Buy article online - an online subscription or single-article purchase is required to access this article.
Download citation
Download citation
link to html
Transmetallation of the dilithium salt of (3,5-dimethyphenyl­amino)(isodicyclopentadienyl)dimethylsilane by treatment with zirconium tetrachloride in a 2:1 ratio leads to the substitution of all four chloride ligands. With the applied stoichiometry, the title complex, [Zr(C20H25NSi)2]·C4H10O, was obtained and crystallized from diethyl ether. X-ray diffraction characterization showed that both isodi­cyclo­penta­dienyl ligands (alternatively called 4,5,6,7-tetrahydro-4,7-methano-1H-indene) are complexed to the metal on their exo face in a completely stereoselective manner and that they are [eta]5-bonded to the Zr atom.

Supporting information

cif

Crystallographic Information File (CIF) https://doi.org/10.1107/S0108270103000751/sq1005sup1.cif
Contains datablocks global, I

hkl

Structure factor file (CIF format) https://doi.org/10.1107/S0108270103000751/sq1005Isup2.hkl
Contains datablock I

CCDC reference: 205300

Comment top

`Constrained geometry' (CG) catalysts can be obtained via different methods. Group 4 ansa monocyclopentadienyl amido complexes can be synthesized by the amine-elimination reaction with excellent results (Hughes et al., 1993; Herrmann & Morawietz, 1994; Carpenetti et al., 1996). When use is made of the synthetic pathway first employed by Bercaw (Shapiro et al., 1990, 1994) and then by Okuda (Okuda, 1990; Okuda et al., 1995), the CG catalyst yield is strongly influenced by the degree of cyclopentadienyl (Cp) substitution. Unsubstituted Cp rings give ansa-Cp amido complexes in very low yield, whereas reactions with substituted Cp rings are quite efficient. We have demonstrated previously that the classical half-sandwich synthetic strategy can be readily adapted to the preparation of isodicyclopentadienyl amido zirconium dichloro complexes (Gentil et al., 2000) by reaction with solid zirconium tetrachloride. In this paper, we report the preparation and structure of the complex bis{N-(3,5-dimethylphenyl)-N-[(η5-isodicyclopentadien- 2-yl)dimethylsilyl]amido-κN}zirconium(II) diethyl ether solvate, obtained by the use of high amido dilithium salt concentrations relative to zirconium tetrachloride. \sch

Complex (I) has approximate C2 symmetry. The ligand has a constrained geometry, which is characterized by the small values of 94.46 (9) and 94.67 (9)°, respectively, for the N1—Si2—C3 and N2—Si1—C13 angles. Further evidence of the constrained nature of this ligand is seen in the displacement of each Si atom from its adjacent Cp ring: the angle between the Si1—C13 bond and its adjacent Cp ring is 25.8 (1)°, and the angle between the Si2—C3 bond and its adjacent Cp ring is 25.5 (1)°.

This Zr complex displays features characteristic of non-bridged isodicyclopentadienyl zirconium complexes (Gallucci et al., 1987; Gobley et al., 1998). The Cg1—Zr—Cg2 angle of 134.17 (4)°, where Cg1 and Cg2 are the centroids of the C1—C5 and C11—C15 rings, respectively, is slightly larger than the corresponding angles in (isodiCp)2ZrCl2 (129.0°) and (isodiCpPPh2)2ZrCl2 [129.02 (5)°]. The isodicyclopentadienyl ligands are found to be in a gauche-like configuration with respect to each other (Gobley et al., 1998).

The metal-Cring distances [2.461–2.623 (2) Å for atoms C1—C5 and 2.461–2.615 (2) Å for atoms C11—C15] are also larger than for the two above-mentioned isodicyclopentadienyl complexes. The shorter Zr—C ring distances involve atoms C3 and C13, which are both bonded to Si atoms. These short distances are likely to be due to the constrained geometry of this ligand. To the best of our knowledge, the Zr—C1 and Zr—C15 distances of 2.623 (2) and 2.615 (2) Å, respectively, are the largest observed for Zr—C bonds in isodicyclopentadienyl complexes. Both the Cp—Zr—Cp angle and the Zr—Cring distances are comparable with those in the doubly bridged amido spiro metallocene Zr[CpSi(CH3)2N-phenyl]2 reported by Herrmann et al. (1994).

As observed in all structures involving an isodicyclopentadienyl ligand with exo complexation, there is a slight bending in this ligand about the bond common to the Cp ring and the norbornane fragment, and this bending is in the endo direction. The dihedral angle between the least-squares planes defined by C1—C5 and C1—C5—C6—C9 is 10.6 (1)°, while the angle between the planes defined by C11—C15 and C11—C15—C16—C19 is 11.0 (1)°. These values are midway between those for an isodiCp half-sandwich zirconium complex [9.5 (1)° for exo-isodiCpSiMe2N-tBuZr(CH2SiMe3)2 (Gentil et al., 2000)] and a bis(isodiCp) zirconium dichloride complex [13.0 (3) and 14.1 (4)° for (isodiCpPPh2)2ZrCl2 (Gobley et al., 1998)].

The Zr—N bond lengths of 2.143 (2) Å for N1 and 2.135 (2) Å for N2 are longer than the Zr—N bond length of 2.086 (1) Å in the exo-isodiCpSiMe2N-tBuZr(CH2SiMe3)2 complex (Gentil et al., 2000), but are quite comparable with the Zr—N bond lengths of 2.142 (2) and 2.143 (2) Å in (η5-C5H4—CHMe-NPh-κN)2Zr (Kunz et al., 2002) and 2.137 (2) and 2.127 (2) Å in [η5-C5H4—Si(Me)2—NPh-κN]2Zr (Herrmann et al., 1994). The sums of the bond angles at the two N atoms are essentially 360° (360.0° for N1 and 359.9° for N2), indicative of trigonal-planar N atoms.

