Literature DB >> 22346888

3-Anilino-1-ferrocenylpropan-1-one.

Zorica Leka, Sladjana B Novaković, Dragana Stevanović, Goran A Bogdanović, Rastko D Vukićević.   

Abstract

In the title ferrocene derivative, [Fe(C(5)H(5))(C(14)H(14)NO)], the dihedral angle between the mean planes of the phenyl ring and the substituted cyclo-penta-dienyl ring is 84.4 (1)°. The mol-ecules are connected into centrosymmetric dimers via N-H⋯O hydrogen bonds. In addition, C-H⋯O and C-H⋯N contacts stabilize the crystal packing.

Entities:  

Year:  2012        PMID: 22346888      PMCID: PMC3274941          DOI: 10.1107/S1600536812003492

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


Related literature

For the physico-chemical properties of ferrocene-based compounds, see: Togni & Hayashi (1995 ▶). For related crystal structures and details of the synthesis, see: Damljanović et al. (2011 ▶); Stevanović et al. (2012 ▶); Leka, Novaković, Stevanović et al. (2012 ▶); Leka, Novaković, Pejović et al. (2012 ▶).

Experimental

Crystal data

[Fe(C5H5)(n class="Chemical">C14H14NO)] M = 333.20 Triclinic, a = 7.605 (3) Å b = 9.748 (3) Å c = 12.098 (4) Å α = 86.036 (4)° β = 73.869 (4)° γ = 68.684 (3)° V = 802.1 (5) Å3 Z = 2 Mo Kα radiation μ = 0.94 mm−1 T = 293 K 0.26 × 0.25 × 0.18 mm

Data collection

Enraf–Nonius CAD-4 diffractometer 3395 measured reflections 3143 independent reflections 2449 reflections with I > 2σ(I) R int = 0.017 3 standard reflections every 60 min intensity decay: none

