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Acta Crystallogr Sect E Struct Rep Online. 2008 February 1; 64(Pt 2): m265.
Published online 2008 January 4. doi:  10.1107/S1600536807067384
PMCID: PMC2960418

1-(2,4-Dinitro­phen­yl)-5-ferrocenyl-3-methyl-1H-pyrazole

Abstract

In the title compound, [Fe(C5H5)(C15H11N4O4)], the dinitro­phenyl and cyclo­penta­dienyl rings make dihedral angles of 53.61 (6) and 23.11 (9)°, respectively, with the pyrazole unit. The two cyclo­penta­dienyl rings are in an eclipsed conformation. The crystal structure is stabilized by inter­molecular C—H(...)O inter­actions, which link mol­ecules into chains parallel to the b axis.

Related literature

For related literature, see: Beer et al. (1998 [triangle]); Erasmus et al. (1996 [triangle]); Fabbrizzi & Poggi (1995 [triangle]); Gilchrist (1997 [triangle]); Basurto et al. (2007 [triangle]); Shi et al. (2005 [triangle]).

An external file that holds a picture, illustration, etc.
Object name is e-64-0m265-scheme1.jpg

Experimental

Crystal data

  • [Fe(C5H5)(C15H11N4O4)]
  • M r = 432.22
  • Triclinic, An external file that holds a picture, illustration, etc.
Object name is e-64-0m265-efi1.jpg
  • a = 7.1073 (2) Å
  • b = 11.5339 (3) Å
  • c = 11.7575 (3) Å
  • α = 103.822 (1)°
  • β = 93.061 (1)°
  • γ = 98.822 (2)°
  • V = 920.76 (4) Å3
  • Z = 2
  • Mo Kα radiation
  • μ = 0.85 mm−1
  • T = 293 (2) K
  • 0.25 × 0.15 × 0.15 mm

Data collection

  • Bruker Kappa APEXII diffractometer
  • Absorption correction: multi-scan (SADABS; Sheldrick, 1996 [triangle]) T min = 0.815, T max = 0.882
  • 24588 measured reflections
  • 6096 independent reflections
  • 4741 reflections with I > 2σ(I)
  • R int = 0.027

Refinement

  • R[F 2 > 2σ(F 2)] = 0.036
  • wR(F 2) = 0.107
  • S = 1.01
  • 6096 reflections
  • 263 parameters
  • 10 restraints
  • H-atom parameters constrained
  • Δρmax = 0.38 e Å−3
  • Δρmin = −0.25 e Å−3

Data collection: APEX2 (Bruker, 2004 [triangle]); cell refinement: APEX2; data reduction: SAINT (Bruker, 2004 [triangle]); program(s) used to solve structure: SHELXS97 (Sheldrick, 1997 [triangle]); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997 [triangle]); molecular graphics: PLATON (Spek, 2003 [triangle]); software used to prepare material for publication: SHELXL97 and PARST (Nardelli, 1995 [triangle]).

Table 1
Hydrogen-bond geometry (Å, °)

Supplementary Material

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536807067384/gk2122sup1.cif

Structure factors: contains datablocks I. DOI: 10.1107/S1600536807067384/gk2122Isup2.hkl

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

Acknowledgments

We thank the CSIR, India, for financial support.

supplementary crystallographic information

Comment

The design of molecular receptors having the ability to selectively bind and sense cationic, anionic or even neutral guests via a macroscopic physical response is an area of intense activity (Fabbrizzi et al., 1995). Chemical sensors bearing ferrocene nuclei as part of the sensing unit have been widely studied (Basurto et al., 2007). Ferrocene has largely proved to be a simple and remarkably robust building block for the construction of redox-responsive receptors (Beer et al., 1998). To build a sensor molecule with dual response (redox &optical), the title compound has been synthesized and studied to understand the above said properties.

The pyrazole ring has delocalized bonds (Gilchrist,1997; Shi et al., 2005). The substitued cyclopentadienyl rings are parallel to each other. The cyclopentadienyl rings are oriented at angles of 23.11 (9)° and 23.45 (7)° with respect to the planar pyrazole ring. Furthermore, the pyrazole and dinitrophenyl rings make a dihedral angle of 53.61 (6) °. The nitro groups are planar and oriented at angles of 26.61 (12)° and 9.53 (10)° to the phenyl ring. The two cyclopentadienyl rings of the ferrocenyl group are in a nearly eclipsed conformation (Erasmus et al., 1996).

