Literature DB >> 21580890

1-Ferrocenylmeth-yl-1H-imidazole.

Vincent O Nyamori1, Muhammad D Bala.   

Abstract

In the title compound, [Fe(C(5)H(5))(C(9)H(9)N(2))], the distances of the Fe atom from the centroids of the unsubstituted and the substituted cyclo-penta-dienyl (cp) rings are 1.639 (1) and 1.647 (1) Å, respectively. The ferrocenyl unit deviates from an eclipsed geometry with tilted cp rings; the inter-planar angle between the cp and imidazole rings is 114.11 (4)°.

Entities:  

Year:  2008        PMID: 21580890      PMCID: PMC2959733          DOI: 10.1107/S1600536808029231

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


Related literature

For a related structure, see: Hua et al. (2004 ▶). For applications of aryl­imidazoles, see: Broggini & Togni (2002 ▶); César et al. (2004 ▶); Cozzi et al. (1993 ▶); Herrmann & Köcher (1997 ▶); Lee & Nolan (2000 ▶); Ohmori et al. (1996 ▶); Snegur et al. (2004 ▶).

Experimental

Crystal data

[Fe(C5H5)(C9H9N2)] M = 266.12 Monoclinic, a = 14.8914 (6) Å b = 7.5587 (3) Å c = 10.7854 (4) Å β = 96.862 (2)° V = 1205.30 (8) Å3 Z = 4 Mo Kα radiation μ = 1.23 mm−1 T = 293 (2) K 0.39 × 0.26 × 0.05 mm

Data collection

Bruker APEXII CCD area-detector diffractometer Absorption correction: integration (XPREP; Bruker, 2005 ▶) T min = 0.646, T max = 0.941 17808 measured reflections 2904 independent reflections 1852 reflections with I > 2σ(I) R int = 0.054

