Literature DB >> 21200556

Benzyl 5-ferrocenyl-3-(4-methyl-phen-yl)-2-pyrazoline-1-dithio-carboxyl-ate.

Xiao-Lan Liu1, Ben-Wan Tong, Yue Zhao, Jun Ye, Yong-Hong Liu.   

Abstract

In the title compound, [Fe(C(5)H(5))(C(23)H(21)N(2)S(2))], the <span class="Chemical">cyclo-penta-dienyl rings of the <class="Chemical">span class="Chemical">ferrocenyl unit deviate slightly from the eclipsed form. In the pyrazoline ring, the N atom bonded to S-benzyl dithio-carbazate exhibits unconventional sp(2)-hybrid character in order to form an extended conjugated system. The pyrazoline ring displays an envelope conformation. The mol-ecules are linked into chains along the b axis via C-H⋯S inter-molecular hydrogen bonds.

Entities:  

Year:  2007        PMID: 21200556      PMCID: PMC2915138          DOI: 10.1107/S1600536807066536

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


Related literature

For related literature, see: Fahrni et al. (2003 ▶); Huang & Katzenellenbogen (2000 ▶); Huang et al. (1998 ▶); Liu et al. (2007 ▶); Rivett et al. (1979 ▶); Shi et al. (2004 ▶); Sun et al. (2004 ▶); Wiley et al. (1958 ▶); <span class="Disease">Wilkinson et al. (1990 ▶).

Experimental

Crystal data

[<span class="Chemical">Fe(C5H5)(<class="Chemical">span class="Chemical">C23H21N2S2)] M = 510.50 Triclinic, a = 9.178 (1) Å b = 10.468 (2) Å c = 13.216 (2) Å α = 99.37 (1)° β = 101.55 (2)° γ = 96.12 (1)° V = 1214.6 (3) Å3 Z = 2 Mo Kα radiation μ = 0.81 mm−1 T = 296 (2) K 0.33 × 0.31 × 0.28 mm

Data collection

Bruker SMART <span class="Gene">APEX CCD area-detector diffractometer Absorption correction: multi-scan (SADABS; Bruker, 2002 ▶) T min = 0.776, T max = 0.805 10742 measured reflections 5528 independent reflections 5035 reflections with I > 2σ(I) R int = 0.019

