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The structure of the title compound, [Fe(C22H28N4O2)]Cl {also known as [N,N′-bis[3-(salicylideneamino)prop­yl]ethane-1,2-diamine]iron(III) chloride}, has crystallographic symmetry with both the Fe and Cl atoms lying on twofold axes. The structure adopts a conformation where the phenolate O atoms are trans. The geometry about the Fe center is distorted octahedral due to the restrictions imposed by the bite angles of the chelate rings. The structure displays N—H...Cl hydrogen bonding.

Supporting information

cif

Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807049999/pr2016sup1.cif
Contains datablocks I, global

hkl

Structure factor file (CIF format) https://doi.org/10.1107/S1600536807049999/pr2016Isup2.hkl
Contains datablock I

CCDC reference: 667170

Key indicators

  • Single-crystal X-ray study
  • T = 293 K
  • Mean [sigma](C-C) = 0.006 Å
  • R factor = 0.040
  • wR factor = 0.114
  • Data-to-parameter ratio = 12.2

checkCIF/PLATON results

No syntax errors found



Alert level A PLAT073_ALERT_1_A H-atoms ref, but _hydrogen_treatment reported as constr
Alert level B PLAT027_ALERT_3_B _diffrn_reflns_theta_full (too) Low ............ 24.97 Deg.
Alert level C PLAT062_ALERT_4_C Rescale T(min) & T(max) by ..................... 1.09 PLAT125_ALERT_4_C No _symmetry_space_group_name_Hall Given ....... ? PLAT152_ALERT_1_C Supplied and Calc Volume s.u. Inconsistent ..... ? PLAT245_ALERT_2_C U(iso) H3A Smaller than U(eq) C3 by ... 0.01 AngSq PLAT352_ALERT_3_C Short N-H Bond (0.87A) N2 - H2N ... 0.75 Ang. PLAT710_ALERT_4_C Delete 1-2-3 or 2-3-4 Linear Torsion Angle ... # 1 O1 -FE -O1 -C2 -173.30 0.30 2.555 1.555 1.555 1.555 PLAT710_ALERT_4_C Delete 1-2-3 or 2-3-4 Linear Torsion Angle ... # 9 N2 -FE -N1 -C7 67.00 1.20 2.555 1.555 1.555 1.555 PLAT710_ALERT_4_C Delete 1-2-3 or 2-3-4 Linear Torsion Angle ... # 14 N2 -FE -N1 -C8 -101.80 1.10 2.555 1.555 1.555 1.555 PLAT710_ALERT_4_C Delete 1-2-3 or 2-3-4 Linear Torsion Angle ... # 19 N1 -FE -N2 -C11 39.20 1.20 2.555 1.555 1.555 1.555 PLAT710_ALERT_4_C Delete 1-2-3 or 2-3-4 Linear Torsion Angle ... # 24 N1 -FE -N2 -C10 -86.90 1.20 2.555 1.555 1.555 1.555 PLAT790_ALERT_4_C Centre of Gravity not Within Unit Cell: Resd. # 2 Cl
Alert level G ABSTM02_ALERT_3_G When printed, the submitted absorption T values will be replaced by the scaled T values. Since the ratio of scaled T's is identical to the ratio of reported T values, the scaling does not imply a change to the absorption corrections used in the study. Ratio of Tmax expected/reported 1.086 Tmax scaled 0.794 Tmin scaled 0.626 ABSTY01_ALERT_1_G Extra text has been found in the _exptl_absorpt_correction_type field, which should be only a single keyword. A literature citation should be included in the _exptl_absorpt_process_details field. PLAT199_ALERT_1_G Check the Reported _cell_measurement_temperature 293 K PLAT200_ALERT_1_G Check the Reported _diffrn_ambient_temperature . 293 K PLAT793_ALERT_1_G Check the Absolute Configuration of N2 = ... S PLAT794_ALERT_5_G Check Predicted Bond Valency for Fe (9) 4.22
1 ALERT level A = In general: serious problem 1 ALERT level B = Potentially serious problem 11 ALERT level C = Check and explain 6 ALERT level G = General alerts; check 6 ALERT type 1 CIF construction/syntax error, inconsistent or missing data 1 ALERT type 2 Indicator that the structure model may be wrong or deficient 3 ALERT type 3 Indicator that the structure quality may be low 8 ALERT type 4 Improvement, methodology, query or suggestion 1 ALERT type 5 Informative message, check