Refinement

R[F 2 > 2σ(F 2)] = 0.034 wR(F 2) = 0.091 S = 1.05 3143 reflections 203 parameters H atoms treated by a mixture of independent and constrained refinement Δρmax = 0.21 e Å−3 Δρmin = −0.21 e Å−3 Data collection: CAD-4 Software (Enraf–Nonius, 1989 ▶); cell refinement: CAD-4 Software; data reduction: CAD-4 Software; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: ORTEP-3 (Farrugia, 1997 ▶) and POV-RAY (Persistence of Vision, 2004 ▶); software used to prepare material for publication: WinGX (Farrugia, 1999 ▶), PLATON (Spek, 2009 ▶) and PARST (Nardelli, 1995 ▶). Crystal structure: contains datablock(s) I, global. DOI: 10.1107/S1600536812003492/bt5790sup1.cif Structure factors: contains datablock(s) I. DOI: 10.1107/S1600536812003492/bt5790Isup2.hkl Additional supplementary materials: crystallographic information; 3D view; checkCIF report
[Fe(C5H5)(C14H14NO)]Z = 2
Mr = 333.20F(000) = 348
Triclinic, P1Dx = 1.380 Mg m3
Hall symbol: -P 1Mo Kα radiation, λ = 0.71073 Å
a = 7.605 (3) ÅCell parameters from 25 reflections
b = 9.748 (3) Åθ = 10.3–15.4°
c = 12.098 (4) ŵ = 0.94 mm1
α = 86.036 (4)°T = 293 K
β = 73.869 (4)°Prismatic, orange
γ = 68.684 (3)°0.26 × 0.25 × 0.18 mm
V = 802.1 (5) Å3
Enraf–Nonius CAD-4 diffractometerRint = 0.017
Radiation source: fine-focus sealed tubeθmax = 26.0°, θmin = 1.8°
graphiteh = 0→9
ω/2θ scansk = −11→11
3395 measured reflectionsl = −14→14
3143 independent reflections3 standard reflections every 60 min
2449 reflections with I > 2σ(I) intensity decay: none
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.034Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.091H atoms treated by a mixture of independent and constrained refinement
S = 1.05w = 1/[σ2(Fo2) + (0.0483P)2 + 0.0454P] where P = (Fo2 + 2Fc2)/3
3143 reflections(Δ/σ)max = 0.001
203 parametersΔρmax = 0.21 e Å3
0 restraintsΔρmin = −0.20 e Å3
xyzUiso*/Ueq
Fe01−0.00076 (5)0.31825 (3)0.71233 (3)0.04475 (12)
O10.2742 (2)0.01729 (17)0.48442 (13)0.0510 (4)
N10.4975 (3)−0.2119 (2)0.64319 (17)0.0458 (4)
C1−0.0181 (3)0.1691 (2)0.61151 (18)0.0394 (5)
C2−0.1759 (3)0.2006 (2)0.7152 (2)0.0461 (5)
H2−0.20000.13260.76950.055*
C3−0.2883 (3)0.3525 (3)0.7207 (2)0.0546 (6)
H3−0.39920.40200.77920.065*
C4−0.2033 (4)0.4165 (3)0.6219 (2)0.0569 (6)
H4−0.24930.51550.60460.068*