Refinement

R[F 2 > 2σ(F 2)] = 0.028 wR(F 2) = 0.088 S = 0.99 5528 reflections 299 parameters H-atom parameters constrained Δρmax = 0.44 e Å−3 Δρmin = −0.22 e Å−3 Data collection: SMART (Bruker, 2002 ▶); cell refinement: SAINT (Bruker, 2002 ▶); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 1990 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997 ▶); molecular graphics: PLATON (Spek, 2003 ▶); software used to prepare material for publication: SHELXTL (Bruker, 2002 ▶). Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536807066536/pv2048sup1.cif Structure factors: contains datablocks I. DOI: 10.1107/S1600536807066536/pv2048Isup2.hkl Additional supplementary materials: crystallographic information; 3D view; checkCIF report
[Fe(C5H5)(C23H21N2S2)]Z = 2
Mr = 510.50F000 = 532.0
Triclinic, P1Dx = 1.396 Mg m3
Hall symbol: - P 1Melting point: 345(2) K
a = 9.178 (1) ÅMo Kα radiation λ = 0.71073 Å
b = 10.468 (2) ÅCell parameters from 7052 reflections
c = 13.216 (2) Åθ = 2.3–27.6º
α = 99.37 (1)ºµ = 0.81 mm1
β = 101.55 (2)ºT = 296 (2) K
γ = 96.12 (1)ºBlock, yellow
V = 1214.6 (3) Å30.33 × 0.31 × 0.28 mm
Bruker SMART APEX CCD area-detector diffractometer5528 independent reflections
Radiation source: fine-focus sealed tube5035 reflections with I > 2σ(I)
Monochromator: graphiteRint = 0.019
T = 296(2) Kθmax = 27.7º
φ and ω scansθmin = 2.3º
Absorption correction: multi-scan(SADABS; Bruker, 2002)h = −10→10
Tmin = 0.776, Tmax = 0.805k = −12→12
10742 measured reflectionsl = −15→15
Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.028H-atom parameters constrained
wR(F2) = 0.088  w = 1/[σ2(Fo2) + (0.0552P)2 + 0.4985P] where P = (Fo2 + 2Fc2)/3
S = 0.99(Δ/σ)max = 0.007
5528 reflectionsΔρmax = 0.44 e Å3
299 parametersΔρmin = −0.22 e Å3
Primary atom site location: structure-invariant direct methodsExtinction correction: none
Experimental. Analysis calculated for C18H16N4OS2: C 65.87, H 5.13, N 5.49%; found: C 65.82, H 5.11, N 5.51%. IR (KBr, cm-1): ν(C=N), ν(S=C) and ν(N–N) 1559 (m), 1245 (s) and 1037 (w) cm-1. 1H NMR (600 MHz, CDCl3,δ, p.p.m.): 7.23–7.76 (m, 9H, ArH), 6.04 (broad, 1H, CH), 4.50–4.47 (d, 1H, CH2), 4.41–4.39 (d, 1H, CH2), 4.15 (s, 5H, C5H5), 4.03 (s, 1H, C5H4), 4.12 (s, 1H, C5H4), 4.19 (s, 1H, C5H4), 4.71 (s, 1H, C5H4), 3.72 (s, 2H, ArCH2), 2.41 (s, 3H, CH3) p.p.m..
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
Fe10.56551 (3)−0.22018 (2)0.364537 (18)0.02183 (10)
S10.64012 (5)0.30267 (4)0.12369 (4)0.02864 (13)
S20.72753 (5)0.03133 (4)0.06920 (3)0.02501 (12)
N10.52328 (15)0.09334 (13)0.17619 (11)0.0209 (3)
N20.43248 (16)0.18040 (13)0.21361 (11)0.0219 (3)