Refinement

R[F 2 > 2σ(F 2)] = 0.040 wR(F 2) = 0.114 S = 1.00 2904 reflections 154 parameters H-atom parameters constrained Δρmax = 0.63 e Å−3 Δρmin = −0.38 e Å−3 Data collection: APEX2 (Bruker, 2005 ▶); cell refinement: SAINT-Plus (Bruker, 2005 ▶); data reduction: SAINT-Plus; program(s) used to solve structure: SHELXTL (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXTL; molecular graphics: PLATON (Spek, 2003 ▶) and ORTEP-3 (Farrugia, 1997 ▶); software used to prepare material for publication: SHELXTL. Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536808029231/dn2373sup1.cif Structure factors: contains datablocks I. DOI: 10.1107/S1600536808029231/dn2373Isup2.hkl Additional supplementary materials: crystallographic information; 3D view; checkCIF report
[Fe(C5H5)(C9H9N2)]F(000) = 552
Mr = 266.12Dx = 1.467 Mg m3
Monoclinic, P21/cMo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ybcCell parameters from 3993 reflections
a = 14.8914 (6) Åθ = 2.8–26.6°
b = 7.5587 (3) ŵ = 1.23 mm1
c = 10.7854 (4) ÅT = 293 K
β = 96.862 (2)°Plate, yellow
V = 1205.30 (8) Å30.39 × 0.26 × 0.05 mm
Z = 4
Bruker APEXII CCD area-detector diffractometer2904 independent reflections
Radiation source: fine-focus sealed tube1852 reflections with I > 2σ(I)
graphiteRint = 0.054
φ and ω scansθmax = 28.0°, θmin = 1.4°
Absorption correction: integration (XPREP; Bruker, 2005)h = −19→18
Tmin = 0.646, Tmax = 0.941k = −9→9
17808 measured reflectionsl = −14→14
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 = 1.00w = 1/[σ2(Fo2) + (0.0573P)2 + 0.4185P] where P = (Fo2 + 2Fc2)/3
2904 reflections(Δ/σ)max = 0.015
154 parametersΔρmax = 0.63 e Å3
0 restraintsΔρmin = −0.38 e Å3
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.
xyzUiso*/Ueq
C10.74936 (18)−0.0973 (4)0.4338 (2)0.0367 (6)
C20.7628 (2)−0.2266 (4)0.3419 (3)0.0426 (7)
H20.7177−0.27800.28630.051*
C30.8561 (2)−0.2636 (4)0.3494 (3)0.0464 (7)
H30.8832−0.34340.29960.056*
C40.9012 (2)−0.1589 (4)0.4453 (3)0.0465 (7)
H40.9633−0.15680.46950.056*
C50.8361 (2)−0.0576 (4)0.4985 (3)0.0412 (7)
H50.84770.02160.56450.049*
C60.6610 (2)−0.0148 (4)0.4525 (3)0.0473 (7)
H6A0.67170.10440.48410.057*
H6B0.6239−0.00650.37240.057*
C70.5876 (2)−0.2876 (4)0.5291 (3)0.0520 (8)
H70.6011−0.36730.46830.062*
C80.5399 (2)−0.3206 (5)0.6267 (3)0.0517 (8)
H80.5150−0.42960.64340.062*
C90.5771 (2)−0.0511 (4)0.6399 (3)0.0483 (8)
H90.58350.06570.66670.058*
C100.7592 (4)0.1645 (8)0.1970 (6)0.104 (2)
H100.69640.17230.18860.125*
C110.8049 (4)0.0625 (7)0.1300 (4)0.0887 (15)
H110.7791−0.01200.06690.106*
C120.8918 (3)0.0786 (6)0.1630 (4)0.0750 (12)
H120.93650.01840.12680.090*
C130.9071 (4)0.1987 (7)0.2598 (5)0.0973 (18)
H130.96250.23370.30170.117*
C140.8167 (6)0.2588 (5)0.2818 (5)0.123 (3)
H140.80170.34160.33970.148*
N10.61150 (15)−0.1138 (3)0.5390 (2)0.0407 (5)
N20.53352 (17)−0.1716 (4)0.6965 (2)0.0518 (7)