The molecules in crystal are connected via intermolecular C—H···O interaction into a chain extended along the [010] direction.

Experimental

2,4-Dinitrophenylhydrazine (1 g, 5 mmol) was added to a solution of ferrocenoylacetone (1.35 g, 5 mmol) and a catalytic amount of p-toluenesulfonic acid in 50 ml of toluene. Tthe mixture was refluxed with a Dean-Stark apparatus for 14 h. The solvent was evaporated under vacuum, and the resulting black residue was chromatographed on a silica-gel column using petroleum ether-ethylacetate (9:1) mixture as eluent. The red band was collected which offered dark-red crystal. (62% yield, m.p. 433–435 K).

Refinement

H atoms were geometrically positioned (C—H = 0.93 - 0.98 Å) and treated as riding on their parent atoms, with Uiso(H) = 1.2Ueq(C) or 1.5Ueq(methyl C). The cyclopentadienyl group C15—C19 was refined as a rigid group.

Figures

Fig. 1.
ORTEP plot of the title molecule with displecement ellipsoids drawn at 20% probability level.
Fig. 2.
Crystal packing of the title compound viewed down the c axis.

Crystal data

[Fe(C5H5)(C15H11N4O4)]Z = 2
Mr = 432.22F000 = 444
Triclinic, P1Dx = 1.559 Mg m3
Hall symbol: -P 1Mo Kα radiation λ = 0.71073 Å
a = 7.1073 (2) ÅCell parameters from 2637 reflections
b = 11.5339 (3) Åθ = 2.2–25º
c = 11.7575 (3) ŵ = 0.86 mm1
α = 103.822 (1)ºT = 293 (2) K
β = 93.061 (1)ºPrism, black
γ = 98.822 (2)º0.25 × 0.15 × 0.15 mm
V = 920.76 (4) Å3

Data collection

Bruker APEXII Kappa diffractometer6096 independent reflections
Radiation source: fine-focus sealed tube4741 reflections with I > 2σ(I)
Monochromator: graphiteRint = 0.027
T = 293(2) Kθmax = 31.5º
ω and [var phi] scansθmin = 2.2º
Absorption correction: multi-scan(SADABS; Sheldrick, 1996)h = −10→10
Tmin = 0.815, Tmax = 0.882k = −16→16
24588 measured reflectionsl = −17→17

Refinement

Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.036H-atom parameters constrained
wR(F2) = 0.107  w = 1/[σ2(Fo2) + (0.0588P)2 + 0.1435P] where P = (Fo2 + 2Fc2)/3
S = 1.01(Δ/σ)max < 0.001
6096 reflectionsΔρmax = 0.38 e Å3
263 parametersΔρmin = −0.25 e Å3
10 restraintsExtinction correction: none
Primary atom site location: structure-invariant direct methods

