Literature DB >> 21583733

(Diethyl ether){1-[2-(1-methyl-1H-imidazol-2-yl-κN)-1,1-diphenyl-ethyl]-(1,2,3,3a,7a-η)-inden-yl}lithium(I).

Guofeng Sun1, Chong Tian, Wanli Nie, Maxim V Borzov.   

Abstract

In the title compound, [Li(C(27)H(23)N(2))(C(4)H(10)O)], the Li atom possesses a nearly planar trigonal coordination environment (assuming the cyclo-penta-dienyl ring of the indenyl group occupies one coordination place). The diethyl ether ligand adopts a nearly planar W-type conformation.

Entities:  

Year:  2009        PMID: 21583733      PMCID: PMC2977547          DOI: 10.1107/S1600536809011556

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


Related literature

For the structural parameters of compounds with the (η5-1H-inden­yl)lithium fragment, see: Schumann et al. (2001 ▶); Cipot et al. (2003 ▶); Wang et al. (2005 ▶); Dinnebier et al. (1999 ▶); Feng et al. (2005 ▶); Faure et al. (2000 ▶); Cheng et al. (2004 ▶); Jones & Alan (2005 ▶). For the (η5-9H-fluoren­yl)lithium counterpart of a similar structure, see: Culp & Cowley (1996 ▶). For the synthesis, see: Krut’ko et al. (2006 ▶).

Experimental

Crystal data

[Li(C27H23N2)(C4H10O)] M = 456.53 Orthorhombic, a = 19.620 (2) Å b = 12.8763 (13) Å c = 20.698 (2) Å V = 5229.0 (9) Å3 Z = 8 Mo Kα radiation μ = 0.07 mm−1 T = 293 K 0.32 × 0.21 × 0.11 mm

Data collection

Bruker SMART APEXII CCD diffractometer Absorption correction: multi-scan (SADABS; Sheldrick, 1996 ▶) T min = 0.978, T max = 0.992 24751 measured reflections 4595 independent reflections 2357 reflections with I > 2σ(I) R int = 0.056

