Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807019095/hb2379sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536807019095/hb2379Isup2.hkl |
CCDC reference: 647608
Key indicators
- Single-crystal X-ray study
- T = 150 K
- Mean (C-C) = 0.004 Å
- R factor = 0.054
- wR factor = 0.148
- Data-to-parameter ratio = 16.8
checkCIF/PLATON results
No syntax errors found
Alert level B PLAT230_ALERT_2_B Hirshfeld Test Diff for N24 - C114 .. 8.14 su
Alert level C DIFMX01_ALERT_2_C The maximum difference density is > 0.1*ZMAX*0.75 _refine_diff_density_max given = 1.233 Test value = 1.050 DIFMX02_ALERT_1_C The maximum difference density is > 0.1*ZMAX*0.75 The relevant atom site should be identified. PLAT094_ALERT_2_C Ratio of Maximum / Minimum Residual Density .... 2.50 PLAT097_ALERT_2_C Maximum (Positive) Residual Density ............ 1.23 e/A PLAT180_ALERT_3_C Check Cell Rounding: # of Values Ending with 0 = 3 PLAT220_ALERT_2_C Large Non-Solvent C Ueq(max)/Ueq(min) ... 3.48 Ratio PLAT222_ALERT_3_C Large Non-Solvent H Ueq(max)/Ueq(min) ... 3.95 Ratio PLAT230_ALERT_2_C Hirshfeld Test Diff for O12 - N32 .. 5.94 su PLAT480_ALERT_4_C Long H...A H-Bond Reported H10A .. O24 .. 2.66 Ang. PLAT480_ALERT_4_C Long H...A H-Bond Reported H10C .. O23 .. 2.70 Ang. PLAT480_ALERT_4_C Long H...A H-Bond Reported H10E .. O22 .. 2.63 Ang.
0 ALERT level A = In general: serious problem 1 ALERT level B = Potentially serious problem 11 ALERT level C = Check and explain 0 ALERT level G = General alerts; check 1 ALERT type 1 CIF construction/syntax error, inconsistent or missing data 6 ALERT type 2 Indicator that the structure model may be wrong or deficient 2 ALERT type 3 Indicator that the structure quality may be low 3 ALERT type 4 Improvement, methodology, query or suggestion 0 ALERT type 5 Informative message, check
The synthesis of the title compound, (I), is described by Slagt et al. (2004). For related structures, see: Delugeard & Messager (1975); Steenwinkel et al. (1997). For related literature, see: Altomare et al. (1999); Mackay (1984).
Compound(I) was prepared according to a literature procedure by Slagt et al. (2004). Yellow crystals for data collection were obtained by recrystallization from petroleum ether (bp. 333 - 353 K).
All the hydrogen atoms were introduced in geometrically idealized positions (C—H = 0.95–0.99 Å) and refined as riding with Uiso(H) = 1.2Ueq(C) or 1.5Ueq(methyl C). C114 and C124 were restrained to approximate to isotropic behavior. The highest difference peak is 0.88Å from H11L and the deepest difference hole is 0.96Å from N24.
Organometallic transition metal complexes based on the NCN pincer ligand (NCN = 2,6-bis[(dimethylamino)methyl]phenyl) are found in numerous applications, e.g. in catalysis. Variations of the para substituent of the NCN pincer ligand have drawn interest for several reasons. The electronic properties can be fine-tuned by choosing the appropriate substituent and result in a variation of the catalytic, spectroscopic and diagnostic properties. Therefore we report here the structure of the title compound, (I), which is a nitro functionilized NCN pincer ligand in the para position. The asymmetric unit of (I) consist of four independent C15H27N3O2Si molecules (Fig. 1). All four molecules have essentially the same geometry as can be seen in Fig. 2 in a quaternion fit (Mackay, 1984).
The coordination geometries of the Si atoms are slightly distorted tetrahedral, with the largest deviation for the angles C13X-SiX-C15X (X = 1, 2, 3 and 4) of 7° from the ideal value of 109°. The Si distances to the methyl groups vary between 1.864 (3) and 1.887 (3) Å, while the Si—C distances to the aromatic ring are longer [1.916 (2) - 1.922 (2) Å]. Similar geometric parameters were found in [(Me3Si)2{C6(CH2NMe2)4}] reported by Steenwinkel et al. (1997). The deviation of the Si atom of the SiMe3 group with respect to the plane of the aromatic ring varies between 0.264 (1) and 0.288 (1) Å.
The nitro groups are coplanar with the phenyl ring with torsion angles between -1.3 (3) and 5.5 (3) °. The N—O distances range of the nitro group is 1.216 (3) to 1.234 (3) Å, the O—N—O angles vary between 123.1 (2) to 123.7 (2)° and the C—N—O angles lay between 117.7 (2) and 118.9 (2)°. These geometric parameters agree well with those found in m-nitro-N,N-dimethylaniline (Delugeard & Messager, 1975). The N atoms of the nitro group are in the plane of the aromatic ring, with a deviation of 0.057 (3) to 0.073 (2) Å.
The torsion angles C9X—N1X—C7X—C2X (-179.8 (2) - -177.6 (2)°) and C12X—N2X—C10X—C6X (158.5 (3) - 165.9 (2)°) of the N(CH3)2 groups result in a non crystallographic CS symmetry, with N atoms mutually trans. The N atoms of the N(CH3)2 groups show the largest difference with respect to the plane of the aromatic ring, N1X with 1.388 (3) to 1.469 (2) and N2X with 0.712 (2) to 0.816 (2) Å.
The molecules have acute intramolecular C—H···N contacts with H···N distances between 2.39 and 2.43 Å. The geometry of the involved N2X atoms are tetrahedral, the C—N—C angles vary between 110.0 (2) and 111.4 (2)°. The free electron pairs of the N atoms are pointing in the direction of the H atoms and therefore we assume the presence of C—H···N hydrogen bonds. Intermolecular C—H···O contacts occur between H10Y (Y = A, C, E and G) and O2X with a range of 2.63 and 2.70Å and connect two molecules into dimeric structures (Fig. 2), respectively (Table 1).