Special details

Experimental. Spectral data: LC Mass:[M]+:432(m/e);1H NMR (CDCl3, 400 MHz, \d in p.p.m.): 2.34 (3H, s, CH~3~), 4.24(7H, s, Fc), 4.13 (2H, s, Fc), 7.56 (1H, d, Ar, J~0~=8.6 MHz), 8.40 (1H, d, Ar, J~0~=8.6 MHz),8.72 (1H, s, Ar).
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
C10.5094 (2)0.03689 (14)0.34324 (13)0.0422 (3)
C20.5263 (3)−0.08426 (16)0.31250 (14)0.0498 (4)
H20.6393−0.10810.28700.060*
C30.3723 (3)−0.16830 (14)0.32047 (14)0.0512 (4)
C40.2039 (3)−0.13645 (15)0.35988 (15)0.0529 (4)
H40.1039−0.19490.36880.063*
C50.1875 (3)−0.01628 (15)0.38571 (14)0.0470 (3)
H50.07310.00630.41020.056*
C60.3372 (2)0.07273 (13)0.37625 (12)0.0384 (3)
C70.2340 (3)0.35505 (15)0.50396 (14)0.0467 (3)
C80.2893 (3)0.37968 (14)0.39813 (14)0.0464 (3)
H80.29520.45300.37750.056*
C90.3328 (2)0.27444 (13)0.33134 (12)0.0386 (3)
C100.3901 (2)0.24686 (13)0.21167 (12)0.0391 (3)
C110.3667 (3)0.13264 (15)0.12710 (14)0.0483 (4)
H110.31000.05400.13920.058*
C120.4404 (3)0.1534 (2)0.02226 (15)0.0589 (5)
H120.44230.0914−0.05080.071*
C130.5071 (3)0.2775 (2)0.04050 (17)0.0611 (5)
H130.56320.3171−0.01780.073*
C140.4769 (2)0.33690 (18)0.15634 (15)0.0507 (4)
H140.50940.42420.19230.061*
C15−0.0579 (3)0.1718 (2)0.0393 (2)0.0712 (5)
H15−0.11290.09530.05640.085*
C16−0.0325 (3)0.2853 (2)0.1168 (2)0.0706 (5)
H16−0.06650.30200.19810.085*
C170.0510 (4)0.3715 (2)0.0615 (3)0.0817 (6)
H170.08350.45910.09600.098*
C180.0794 (4)0.3085 (3)−0.0561 (2)0.0858 (6)
H180.13350.3446−0.11720.103*
C190.0095 (3)0.1847 (3)−0.0667 (2)0.0784 (5)
H190.00950.1186−0.13690.094*
C200.1706 (3)0.44028 (19)0.60557 (17)0.0650 (5)
H20A0.03870.44520.58920.098*
H20B0.24720.51920.61780.098*
H20C0.18520.41130.67500.098*
Fe10.22444 (3)0.247896 (19)0.064950 (18)0.03941 (8)
N10.6829 (2)0.12430 (16)0.34359 (15)0.0571 (4)
N20.3891 (4)−0.29740 (15)0.28358 (15)0.0726 (5)
N30.2412 (2)0.24113 (13)0.50543 (11)0.0473 (3)
N40.3046 (2)0.19276 (11)0.39851 (11)0.0410 (3)
O10.7007 (2)0.22452 (14)0.40943 (16)0.0728 (4)
O20.8042 (3)0.08766 (19)0.28032 (19)0.0951 (6)