C5−0.0372 (4)0.3057 (2)0.5537 (2)0.0480 (5)
H50.04490.31870.48410.058*
C60.2740 (5)0.2429 (4)0.7347 (4)0.0846 (10)
H60.37570.15680.70170.102*
C70.1301 (8)0.2555 (5)0.8412 (4)0.1119 (16)
H70.11890.17960.89040.134*
C80.0069 (6)0.4060 (5)0.8582 (3)0.0975 (13)
H8−0.09970.44770.92140.117*
C90.0746 (5)0.4800 (4)0.7630 (3)0.0807 (9)
H90.01990.58010.75120.097*
C100.2371 (4)0.3796 (4)0.6889 (3)0.0771 (9)
H100.30960.40160.61910.093*
C110.1447 (3)0.0293 (2)0.57366 (17)0.0373 (4)
C120.1448 (3)−0.1032 (2)0.64668 (18)0.0402 (5)
H12B0.0398−0.13340.64020.048*
H12A0.1188−0.07520.72670.048*
C130.3384 (3)−0.2331 (2)0.61176 (19)0.0451 (5)
H13A0.3196−0.32060.64780.054*
H13B0.3752−0.25010.52900.054*
C140.5038 (3)−0.2122 (2)0.75672 (19)0.0414 (5)
C150.3963 (4)−0.2745 (3)0.8440 (2)0.0554 (6)
H150.3092−0.31210.82830.066*
C160.4193 (4)−0.2805 (4)0.9544 (2)0.0714 (8)
H160.3476−0.32321.01160.086*
C170.5448 (5)−0.2254 (4)0.9813 (2)0.0772 (9)
H170.5602−0.23171.05530.093*
C180.6488 (4)−0.1596 (3)0.8953 (2)0.0681 (7)
H180.7327−0.11970.91220.082*
C190.6284 (3)−0.1532 (3)0.7854 (2)0.0519 (6)
H190.6989−0.10880.72910.062*
H1N0.546 (3)−0.161 (3)0.600 (2)0.044 (7)*
U11U22U33U12U13U23
Fe010.04078 (19)0.04572 (19)0.0522 (2)−0.01795 (14)−0.01521 (14)−0.00289 (13)
O10.0527 (10)0.0508 (9)0.0448 (9)−0.0228 (8)−0.0013 (7)0.0055 (7)
N10.0391 (10)0.0494 (11)0.0490 (11)−0.0190 (9)−0.0103 (9)0.0123 (9)
C10.0382 (11)0.0417 (11)0.0448 (11)−0.0191 (9)−0.0152 (9)0.0021 (9)
C20.0380 (11)0.0497 (13)0.0538 (13)−0.0216 (10)−0.0096 (10)0.0024 (10)
C30.0386 (12)0.0520 (13)0.0711 (16)−0.0138 (11)−0.0136 (11)−0.0048 (12)
C40.0558 (15)0.0407 (12)0.0758 (17)−0.0088 (11)−0.0326 (13)0.0045 (11)
C50.0562 (14)0.0460 (12)0.0485 (12)−0.0222 (11)−0.0214 (11)0.0097 (10)
C60.0646 (19)0.077 (2)0.124 (3)−0.0120 (16)−0.056 (2)−0.018 (2)
C70.167 (4)0.134 (4)0.114 (3)−0.103 (4)−0.109 (3)0.056 (3)
C80.095 (3)0.155 (4)0.068 (2)−0.074 (3)−0.0120 (18)−0.038 (2)
C90.0660 (19)0.0687 (18)0.117 (3)−0.0305 (16)−0.0230 (18)−0.0293 (18)
C100.0559 (17)0.091 (2)0.096 (2)−0.0390 (17)−0.0160 (16)−0.0179 (18)
C110.0383 (11)0.0425 (11)0.0383 (11)−0.0211 (9)−0.0133 (9)0.0044 (8)
C120.0367 (11)0.0430 (11)0.0446 (11)−0.0193 (9)−0.0110 (9)0.0064 (9)
C130.0473 (13)0.0392 (11)0.0501 (12)−0.0178 (10)−0.0124 (10)0.0022 (9)