Despite the presence of four independent molecules there is no pseudo- translational symmetry present. The corresponding <|E2-1|> value of 0.985 is close to the expected value of 0.968 for a centrosymmetric structure (SHELXS97, Sheldrick, 1997). An additional test on pseudo-translational symmetry as implemented in the program SIR97 (Altomare et al., 1999) also did not give an indication for pseudo-translational symmetry. The analyses of the normal probability distribution of equivalent bond distances shows that all distances are distributed normally, except three outliers. These outliers belong to the substituents of N24. The corresponding C atoms (C104, C114 and C124) also show rather high anisotropic displacement parameters, which are the reason for the anomalous C—N bonds.
The synthesis of the title compound, (I), is described by Slagt et al. (2004). For related structures, see: Delugeard & Messager (1975); Steenwinkel et al. (1997). For related literature, see: Altomare et al. (1999); Mackay (1984).
Data collection: COLLECT (Nonius, 1999); cell refinement: DENZO (Otwinowski & Minor, 1997); data reduction: DENZO; program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: PLATON (Spek, 2003); software used to prepare material for publication: manual editing of SHELXL97 (Sheldrick, 1997) output.
C15H27N3O2Si | Z = 8 |
Mr = 309.49 | F(000) = 1344 |
Triclinic, P1 | Dx = 1.156 Mg m−3 |
Hall symbol: -P 1 | Mo Kα radiation, λ = 0.71073 Å |
a = 14.2353 (2) Å | Cell parameters from 71004 reflections |
b = 16.1402 (2) Å | θ = 1.0–27.5° |
c = 17.1387 (3) Å | µ = 0.14 mm−1 |
α = 75.0826 (7)° | T = 150 K |
β = 73.6940 (8)° | Plate, yellow |
γ = 73.5679 (9)° | 0.38 × 0.20 × 0.10 mm |
V = 3556.63 (9) Å3 |
Nonius KappaCCD diffractometer | 9550 reflections with I > 2σ(I) |
Radiation source: rotating anode | Rint = 0.042 |
Graphite monochromator | θmax = 25.5°, θmin = 1.5° |
φ and ω scans | h = −15→17 |
37090 measured reflections | k = −17→19 |
13201 independent reflections | l = −20→20 |
Refinement on F2 | Primary atom site location: structure-invariant direct methods |
Least-squares matrix: full | Secondary atom site location: difference Fourier map |
R[F2 > 2σ(F2)] = 0.054 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.148 | H-atom parameters constrained |
S = 1.04 | w = 1/[σ2(Fo2) + (0.0674P)2 + 1.78P] where P = (Fo2 + 2Fc2)/3 |
13201 reflections | (Δ/σ)max = 0.001 |
785 parameters | Δρmax = 1.23 e Å−3 |
12 restraints | Δρmin = −0.49 e Å−3 |
C15H27N3O2Si | γ = 73.5679 (9)° |
Mr = 309.49 | V = 3556.63 (9) Å3 |
Triclinic, P1 | Z = 8 |
a = 14.2353 (2) Å | Mo Kα radiation |
b = 16.1402 (2) Å | µ = 0.14 mm−1 |
c = 17.1387 (3) Å | T = 150 K |
α = 75.0826 (7)° | 0.38 × 0.20 × 0.10 mm |
β = 73.6940 (8)° |
Nonius KappaCCD diffractometer | 9550 reflections with I > 2σ(I) |
37090 measured reflections | Rint = 0.042 |
13201 independent reflections |
R[F2 > 2σ(F2)] = 0.054 | 12 restraints |
wR(F2) = 0.148 | H-atom parameters constrained |
S = 1.04 | Δρmax = 1.23 e Å−3 |
13201 reflections | Δρmin = −0.49 e Å−3 |
785 parameters |
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. |
x | y | z | Uiso*/Ueq | ||
Si1 | 0.19786 (5) | 0.34606 (5) | 0.51366 (4) | 0.03571 (18) | |
O11 | 0.08556 (16) | 0.14027 (14) | 0.91934 (12) | 0.0540 (5) | |
O21 | 0.21565 (15) | 0.04222 (12) | 0.87465 (12) | 0.0489 (5) | |
N11 | 0.27173 (14) | 0.13914 (14) | 0.50287 (13) | 0.0343 (5) | |
N21 | −0.07639 (15) | 0.37310 (13) | 0.73811 (12) | 0.0332 (5) | |