O30.5291 (3)−0.32384 (15)0.23593 (15)0.0900 (6)
O40.2588 (4)−0.37005 (15)0.3009 (2)0.1185 (8)

Atomic displacement parameters (Å2)

U11U22U33U12U13U23
C10.0503 (8)0.0398 (7)0.0421 (7)0.0131 (6)0.0009 (6)0.0189 (6)
C20.0665 (10)0.0494 (9)0.0442 (8)0.0288 (8)0.0083 (7)0.0198 (7)
C30.0860 (13)0.0318 (7)0.0396 (7)0.0181 (8)−0.0010 (7)0.0129 (6)
C40.0735 (12)0.0377 (8)0.0477 (8)0.0022 (8)0.0003 (8)0.0169 (6)
C50.0546 (9)0.0441 (8)0.0456 (8)0.0109 (7)0.0064 (7)0.0156 (6)
C60.0527 (8)0.0322 (6)0.0334 (6)0.0123 (6)0.0002 (5)0.0119 (5)
C70.0562 (9)0.0412 (8)0.0423 (7)0.0166 (7)0.0008 (6)0.0055 (6)
C80.0620 (10)0.0333 (7)0.0458 (8)0.0162 (7)0.0000 (7)0.0094 (6)
C90.0474 (8)0.0330 (6)0.0374 (6)0.0113 (6)−0.0019 (5)0.0113 (5)
C100.0429 (7)0.0403 (7)0.0376 (6)0.0151 (6)−0.0008 (5)0.0127 (5)
C110.0639 (10)0.0451 (8)0.0408 (7)0.0264 (7)−0.0015 (7)0.0108 (6)
C120.0645 (11)0.0810 (13)0.0396 (8)0.0435 (10)0.0051 (7)0.0120 (8)
C130.0450 (9)0.0962 (16)0.0514 (9)0.0185 (9)0.0093 (7)0.0315 (10)
C140.0434 (8)0.0590 (10)0.0516 (9)0.0024 (7)−0.0028 (7)0.0232 (8)
C150.0454 (10)0.0815 (10)0.0814 (11)0.0065 (9)−0.0104 (9)0.0163 (9)
C160.0478 (10)0.0945 (13)0.0715 (10)0.0339 (10)0.0015 (8)0.0117 (8)
C170.0743 (14)0.0694 (10)0.1093 (14)0.0405 (10)−0.0153 (11)0.0251 (9)
C180.0756 (14)0.1228 (15)0.0822 (11)0.0391 (12)−0.0092 (10)0.0602 (12)
C190.0677 (13)0.1053 (12)0.0567 (8)0.0298 (11)−0.0220 (8)0.0065 (9)
C200.0869 (14)0.0567 (11)0.0522 (10)0.0314 (10)0.0096 (9)0.0020 (8)
Fe10.03942 (12)0.04333 (13)0.03942 (12)0.01542 (9)−0.00190 (8)0.01395 (9)
N10.0497 (8)0.0612 (10)0.0707 (10)0.0128 (7)0.0001 (7)0.0357 (8)
N20.1285 (18)0.0403 (8)0.0541 (9)0.0290 (10)−0.0004 (10)0.0142 (7)
N30.0641 (9)0.0435 (7)0.0376 (6)0.0190 (6)0.0080 (6)0.0094 (5)
N40.0573 (8)0.0325 (6)0.0365 (6)0.0155 (5)0.0044 (5)0.0102 (5)
O10.0628 (9)0.0566 (8)0.0960 (11)−0.0018 (7)−0.0147 (8)0.0257 (8)
O20.0702 (10)0.1045 (14)0.1224 (16)0.0192 (10)0.0402 (11)0.0418 (12)
O30.1459 (17)0.0619 (10)0.0723 (10)0.0583 (11)0.0112 (10)0.0105 (8)
O40.177 (2)0.0373 (8)0.147 (2)0.0134 (11)0.0416 (17)0.0319 (10)

