Literature DB >> 21580348

1-[3,5-Bis(4-fluoro-phen-yl)-4,5-dihydro-1H-pyrazol-1-yl]ethanone.

Hoong-Kun Fun, Madhukar Hemamalini, S Samshuddin, B Narayana, H S Yathirajan.   

Abstract

In the asymmetric unit of the title compound, C(17)H(14)F(2)N(2)O, there are three independent mol-ecules (A, B and C) which differ slightly in the relative orientations of the two fluoro-phenyl rings. In mol-ecules A and C one of the fluoro-phenyl rings is disordered over two positions, with occupancy ratios of 0.72 (2):0.28 (2) for mol-ecule A and 0.67 (2):0.33 (2) for mol-ecule C. The dihedral angle between the two fluoro-phenyl rings in the independent mol-ecules lie in the range 70.3 (3)-84.0 (3)°. In the crystal structure, the mol-ecules are linked via inter-molecular C-H⋯O and C-H⋯F hydrogen bonds and π⋯π stacking inter-actions [centroid-centroid distance = 3.7508 (13) Å], forming a three-dimensional network.

Entities:  

Year:  2010        PMID: 21580348      PMCID: PMC2983722          DOI: 10.1107/S1600536810004435

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


Related literature

For the biological activity of pyrazoline derivatives, see: Amir et al. (2008 ▶); Garge et al. (1971 ▶); Hes et al. (1978 ▶); Manna et al. (2005 ▶); Regaila et al. (1979 ▶). For the role of pyrazolines in organic synthesis, see: Bhaskarreddy et al. (1997 ▶); Klimova et al. (1999 ▶). For related structures, see: Anuradha et al. (2008 ▶); Jian et al. (2006 ▶); Jian & Wang (2006 ▶); Lu et al. (2008 ▶); Wang et al. (2005 ▶). For the stability of the temperature controller used in the data collection, see: Cosier & Glazer (1986 ▶).

Experimental

Crystal data

C17H14F2N2O M = 300.30 Triclinic, a = 7.1447 (1) Å b = 17.2332 (3) Å c = 18.4871 (4) Å α = 102.880 (1)° β = 97.941 (1)° γ = 96.373 (1)° V = 2173.86 (7) Å3 Z = 6 Mo Kα radiation μ = 0.11 mm−1 T = 100 K 0.40 × 0.27 × 0.21 mm

Data collection

Bruker SMART APEXII CCD area-detector diffractometer Absorption correction: multi-scan (SADABS; Bruker, 2009 ▶) T min = 0.960, T max = 0.978 40717 measured reflections 12544 independent reflections 6078 reflections with I > 2σ(I) R int = 0.039