Fe10.83161 (2)−0.00206 (5)0.31303 (3)0.03545 (14)
U11U22U33U12U13U23
C10.0351 (14)0.0369 (15)0.0384 (14)−0.0031 (12)0.0057 (11)0.0063 (11)
C20.0457 (17)0.0350 (15)0.0472 (16)−0.0136 (13)0.0058 (13)−0.0007 (12)
C30.0472 (17)0.0345 (15)0.0586 (18)0.0027 (13)0.0106 (14)0.0007 (13)
C40.0345 (15)0.0484 (17)0.0556 (18)0.0019 (13)0.0013 (13)0.0107 (14)
C50.0464 (17)0.0405 (15)0.0359 (14)−0.0038 (13)0.0016 (12)0.0027 (11)
C60.0422 (15)0.0494 (18)0.0523 (17)0.0031 (14)0.0142 (13)0.0135 (14)
C70.059 (2)0.0536 (19)0.0461 (17)−0.0088 (15)0.0189 (15)−0.0071 (14)
C80.0466 (17)0.063 (2)0.0465 (17)−0.0092 (15)0.0106 (14)0.0064 (15)
C90.0448 (17)0.0511 (19)0.0506 (18)0.0072 (14)0.0129 (14)−0.0042 (14)
C100.090 (3)0.097 (4)0.135 (5)0.044 (3)0.049 (3)0.084 (4)
C110.107 (4)0.097 (3)0.058 (2)−0.029 (3)−0.009 (2)0.035 (2)
C120.088 (3)0.074 (3)0.072 (3)0.008 (2)0.042 (2)0.024 (2)
C130.107 (4)0.097 (4)0.082 (3)−0.069 (3)−0.015 (3)0.041 (3)
C140.286 (9)0.0223 (19)0.081 (3)0.009 (3)0.104 (5)0.0110 (18)
N10.0374 (13)0.0450 (14)0.0411 (13)−0.0004 (11)0.0108 (10)0.0031 (11)
N20.0479 (15)0.0667 (18)0.0434 (14)0.0045 (13)0.0161 (12)0.0017 (13)
Fe10.0377 (2)0.0310 (2)0.0387 (2)−0.00352 (17)0.00896 (15)0.00289 (17)
C1—C21.423 (4)C8—N21.365 (4)
C1—C51.424 (4)C8—H80.9300
C1—C61.492 (4)C9—N21.311 (4)
C1—Fe12.024 (3)C9—N11.343 (4)
C2—C31.410 (4)C9—H90.9300
C2—Fe12.026 (3)C10—C111.303 (7)
C2—H20.9300C10—C141.375 (8)
C3—C41.408 (4)C10—Fe11.998 (4)
C3—Fe12.040 (3)C10—H100.9300
C3—H30.9300C11—C121.305 (6)
C4—C51.410 (4)C11—Fe12.026 (4)
C4—Fe12.040 (3)C11—H110.9300
C4—H40.9300C12—C131.382 (6)
C5—Fe12.037 (3)C12—Fe12.035 (3)
C5—H50.9300C12—H120.9300
C6—N11.463 (3)C13—C141.467 (8)
C6—H6A0.9700C13—Fe12.013 (3)
C6—H6B0.9700C13—H130.9300
C7—C81.361 (4)C14—Fe12.008 (4)
C7—N11.362 (4)C14—H140.9300
C7—H70.9300
C2—C1—C5106.9 (2)Fe1—C12—H12126.3
C2—C1—C6125.5 (3)C12—C13—C14104.7 (4)
C5—C1—C6127.5 (3)C12—C13—Fe170.9 (2)
C2—C1—Fe169.49 (15)C14—C13—Fe168.4 (2)
C5—C1—Fe169.97 (15)C12—C13—H13127.7
C6—C1—Fe1123.35 (19)C14—C13—H13127.7
C3—C2—C1108.4 (2)Fe1—C13—H13124.7
C3—C2—Fe170.25 (16)C10—C14—C13104.1 (4)
C1—C2—Fe169.36 (15)C10—C14—Fe169.5 (2)
C3—C2—H2125.8C13—C14—Fe168.8 (2)
C1—C2—H2125.8C10—C14—H14128.0
Fe1—C2—H2126.2C13—C14—H14128.0
C4—C3—C2108.1 (3)Fe1—C14—H14125.4
C4—C3—Fe169.80 (17)C9—N1—C7106.4 (2)
C2—C3—Fe169.15 (16)C9—N1—C6127.4 (3)
C4—C3—H3126.0C7—N1—C6126.2 (2)
C2—C3—H3126.0C9—N2—C8104.2 (2)
Fe1—C3—H3126.7C10—Fe1—C1440.1 (2)
C3—C4—C5108.3 (3)C10—Fe1—C1368.0 (2)
C3—C4—Fe169.82 (17)C14—Fe1—C1342.8 (2)
C5—C4—Fe169.66 (16)C10—Fe1—C1107.71 (16)
C3—C4—H4125.9C14—Fe1—C1113.20 (19)
C5—C4—H4125.9C13—Fe1—C1148.6 (2)
Fe1—C4—H4126.2C10—Fe1—C2112.3 (2)
C4—C5—C1108.3 (3)C14—Fe1—C2143.2 (3)
C4—C5—Fe169.87 (17)C13—Fe1—C2170.3 (2)
C1—C5—Fe168.97 (15)C1—Fe1—C241.15 (11)
C4—C5—H5125.9C10—Fe1—C1137.8 (2)
C1—C5—H5125.9C14—Fe1—C1166.1 (2)
Fe1—C5—H5126.9C13—Fe1—C1165.89 (18)
N1—C6—C1113.1 (2)C1—Fe1—C11130.50 (18)