Geometric parameters (Å, °)

C1—C21.383 (2)C13—C141.414 (3)
C1—C61.396 (2)C13—Fe12.0328 (18)
C1—N11.468 (2)C13—H130.9800
C2—C31.369 (3)C14—Fe12.0325 (17)
C2—H20.9300C14—H140.9800
C3—C41.376 (3)C15—C161.384 (3)
C3—N21.474 (2)C15—C191.391 (4)
C4—C51.371 (2)C15—Fe12.039 (2)
C4—H40.9300C15—H150.9800
C5—C61.389 (2)C16—C171.390 (4)
C5—H50.9300C16—Fe12.031 (2)
C6—N41.4036 (18)C16—H160.9800
C7—N31.327 (2)C17—C181.441 (4)
C7—C81.404 (2)C17—Fe12.0285 (19)
C7—C201.493 (2)C17—H170.9800
C8—C91.368 (2)C18—C191.411 (4)
C8—H80.9300C18—Fe12.0290 (18)
C9—N41.3658 (18)C18—H180.9800
C9—C101.461 (2)C19—Fe12.032 (2)
C10—C111.429 (2)C19—H190.9800
C10—C141.432 (2)C20—H20A0.9600
C10—Fe12.0394 (13)C20—H20B0.9600
C11—C121.422 (2)C20—H20C0.9600
C11—Fe12.0299 (15)N1—O11.212 (2)
C11—H110.9800N1—O21.227 (2)
C12—C131.398 (3)N2—O41.210 (3)
C12—Fe12.0318 (17)N2—O31.212 (3)
C12—H120.9800N3—N41.3775 (18)
C2—C1—C6121.03 (15)Fe1—C17—H17126.3
C2—C1—N1116.47 (15)C19—C18—C17106.3 (2)
C6—C1—N1122.45 (14)C19—C18—Fe169.78 (11)
C3—C2—C1118.33 (16)C17—C18—Fe169.17 (11)
C3—C2—H2120.8C19—C18—H18126.9
C1—C2—H2120.8C17—C18—H18126.9
C2—C3—C4122.51 (15)Fe1—C18—H18126.9
C2—C3—N2117.97 (18)C15—C19—C18108.7 (2)
C4—C3—N2119.51 (18)C15—C19—Fe170.27 (12)
C5—C4—C3118.24 (16)C18—C19—Fe169.55 (12)
C5—C4—H4120.9C15—C19—H19125.7
C3—C4—H4120.9C18—C19—H19125.7
C4—C5—C6121.72 (17)Fe1—C19—H19125.7
C4—C5—H5119.1C7—C20—H20A109.5
C6—C5—H5119.1C7—C20—H20B109.5
C5—C6—C1117.96 (14)H20A—C20—H20B109.5
C5—C6—N4117.92 (14)C7—C20—H20C109.5
C1—C6—N4124.11 (14)H20A—C20—H20C109.5
N3—C7—C8111.62 (14)H20B—C20—H20C109.5
N3—C7—C20121.14 (16)C17—Fe1—C1841.62 (11)
C8—C7—C20127.23 (16)C17—Fe1—C11159.40 (10)
C9—C8—C7106.43 (14)C18—Fe1—C11156.84 (10)
C9—C8—H8126.8C17—Fe1—C1640.04 (11)
C7—C8—H8126.8C18—Fe1—C1668.37 (10)
N4—C9—C8105.52 (13)C11—Fe1—C16123.17 (9)
N4—C9—C10124.59 (13)C17—Fe1—C12158.55 (11)
C8—C9—C10129.85 (14)C18—Fe1—C12121.65 (10)
C11—C10—C14107.16 (14)C11—Fe1—C1240.99 (7)
C11—C10—C9129.07 (14)C16—Fe1—C12159.78 (10)
C14—C10—C9123.73 (14)C17—Fe1—C1968.40 (11)
C11—C10—Fe169.09 (8)C18—Fe1—C1940.67 (11)
C14—C10—Fe169.15 (8)C11—Fe1—C19121.03 (10)
C9—C10—Fe1124.97 (10)C16—Fe1—C1967.29 (10)
C12—C11—C10107.78 (16)C12—Fe1—C19107.79 (9)
C12—C11—Fe169.58 (9)C17—Fe1—C14107.97 (10)
C10—C11—Fe169.80 (8)C18—Fe1—C14124.35 (10)
C12—C11—H11126.1C11—Fe1—C1469.05 (7)
C10—C11—H11126.1C16—Fe1—C14122.61 (9)
Fe1—C11—H11126.1C12—Fe1—C1468.44 (8)
C13—C12—C11108.44 (16)C19—Fe1—C14161.20 (10)
C13—C12—Fe169.92 (10)C17—Fe1—C13123.33 (11)
C11—C12—Fe169.43 (9)C18—Fe1—C13108.12 (10)
C13—C12—H12125.8C11—Fe1—C1368.55 (8)