C140.0320 (10)0.0373 (10)0.0487 (12)−0.0079 (9)−0.0080 (9)0.0049 (9)
C150.0509 (14)0.0659 (15)0.0574 (14)−0.0319 (12)−0.0152 (11)0.0138 (12)
C160.0685 (19)0.100 (2)0.0539 (15)−0.0450 (17)−0.0138 (13)0.0213 (15)
C170.074 (2)0.111 (3)0.0522 (15)−0.0374 (18)−0.0210 (14)0.0063 (16)
C180.0594 (17)0.086 (2)0.0691 (17)−0.0334 (15)−0.0214 (14)−0.0047 (15)
C190.0422 (13)0.0558 (14)0.0596 (14)−0.0232 (11)−0.0099 (11)0.0051 (11)
Fe01—C72.021 (3)C6—H60.9300
Fe01—C12.023 (2)C7—C81.417 (6)
Fe01—C52.031 (2)C7—H70.9300
Fe01—C62.037 (3)C8—C91.392 (5)
Fe01—C82.038 (3)C8—H80.9300
Fe01—C22.042 (2)C9—C101.383 (4)
Fe01—C92.043 (3)C9—H90.9300
Fe01—C102.046 (3)C10—H100.9300
Fe01—C42.051 (2)C11—C121.513 (3)
Fe01—C32.063 (3)C12—C131.524 (3)
O1—C111.221 (2)C12—H12B0.9700
N1—C141.387 (3)C12—H12A0.9700
N1—C131.449 (3)C13—H13A0.9700
N1—H1N0.80 (2)C13—H13B0.9700
C1—C21.434 (3)C14—C151.394 (3)
C1—C51.439 (3)C14—C191.399 (3)
C1—C111.464 (3)C15—C161.390 (4)
C2—C31.410 (3)C15—H150.9300
C2—H20.9300C16—C171.369 (4)
C3—C41.413 (4)C16—H160.9300
C3—H30.9300C17—C181.393 (4)
C4—C51.413 (3)C17—H170.9300
C4—H40.9300C18—C191.375 (4)
C5—H50.9300C18—H180.9300
C6—C101.369 (5)C19—H190.9300
C6—C71.420 (6)
C7—Fe01—C1121.56 (15)Fe01—C4—H4126.7
C7—Fe01—C5156.29 (18)C4—C5—C1107.5 (2)
C1—Fe01—C541.58 (9)C4—C5—Fe0170.49 (14)
C7—Fe01—C640.95 (17)C1—C5—Fe0168.90 (12)
C1—Fe01—C6108.24 (11)C4—C5—H5126.2
C5—Fe01—C6119.96 (13)C1—C5—H5126.2
C7—Fe01—C840.86 (17)Fe01—C5—H5125.9
C1—Fe01—C8157.53 (15)C10—C6—C7108.1 (3)
C5—Fe01—C8160.08 (16)C10—C6—Fe0170.77 (17)
C6—Fe01—C867.93 (15)C7—C6—Fe0168.91 (19)
C7—Fe01—C2109.56 (13)C10—C6—H6126.0
C1—Fe01—C241.32 (9)C7—C6—H6126.0
C5—Fe01—C269.15 (9)Fe01—C6—H6125.9
C6—Fe01—C2127.82 (13)C8—C7—C6106.8 (3)
C8—Fe01—C2122.33 (13)C8—C7—Fe0170.2 (2)
C7—Fe01—C967.70 (16)C6—C7—Fe0170.15 (19)
C1—Fe01—C9160.84 (12)C8—C7—H7126.6
C5—Fe01—C9123.30 (13)C6—C7—H7126.6
C6—Fe01—C966.68 (13)Fe01—C7—H7124.7
C8—Fe01—C939.90 (15)C9—C8—C7107.4 (3)
C2—Fe01—C9156.23 (12)C9—C8—Fe0170.27 (17)
C7—Fe01—C1067.42 (16)C7—C8—Fe0168.94 (18)
C1—Fe01—C10124.95 (11)C9—C8—H8126.3
C5—Fe01—C10106.64 (12)C7—C8—H8126.3
C6—Fe01—C1039.17 (14)Fe01—C8—H8126.1
C8—Fe01—C1066.99 (14)C10—C9—C8108.6 (3)
C2—Fe01—C10163.30 (11)C10—C9—Fe0170.35 (16)
C9—Fe01—C1039.54 (12)C8—C9—Fe0169.84 (17)
C7—Fe01—C4162.65 (19)C10—C9—H9125.7
C1—Fe01—C468.75 (9)C8—C9—H9125.7
