+), 368 (2, [M—CH3]+), 340 (36, [M—C(O)NH]+), 271 (35, [P(O)(N(CH3)(C6H11))2]+), 112 (100, [N(CH3)(C6H11)]+), 97 (58, [CF3C(O)]+), 69 (98, [CF3]+). Synthesis of [NH2CH3C6H11][CF3CONPO(NCH3C6H11)2] Lithium hydroxide (0.04 g, 1.6 mmol) was added to a solution of CF3CONHPO(NCH3C6H11)2 (0.62 g, 1.6 mmol) in 10 ml of aqueous methanol (1:3). The solution was stirred at room temperature for 24 h. Colorless single-crystal was obtained after a week at room temperature. Yield: 0.48 g, 60%. Anal. Calc. for C23H44F3N4O2P: C, 55.59; H, 8.86; N, 11.28. Found: C, 55.47; H, 8.80; N, 11.52%. 31P NMR ([D6]DMSO): 18.61. 13C NMR ([D6]DMSO): 23.84 (s), 24.83 (s), 25.37 (s), 25.87 (s), 27.20 (d, J(P,C)=3.9 Hz), 28.69 (s), 29.70 (s), 30.38 (s), 53.48 (s), 56.72 (s), 137.58 (dq, CF3), 157.14 (q, C?O). IR (KBr, cm-1): 3338, 3058, 2936, 2849, 2690, 2624, 1689 (C?O), 1631, 1601, 1553, 1520, 1430, 1375, 1220, 1067, 987, 896, 769, 682.

Refinement

The hydrogen atoms of NH2 group were found in difference Fourier synthesis. The H(C) atom positions were calculated. All hydrogen atoms were refined in isotropic approximation in riding model with with the Uiso(H) parameters equal to 1.2 Ueq(Ci), for methyl groups equal to 1.5 Ueq(Cii), where U(Ci) and U(Cii) are respectively the equivalent thermal parameters of the carbon atoms to which corresponding H atoms are bonded.

Figures

Fig. 1.
General view of [NH2CH3C6H11][CF3CONPO(NCH3C6H11)2] in representation of atoms via thermal ellipsoids at 50% probability level (all hydrogen atoms except H(4 N A) and H(4NB) are omitted for clarity).
Fig. 2.
The fragment of crystal packing of [NH2CH3C6H11][CF3CONPO(NCH3C6H11)2] along the crystallographic plane ab (all hydrogen atoms except H(4 N A)and H(4NB) are omitted for clarity).
Fig. 3.
A view of C—H···O hydrogen bonds in [NH2CH3C6H11][CF3CONPO(NCH3C6H11)2].
Fig. 4.
A view of C—H···F hydrogen bonds in [NH2CH3C6H11][CF3CONPO(NCH3C6H11)2].

Crystal data

C7H16N+·C16H28F3N3O2PF(000) = 1072
Mr = 496.59Dx = 1.260 Mg m3
Monoclinic, P21/cMo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ybcCell parameters from 365 reflections
a = 9.183 (3) Åθ = 2–25°
b = 30.893 (7) ŵ = 0.15 mm1
c = 9.241 (2) ÅT = 120 K
β = 93.039 (7)°Prism, colorless
V = 2617.9 (12) Å30.40 × 0.30 × 0.25 mm
Z = 4

Data collection

Bruker SMART 1000 CCD area-detector diffractometer5148 independent reflections
Radiation source: fine-focus sealed tube2673 reflections with I > 2σ(I)
graphiteRint = 0.064
[var phi] and ω scansθmax = 26.0°, θmin = 2.2°
Absorption correction: multi-scan (SADABS; Sheldrick, 1996)h = −11→11
Tmin = 0.947, Tmax = 0.969k = −38→37
23153 measured reflectionsl = −11→11

Refinement

Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.060Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.113H-atom parameters constrained
S = 1.08w = 1/[σ2(Fo2) + (0.0126P)2 + 2.4P] where P = (Fo2 + 2Fc2)/3
5148 reflections(Δ/σ)max = 0.004
304 parametersΔρmax = 0.33 e Å3
0 restraintsΔρmin = −0.32 e Å3