Refinement

R[F 2 > 2σ(F 2)] = 0.048 wR(F 2) = 0.152 S = 1.02 4595 reflections 320 parameters 7 restraints H-atom parameters constrained Δρmax = 0.32 e Å−3 Δρmin = −0.20 e Å−3 Data collection: APEX2 (Bruker, 2007 ▶); cell refinement: SAINT (Bruker, 2007 ▶); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: SHELXTL (Sheldrick, 2008 ▶); software used to prepare material for publication: SHELXL97. Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536809011556/dn2437sup1.cif Structure factors: contains datablocks I. DOI: 10.1107/S1600536809011556/dn2437Isup2.hkl Additional supplementary materials: crystallographic information; 3D view; checkCIF report
[Li(C27H23N2)(C4H10O)]F(000) = 1952
Mr = 456.53Dx = 1.160 Mg m3
Orthorhombic, PbcaMo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ac 2abCell parameters from 4629 reflections
a = 19.620 (2) Åθ = 2.2–21.0°
b = 12.8763 (13) ŵ = 0.07 mm1
c = 20.698 (2) ÅT = 293 K
V = 5229.0 (9) Å3Prism, green
Z = 80.32 × 0.21 × 0.11 mm
Bruker SMART APEX diffractometer4595 independent reflections
Radiation source: fine-focus sealed tube2357 reflections with I > 2σ(I)
graphiteRint = 0.056
φ and ω scansθmax = 25.0°, θmin = 2.0°
Absorption correction: multi-scan (SADABS; Sheldrick, 1996)h = −20→23
Tmin = 0.978, Tmax = 0.992k = −15→15
24751 measured reflectionsl = −24→24
Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.048H-atom parameters constrained
wR(F2) = 0.152w = 1/[σ2(Fo2) + (0.0739P)2] where P = (Fo2 + 2Fc2)/3
S = 1.02(Δ/σ)max < 0.001
4595 reflectionsΔρmax = 0.32 e Å3
320 parametersΔρmin = −0.20 e Å3
7 restraintsExtinction correction: SHELXL97 (Sheldrick, 2008), Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4
Primary atom site location: structure-invariant direct methodsExtinction coefficient: 0.0022 (5)
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
Li10.13031 (19)0.1533 (3)0.39839 (18)0.0771 (11)
N10.07860 (10)−0.12724 (15)0.31605 (9)0.0698 (6)
N20.09933 (9)0.00828 (15)0.37892 (9)0.0687 (5)
C10.12154 (11)−0.04750 (18)0.32932 (10)0.0599 (6)
C20.02674 (13)−0.1227 (2)0.35940 (13)0.0855 (8)
H2−0.0111−0.16850.36220.103*
C30.03967 (13)−0.0401 (2)0.39760 (13)0.0844 (8)
H30.0116−0.01830.43250.101*
C40.08482 (13)−0.2031 (2)0.26429 (13)0.0920 (8)
H4A0.0831−0.16750.22250.138*
H4B0.0472−0.25300.26710.138*
H4C0.1283−0.23990.26840.138*