C5—Fe01—C440.49 (10)Fe01—C9—H9125.7
C6—Fe01—C4154.06 (15)C6—C10—C9109.2 (3)
C8—Fe01—C4124.72 (16)C6—C10—Fe0170.06 (18)
C2—Fe01—C467.94 (10)C9—C10—Fe0170.11 (17)
C9—Fe01—C4107.24 (13)C6—C10—H10125.4
C10—Fe01—C4120.04 (14)C9—C10—H10125.4
C7—Fe01—C3126.91 (17)Fe01—C10—H10126.0
C1—Fe01—C368.67 (9)O1—C11—C1121.74 (18)
C5—Fe01—C368.33 (10)O1—C11—C12120.34 (18)
C6—Fe01—C3164.78 (15)C1—C11—C12117.89 (17)
C8—Fe01—C3108.87 (13)C11—C12—C13112.81 (17)
C2—Fe01—C340.18 (9)C11—C12—H12B109.0
C9—Fe01—C3121.15 (12)C13—C12—H12B109.0
C10—Fe01—C3154.80 (13)C11—C12—H12A109.0
C4—Fe01—C340.17 (10)C13—C12—H12A109.0
C14—N1—C13122.08 (19)H12B—C12—H12A107.8
C14—N1—H1N117.2 (17)N1—C13—C12113.66 (18)
C13—N1—H1N113.7 (17)N1—C13—H13A108.8
C2—C1—C5107.12 (19)C12—C13—H13A108.8
C2—C1—C11127.89 (19)N1—C13—H13B108.8
C5—C1—C11124.78 (19)C12—C13—H13B108.8
C2—C1—Fe0170.05 (12)H13A—C13—H13B107.7
C5—C1—Fe0169.52 (12)N1—C14—C15122.8 (2)
C11—C1—Fe01121.47 (14)N1—C14—C19119.3 (2)
C3—C2—C1108.2 (2)C15—C14—C19117.8 (2)
C3—C2—Fe0170.69 (14)C16—C15—C14120.0 (2)
C1—C2—Fe0168.63 (12)C16—C15—H15120.0
C3—C2—H2125.9C14—C15—H15120.0
C1—C2—H2125.9C17—C16—C15121.8 (3)
Fe01—C2—H2126.4C17—C16—H16119.1
C2—C3—C4108.2 (2)C15—C16—H16119.1
C2—C3—Fe0169.13 (13)C16—C17—C18118.5 (3)
C4—C3—Fe0169.46 (14)C16—C17—H17120.8
C2—C3—H3125.9C18—C17—H17120.8
C4—C3—H3125.9C19—C18—C17120.5 (3)
Fe01—C3—H3127.1C19—C18—H18119.7
C5—C4—C3108.9 (2)C17—C18—H18119.7
C5—C4—Fe0169.02 (13)C18—C19—C14121.3 (2)
C3—C4—Fe0170.36 (14)C18—C19—H19119.3
C5—C4—H4125.5C14—C19—H19119.3
C3—C4—H4125.5
C7—Fe01—C1—C284.1 (2)C2—Fe01—C6—C10165.22 (17)
C5—Fe01—C1—C2−118.02 (18)C9—Fe01—C6—C10−36.8 (2)
C6—Fe01—C1—C2127.09 (18)C4—Fe01—C6—C1044.6 (3)
C8—Fe01—C1—C250.9 (4)C3—Fe01—C6—C10−161.0 (4)
C9—Fe01—C1—C2−161.7 (3)C1—Fe01—C6—C7−117.5 (2)
C10—Fe01—C1—C2167.13 (16)C5—Fe01—C6—C7−161.5 (2)
C4—Fe01—C1—C2−80.32 (15)C8—Fe01—C6—C738.9 (2)
C3—Fe01—C1—C2−37.06 (14)C2—Fe01—C6—C7−75.6 (3)
C7—Fe01—C1—C5−157.9 (2)C9—Fe01—C6—C782.3 (2)
C6—Fe01—C1—C5−114.89 (18)C10—Fe01—C6—C7119.1 (3)
C8—Fe01—C1—C5168.9 (3)C4—Fe01—C6—C7163.8 (3)
C2—Fe01—C1—C5118.02 (18)C3—Fe01—C6—C7−41.8 (5)
C9—Fe01—C1—C5−43.7 (4)C10—C6—C7—C8−0.8 (3)
C10—Fe01—C1—C5−74.85 (19)Fe01—C6—C7—C8−61.0 (2)
C4—Fe01—C1—C537.70 (14)C10—C6—C7—Fe0160.2 (2)
C3—Fe01—C1—C580.96 (15)C1—Fe01—C7—C8−161.36 (19)