Refinement

R[F 2 > 2σ(F 2)] = 0.078 wR(F 2) = 0.242 S = 1.03 12544 reflections 726 parameters 510 restraints H-atom parameters constrained Δρmax = 0.32 e Å−3 Δρmin = −0.22 e Å−3 Data collection: APEX2 (Bruker, 2009 ▶); cell refinement: SAINT (Bruker, 2009 ▶); data reduction: SAINT; program(s) used to solve structure: SHELXTL (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXTL; molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL and PLATON (Spek, 2009 ▶). Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536810004435/ci5026sup1.cif Structure factors: contains datablocks I. DOI: 10.1107/S1600536810004435/ci5026Isup2.hkl Additional supplementary materials: crystallographic information; 3D view; checkCIF report
C17H14F2N2OZ = 6
Mr = 300.30F(000) = 936
Triclinic, P1Dx = 1.376 Mg m3
Hall symbol: -P 1Mo Kα radiation, λ = 0.71073 Å
a = 7.1447 (1) ÅCell parameters from 8334 reflections
b = 17.2332 (3) Åθ = 2.9–30.0°
c = 18.4871 (4) ŵ = 0.11 mm1
α = 102.880 (1)°T = 100 K
β = 97.941 (1)°Block, colourless
γ = 96.373 (1)°0.40 × 0.27 × 0.21 mm
V = 2173.86 (7) Å3
Bruker SMART APEXII CCD area-detector diffractometer12544 independent reflections
Radiation source: fine-focus sealed tube6078 reflections with I > 2σ(I)
graphiteRint = 0.039
φ and ω scansθmax = 30.0°, θmin = 1.2°
Absorption correction: multi-scan (SADABS; Bruker, 2009)h = −10→10
Tmin = 0.960, Tmax = 0.978k = −22→24
40717 measured reflectionsl = −20→25
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.078Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.242H-atom parameters constrained
S = 1.03w = 1/[σ2(Fo2) + (0.1087P)2 + 0.1919P] where P = (Fo2 + 2Fc2)/3
12544 reflections(Δ/σ)max = 0.002
726 parametersΔρmax = 0.32 e Å3
510 restraintsΔρmin = −0.22 e Å3
Experimental. The crystal was placed in the cold stream of an Oxford Cryosystems Cobra open-flow nitrogen cryostat (Cosier & Glazer, 1986) operating at 100.0 (1) k.
Geometry. All s.u.'s (except the s.u. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell s.u.'s are taken into account individually in the estimation of s.u.'s in distances, angles and torsion angles; correlations between s.u.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell s.u.'s is used for estimating s.u.'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 > 2σ(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)
F2A0.4613 (3)0.09609 (11)0.49187 (11)0.1240 (6)
O1A0.9145 (2)−0.05242 (8)0.25336 (9)0.0730 (5)
N1A0.9407 (2)0.11515 (8)0.17523 (8)0.0456 (4)
N2A0.9414 (2)0.06841 (9)0.22753 (8)0.0512 (4)
F1A1.1097 (13)0.42500 (19)0.0516 (2)0.0741 (14)0.72 (2)
C1A1.1010 (14)0.3317 (5)0.2059 (4)0.0436 (16)0.72 (2)
H1AA1.12660.34560.25830.052*0.72 (2)
C2A1.1175 (13)0.3910 (4)0.1671 (3)0.0483 (15)0.72 (2)
H2AA1.14740.44510.19220.058*0.72 (2)
C3A1.0883 (11)0.3676 (3)0.0906 (3)0.0477 (12)0.72 (2)
C4A1.0423 (10)0.2887 (3)0.0501 (3)0.0489 (11)0.72 (2)
H4AA1.02520.2754−0.00220.059*0.72 (2)
C5A1.0224 (9)0.2300 (4)0.0894 (4)0.0431 (11)0.72 (2)
H5AA0.99270.17610.06360.052*0.72 (2)
C6A1.0466 (13)0.2513 (4)0.1680 (4)0.0364 (12)0.72 (2)
F1X1.002 (4)0.4294 (6)0.0552 (7)0.097 (5)0.28 (2)
C1X1.055 (3)0.3297 (12)0.2090 (11)0.041 (4)0.28 (2)
H1XA1.08060.34440.26140.050*0.28 (2)
C2X1.062 (3)0.3898 (12)0.1703 (9)0.052 (4)0.28 (2)
H2XA1.10140.44320.19640.062*0.28 (2)
C3X1.011 (3)0.3712 (8)0.0948 (8)0.061 (4)0.28 (2)
C4X0.966 (4)0.2924 (8)0.0541 (9)0.071 (4)0.28 (2)
H4XA0.93970.27910.00180.086*0.28 (2)
C5X0.962 (4)0.2339 (10)0.0943 (10)0.066 (5)0.28 (2)
H5XA0.92260.18100.06710.079*0.28 (2)
C6X1.012 (4)0.2471 (11)0.1724 (11)0.054 (5)0.28 (2)
C7A1.0168 (3)0.18737 (10)0.21017 (10)0.0451 (4)
C8A1.0795 (3)0.19916 (12)0.29317 (11)0.0615 (6)
H8AA1.01700.23990.32180.074*
H8AB1.21680.21430.30710.074*
C9A1.0154 (3)0.11514 (11)0.30573 (10)0.0550 (5)
H9AA1.12760.09370.32580.066*
C10A0.8666 (3)0.11110 (11)0.35581 (10)0.0523 (5)
C11A0.8752 (3)0.06103 (12)0.40491 (12)0.0629 (6)
H11A0.97470.03070.40760.075*
C12A0.7375 (4)0.05556 (14)0.45006 (14)0.0797 (7)
H12A0.74320.02150.48270.096*
C13A0.5947 (4)0.10047 (15)0.44597 (15)0.0770 (7)
C14A0.5789 (3)0.15065 (14)0.39909 (13)0.0708 (6)
H14A0.47830.18050.39730.085*