Comment top

Metal complexes of linear hexadentate ligands have fascinated inorganic chemists since their first report in 1947 (Dwyer & Lions, 1947). The first such report of a Fe complex of a linear FeN4O2 ligand (i.e. a ligand in which all the N and O donor atoms are linked in a straight chain with no branching) derived from the Schiff base condensation of salicylaldehyde and triethylenetetraamine was in 1955 (Das Sarma & Bailar, 1955). However, this interest lapsed for several years until the discovery that such complexes exhibited spin-crossover magnetic behavior (Sinn et al., 1978). Hexadentate linear FeN4O2 ligands derived from the Schiff base condensation of salicylaldehyde and linear tetramines can be characterized by the number of linking carbon atoms in the tetramine backbone (see Scheme 1). The structures of Fe complexes of Sal222 (Sinn et al., 1978; Hayami et al., 1997; Floquet et al., 2004; Dorbes et al., 2005; Bera et al., 2005; Nishida et al., 1987; Salmon et al., 1999; McPartlin et al., 1978; Maeda et al., 1991; Boinnard et al., 1994), Sal232 (Hayami et al., 1997), Sal323 (Hayami et al., 1997; Ito et al., 1983), and Sal333 (Ito et al., 1983) have been reported. When chelating to Fe, as the number of carbon atoms in the tetramine backbone increases from 6 to 9, the conformation adopted by the ligand changes from a cis-FeN4O2 to a trans-FeN4O2 arrangement for the phenolic O donors. All structurally characterized Fe complexes with Sal222 have adopted the cis-FeN4O2 conformation while all those with either Sal323 or Sal333 have adopted the trans-FeN4O2 conformation. Further, it has been observed that the angles subtended at the Fe center reflect the magnetic properties of the compound (Hayami et al., 1997; Nishida et al., 1987) with low-spin compounds having angles closer to 90° and 180°. While several structures containing the 323 backbone have been structurally characterized, there is no report of a structure containing a chloride anion. There is a report of an isomorphous and isostructural Mn derivative (Zhu et al., 2002).

In the structure of I both the Fe of the cation and Cl anion lie on crystallographic 2 fold axes. The cation has adopted a conformation in which the phenolic O donors are trans to each other. The cis and trans bond angles subtended at the Fe center range from 84.96 (12) to 94.36 (17)° and 173.15 (13) to 174.73 (15)° respectively, indicating that the Fe is low spin. The Fe—O (1.882 (2) Å) and Fe—N bond lengths [1.957 (3)and 2.018 (3) Å] also reflect this.

Related literature top

For related literature, see: Bera et al. (2005); Boinnard et al. (1994); Das Sarma & Bailar (1955); Dorbes et al. (2005); Dwyer & Lions (1947); Floquet et al. (2004); Gultneh et al. (2006); Harpstrite et al. (2003); Hayami et al. (1997); Ito et al. (1983); Maeda et al. (1991); McPartlin et al. (1978); Nishida et al. (1987); Salmon et al. (1999); Sinn et al. (1978); Yisgedu et al. (2007); Butcher et al. (2007); Zhu et al. (2002).

Experimental top

To 4.0 g (20 mmol) of 1,5,8,12-tetraazadodecane in 15 ml of ethanol was added 6.0 g (40 mmol) of salicylaldehyde in 10 ml of ethanol drop-wise. The deep yellow solution was left to stir for half an hour and a crystalline product resulted (H~2~L). To 0.85 g of H~2~L dissolved in 10.0 ml of methanol was added 0.58 g of FeCl3.xH2O. The solution became violet and a red-purple solid precipitated. This was stirred overnight, the solid filtered, washed with methanol and dried. Crystallization was effected by slow evaporation of a DMF solution of the complex.

Refinement top

The H atoms were idealized with C—H distances of 0.93 (aromatic C—H), and 0.97 (CH~2~) \%A and Uĩso~(H) = 1.2U~eq~(C). The amine H atoms were refined isotropically.