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.
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.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2)

xyzUiso*/Ueq
P10.59626 (9)0.11209 (3)0.00482 (9)0.0277 (2)
F10.8519 (2)0.13212 (8)−0.3599 (2)0.0674 (7)
F21.0171 (2)0.15024 (6)−0.2005 (2)0.0605 (6)
F31.0165 (2)0.08688 (6)−0.2932 (2)0.0498 (5)
O10.5406 (2)0.06625 (6)0.0163 (2)0.0306 (5)
O20.9035 (2)0.07648 (7)−0.0331 (2)0.0381 (6)
N10.7111 (3)0.12011 (8)−0.1208 (3)0.0285 (6)
N20.4692 (3)0.14801 (7)−0.0417 (3)0.0250 (6)
N30.6583 (3)0.12719 (7)0.1670 (3)0.0280 (6)
N40.3080 (3)0.01010 (8)0.0416 (3)0.0300 (6)
H4NA0.38100.03190.04270.029 (9)*
H4NB0.3547−0.01720.03500.051 (11)*
C10.8390 (3)0.10240 (10)−0.1197 (3)0.0302 (8)
C20.9298 (3)0.11769 (11)−0.2449 (4)0.0330 (8)
C30.3392 (3)0.14748 (10)0.0448 (3)0.0348 (8)
H3A0.29590.17650.04550.052*
H3B0.36720.13870.14440.052*
H3C0.26790.12690.00230.052*
C40.4473 (3)0.16366 (9)−0.1935 (3)0.0259 (7)
H4A0.54660.1700−0.22770.031*
C50.3796 (3)0.13003 (10)−0.2974 (3)0.0317 (8)
H5A0.28080.1225−0.26740.038*
H5B0.43950.1034−0.29290.038*
C60.3694 (4)0.14714 (11)−0.4532 (3)0.0411 (9)
H6A0.46890.1512−0.48730.049*
H6B0.31860.1256−0.51700.049*
C70.2875 (4)0.18992 (11)−0.4631 (4)0.0443 (9)
H7A0.28890.2012−0.56330.053*
H7B0.18450.1851−0.44060.053*
C80.3553 (4)0.22305 (10)−0.3587 (4)0.0411 (9)
H8A0.29650.2499−0.36380.049*
H8B0.45470.2302−0.38770.049*
C90.3634 (4)0.20606 (10)−0.2029 (3)0.0340 (8)
H9A0.41250.2277−0.13810.041*
H9B0.26360.2015−0.17030.041*
C100.6862 (4)0.09517 (10)0.2826 (3)0.0391 (9)
H10A0.68660.10960.37700.059*
H10B0.78110.08150.27090.059*
H10C0.60950.07310.27690.059*
C110.7380 (3)0.16853 (9)0.1839 (3)0.0292 (8)
H11A0.72510.18400.08890.035*
C120.9025 (3)0.16295 (10)0.2143 (4)0.0357 (8)
H12A0.92040.14770.30790.043*
H12B0.94240.14490.13740.043*
C130.9808 (4)0.20648 (11)0.2202 (4)0.0472 (10)
H13A1.08590.20190.24480.057*
H13B0.97100.22050.12390.057*
C140.9170 (4)0.23579 (11)0.3327 (4)0.0504 (10)
H14A0.96580.26430.33140.060*
H14B0.93570.22300.43020.060*
C150.7527 (4)0.24187 (11)0.3035 (4)0.0482 (10)
H15A0.73420.25740.21060.058*
H15B0.71330.25970.38150.058*
C160.6749 (4)0.19793 (10)0.2965 (4)0.0403 (9)
H16A0.68490.18380.39270.048*
H16B0.56970.20240.27220.048*
C170.2070 (3)0.01882 (10)−0.0858 (3)0.0367 (9)
H17A0.26350.0236−0.17150.055*
H17B0.14900.0447−0.06740.055*
H17C0.1420−0.0060−0.10260.055*
C180.2394 (3)0.00821 (10)0.1845 (3)0.0299 (8)
H18A0.1527−0.01140.17450.036*
C190.3478 (4)−0.01118 (10)0.2964 (3)0.0364 (9)
H19A0.43630.00710.30500.044*
H19B0.3770−0.04040.26460.044*
C200.2801 (4)−0.01433 (11)0.4438 (3)0.0430 (9)
H20A0.1985−0.03530.43750.052*
H20B0.3541−0.02520.51670.052*
C210.2246 (4)0.02903 (11)0.4918 (4)0.0454 (10)
H21A0.30800.04890.51070.054*
H21B0.17450.02540.58330.054*
C220.1197 (4)0.04878 (11)0.3780 (3)0.0437 (9)
H22A0.09020.07790.41020.052*
H22B0.03090.03060.36740.052*
C230.1878 (4)0.05249 (10)0.2320 (3)0.0357 (8)
H23A0.11510.06410.15900.043*
H23B0.27140.07280.23970.043*