C50.18531 (10)−0.02763 (18)0.29257 (10)0.0609 (6)
H5A0.1939−0.08750.26370.073*
H5B0.2237−0.02360.32350.073*
C60.18485 (9)0.07348 (17)0.25096 (9)0.0568 (6)
C110.17977 (10)0.16801 (17)0.29535 (9)0.0578 (6)
C120.13052 (12)0.24721 (19)0.29777 (11)0.0704 (6)
H120.09180.25130.27030.084*
C130.14622 (13)0.31901 (19)0.34603 (12)0.0781 (7)
H130.11990.37820.35730.094*
C140.20755 (13)0.2886 (2)0.37489 (11)0.0714 (7)
C150.22949 (11)0.19385 (19)0.34335 (10)0.0629 (6)
C160.29167 (12)0.1485 (2)0.36330 (10)0.0745 (7)
H160.30730.08640.34340.089*
C170.32949 (13)0.1942 (3)0.41150 (13)0.0918 (9)
H170.37140.16360.42430.110*
C180.30745 (17)0.2848 (3)0.44184 (12)0.0943 (9)
H180.33440.31430.47530.113*
C190.24817 (16)0.3318 (2)0.42462 (12)0.0883 (8)
H190.23400.39350.44590.106*
C210.12573 (10)0.06018 (17)0.20274 (10)0.0585 (6)
C220.05774 (11)0.06908 (17)0.22160 (11)0.0648 (6)
H220.04730.09150.26420.078*
C230.00511 (12)0.0457 (2)0.17914 (14)0.0782 (7)
H23−0.04080.05220.19320.094*
C240.01830 (14)0.0137 (2)0.11771 (14)0.0860 (8)
H24−0.0180−0.00080.08870.103*
C250.08479 (14)0.0028 (2)0.09833 (12)0.0858 (8)
H250.0946−0.02090.05590.103*
C260.13787 (12)0.02615 (19)0.14016 (10)0.0714 (7)
H260.18350.01870.12560.086*
C310.25269 (11)0.0834 (2)0.21395 (9)0.0674 (7)
C320.26254 (12)0.1724 (2)0.17666 (11)0.0826 (8)
H320.22800.22410.17510.099*
C330.32247 (17)0.1862 (3)0.14166 (13)0.1068 (11)
H330.32840.24600.11540.128*
C340.37300 (17)0.1127 (4)0.14541 (17)0.1193 (14)
H340.41430.12260.12220.143*
C350.36456 (14)0.0259 (3)0.18195 (15)0.1050 (11)
H350.4001−0.02410.18420.126*
C360.30438 (11)0.0097 (2)0.21600 (11)0.0798 (7)
H360.2986−0.05180.24070.096*
O10.10490 (8)0.17992 (15)0.49122 (8)0.0859 (5)
C410.06321 (18)0.2679 (2)0.50301 (14)0.1134 (10)
H41A0.08710.33190.48930.136*
H41B0.05300.27350.54970.136*
C42−0.00153 (17)0.2555 (3)0.46558 (18)0.1471 (15)
H42A0.00860.25700.41920.221*
H42C−0.03270.31230.47630.221*
H42B−0.02280.18900.47670.221*
C430.15656 (18)0.1729 (3)0.54066 (14)0.1278 (12)
H43B0.13500.16400.58350.153*
H43A0.18410.23730.54150.153*
C440.19980 (19)0.0846 (4)0.52646 (17)0.1513 (16)
H44A0.22890.10090.48930.227*
H44B0.17140.02420.51630.227*
H44C0.22830.06910.56410.227*
U11U22U33U12U13U23
Li10.073 (3)0.080 (3)0.079 (2)−0.002 (2)0.0148 (19)0.000 (2)
N10.0699 (13)0.0588 (14)0.0808 (13)−0.0005 (11)0.0005 (10)0.0118 (11)
N20.0691 (12)0.0674 (13)0.0694 (11)0.0065 (11)0.0155 (10)0.0098 (10)