C7—Fe01—C1—C11−38.9 (3)C5—Fe01—C7—C8160.3 (3)
C5—Fe01—C1—C11119.0 (2)C6—Fe01—C7—C8117.1 (3)
C6—Fe01—C1—C114.1 (2)C2—Fe01—C7—C8−117.2 (2)
C8—Fe01—C1—C11−72.1 (4)C9—Fe01—C7—C837.5 (2)
C2—Fe01—C1—C11−122.9 (2)C10—Fe01—C7—C880.4 (2)
C9—Fe01—C1—C1175.4 (4)C4—Fe01—C7—C8−38.7 (5)
C10—Fe01—C1—C1144.2 (2)C3—Fe01—C7—C8−75.5 (3)
C4—Fe01—C1—C11156.73 (19)C1—Fe01—C7—C681.5 (2)
C3—Fe01—C1—C11−160.01 (19)C5—Fe01—C7—C643.2 (4)
C5—C1—C2—C3−0.1 (2)C8—Fe01—C7—C6−117.1 (3)
C11—C1—C2—C3174.7 (2)C2—Fe01—C7—C6125.7 (2)
Fe01—C1—C2—C359.83 (16)C9—Fe01—C7—C6−79.6 (2)
C5—C1—C2—Fe01−59.92 (15)C10—Fe01—C7—C6−36.69 (19)
C11—C1—C2—Fe01114.9 (2)C4—Fe01—C7—C6−155.8 (4)
C7—Fe01—C2—C3124.5 (2)C3—Fe01—C7—C6167.35 (18)
C1—Fe01—C2—C3−119.5 (2)C6—C7—C8—C90.9 (4)
C5—Fe01—C2—C3−80.70 (16)Fe01—C7—C8—C9−60.0 (2)
C6—Fe01—C2—C3166.91 (19)C6—C7—C8—Fe0161.0 (2)
C8—Fe01—C2—C381.0 (2)C7—Fe01—C8—C9118.6 (3)
C9—Fe01—C2—C345.6 (4)C1—Fe01—C8—C9164.0 (2)
C10—Fe01—C2—C3−159.0 (4)C5—Fe01—C8—C9−38.0 (5)
C4—Fe01—C2—C3−37.07 (15)C6—Fe01—C8—C979.6 (2)
C7—Fe01—C2—C1−115.9 (2)C2—Fe01—C8—C9−158.67 (18)
C5—Fe01—C2—C138.82 (13)C10—Fe01—C8—C937.0 (2)
C6—Fe01—C2—C1−73.6 (2)C4—Fe01—C8—C9−74.5 (2)
C8—Fe01—C2—C1−159.45 (19)C3—Fe01—C8—C9−116.3 (2)
C9—Fe01—C2—C1165.2 (3)C1—Fe01—C8—C745.4 (4)
C10—Fe01—C2—C1−39.5 (5)C5—Fe01—C8—C7−156.6 (3)
C4—Fe01—C2—C182.46 (14)C6—Fe01—C8—C7−39.0 (2)
C3—Fe01—C2—C1119.5 (2)C2—Fe01—C8—C782.8 (3)
C1—C2—C3—C40.1 (3)C9—Fe01—C8—C7−118.6 (3)
Fe01—C2—C3—C458.62 (17)C10—Fe01—C8—C7−81.6 (3)
C1—C2—C3—Fe01−58.54 (15)C4—Fe01—C8—C7166.9 (2)
C7—Fe01—C3—C2−76.1 (2)C3—Fe01—C8—C7125.1 (3)
C1—Fe01—C3—C238.08 (14)C7—C8—C9—C10−0.7 (4)
C5—Fe01—C3—C282.93 (15)Fe01—C8—C9—C10−59.9 (2)
C6—Fe01—C3—C2−43.0 (5)C7—C8—C9—Fe0159.2 (2)
C8—Fe01—C3—C2−118.1 (2)C7—Fe01—C9—C1081.1 (3)
C9—Fe01—C3—C2−160.32 (17)C1—Fe01—C9—C10−41.8 (5)
C10—Fe01—C3—C2166.0 (2)C5—Fe01—C9—C10−75.1 (2)
C4—Fe01—C3—C2120.0 (2)C6—Fe01—C9—C1036.5 (2)
C7—Fe01—C3—C4163.9 (2)C8—Fe01—C9—C10119.5 (3)
C1—Fe01—C3—C4−81.92 (15)C2—Fe01—C9—C10169.2 (3)
C5—Fe01—C3—C4−37.07 (14)C4—Fe01—C9—C10−116.6 (2)
C6—Fe01—C3—C4−163.0 (4)C3—Fe01—C9—C10−158.2 (2)
C8—Fe01—C3—C4121.9 (2)C7—Fe01—C9—C8−38.4 (3)
C2—Fe01—C3—C4−120.0 (2)C1—Fe01—C9—C8−161.3 (3)
C9—Fe01—C3—C479.7 (2)C5—Fe01—C9—C8165.5 (2)
C10—Fe01—C3—C446.0 (3)C6—Fe01—C9—C8−83.0 (3)
C2—C3—C4—C50.0 (3)C2—Fe01—C9—C849.7 (4)