Experimental top

All experiments were conducted under an argon atmosphere. The solvents were dried and distilled prior to use. (3,5-Dimethylphenylamino)(dimethyl)(isodicyclopentadienyl)silane was prepared according to published methods, using chlorodimethyl(isodicyclopentadienyl)silane (Gentil et al., 2000) and solid lithium (3,5-dimethyl)phenylamine in diethyl ether. To a solution of (3,5-dimethylphenylamino)(dimethyl)(isodicyclopentadienyl)silane (3.04 mmol, 897 mg) in diethyl ether (15 ml) at 195 K was slowly added n-butyllithium (6.1 mmol, 3.8 ml of a 1.6 M solution in hexane). The mixture was allowed to warm to room temperature, refluxed overnight, and filtered. The pale-yellow precipitate was washed three times with diethyl ether and dried in vacuo (628 mg, 69%). The pale-yellow powder was then placed in diethyl ether (15 ml) and the suspension treated gradually with solid zirconium tetrachloride (1.05 mmol, 244 mg, 0.5 equivalents). The mixture was warmed to room temperature and stirred for 48 h, and the resulting suspension was filtered off. Concentration of the filtrate and cooling to 253 K over a period of 2 d afforded colourless crystals of (I) (164 mg, 20% yield).

Refinement top

Besides the Zr complex, the asymmetric unit of (I) contains a diethyl ether solvent molecule. The methyl group H atoms were added at calculated positions using a riding model with Uiso(H) = 1.5Ueq(C). For each methyl group, the torsion angle which defines the orientation about the Si—C or the C—C bond was refined. The remaining H atoms were included in the model at calculated positions using a riding model with Uiso(H) = 1.2Ueq(C). Data integration was done with DENZO (Otwinowski & Minor, 1997). Scaling and merging of the data were done with SCALEPACK (Otwinowski & Minor, 1997); application of an absorption correction is inherent in this treatment and is reflected in the scale factor range of 9.93 to 11.54 for the frames. PLATON (Spek, 1990) was used to calculate some metric parameters.

Computing details top

Data collection: COLLECT (Nonius, 1999); cell refinement: DENZO (Otwinowski & Minor, 1997); data reduction: DENZO (Otwinowski & Minor, 1997); program(s) used to solve structure: SHELXS86 (Sheldrick, 1990); program(s) used to refine structure: SHELXL93 (Sheldrick, 1993); molecular graphics: ORTEPII (Johnson, 1976).

Figures top
[Figure 1] Fig. 1. A view of the molecule of complex (I), with displacement ellipsoids drawn at the 50% probability level. H atoms have been omitted for clarity.
bis{N-(3,5-dimethylphenyl)-N-[(η5-isodicyclopentadien- 2-yl)dimethylsilyl]amido-κN}zirconium(II) diethyl ether solvate top
Crystal data top
[Zr(C20H25NSi)2]·C4H10OZ = 2
Mr = 780.34F(000) = 828
Triclinic, P1Dx = 1.289 Mg m3
a = 10.7036 (2) ÅMo Kα radiation, λ = 0.71073 Å
b = 11.6479 (2) ÅCell parameters from 9071 reflections
c = 17.4618 (3) Åθ = 2.0–27.5°
α = 70.848 (1)°µ = 0.37 mm1
β = 78.069 (1)°T = 150 K
γ = 84.194 (1)°Square plate, colourless
V = 2010.81 (6) Å30.35 × 0.35 × 0.04 mm
Data collection top
Nonius Kappa CCD area-detector
diffractometer
7028 reflections with I > 2σ(I)
Radiation source: fine-focus sealed tubeRint = 0.051
Graphite monochromatorθmax = 27.5°, θmin = 2.0°
ϕ and ω scansh = 013
50007 measured reflectionsk = 1415
9121 independent reflectionsl = 2122
Refinement top
Refinement on F20 constraints
Least-squares matrix: fullPrimary atom site location: structure-invariant direct methods
R[F2 > 2σ(F2)] = 0.038Secondary atom site location: difference Fourier map
wR(F2) = 0.077H-atom parameters constrained
S = 1.03 w = 1/[σ2(Fo2) + (0.0319P)2 + 1.2411P]
where P = (Fo2 + 2Fc2)/3
9118 reflections(Δ/σ)max = 0.037
461 parametersΔρmax = 0.51 e Å3
0 restraintsΔρmin = 0.33 e Å3
Crystal data top
[Zr(C20H25NSi)2]·C4H10Oγ = 84.194 (1)°
Mr = 780.34V = 2010.81 (6) Å3
Triclinic, P1Z = 2
a = 10.7036 (2) ÅMo Kα radiation
b = 11.6479 (2) ŵ = 0.37 mm1
c = 17.4618 (3) ÅT = 150 K
α = 70.848 (1)°0.35 × 0.35 × 0.04 mm
β = 78.069 (1)°
Data collection top
Nonius Kappa CCD area-detector
diffractometer
7028 reflections with I > 2σ(I)
50007 measured reflectionsRint = 0.051
9121 independent reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0380 restraints
wR(F2) = 0.077H-atom parameters constrained
S = 1.03Δρmax = 0.51 e Å3
9118 reflectionsΔρmin = 0.33 e Å3
461 parameters
Special details top

Experimental. All work was done at 150 K using an Oxford Cryosystems Cryostream Cooler. A hemisphere of data was measured with a redundancy factor of 2.8, which means that 90% of the data was measured at least 2.8 times. A combination of ϕ and ω scans with a frame width of 1.0° was used for data collection.

1H and 13C NMR spectra were recorded with a Bruker DRX500 spectrometer. 1H NMR (C6D6, δ, p.p.m.): 6.92 (s, 1H, Ar), 6.65 (s, 2H, Ar), 5.60 (s, 2H, peripheral), 3.09 (br s, 2H, bridgehead), 2.39 (s, 6H, CH3), 1.81 (dm, 1H, syn-methano bridge), 1.67 (dm, 2H, exo-ethano bridge), 1.39 (dm, 1H, anti-methano bridge), 1.03 (dm, 2H, endo-ethano bridge), 0.85 (s, 3H, SiCH3), 0.70 (s, 3H, SiCH3); 13C NMR (C6D6, δ, p.p.m.): 148.3 (quaternary), 137.7 (Ar ipso), 123.0 (Ar para), 121.6 (Ar ortho), 110.5 (Ar meta), 103.8 (peripheral), 50.1 (methano bridge), 40.5 (bridgehead), 29.8 (ethano bridge), 21.9 (CH3), 3.0 (SiCH3), −1.3 (SiCH3).