Structure description top

Metal complexes of linear hexadentate ligands have fascinated inorganic chemists since their first report in 1947 (Dwyer & Lions, 1947). The first such report of a Fe complex of a linear FeN4O2 ligand derived from the Schiff base condensation of salicylaldehyde and triethylenetetraamine (Sal222, see Figure 1) was in 1955 (Das Sarma & Bailer, 1955). However, this interest lapsed for several years until the discovery that such complexes exhibited spin-crossover magnetic behavior (Sinn et al., 1978). Hexadentate linear FeN4O2 ligands derived from the Schiff base condensation of salicylaldehyde and linear tetramines can be characterized by the number of linking carbon atoms in the tetramine backbone (see Figure 1). The structures of Fe complexes of Sal222 (Sinn et al., 1978; Hayami et al., 1997; Floquet et al., 2004; Dorbes et al., 2005; Bera et al., 2005; Nishida et al., 1987; Salmon et al., 1999; McPartlin et al., 1978; Maeda et al., 1991; Boinnard et al., 1994), Sal232 (Hayami et al., 1997), Sal323 (Hayami et al., 1997; Ito et al., 1983), and Sal333 (Ito et al., 1983) have been reported. When chelating to Fe, as the number of carbon atoms in the tetramine backbone increases from 6 to 9, the conformation adopted by the ligand changes from a cis-FeN4O2 to a trans-FeN4O2 arrangement for the phenolic O donors. All structurally characterized Fe complexes with Sal222 have adopted the cis-FeN4O2 conformation while all those with either Sal323 or Sal333 have adopted the trans-FeN4O2 conformation. Further, it has been observed that the angles subtended at the Fe center reflect the magnetic properties of the compound (Hayami et al., 1997;Nishida et al., 1987) with low-spin compounds having such angles closer to 90° and 180°.

Computing details top

Data collection: XSCANS (Bruker, 1997); cell refinement: XSCANS (Bruker, 1997); data reduction: XSCANS (Bruker, 1997); program(s) used to solve structure: SHELXS97 (Sheldrick, 1990); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: SHELXTL (Bruker, 2000); software used to prepare material for publication: SHELXTL (Bruker, 2000).

Figures top
[Figure 1] Fig. 1. The cation with numbering scheme used. Ellipsoids are drawn at the 20% probabilty level.
[Figure 2] Fig. 2. The packing arrangement viewed down the a axis showing the N—H···Cl hydrogen bonding interactions.
[Figure 3] Fig. 3. Sal222, Sal232, Sal323 and Sal333.
[2,2'-(2,6,9,13-Tetraazatetradeca-1,13-diene-1,14-diyl)diphenolato]iron(III) chloride top
Crystal data top
[Fe(C22H28N4O2)]ClDx = 1.461 Mg m3
Mr = 471.78Mo Kα radiation, λ = 0.71073 Å
Orthorhombic, PccnCell parameters from 52 reflections
a = 7.5156 (15) Åθ = 2.5–27.6°
b = 16.161 (3) ŵ = 0.86 mm1
c = 17.654 (4) ÅT = 293 K
V = 2144.2 (7) Å3Prism, black
Z = 40.47 × 0.35 × 0.27 mm
F(000) = 988
Data collection top
Bruker P4
diffractometer
1284 reflections with I > 2σ(I)
Radiation source: fine-focus sealed tubeRint = 0.000
Graphite monochromatorθmax = 25.0°, θmin = 2.3°
ω scansh = 08
Absorption correction: ψ scans
(North et al., 1968)
k = 019
Tmin = 0.576, Tmax = 0.731l = 020
1873 measured reflections3 standard reflections every 97 reflections
1873 independent reflections intensity decay: none
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.040Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.114H-atom parameters constrained
S = 1.05 w = 1/[σ2(Fo2) + (0.0362P)2 + 2.7631P]
where P = (Fo2 + 2Fc2)/3
1873 reflections(Δ/σ)max < 0.001
154 parametersΔρmax = 0.39 e Å3
0 restraintsΔρmin = 0.44 e Å3
Crystal data top
[Fe(C22H28N4O2)]ClV = 2144.2 (7) Å3
Mr = 471.78Z = 4
Orthorhombic, PccnMo Kα radiation
a = 7.5156 (15) ŵ = 0.86 mm1
b = 16.161 (3) ÅT = 293 K
c = 17.654 (4) Å0.47 × 0.35 × 0.27 mm
Data collection top
Bruker P4
diffractometer
1284 reflections with I > 2σ(I)
Absorption correction: ψ scans
(North et al., 1968)
Rint = 0.000
Tmin = 0.576, Tmax = 0.7313 standard reflections every 97 reflections
1873 measured reflections intensity decay: none
1873 independent reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0400 restraints
wR(F2) = 0.114H-atom parameters constrained
S = 1.05Δρmax = 0.39 e Å3
1873 reflectionsΔρmin = 0.44 e Å3
154 parameters
Special details top