C15A0.7175 (3)0.15619 (12)0.35381 (11)0.0613 (6)
H15A0.71020.19070.32170.074*
C16A0.8997 (3)−0.01320 (11)0.20599 (11)0.0527 (5)
C17A0.8353 (3)−0.04987 (11)0.12432 (12)0.0621 (6)
H17A0.8408−0.10660.11420.093*
H17B0.9171−0.02550.09600.093*
H17C0.7064−0.04120.11000.093*
F1B0.6346 (2)−0.09751 (7)0.94366 (8)0.0912 (5)
F2B1.2124 (3)0.23406 (10)0.50335 (11)0.1207 (6)
O1B0.7863 (3)0.38636 (8)0.74826 (9)0.0774 (5)
N1B0.7612 (2)0.21708 (8)0.82439 (8)0.0474 (4)
N2B0.7549 (2)0.26485 (9)0.77306 (9)0.0544 (4)
C1B0.5996 (3)0.00176 (11)0.79147 (11)0.0512 (5)
H1BA0.5638−0.01100.73940.061*
C2B0.5897 (3)−0.05886 (11)0.82958 (12)0.0572 (5)
H2BA0.5488−0.11220.80380.069*
C3B0.6414 (3)−0.03835 (11)0.90579 (12)0.0575 (5)
C4B0.6973 (3)0.03970 (11)0.94695 (12)0.0590 (5)
H4BA0.72710.05180.99920.071*
C5B0.7078 (3)0.09941 (11)0.90838 (11)0.0516 (5)
H5BA0.74580.15260.93510.062*
C6B0.6628 (2)0.08176 (10)0.83014 (10)0.0437 (4)
C7B0.6789 (3)0.14553 (11)0.78974 (10)0.0458 (4)
C8B0.6035 (3)0.13564 (12)0.70780 (11)0.0644 (6)
H8BA0.46530.12290.69730.077*
H8BB0.65760.09380.67650.077*
C9B0.6710 (3)0.21961 (12)0.69536 (11)0.0564 (5)
H9BA0.55990.24300.67730.068*
C10B0.8155 (3)0.22149 (11)0.64289 (10)0.0517 (5)
C11B0.8024 (3)0.27024 (12)0.59256 (11)0.0616 (5)
H11B0.70220.30020.59000.074*
C12B0.9375 (4)0.27470 (14)0.54602 (13)0.0791 (7)
H12B0.92950.30770.51250.095*
C13B1.0813 (4)0.23014 (14)0.55029 (14)0.0749 (7)
C14B1.1007 (3)0.18113 (13)0.59823 (13)0.0694 (6)
H14B1.20150.15140.59980.083*
C15B0.9645 (3)0.17688 (12)0.64496 (11)0.0596 (5)
H15B0.97410.14350.67810.071*
C16B0.8064 (3)0.34635 (11)0.79500 (12)0.0595 (5)
C17B0.8895 (4)0.38121 (11)0.87589 (12)0.0752 (7)
H17D0.93140.43780.88370.113*
H17E0.99640.35510.88960.113*
H17F0.79440.37310.90650.113*
F2C0.1119 (3)0.42973 (11)0.48513 (12)0.1249 (6)
O1C0.6321 (3)0.28974 (9)0.26097 (9)0.0863 (6)
N1C0.6015 (2)0.45434 (8)0.18017 (8)0.0458 (4)
N2C0.6263 (2)0.40862 (9)0.23277 (9)0.0518 (4)
F1C0.6000 (10)0.7682 (4)0.0556 (5)0.0767 (13)0.67 (2)
C1C0.712 (2)0.6756 (5)0.2086 (5)0.0469 (16)0.67 (2)
H1CA0.77130.68960.25880.056*0.67 (2)
C2C0.6924 (16)0.7348 (5)0.1691 (4)0.0506 (17)0.67 (2)
H2CA0.73180.78890.19260.061*0.67 (2)
C3C0.6135 (11)0.7112 (4)0.0953 (4)0.0487 (13)0.67 (2)
C4C0.5451 (11)0.6328 (3)0.0575 (4)0.0527 (12)0.67 (2)
H4CA0.49240.61960.00670.063*0.67 (2)
C5C0.5571 (12)0.5745 (4)0.0975 (4)0.0461 (12)0.67 (2)
H5CA0.50680.52120.07410.055*0.67 (2)
C6C0.6446 (13)0.5950 (5)0.1731 (4)0.0395 (14)0.67 (2)
F1Y0.671 (5)0.7647 (9)0.0556 (10)0.123 (6)0.33 (2)
C1Y0.718 (5)0.6637 (12)0.2093 (10)0.057 (4)0.33 (2)
H1YA0.74730.67760.26150.068*0.33 (2)
C2Y0.733 (3)0.7245 (11)0.1713 (9)0.056 (4)0.33 (2)
H2YA0.78200.77710.19760.068*0.33 (2)
C3Y0.676 (3)0.7066 (8)0.0951 (9)0.064 (4)0.33 (2)
C4Y0.623 (4)0.6273 (7)0.0549 (8)0.075 (4)0.33 (2)
H4YA0.58640.61450.00290.090*0.33 (2)
C5Y0.626 (3)0.5680 (8)0.0937 (8)0.056 (3)0.33 (2)
H5YA0.60510.51480.06600.068*0.33 (2)
C6Y0.660 (3)0.5826 (11)0.1730 (8)0.057 (4)0.33 (2)
C7C0.6597 (2)0.52828 (10)0.21396 (10)0.0450 (4)
C8C0.7417 (3)0.54173 (12)0.29583 (11)0.0606 (5)
H8CA0.68400.58230.32700.073*
H8CB0.87910.55770.30490.073*
C9C0.6887 (3)0.45806 (11)0.31055 (11)0.0552 (5)
H9CA0.80330.44050.33370.066*
C10C0.5332 (3)0.45217 (11)0.35786 (10)0.0506 (5)
C11C0.5377 (3)0.40019 (12)0.40562 (11)0.0615 (5)
H11C0.63780.37030.40900.074*
C12C0.3949 (4)0.39252 (14)0.44809 (14)0.0780 (7)
H12C0.39760.35770.47990.094*
C13C0.2514 (4)0.43678 (15)0.44227 (15)0.0762 (7)
C14C0.2400 (3)0.48843 (13)0.39656 (13)0.0682 (6)
H14C0.13890.51790.39390.082*
C15C0.3827 (3)0.49603 (12)0.35406 (11)0.0572 (5)
H15C0.37750.53110.32250.069*
C16C0.6052 (3)0.32713 (11)0.21266 (12)0.0598 (5)
C17C0.5497 (4)0.28828 (11)0.13118 (12)0.0732 (7)
H17G0.56670.23270.12240.110*
H17H0.62850.31490.10330.110*
H17I0.41820.29210.11510.110*
U11U22U33U12U13U23
F2A0.1377 (15)0.1098 (12)0.1409 (15)0.0033 (11)0.0792 (13)0.0377 (11)
O1A0.1061 (12)0.0531 (8)0.0716 (10)0.0171 (8)0.0127 (9)0.0381 (8)
N1A0.0561 (9)0.0378 (8)0.0454 (9)0.0016 (6)0.0047 (7)0.0202 (7)
N2A0.0690 (10)0.0413 (8)0.0442 (9)−0.0003 (7)0.0014 (7)0.0215 (7)
F1A0.123 (4)0.0429 (10)0.0600 (13)−0.0076 (16)0.0184 (17)0.0272 (9)
C1A0.044 (4)0.042 (2)0.039 (2)−0.0108 (19)0.005 (2)0.0067 (15)