N31 | 0.15340 (18) | 0.11250 (14) | 0.86384 (14) | 0.0388 (5) | |
C11 | 0.17791 (17) | 0.26834 (16) | 0.61963 (15) | 0.0307 (5) | |
C21 | 0.24341 (17) | 0.18426 (16) | 0.63599 (15) | 0.0319 (5) | |
C31 | 0.23543 (18) | 0.13435 (16) | 0.71567 (15) | 0.0332 (6) | |
H31 | 0.2810 | 0.0791 | 0.7262 | 0.040* | |
C41 | 0.16114 (18) | 0.16533 (16) | 0.77939 (15) | 0.0318 (6) | |
C51 | 0.09055 (18) | 0.24305 (15) | 0.76585 (15) | 0.0311 (5) | |
H51 | 0.0376 | 0.2615 | 0.8102 | 0.037* | |
C61 | 0.09812 (17) | 0.29399 (15) | 0.68619 (15) | 0.0294 (5) | |
C71 | 0.31902 (18) | 0.14127 (18) | 0.56785 (16) | 0.0378 (6) | |
H71A | 0.3727 | 0.1743 | 0.5432 | 0.045* | |
H71B | 0.3504 | 0.0804 | 0.5918 | 0.045* | |
C81 | 0.18901 (19) | 0.09441 (17) | 0.53594 (17) | 0.0394 (6) | |
H81A | 0.1598 | 0.0939 | 0.4907 | 0.059* | |
H81B | 0.1375 | 0.1255 | 0.5766 | 0.059* | |
H81C | 0.2141 | 0.0337 | 0.5627 | 0.059* | |
C91 | 0.3470 (2) | 0.0949 (2) | 0.43974 (19) | 0.0515 (7) | |
H91A | 0.3739 | 0.0340 | 0.4649 | 0.077* | |
H91B | 0.4018 | 0.1259 | 0.4166 | 0.077* | |
H91C | 0.3158 | 0.0951 | 0.3955 | 0.077* | |
C101 | 0.01617 (18) | 0.37804 (16) | 0.67543 (15) | 0.0337 (6) | |
H10A | 0.0408 | 0.4284 | 0.6784 | 0.040* | |
H10B | 0.0020 | 0.3889 | 0.6199 | 0.040* | |
C111 | −0.1303 (2) | 0.31734 (18) | 0.72233 (18) | 0.0454 (7) | |
H11A | −0.1910 | 0.3138 | 0.7665 | 0.068* | |
H11B | −0.0871 | 0.2582 | 0.7210 | 0.068* | |
H11C | −0.1492 | 0.3423 | 0.6689 | 0.068* | |
C121 | −0.1409 (2) | 0.46004 (18) | 0.74324 (18) | 0.0501 (7) | |
H12A | −0.1638 | 0.4856 | 0.6915 | 0.075* | |
H12B | −0.1032 | 0.4979 | 0.7520 | 0.075* | |
H12C | −0.1991 | 0.4553 | 0.7897 | 0.075* | |
C131 | 0.3315 (2) | 0.3301 (2) | 0.45396 (18) | 0.0516 (8) | |
H13A | 0.3499 | 0.2769 | 0.4305 | 0.077* | |
H13B | 0.3755 | 0.3239 | 0.4910 | 0.077* | |
H13C | 0.3392 | 0.3812 | 0.4091 | 0.077* | |
C141 | 0.1148 (2) | 0.33701 (19) | 0.45041 (17) | 0.0445 (7) | |
H14A | 0.1260 | 0.3768 | 0.3965 | 0.067* | |
H14B | 0.0443 | 0.3532 | 0.4795 | 0.067* | |
H14C | 0.1304 | 0.2763 | 0.4421 | 0.067* | |
C151 | 0.1683 (2) | 0.46361 (18) | 0.52766 (18) | 0.0508 (7) | |
H15A | 0.1961 | 0.5002 | 0.4758 | 0.076* | |
H15B | 0.1982 | 0.4662 | 0.5717 | 0.076* | |
H15C | 0.0953 | 0.4855 | 0.5428 | 0.076* | |
Si2 | −0.05642 (5) | 0.80583 (4) | 0.77250 (4) | 0.03175 (17) | |
O22 | 0.39778 (13) | 0.91426 (12) | 0.68916 (13) | 0.0487 (5) | |
O12 | 0.41794 (14) | 0.86254 (15) | 0.57979 (13) | 0.0551 (5) | |
N12 | −0.05073 (15) | 0.98467 (13) | 0.82475 (12) | 0.0334 (5) | |
N22 | 0.14627 (15) | 0.81032 (13) | 0.50733 (12) | 0.0331 (5) | |
N32 | 0.36744 (16) | 0.88291 (14) | 0.64502 (15) | 0.0384 (5) | |
C12 | 0.06978 (17) | 0.84025 (15) | 0.72870 (14) | 0.0283 (5) | |
C22 | 0.10688 (18) | 0.88324 (15) | 0.77254 (15) | 0.0305 (5) | |
C32 | 0.20409 (18) | 0.89615 (15) | 0.74547 (15) | 0.0331 (6) | |
H32 | 0.2293 | 0.9229 | 0.7762 | 0.040* | |
C42 | 0.26385 (17) | 0.86969 (15) | 0.67344 (16) | 0.0315 (5) | |
C52 | 0.22868 (17) | 0.83465 (15) | 0.62492 (15) | 0.0300 (5) | |
H52 | 0.2700 | 0.8201 | 0.5740 | 0.036* | |
C62 | 0.13120 (17) | 0.82098 (14) | 0.65202 (15) | 0.0282 (5) | |
C72 | 0.04166 (19) | 0.92473 (17) | 0.84474 (15) | 0.0357 (6) | |
H72A | 0.0240 | 0.8779 | 0.8926 | 0.043* | |
H72B | 0.0799 | 0.9577 | 0.8609 | 0.043* | |
C82 | −0.02987 (19) | 1.05283 (16) | 0.75183 (17) | 0.0385 (6) | |
H82A | 0.0102 | 1.0877 | 0.7621 | 0.058* | |
H82B | −0.0934 | 1.0913 | 0.7404 | 0.058* | |
H82C | 0.0076 | 1.0253 | 0.7041 | 0.058* | |