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 on F2 for ALL reflections except for 3 with very negative F2 or flagged by the user for potential systematic errors. Weighted R-factors wR and all goodnesses of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The observed criterion 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
Zr0.39150 (2)0.04658 (2)0.256091 (13)0.01798 (7)
Si10.60202 (5)0.04139 (6)0.13603 (4)0.02049 (14)
Si20.32191 (6)0.21426 (6)0.36521 (4)0.02163 (14)
O0.8742 (2)0.6112 (2)0.21117 (11)0.0403 (4)
N10.4006 (2)0.2236 (2)0.26655 (11)0.0212 (4)
N20.5841 (2)0.0194 (2)0.23123 (11)0.0204 (4)
C10.3787 (2)0.1409 (2)0.39085 (13)0.0224 (5)
C20.4030 (2)0.0373 (2)0.40897 (13)0.0228 (5)
H20.47770.02540.426420.027*
C30.2965 (2)0.0477 (2)0.39682 (13)0.0216 (5)
C40.2052 (2)0.0089 (2)0.37240 (13)0.0227 (5)
H40.12350.02450.361630.027*
C50.2579 (2)0.1233 (2)0.36712 (13)0.0234 (5)
C60.2240 (2)0.2443 (2)0.36336 (15)0.0287 (5)
H60.15880.24170.329200.034*
C70.1964 (2)0.3274 (2)0.4548 (2)0.0341 (6)
H7A0.13420.28730.48920.041*
H7B0.16270.40590.45920.041*
C80.3288 (2)0.3465 (2)0.48108 (15)0.0324 (6)
H8A0.35550.43370.497630.039*
H8B0.32700.31510.527550.039*
C90.4197 (2)0.2726 (2)0.40241 (14)0.0274 (5)
H90.51310.29310.400170.033*
C100.3599 (2)0.2951 (2)0.33567 (15)0.0321 (6)
H10A0.36080.38240.340780.038*
H10B0.39990.24770.279060.038*
C110.2254 (2)0.0547 (2)0.16633 (13)0.0210 (5)
C120.3199 (2)0.0363 (2)0.15759 (13)0.0216 (5)
H120.30700.12120.174730.026*
C130.4393 (2)0.0221 (2)0.11817 (13)0.0212 (5)
C140.4125 (2)0.1500 (2)0.10134 (13)0.0206 (5)
H140.47280.21180.074520.025*
C150.2826 (2)0.1689 (2)0.13095 (13)0.0202 (5)
C160.1762 (2)0.2654 (2)0.12446 (13)0.0239 (5)
H160.19980.34870.119800.029*
C170.1116 (2)0.2553 (2)0.05503 (15)0.0291 (5)
H17A0.17580.25680.004960.035*
H17B0.04740.32230.040460.035*
C180.0472 (2)0.1302 (2)0.09400 (15)0.0306 (6)
H18A0.08110.07500.061260.037*
H18B0.04660.14020.097630.037*
C190.0824 (2)0.0802 (2)0.18159 (14)0.0252 (5)
H190.02930.01360.223060.030*
C200.0770 (2)0.2014 (2)0.20089 (14)0.0275 (5)
H20A0.00850.24280.200830.033*
H20B0.10520.19120.253360.033*
C210.1678 (2)0.3047 (2)0.37536 (15)0.0308 (6)
H21A0.18580.39080.36110.046*
H21B0.12130.27560.43230.046*
H21C0.11580.29490.33800.046*
C220.4251 (2)0.2503 (2)0.42732 (15)0.0327 (6)
H22A0.37950.23410.48440.049*
H22B0.44650.33620.40390.049*
H22C0.50380.19940.42640.049*
C230.6299 (2)0.1999 (2)0.13303 (15)0.0286 (5)
H23A0.62950.20110.07720.043*
H23B0.56210.25080.17210.043*
H23C0.71280.23150.14820.043*
C240.7281 (2)0.0518 (2)0.05696 (14)0.0295 (5)
H24A0.72170.04920.00240.044*
H24B0.81230.01940.06930.044*
H24C0.71670.13620.05750.044*
C250.6768 (2)0.0481 (2)0.28281 (13)0.0204 (5)
C260.7339 (2)0.1643 (2)0.30747 (13)0.0222 (5)
H260.71330.22480.287030.027*
C270.8202 (2)0.1937 (2)0.36114 (13)0.0234 (5)
C280.8531 (2)0.1037 (2)0.38912 (13)0.0239 (5)
H280.91300.12270.425150.029*
C290.7995 (2)0.0137 (2)0.36504 (13)0.0216 (5)
C300.7113 (2)0.0394 (2)0.31281 (13)0.0212 (5)
H300.67330.11890.296990.025*
C310.8726 (2)0.3230 (2)0.3913 (2)0.0339 (6)
H31A0.93760.32630.42410.051*
H31B0.91100.35020.34380.051*
H31C0.80310.37620.42530.051*
C320.8339 (2)0.1110 (2)0.39588 (14)0.0279 (5)
H32A0.75850.13470.43070.042*
H32B0.86370.18200.348800.042*
H32C0.90180.07950.42810.042*
C330.4538 (2)0.3289 (2)0.20567 (13)0.0202 (5)
C340.5777 (2)0.3239 (2)0.16038 (13)0.0210 (5)
H340.62560.24900.171540.025*
C350.6323 (2)0.4257 (2)0.09968 (13)0.0231 (5)
C360.5613 (2)0.5351 (2)0.08268 (14)0.0242 (5)
H360.59740.60480.040600.029*
C370.4388 (2)0.5437 (2)0.12632 (14)0.0242 (5)
C380.3867 (2)0.4408 (2)0.18761 (14)0.0240 (5)
H380.30320.44700.218030.029*