C10.0592 (14)0.0545 (15)0.0658 (13)0.0027 (12)0.0029 (11)0.0134 (11)
C20.0740 (18)0.080 (2)0.1020 (19)−0.0060 (15)0.0127 (16)0.0216 (17)
C30.0792 (18)0.084 (2)0.0903 (18)0.0069 (15)0.0261 (14)0.0216 (16)
C40.105 (2)0.0691 (18)0.101 (2)−0.0129 (15)−0.0075 (16)−0.0036 (16)
C50.0561 (13)0.0621 (15)0.0644 (13)0.0083 (11)0.0015 (10)0.0001 (11)
C60.0505 (12)0.0647 (15)0.0553 (11)0.0039 (10)0.0036 (10)0.0076 (10)
C110.0573 (13)0.0586 (15)0.0576 (12)−0.0002 (11)0.0056 (10)0.0064 (11)
C120.0753 (16)0.0618 (16)0.0741 (15)0.0017 (13)−0.0015 (12)0.0108 (13)
C130.096 (2)0.0555 (16)0.0830 (16)0.0026 (14)0.0119 (15)0.0007 (13)
C140.0816 (18)0.0638 (17)0.0689 (15)−0.0199 (14)0.0126 (13)0.0063 (13)
C150.0610 (14)0.0717 (17)0.0559 (12)−0.0118 (12)0.0086 (11)0.0047 (11)
C160.0617 (15)0.098 (2)0.0638 (13)−0.0071 (13)0.0041 (12)0.0044 (13)
C170.0727 (17)0.131 (3)0.0716 (16)−0.0215 (18)−0.0024 (14)0.0006 (17)
C180.098 (2)0.113 (3)0.0716 (17)−0.040 (2)0.0002 (16)−0.0015 (18)
C190.108 (2)0.081 (2)0.0754 (17)−0.0330 (18)0.0137 (16)−0.0046 (14)
C210.0571 (14)0.0577 (15)0.0606 (13)0.0016 (10)−0.0011 (10)0.0089 (11)
C220.0566 (14)0.0634 (16)0.0743 (14)0.0019 (11)−0.0034 (12)0.0054 (12)
C230.0599 (15)0.0754 (19)0.0991 (19)0.0021 (13)−0.0080 (14)0.0075 (15)
C240.0766 (19)0.089 (2)0.0928 (19)−0.0124 (15)−0.0246 (15)0.0046 (16)
C250.097 (2)0.092 (2)0.0691 (16)−0.0149 (16)−0.0119 (14)−0.0037 (14)
C260.0684 (16)0.0810 (18)0.0648 (14)−0.0056 (13)−0.0023 (12)0.0010 (12)
C310.0559 (14)0.0929 (19)0.0535 (12)−0.0075 (13)0.0004 (11)−0.0026 (13)
C320.0733 (17)0.107 (2)0.0674 (14)−0.0184 (15)0.0080 (12)0.0037 (15)
C330.102 (2)0.145 (3)0.0737 (17)−0.044 (2)0.0214 (17)−0.0050 (18)
C340.075 (2)0.185 (4)0.099 (2)−0.038 (2)0.0293 (19)−0.045 (3)
C350.0653 (19)0.158 (3)0.092 (2)0.0040 (19)0.0110 (16)−0.038 (2)
C360.0557 (15)0.115 (2)0.0692 (15)0.0071 (15)0.0063 (12)−0.0151 (14)
O10.0886 (12)0.0925 (14)0.0765 (11)0.0028 (10)0.0090 (9)0.0092 (9)
C410.157 (3)0.084 (2)0.100 (2)0.008 (2)0.0438 (19)−0.0075 (17)
C420.115 (3)0.135 (3)0.191 (4)0.033 (2)0.034 (2)0.039 (3)
C430.129 (3)0.180 (4)0.0742 (18)−0.011 (2)0.0022 (17)0.020 (2)
C440.125 (3)0.208 (4)0.121 (3)0.041 (3)0.012 (2)0.070 (3)
Li1—N22.004 (5)C18—C191.359 (4)
Li1—O12.015 (4)C18—H180.9500
Li1—C152.315 (4)C19—H190.9500
Li1—C112.351 (4)C21—C261.388 (3)