C92 | −0.1088 (2) | 1.0258 (2) | 0.89534 (18) | 0.0492 (7) | |
H92A | −0.1722 | 1.0636 | 0.8829 | 0.074* | |
H92B | −0.0702 | 1.0613 | 0.9063 | 0.074* | |
H92C | −0.1232 | 0.9800 | 0.9442 | 0.074* | |
C102 | 0.09651 (17) | 0.78482 (16) | 0.59340 (14) | 0.0309 (5) | |
H10C | 0.1106 | 0.7198 | 0.6089 | 0.037* | |
H10D | 0.0230 | 0.8069 | 0.5997 | 0.037* | |
C112 | 0.1096 (2) | 0.90263 (18) | 0.47511 (18) | 0.0483 (7) | |
H11D | 0.0382 | 0.9136 | 0.4752 | 0.072* | |
H11E | 0.1477 | 0.9184 | 0.4183 | 0.072* | |
H11F | 0.1180 | 0.9384 | 0.5100 | 0.072* | |
C122 | 0.1355 (2) | 0.7562 (2) | 0.45584 (17) | 0.0469 (7) | |
H12D | 0.1763 | 0.7700 | 0.3998 | 0.070* | |
H12E | 0.0648 | 0.7683 | 0.4536 | 0.070* | |
H12F | 0.1582 | 0.6939 | 0.4795 | 0.070* | |
C132 | −0.0967 (2) | 0.78689 (18) | 0.88807 (16) | 0.0456 (7) | |
H13D | −0.1519 | 0.7563 | 0.9065 | 0.068* | |
H13E | −0.1195 | 0.8436 | 0.9061 | 0.068* | |
H13F | −0.0399 | 0.7509 | 0.9122 | 0.068* | |
C142 | −0.15694 (19) | 0.88781 (18) | 0.72455 (17) | 0.0425 (7) | |
H14D | −0.1676 | 0.9447 | 0.7400 | 0.064* | |
H14E | −0.2196 | 0.8672 | 0.7444 | 0.064* | |
H14F | −0.1363 | 0.8944 | 0.6641 | 0.064* | |
C152 | −0.0437 (2) | 0.69426 (18) | 0.75079 (18) | 0.0459 (7) | |
H15D | −0.1002 | 0.6693 | 0.7862 | 0.069* | |
H15E | 0.0195 | 0.6553 | 0.7623 | 0.069* | |
H15F | −0.0439 | 0.7000 | 0.6925 | 0.069* | |
Si3 | 0.29048 (5) | 0.70281 (5) | 0.98179 (4) | 0.03332 (17) | |
O13 | 0.41790 (15) | 0.64199 (14) | 0.58179 (12) | 0.0546 (5) | |
O23 | 0.28075 (15) | 0.59530 (13) | 0.62388 (11) | 0.0467 (5) | |
N13 | 0.22553 (15) | 0.51868 (13) | 0.99528 (12) | 0.0340 (5) | |
N23 | 0.57115 (15) | 0.70262 (14) | 0.76667 (13) | 0.0377 (5) | |
N33 | 0.34566 (17) | 0.62428 (14) | 0.63587 (13) | 0.0368 (5) | |
C13 | 0.31410 (17) | 0.66755 (15) | 0.87812 (14) | 0.0283 (5) | |
C23 | 0.25061 (17) | 0.62266 (15) | 0.86245 (15) | 0.0303 (5) | |
C33 | 0.26030 (18) | 0.60985 (15) | 0.78295 (15) | 0.0324 (6) | |
H33 | 0.2153 | 0.5825 | 0.7724 | 0.039* | |
C43 | 0.33587 (18) | 0.63730 (15) | 0.71989 (14) | 0.0303 (5) | |
C53 | 0.40531 (18) | 0.67382 (15) | 0.73310 (15) | 0.0302 (5) | |
H53 | 0.4593 | 0.6887 | 0.6892 | 0.036* | |
C63 | 0.39484 (17) | 0.68850 (15) | 0.81224 (14) | 0.0278 (5) | |
C73 | 0.17633 (18) | 0.57911 (17) | 0.93075 (15) | 0.0351 (6) | |
H73A | 0.1219 | 0.6248 | 0.9557 | 0.042* | |
H73B | 0.1457 | 0.5461 | 0.9071 | 0.042* | |
C83 | 0.3087 (2) | 0.45113 (17) | 0.96122 (17) | 0.0409 (6) | |
H83A | 0.2832 | 0.4168 | 0.9356 | 0.061* | |
H83B | 0.3396 | 0.4120 | 1.0058 | 0.061* | |
H83C | 0.3589 | 0.4793 | 0.9194 | 0.061* | |
C93 | 0.1520 (2) | 0.47654 (19) | 1.05929 (17) | 0.0475 (7) | |
H93A | 0.1844 | 0.4380 | 1.1033 | 0.071* | |
H93B | 0.1257 | 0.4416 | 1.0349 | 0.071* | |
H93C | 0.0967 | 0.5218 | 1.0825 | 0.071* | |
C103 | 0.47548 (17) | 0.72712 (16) | 0.82299 (15) | 0.0316 (5) | |
H10E | 0.4531 | 0.7921 | 0.8133 | 0.038* | |
H10F | 0.4841 | 0.7064 | 0.8807 | 0.038* | |
C113 | 0.6176 (2) | 0.6108 (2) | 0.7890 (2) | 0.0577 (8) | |
H11G | 0.5715 | 0.5749 | 0.7908 | 0.087* | |
H11H | 0.6330 | 0.5994 | 0.8435 | 0.087* | |
H11I | 0.6798 | 0.5957 | 0.7477 | 0.087* | |
C123 | 0.6386 (2) | 0.7573 (2) | 0.7638 (2) | 0.0598 (9) | |
H12G | 0.6570 | 0.7439 | 0.8174 | 0.090* | |
H12H | 0.6047 | 0.8195 | 0.7517 | 0.090* | |
H12I | 0.6994 | 0.7451 | 0.7203 | 0.090* | |
C133 | 0.1578 (2) | 0.71583 (19) | 1.04220 (17) | 0.0451 (7) | |
H13G | 0.1481 | 0.7474 | 1.0867 | 0.068* | |