C390.7680 (2)0.4189 (2)0.0547 (2)0.0354 (6)
H39A0.82340.46120.07410.053*
H39B0.77150.45760.00470.053*
H39C0.79720.33360.06550.053*
C400.3608 (2)0.6615 (2)0.1076 (2)0.0331 (6)
H40A0.31430.67290.15940.050*
H40B0.29970.65880.07350.050*
H40C0.41760.72920.07790.050*
C410.8483 (3)0.4862 (3)0.2493 (2)0.0562 (8)
H41A0.89670.45100.29480.067*
H41B0.87560.44200.20860.067*
C420.7091 (3)0.4729 (3)0.2823 (2)0.0526 (8)
H42A0.69110.38660.30920.079*
H42B0.66170.50640.23690.079*
H42C0.68250.51700.32240.079*
C431.0030 (3)0.6371 (3)0.1759 (2)0.0565 (8)
H43A1.03210.59970.13160.068*
H43B1.05700.60280.21840.068*
C441.0153 (3)0.7716 (3)0.1413 (2)0.0583 (9)
H44A1.10550.79050.11950.087*
H44B0.98260.80850.18500.087*
H44C0.96610.80440.09690.087*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Zr0.01738 (11)0.01934 (12)0.01615 (11)0.00010 (8)0.00245 (8)0.00473 (8)
Si10.0174 (3)0.0255 (3)0.0198 (3)0.0025 (2)0.0041 (2)0.0093 (3)
Si20.0228 (3)0.0229 (3)0.0184 (3)0.0004 (3)0.0013 (2)0.0071 (3)
O0.0403 (10)0.0329 (11)0.0435 (11)0.0075 (8)0.0060 (9)0.0102 (9)
N10.0222 (9)0.0196 (10)0.0192 (9)0.0002 (8)0.0011 (8)0.0048 (8)
N20.0195 (9)0.0227 (10)0.0195 (9)0.0016 (7)0.0052 (8)0.0072 (8)
C10.0241 (11)0.0231 (12)0.0165 (11)0.0040 (9)0.0026 (9)0.0013 (9)
C20.0221 (11)0.0281 (13)0.0151 (11)0.0034 (9)0.0030 (9)0.0022 (9)
C30.0233 (11)0.0236 (12)0.0142 (11)0.0014 (9)0.0006 (9)0.0035 (9)
C40.0194 (11)0.0254 (13)0.0180 (11)0.0018 (9)0.0004 (9)0.0015 (9)
C50.0231 (11)0.0236 (13)0.0202 (11)0.0052 (9)0.0026 (9)0.0022 (10)
C60.0310 (13)0.0243 (13)0.0301 (13)0.0045 (10)0.0096 (11)0.0044 (11)
C70.0367 (14)0.0267 (14)0.0343 (14)0.0092 (11)0.0056 (11)0.0015 (11)
C80.0384 (14)0.0245 (13)0.0290 (13)0.0047 (11)0.0062 (11)0.0004 (11)
C90.0284 (12)0.0227 (13)0.0283 (13)0.0007 (10)0.0065 (10)0.0036 (10)
C100.0420 (14)0.0255 (14)0.0272 (13)0.0028 (11)0.0052 (11)0.0066 (11)
C110.0201 (11)0.0258 (13)0.0181 (11)0.0002 (9)0.0049 (9)0.0075 (10)
C120.0228 (11)0.0239 (12)0.0212 (11)0.0014 (9)0.0065 (9)0.0095 (10)
C130.0216 (11)0.0269 (13)0.0165 (11)0.0032 (9)0.0054 (9)0.0088 (9)
C140.0200 (11)0.0261 (13)0.0144 (10)0.0021 (9)0.0024 (9)0.0048 (9)
C150.0208 (11)0.0217 (12)0.0171 (11)0.0018 (9)0.0058 (9)0.0040 (9)
C160.0231 (11)0.0224 (12)0.0244 (12)0.0028 (9)0.0050 (9)0.0055 (10)
C170.0223 (12)0.0374 (15)0.0269 (13)0.0062 (10)0.0086 (10)0.0087 (11)
C180.0223 (12)0.039 (2)0.0343 (14)0.0049 (10)0.0113 (11)0.0141 (12)
C190.0189 (11)0.0287 (13)0.0261 (12)0.0016 (9)0.0013 (9)0.0077 (10)
C200.0228 (12)0.0332 (14)0.0254 (12)0.0058 (10)0.0037 (10)0.0101 (11)
C210.0320 (13)0.0331 (15)0.0248 (13)0.0032 (11)0.0019 (10)0.0114 (11)
C220.0376 (14)0.0339 (15)0.0284 (13)0.0049 (11)0.0056 (11)0.0114 (11)
C230.0256 (12)0.0317 (14)0.0324 (13)0.0047 (10)0.0063 (10)0.0165 (11)
C240.0243 (12)0.0365 (15)0.0268 (13)0.0009 (10)0.0032 (10)0.0105 (11)
C250.0163 (10)0.0271 (13)0.0156 (11)0.0022 (9)0.0007 (8)0.0057 (9)
C260.0211 (11)0.0249 (13)0.0220 (11)0.0005 (9)0.0057 (9)0.0084 (10)
C270.0187 (11)0.0259 (13)0.0224 (12)0.0004 (9)0.0029 (9)0.0042 (10)
C280.0193 (11)0.0321 (14)0.0187 (11)0.0028 (10)0.0049 (9)0.0048 (10)
C290.0185 (11)0.0278 (13)0.0175 (11)0.0042 (9)0.0009 (9)0.0072 (10)
C300.0201 (11)0.0226 (12)0.0199 (11)0.0017 (9)0.0032 (9)0.0064 (10)
C310.0314 (13)0.0317 (15)0.0388 (15)0.0044 (11)0.0172 (12)0.0065 (12)
C320.0269 (12)0.0347 (14)0.0234 (12)0.0061 (10)0.0026 (10)0.0108 (11)
C330.0241 (11)0.0197 (12)0.0175 (11)0.0029 (9)0.0042 (9)0.0060 (9)
C340.0239 (11)0.0173 (12)0.0217 (11)0.0010 (9)0.0049 (9)0.0061 (9)
C350.0250 (11)0.0241 (13)0.0211 (12)0.0039 (10)0.0018 (9)0.0090 (10)
C360.0301 (12)0.0184 (12)0.0221 (12)0.0065 (10)0.0052 (10)0.0017 (9)