Li1—C142.360 (5)C21—C221.395 (3)
Li1—C122.408 (5)C22—C231.389 (3)
Li1—C132.414 (5)C22—H220.9500
Li—Cp2.041 (4)C23—C241.361 (3)
N1—C11.356 (3)C23—H230.9500
N1—C21.358 (3)C24—C251.372 (3)
N1—C41.455 (3)C24—H240.9500
N2—C11.326 (3)C25—C261.387 (3)
N2—C31.381 (3)C25—H250.9500
C1—C51.486 (3)C26—H260.9500
C2—C31.349 (4)C31—C361.390 (3)
C2—H20.9500C31—C321.395 (3)
C3—H30.9500C32—C331.393 (3)
C4—H4A0.9800C32—H320.9500
C4—H4B0.9800C33—C341.373 (5)
C4—H4C0.9800C33—H330.9500
C5—C61.561 (3)C34—C351.359 (5)
C5—H5A0.9900C34—H340.9500
C5—H5B0.9900C35—C361.391 (4)
C6—C111.528 (3)C35—H350.9500
C6—C211.540 (3)C36—H360.9500
C6—C311.541 (3)O1—C411.419 (3)
C11—C121.406 (3)O1—C431.443 (3)
C11—C151.431 (3)C41—C421.496 (4)
C12—C131.396 (3)C41—H41A0.9900
C12—H120.9500C41—H41B0.9900
C13—C141.399 (3)C42—H42A0.9800
C13—H130.9500C42—H42C0.9800
C14—C191.416 (3)C42—H42B0.9800
C14—C151.449 (3)C43—C441.448 (5)
C15—C161.414 (3)C43—H43B0.9900
C16—C171.376 (3)C43—H43A0.9900
C16—H160.9500C44—H44A0.9800
C17—C181.393 (4)C44—H44B0.9800
C17—H170.9500C44—H44C0.9800
N2—Li1—O1105.98 (19)C11—C15—C14107.8 (2)
N2—Li1—C15111.48 (19)C16—C15—Li1119.22 (18)
O1—Li1—C15129.7 (2)C11—C15—Li173.52 (15)
N2—Li1—C1191.03 (16)C14—C15—Li173.66 (16)
O1—Li1—C11162.5 (2)C17—C16—C15120.0 (3)
C15—Li1—C1135.73 (9)C17—C16—H16120.0
N2—Li1—C14147.2 (2)C15—C16—H16120.0
O1—Li1—C14103.28 (19)C16—C17—C18121.2 (3)
C15—Li1—C1436.10 (10)C16—C17—H17119.4
C11—Li1—C1459.22 (12)C18—C17—H17119.4
N2—Li1—C12107.12 (19)C19—C18—C17121.4 (3)
O1—Li1—C12137.7 (2)C19—C18—H18119.3
C15—Li1—C1257.28 (12)C17—C18—H18119.3
C11—Li1—C1234.33 (9)C18—C19—C14119.8 (3)
C14—Li1—C1256.62 (12)C18—C19—H19120.1
N2—Li1—C13140.6 (2)C14—C19—H19120.1
O1—Li1—C13108.04 (19)C26—C21—C22116.83 (19)
C15—Li1—C1358.04 (13)C26—C21—C6120.71 (18)
C11—Li1—C1357.85 (12)C22—C21—C6122.00 (18)
C14—Li1—C1334.06 (10)C23—C22—C21121.1 (2)
C12—Li1—C1333.64 (10)C23—C22—H22119.5
C1—N1—C2107.4 (2)C21—C22—H22119.5
C1—N1—C4127.3 (2)C24—C23—C22121.0 (2)
C2—N1—C4125.3 (2)C24—C23—H23119.5
C1—N2—C3104.5 (2)C22—C23—H23119.5
C1—N2—Li1124.08 (18)C23—C24—C25119.0 (2)
C3—N2—Li1128.4 (2)C23—C24—H24120.5
N2—C1—N1111.26 (19)C25—C24—H24120.5
N2—C1—C5125.4 (2)C24—C25—C26120.6 (2)
N1—C1—C5123.3 (2)C24—C25—H25119.7
C3—C2—N1106.3 (2)C26—C25—H25119.7
C3—C2—H2126.8C25—C26—C21121.5 (2)
N1—C2—H2126.8C25—C26—H26119.3
C2—C3—N2110.5 (2)C21—C26—H26119.3