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) top
xyzUiso*/Ueq
Fe0.25000.25000.45616 (4)0.0252 (2)
Cl0.25000.25000.64500 (8)0.0477 (4)
O10.1430 (3)0.35514 (14)0.46105 (14)0.0328 (6)
N10.0734 (4)0.21620 (19)0.38082 (17)0.0290 (7)
N20.0916 (4)0.2076 (2)0.53991 (19)0.0321 (8)
H2N0.018 (5)0.239 (3)0.543 (2)0.036 (12)*
C10.0179 (5)0.3553 (2)0.3355 (2)0.0306 (8)
C20.0830 (5)0.3955 (2)0.4010 (2)0.0304 (9)
C30.0817 (5)0.4824 (2)0.4026 (3)0.0387 (10)
H3A0.12540.51000.44500.027 (10)*
C40.0173 (6)0.5272 (3)0.3428 (3)0.0458 (11)
H4A0.02120.58470.34430.053 (13)*
C50.0538 (6)0.4877 (3)0.2800 (3)0.0500 (12)
H5A0.10040.51850.24020.073 (16)*
C60.0553 (6)0.4032 (3)0.2768 (2)0.0426 (10)
H6A0.10550.37690.23510.039 (11)*
C70.0010 (5)0.2664 (2)0.3343 (2)0.0314 (9)
H7A0.07290.24370.29680.032 (9)*
C80.0042 (5)0.1322 (2)0.3848 (2)0.0365 (10)
H8A0.08980.09120.38240.034 (11)*
H8B0.08330.12350.34220.034 (11)*
C90.1069 (5)0.1228 (2)0.4585 (2)0.0436 (11)
H9A0.19530.16640.46140.042 (11)*
H9B0.16970.07030.45750.051 (12)*
C100.0070 (6)0.1259 (2)0.5292 (2)0.0420 (10)
H10A0.06640.11350.57300.072 (16)*
H10B0.09870.08380.52590.048 (12)*
C110.1977 (5)0.2105 (3)0.6102 (2)0.0455 (11)
H11A0.27770.16340.61240.063 (14)*
H11B0.11990.20850.65400.057 (13)*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Fe0.0230 (3)0.0250 (3)0.0277 (4)0.0014 (3)0.0000.000
Cl0.0391 (7)0.0573 (9)0.0468 (8)0.0180 (8)0.0000.000
O10.0354 (15)0.0276 (13)0.0353 (15)0.0095 (11)0.0071 (12)0.0031 (11)
N10.0256 (17)0.0286 (15)0.0327 (17)0.0019 (13)0.0018 (14)0.0032 (13)
N20.0294 (18)0.0321 (18)0.0349 (19)0.0075 (15)0.0068 (15)0.0045 (15)
C10.025 (2)0.037 (2)0.030 (2)0.0020 (17)0.0002 (16)0.0018 (16)
C20.022 (2)0.030 (2)0.039 (2)0.0037 (16)0.0028 (16)0.0007 (17)
C30.035 (2)0.028 (2)0.053 (3)0.0043 (18)0.000 (2)0.0046 (19)
C40.039 (2)0.034 (2)0.064 (3)0.0079 (19)0.007 (2)0.011 (2)
C50.047 (3)0.050 (3)0.053 (3)0.008 (2)0.001 (2)0.023 (2)
C60.036 (2)0.059 (3)0.033 (2)0.001 (2)0.0002 (19)0.005 (2)
C70.0231 (17)0.044 (2)0.0272 (18)0.0008 (16)0.0020 (16)0.0080 (17)
C80.028 (2)0.034 (2)0.047 (2)0.0030 (17)0.0037 (18)0.0104 (18)
C90.032 (2)0.030 (2)0.069 (3)0.0091 (17)0.011 (2)0.005 (2)
C100.045 (2)0.031 (2)0.049 (3)0.0005 (19)0.014 (2)0.0071 (19)
C110.035 (2)0.075 (3)0.027 (2)0.011 (2)0.0061 (17)0.0108 (19)
Geometric parameters (Å, º) top
Fe—O11.882 (2)C4—C51.387 (6)
Fe—O1i1.882 (2)C4—H4A0.9300
Fe—N11.957 (3)C5—C61.367 (6)
Fe—N1i1.957 (3)C5—H5A0.9300
Fe—N2i2.018 (3)C6—H6A0.9300
Fe—N22.018 (3)C7—H7A0.9300
O1—C21.323 (4)C8—C91.520 (5)
N1—C71.283 (5)C8—H8A0.9700
N1—C81.479 (5)C8—H8B0.9700
N2—C111.476 (5)C9—C101.515 (6)