C2A0.058 (4)0.0319 (16)0.051 (2)−0.010 (2)0.0107 (19)0.0091 (14)
C3A0.060 (3)0.0363 (15)0.0505 (18)−0.0030 (17)0.0139 (19)0.0195 (13)
C4A0.066 (3)0.0417 (16)0.0386 (17)−0.0042 (17)0.0114 (18)0.0132 (13)
C5A0.055 (3)0.0323 (15)0.0397 (18)−0.0034 (15)0.0084 (17)0.0088 (13)
C6A0.034 (2)0.0368 (19)0.040 (2)−0.0050 (15)0.0039 (14)0.0207 (17)
F1X0.151 (13)0.049 (3)0.090 (5)−0.012 (5)0.008 (6)0.037 (3)
C1X0.041 (9)0.035 (4)0.051 (5)−0.006 (4)0.024 (5)0.014 (3)
C2X0.056 (9)0.037 (4)0.059 (5)−0.011 (5)0.020 (5)0.008 (4)
C3X0.073 (9)0.043 (4)0.065 (5)−0.013 (5)0.012 (6)0.022 (4)
C4X0.104 (12)0.051 (5)0.056 (5)−0.017 (7)0.016 (7)0.019 (4)
C5X0.099 (12)0.039 (5)0.055 (5)−0.012 (7)0.016 (7)0.013 (4)
C6X0.064 (11)0.041 (5)0.044 (5)−0.018 (5)0.007 (6)−0.003 (5)
C7A0.0499 (10)0.0398 (9)0.0447 (11)−0.0031 (8)0.0025 (8)0.0165 (8)
C8A0.0758 (14)0.0540 (12)0.0491 (12)−0.0158 (10)−0.0053 (10)0.0227 (10)
C9A0.0645 (12)0.0543 (11)0.0447 (11)−0.0010 (9)−0.0061 (9)0.0230 (9)
C10A0.0677 (13)0.0455 (10)0.0398 (10)−0.0049 (9)−0.0070 (9)0.0182 (9)
C11A0.0840 (15)0.0545 (12)0.0549 (13)0.0068 (10)0.0051 (11)0.0287 (10)
C12A0.117 (2)0.0615 (14)0.0678 (16)−0.0007 (14)0.0212 (15)0.0347 (12)
C13A0.0909 (18)0.0617 (14)0.0769 (17)−0.0080 (13)0.0264 (14)0.0155 (13)
C14A0.0716 (15)0.0642 (14)0.0698 (15)0.0057 (11)0.0023 (12)0.0099 (12)
C15A0.0786 (15)0.0510 (11)0.0498 (12)0.0030 (10)−0.0097 (11)0.0187 (10)
C16A0.0621 (12)0.0418 (10)0.0611 (13)0.0092 (8)0.0108 (10)0.0258 (10)
C17A0.0827 (15)0.0387 (10)0.0664 (14)0.0049 (9)0.0156 (11)0.0160 (10)
F1B0.1521 (14)0.0463 (7)0.0769 (9)−0.0046 (7)0.0106 (9)0.0329 (7)
F2B0.1402 (15)0.1065 (12)0.1281 (14)−0.0002 (10)0.0764 (12)0.0311 (11)
O1B0.1182 (13)0.0545 (8)0.0744 (10)0.0239 (8)0.0208 (9)0.0383 (8)
N1B0.0634 (10)0.0389 (8)0.0458 (9)0.0084 (7)0.0122 (7)0.0200 (7)
N2B0.0790 (11)0.0437 (9)0.0444 (9)0.0061 (8)0.0083 (8)0.0216 (7)
C1B0.0632 (12)0.0436 (10)0.0438 (11)−0.0027 (8)0.0104 (9)0.0083 (9)
C2B0.0758 (14)0.0340 (9)0.0596 (13)−0.0017 (9)0.0122 (10)0.0108 (9)
C3B0.0749 (14)0.0400 (10)0.0610 (14)0.0002 (9)0.0114 (11)0.0235 (10)
C4B0.0797 (14)0.0458 (11)0.0491 (12)−0.0032 (9)0.0018 (10)0.0181 (9)
C5B0.0676 (12)0.0363 (9)0.0467 (11)−0.0037 (8)0.0010 (9)0.0119 (8)
C6B0.0463 (10)0.0387 (9)0.0468 (11)0.0009 (7)0.0074 (8)0.0146 (8)
C7B0.0499 (10)0.0434 (10)0.0445 (11)0.0005 (8)0.0066 (8)0.0157 (8)
C8B0.0770 (14)0.0614 (13)0.0510 (12)−0.0118 (10)−0.0034 (10)0.0255 (10)
C9B0.0654 (13)0.0566 (11)0.0477 (12)0.0016 (9)−0.0025 (9)0.0247 (10)
C10B0.0679 (12)0.0462 (10)0.0371 (10)−0.0036 (9)−0.0063 (9)0.0170 (8)
C11B0.0828 (15)0.0537 (12)0.0518 (12)0.0065 (10)0.0032 (11)0.0271 (10)
C12B0.119 (2)0.0616 (14)0.0610 (15)−0.0049 (14)0.0171 (14)0.0315 (12)
C13B0.0900 (18)0.0596 (14)0.0729 (16)−0.0089 (12)0.0261 (14)0.0135 (12)
C14B0.0735 (15)0.0636 (14)0.0647 (15)0.0058 (11)0.0044 (12)0.0089 (12)
C15B0.0762 (14)0.0528 (11)0.0470 (12)0.0067 (10)−0.0060 (10)0.0178 (9)
C16B0.0845 (15)0.0431 (11)0.0626 (14)0.0166 (10)0.0238 (11)0.0265 (10)
C17B0.130 (2)0.0381 (10)0.0620 (14)0.0134 (12)0.0289 (14)0.0122 (10)
F2C0.1355 (15)0.1059 (12)0.1501 (16)0.0022 (10)0.0853 (13)0.0360 (11)
O1C0.1375 (16)0.0627 (9)0.0793 (11)0.0351 (10)0.0268 (10)0.0446 (9)
N1C0.0557 (9)0.0376 (8)0.0477 (9)0.0036 (6)0.0081 (7)0.0195 (7)
N2C0.0712 (11)0.0433 (8)0.0447 (9)0.0048 (7)0.0063 (8)0.0222 (7)
F1C0.117 (3)0.0422 (15)0.081 (2)0.0150 (16)0.021 (2)0.0325 (15)
C1C0.059 (3)0.030 (3)0.046 (3)−0.006 (2)0.006 (2)0.005 (2)
C2C0.072 (4)0.025 (2)0.060 (3)0.007 (2)0.022 (2)0.0142 (17)
C3C0.059 (3)0.0343 (18)0.060 (2)0.0096 (17)0.020 (2)0.0203 (16)
C4C0.072 (3)0.0406 (18)0.047 (2)0.011 (2)0.006 (2)0.0161 (15)
C5C0.059 (3)0.0294 (17)0.0475 (19)0.0037 (18)0.004 (2)0.0092 (14)
C6C0.055 (3)0.025 (2)0.044 (2)0.0003 (18)0.018 (2)0.0181 (19)
F1Y0.238 (17)0.042 (4)0.075 (6)−0.013 (7)−0.019 (9)0.031 (4)
C1Y0.093 (9)0.035 (6)0.050 (6)−0.001 (6)0.027 (6)0.023 (4)
C2Y0.078 (9)0.023 (5)0.059 (5)0.007 (5)−0.004 (5)0.001 (4)
C3Y0.098 (11)0.035 (4)0.058 (5)−0.002 (5)0.003 (6)0.020 (4)
C4Y0.119 (11)0.036 (4)0.054 (5)−0.002 (6)−0.022 (7)0.007 (3)
C5Y0.081 (9)0.033 (4)0.051 (4)0.001 (5)−0.007 (5)0.015 (3)