Atomic displacement parameters (Å2)

U11U22U33U12U13U23
P10.0272 (5)0.0257 (5)0.0301 (5)−0.0010 (4)0.0017 (4)0.0008 (4)
F10.0449 (13)0.112 (2)0.0460 (13)0.0198 (13)0.0116 (11)0.0314 (13)
F20.0560 (14)0.0487 (13)0.0793 (16)−0.0186 (11)0.0286 (12)−0.0111 (12)
F30.0466 (13)0.0509 (13)0.0535 (13)0.0069 (10)0.0170 (10)−0.0057 (11)
O10.0307 (12)0.0241 (12)0.0372 (13)−0.0017 (10)0.0042 (10)0.0018 (10)
O20.0367 (14)0.0360 (14)0.0416 (14)0.0078 (11)0.0014 (11)0.0029 (11)
N10.0212 (14)0.0337 (16)0.0304 (15)0.0044 (12)0.0008 (12)0.0002 (12)
N20.0265 (15)0.0242 (14)0.0249 (14)−0.0005 (11)0.0056 (12)0.0033 (11)
N30.0345 (16)0.0223 (14)0.0268 (15)−0.0040 (12)−0.0019 (12)0.0018 (12)
N40.0331 (16)0.0260 (16)0.0308 (16)0.0019 (13)0.0009 (13)0.0012 (12)
C10.031 (2)0.0290 (19)0.0299 (19)−0.0028 (16)−0.0004 (16)−0.0024 (15)
C20.0264 (19)0.032 (2)0.040 (2)0.0042 (16)−0.0021 (16)−0.0007 (16)
C30.036 (2)0.0320 (19)0.037 (2)0.0024 (16)0.0092 (17)0.0039 (16)
C40.0234 (17)0.0253 (17)0.0294 (18)0.0005 (14)0.0044 (14)0.0060 (14)
C50.0325 (19)0.0283 (18)0.0338 (19)0.0005 (15)−0.0027 (15)0.0034 (15)
C60.050 (2)0.039 (2)0.034 (2)−0.0105 (18)−0.0064 (17)−0.0030 (17)
C70.040 (2)0.048 (2)0.044 (2)−0.0035 (18)−0.0075 (18)0.0165 (19)
C80.044 (2)0.032 (2)0.047 (2)0.0049 (17)−0.0007 (18)0.0093 (17)
C90.037 (2)0.0297 (19)0.036 (2)−0.0004 (15)0.0036 (16)0.0043 (16)
C100.054 (2)0.0310 (19)0.031 (2)−0.0043 (17)−0.0053 (17)0.0073 (16)
C110.035 (2)0.0261 (18)0.0258 (18)−0.0052 (15)−0.0029 (15)0.0027 (14)
C120.036 (2)0.038 (2)0.033 (2)−0.0044 (16)0.0010 (16)−0.0048 (16)
C130.043 (2)0.053 (2)0.045 (2)−0.0163 (19)−0.0068 (19)0.0032 (19)
C140.060 (3)0.035 (2)0.054 (3)−0.0102 (19)−0.015 (2)−0.0093 (19)
C150.053 (3)0.036 (2)0.055 (3)0.0040 (18)−0.005 (2)−0.0125 (19)
C160.040 (2)0.033 (2)0.047 (2)0.0020 (17)−0.0012 (18)−0.0059 (17)
C170.041 (2)0.041 (2)0.0278 (19)0.0017 (17)−0.0061 (16)0.0043 (16)
C180.032 (2)0.0329 (19)0.0247 (18)−0.0010 (15)0.0033 (15)0.0027 (15)
C190.041 (2)0.031 (2)0.036 (2)0.0006 (16)−0.0051 (17)0.0008 (16)
C200.058 (3)0.038 (2)0.032 (2)−0.0026 (18)−0.0092 (18)0.0079 (17)
C210.062 (3)0.047 (2)0.027 (2)−0.001 (2)0.0042 (18)−0.0015 (17)
C220.051 (2)0.045 (2)0.036 (2)0.0031 (18)0.0105 (18)−0.0010 (18)
C230.042 (2)0.034 (2)0.031 (2)0.0049 (16)−0.0007 (16)0.0026 (15)