C11—C12—H12125.8C16—Fe1—C13158.67 (11)
Fe1—C12—H12125.8C12—Fe1—C1340.23 (9)
C12—C13—C14108.75 (16)C19—Fe1—C13124.66 (9)
C12—C13—Fe169.85 (11)C14—Fe1—C1340.72 (8)
C14—C13—Fe169.63 (10)C17—Fe1—C1567.57 (11)
C12—C13—H13125.6C18—Fe1—C1568.07 (11)
C14—C13—H13125.6C11—Fe1—C15106.92 (9)
Fe1—C13—H13125.6C16—Fe1—C1539.76 (10)
C13—C14—C10107.86 (17)C12—Fe1—C15123.95 (10)
C13—C14—Fe169.65 (11)C19—Fe1—C1539.96 (10)
C10—C14—Fe169.66 (9)C14—Fe1—C15157.41 (9)
C13—C14—H14126.1C13—Fe1—C15160.32 (10)
C10—C14—H14126.1C17—Fe1—C10123.26 (9)
Fe1—C14—H14126.1C18—Fe1—C10161.03 (10)
C16—C15—C19108.5 (2)C11—Fe1—C1041.11 (6)
C16—C15—Fe169.83 (12)C16—Fe1—C10107.29 (8)
C19—C15—Fe169.77 (13)C12—Fe1—C1068.91 (6)
C16—C15—H15125.8C19—Fe1—C10156.41 (10)
C19—C15—H15125.8C14—Fe1—C1041.19 (6)
Fe1—C15—H15125.8C13—Fe1—C1068.82 (7)
C15—C16—C17109.2 (2)C15—Fe1—C10121.20 (8)
C15—C16—Fe170.41 (12)O1—N1—O2124.75 (19)
C17—C16—Fe169.88 (13)O1—N1—C1118.46 (17)
C15—C16—H16125.4O2—N1—C1116.70 (18)
C17—C16—H16125.4O4—N2—O3124.54 (19)
Fe1—C16—H16125.4O4—N2—C3117.2 (2)
C16—C17—C18107.3 (2)O3—N2—C3118.2 (2)
C16—C17—Fe170.08 (11)C7—N3—N4103.94 (12)
C18—C17—Fe169.21 (12)C9—N4—N3112.48 (11)
C16—C17—H17126.3C9—N4—C6129.99 (12)
C18—C17—H17126.3N3—N4—C6117.48 (11)
C6—C1—C2—C3−3.0 (2)C13—C12—Fe1—C1880.62 (15)
N1—C1—C2—C3174.66 (14)C11—C12—Fe1—C18−159.58 (13)
C1—C2—C3—C4−1.3 (2)C13—C12—Fe1—C11−119.80 (16)
C1—C2—C3—N2177.89 (14)C13—C12—Fe1—C16−164.5 (2)
C2—C3—C4—C53.7 (2)C11—C12—Fe1—C16−44.7 (3)
N2—C3—C4—C5−175.45 (15)C13—C12—Fe1—C19123.06 (13)
C3—C4—C5—C6−1.9 (2)C11—C12—Fe1—C19−117.14 (13)
C4—C5—C6—C1−2.2 (2)C13—C12—Fe1—C14−37.36 (10)
C4—C5—C6—N4176.74 (14)C11—C12—Fe1—C1482.44 (12)
C2—C1—C6—C54.7 (2)C11—C12—Fe1—C13119.80 (16)
N1—C1—C6—C5−172.86 (14)C13—C12—Fe1—C15164.08 (12)
C2—C1—C6—N4−174.17 (13)C11—C12—Fe1—C15−76.12 (14)
N1—C1—C6—N48.3 (2)C13—C12—Fe1—C10−81.74 (11)
N3—C7—C8—C90.0 (2)C11—C12—Fe1—C1038.06 (10)
C20—C7—C8—C9−179.23 (18)C15—C19—Fe1—C17−80.42 (17)
C7—C8—C9—N4−0.63 (18)C18—C19—Fe1—C1739.38 (16)
C7—C8—C9—C10177.00 (16)C15—C19—Fe1—C18−119.8 (2)
N4—C9—C10—C1123.5 (2)C15—C19—Fe1—C1179.09 (17)
C8—C9—C10—C11−153.74 (17)C18—C19—Fe1—C11−161.12 (15)
N4—C9—C10—C14−159.30 (15)C15—C19—Fe1—C16−37.04 (15)
C8—C9—C10—C1423.5 (3)C18—C19—Fe1—C1682.75 (17)
N4—C9—C10—Fe1113.88 (15)C15—C19—Fe1—C12122.03 (15)
C8—C9—C10—Fe1−63.4 (2)C18—C19—Fe1—C12−118.18 (16)
C14—C10—C11—C120.56 (18)C15—C19—Fe1—C14−162.7 (2)
C9—C10—C11—C12178.14 (15)C18—C19—Fe1—C14−42.9 (4)
Fe1—C10—C11—C1259.44 (11)C15—C19—Fe1—C13163.18 (15)
C14—C10—C11—Fe1−58.88 (11)C18—C19—Fe1—C13−77.02 (18)