C6Y0.073 (7)0.030 (5)0.053 (5)−0.002 (5)−0.019 (5)−0.003 (4)
C7C0.0490 (10)0.0410 (10)0.0445 (11)−0.0046 (8)0.0043 (8)0.0166 (8)
C8C0.0690 (13)0.0567 (12)0.0504 (12)−0.0149 (9)−0.0031 (10)0.0211 (10)
C9C0.0603 (12)0.0562 (12)0.0493 (12)−0.0026 (9)−0.0034 (9)0.0260 (10)
C10C0.0608 (12)0.0488 (10)0.0387 (10)−0.0041 (9)−0.0053 (8)0.0174 (8)
C11C0.0801 (15)0.0575 (12)0.0516 (12)0.0080 (10)0.0051 (11)0.0277 (10)
C12C0.111 (2)0.0615 (14)0.0675 (16)−0.0037 (14)0.0241 (14)0.0316 (12)
C13C0.0844 (17)0.0630 (14)0.0797 (17)−0.0094 (12)0.0307 (14)0.0134 (13)
C14C0.0655 (14)0.0614 (13)0.0707 (15)0.0018 (10)0.0034 (12)0.0099 (12)
C15C0.0665 (13)0.0533 (11)0.0484 (12)0.0012 (9)−0.0063 (10)0.0187 (9)
C16C0.0784 (14)0.0439 (11)0.0679 (14)0.0164 (10)0.0197 (11)0.0281 (10)
C17C0.1102 (19)0.0383 (10)0.0728 (16)0.0099 (11)0.0195 (14)0.0147 (11)
F2A—C13A1.368 (3)C8B—C9B1.550 (3)
O1A—C16A1.220 (2)C8B—H8BA0.97
N1A—C7A1.287 (2)C8B—H8BB0.97
N1A—N2A1.3895 (18)C9B—C10B1.514 (3)
N2A—C16A1.360 (2)C9B—H9BA0.98
N2A—C9A1.481 (2)C10B—C15B1.382 (3)
F1A—C3A1.355 (4)C10B—C11B1.386 (2)
C1A—C2A1.379 (6)C11B—C12B1.386 (3)
C1A—C6A1.390 (6)C11B—H11B0.93
C1A—H1AA0.93C12B—C13B1.353 (4)
C2A—C3A1.360 (5)C12B—H12B0.93
C2A—H2AA0.93C13B—C14B1.358 (3)
C3A—C4A1.377 (5)C14B—C15B1.394 (3)
C4A—C5A1.376 (5)C14B—H14B0.93
C4A—H4AA0.93C15B—H15B0.93
C5A—C6A1.399 (6)C16B—C17B1.492 (3)
C5A—H5AA0.93C17B—H17D0.96
C6A—C7A1.497 (6)C17B—H17E0.96
F1X—C3X1.369 (11)C17B—H17F0.96
C1X—C2X1.385 (13)F2C—C13C1.368 (3)
C1X—C6X1.413 (13)O1C—C16C1.219 (2)
C1X—H1XA0.93N1C—C7C1.282 (2)
C2X—C3X1.348 (13)N1C—N2C1.3867 (18)
C2X—H2XA0.93N2C—C16C1.356 (2)
C3X—C4X1.377 (12)N2C—C9C1.478 (2)
C4X—C5X1.379 (13)F1C—C3C1.355 (6)
C4X—H4XA0.93C1C—C2C1.390 (7)
C5X—C6X1.399 (14)C1C—C6C1.396 (6)
C5X—H5XA0.93C1C—H1CA0.93
C6X—C7A1.367 (18)C2C—C3C1.354 (7)
C7A—C8A1.499 (2)C2C—H2CA0.93
C8A—C9A1.547 (2)C3C—C4C1.375 (6)
C8A—H8AA0.97C4C—C5C1.376 (6)
C8A—H8AB0.97C4C—H4CA0.93
C9A—C10A1.509 (3)C5C—C6C1.400 (7)
C9A—H9AA0.98C5C—H5CA0.93
C10A—C11A1.385 (2)C6C—C7C1.516 (7)
C10A—C15A1.388 (3)F1Y—C3Y1.365 (11)
C11A—C12A1.384 (3)C1Y—C2Y1.388 (13)
C11A—H11A0.93C1Y—C6Y1.396 (12)
C12A—C13A1.351 (4)C1Y—H1YA0.93
C12A—H12A0.93C2Y—C3Y1.367 (12)
C13A—C14A1.357 (3)C2Y—H2YA0.93
C14A—C15A1.391 (3)C3Y—C4Y1.384 (11)
C14A—H14A0.93C4Y—C5Y1.373 (11)
C15A—H15A0.93C4Y—H4YA0.93
C16A—C17A1.486 (3)C5Y—C6Y1.412 (12)
C17A—H17A0.96C5Y—H5YA0.93
C17A—H17B0.96C6Y—C7C1.329 (16)
C17A—H17C0.96C7C—C8C1.502 (2)
F1B—C3B1.360 (2)C8C—C9C1.542 (2)
F2B—C13B1.368 (3)C8C—H8CA0.97
O1B—C16B1.223 (2)C8C—H8CB0.97
N1B—C7B1.288 (2)C9C—C10C1.514 (3)
N1B—N2B1.3873 (18)C9C—H9CA0.98
N2B—C16B1.365 (2)C10C—C15C1.384 (3)
N2B—C9B1.480 (2)C10C—C11C1.391 (2)
C1B—C2B1.385 (2)C11C—C12C1.383 (3)
C1B—C6B1.396 (2)C11C—H11C0.93
C1B—H1BA0.93C12C—C13C1.351 (4)
C2B—C3B1.361 (3)C12C—H12C0.93
C2B—H2BA0.93C13C—C14C1.358 (3)
C3B—C4B1.374 (3)C14C—C15C1.383 (3)
C4B—C5B1.377 (2)C14C—H14C0.93
C4B—H4BA0.93C15C—H15C0.93
C5B—C6B1.394 (3)C16C—C17C1.483 (3)
C5B—H5BA0.93C17C—H17G0.96
C6B—C7B1.463 (2)C17C—H17H0.96
C7B—C8B1.501 (3)C17C—H17I0.96
C7A—N1A—N2A108.01 (14)N2B—C9B—C8B101.28 (14)
C16A—N2A—N1A121.67 (15)C10B—C9B—C8B115.55 (17)
C16A—N2A—C9A124.59 (15)N2B—C9B—H9BA109.5
N1A—N2A—C9A113.27 (13)C10B—C9B—H9BA109.5
C2A—C1A—C6A121.0 (5)C8B—C9B—H9BA109.5
C2A—C1A—H1AA119.5C15B—C10B—C11B118.6 (2)
C6A—C1A—H1AA119.5C15B—C10B—C9B121.48 (16)
C3A—C2A—C1A117.5 (5)C11B—C10B—C9B119.88 (18)
C3A—C2A—H2AA121.2C12B—C11B—C10B120.5 (2)
C1A—C2A—H2AA121.2C12B—C11B—H11B119.7
F1A—C3A—C2A118.2 (4)C10B—C11B—H11B119.7
F1A—C3A—C4A117.7 (4)C13B—C12B—C11B118.7 (2)
C2A—C3A—C4A124.1 (4)C13B—C12B—H12B120.6
C5A—C4A—C3A117.9 (5)C11B—C12B—H12B120.6
C5A—C4A—H4AA121.0C12B—C13B—C14B123.3 (2)
C3A—C4A—H4AA121.0C12B—C13B—F2B118.3 (2)
C4A—C5A—C6A120.1 (5)C14B—C13B—F2B118.4 (2)
C4A—C5A—H5AA119.9C13B—C14B—C15B117.8 (2)
C6A—C5A—H5AA119.9C13B—C14B—H14B121.1
C1A—C6A—C5A119.2 (5)C15B—C14B—H14B121.1
C1A—C6A—C7A121.0 (5)C10B—C15B—C14B121.08 (19)
C5A—C6A—C7A119.8 (5)C10B—C15B—H15B119.5
C2X—C1X—C6X122.8 (15)C14B—C15B—H15B119.5
C2X—C1X—H1XA118.6O1B—C16B—N2B119.4 (2)
C6X—C1X—H1XA118.6O1B—C16B—C17B123.72 (18)
C3X—C2X—C1X120.2 (15)N2B—C16B—C17B116.87 (16)
C3X—C2X—H2XA119.9C16B—C17B—H17D109.5
C1X—C2X—H2XA119.9C16B—C17B—H17E109.5