H13H | 0.1430 | 0.6576 | 1.0663 | 0.068* | |
H13I | 0.1125 | 0.7493 | 1.0054 | 0.068* | |
C143 | 0.3769 (2) | 0.62534 (19) | 1.04663 (17) | 0.0470 (7) | |
H14G | 0.3601 | 0.5675 | 1.0630 | 0.070* | |
H14H | 0.3694 | 0.6482 | 1.0963 | 0.070* | |
H14I | 0.4465 | 0.6196 | 1.0146 | 0.070* | |
C153 | 0.3102 (2) | 0.81781 (19) | 0.96185 (19) | 0.0515 (7) | |
H15G | 0.2843 | 0.8409 | 1.0133 | 0.077* | |
H15H | 0.2744 | 0.8558 | 0.9197 | 0.077* | |
H15I | 0.3821 | 0.8165 | 0.9422 | 0.077* | |
Si4 | 0.55029 (5) | 0.15980 (5) | 0.72471 (4) | 0.03316 (17) | |
O14 | 0.08172 (14) | 0.36777 (13) | 0.91013 (13) | 0.0543 (5) | |
O24 | 0.10430 (13) | 0.46304 (12) | 0.79620 (13) | 0.0485 (5) | |
N14 | 0.55441 (15) | 0.36854 (13) | 0.66671 (12) | 0.0326 (5) | |
N24 | 0.3467 (2) | 0.1327 (2) | 0.98601 (16) | 0.0700 (8) | |
N34 | 0.13342 (15) | 0.39411 (14) | 0.84303 (15) | 0.0379 (5) | |
C14 | 0.42679 (17) | 0.23832 (15) | 0.76472 (15) | 0.0293 (5) | |
C24 | 0.39319 (17) | 0.32353 (16) | 0.71871 (14) | 0.0300 (5) | |
C34 | 0.29717 (18) | 0.37357 (16) | 0.74374 (15) | 0.0330 (6) | |
H34 | 0.2743 | 0.4291 | 0.7110 | 0.040* | |
C44 | 0.23527 (17) | 0.34188 (15) | 0.81653 (15) | 0.0310 (5) | |
C54 | 0.26766 (17) | 0.26353 (16) | 0.86741 (15) | 0.0312 (5) | |
H54 | 0.2255 | 0.2448 | 0.9191 | 0.037* | |
C64 | 0.36321 (16) | 0.21212 (15) | 0.84199 (15) | 0.0280 (5) | |
C74 | 0.46169 (18) | 0.36776 (17) | 0.64528 (15) | 0.0348 (6) | |
H74A | 0.4789 | 0.3361 | 0.5990 | 0.042* | |
H74B | 0.4262 | 0.4290 | 0.6266 | 0.042* | |
C84 | 0.5334 (2) | 0.41329 (18) | 0.73570 (16) | 0.0398 (6) | |
H84A | 0.5968 | 0.4130 | 0.7478 | 0.060* | |
H84B | 0.4927 | 0.3827 | 0.7847 | 0.060* | |
H84C | 0.4965 | 0.4742 | 0.7209 | 0.060* | |
C94 | 0.6186 (2) | 0.4121 (2) | 0.59433 (17) | 0.0471 (7) | |
H94A | 0.5835 | 0.4732 | 0.5779 | 0.071* | |
H94B | 0.6340 | 0.3811 | 0.5484 | 0.071* | |
H94C | 0.6812 | 0.4110 | 0.6083 | 0.071* | |
C104 | 0.39355 (18) | 0.12733 (17) | 0.90208 (16) | 0.0369 (6) | |
H10G | 0.3757 | 0.0789 | 0.8880 | 0.044* | |
H10H | 0.4674 | 0.1129 | 0.8955 | 0.044* | |
C114 | 0.3908 (4) | 0.1798 (3) | 1.0148 (3) | 0.0974 (13) | |
H11J | 0.4618 | 0.1506 | 1.0119 | 0.146* | |
H11K | 0.3568 | 0.1836 | 1.0725 | 0.146* | |
H11L | 0.3856 | 0.2393 | 0.9809 | 0.146* | |
C124 | 0.3456 (3) | 0.0442 (3) | 1.0387 (2) | 0.0873 (12) | |
H12J | 0.4145 | 0.0123 | 1.0421 | 0.131* | |
H12K | 0.3163 | 0.0114 | 1.0145 | 0.131* | |
H12L | 0.3052 | 0.0503 | 1.0945 | 0.131* | |
C134 | 0.5957 (2) | 0.1800 (2) | 0.60985 (17) | 0.0481 (7) | |
H13J | 0.6220 | 0.2335 | 0.5914 | 0.072* | |
H13K | 0.5399 | 0.1874 | 0.5839 | 0.072* | |
H13L | 0.6492 | 0.1298 | 0.5938 | 0.072* | |
C144 | 0.65055 (19) | 0.16092 (19) | 0.77505 (18) | 0.0446 (7) | |
H14J | 0.7103 | 0.1151 | 0.7595 | 0.067* | |
H14K | 0.6261 | 0.1497 | 0.8354 | 0.067* | |
H14L | 0.6678 | 0.2186 | 0.7567 | 0.067* | |
C154 | 0.5303 (2) | 0.04458 (18) | 0.74791 (19) | 0.0509 (7) | |
H15J | 0.4659 | 0.0465 | 0.7367 | 0.076* | |
H15K | 0.5299 | 0.0185 | 0.8063 | 0.076* | |
H15L | 0.5848 | 0.0088 | 0.7128 | 0.076* |
U11 | U22 | U33 | U12 | U13 | U23 | |
Si1 | 0.0380 (4) | 0.0410 (4) | 0.0310 (4) | −0.0191 (3) | −0.0046 (3) | −0.0041 (3) |
O11 | 0.0621 (13) | 0.0559 (13) | 0.0321 (11) | −0.0048 (11) | −0.0079 (10) | −0.0004 (10) |
O21 | 0.0582 (12) | 0.0401 (11) | 0.0489 (12) | −0.0028 (10) | −0.0286 (10) | −0.0006 (9) |
N11 | 0.0275 (10) | 0.0430 (12) | 0.0342 (12) | −0.0098 (9) | −0.0029 (9) | −0.0132 (10) |