C50.3598 (2)−0.28594 (18)0.38988 (16)0.0310 (4)
H50.2866−0.23470.40340.037*
C40.4760 (2)−0.31695 (18)0.46642 (16)0.0322 (4)
H40.4920−0.28970.53880.039*
C30.5633 (2)−0.39647 (18)0.41353 (16)0.0342 (4)
H30.6465−0.43050.44520.041*
C20.5017 (2)−0.41532 (18)0.30377 (16)0.0351 (4)
H20.5376−0.46370.25090.042*
C10.3750 (2)−0.34678 (18)0.28908 (16)0.0324 (4)
H10.3133−0.34270.22500.039*
C60.6003 (2)−0.01980 (17)0.39096 (14)0.0262 (4)
H60.53850.03570.41750.031*
C70.7219 (2)−0.06716 (19)0.45157 (15)0.0340 (4)
H70.7534−0.04830.52450.041*
C80.7865 (2)−0.1481 (2)0.38121 (17)0.0365 (5)
H80.8680−0.19170.40010.044*
C90.7059 (2)−0.15140 (18)0.27690 (15)0.0287 (4)
H90.7257−0.19720.21580.034*
C100.58923 (19)−0.07210 (16)0.28218 (13)0.0218 (3)
C110.47914 (18)−0.04276 (16)0.19133 (13)0.0212 (3)
H110.4742−0.10630.12710.025*
C120.32107 (19)−0.03292 (16)0.21151 (14)0.0230 (4)
H12A0.2439−0.07460.15000.028*
H12B0.3063−0.07250.27080.028*
C130.31983 (18)0.11285 (16)0.23500 (12)0.0211 (3)
C140.20317 (18)0.17603 (17)0.27623 (13)0.0219 (3)
C150.0737 (2)0.10168 (18)0.28749 (14)0.0271 (4)
H150.06070.01110.26770.033*
C16−0.0357 (2)0.16144 (19)0.32793 (14)0.0309 (4)
H16−0.12120.11030.33490.037*
C17−0.0196 (2)0.2960 (2)0.35799 (14)0.0309 (4)
C180.1102 (2)0.37050 (18)0.34690 (14)0.0296 (4)
H180.12300.46110.36710.036*
C190.2197 (2)0.31208 (17)0.30645 (14)0.0260 (4)
H190.30480.36350.29930.031*
C20−0.1389 (2)0.3607 (3)0.40227 (19)0.0483 (6)
H20A−0.23640.31530.36580.072*
H20B−0.13130.45020.39340.072*
H20C−0.12460.35760.47580.072*
C210.62648 (18)0.13289 (16)0.12474 (13)0.0210 (3)
C220.7966 (2)0.32849 (18)0.06058 (17)0.0356 (5)
H22A0.88410.29760.09780.043*
H22B0.77060.2810−0.01150.043*
C230.8295 (2)0.47341 (17)0.06311 (14)0.0263 (4)
C280.7407 (2)0.5341 (2)−0.00745 (16)0.0370 (5)
H280.65660.4858−0.05490.044*
C270.7770 (3)0.6667 (2)−0.00738 (18)0.0442 (5)
H270.71810.7062−0.05570.053*
C260.8997 (2)0.73954 (19)0.06398 (19)0.0405 (5)
H260.92460.82790.06360.049*
C250.9849 (2)0.6807 (2)0.13578 (19)0.0408 (5)
H251.06640.73000.18530.049*
C240.9504 (2)0.54858 (19)0.13486 (17)0.0344 (4)
H241.00970.50980.18340.041*
U11U22U33U12U13U23
Fe10.02452 (15)0.02086 (15)0.02275 (15)0.00548 (10)0.00666 (11)0.00855 (10)
S10.0313 (2)0.0201 (2)0.0413 (3)0.00543 (17)0.0205 (2)0.00872 (19)
S20.0281 (2)0.0247 (2)0.0256 (2)0.00900 (17)0.01053 (18)0.00548 (17)
N10.0250 (7)0.0185 (7)0.0220 (7)0.0066 (5)0.0085 (6)0.0057 (5)
N20.0242 (7)0.0224 (7)0.0221 (7)0.0077 (6)0.0085 (6)0.0064 (6)
C50.0291 (9)0.0274 (9)0.0412 (11)0.0029 (7)0.0142 (8)0.0125 (8)
C40.0403 (11)0.0297 (10)0.0319 (10)0.0035 (8)0.0138 (8)0.0148 (8)