C2X—C3X—F1X121.8 (12)H17D—C17B—H17E109.5
C2X—C3X—C4X121.1 (12)C16B—C17B—H17F109.5
F1X—C3X—C4X117.1 (12)H17D—C17B—H17F109.5
C3X—C4X—C5X117.1 (13)H17E—C17B—H17F109.5
C3X—C4X—H4XA121.4C7C—N1C—N2C108.00 (14)
C5X—C4X—H4XA121.4C16C—N2C—N1C122.17 (16)
C4X—C5X—C6X125.9 (14)C16C—N2C—C9C124.71 (15)
C4X—C5X—H5XA117.1N1C—N2C—C9C113.01 (13)
C6X—C5X—H5XA117.1C2C—C1C—C6C120.1 (6)
C7A—C6X—C5X124.4 (15)C2C—C1C—H1CA119.9
C7A—C6X—C1X123.0 (14)C6C—C1C—H1CA119.9
C5X—C6X—C1X112.6 (14)C3C—C2C—C1C117.9 (6)
N1A—C7A—C6X119.1 (8)C3C—C2C—H2CA121.1
N1A—C7A—C6A120.7 (3)C1C—C2C—H2CA121.1
N1A—C7A—C8A114.60 (15)C2C—C3C—F1C118.3 (6)
C6X—C7A—C8A125.8 (8)C2C—C3C—C4C124.4 (6)
C6A—C7A—C8A124.6 (3)F1C—C3C—C4C117.4 (6)
C7A—C8A—C9A102.63 (15)C3C—C4C—C5C117.8 (6)
C7A—C8A—H8AA111.2C3C—C4C—H4CA121.1
C9A—C8A—H8AA111.2C5C—C4C—H4CA121.1
C7A—C8A—H8AB111.2C4C—C5C—C6C120.3 (5)
C9A—C8A—H8AB111.2C4C—C5C—H5CA119.9
H8AA—C8A—H8AB109.2C6C—C5C—H5CA119.9
N2A—C9A—C10A111.54 (15)C1C—C6C—C5C119.5 (6)
N2A—C9A—C8A101.25 (13)C1C—C6C—C7C122.2 (6)
C10A—C9A—C8A116.02 (17)C5C—C6C—C7C118.2 (5)
N2A—C9A—H9AA109.2C2Y—C1Y—C6Y123.4 (14)
C10A—C9A—H9AA109.2C2Y—C1Y—H1YA118.3
C8A—C9A—H9AA109.2C6Y—C1Y—H1YA118.3
C11A—C10A—C15A118.2 (2)C3Y—C2Y—C1Y119.5 (13)
C11A—C10A—C9A120.21 (18)C3Y—C2Y—H2YA120.2
C15A—C10A—C9A121.60 (17)C1Y—C2Y—H2YA120.2
C12A—C11A—C10A120.8 (2)F1Y—C3Y—C2Y122.2 (13)
C12A—C11A—H11A119.6F1Y—C3Y—C4Y117.5 (12)
C10A—C11A—H11A119.6C2Y—C3Y—C4Y120.2 (11)
C13A—C12A—C11A118.9 (2)C5Y—C4Y—C3Y118.4 (11)
C13A—C12A—H12A120.6C5Y—C4Y—H4YA120.8
C11A—C12A—H12A120.6C3Y—C4Y—H4YA120.8
C12A—C13A—C14A123.0 (2)C4Y—C5Y—C6Y124.3 (12)
C12A—C13A—F2A118.6 (2)C4Y—C5Y—H5YA117.9
C14A—C13A—F2A118.4 (3)C6Y—C5Y—H5YA117.9
C13A—C14A—C15A118.1 (2)C7C—C6Y—C1Y118.9 (13)
C13A—C14A—H14A121.0C7C—C6Y—C5Y127.3 (13)
C15A—C14A—H14A121.0C1Y—C6Y—C5Y113.4 (13)
C10A—C15A—C14A121.08 (19)N1C—C7C—C6Y118.2 (7)
C10A—C15A—H15A119.5N1C—C7C—C8C114.27 (15)
C14A—C15A—H15A119.5C6Y—C7C—C8C127.2 (7)
O1A—C16A—N2A119.64 (18)N1C—C7C—C6C121.6 (3)
O1A—C16A—C17A123.35 (17)C8C—C7C—C6C124.1 (3)
N2A—C16A—C17A117.00 (15)C7C—C8C—C9C102.18 (15)
C16A—C17A—H17A109.5C7C—C8C—H8CA111.3
C16A—C17A—H17B109.5C9C—C8C—H8CA111.3
H17A—C17A—H17B109.5C7C—C8C—H8CB111.3
C16A—C17A—H17C109.5C9C—C8C—H8CB111.3
H17A—C17A—H17C109.5H8CA—C8C—H8CB109.2
H17B—C17A—H17C109.5N2C—C9C—C10C111.47 (15)
C7B—N1B—N2B108.18 (15)N2C—C9C—C8C100.87 (13)
C16B—N2B—N1B121.94 (16)C10C—C9C—C8C115.30 (17)
C16B—N2B—C9B124.58 (15)N2C—C9C—H9CA109.6
N1B—N2B—C9B113.25 (14)C10C—C9C—H9CA109.6
C2B—C1B—C6B120.88 (18)C8C—C9C—H9CA109.6
C2B—C1B—H1BA119.6C15C—C10C—C11C118.38 (19)
C6B—C1B—H1BA119.6C15C—C10C—C9C121.91 (16)
C3B—C2B—C1B118.29 (17)C11C—C10C—C9C119.70 (18)
C3B—C2B—H2BA120.9C12C—C11C—C10C120.7 (2)
C1B—C2B—H2BA120.9C12C—C11C—H11C119.7
F1B—C3B—C2B118.77 (17)C10C—C11C—H11C119.7
F1B—C3B—C4B117.96 (18)C13C—C12C—C11C118.5 (2)
C2B—C3B—C4B123.26 (17)C13C—C12C—H12C120.7
C3B—C4B—C5B117.89 (18)C11C—C12C—H12C120.7
C3B—C4B—H4BA121.1C12C—C13C—C14C123.2 (2)
C5B—C4B—H4BA121.1C12C—C13C—F2C118.2 (2)
C4B—C5B—C6B121.40 (17)C14C—C13C—F2C118.5 (2)
C4B—C5B—H5BA119.3C13C—C14C—C15C118.2 (2)
C6B—C5B—H5BA119.3C13C—C14C—H14C120.9
C5B—C6B—C1B118.20 (16)C15C—C14C—H14C120.9
C5B—C6B—C7B120.86 (16)C14C—C15C—C10C120.96 (19)
C1B—C6B—C7B120.94 (17)C14C—C15C—H15C119.5
N1B—C7B—C6B120.47 (16)C10C—C15C—H15C119.5
N1B—C7B—C8B114.47 (15)O1C—C16C—N2C119.7 (2)
C6B—C7B—C8B125.06 (16)O1C—C16C—C17C123.49 (18)
C7B—C8B—C9B102.45 (15)N2C—C16C—C17C116.85 (16)
C7B—C8B—H8BA111.3C16C—C17C—H17G109.5
C9B—C8B—H8BA111.3C16C—C17C—H17H109.5
C7B—C8B—H8BB111.3H17G—C17C—H17H109.5
C9B—C8B—H8BB111.3C16C—C17C—H17I109.5
H8BA—C8B—H8BB109.2H17G—C17C—H17I109.5
N2B—C9B—C10B111.14 (16)H17H—C17C—H17I109.5
C7A—N1A—N2A—C16A−168.87 (17)C16B—N2B—C9B—C8B−168.37 (19)
C7A—N1A—N2A—C9A3.5 (2)N1B—N2B—C9B—C8B6.1 (2)
C6A—C1A—C2A—C3A−3.3 (11)C7B—C8B—C9B—N2B−5.5 (2)
C1A—C2A—C3A—F1A−178.0 (6)C7B—C8B—C9B—C10B114.70 (18)
C1A—C2A—C3A—C4A0.5 (9)N2B—C9B—C10B—C15B73.5 (2)
F1A—C3A—C4A—C5A179.3 (4)C8B—C9B—C10B—C15B−41.2 (2)
C2A—C3A—C4A—C5A0.8 (7)N2B—C9B—C10B—C11B−104.97 (19)
C3A—C4A—C5A—C6A0.7 (7)C8B—C9B—C10B—C11B140.37 (18)
C2A—C1A—C6A—C5A4.8 (12)C15B—C10B—C11B—C12B−0.8 (3)
C2A—C1A—C6A—C7A−176.1 (7)C9B—C10B—C11B—C12B177.75 (19)
C4A—C5A—C6A—C1A−3.4 (11)C10B—C11B—C12B—C13B0.5 (3)