Geometric parameters (Å, °)

P1—O11.511 (2)C10—H10B0.9800
P1—N11.629 (3)C10—H10C0.9800
P1—N31.643 (2)C11—C161.519 (4)
P1—N21.651 (2)C11—C121.531 (4)
F1—C21.326 (3)C11—H11A1.0000
F2—C21.337 (3)C12—C131.525 (4)
F3—C21.333 (3)C12—H12A0.9900
O2—C11.258 (3)C12—H12B0.9900
N1—C11.295 (4)C13—C141.520 (5)
N2—C31.472 (3)C13—H13A0.9900
N2—C41.487 (3)C13—H13B0.9900
N3—C101.468 (4)C14—C151.530 (5)
N3—C111.476 (3)C14—H14A0.9900
N4—C171.484 (4)C14—H14B0.9900
N4—C181.494 (4)C15—C161.534 (4)
N4—H4NA0.9502C15—H15A0.9900
N4—H4NB0.9499C15—H15B0.9900
C1—C21.536 (4)C16—H16A0.9900
C3—H3A0.9800C16—H16B0.9900
C3—H3B0.9800C17—H17A0.9800
C3—H3C0.9800C17—H17B0.9800
C4—C91.520 (4)C17—H17C0.9800
C4—C51.525 (4)C18—C231.520 (4)
C4—H4A1.0000C18—C191.520 (4)
C5—C61.531 (4)C18—H18A1.0000
C5—H5A0.9900C19—C201.530 (4)
C5—H5B0.9900C19—H19A0.9900
C6—C71.521 (4)C19—H19B0.9900
C6—H6A0.9900C20—C211.509 (4)
C6—H6B0.9900C20—H20A0.9900
C7—C81.517 (4)C20—H20B0.9900
C7—H7A0.9900C21—C221.516 (4)
C7—H7B0.9900C21—H21A0.9900
C8—C91.531 (4)C21—H21B0.9900
C8—H8A0.9900C22—C231.521 (4)
C8—H8B0.9900C22—H22A0.9900
C9—H9A0.9900C22—H22B0.9900
C9—H9B0.9900C23—H23A0.9900
C10—H10A0.9800C23—H23B0.9900
O1—P1—N1115.26 (13)N3—C11—C12113.6 (2)
O1—P1—N3107.72 (12)C16—C11—C12110.5 (3)
N1—P1—N3113.65 (13)N3—C11—H11A106.5
O1—P1—N2114.29 (12)C16—C11—H11A106.5
N1—P1—N2100.79 (12)C12—C11—H11A106.5
N3—P1—N2104.66 (12)C13—C12—C11111.5 (3)
C1—N1—P1123.4 (2)C13—C12—H12A109.3
C3—N2—C4116.3 (2)C11—C12—H12A109.3
C3—N2—P1115.67 (19)C13—C12—H12B109.3
C4—N2—P1121.53 (19)C11—C12—H12B109.3
C10—N3—C11116.1 (2)H12A—C12—H12B108.0
C10—N3—P1120.7 (2)C14—C13—C12110.6 (3)
C11—N3—P1119.19 (19)C14—C13—H13A109.5
C17—N4—C18115.7 (2)C12—C13—H13A109.5
C17—N4—H4NA106.9C14—C13—H13B109.5
C18—N4—H4NA110.4C12—C13—H13B109.5
C17—N4—H4NB112.1H13A—C13—H13B108.1
C18—N4—H4NB103.6C13—C14—C15111.4 (3)
H4NA—N4—H4NB108.1C13—C14—H14A109.3
O2—C1—N1132.1 (3)C15—C14—H14A109.3
O2—C1—C2114.8 (3)C13—C14—H14B109.3
N1—C1—C2113.1 (3)C15—C14—H14B109.3
F1—C2—F3106.1 (3)H14A—C14—H14B108.0
F1—C2—F2106.4 (3)C14—C15—C16110.6 (3)
F3—C2—F2106.3 (3)C14—C15—H15A109.5
F1—C2—C1114.6 (3)C16—C15—H15A109.5
F3—C2—C1113.0 (3)C14—C15—H15B109.5
F2—C2—C1109.9 (3)C16—C15—H15B109.5
N2—C3—H3A109.5H15A—C15—H15B108.1
N2—C3—H3B109.5C11—C16—C15111.4 (3)
H3A—C3—H3B109.5C11—C16—H16A109.4
N2—C3—H3C109.5C15—C16—H16A109.4
H3A—C3—H3C109.5C11—C16—H16B109.4
H3B—C3—H3C109.5C15—C16—H16B109.4
N2—C4—C9112.1 (2)H16A—C16—H16B108.0
N2—C4—C5113.8 (2)N4—C17—H17A109.5
C9—C4—C5111.3 (2)N4—C17—H17B109.5
N2—C4—H4A106.4H17A—C17—H17B109.5
C9—C4—H4A106.4N4—C17—H17C109.5