C30.0408 (11)0.0239 (9)0.0443 (12)0.0099 (8)0.0121 (9)0.0180 (8)
C20.0442 (11)0.0213 (9)0.0415 (11)0.0056 (8)0.0147 (9)0.0040 (8)
C10.0332 (10)0.0254 (9)0.0361 (11)−0.0019 (8)0.0038 (8)0.0075 (8)
C60.0326 (9)0.0209 (8)0.0240 (9)0.0000 (7)0.0053 (7)0.0049 (7)
C70.0351 (10)0.0348 (10)0.0268 (10)−0.0067 (8)−0.0032 (8)0.0108 (8)
C80.0236 (9)0.0423 (11)0.0481 (12)0.0062 (8)0.0046 (8)0.0248 (10)
C90.0270 (9)0.0308 (10)0.0356 (10)0.0082 (7)0.0144 (8)0.0153 (8)
C100.0239 (8)0.0201 (8)0.0239 (9)0.0021 (6)0.0076 (7)0.0092 (7)
C110.0268 (9)0.0172 (8)0.0205 (8)0.0040 (6)0.0059 (7)0.0049 (6)
C120.0229 (8)0.0213 (8)0.0254 (9)0.0027 (6)0.0045 (7)0.0071 (7)
C130.0228 (8)0.0230 (8)0.0175 (8)0.0027 (7)0.0024 (6)0.0070 (6)
C140.0220 (8)0.0265 (9)0.0182 (8)0.0054 (7)0.0035 (6)0.0069 (7)
C150.0267 (9)0.0270 (9)0.0270 (9)0.0011 (7)0.0051 (7)0.0059 (7)
C160.0214 (9)0.0424 (11)0.0280 (9)−0.0021 (8)0.0073 (7)0.0060 (8)
C170.0268 (9)0.0444 (11)0.0221 (9)0.0080 (8)0.0075 (7)0.0032 (8)
C180.0331 (10)0.0283 (9)0.0277 (9)0.0078 (8)0.0082 (8)0.0020 (7)
C190.0250 (9)0.0260 (9)0.0287 (9)0.0034 (7)0.0084 (7)0.0074 (7)
C200.0334 (11)0.0616 (15)0.0477 (13)0.0092 (10)0.0175 (10)−0.0079 (11)
C210.0222 (8)0.0217 (8)0.0190 (8)0.0035 (6)0.0030 (6)0.0054 (6)
C220.0384 (11)0.0265 (10)0.0497 (12)0.0037 (8)0.0282 (9)0.0076 (9)
C230.0271 (9)0.0252 (9)0.0320 (10)0.0048 (7)0.0171 (8)0.0077 (7)
C280.0345 (10)0.0428 (12)0.0327 (11)0.0070 (9)0.0050 (8)0.0066 (9)
C270.0503 (13)0.0474 (13)0.0487 (13)0.0257 (11)0.0184 (10)0.0276 (10)
C260.0370 (11)0.0266 (10)0.0701 (15)0.0109 (8)0.0301 (11)0.0178 (10)
C250.0266 (10)0.0321 (11)0.0620 (14)0.0017 (8)0.0098 (9)0.0055 (10)
C240.0290 (10)0.0342 (10)0.0439 (11)0.0074 (8)0.0086 (8)0.0159 (9)
Fe1—C82.0428 (19)C10—C111.502 (2)
Fe1—C22.0452 (19)C11—C121.538 (2)
Fe1—C12.0460 (19)C11—H110.9800
Fe1—C92.0474 (18)C12—C131.509 (2)
Fe1—C62.0488 (17)C12—H12A0.9700
Fe1—C72.0487 (19)C12—H12B0.9700
Fe1—C52.0493 (18)C13—C141.466 (2)
Fe1—C102.0510 (16)C14—C151.397 (2)
Fe1—C32.0521 (18)C14—C191.398 (2)
Fe1—C42.0549 (18)C15—C161.388 (3)
S1—C211.7708 (17)C15—H150.9300
S1—C221.8167 (18)C16—C171.383 (3)
S2—C211.6608 (17)C16—H160.9300
N1—C211.340 (2)C17—C181.399 (3)
N1—N21.3964 (19)C17—C201.512 (3)
N1—C111.495 (2)C18—C191.382 (3)
N2—C131.294 (2)C18—H180.9300
C5—C11.420 (3)C19—H190.9300
C5—C41.419 (3)C20—H20A0.9600
C5—H50.9300C20—H20B0.9600
C4—C31.414 (3)C20—H20C0.9600
C4—H40.9300C22—C231.508 (2)
C3—C21.420 (3)C22—H22A0.9700
C3—H30.9300C22—H22B0.9700
C2—C11.428 (3)C23—C241.378 (3)
C2—H20.9300C23—C281.392 (3)
C1—H10.9300C28—C271.392 (3)
C6—C71.422 (3)C28—H280.9300
C6—C101.432 (2)C27—C261.377 (3)