Fe01—C3—C4—C558.38 (17)C10—Fe01—C9—C8−119.5 (3)
C2—C3—C4—Fe01−58.41 (17)C4—Fe01—C9—C8124.0 (2)
C7—Fe01—C4—C5−168.4 (4)C3—Fe01—C9—C882.3 (3)
C1—Fe01—C4—C5−38.69 (13)C7—C6—C10—C90.4 (3)
C6—Fe01—C4—C549.5 (3)Fe01—C6—C10—C959.4 (2)
C8—Fe01—C4—C5161.79 (17)C7—C6—C10—Fe01−59.0 (2)
C2—Fe01—C4—C5−83.30 (15)C8—C9—C10—C60.2 (4)
C9—Fe01—C4—C5121.45 (16)Fe01—C9—C10—C6−59.4 (2)
C10—Fe01—C4—C580.33 (17)C8—C9—C10—Fe0159.6 (2)
C3—Fe01—C4—C5−120.4 (2)C7—Fe01—C10—C638.3 (2)
C7—Fe01—C4—C3−48.0 (5)C1—Fe01—C10—C6−75.3 (2)
C1—Fe01—C4—C381.69 (15)C5—Fe01—C10—C6−117.3 (2)
C5—Fe01—C4—C3120.4 (2)C8—Fe01—C10—C682.8 (3)
C6—Fe01—C4—C3169.9 (2)C2—Fe01—C10—C6−44.5 (5)
C8—Fe01—C4—C3−77.8 (2)C9—Fe01—C10—C6120.2 (3)
C2—Fe01—C4—C337.08 (14)C4—Fe01—C10—C6−159.2 (2)
C9—Fe01—C4—C3−118.17 (17)C3—Fe01—C10—C6168.4 (3)
C10—Fe01—C4—C3−159.29 (15)C7—Fe01—C10—C9−81.9 (3)
C3—C4—C5—C10.0 (3)C1—Fe01—C10—C9164.5 (2)
Fe01—C4—C5—C159.18 (15)C5—Fe01—C10—C9122.6 (2)
C3—C4—C5—Fe01−59.20 (17)C6—Fe01—C10—C9−120.2 (3)
C2—C1—C5—C40.1 (2)C8—Fe01—C10—C9−37.4 (2)
C11—C1—C5—C4−174.96 (19)C2—Fe01—C10—C9−164.7 (4)
Fe01—C1—C5—C4−60.18 (16)C4—Fe01—C10—C980.6 (2)
C2—C1—C5—Fe0160.26 (15)C3—Fe01—C10—C948.2 (4)
C11—C1—C5—Fe01−114.8 (2)C2—C1—C11—O1−177.9 (2)
C7—Fe01—C5—C4171.4 (3)C5—C1—C11—O1−3.9 (3)
C1—Fe01—C5—C4118.6 (2)Fe01—C1—C11—O1−89.6 (2)
C6—Fe01—C5—C4−157.43 (17)C2—C1—C11—C124.3 (3)
C8—Fe01—C5—C4−48.9 (4)C5—C1—C11—C12178.23 (19)
C2—Fe01—C5—C480.04 (16)Fe01—C1—C11—C1292.5 (2)
C9—Fe01—C5—C4−77.10 (19)O1—C11—C12—C1313.0 (3)
C10—Fe01—C5—C4−117.04 (17)C1—C11—C12—C13−169.09 (17)
C3—Fe01—C5—C436.79 (15)C14—N1—C13—C1270.6 (3)
C7—Fe01—C5—C152.8 (4)C11—C12—C13—N172.3 (2)
C6—Fe01—C5—C183.95 (18)C13—N1—C14—C1519.6 (3)
C8—Fe01—C5—C1−167.5 (3)C13—N1—C14—C19−163.0 (2)
C2—Fe01—C5—C1−38.59 (13)N1—C14—C15—C16175.5 (2)
C9—Fe01—C5—C1164.27 (14)C19—C14—C15—C16−1.9 (4)
C10—Fe01—C5—C1124.33 (15)C14—C15—C16—C170.6 (5)
C4—Fe01—C5—C1−118.6 (2)C15—C16—C17—C181.1 (5)
C3—Fe01—C5—C1−81.84 (14)C16—C17—C18—C19−1.3 (5)
C7—Fe01—C6—C10−119.1 (3)C17—C18—C19—C14−0.1 (4)
C1—Fe01—C6—C10123.40 (19)N1—C14—C19—C18−175.8 (2)
C5—Fe01—C6—C1079.4 (2)C15—C14—C19—C181.7 (4)
C8—Fe01—C6—C10−80.2 (2)
D—H···AD—HH···AD···AD—H···A
N1—H1N···O1i0.80 (3)2.30 (3)3.082 (3)164 (2)
C19—H19···O1i0.932.653.425 (3)141
C4—H4···N1ii0.932.633.489 (3)153
Table 1