N1—C6—H6A109.0C2—Fe1—C11107.92 (16)
C1—C6—H6A109.0C10—Fe1—C1264.48 (18)
N1—C6—H6B109.0C14—Fe1—C1267.83 (18)
C1—C6—H6B109.0C13—Fe1—C1239.91 (19)
H6A—C6—H6B107.8C1—Fe1—C12167.51 (17)
C8—C7—N1105.8 (3)C2—Fe1—C12130.71 (17)
C8—C7—H7127.1C11—Fe1—C1237.50 (18)
N1—C7—H7127.1C10—Fe1—C5134.2 (2)
C7—C8—N2110.7 (3)C14—Fe1—C5110.93 (16)
C7—C8—H8124.7C13—Fe1—C5118.80 (16)
N2—C8—H8124.7C1—Fe1—C541.06 (11)
N2—C9—N1113.0 (3)C2—Fe1—C568.54 (12)
N2—C9—H9123.5C11—Fe1—C5170.4 (2)
N1—C9—H9123.5C12—Fe1—C5151.27 (17)
C11—C10—C14110.5 (5)C10—Fe1—C4174.5 (2)
C11—C10—Fe172.3 (3)C14—Fe1—C4136.4 (3)
C14—C10—Fe170.3 (3)C13—Fe1—C4112.53 (16)
C11—C10—H10124.8C1—Fe1—C468.85 (11)
C14—C10—H10124.8C2—Fe1—C468.27 (12)
Fe1—C10—H10124.2C11—Fe1—C4147.7 (2)
C10—C11—C12111.1 (5)C12—Fe1—C4119.68 (16)
C10—C11—Fe169.9 (3)C5—Fe1—C440.47 (12)
C12—C11—Fe171.6 (2)C10—Fe1—C3143.3 (2)
C10—C11—H11124.4C14—Fe1—C3175.9 (3)
C12—C11—H11124.4C13—Fe1—C3133.8 (2)
Fe1—C11—H11125.6C1—Fe1—C368.89 (12)
C11—C12—C13109.7 (5)C2—Fe1—C340.59 (12)
C11—C12—Fe170.9 (2)C11—Fe1—C3115.5 (2)
C13—C12—Fe169.2 (2)C12—Fe1—C3110.95 (16)
C11—C12—H12125.2C5—Fe1—C368.13 (12)
C13—C12—H12125.2C4—Fe1—C340.37 (12)
C5—C1—C2—C3−0.7 (3)C5—C1—Fe1—C11−173.4 (3)
C6—C1—C2—C3176.6 (3)C6—C1—Fe1—C11−51.0 (4)
Fe1—C1—C2—C359.6 (2)C2—C1—Fe1—C1254.4 (7)
C5—C1—C2—Fe1−60.26 (19)C5—C1—Fe1—C12172.2 (7)
C6—C1—C2—Fe1117.0 (3)C6—C1—Fe1—C12−65.4 (8)
C1—C2—C3—C40.1 (3)C2—C1—Fe1—C5−117.8 (2)
Fe1—C2—C3—C459.1 (2)C6—C1—Fe1—C5122.4 (3)
C1—C2—C3—Fe1−59.04 (19)C2—C1—Fe1—C4−80.75 (18)
C2—C3—C4—C50.5 (3)C5—C1—Fe1—C437.09 (17)
Fe1—C3—C4—C559.3 (2)C6—C1—Fe1—C4159.5 (3)
C2—C3—C4—Fe1−58.7 (2)C2—C1—Fe1—C3−37.33 (17)
C3—C4—C5—C1−0.9 (3)C5—C1—Fe1—C380.52 (19)
Fe1—C4—C5—C158.42 (19)C6—C1—Fe1—C3−157.1 (3)
C3—C4—C5—Fe1−59.4 (2)C3—C2—Fe1—C10148.6 (3)
C2—C1—C5—C41.0 (3)C1—C2—Fe1—C10−91.8 (3)
C6—C1—C5—C4−176.2 (3)C3—C2—Fe1—C14−177.6 (3)
Fe1—C1—C5—C4−59.0 (2)C1—C2—Fe1—C14−58.0 (3)
C2—C1—C5—Fe159.95 (18)C3—C2—Fe1—C1−119.6 (2)
C6—C1—C5—Fe1−117.2 (3)C3—C2—Fe1—C11108.5 (3)
C2—C1—C6—N189.2 (3)C1—C2—Fe1—C11−131.9 (2)
C5—C1—C6—N1−94.1 (3)C3—C2—Fe1—C1273.8 (3)
Fe1—C1—C6—N1176.54 (19)C1—C2—Fe1—C12−166.6 (2)
N1—C7—C8—N20.1 (4)C3—C2—Fe1—C5−81.00 (19)
C14—C10—C11—C120.3 (5)C1—C2—Fe1—C538.61 (16)
Fe1—C10—C11—C12−59.9 (3)C3—C2—Fe1—C4−37.32 (18)
C14—C10—C11—Fe160.2 (3)C1—C2—Fe1—C482.29 (18)
C10—C11—C12—C130.5 (5)C1—C2—Fe1—C3119.6 (2)
Fe1—C11—C12—C13−58.5 (3)C12—C11—Fe1—C10121.7 (5)
C10—C11—C12—Fe158.9 (3)C10—C11—Fe1—C14−37.5 (4)
C11—C12—C13—C14−1.0 (5)C12—C11—Fe1—C1484.2 (4)
Fe1—C12—C13—C14−60.5 (2)C10—C11—Fe1—C13−84.6 (4)
C11—C12—C13—Fe159.5 (3)C12—C11—Fe1—C1337.1 (3)
C11—C10—C14—C13−0.9 (5)C10—C11—Fe1—C163.3 (4)
Fe1—C10—C14—C1360.5 (3)C12—C11—Fe1—C1−174.9 (3)
C11—C10—C14—Fe1−61.4 (3)C10—C11—Fe1—C2103.5 (4)
C12—C13—C14—C101.1 (4)C12—C11—Fe1—C2−134.8 (3)
Fe1—C13—C14—C10−61.0 (3)C10—C11—Fe1—C12−121.7 (5)
C12—C13—C14—Fe162.1 (3)C10—C11—Fe1—C4−179.0 (3)