N2—C101.478 (5)C9—H9A0.9700
N2—H2N0.75 (4)C9—H9B0.9700
C1—C61.406 (5)C10—H10A0.9700
C1—C21.414 (5)C10—H10B0.9700
C1—C71.443 (5)C11—C11i1.500 (9)
C2—C31.406 (5)C11—H11A0.9700
C3—C41.369 (6)C11—H11B0.9700
C3—H3A0.9300
O1—Fe—O1i174.73 (15)C3—C4—H4A119.7
O1—Fe—N189.62 (12)C5—C4—H4A119.7
O1i—Fe—N193.97 (12)C6—C5—C4119.8 (4)
O1—Fe—N1i93.97 (12)C6—C5—H5A120.1
O1i—Fe—N1i89.62 (12)C4—C5—H5A120.1
N1—Fe—N1i94.36 (17)C5—C6—C1121.1 (4)
O1—Fe—N2i84.96 (12)C5—C6—H6A119.5
O1i—Fe—N2i91.18 (12)C1—C6—H6A119.5
N1—Fe—N2i173.15 (13)N1—C7—C1125.2 (3)
N1i—Fe—N2i90.19 (13)N1—C7—H7A117.4
O1—Fe—N291.18 (12)C1—C7—H7A117.4
O1i—Fe—N284.96 (12)N1—C8—C9109.5 (3)
N1—Fe—N290.19 (13)N1—C8—H8A109.8
N1i—Fe—N2173.15 (13)C9—C8—H8A109.8
N2i—Fe—N285.8 (2)N1—C8—H8B109.8
C2—O1—Fe123.6 (2)C9—C8—H8B109.8
C7—N1—C8116.1 (3)H8A—C8—H8B108.2
C7—N1—Fe123.7 (3)C10—C9—C8114.5 (3)
C8—N1—Fe119.4 (2)C10—C9—H9A108.6
C11—N2—C10111.6 (3)C8—C9—H9A108.6
C11—N2—Fe106.7 (2)C10—C9—H9B108.6
C10—N2—Fe117.6 (3)C8—C9—H9B108.6
C11—N2—H2N108 (3)H9A—C9—H9B107.6
C10—N2—H2N107 (3)N2—C10—C9112.2 (3)
Fe—N2—H2N106 (3)N2—C10—H10A109.2
C6—C1—C2119.1 (4)C9—C10—H10A109.2
C6—C1—C7119.8 (4)N2—C10—H10B109.2
C2—C1—C7120.2 (3)C9—C10—H10B109.2
O1—C2—C3118.6 (3)H10A—C10—H10B107.9
O1—C2—C1123.1 (3)N2—C11—C11i108.0 (3)
C3—C2—C1118.2 (4)N2—C11—H11A110.1
C4—C3—C2121.0 (4)C11i—C11—H11A110.1
C4—C3—H3A119.5N2—C11—H11B110.1
C2—C3—H3A119.5C11i—C11—H11B110.1
C3—C4—C5120.6 (4)H11A—C11—H11B108.4
O1i—Fe—O1—C2173.3 (3)Fe—O1—C2—C3151.3 (3)
N1—Fe—O1—C240.4 (3)Fe—O1—C2—C129.5 (5)
N1i—Fe—O1—C253.9 (3)C6—C1—C2—O1175.3 (3)
N2i—Fe—O1—C2143.8 (3)C7—C1—C2—O15.7 (5)
N2—Fe—O1—C2130.6 (3)C6—C1—C2—C33.9 (5)
O1—Fe—N1—C729.5 (3)C7—C1—C2—C3173.4 (4)
O1i—Fe—N1—C7154.4 (3)O1—C2—C3—C4178.4 (4)
N1i—Fe—N1—C764.4 (3)C1—C2—C3—C40.8 (6)
N2i—Fe—N1—C767.0 (12)C2—C3—C4—C52.1 (6)
N2—Fe—N1—C7120.7 (3)C3—C4—C5—C61.8 (7)
O1—Fe—N1—C8139.4 (3)C4—C5—C6—C11.4 (7)
O1i—Fe—N1—C836.8 (3)C2—C1—C6—C54.3 (6)
N1i—Fe—N1—C8126.7 (3)C7—C1—C6—C5173.9 (4)
N2i—Fe—N1—C8101.8 (11)C8—N1—C7—C1162.0 (4)
N2—Fe—N1—C848.2 (3)Fe—N1—C7—C17.2 (5)
O1—Fe—N2—C1199.5 (3)C6—C1—C7—N1173.4 (4)
O1i—Fe—N2—C1176.9 (3)C2—C1—C7—N117.1 (6)
N1—Fe—N2—C11170.9 (3)C7—N1—C8—C9106.7 (4)
N1i—Fe—N2—C1139.2 (12)Fe—N1—C8—C963.0 (4)
N2i—Fe—N2—C1114.7 (2)N1—C8—C9—C1065.7 (4)
O1—Fe—N2—C10134.3 (3)C11—N2—C10—C9178.3 (3)
O1i—Fe—N2—C1049.2 (3)Fe—N2—C10—C958.0 (4)
N1—Fe—N2—C1044.7 (3)C8—C9—C10—N265.0 (4)
N1i—Fe—N2—C1086.9 (12)C10—N2—C11—C11i170.8 (4)
N2i—Fe—N2—C10140.8 (3)Fe—N2—C11—C11i41.1 (4)
Symmetry code: (i) x+1/2, y+1/2, z.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N2—H2N···Cl0.75 (4)2.70 (4)3.241 (3)131 (4)