C9—C10—C11—Fe1118.70 (15)C18—C19—Fe1—C15119.8 (2)
C10—C11—C12—C13−0.36 (19)C15—C19—Fe1—C1044.1 (3)
Fe1—C11—C12—C1359.22 (12)C18—C19—Fe1—C10163.93 (18)
C10—C11—C12—Fe1−59.58 (11)C13—C14—Fe1—C17−120.57 (14)
C11—C12—C13—C140.0 (2)C10—C14—Fe1—C17120.32 (13)
Fe1—C12—C13—C1458.93 (12)C13—C14—Fe1—C18−77.49 (16)
C11—C12—C13—Fe1−58.92 (12)C10—C14—Fe1—C18163.41 (12)
C12—C13—C14—C100.3 (2)C13—C14—Fe1—C1181.06 (13)
Fe1—C13—C14—C1059.40 (11)C10—C14—Fe1—C11−38.04 (9)
C12—C13—C14—Fe1−59.07 (13)C13—C14—Fe1—C16−162.16 (13)
C11—C10—C14—C13−0.55 (18)C10—C14—Fe1—C1678.74 (13)
C9—C10—C14—C13−178.29 (14)C13—C14—Fe1—C1236.93 (12)
Fe1—C10—C14—C13−59.39 (12)C10—C14—Fe1—C12−82.17 (11)
C11—C10—C14—Fe158.84 (11)C13—C14—Fe1—C19−45.0 (3)
C9—C10—C14—Fe1−118.89 (14)C10—C14—Fe1—C19−164.1 (3)
C19—C15—C16—C170.0 (2)C10—C14—Fe1—C13−119.10 (16)
Fe1—C15—C16—C1759.27 (15)C13—C14—Fe1—C15164.8 (2)
C19—C15—C16—Fe1−59.27 (15)C10—C14—Fe1—C1545.7 (3)
C15—C16—C17—C18−0.2 (2)C13—C14—Fe1—C10119.10 (16)
Fe1—C16—C17—C1859.42 (14)C12—C13—Fe1—C17−161.33 (13)
C15—C16—C17—Fe1−59.60 (15)C14—C13—Fe1—C1778.58 (15)
C16—C17—C18—C190.3 (2)C12—C13—Fe1—C18−117.91 (13)
Fe1—C17—C18—C1960.25 (14)C14—C13—Fe1—C18122.00 (14)
C16—C17—C18—Fe1−59.97 (14)C12—C13—Fe1—C1137.71 (10)
C16—C15—C19—C180.2 (2)C14—C13—Fe1—C11−82.39 (11)
Fe1—C15—C19—C18−59.13 (15)C12—C13—Fe1—C16165.3 (2)
C16—C15—C19—Fe159.31 (15)C14—C13—Fe1—C1645.2 (3)
C17—C18—C19—C15−0.3 (2)C14—C13—Fe1—C12−120.09 (15)
Fe1—C18—C19—C1559.58 (15)C12—C13—Fe1—C19−75.98 (15)
C17—C18—C19—Fe1−59.85 (14)C14—C13—Fe1—C19163.93 (13)
C16—C17—Fe1—C18118.5 (2)C12—C13—Fe1—C14120.09 (15)
C16—C17—Fe1—C11−41.5 (3)C12—C13—Fe1—C15−42.5 (3)
C18—C17—Fe1—C11−160.0 (2)C14—C13—Fe1—C15−162.6 (2)
C18—C17—Fe1—C16−118.5 (2)C12—C13—Fe1—C1081.98 (10)
C16—C17—Fe1—C12163.7 (2)C14—C13—Fe1—C10−38.11 (10)
C18—C17—Fe1—C1245.2 (3)C16—C15—Fe1—C17−36.98 (16)
C16—C17—Fe1—C1979.97 (16)C19—C15—Fe1—C1782.68 (18)
C18—C17—Fe1—C19−38.50 (16)C16—C15—Fe1—C18−82.10 (17)
C16—C17—Fe1—C14−119.65 (14)C19—C15—Fe1—C1837.57 (16)
C18—C17—Fe1—C14121.88 (16)C16—C15—Fe1—C11121.91 (15)
C16—C17—Fe1—C13−161.88 (13)C19—C15—Fe1—C11−118.42 (15)
C18—C17—Fe1—C1379.65 (18)C19—C15—Fe1—C16119.7 (2)
C16—C17—Fe1—C1536.73 (15)C16—C15—Fe1—C12163.64 (13)
C18—C17—Fe1—C15−81.74 (17)C19—C15—Fe1—C12−76.69 (17)
C16—C17—Fe1—C10−76.82 (16)C16—C15—Fe1—C19−119.7 (2)
C18—C17—Fe1—C10164.72 (14)C16—C15—Fe1—C1445.9 (3)
C19—C18—Fe1—C17−117.4 (2)C19—C15—Fe1—C14165.6 (2)
C19—C18—Fe1—C1144.8 (3)C16—C15—Fe1—C13−164.6 (2)
C17—C18—Fe1—C11162.2 (2)C19—C15—Fe1—C13−45.0 (3)
C19—C18—Fe1—C16−79.89 (16)C16—C15—Fe1—C1079.35 (16)