N2—C9—N1—C70.6 (4)C12—C11—Fe1—C4−57.3 (5)
N2—C9—N1—C6177.8 (3)C10—C11—Fe1—C3146.6 (3)
C8—C7—N1—C9−0.4 (3)C12—C11—Fe1—C3−91.7 (3)
C8—C7—N1—C6−177.6 (3)C11—C12—Fe1—C10−35.3 (4)
C1—C6—N1—C9127.7 (3)C13—C12—Fe1—C1085.6 (4)
C1—C6—N1—C7−55.7 (4)C11—C12—Fe1—C14−79.2 (4)
N1—C9—N2—C8−0.5 (4)C13—C12—Fe1—C1441.6 (3)
C7—C8—N2—C90.3 (4)C11—C12—Fe1—C13−120.8 (5)
C11—C10—Fe1—C14120.3 (5)C11—C12—Fe1—C118.1 (9)
C11—C10—Fe1—C1378.7 (3)C13—C12—Fe1—C1138.9 (7)
C14—C10—Fe1—C13−41.6 (3)C11—C12—Fe1—C263.0 (4)
C11—C10—Fe1—C1−134.5 (3)C13—C12—Fe1—C2−176.2 (3)
C14—C10—Fe1—C1105.2 (3)C13—C12—Fe1—C11120.8 (5)
C11—C10—Fe1—C2−90.8 (3)C11—C12—Fe1—C5−172.6 (3)
C14—C10—Fe1—C2148.9 (3)C13—C12—Fe1—C5−51.8 (5)
C14—C10—Fe1—C11−120.3 (5)C11—C12—Fe1—C4148.8 (3)
C11—C10—Fe1—C1235.0 (3)C13—C12—Fe1—C4−90.3 (3)
C14—C10—Fe1—C12−85.3 (3)C11—C12—Fe1—C3105.0 (3)
C11—C10—Fe1—C5−172.0 (3)C13—C12—Fe1—C3−134.2 (3)
C14—C10—Fe1—C567.7 (4)C4—C5—Fe1—C10−178.0 (3)
C11—C10—Fe1—C3−56.3 (4)C1—C5—Fe1—C1062.0 (3)
C14—C10—Fe1—C3−176.6 (3)C4—C5—Fe1—C14−138.3 (3)
C13—C14—Fe1—C10−115.0 (4)C1—C5—Fe1—C14101.7 (3)
C10—C14—Fe1—C13115.0 (4)C4—C5—Fe1—C13−91.7 (3)
C10—C14—Fe1—C1−90.3 (3)C1—C5—Fe1—C13148.4 (3)
C13—C14—Fe1—C1154.7 (3)C4—C5—Fe1—C1119.9 (2)
C10—C14—Fe1—C2−52.9 (4)C4—C5—Fe1—C281.24 (19)
C13—C14—Fe1—C2−168.0 (2)C1—C5—Fe1—C2−38.70 (17)
C10—C14—Fe1—C1135.4 (3)C4—C5—Fe1—C12−56.6 (4)
C13—C14—Fe1—C11−79.7 (3)C1—C5—Fe1—C12−176.5 (3)
C10—C14—Fe1—C1276.2 (3)C1—C5—Fe1—C4−119.9 (2)
C13—C14—Fe1—C12−38.8 (3)C4—C5—Fe1—C337.41 (17)
C10—C14—Fe1—C5−134.7 (3)C1—C5—Fe1—C3−82.53 (18)
C13—C14—Fe1—C5110.3 (3)C3—C4—Fe1—C14−176.2 (3)
C10—C14—Fe1—C4−173.5 (3)C5—C4—Fe1—C1464.3 (3)
C13—C14—Fe1—C471.5 (3)C3—C4—Fe1—C13−132.0 (3)
C12—C13—Fe1—C10−76.1 (3)C5—C4—Fe1—C13108.5 (3)
C14—C13—Fe1—C1039.1 (3)C3—C4—Fe1—C181.89 (19)
C12—C13—Fe1—C14−115.2 (4)C5—C4—Fe1—C1−37.61 (17)
C12—C13—Fe1—C1−164.2 (3)C3—C4—Fe1—C237.52 (17)
C14—C13—Fe1—C1−49.0 (4)C5—C4—Fe1—C2−81.98 (18)
C12—C13—Fe1—C11−34.9 (3)C3—C4—Fe1—C11−51.9 (4)
C14—C13—Fe1—C1180.2 (3)C5—C4—Fe1—C11−171.4 (3)
C14—C13—Fe1—C12115.2 (4)C3—C4—Fe1—C12−88.0 (2)
C12—C13—Fe1—C5154.5 (3)C5—C4—Fe1—C12152.5 (2)
C14—C13—Fe1—C5−90.4 (3)C3—C4—Fe1—C5119.5 (3)
C12—C13—Fe1—C4109.9 (3)C5—C4—Fe1—C3−119.5 (3)
C14—C13—Fe1—C4−135.0 (3)C4—C3—Fe1—C10−173.4 (3)
C12—C13—Fe1—C368.0 (3)C2—C3—Fe1—C10−53.8 (3)
C14—C13—Fe1—C3−176.8 (3)C4—C3—Fe1—C1372.0 (3)
C2—C1—Fe1—C10103.8 (3)C2—C3—Fe1—C13−168.4 (2)
C5—C1—Fe1—C10−138.3 (3)C4—C3—Fe1—C1−81.78 (19)
C6—C1—Fe1—C10−15.9 (3)C2—C3—Fe1—C137.83 (17)
C2—C1—Fe1—C14146.4 (3)C4—C3—Fe1—C2−119.6 (3)
C5—C1—Fe1—C14−95.7 (3)C4—C3—Fe1—C11152.3 (2)
C6—C1—Fe1—C1426.7 (4)C2—C3—Fe1—C11−88.1 (2)
C2—C1—Fe1—C13−179.6 (3)C4—C3—Fe1—C12111.6 (2)
C5—C1—Fe1—C13−61.8 (4)C2—C3—Fe1—C12−128.8 (2)
C6—C1—Fe1—C1360.6 (4)C4—C3—Fe1—C5−37.50 (18)
C5—C1—Fe1—C2117.8 (2)C2—C3—Fe1—C582.10 (18)
C6—C1—Fe1—C2−119.7 (3)C2—C3—Fe1—C4119.6 (3)
C2—C1—Fe1—C1168.7 (3)
  5 in total