C2—C3—H3124.7C36—C31—C32118.5 (2)
N2—C3—H3124.7C36—C31—C6123.9 (2)
N1—C4—H4A109.5C32—C31—C6117.6 (2)
N1—C4—H4B109.5C33—C32—C31120.6 (3)
H4A—C4—H4B109.5C33—C32—H32119.7
N1—C4—H4C109.5C31—C32—H32119.7
H4A—C4—H4C109.5C34—C33—C32119.5 (3)
H4B—C4—H4C109.5C34—C33—H33120.3
C1—C5—C6114.90 (16)C32—C33—H33120.3
C1—C5—H5A108.5C35—C34—C33120.7 (3)
C6—C5—H5A108.5C35—C34—H34119.7
C1—C5—H5B108.5C33—C34—H34119.7
C6—C5—H5B108.5C34—C35—C36120.6 (3)
H5A—C5—H5B107.5C34—C35—H35119.7
C11—C6—C21115.41 (16)C36—C35—H35119.7
C11—C6—C31106.80 (17)C31—C36—C35120.1 (3)
C21—C6—C31109.73 (16)C31—C36—H36119.9
C11—C6—C5109.45 (16)C35—C36—H36119.9
C21—C6—C5105.62 (16)C41—O1—C43109.5 (3)
C31—C6—C5109.79 (17)C41—O1—Li1116.3 (2)
C12—C11—C15106.0 (2)C43—O1—Li1119.5 (2)
C12—C11—C6130.09 (19)O1—C41—C42108.4 (3)
C15—C11—C6123.91 (19)O1—C41—H41A110.0
C12—C11—Li175.08 (16)C42—C41—H41A110.0
C15—C11—Li170.76 (14)O1—C41—H41B110.0
C6—C11—Li1120.53 (17)C42—C41—H41B110.0
C13—C12—C11110.8 (2)H41A—C41—H41B108.4
C13—C12—Li173.38 (17)C41—C42—H42A109.5
C11—C12—Li170.59 (15)C41—C42—H42C109.5
C13—C12—H12124.6H42A—C42—H42C109.5
C11—C12—H12124.6C41—C42—H42B109.5
Li1—C12—H12123.0H42A—C42—H42B109.5
C12—C13—C14108.1 (2)H42C—C42—H42B109.5
C12—C13—Li172.97 (17)O1—C43—C44108.5 (3)
C14—C13—Li170.87 (16)O1—C43—H43B110.0
C12—C13—H13126.0C44—C43—H43B110.0
C14—C13—H13126.0O1—C43—H43A110.0
Li1—C13—H13121.9C44—C43—H43A110.0
C13—C14—C19133.2 (3)H43B—C43—H43A108.4
C13—C14—C15107.4 (2)C43—C44—H44A109.5
C19—C14—C15119.4 (3)C43—C44—H44B109.5
C13—C14—Li175.07 (17)H44A—C44—H44B109.5
C19—C14—Li1120.11 (18)C43—C44—H44C109.5
C15—C14—Li170.24 (15)H44A—C44—H44C109.5
C16—C15—C11134.0 (2)H44B—C44—H44C109.5
C16—C15—C14118.2 (2)
O1—Li1—N2—C1−162.01 (19)C15—Li1—C14—C19−113.3 (3)
C15—Li1—N2—C1−16.2 (3)C11—Li1—C14—C19−151.4 (3)
C11—Li1—N2—C113.9 (3)C12—Li1—C14—C19168.0 (3)
C14—Li1—N2—C1−9.5 (5)C13—Li1—C14—C19131.6 (3)
C12—Li1—N2—C144.7 (3)N2—Li1—C14—C15−10.6 (4)
C13—Li1—N2—C149.1 (4)O1—Li1—C14—C15142.3 (2)
O1—Li1—N2—C340.8 (3)C11—Li1—C14—C15−38.10 (13)
C15—Li1—N2—C3−173.4 (2)C12—Li1—C14—C15−78.75 (15)
C11—Li1—N2—C3−143.4 (2)C13—Li1—C14—C15−115.1 (2)
C14—Li1—N2—C3−166.7 (3)C12—C11—C15—C16−177.6 (2)
C12—Li1—N2—C3−112.6 (2)C6—C11—C15—C160.5 (4)
C13—Li1—N2—C3−108.1 (3)Li1—C11—C15—C16115.0 (3)
C3—N2—C1—N10.5 (2)C12—C11—C15—C141.2 (2)
Li1—N2—C1—N1−161.28 (19)C6—C11—C15—C14179.34 (17)