C17—C18—Fe1—C1637.47 (16)C19—C15—Fe1—C10−160.98 (14)
C19—C18—Fe1—C1280.40 (18)C11—C10—Fe1—C17161.99 (13)
C17—C18—Fe1—C12−162.24 (16)C14—C10—Fe1—C17−79.09 (15)
C17—C18—Fe1—C19117.4 (2)C9—C10—Fe1—C1738.21 (18)
C19—C18—Fe1—C14164.58 (14)C11—C10—Fe1—C18−165.4 (3)
C17—C18—Fe1—C14−78.06 (18)C14—C10—Fe1—C18−46.5 (3)
C19—C18—Fe1—C13122.51 (16)C9—C10—Fe1—C1870.8 (3)
C17—C18—Fe1—C13−120.13 (17)C14—C10—Fe1—C11118.92 (15)
C19—C18—Fe1—C15−36.93 (15)C9—C10—Fe1—C11−123.78 (18)
C17—C18—Fe1—C1580.43 (17)C11—C10—Fe1—C16120.99 (12)
C19—C18—Fe1—C10−160.1 (2)C14—C10—Fe1—C16−120.09 (13)
C17—C18—Fe1—C10−42.7 (3)C9—C10—Fe1—C16−2.79 (16)
C12—C11—Fe1—C17−166.3 (3)C11—C10—Fe1—C12−37.96 (11)
C10—C11—Fe1—C17−47.3 (3)C14—C10—Fe1—C1280.96 (12)
C12—C11—Fe1—C1849.0 (3)C9—C10—Fe1—C12−161.75 (16)
C10—C11—Fe1—C18168.0 (2)C11—C10—Fe1—C1948.3 (2)
C12—C11—Fe1—C16163.11 (13)C14—C10—Fe1—C19167.2 (2)
C10—C11—Fe1—C16−77.93 (13)C9—C10—Fe1—C19−75.5 (2)
C10—C11—Fe1—C12118.96 (16)C11—C10—Fe1—C14−118.92 (15)
C12—C11—Fe1—C1981.45 (15)C9—C10—Fe1—C14117.30 (17)
C10—C11—Fe1—C19−159.59 (12)C11—C10—Fe1—C13−81.24 (12)
C12—C11—Fe1—C14−80.84 (13)C14—C10—Fe1—C1337.68 (12)
C10—C11—Fe1—C1438.12 (10)C9—C10—Fe1—C13154.98 (15)
C12—C11—Fe1—C13−37.03 (12)C11—C10—Fe1—C1579.82 (13)
C10—C11—Fe1—C1381.94 (11)C14—C10—Fe1—C15−161.26 (12)
C12—C11—Fe1—C15122.68 (13)C9—C10—Fe1—C15−43.96 (16)
C10—C11—Fe1—C15−118.36 (12)C2—C1—N1—O1−151.82 (15)
C12—C11—Fe1—C10−118.96 (16)C6—C1—N1—O125.8 (2)
C15—C16—Fe1—C17120.2 (2)C2—C1—N1—O224.8 (2)
C15—C16—Fe1—C1881.29 (17)C6—C1—N1—O2−157.56 (17)
C17—C16—Fe1—C18−38.91 (16)C2—C3—N2—O4173.5 (2)
C15—C16—Fe1—C11−75.99 (16)C4—C3—N2—O4−7.3 (3)
C17—C16—Fe1—C11163.82 (14)C2—C3—N2—O3−8.1 (3)
C15—C16—Fe1—C12−42.5 (3)C4—C3—N2—O3171.12 (17)
C17—C16—Fe1—C12−162.7 (2)C8—C7—N3—N40.66 (19)
C15—C16—Fe1—C1937.22 (16)C20—C7—N3—N4179.92 (17)
C17—C16—Fe1—C19−82.97 (17)C8—C9—N4—N31.10 (18)
C15—C16—Fe1—C14−160.88 (13)C10—C9—N4—N3−176.70 (14)
C17—C16—Fe1—C1478.93 (16)C8—C9—N4—C6−176.26 (16)
C15—C16—Fe1—C13165.8 (2)C10—C9—N4—C65.9 (3)
C17—C16—Fe1—C1345.6 (3)C7—N3—N4—C9−1.10 (18)
C17—C16—Fe1—C15−120.2 (2)C7—N3—N4—C6176.62 (14)
C15—C16—Fe1—C10−118.31 (14)C5—C6—N4—C9−127.16 (17)
C17—C16—Fe1—C10121.50 (15)C1—C6—N4—C951.7 (2)
C13—C12—Fe1—C1747.0 (3)C5—C6—N4—N355.59 (19)
C11—C12—Fe1—C17166.8 (2)C1—C6—N4—N3−125.57 (16)

Hydrogen-bond geometry (Å, °)

D—H···AD—HH···AD···AD—H···A
C8—H8···O4i0.932.463.380 (3)170

Symmetry codes: (i) x, y+1, z.

Footnotes

Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: GK2122).

References

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