C370.0272 (12)0.0199 (12)0.0287 (13)0.0012 (9)0.0104 (10)0.0086 (10)
C380.0218 (11)0.0251 (13)0.0256 (12)0.0003 (9)0.0040 (10)0.0088 (10)
C390.0320 (13)0.0284 (14)0.040 (2)0.0052 (11)0.0026 (12)0.0071 (12)
C400.0303 (13)0.0220 (13)0.043 (2)0.0017 (10)0.0096 (12)0.0047 (11)
C410.073 (2)0.035 (2)0.065 (2)0.010 (2)0.022 (2)0.018 (2)
C420.076 (2)0.039 (2)0.044 (2)0.018 (2)0.020 (2)0.0046 (14)
C430.039 (2)0.062 (2)0.062 (2)0.0126 (15)0.0011 (15)0.018 (2)
C440.033 (2)0.063 (2)0.061 (2)0.0000 (15)0.0011 (15)0.003 (2)
Geometric parameters (Å, º) top
Zr—N22.135 (2)C18—H18B0.99
Zr—N12.143 (2)C19—C201.549 (3)
Zr—C132.461 (2)C19—H191.00
Zr—C32.461 (2)C20—H20A0.99
Zr—C42.499 (2)C20—H20B0.99
Zr—C122.502 (2)C21—H21A0.98
Zr—C142.544 (2)C21—H21B0.98
Zr—C22.549 (2)C21—H21C0.98
Zr—C52.575 (2)C22—H22A0.98
Zr—C112.579 (2)C22—H22B0.98
Zr—C152.615 (2)C22—H22C0.98
Zr—C12.623 (2)C23—H23A0.98
Si1—N21.733 (2)C23—H23B0.98
Si1—C231.856 (2)C23—H23C0.98
Si1—C241.857 (2)C24—H24A0.98
Si1—C131.869 (2)C24—H24B0.98
Si2—N11.728 (2)C24—H24C0.98
Si2—C221.860 (2)C25—C261.396 (3)
Si2—C31.867 (2)C25—C301.399 (3)
Si2—C211.874 (2)C26—C271.390 (3)
O—C431.408 (3)C26—H260.95
O—C411.416 (3)C27—C281.394 (3)
N1—C331.412 (3)C27—C311.514 (3)
N2—C251.418 (3)C28—C291.393 (3)
C1—C21.404 (3)C28—H280.95
C1—C51.414 (3)C29—C301.390 (3)
C1—C91.512 (3)C29—C321.509 (3)
C2—C31.435 (3)C30—H300.95
C2—H20.95C31—H31A0.98
C3—C41.435 (3)C31—H31B0.98
C4—C51.417 (3)C31—H31C0.98
C4—H40.95C32—H32A0.98
C5—C61.515 (3)C32—H32B0.98
C6—C71.556 (3)C32—H32C0.98
C6—C101.557 (3)C33—C381.396 (3)
C6—H61.00C33—C341.403 (3)
C7—C81.551 (3)C34—C351.389 (3)
C7—H7A0.99C34—H340.95
C7—H7B0.99C35—C361.392 (3)
C8—C91.554 (3)C35—C391.510 (3)
C8—H8A0.99C36—C371.386 (3)
C8—H8B0.99C36—H360.95
C9—C101.542 (3)C37—C381.392 (3)
C9—H91.00C37—C401.507 (3)
C10—H10A0.99C38—H380.95
C10—H10B0.99C39—H39A0.98
C11—C121.413 (3)C39—H39B0.98
C11—C151.413 (3)C39—H39C0.98
C11—C191.514 (3)C40—H40A0.98
C12—C131.440 (3)C40—H40B0.98
C12—H120.95C40—H40C0.98
C13—C141.431 (3)C41—C421.487 (4)
C14—C151.401 (3)C41—H41A0.99
C14—H140.95C41—H41B0.99
C15—C161.511 (3)C42—H42A0.98
C16—C201.545 (3)C42—H42B0.98
C16—C171.555 (3)C42—H42C0.98
C16—H161.00C43—C441.492 (4)
C17—C181.556 (3)C43—H43A0.99
C17—H17A0.99C43—H43B0.99
C17—H17B0.99C44—H44A0.98
C18—C191.559 (3)C44—H44B0.98
C18—H18A0.99C44—H44C0.98
N2—Zr—N1106.64 (7)C11—C12—H12126.0
N2—Zr—C1370.03 (7)C13—C12—H12126.0
N1—Zr—C13118.92 (7)Zr—C12—H12117.6
N2—Zr—C3119.32 (7)C14—C13—C12106.4 (2)
N1—Zr—C369.59 (7)C14—C13—Si1119.3 (2)
C13—Zr—C3166.38 (7)C12—C13—Si1126.6 (2)
N2—Zr—C4136.22 (7)C14—C13—Zr76.61 (12)
N1—Zr—C492.99 (7)C12—C13—Zr74.73 (12)
C13—Zr—C4132.75 (7)Si1—C13—Zr89.79 (8)
C3—Zr—C433.63 (7)C15—C14—C13108.7 (2)
N2—Zr—C1293.51 (7)C15—C14—Zr77.05 (12)
N1—Zr—C12135.66 (7)C13—C14—Zr70.21 (12)
C13—Zr—C1233.72 (7)C15—C14—H14125.6
C3—Zr—C12132.69 (7)C13—C14—H14125.6
C4—Zr—C1299.09 (7)Zr—C14—H14118.9
N2—Zr—C1487.02 (7)C14—C15—C11108.5 (2)
N1—Zr—C1487.17 (7)C14—C15—C16142.6 (2)
C13—Zr—C1433.18 (7)C11—C15—C16107.4 (2)
C3—Zr—C14148.44 (7)C14—C15—Zr71.47 (12)
C4—Zr—C14133.66 (7)C11—C15—Zr72.80 (12)
C12—Zr—C1454.22 (7)C16—C15—Zr130.43 (14)
N2—Zr—C287.62 (7)C15—C16—C20100.3 (2)
N1—Zr—C286.78 (7)C15—C16—C17104.4 (2)
C13—Zr—C2149.41 (7)C20—C16—C1799.8 (2)
C3—Zr—C233.22 (7)C15—C16—H16116.6
C4—Zr—C254.14 (7)C20—C16—H16116.6
C12—Zr—C2134.12 (7)C17—C16—H16116.6
C14—Zr—C2170.44 (7)C16—C17—C18103.5 (2)
N2—Zr—C5109.38 (7)C16—C17—H17A111.1
N1—Zr—C5123.02 (7)C18—C17—H17A111.1
C13—Zr—C5114.21 (7)C16—C17—H17B111.1
C3—Zr—C554.58 (7)C18—C17—H17B111.1
C4—Zr—C532.40 (7)H17A—C17—H17B109.0
C12—Zr—C584.04 (7)C17—C18—C19104.1 (2)
C14—Zr—C5136.53 (7)C17—C18—H18A110.9