C3—N2—C1—C5−179.0 (2)Li1—C11—C15—C14−66.22 (17)
Li1—N2—C1—C519.3 (3)C12—C11—C15—Li167.45 (18)
C2—N1—C1—N2−0.4 (2)C6—C11—C15—Li1−114.4 (2)
C4—N1—C1—N2178.2 (2)C13—C14—C15—C16178.70 (19)
C2—N1—C1—C5179.1 (2)C19—C14—C15—C16−0.7 (3)
C4—N1—C1—C5−2.3 (3)Li1—C14—C15—C16−114.8 (2)
C1—N1—C2—C30.1 (3)C13—C14—C15—C11−0.3 (2)
C4—N1—C2—C3−178.5 (2)C19—C14—C15—C11−179.71 (18)
N1—C2—C3—N20.1 (3)Li1—C14—C15—C1166.12 (17)
C1—N2—C3—C2−0.4 (3)C13—C14—C15—Li1−66.46 (19)
Li1—N2—C3—C2160.3 (2)C19—C14—C15—Li1114.2 (2)
N2—C1—C5—C6−68.5 (3)N2—Li1—C15—C16−72.6 (3)
N1—C1—C5—C6112.1 (2)O1—Li1—C15—C1662.8 (4)
C1—C5—C6—C1164.7 (2)C11—Li1—C15—C16−131.6 (3)
C1—C5—C6—C21−60.1 (2)C14—Li1—C15—C16113.6 (3)
C1—C5—C6—C31−178.38 (18)C12—Li1—C15—C16−169.6 (2)
C21—C6—C11—C12−2.4 (3)C13—Li1—C15—C16150.3 (2)
C31—C6—C11—C12119.9 (2)N2—Li1—C15—C1159.1 (2)
C5—C6—C11—C12−121.3 (2)O1—Li1—C15—C11−165.6 (3)
C21—C6—C11—C15179.99 (18)C14—Li1—C15—C11−114.8 (2)
C31—C6—C11—C15−57.7 (2)C12—Li1—C15—C11−38.02 (13)
C5—C6—C11—C1561.1 (2)C13—Li1—C15—C11−78.07 (15)
C21—C6—C11—Li193.7 (2)N2—Li1—C15—C14173.8 (2)
C31—C6—C11—Li1−144.04 (18)O1—Li1—C15—C14−50.8 (3)
C5—C6—C11—Li1−25.2 (2)C11—Li1—C15—C14114.8 (2)
N2—Li1—C11—C12119.73 (19)C12—Li1—C15—C1476.77 (16)
O1—Li1—C11—C12−73.6 (8)C13—Li1—C15—C1436.72 (13)
C15—Li1—C11—C12−113.2 (2)C11—C15—C16—C17178.8 (2)
C14—Li1—C11—C12−74.73 (16)C14—C15—C16—C170.1 (3)
C13—Li1—C11—C12−34.59 (14)Li1—C15—C16—C17−86.1 (3)
N2—Li1—C11—C15−127.0 (2)C15—C16—C17—C180.6 (4)
O1—Li1—C11—C1539.6 (7)C16—C17—C18—C19−0.6 (4)
C14—Li1—C11—C1538.51 (14)C17—C18—C19—C140.0 (4)
C12—Li1—C11—C15113.2 (2)C13—C14—C19—C18−178.5 (2)
C13—Li1—C11—C1578.65 (15)C15—C14—C19—C180.6 (3)
N2—Li1—C11—C6−8.3 (2)Li1—C14—C19—C1883.6 (3)
O1—Li1—C11—C6158.3 (7)C11—C6—C21—C26141.1 (2)
C15—Li1—C11—C6118.7 (2)C31—C6—C21—C2620.4 (3)
C14—Li1—C11—C6157.20 (19)C5—C6—C21—C26−97.8 (2)
C12—Li1—C11—C6−128.1 (2)C11—C6—C21—C22−46.9 (3)
C13—Li1—C11—C6−162.66 (19)C31—C6—C21—C22−167.6 (2)
C15—C11—C12—C13−1.7 (2)C5—C6—C21—C2274.1 (2)
C6—C11—C12—C13−179.66 (19)C26—C21—C22—C23−0.6 (3)
Li1—C11—C12—C1362.8 (2)C6—C21—C22—C23−172.9 (2)
C15—C11—C12—Li1−64.47 (17)C21—C22—C23—C24−0.2 (4)
C6—C11—C12—Li1117.6 (2)C22—C23—C24—C251.2 (4)
N2—Li1—C12—C13174.9 (2)C23—C24—C25—C26−1.4 (4)
O1—Li1—C12—C1334.8 (3)C24—C25—C26—C210.6 (4)
C15—Li1—C12—C13−80.20 (17)C22—C21—C26—C250.4 (3)
C11—Li1—C12—C13−119.8 (2)C6—C21—C26—C25172.8 (2)