N21 | 0.0373 (11) | 0.0282 (11) | 0.0312 (12) | −0.0012 (9) | −0.0060 (9) | −0.0092 (9) |
N31 | 0.0481 (13) | 0.0372 (13) | 0.0369 (13) | −0.0120 (11) | −0.0216 (12) | −0.0015 (10) |
C11 | 0.0322 (13) | 0.0346 (14) | 0.0317 (14) | −0.0121 (11) | −0.0096 (11) | −0.0094 (11) |
C21 | 0.0254 (12) | 0.0385 (14) | 0.0366 (14) | −0.0102 (11) | −0.0087 (11) | −0.0105 (11) |
C31 | 0.0308 (13) | 0.0340 (14) | 0.0395 (15) | −0.0051 (11) | −0.0163 (12) | −0.0084 (11) |
C41 | 0.0378 (13) | 0.0337 (14) | 0.0299 (14) | −0.0126 (11) | −0.0150 (11) | −0.0034 (11) |
C51 | 0.0345 (13) | 0.0330 (13) | 0.0295 (14) | −0.0098 (11) | −0.0095 (11) | −0.0076 (11) |
C61 | 0.0340 (13) | 0.0284 (13) | 0.0303 (13) | −0.0096 (10) | −0.0102 (11) | −0.0072 (10) |
C71 | 0.0267 (13) | 0.0450 (16) | 0.0435 (16) | −0.0061 (11) | −0.0090 (12) | −0.0128 (12) |
C81 | 0.0428 (15) | 0.0392 (15) | 0.0421 (16) | −0.0166 (12) | −0.0125 (13) | −0.0067 (12) |
C91 | 0.0441 (16) | 0.062 (2) | 0.0482 (18) | −0.0079 (14) | −0.0031 (14) | −0.0235 (15) |
C101 | 0.0411 (14) | 0.0317 (14) | 0.0269 (13) | −0.0072 (11) | −0.0072 (11) | −0.0050 (11) |
C111 | 0.0388 (15) | 0.0434 (16) | 0.0541 (18) | −0.0070 (13) | −0.0129 (14) | −0.0093 (14) |
C121 | 0.0572 (18) | 0.0376 (16) | 0.0433 (17) | 0.0029 (13) | −0.0026 (14) | −0.0117 (13) |
C131 | 0.0492 (17) | 0.0601 (19) | 0.0486 (18) | −0.0311 (15) | 0.0033 (14) | −0.0107 (15) |
C141 | 0.0523 (17) | 0.0473 (17) | 0.0373 (16) | −0.0223 (14) | −0.0152 (13) | 0.0040 (13) |
C151 | 0.0631 (19) | 0.0432 (17) | 0.0440 (17) | −0.0240 (15) | −0.0045 (15) | 0.0000 (13) |
Si2 | 0.0319 (4) | 0.0326 (4) | 0.0283 (4) | −0.0095 (3) | −0.0046 (3) | −0.0017 (3) |
O22 | 0.0396 (10) | 0.0519 (12) | 0.0664 (14) | −0.0135 (9) | −0.0222 (10) | −0.0166 (10) |
O12 | 0.0357 (10) | 0.0824 (16) | 0.0531 (13) | −0.0224 (10) | 0.0006 (10) | −0.0249 (12) |
N12 | 0.0353 (11) | 0.0333 (12) | 0.0296 (12) | −0.0020 (9) | −0.0073 (9) | −0.0090 (9) |
N22 | 0.0342 (11) | 0.0376 (12) | 0.0294 (11) | −0.0125 (9) | −0.0013 (9) | −0.0114 (9) |
N32 | 0.0315 (11) | 0.0357 (12) | 0.0510 (15) | −0.0062 (10) | −0.0185 (11) | −0.0047 (11) |
C12 | 0.0300 (12) | 0.0249 (12) | 0.0281 (13) | −0.0017 (10) | −0.0115 (10) | −0.0017 (10) |
C22 | 0.0353 (13) | 0.0277 (13) | 0.0280 (13) | −0.0026 (10) | −0.0144 (11) | −0.0017 (10) |
C32 | 0.0362 (13) | 0.0307 (13) | 0.0360 (15) | −0.0039 (11) | −0.0189 (12) | −0.0051 (11) |
C42 | 0.0277 (12) | 0.0267 (13) | 0.0398 (15) | −0.0036 (10) | −0.0135 (11) | −0.0020 (11) |
C52 | 0.0271 (12) | 0.0268 (13) | 0.0341 (14) | −0.0024 (10) | −0.0073 (11) | −0.0062 (10) |
C62 | 0.0288 (12) | 0.0226 (12) | 0.0329 (14) | −0.0037 (10) | −0.0100 (11) | −0.0037 (10) |
C72 | 0.0423 (14) | 0.0388 (15) | 0.0291 (14) | −0.0077 (12) | −0.0133 (12) | −0.0075 (11) |
C82 | 0.0389 (14) | 0.0310 (14) | 0.0458 (16) | −0.0062 (11) | −0.0147 (12) | −0.0038 (12) |
C92 | 0.0500 (17) | 0.0538 (18) | 0.0417 (17) | −0.0023 (14) | −0.0064 (14) | −0.0200 (14) |
C102 | 0.0283 (12) | 0.0336 (14) | 0.0324 (14) | −0.0086 (10) | −0.0036 (11) | −0.0109 (11) |
C112 | 0.0608 (18) | 0.0467 (17) | 0.0439 (17) | −0.0204 (14) | −0.0210 (15) | −0.0009 (13) |
C122 | 0.0471 (16) | 0.0626 (19) | 0.0385 (16) | −0.0221 (14) | 0.0015 (13) | −0.0243 (14) |
C132 | 0.0572 (17) | 0.0414 (16) | 0.0322 (15) | −0.0141 (14) | −0.0022 (13) | −0.0023 (12) |
C142 | 0.0322 (14) | 0.0485 (17) | 0.0450 (17) | −0.0123 (12) | −0.0088 (12) | −0.0023 (13) |
C152 | 0.0505 (16) | 0.0435 (16) | 0.0461 (17) | −0.0231 (14) | −0.0034 (14) | −0.0072 (13) |