Experimental details

Crystal data
Chemical formula[Fe(C22H28N4O2)]Cl
Mr471.78
Crystal system, space groupOrthorhombic, Pccn
Temperature (K)293
a, b, c (Å)7.5156 (15), 16.161 (3), 17.654 (4)
V3)2144.2 (7)
Z4
Radiation typeMo Kα
µ (mm1)0.86
Crystal size (mm)0.47 × 0.35 × 0.27
Data collection
DiffractometerBruker P4
Absorption correctionψ scans
(North et al., 1968)
Tmin, Tmax0.576, 0.731
No. of measured, independent and
observed [I > 2σ(I)] reflections
1873, 1873, 1284
Rint0.000
(sin θ/λ)max1)0.594
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.040, 0.114, 1.05
No. of reflections1873
No. of parameters154
H-atom treatmentH-atom parameters constrained
Δρmax, Δρmin (e Å3)0.39, 0.44

Computer programs: XSCANS (Bruker, 1997), SHELXS97 (Sheldrick, 1990), SHELXL97 (Sheldrick, 1997), SHELXTL (Bruker, 2000).

Selected geometric parameters (Å, º) top
Fe—O11.882 (2)Fe—N22.018 (3)
Fe—N11.957 (3)
O1—Fe—O1i174.73 (15)N1—Fe—N2i173.15 (13)
O1—Fe—N189.62 (12)O1—Fe—N291.18 (12)
O1i—Fe—N193.97 (12)N1—Fe—N290.19 (13)
N1—Fe—N1i94.36 (17)N2i—Fe—N285.8 (2)
O1—Fe—N2i84.96 (12)
Symmetry code: (i) x+1/2, y+1/2, z.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N2—H2N···Cl0.75 (4)2.70 (4)3.241 (3)131 (4)
 

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