C5—C4—H4A106.4H17A—C17—H17C109.5
C4—C5—C6111.1 (2)H17B—C17—H17C109.5
C4—C5—H5A109.4N4—C18—C23111.9 (2)
C6—C5—H5A109.4N4—C18—C19108.9 (2)
C4—C5—H5B109.4C23—C18—C19111.2 (3)
C6—C5—H5B109.4N4—C18—H18A108.2
H5A—C5—H5B108.0C23—C18—H18A108.2
C7—C6—C5111.2 (3)C19—C18—H18A108.2
C7—C6—H6A109.4C18—C19—C20110.4 (3)
C5—C6—H6A109.4C18—C19—H19A109.6
C7—C6—H6B109.4C20—C19—H19A109.6
C5—C6—H6B109.4C18—C19—H19B109.6
H6A—C6—H6B108.0C20—C19—H19B109.6
C8—C7—C6111.3 (3)H19A—C19—H19B108.1
C8—C7—H7A109.4C21—C20—C19111.4 (3)
C6—C7—H7A109.4C21—C20—H20A109.3
C8—C7—H7B109.4C19—C20—H20A109.3
C6—C7—H7B109.4C21—C20—H20B109.3
H7A—C7—H7B108.0C19—C20—H20B109.3
C7—C8—C9111.4 (3)H20A—C20—H20B108.0
C7—C8—H8A109.3C20—C21—C22111.5 (3)
C9—C8—H8A109.3C20—C21—H21A109.3
C7—C8—H8B109.3C22—C21—H21A109.3
C9—C8—H8B109.3C20—C21—H21B109.3
H8A—C8—H8B108.0C22—C21—H21B109.3
C4—C9—C8110.4 (3)H21A—C21—H21B108.0
C4—C9—H9A109.6C21—C22—C23111.7 (3)
C8—C9—H9A109.6C21—C22—H22A109.3
C4—C9—H9B109.6C23—C22—H22A109.3
C8—C9—H9B109.6C21—C22—H22B109.3
H9A—C9—H9B108.1C23—C22—H22B109.3
N3—C10—H10A109.5H22A—C22—H22B107.9
N3—C10—H10B109.5C18—C23—C22109.7 (3)
H10A—C10—H10B109.5C18—C23—H23A109.7
N3—C10—H10C109.5C22—C23—H23A109.7
H10A—C10—H10C109.5C18—C23—H23B109.7
H10B—C10—H10C109.5C22—C23—H23B109.7
N3—C11—C16112.6 (3)H23A—C23—H23B108.2
O1—P1—N1—C1−64.8 (3)C4—C5—C6—C7−54.9 (4)
N3—P1—N1—C160.3 (3)C5—C6—C7—C855.0 (4)
N2—P1—N1—C1171.7 (2)C6—C7—C8—C9−55.9 (4)
O1—P1—N2—C351.3 (2)N2—C4—C9—C8174.9 (2)
N1—P1—N2—C3175.5 (2)C5—C4—C9—C8−56.4 (3)
N3—P1—N2—C3−66.3 (2)C7—C8—C9—C456.4 (4)
O1—P1—N2—C4−99.4 (2)C10—N3—C11—C16−75.6 (3)
N1—P1—N2—C424.9 (2)P1—N3—C11—C16126.7 (2)
N3—P1—N2—C4143.0 (2)C10—N3—C11—C1251.0 (4)
O1—P1—N3—C1014.9 (3)P1—N3—C11—C12−106.8 (3)
N1—P1—N3—C10−114.1 (2)N3—C11—C12—C13176.0 (3)
N2—P1—N3—C10136.9 (2)C16—C11—C12—C13−56.3 (4)
O1—P1—N3—C11171.6 (2)C11—C12—C13—C1456.4 (4)
N1—P1—N3—C1142.6 (3)C12—C13—C14—C15−56.2 (4)
N2—P1—N3—C11−66.4 (2)C13—C14—C15—C1655.9 (4)
P1—N1—C1—O21.1 (5)N3—C11—C16—C15−175.8 (3)
P1—N1—C1—C2−176.0 (2)C12—C11—C16—C1556.0 (4)
O2—C1—C2—F1157.9 (3)C14—C15—C16—C11−55.9 (4)
N1—C1—C2—F1−24.4 (4)C17—N4—C18—C23−69.9 (3)
O2—C1—C2—F336.2 (4)C17—N4—C18—C19166.7 (3)
N1—C1—C2—F3−146.1 (3)N4—C18—C19—C20−179.0 (3)
O2—C1—C2—F2−82.3 (3)C23—C18—C19—C2057.2 (3)
N1—C1—C2—F295.3 (3)C18—C19—C20—C21−55.3 (4)
C3—N2—C4—C948.6 (3)C19—C20—C21—C2254.5 (4)
P1—N2—C4—C9−161.0 (2)C20—C21—C22—C23−55.5 (4)
C3—N2—C4—C5−78.8 (3)N4—C18—C23—C22−179.7 (3)
P1—N2—C4—C571.7 (3)C19—C18—C23—C22−57.7 (4)
N2—C4—C5—C6−176.2 (2)C21—C22—C23—C1856.5 (4)
C9—C4—C5—C656.0 (3)