C2—Zr—C552.94 (7)C19—C18—H18A110.9
N2—Zr—C11123.37 (7)C17—C18—H18B110.9
N1—Zr—C11108.88 (7)C19—C18—H18B110.9
C13—Zr—C1154.48 (7)H18A—C18—H18B109.0
C3—Zr—C11113.78 (7)C11—C19—C20100.4 (2)
C4—Zr—C1183.82 (7)C11—C19—C18104.9 (2)
C12—Zr—C1132.25 (7)C20—C19—C1899.1 (2)
C14—Zr—C1152.94 (7)C11—C19—H19116.6
C2—Zr—C11136.34 (7)C20—C19—H19116.6
C5—Zr—C1185.78 (7)C18—C19—H19116.6
N2—Zr—C15118.22 (7)C16—C20—C1995.8 (2)
N1—Zr—C1582.66 (7)C16—C20—H20A112.6
C13—Zr—C1553.85 (7)C19—C20—H20A112.6
C3—Zr—C15120.93 (7)C16—C20—H20B112.6
C4—Zr—C15102.58 (7)C19—C20—H20B112.6
C12—Zr—C1553.12 (7)H20A—C20—H20B110.1
C14—Zr—C1531.48 (6)Si2—C21—H21A109.5
C2—Zr—C15153.93 (7)Si2—C21—H21B109.5
C5—Zr—C15115.13 (7)H21A—C21—H21B109.5
C11—Zr—C1531.57 (7)Si2—C21—H21C109.5
N2—Zr—C183.20 (7)H21A—C21—H21C109.5
N1—Zr—C1117.94 (7)H21B—C21—H21C109.5
C13—Zr—C1121.81 (7)Si2—C22—H22A109.5
C3—Zr—C153.91 (7)Si2—C22—H22B109.5
C4—Zr—C153.14 (7)H22A—C22—H22B109.5
C12—Zr—C1103.11 (7)Si2—C22—H22C109.5
C14—Zr—C1154.74 (7)H22A—C22—H22C109.5
C2—Zr—C131.46 (7)H22B—C22—H22C109.5
C5—Zr—C131.56 (7)Si1—C23—H23A109.5
C11—Zr—C1115.25 (7)Si1—C23—H23B109.5
C15—Zr—C1146.16 (7)H23A—C23—H23B109.5
N2—Si1—C23117.41 (10)Si1—C23—H23C109.5
N2—Si1—C24113.17 (10)H23A—C23—H23C109.5
C23—Si1—C24107.41 (11)H23B—C23—H23C109.5
N2—Si1—C1394.67 (9)Si1—C24—H24A109.5
C23—Si1—C13112.83 (10)Si1—C24—H24B109.5
C24—Si1—C13110.99 (10)H24A—C24—H24B109.5
C23—Si1—Zr125.89 (8)Si1—C24—H24C109.5
C24—Si1—Zr126.65 (8)H24A—C24—H24C109.5
C13—Si1—Zr52.92 (6)H24B—C24—H24C109.5
N1—Si2—C22112.82 (10)C26—C25—C30117.6 (2)
N1—Si2—C394.46 (9)C26—C25—N2121.9 (2)
C22—Si2—C3111.85 (11)C30—C25—N2120.5 (2)
N1—Si2—C21117.18 (10)C27—C26—C25121.7 (2)
C22—Si2—C21107.90 (11)C27—C26—H26119.1
C3—Si2—C21112.22 (11)C25—C26—H26119.1
C22—Si2—Zr127.16 (8)C26—C27—C28119.0 (2)
C3—Si2—Zr52.75 (7)C26—C27—C31120.0 (2)
C21—Si2—Zr124.87 (8)C28—C27—C31120.9 (2)
C43—O—C41115.5 (2)C29—C28—C27121.0 (2)
C33—N1—Si2126.07 (15)C29—C28—H28119.5
C33—N1—Zr128.32 (14)C27—C28—H28119.5
Si2—N1—Zr105.55 (9)C30—C29—C28118.6 (2)
C25—N2—Si1126.21 (14)C30—C29—C32120.3 (2)
C25—N2—Zr128.38 (14)C28—C29—C32121.1 (2)
Si1—N2—Zr105.27 (8)C29—C30—C25122.1 (2)
C2—C1—C5108.3 (2)C29—C30—H30118.9
C2—C1—C9143.2 (2)C25—C30—H30118.9
C5—C1—C9107.0 (2)C27—C31—H31A109.5
C2—C1—Zr71.35 (12)C27—C31—H31B109.5
C5—C1—Zr72.34 (12)H31A—C31—H31B109.5
C9—C1—Zr130.39 (15)C27—C31—H31C109.5
C1—C2—C3108.9 (2)H31A—C31—H31C109.5
C1—C2—Zr77.18 (12)H31B—C31—H31C109.5
C3—C2—Zr70.04 (12)C29—C32—H32A109.5
C1—C2—H2125.6C29—C32—H32B109.5
C3—C2—H2125.6H32A—C32—H32B109.5
Zr—C2—H2118.9C29—C32—H32C109.5
C2—C3—C4106.4 (2)H32A—C32—H32C109.5
C2—C3—Si2119.9 (2)H32B—C32—H32C109.5
C4—C3—Si2126.3 (2)C38—C33—C34117.4 (2)
C2—C3—Zr76.74 (12)C38—C33—N1122.2 (2)
C4—C3—Zr74.62 (12)C34—C33—N1120.4 (2)
Si2—C3—Zr90.11 (8)C35—C34—C33121.7 (2)
C5—C4—C3108.2 (2)C35—C34—H34119.1
C5—C4—Zr76.76 (12)C33—C34—H34119.1
C3—C4—Zr71.75 (12)C34—C35—C36119.0 (2)
C5—C4—H4125.9C34—C35—C39120.5 (2)
C3—C4—H4125.9C36—C35—C39120.4 (2)
Zr—C4—H4117.5C37—C36—C35120.9 (2)
C1—C5—C4108.2 (2)C37—C36—H36119.5
C1—C5—C6106.8 (2)C35—C36—H36119.5
C4—C5—C6143.1 (2)C36—C37—C38119.0 (2)
C1—C5—Zr76.10 (12)C36—C37—C40121.2 (2)
C4—C5—Zr70.85 (12)C38—C37—C40119.8 (2)
C6—C5—Zr129.4 (2)C37—C38—C33121.9 (2)
C5—C6—C7105.0 (2)C37—C38—H38119.0
C5—C6—C1099.9 (2)C33—C38—H38119.0
C7—C6—C1099.5 (2)C35—C39—H39A109.5
C5—C6—H6116.6C35—C39—H39B109.5
C7—C6—H6116.6H39A—C39—H39B109.5
C10—C6—H6116.6C35—C39—H39C109.5
C8—C7—C6103.8 (2)H39A—C39—H39C109.5
C8—C7—H7A111.0H39B—C39—H39C109.5
C6—C7—H7A111.0C37—C40—H40A109.5
C8—C7—H7B111.0C37—C40—H40B109.5
C6—C7—H7B111.0H40A—C40—H40B109.5
H7A—C7—H7B109.0C37—C40—H40C109.5
C7—C8—C9103.9 (2)H40A—C40—H40C109.5