Si3 | 0.0346 (4) | 0.0365 (4) | 0.0263 (4) | −0.0035 (3) | −0.0043 (3) | −0.0095 (3) |
O13 | 0.0582 (13) | 0.0804 (15) | 0.0296 (11) | −0.0283 (12) | 0.0004 (10) | −0.0157 (10) |
O23 | 0.0571 (12) | 0.0539 (12) | 0.0385 (11) | −0.0176 (10) | −0.0197 (9) | −0.0101 (9) |
N13 | 0.0325 (11) | 0.0365 (12) | 0.0299 (12) | −0.0085 (9) | −0.0025 (9) | −0.0052 (9) |
N23 | 0.0349 (11) | 0.0464 (13) | 0.0340 (12) | −0.0130 (10) | −0.0010 (10) | −0.0147 (10) |
N33 | 0.0446 (13) | 0.0355 (12) | 0.0320 (12) | −0.0061 (10) | −0.0147 (11) | −0.0060 (10) |
C13 | 0.0274 (12) | 0.0260 (12) | 0.0265 (13) | 0.0008 (10) | −0.0069 (10) | −0.0034 (10) |
C23 | 0.0264 (12) | 0.0306 (13) | 0.0314 (14) | −0.0008 (10) | −0.0090 (10) | −0.0051 (10) |
C33 | 0.0323 (13) | 0.0307 (13) | 0.0351 (15) | −0.0036 (11) | −0.0133 (11) | −0.0056 (11) |
C43 | 0.0359 (13) | 0.0274 (13) | 0.0263 (13) | −0.0025 (10) | −0.0106 (11) | −0.0043 (10) |
C53 | 0.0346 (13) | 0.0256 (12) | 0.0264 (13) | −0.0040 (10) | −0.0061 (11) | −0.0024 (10) |
C63 | 0.0316 (12) | 0.0236 (12) | 0.0259 (13) | −0.0018 (10) | −0.0081 (10) | −0.0040 (10) |
C73 | 0.0286 (13) | 0.0400 (15) | 0.0355 (15) | −0.0058 (11) | −0.0069 (11) | −0.0078 (12) |
C83 | 0.0457 (15) | 0.0354 (15) | 0.0400 (16) | −0.0045 (12) | −0.0100 (13) | −0.0095 (12) |
C93 | 0.0466 (16) | 0.0546 (18) | 0.0372 (16) | −0.0215 (14) | −0.0006 (13) | −0.0002 (13) |
C103 | 0.0367 (13) | 0.0303 (13) | 0.0265 (13) | −0.0086 (11) | −0.0032 (11) | −0.0066 (10) |
C113 | 0.0454 (17) | 0.060 (2) | 0.073 (2) | 0.0055 (15) | −0.0229 (16) | −0.0304 (17) |
C123 | 0.0517 (18) | 0.088 (2) | 0.0499 (19) | −0.0394 (18) | 0.0070 (15) | −0.0251 (17) |
C133 | 0.0449 (16) | 0.0478 (17) | 0.0378 (16) | −0.0039 (13) | −0.0006 (13) | −0.0165 (13) |
C143 | 0.0492 (16) | 0.0581 (18) | 0.0330 (15) | −0.0063 (14) | −0.0146 (13) | −0.0084 (13) |
C153 | 0.0602 (19) | 0.0467 (17) | 0.0481 (18) | −0.0135 (15) | 0.0026 (15) | −0.0244 (14) |
Si4 | 0.0293 (4) | 0.0376 (4) | 0.0333 (4) | −0.0046 (3) | −0.0051 (3) | −0.0135 (3) |
O14 | 0.0360 (10) | 0.0555 (13) | 0.0556 (14) | −0.0011 (9) | 0.0036 (10) | −0.0090 (11) |
O24 | 0.0369 (10) | 0.0397 (11) | 0.0669 (14) | 0.0007 (9) | −0.0191 (10) | −0.0091 (10) |
N14 | 0.0347 (11) | 0.0387 (12) | 0.0258 (11) | −0.0130 (9) | −0.0053 (9) | −0.0054 (9) |
N24 | 0.0632 (17) | 0.0716 (19) | 0.0392 (16) | 0.0179 (15) | −0.0012 (13) | 0.0031 (14) |
N34 | 0.0301 (11) | 0.0351 (13) | 0.0518 (15) | −0.0024 (10) | −0.0149 (11) | −0.0133 (11) |
C14 | 0.0270 (12) | 0.0335 (13) | 0.0325 (14) | −0.0093 (10) | −0.0089 (10) | −0.0103 (11) |
C24 | 0.0315 (13) | 0.0350 (14) | 0.0278 (13) | −0.0097 (11) | −0.0115 (10) | −0.0058 (10) |
C34 | 0.0342 (13) | 0.0318 (13) | 0.0368 (15) | −0.0064 (11) | −0.0161 (12) | −0.0056 (11) |
C44 | 0.0277 (12) | 0.0302 (13) | 0.0397 (15) | −0.0056 (10) | −0.0121 (11) | −0.0108 (11) |
C54 | 0.0283 (12) | 0.0350 (14) | 0.0329 (14) | −0.0110 (11) | −0.0042 (11) | −0.0099 (11) |
C64 | 0.0257 (12) | 0.0288 (13) | 0.0324 (14) | −0.0080 (10) | −0.0080 (10) | −0.0074 (10) |
C74 | 0.0390 (14) | 0.0386 (15) | 0.0274 (14) | −0.0102 (11) | −0.0108 (11) | −0.0019 (11) |
C84 | 0.0429 (15) | 0.0411 (15) | 0.0408 (16) | −0.0109 (12) | −0.0107 (13) | −0.0142 (12) |
C94 | 0.0455 (16) | 0.0554 (18) | 0.0383 (16) | −0.0216 (14) | −0.0023 (13) | −0.0021 (14) |
C104 | 0.0302 (13) | 0.0355 (14) | 0.0390 (16) | −0.0069 (11) | −0.0051 (11) | −0.0007 (12) |
C114 | 0.105 (2) | 0.097 (2) | 0.085 (2) | −0.0003 (16) | −0.0282 (16) | −0.0263 (16) |