C4A—C5A—C6A—C7A177.5 (5)C11B—C12B—C13B—C14B−0.2 (4)
C6X—C1X—C2X—C3X5(3)C11B—C12B—C13B—F2B179.1 (2)
C1X—C2X—C3X—F1X175.1 (15)C12B—C13B—C14B—C15B0.2 (4)
C1X—C2X—C3X—C4X−5(2)F2B—C13B—C14B—C15B−179.1 (2)
C2X—C3X—C4X—C5X5(2)C11B—C10B—C15B—C14B0.7 (3)
F1X—C3X—C4X—C5X−175.6 (12)C9B—C10B—C15B—C14B−177.75 (18)
C3X—C4X—C5X—C6X−5(2)C13B—C14B—C15B—C10B−0.4 (3)
C4X—C5X—C6X—C7A−176.1 (18)N1B—N2B—C16B—O1B−175.16 (17)
C4X—C5X—C6X—C1X5(3)C9B—N2B—C16B—O1B−1.1 (3)
C2X—C1X—C6X—C7A176 (2)N1B—N2B—C16B—C17B6.2 (3)
C2X—C1X—C6X—C5X−5(3)C9B—N2B—C16B—C17B−179.76 (19)
N2A—N1A—C7A—C6X−172.3 (15)C7C—N1C—N2C—C16C−169.85 (17)
N2A—N1A—C7A—C6A176.6 (4)C7C—N1C—N2C—C9C6.5 (2)
N2A—N1A—C7A—C8A−0.3 (2)C6C—C1C—C2C—C3C−2.9 (18)
C5X—C6X—C7A—N1A−12 (3)C1C—C2C—C3C—F1C−177.5 (10)
C1X—C6X—C7A—N1A166.6 (18)C1C—C2C—C3C—C4C2.7 (14)
C5X—C6X—C7A—C6A90 (7)C2C—C3C—C4C—C5C0.2 (9)
C1X—C6X—C7A—C6A−91 (7)F1C—C3C—C4C—C5C−179.6 (5)
C5X—C6X—C7A—C8A176.6 (16)C3C—C4C—C5C—C6C−2.9 (8)
C1X—C6X—C7A—C8A−4(3)C2C—C1C—C6C—C5C0.3 (18)
C1A—C6A—C7A—N1A170.0 (6)C2C—C1C—C6C—C7C−178.9 (10)
C5A—C6A—C7A—N1A−10.9 (9)C4C—C5C—C6C—C1C2.7 (12)
C1A—C6A—C7A—C6X87 (6)C4C—C5C—C6C—C7C−178.1 (5)
C5A—C6A—C7A—C6X−94 (6)C6Y—C1Y—C2Y—C3Y5(4)
C1A—C6A—C7A—C8A−13.4 (10)C1Y—C2Y—C3Y—F1Y174 (2)
C5A—C6A—C7A—C8A165.7 (5)C1Y—C2Y—C3Y—C4Y−7(3)
N1A—C7A—C8A—C9A−2.7 (2)F1Y—C3Y—C4Y—C5Y−179.6 (12)
C6X—C7A—C8A—C9A168.6 (16)C2Y—C3Y—C4Y—C5Y1(2)
C6A—C7A—C8A—C9A−179.4 (5)C3Y—C4Y—C5Y—C6Y7(2)
C16A—N2A—C9A—C10A−68.8 (2)C2Y—C1Y—C6Y—C7C176 (3)
N1A—N2A—C9A—C10A119.06 (16)C2Y—C1Y—C6Y—C5Y3(4)
C16A—N2A—C9A—C8A167.22 (18)C4Y—C5Y—C6Y—C7C178.1 (15)
N1A—N2A—C9A—C8A−4.9 (2)C4Y—C5Y—C6Y—C1Y−9(3)
C7A—C8A—C9A—N2A4.23 (19)N2C—N1C—C7C—C6Y176.0 (12)
C7A—C8A—C9A—C10A−116.68 (18)N2C—N1C—C7C—C8C2.6 (2)
N2A—C9A—C10A—C11A102.35 (19)N2C—N1C—C7C—C6C−177.3 (4)
C8A—C9A—C10A—C11A−142.43 (18)C1Y—C6Y—C7C—N1C178 (2)
N2A—C9A—C10A—C15A−77.0 (2)C5Y—C6Y—C7C—N1C−9(3)
C8A—C9A—C10A—C15A38.2 (2)C1Y—C6Y—C7C—C8C−9(3)
C15A—C10A—C11A—C12A0.7 (3)C5Y—C6Y—C7C—C8C163.3 (15)
C9A—C10A—C11A—C12A−178.70 (19)C1Y—C6Y—C7C—C6C56 (8)
C10A—C11A—C12A—C13A−0.5 (4)C5Y—C6Y—C7C—C6C−131 (10)
C11A—C12A—C13A—C14A0.4 (4)C1C—C6C—C7C—N1C−178.1 (9)
C11A—C12A—C13A—F2A−178.6 (2)C5C—C6C—C7C—N1C2.8 (9)
C12A—C13A—C14A—C15A−0.5 (4)C1C—C6C—C7C—C6Y−117 (9)
F2A—C13A—C14A—C15A178.6 (2)C5C—C6C—C7C—C6Y64 (8)
C11A—C10A—C15A—C14A−0.8 (3)C1C—C6C—C7C—C8C2.0 (12)
C9A—C10A—C15A—C14A178.59 (18)C5C—C6C—C7C—C8C−177.1 (5)
C13A—C14A—C15A—C10A0.7 (3)N1C—C7C—C8C—C9C−9.8 (2)
N1A—N2A—C16A—O1A175.02 (16)C6Y—C7C—C8C—C9C177.4 (13)
C9A—N2A—C16A—O1A3.5 (3)C6C—C7C—C8C—C9C170.1 (4)
N1A—N2A—C16A—C17A−5.7 (3)C16C—N2C—C9C—C10C−72.8 (2)
C9A—N2A—C16A—C17A−177.21 (18)N1C—N2C—C9C—C10C110.90 (16)
C7B—N1B—N2B—C16B170.59 (18)C16C—N2C—C9C—C8C164.28 (18)
C7B—N1B—N2B—C9B−4.1 (2)N1C—N2C—C9C—C8C−12.0 (2)
C6B—C1B—C2B—C3B0.6 (3)C7C—C8C—C9C—N2C11.94 (19)
C1B—C2B—C3B—F1B−179.15 (18)C7C—C8C—C9C—C10C−108.26 (18)
C1B—C2B—C3B—C4B2.1 (3)N2C—C9C—C10C—C15C−80.1 (2)
F1B—C3B—C4B—C5B178.73 (18)C8C—C9C—C10C—C15C34.1 (2)
C2B—C3B—C4B—C5B−2.5 (3)N2C—C9C—C10C—C11C98.58 (19)
C3B—C4B—C5B—C6B0.2 (3)C8C—C9C—C10C—C11C−147.21 (17)
C4B—C5B—C6B—C1B2.3 (3)C15C—C10C—C11C—C12C0.1 (3)
C4B—C5B—C6B—C7B−178.54 (18)C9C—C10C—C11C—C12C−178.56 (19)
C2B—C1B—C6B—C5B−2.7 (3)C10C—C11C—C12C—C13C−0.2 (4)
C2B—C1B—C6B—C7B178.12 (17)C11C—C12C—C13C—C14C0.2 (4)
N2B—N1B—C7B—C6B−179.56 (15)C11C—C12C—C13C—F2C−179.2 (2)
N2B—N1B—C7B—C8B−0.1 (2)C12C—C13C—C14C—C15C−0.1 (4)
C5B—C6B—C7B—N1B10.3 (3)F2C—C13C—C14C—C15C179.2 (2)
C1B—C6B—C7B—N1B−170.53 (17)C13C—C14C—C15C—C10C0.1 (3)
C5B—C6B—C7B—C8B−169.09 (19)C11C—C10C—C15C—C14C−0.1 (3)
C1B—C6B—C7B—C8B10.1 (3)C9C—C10C—C15C—C14C178.58 (18)
N1B—C7B—C8B—C9B3.8 (2)N1C—N2C—C16C—O1C178.61 (17)
C6B—C7B—C8B—C9B−176.74 (18)C9C—N2C—C16C—O1C2.7 (3)
C16B—N2B—C9B—C10B68.4 (2)N1C—N2C—C16C—C17C−1.3 (3)
N1B—N2B—C9B—C10B−117.15 (16)C9C—N2C—C16C—C17C−177.25 (19)
D—H···AD—HH···AD···AD—H···A
C12A—H12A···F2Ai0.932.533.294 (3)139
C12B—H12B···F2Cii0.932.533.309 (3)141
C12C—H12C···F2Biii0.932.533.320 (3)143
C17A—H17A···F1Civ0.962.533.276 (8)134
C17B—H17D···F1Av0.962.473.309 (4)146
C17C—H17G···F1Bi0.962.553.311 (2)137
C15A—H15A···O1C0.932.323.225 (3)165
C15B—H15B···O1Avi0.932.363.262 (3)162
C15C—H15C···O1Bvii0.932.423.281 (3)153
Table 1