C7—C8—H8A111.0H40B—C40—H40C109.5
C9—C8—H8A111.0O—C41—C42109.4 (2)
C7—C8—H8B111.0O—C41—H41A109.8
C9—C8—H8B111.0C42—C41—H41A109.8
H8A—C8—H8B109.0O—C41—H41B109.8
C1—C9—C10100.1 (2)C42—C41—H41B109.8
C1—C9—C8105.3 (2)H41A—C41—H41B108.3
C10—C9—C899.8 (2)C41—C42—H42A109.5
C1—C9—H9116.4C41—C42—H42B109.5
C10—C9—H9116.4H42A—C42—H42B109.5
C8—C9—H9116.4C41—C42—H42C109.5
C9—C10—C695.5 (2)H42A—C42—H42C109.5
C9—C10—H10A112.6H42B—C42—H42C109.5
C6—C10—H10A112.6O—C43—C44109.0 (2)
C9—C10—H10B112.6O—C43—H43A109.9
C6—C10—H10B112.6C44—C43—H43A109.9
H10A—C10—H10B110.1O—C43—H43B109.9
C12—C11—C15108.3 (2)C44—C43—H43B109.9
C12—C11—C19143.2 (2)H43A—C43—H43B108.3
C15—C11—C19106.6 (2)C43—C44—H44A109.5
C12—C11—Zr70.90 (11)C43—C44—H44B109.5
C15—C11—Zr75.64 (12)H44A—C44—H44B109.5
C19—C11—Zr130.16 (14)C43—C44—H44C109.5
C11—C12—C13108.0 (2)H44A—C44—H44C109.5
C11—C12—Zr76.85 (12)H44B—C44—H44C109.5
C13—C12—Zr71.55 (11)
C22—Si2—N1—C3361.7 (2)C23—Si1—C13—C1247.9 (2)
C3—Si2—N1—C33177.7 (2)C24—Si1—C13—C12168.5 (2)
C21—Si2—N1—C3364.5 (2)C12—C13—C14—C151.3 (2)
Zr—Si2—N1—C33177.4 (2)Si1—C13—C14—C15150.1 (2)
C22—Si2—N1—Zr120.82 (11)C13—C14—C15—C110.3 (2)
C3—Si2—N1—Zr4.85 (10)C13—C14—C15—C16163.0 (3)
C21—Si2—N1—Zr112.96 (11)C12—C11—C15—C140.9 (2)
Zr—Si2—N1—Zr0.0C19—C11—C15—C14168.8 (2)
N2—Zr—N1—C3363.0 (2)C12—C11—C15—C16168.2 (2)
N2—Zr—N1—Si2119.64 (8)C19—C11—C15—C160.3 (2)
C23—Si1—N2—C2561.7 (2)C14—C15—C16—C20165.0 (3)
C24—Si1—N2—C2564.3 (2)C11—C15—C16—C2032.2 (2)
C13—Si1—N2—C25179.5 (2)C14—C15—C16—C1792.0 (3)
C23—Si1—N2—Zr114.26 (10)C11—C15—C16—C1770.9 (2)
C24—Si1—N2—Zr119.70 (10)C15—C16—C17—C1868.4 (2)
C13—Si1—N2—Zr4.49 (10)C20—C16—C17—C1835.0 (2)
N1—Zr—N2—C2565.1 (2)C16—C17—C18—C190.6 (2)
N1—Zr—N2—Si1118.98 (9)C12—C11—C19—C20166.8 (3)
C5—C1—C2—C30.1 (2)C15—C11—C19—C2032.6 (2)
C9—C1—C2—C3162.9 (3)C12—C11—C19—C1890.8 (3)
C1—C2—C3—C41.2 (2)C15—C11—C19—C1869.8 (2)
C1—C2—C3—Si2150.4 (2)C17—C18—C19—C1167.6 (2)
N1—Si2—C3—C270.7 (2)C17—C18—C19—C2035.8 (2)
C22—Si2—C3—C246.1 (2)C15—C16—C20—C1949.7 (2)
C21—Si2—C3—C2167.5 (2)C17—C16—C20—C1957.1 (2)
N1—Si2—C3—C474.9 (2)C11—C19—C20—C1650.0 (2)
C22—Si2—C3—C4168.3 (2)C18—C19—C20—C1657.0 (2)
C21—Si2—C3—C446.8 (2)Si1—N2—C25—C2654.2 (3)
C2—C3—C4—C52.1 (2)Zr—N2—C25—C26120.9 (2)
Si2—C3—C4—C5147.2 (2)Si1—N2—C25—C30127.7 (2)
C2—C1—C5—C41.4 (2)Zr—N2—C25—C3057.2 (3)
C9—C1—C5—C4168.1 (2)C30—C25—C26—C271.2 (3)
C2—C1—C5—C6169.8 (2)N2—C25—C26—C27176.9 (2)
C9—C1—C5—C60.4 (2)C25—C26—C27—C281.9 (3)
Zr—C1—C5—C6127.5 (2)C25—C26—C27—C31175.5 (2)
C3—C4—C5—C12.1 (2)C26—C27—C28—C291.0 (3)
C3—C4—C5—C6163.5 (3)C31—C27—C28—C29176.4 (2)
C1—C5—C6—C770.3 (2)C27—C28—C29—C300.5 (3)
C4—C5—C6—C791.2 (3)C27—C28—C29—C32179.4 (2)
C1—C5—C6—C1032.4 (2)C28—C29—C30—C251.1 (3)
C4—C5—C6—C10166.1 (3)C32—C29—C30—C25180.0 (2)
C5—C6—C7—C867.8 (2)C26—C25—C30—C290.3 (3)
C10—C6—C7—C835.2 (2)N2—C25—C30—C29178.5 (2)
C6—C7—C8—C90.0 (2)Si2—N1—C33—C3847.2 (3)
C2—C1—C9—C10163.5 (3)Zr—N1—C33—C38129.6 (2)
C5—C1—C9—C1033.4 (2)Si2—N1—C33—C34133.1 (2)
C2—C1—C9—C893.3 (3)Zr—N1—C33—C3450.0 (3)
C5—C1—C9—C869.8 (2)C38—C33—C34—C350.2 (3)
C7—C8—C9—C167.9 (2)N1—C33—C34—C35179.5 (2)
C7—C8—C9—C1035.6 (2)C33—C34—C35—C360.9 (3)
C1—C9—C10—C650.8 (2)C33—C34—C35—C39177.2 (2)
C8—C9—C10—C656.8 (2)C34—C35—C36—C371.1 (3)
C5—C6—C10—C950.5 (2)C39—C35—C36—C37177.0 (2)
C7—C6—C10—C956.7 (2)C35—C36—C37—C380.3 (3)
C15—C11—C12—C131.7 (2)C35—C36—C37—C40179.3 (2)
C19—C11—C12—C13162.1 (3)C36—C37—C38—C330.8 (3)
C11—C12—C13—C141.8 (2)C40—C37—C38—C33178.2 (2)
C11—C12—C13—Si1146.9 (2)C34—C33—C38—C371.1 (3)
N2—Si1—C13—C1470.7 (2)N1—C33—C38—C37178.6 (2)
C23—Si1—C13—C14166.9 (2)C43—O—C41—C42179.1 (3)
C24—Si1—C13—C1446.3 (2)C41—O—C43—C44177.8 (3)
N2—Si1—C13—C1274.4 (2)