C6—H60.9300C27—H270.9300
C7—C81.416 (3)C26—C251.374 (3)
C7—H70.9300C26—H260.9300
C8—C91.421 (3)C25—C241.383 (3)
C8—H80.9300C25—H250.9300
C9—C101.429 (2)C24—H240.9300
C9—H90.9300
C8—Fe1—C2116.95 (9)C6—C7—Fe169.69 (10)
C8—Fe1—C1151.92 (9)C8—C7—H7126.1
C2—Fe1—C140.85 (8)C6—C7—H7126.1
C8—Fe1—C940.66 (8)Fe1—C7—H7126.3
C2—Fe1—C9106.49 (8)C7—C8—C9108.51 (17)
C1—Fe1—C9118.79 (8)C7—C8—Fe169.98 (11)
C8—Fe1—C668.20 (8)C9—C8—Fe169.85 (10)
C2—Fe1—C6166.18 (8)C7—C8—H8125.7
C1—Fe1—C6129.18 (7)C9—C8—H8125.7
C9—Fe1—C668.42 (7)Fe1—C8—H8126.0
C8—Fe1—C740.49 (9)C8—C9—C10108.07 (17)
C2—Fe1—C7151.03 (8)C8—C9—Fe169.49 (11)
C1—Fe1—C7166.78 (8)C10—C9—Fe169.73 (9)
C9—Fe1—C768.41 (8)C8—C9—H9126.0
C6—Fe1—C740.62 (8)C10—C9—H9126.0
C8—Fe1—C5164.95 (8)Fe1—C9—H9126.4
C2—Fe1—C568.37 (8)C9—C10—C6107.23 (15)
C1—Fe1—C540.57 (8)C9—C10—C11127.04 (15)
C9—Fe1—C5153.95 (8)C6—C10—C11125.67 (15)
C6—Fe1—C5110.18 (7)C9—C10—Fe169.46 (9)
C7—Fe1—C5128.59 (8)C6—C10—Fe169.47 (9)
C8—Fe1—C1068.59 (7)C11—C10—Fe1128.36 (11)
C2—Fe1—C10127.05 (8)N1—C11—C10109.61 (13)
C1—Fe1—C10108.77 (7)N1—C11—C12100.44 (12)
C9—Fe1—C1040.81 (7)C10—C11—C12114.22 (14)
C6—Fe1—C1040.88 (7)N1—C11—H11110.7
C7—Fe1—C1068.72 (7)C10—C11—H11110.7
C5—Fe1—C10120.71 (7)C12—C11—H11110.7
C8—Fe1—C3106.16 (8)C13—C12—C11102.75 (13)
C2—Fe1—C340.56 (8)C13—C12—H12A111.2
C1—Fe1—C368.31 (8)C11—C12—H12A111.2
C9—Fe1—C3125.60 (8)C13—C12—H12B111.2
C6—Fe1—C3152.81 (8)C11—C12—H12B111.2
C7—Fe1—C3117.78 (8)H12A—C12—H12B109.1
C5—Fe1—C368.04 (8)N2—C13—C14121.50 (15)
C10—Fe1—C3164.02 (8)N2—C13—C12113.60 (15)
C8—Fe1—C4126.35 (8)C14—C13—C12124.88 (14)
C2—Fe1—C468.10 (8)C15—C14—C19118.43 (16)
C1—Fe1—C468.15 (8)C15—C14—C13120.79 (15)
C9—Fe1—C4163.37 (8)C19—C14—C13120.77 (15)
C6—Fe1—C4120.38 (8)C16—C15—C14120.77 (17)
C7—Fe1—C4108.22 (8)C16—C15—H15119.6
C5—Fe1—C440.46 (8)C14—C15—H15119.6
C10—Fe1—C4154.75 (7)C17—C16—C15120.92 (17)
C3—Fe1—C440.27 (8)C17—C16—H16119.5
C21—S1—C22101.89 (8)C15—C16—H16119.5
C21—N1—N2120.26 (13)C16—C17—C18118.34 (17)
C21—N1—C11127.22 (14)C16—C17—C20120.75 (18)
N2—N1—C11112.25 (12)C18—C17—C20120.91 (19)
C13—N2—N1108.02 (13)C19—C18—C17121.25 (17)
C1—C5—C4108.06 (17)C19—C18—H18119.4
C1—C5—Fe169.59 (11)C17—C18—H18119.4
C4—C5—Fe169.98 (11)C18—C19—C14120.30 (16)
C1—C5—H5126.0C18—C19—H19119.9
C4—C5—H5126.0C14—C19—H19119.9
Fe1—C5—H5126.0C17—C20—H20A109.5
C3—C4—C5108.19 (17)C17—C20—H20B109.5
C3—C4—Fe169.76 (10)H20A—C20—H20B109.5
C5—C4—Fe169.56 (10)C17—C20—H20C109.5
C3—C4—H4125.9H20A—C20—H20C109.5
C5—C4—H4125.9H20B—C20—H20C109.5
Fe1—C4—H4126.4N1—C21—S2122.65 (13)
C4—C3—C2108.20 (17)N1—C21—S1112.19 (12)
C4—C3—Fe169.97 (10)S2—C21—S1125.16 (10)