Hydrogen-bond geometry (Å, °)

D—H···AD—HH···AD···AD—H···A
N4—H4NA···O10.951.842.771 (3)167
N4—H4NB···O1i0.951.872.804 (3)168

Symmetry codes: (i) −x+1, −y, −z.

Footnotes

Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: NG2519).

References

  • Brandenburg, K. (2001). DIAMOND Crystal Impact GbR, Bonn, Germany.
  • Bruker (1998). SAINT-Plus and SMART Bruker AXS Inc., Madison, Wisconsin, USA.
  • Corbridge, D. E. C. (1995). Phosphorus, an Outline of its Chemistry, Biochemistry and Technology, 5th ed., p. 1179. New York: Elsevier Science.
  • Sheldrick, G. M. (1996). SADABS University of Göttingen, Germany.
  • Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. [PubMed]
  • Shokol, V. A., Kisilenko, A. A. & Derkach, G. I. (1969). Zh. Obshch. Khim.39, 1492–1497.
  • Trush, V. A., Gubina, K. E., Amirkhanov, V. M., Swiatek-Kozlowska, J. & Domasevitch, K. V. (2005). Polyhedron, 24, 1007–1014.
  • Yazdanbakhsh, M. & Sabbaghi, F. (2007). Acta Cryst. E63, o4318.

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