Hydrogen-bond geometry (Å, °)

D—H⋯AD—HH⋯ADAD—H⋯A
C12A—H12A⋯F2Ai0.932.533.294 (3)139
C12B—H12B⋯F2Cii0.932.533.309 (3)141
C12C—H12C⋯F2Biii0.932.533.320 (3)143
C17A—H17A⋯F1Civ0.962.533.276 (8)134
C17B—H17D⋯F1Av0.962.473.309 (4)146
C17C—H17G⋯F1Bi0.962.553.311 (2)137
C15A—H15A⋯O1C0.932.323.225 (3)165
C15B—H15B⋯O1Avi0.932.363.262 (3)162
C15C—H15C⋯O1Bvii0.932.423.281 (3)153

Symmetry codes: (i) ; (ii) ; (iii) ; (iv) ; (v) ; (vi) ; (vii) .

  7 in total

1.  Synthesis of some pyrazole derivatives and preliminary investigation of their affinity binding to P-glycoprotein.

Authors:  Fedele Manna; Franco Chimenti; Rossella Fioravanti; Adriana Bolasco; Daniela Secci; Paola Chimenti; Cristiano Ferlini; Giovanni Scambia
Journal:  Bioorg Med Chem Lett       Date:  2005-10-15       Impact factor: 2.823

2.  A short history of SHELX.

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

3.  1-[3-(2-Naphth-yl)-5-(3,4,5-trimethoxy-phen-yl)-4,5-dihydro-1H-pyrazol-1-yl]ethanone.

Authors:  Zhi-Ke Lu; Hai-Lin Diao; Shen Li; Bin He
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-07-31

4.  Potential antidiabetics. 8. 4-Arylhydrazono-N'-guanylnitrate-3-methyl-2-pyrazolin-5-ones, 4-arylazo-N'-guanylnitrate-3,5-dimethylpyrazoles, and 4-arylazo-N'-guanylnitrate-3,5-diphenylpyrazoles.

Authors:  H G Garg; C Prakash
Journal:  J Pharm Sci       Date:  1971-02       Impact factor: 3.534

5.  Synthesis and pharmacological evaluation of pyrazoline derivatives as new anti-inflammatory and analgesic agents.

Authors:  Mohammad Amir; Harish Kumar; Suroor A Khan
Journal:  Bioorg Med Chem Lett       Date:  2008-01-07       Impact factor: 2.823

6.  1-[3-(2,4-Dichloro-5-fluoro-phen-yl)-5-(3-methyl-2-thien-yl)-4,5-dihydro-1H-pyrazol-1-yl]ethanone.

Authors:  N Anuradha; A Thiruvalluvar; M Mahalinga; R J Butcher
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-10-22

7.  Structure validation in chemical crystallography.

Authors:  Anthony L Spek
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2009-01-20
  7 in total
  32 in total

1.  3,5-Bis(4-bromo-phen-yl)-1-phenyl-4,5-dihydro-1H-pyrazole.

Authors:  S Samshuddin; B Narayana; H S Yathirajan; A P Safwan; Edward R T Tiekink
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-05-08

2.  3,5-Bis(4-fluoro-phen-yl)-1-phenyl-4,5-dihydro-1H-pyrazole.

Authors:  Jerry P Jasinski; Curtis J Guild; S Samshuddin; B Narayana; H S Yathirajan
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-07-07

3.  3,5-Bis(4-meth-oxy-phen-yl)-1-phenyl-4,5-dihydro-1H-pyrazole.

Authors:  Zeliha Baktır; Mehmet Akkurt; S Samshuddin; B Narayana; H S Yathirajan
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-01-12

4.  5-(4-Bromo-phen-yl)-3-(4-fluoro-phen-yl)-1-phenyl-4,5-dihydro-1H-pyrazole.

Authors:  Hoong-Kun Fun; Tze Shyang Chia; M Sapnakumari; B Narayana; B K Sarojini
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-08-11

5.  1-[5-(4-Bromo-phen-yl)-3-(4-fluoro-phen-yl)-4,5-dihydro-1H-pyrazol-1-yl]butan-1-one.

Authors:  Hoong-Kun Fun; Wan-Sin Loh; M Sapnakumari; B Narayana; B K Sarojini
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-08-08

6.  1-[5-(4-Bromo-phen-yl)-3-(4-fluoro-phen-yl)-4,5-dihydro-1H-pyrazol-1-yl]ethanone.

Authors:  Hoong-Kun Fun; Wan-Sin Loh; M Sapnakumari; B Narayana; B K Sarojini
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-07-28

7.  (2E)-1-(4-Chloro-phen-yl)-3-(4-nitro-phen-yl)prop-2-en-1-one.

Authors:  T S Yamuna; H S Yathirajan; Jerry P Jasinski; Amanda C Keeley; B Narayana; B K Sarojini
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-04-27

8.  1-[3-(4-Fluoro-phen-yl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl]ethanone.

Authors:  Hoong-Kun Fun; Chin Wei Ooi; M Sapnakumari; B Narayana; B K Sarojini
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-08-04

9.  2-[3,5-Bis(4-meth-oxy-phen-yl)-4,5-di-hydro-1H-pyrazol-1-yl]-4,6-bis-(4-meth-oxy-phen-yl)pyrimidine.

Authors:  Rajni Kant; Vivek K Gupta; Kamini Kapoor; S Samshuddin; B Narayana
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-07-10

10.  1-[3-(4-Chloro-phen-yl)-5-(4-meth-oxy-phen-yl)-4,5-dihydro-1H-pyrazol-1-yl]ethanone.

Authors:  Hoong-Kun Fun; Ching Kheng Quah; S Samshuddin; B Narayana; B K Sarojini
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-03-10
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