C2—C3—Fe169.46 (10)C23—C22—S1107.43 (12)
C4—C3—H3125.9C23—C22—H22A110.2
C2—C3—H3125.9S1—C22—H22A110.2
Fe1—C3—H3126.2C23—C22—H22B110.2
C3—C2—C1107.78 (18)S1—C22—H22B110.2
C3—C2—Fe169.98 (11)H22A—C22—H22B108.5
C1—C2—Fe169.60 (10)C24—C23—C28118.41 (17)
C3—C2—H2126.1C24—C23—C22120.43 (17)
C1—C2—H2126.1C28—C23—C22121.16 (18)
Fe1—C2—H2125.9C23—C28—C27120.40 (19)
C5—C1—C2107.77 (18)C23—C28—H28119.8
C5—C1—Fe169.84 (11)C27—C28—H28119.8
C2—C1—Fe169.54 (11)C26—C27—C28120.19 (19)
C5—C1—H1126.1C26—C27—H27119.9
C2—C1—H1126.1C28—C27—H27119.9
Fe1—C1—H1126.1C25—C26—C27119.51 (18)
C7—C6—C10108.33 (16)C25—C26—H26120.2
C7—C6—Fe169.69 (10)C27—C26—H26120.2
C10—C6—Fe169.64 (9)C26—C25—C24120.4 (2)
C7—C6—H6125.8C26—C25—H25119.8
C10—C6—H6125.8C24—C25—H25119.8
Fe1—C6—H6126.4C23—C24—C25121.06 (19)
C8—C7—C6107.85 (17)C23—C24—H24119.5
C8—C7—Fe169.53 (11)C25—C24—H24119.5
C21—N1—N2—C13163.81 (15)C1—Fe1—C7—C6−43.9 (4)
C11—N1—N2—C13−10.50 (18)C9—Fe1—C7—C681.61 (12)
C8—Fe1—C5—C1−151.8 (3)C5—Fe1—C7—C6−75.37 (13)
C2—Fe1—C5—C1−38.01 (11)C10—Fe1—C7—C637.61 (10)
C9—Fe1—C5—C145.3 (2)C3—Fe1—C7—C6−158.46 (11)
C6—Fe1—C5—C1127.27 (11)C4—Fe1—C7—C6−115.72 (12)
C7—Fe1—C5—C1169.42 (11)C6—C7—C8—C90.0 (2)
C10—Fe1—C5—C183.21 (12)Fe1—C7—C8—C959.42 (13)
C3—Fe1—C5—C1−81.85 (12)C6—C7—C8—Fe1−59.37 (13)
C4—Fe1—C5—C1−119.19 (16)C2—Fe1—C8—C7−156.34 (11)
C8—Fe1—C5—C4−32.6 (3)C1—Fe1—C8—C7171.85 (15)
C2—Fe1—C5—C481.18 (12)C9—Fe1—C8—C7119.58 (16)
C1—Fe1—C5—C4119.19 (16)C6—Fe1—C8—C737.76 (11)
C9—Fe1—C5—C4164.52 (16)C5—Fe1—C8—C7−49.0 (3)
C6—Fe1—C5—C4−113.54 (12)C10—Fe1—C8—C781.88 (12)
C7—Fe1—C5—C4−71.39 (14)C3—Fe1—C8—C7−114.07 (12)
C10—Fe1—C5—C4−157.60 (11)C4—Fe1—C8—C7−74.70 (14)
C3—Fe1—C5—C437.34 (12)C2—Fe1—C8—C984.08 (13)
C1—C5—C4—C30.1 (2)C1—Fe1—C8—C952.3 (2)
Fe1—C5—C4—C3−59.26 (13)C6—Fe1—C8—C9−81.83 (12)
C1—C5—C4—Fe159.39 (12)C7—Fe1—C8—C9−119.58 (16)
C8—Fe1—C4—C3−70.49 (15)C5—Fe1—C8—C9−168.6 (3)
C2—Fe1—C4—C337.61 (12)C10—Fe1—C8—C9−37.70 (11)
C1—Fe1—C4—C381.79 (13)C3—Fe1—C8—C9126.35 (12)
C9—Fe1—C4—C3−36.3 (3)C4—Fe1—C8—C9165.72 (11)
C6—Fe1—C4—C3−154.57 (12)C7—C8—C9—C10−0.2 (2)
C7—Fe1—C4—C3−111.74 (13)Fe1—C8—C9—C1059.26 (12)
C5—Fe1—C4—C3119.51 (17)C7—C8—C9—Fe1−59.50 (13)
C10—Fe1—C4—C3169.66 (15)C2—Fe1—C9—C8−112.38 (13)
C8—Fe1—C4—C5170.00 (12)C1—Fe1—C9—C8−154.87 (12)
C2—Fe1—C4—C5−81.90 (13)C6—Fe1—C9—C881.23 (13)
C1—Fe1—C4—C5−37.72 (11)C7—Fe1—C9—C837.40 (12)
C9—Fe1—C4—C5−155.8 (2)C5—Fe1—C9—C8173.27 (16)
C6—Fe1—C4—C585.92 (13)C10—Fe1—C9—C8119.41 (16)
C7—Fe1—C4—C5128.75 (12)C3—Fe1—C9—C8−72.06 (15)
C10—Fe1—C4—C550.2 (2)C4—Fe1—C9—C8−44.0 (3)
C3—Fe1—C4—C5−119.51 (17)C8—Fe1—C9—C10−119.41 (16)
C5—C4—C3—C20.0 (2)C2—Fe1—C9—C10128.21 (11)