1.  A short history of SHELX.

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

Review 2.  Chiral N-heterocyclic carbenes as stereodirecting ligands in asymmetric catalysis.

Authors:  Vincent César; Stéphane Bellemin-Laponnaz; Lutz H Gade
Journal:  Chem Soc Rev       Date:  2004-11-03       Impact factor: 54.564

3.  Efficient cross-coupling reactions of aryl chlorides and bromides with phenyl- or vinyltrimethoxysilane mediated by a Palladium/Imidazolium chloride system

Authors: 
Journal:  Org Lett       Date:  2000-07-13       Impact factor: 6.005

4.  Novel AMPA receptor antagonists: synthesis and structure-activity relationships of 1-hydroxy-7-(1H-imidazol-1-yl)-6-nitro-2,3(1H,4H)- quinoxalinedione and related compounds.

Authors:  J Ohmori; M Shimizu-Sasamata; M Okada; S Sakamoto
Journal:  J Med Chem       Date:  1996-09-27       Impact factor: 7.446

5.  Imidazol-1-yl and pyridin-3-yl derivatives of 4-phenyl-1,4-dihydropyridines combining Ca2+ antagonism and thromboxane A2 synthase inhibition.

Authors:  P Cozzi; G Carganico; D Fusar; M Grossoni; M Menichincheri; V Pinciroli; R Tonani; F Vaghi; P Salvati
Journal:  J Med Chem       Date:  1993-10-01       Impact factor: 7.446

  5 in total
  4 in total

1.  4-ferrocenylphenol.

Authors:  Vincent O Nyamori; Muhammad D Bala
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-11-29

2.  1-(6-Ferrocenylhex-yl)-1H-imidazole.

Authors:  Vincent O Nyamori; Muhammad D Bala; Demetrius C Levendis
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-03-17

3.  1-(4-Carb-oxy-phen-yl)-1H-imidazol-3-ium chloride dihydrate.

Authors:  Zhi-Peng Yu; Wen-Qian Geng; Lin Kong; Hong-Ping Zhou
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-01-22

4.  1-(Ferrocen-1-ylmeth-yl)-3-methyl-imidazol-3-ium iodide.

Authors:  Vincent O Nyamori; Siphesihle M Zulu; Bernard Omondi
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-11-10
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.