Experimental details

Crystal data
Chemical formula[Zr(C20H25NSi)2]·C4H10O
Mr780.34
Crystal system, space groupTriclinic, P1
Temperature (K)150
a, b, c (Å)10.7036 (2), 11.6479 (2), 17.4618 (3)
α, β, γ (°)70.848 (1), 78.069 (1), 84.194 (1)
V3)2010.81 (6)
Z2
Radiation typeMo Kα
µ (mm1)0.37
Crystal size (mm)0.35 × 0.35 × 0.04
Data collection
DiffractometerNonius Kappa CCD area-detector
diffractometer
Absorption correction
No. of measured, independent and
observed [I > 2σ(I)] reflections
50007, 9121, 7028
Rint0.051
(sin θ/λ)max1)0.649
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.038, 0.077, 1.03
No. of reflections9118
No. of parameters461
H-atom treatmentH-atom parameters constrained
Δρmax, Δρmin (e Å3)0.51, 0.33

Computer programs: COLLECT (Nonius, 1999), DENZO (Otwinowski & Minor, 1997), SHELXS86 (Sheldrick, 1990), SHELXL93 (Sheldrick, 1993), ORTEPII (Johnson, 1976).

Selected geometric parameters (Å, º) top
Zr—N22.135 (2)C2—C31.435 (3)
Zr—N12.143 (2)C3—C41.435 (3)
Zr—C132.461 (2)C4—C51.417 (3)
Zr—C32.461 (2)C5—C61.515 (3)
Zr—C42.499 (2)C6—C71.556 (3)
Zr—C122.502 (2)C6—C101.557 (3)
Zr—C142.544 (2)C7—C81.551 (3)
Zr—C22.549 (2)C8—C91.554 (3)
Zr—C52.575 (2)C9—C101.542 (3)
Zr—C112.579 (2)C11—C121.413 (3)
Zr—C152.615 (2)C11—C151.413 (3)
Zr—C12.623 (2)C11—C191.514 (3)
Si1—N21.733 (2)C12—C131.440 (3)
Si1—C131.869 (2)C13—C141.431 (3)
Si2—N11.728 (2)C14—C151.401 (3)
Si2—C31.867 (2)C15—C161.511 (3)
N1—C331.412 (3)C16—C201.545 (3)
N2—C251.418 (3)C16—C171.555 (3)
C1—C21.404 (3)C17—C181.556 (3)
C1—C51.414 (3)C18—C191.559 (3)
C1—C91.512 (3)C19—C201.549 (3)
N2—Zr—N1106.64 (7)C9—C10—C695.5 (2)
N2—Si1—C1394.67 (9)C12—C11—C15108.3 (2)
N1—Si2—C394.46 (9)C12—C11—C19143.2 (2)
C2—C1—C5108.3 (2)C15—C11—C19106.6 (2)
C2—C1—C9143.2 (2)C11—C12—C13108.0 (2)
C5—C1—C9107.0 (2)C14—C13—C12106.4 (2)
C1—C2—C3108.9 (2)C15—C14—C13108.7 (2)
C2—C3—C4106.4 (2)C14—C15—C11108.5 (2)
C5—C4—C3108.2 (2)C14—C15—C16142.6 (2)
C1—C5—C4108.2 (2)C11—C15—C16107.4 (2)
C1—C5—C6106.8 (2)C15—C16—C20100.3 (2)
C4—C5—C6143.1 (2)C15—C16—C17104.4 (2)
C5—C6—C7105.0 (2)C20—C16—C1799.8 (2)
C5—C6—C1099.9 (2)C16—C17—C18103.5 (2)
C7—C6—C1099.5 (2)C17—C18—C19104.1 (2)
C8—C7—C6103.8 (2)C11—C19—C20100.4 (2)
C7—C8—C9103.9 (2)C11—C19—C18104.9 (2)
C1—C9—C10100.1 (2)C20—C19—C1899.1 (2)
C1—C9—C8105.3 (2)C16—C20—C1995.8 (2)
C10—C9—C899.8 (2)
Selected geometric parameters (Å, °) involving Zr and the ring centroids top
Cg1-Zr2.2361 (10)
Cg2-Zr2.2352 (10)
Cg1-Zr-Cg2134.17 (4)
Cg1-Zr-N199.06 (6)
Cg1-Zr-N2107.96 (6)
Cg2-Zr-N1107.47 (6)
Cg2-Zr-N299.44 (6)
Cg1 is the centroid of the C1-C5 ring. Cg2 is the centroid of the C11-C15 ring.
 

Subscribe to Acta Crystallographica Section C: Structural Chemistry

The full text of this article is available to subscribers to the journal.

If you have already registered and are using a computer listed in your registration details, please email support@iucr.org for assistance.

Buy online

You may purchase this article in PDF and/or HTML formats. For purchasers in the European Community who do not have a VAT number, VAT will be added at the local rate. Payments to the IUCr are handled by WorldPay, who will accept payment by credit card in several currencies. To purchase the article, please complete the form below (fields marked * are required), and then click on `Continue'.
E-mail address* 
Repeat e-mail address* 
(for error checking) 

Format*   PDF (US $40)
   HTML (US $40)
   PDF+HTML (US $50)
In order for VAT to be shown for your country javascript needs to be enabled.

VAT number 
(non-UK EC countries only) 
Country* 
 

Terms and conditions of use
Contact us

Follow Acta Cryst. C
Sign up for e-alerts
Follow Acta Cryst. on Twitter
Follow us on facebook
Sign up for RSS feeds