Hydrogen-bond geometry (Å, °)

D—H⋯AD—HH⋯ADAD—H⋯A
N1—H1N⋯O1i0.80 (3)2.30 (3)3.082 (3)164 (2)
C19—H19⋯O1i0.932.653.425 (3)141
C4—H4⋯N1ii0.932.633.489 (3)153

Symmetry codes: (i) ; (ii) .

  5 in total

1.  A new polymorph of 1-ferrocenyl-3-(3-nitroanilino)propan-1-one.

Authors:  Dragana Stevanović; Anka Pejović; Sladjana B Novaković; Goran A Bogdanović; Vladimir Divjaković; Rastko D Vukićević
Journal:  Acta Crystallogr C       Date:  2012-01-14       Impact factor: 1.172

2.  A short history of SHELX.

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

3.  1-Ferrocenyl-3-(3-fluoro-anilino)propan-1-one.

Authors:  Zorica Leka; Sladjana B Novaković; Anka Pejović; Goran A Bogdanović; Rastko D Vukićević
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-01-31

4.  1-Ferrocenyl-3-(4-methyl-anilino)propan-1-one.

Authors:  Zorica Leka; Sladjana B Novaković; Dragana Stevanović; Goran A Bogdanović; Rastko D Vukićević
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-01-31

5.  Structure validation in chemical crystallography.

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

1.  1-Ferrocenyl-3-(3-fluoro-anilino)propan-1-one.

Authors:  Zorica Leka; Sladjana B Novaković; Anka Pejović; Goran A Bogdanović; Rastko D Vukićević
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-01-31

2.  1-Ferrocenyl-3-(4-methyl-anilino)propan-1-one.

Authors:  Zorica Leka; Sladjana B Novaković; Dragana Stevanović; Goran A Bogdanović; Rastko D Vukićević
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-01-31

3.  3-(3-Acetyl-anilino)-1-ferrocenylpropan-1-one.

Authors:  Sladjana B Novaković; Dragana Stevanović; Vladimir Divjaković; Goran A Bogdanović; Rastko D Vukićević
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-06-30

4.  1-Ferrocenyl-3-(2-methyl-anilino)propan-1-one.

Authors:  Zorica Leka; Sladjana B Novaković; Anka Pejović; Goran A Bogdanović; Rastko D Vukićević
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-06-30

5.  2-[(Ferrocen-1-yl)(hy-droxy)meth-yl]prop-2-ene-nitrile.

Authors:  S Selvanayagam; K Ravikumar; S Kathiravan; R Raghunathan
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-11-20
  5 in total

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