Fe1—C4—C3—C2−59.13 (13)C1—Fe1—C9—C1085.72 (12)
C5—C4—C3—Fe159.14 (13)C6—Fe1—C9—C10−38.18 (10)
C8—Fe1—C3—C4127.78 (12)C7—Fe1—C9—C10−82.01 (11)
C2—Fe1—C3—C4−119.45 (17)C5—Fe1—C9—C1053.9 (2)
C1—Fe1—C3—C4−81.37 (13)C3—Fe1—C9—C10168.53 (10)
C9—Fe1—C3—C4167.97 (11)C4—Fe1—C9—C10−163.4 (2)
C6—Fe1—C3—C454.2 (2)C8—C9—C10—C60.34 (19)
C7—Fe1—C3—C485.70 (13)Fe1—C9—C10—C659.45 (11)
C5—Fe1—C3—C4−37.51 (12)C8—C9—C10—C11177.69 (16)
C10—Fe1—C3—C4−163.8 (2)Fe1—C9—C10—C11−123.19 (16)
C8—Fe1—C3—C2−112.77 (13)C8—C9—C10—Fe1−59.12 (12)
C1—Fe1—C3—C238.08 (12)C7—C6—C10—C9−0.31 (19)
C9—Fe1—C3—C2−72.58 (14)Fe1—C6—C10—C9−59.44 (11)
C6—Fe1—C3—C2173.60 (15)C7—C6—C10—C11−177.71 (15)
C7—Fe1—C3—C2−154.85 (12)Fe1—C6—C10—C11123.15 (16)
C5—Fe1—C3—C281.94 (13)C7—C6—C10—Fe159.14 (12)
C10—Fe1—C3—C2−44.4 (3)C8—Fe1—C10—C937.56 (12)
C4—Fe1—C3—C2119.45 (17)C2—Fe1—C10—C9−70.73 (14)
C4—C3—C2—C1−0.1 (2)C1—Fe1—C10—C9−112.63 (12)
Fe1—C3—C2—C1−59.58 (13)C6—Fe1—C10—C9118.56 (15)
C4—C3—C2—Fe159.45 (13)C7—Fe1—C10—C981.19 (12)
C8—Fe1—C2—C383.47 (13)C5—Fe1—C10—C9−155.64 (11)
C1—Fe1—C2—C3−118.83 (17)C3—Fe1—C10—C9−36.0 (3)
C9—Fe1—C2—C3125.99 (12)C4—Fe1—C10—C9168.95 (16)
C6—Fe1—C2—C3−167.7 (3)C8—Fe1—C10—C6−81.00 (12)
C7—Fe1—C2—C350.9 (2)C2—Fe1—C10—C6170.70 (11)
C5—Fe1—C2—C3−81.07 (12)C1—Fe1—C10—C6128.81 (11)
C10—Fe1—C2—C3166.04 (11)C9—Fe1—C10—C6−118.56 (15)
C4—Fe1—C2—C3−37.35 (12)C7—Fe1—C10—C6−37.37 (11)
C8—Fe1—C2—C1−157.71 (12)C5—Fe1—C10—C685.80 (12)
C9—Fe1—C2—C1−115.19 (12)C3—Fe1—C10—C6−154.5 (3)
C6—Fe1—C2—C1−48.9 (4)C4—Fe1—C10—C650.4 (2)
C7—Fe1—C2—C1169.74 (15)C8—Fe1—C10—C11159.15 (17)
C5—Fe1—C2—C137.75 (12)C2—Fe1—C10—C1150.85 (18)
C10—Fe1—C2—C1−75.14 (14)C1—Fe1—C10—C118.96 (17)
C3—Fe1—C2—C1118.83 (17)C9—Fe1—C10—C11121.59 (19)
C4—Fe1—C2—C181.48 (12)C6—Fe1—C10—C11−119.85 (19)
C4—C5—C1—C2−0.2 (2)C7—Fe1—C10—C11−157.23 (17)
Fe1—C5—C1—C259.43 (13)C5—Fe1—C10—C11−34.05 (18)
C4—C5—C1—Fe1−59.63 (13)C3—Fe1—C10—C1185.6 (3)
C3—C2—C1—C50.2 (2)C4—Fe1—C10—C11−69.5 (2)
Fe1—C2—C1—C5−59.62 (12)C21—N1—C11—C1082.3 (2)
C3—C2—C1—Fe159.82 (13)N2—N1—C11—C10−103.92 (15)
C8—Fe1—C1—C5164.87 (15)C21—N1—C11—C12−157.18 (16)
C2—Fe1—C1—C5118.94 (16)N2—N1—C11—C1216.65 (16)
C9—Fe1—C1—C5−159.12 (11)C9—C10—C11—N1−104.11 (18)
C6—Fe1—C1—C5−74.48 (14)C6—C10—C11—N172.8 (2)
C7—Fe1—C1—C5−38.9 (4)Fe1—C10—C11—N1163.79 (12)
C10—Fe1—C1—C5−115.62 (11)C9—C10—C11—C12144.09 (17)
C3—Fe1—C1—C581.13 (12)C6—C10—C11—C12−39.0 (2)
C4—Fe1—C1—C537.62 (11)Fe1—C10—C11—C1252.0 (2)
C8—Fe1—C1—C245.9 (2)N1—C11—C12—C13−15.48 (15)
C9—Fe1—C1—C281.94 (13)C10—C11—C12—C13101.72 (15)
C6—Fe1—C1—C2166.58 (11)N1—N2—C13—C14179.95 (14)
C7—Fe1—C1—C2−157.8 (3)N1—N2—C13—C12−1.10 (19)