C14—Li1—C12—C13−36.81 (14)C11—C6—C31—C36121.2 (2)
N2—Li1—C12—C11−65.30 (19)C21—C6—C31—C36−113.0 (2)
O1—Li1—C12—C11154.6 (3)C5—C6—C31—C362.7 (3)
C15—Li1—C12—C1139.62 (13)C11—C6—C31—C32−58.3 (2)
C14—Li1—C12—C1183.01 (16)C21—C6—C31—C3267.5 (2)
C13—Li1—C12—C11119.8 (2)C5—C6—C31—C32−176.84 (19)
C11—C12—C13—C141.5 (3)C36—C31—C32—C330.8 (3)
Li1—C12—C13—C1462.59 (19)C6—C31—C32—C33−179.6 (2)
C11—C12—C13—Li1−61.06 (18)C31—C32—C33—C34−1.8 (4)
N2—Li1—C13—C12−7.7 (3)C32—C33—C34—C351.2 (5)
O1—Li1—C13—C12−156.2 (2)C33—C34—C35—C360.3 (5)
C15—Li1—C13—C1277.74 (16)C32—C31—C36—C350.7 (3)
C11—Li1—C13—C1235.30 (13)C6—C31—C36—C35−178.8 (2)
C14—Li1—C13—C12116.7 (2)C34—C35—C36—C31−1.3 (4)
N2—Li1—C13—C14−124.4 (3)N2—Li1—O1—C41−124.0 (2)
O1—Li1—C13—C1487.1 (2)C15—Li1—O1—C4198.9 (3)
C15—Li1—C13—C14−38.97 (14)C11—Li1—O1—C4169.9 (8)
C11—Li1—C13—C14−81.41 (16)C14—Li1—O1—C4170.9 (3)
C12—Li1—C13—C14−116.7 (2)C12—Li1—O1—C4116.4 (4)
C12—C13—C14—C19178.5 (2)C13—Li1—O1—C4135.8 (3)
Li1—C13—C14—C19−117.5 (3)N2—Li1—O1—C43101.1 (3)
C12—C13—C14—C15−0.7 (2)C15—Li1—O1—C43−36.0 (4)
Li1—C13—C14—C1563.25 (17)C11—Li1—O1—C43−65.0 (8)
C12—C13—C14—Li1−63.95 (19)C14—Li1—O1—C43−64.0 (3)
N2—Li1—C14—C13104.5 (4)C12—Li1—O1—C43−118.5 (3)
O1—Li1—C14—C13−102.6 (2)C13—Li1—O1—C43−99.1 (3)
C15—Li1—C14—C13115.1 (2)C43—O1—C41—C42−162.1 (3)
C11—Li1—C14—C1377.00 (16)Li1—O1—C41—C4258.7 (3)
C12—Li1—C14—C1336.35 (14)C41—O1—C43—C44−178.1 (3)
N2—Li1—C14—C19−123.9 (4)Li1—O1—C43—C44−40.5 (4)
O1—Li1—C14—C1929.0 (3)
Li1—N22.004 (5)
Li1—O12.015 (4)
Li—Cp2.041 (4)
N2—Li1—O1105.98 (19)
C2—C3—N2110.5 (2)
  2 in total

1.  A short history of SHELX.

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

2.  pi-Indenyl tin(II) and lead(II) compounds.

Authors:  Jamie N Jones; Alan H Cowley
Journal:  Chem Commun (Camb)       Date:  2005-01-21       Impact factor: 6.222

  2 in total
  2 in total

1.  2-{(E)-N-[2-(1H-Inden-3-yl)eth-yl]imino-meth-yl}-1H-imidazole.

Authors:  Zhao Li; Chong Tian; Wanli Nie; Maxim V Borzov
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-04-16

2.  {2-[(η-Cyclo-penta-dien-yl)diphenyl-meth-yl]-1H-imidazolido-κN}bis-(N,N-diethyl-amido)-titanium(IV).

Authors:  Xianfeng Cai; Yingying Xu; Wanli Nie; Maxim V Borzov
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-04-07
  2 in total

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