C5—Fe1—C1—C2−118.94 (16)C11—C12—C13—N211.39 (18)
C10—Fe1—C1—C2125.44 (12)C11—C12—C13—C14−169.70 (15)
C3—Fe1—C1—C2−37.81 (12)N2—C13—C14—C15172.56 (16)
C4—Fe1—C1—C2−81.33 (12)C12—C13—C14—C15−6.3 (2)
C8—Fe1—C6—C7−37.65 (12)N2—C13—C14—C19−8.2 (2)
C2—Fe1—C6—C7−152.3 (3)C12—C13—C14—C19172.93 (16)
C1—Fe1—C6—C7168.21 (12)C19—C14—C15—C16−0.1 (3)
C9—Fe1—C6—C7−81.56 (12)C13—C14—C15—C16179.08 (16)
C5—Fe1—C6—C7126.32 (12)C14—C15—C16—C170.1 (3)
C10—Fe1—C6—C7−119.67 (16)C15—C16—C17—C18−0.2 (3)
C3—Fe1—C6—C745.3 (2)C15—C16—C17—C20−179.84 (18)
C4—Fe1—C6—C782.72 (13)C16—C17—C18—C190.3 (3)
C8—Fe1—C6—C1082.03 (11)C20—C17—C18—C19−179.98 (18)
C2—Fe1—C6—C10−32.7 (4)C17—C18—C19—C14−0.4 (3)
C1—Fe1—C6—C10−72.12 (13)C15—C14—C19—C180.3 (3)
C9—Fe1—C6—C1038.12 (10)C13—C14—C19—C18−178.90 (16)
C7—Fe1—C6—C10119.67 (16)N2—N1—C21—S2−174.50 (11)
C5—Fe1—C6—C10−114.01 (11)C11—N1—C21—S2−1.1 (2)
C3—Fe1—C6—C10164.99 (15)N2—N1—C21—S15.40 (19)
C4—Fe1—C6—C10−157.61 (10)C11—N1—C21—S1178.78 (12)
C10—C6—C7—C80.2 (2)C22—S1—C21—N1175.13 (13)
Fe1—C6—C7—C859.27 (13)C22—S1—C21—S2−4.97 (14)
C10—C6—C7—Fe1−59.11 (12)C21—S1—C22—C23−175.12 (14)
C2—Fe1—C7—C847.6 (2)S1—C22—C23—C24102.92 (18)
C1—Fe1—C7—C8−163.0 (3)S1—C22—C23—C28−78.0 (2)
C9—Fe1—C7—C8−37.54 (11)C24—C23—C28—C272.2 (3)
C6—Fe1—C7—C8−119.15 (16)C22—C23—C28—C27−176.87 (18)
C5—Fe1—C7—C8165.48 (11)C23—C28—C27—C26−1.2 (3)
C10—Fe1—C7—C8−81.54 (12)C28—C27—C26—C25−0.7 (3)
C3—Fe1—C7—C882.39 (13)C27—C26—C25—C241.7 (3)
C4—Fe1—C7—C8125.13 (12)C28—C23—C24—C25−1.2 (3)
C8—Fe1—C7—C6119.15 (16)C22—C23—C24—C25177.82 (18)
C2—Fe1—C7—C6166.76 (15)C26—C25—C24—C23−0.7 (3)
  3 in total

1.  SHELXL: high-resolution refinement.

Authors:  G M Sheldrick; T R Schneider
Journal:  Methods Enzymol       Date:  1997       Impact factor: 1.600

2.  Regioselective synthesis of 1,3,5-triaryl-4-alkylpyrazoles: novel ligands for the estrogen receptor.

Authors:  Y R Huang; J A Katzenellenbogen
Journal:  Org Lett       Date:  2000-09-07       Impact factor: 6.005

3.  Tuning the photoinduced electron-transfer thermodynamics in 1,3,5-triaryl-2-pyrazoline fluorophores: X-ray structures, photophysical characterization, computational analysis, and in vivo evaluation.

Authors:  Christoph J Fahrni; Liuchun Yang; Donald G VanDerveer
Journal:  J Am Chem Soc       Date:  2003-04-02       Impact factor: 15.419

  3 in total
  1 in total

1.  (E)-1-Ferrocenyl-3-phenyl-prop-2-en-1-one.

Authors:  Yong-Hong Liu; Jian-Feng Liu; Pan-Ming Jian; Xiao-Lan Liu
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-07-05
  1 in total

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