C124 | 0.0762 (18) | 0.0835 (18) | 0.0721 (18) | −0.0036 (15) | −0.0071 (15) | 0.0102 (15) |
C134 | 0.0480 (16) | 0.0537 (18) | 0.0416 (17) | −0.0070 (14) | −0.0013 (13) | −0.0222 (14) |
C144 | 0.0299 (13) | 0.0532 (17) | 0.0490 (17) | −0.0031 (12) | −0.0113 (13) | −0.0112 (14) |
C154 | 0.0551 (18) | 0.0430 (17) | 0.0539 (19) | −0.0065 (14) | −0.0052 (15) | −0.0212 (14) |
Si1—C141 | 1.869 (3) | Si3—C133 | 1.864 (3) |
Si1—C131 | 1.870 (3) | Si3—C143 | 1.869 (3) |
Si1—C151 | 1.887 (3) | Si3—C153 | 1.885 (3) |
Si1—C11 | 1.921 (3) | Si3—C13 | 1.916 (2) |
O11—N31 | 1.224 (3) | O13—N33 | 1.222 (3) |
O21—N31 | 1.234 (3) | O23—N33 | 1.231 (3) |
N11—C81 | 1.458 (3) | N13—C93 | 1.461 (3) |
N11—C91 | 1.464 (3) | N13—C83 | 1.463 (3) |
N11—C71 | 1.466 (3) | N13—C73 | 1.469 (3) |
N21—C111 | 1.451 (3) | N23—C113 | 1.440 (4) |
N21—C121 | 1.452 (3) | N23—C103 | 1.448 (3) |
N21—C101 | 1.455 (3) | N23—C123 | 1.460 (3) |
N31—C41 | 1.470 (3) | N33—C43 | 1.471 (3) |
C11—C61 | 1.419 (3) | C13—C63 | 1.416 (3) |
C11—C21 | 1.423 (3) | C13—C23 | 1.422 (3) |
C21—C31 | 1.388 (3) | C23—C33 | 1.393 (3) |
C21—C71 | 1.514 (3) | C23—C73 | 1.511 (3) |
C31—C41 | 1.376 (3) | C33—C43 | 1.375 (3) |
C31—H31 | 0.9500 | C33—H33 | 0.9500 |
C41—C51 | 1.380 (3) | C43—C53 | 1.378 (3) |
C51—C61 | 1.393 (3) | C53—C63 | 1.396 (3) |
C51—H51 | 0.9500 | C53—H53 | 0.9500 |
C61—C101 | 1.527 (3) | C63—C103 | 1.524 (3) |
C71—H71A | 0.9900 | C73—H73A | 0.9900 |
C71—H71B | 0.9900 | C73—H73B | 0.9900 |
C81—H81A | 0.9800 | C83—H83A | 0.9800 |
C81—H81B | 0.9800 | C83—H83B | 0.9800 |
C81—H81C | 0.9800 | C83—H83C | 0.9800 |
C91—H91A | 0.9800 | C93—H93A | 0.9800 |
C91—H91B | 0.9800 | C93—H93B | 0.9800 |
C91—H91C | 0.9800 | C93—H93C | 0.9800 |
C101—H10A | 0.9900 | C103—H10E | 0.9900 |
C101—H10B | 0.9900 | C103—H10F | 0.9900 |
C111—H11A | 0.9800 | C113—H11G | 0.9800 |
C111—H11B | 0.9800 | C113—H11H | 0.9800 |
C111—H11C | 0.9800 | C113—H11I | 0.9800 |
C121—H12A | 0.9800 | C123—H12G | 0.9800 |
C121—H12B | 0.9800 | C123—H12H | 0.9800 |
C121—H12C | 0.9800 | C123—H12I | 0.9800 |
C131—H13A | 0.9800 | C133—H13G | 0.9800 |
C131—H13B | 0.9800 | C133—H13H | 0.9800 |
C131—H13C | 0.9800 | C133—H13I | 0.9800 |
C141—H14A | 0.9800 | C143—H14G | 0.9800 |
C141—H14B | 0.9800 | C143—H14H | 0.9800 |
C141—H14C | 0.9800 | C143—H14I | 0.9800 |
C151—H15A | 0.9800 | C153—H15G | 0.9800 |
C151—H15B | 0.9800 | C153—H15H | 0.9800 |
C151—H15C | 0.9800 | C153—H15I | 0.9800 |
Si2—C132 | 1.870 (3) | Si4—C134 | 1.864 (3) |
Si2—C142 | 1.872 (3) | Si4—C144 | 1.870 (3) |
Si2—C152 | 1.881 (3) | Si4—C154 | 1.885 (3) |
Si2—C12 | 1.922 (2) | Si4—C14 | 1.918 (2) |
O22—N32 | 1.232 (3) | O14—N34 | 1.223 (3) |
O12—N32 | 1.216 (3) | O24—N34 | 1.233 (3) |
N12—C92 | 1.459 (3) | N14—C84 | 1.459 (3) |
N12—C82 | 1.459 (3) | N14—C94 | 1.465 (3) |
N12—C72 | 1.465 (3) | N14—C74 | 1.470 (3) |
N22—C112 | 1.448 (3) | N24—C114 | 1.362 (5) |
N22—C122 | 1.453 (3) | N24—C104 | 1.419 (4) |
N22—C102 | 1.454 (3) | N24—C124 | 1.483 (4) |
N32—C42 | 1.476 (3) | N34—C44 | 1.468 (3) |
C12—C62 | 1.414 (3) | C14—C64 | 1.417 (3) |
C12—C22 | 1.422 (3) | C14—C24 | 1.422 (3) |
C22—C32 | 1.388 (3) | C24—C34 | 1.389 (3) |
C22—C72 | 1.507 (3) | C24—C74 | 1.512 (3) |
C32—C42 | 1.381 (3) | C34—C44 | 1.380 (3) |
C32—H32 | 0.9500 | C34—H34 | 0.9500 |
C42—C52 | 1.378 (3) | C44—C54 | 1.378 (3) |
C52—C62 | 1.396 (3) | C54—C64 | 1.394 (3) |
C52—H52 | 0.9500 | C54—H54 | 0.9500 |
C62—C102 | 1.529 (3) | C64—C104 | 1.520 (3) |
C72—H72A | 0.9900 | C74—H74A | 0.9900 |
C72—H72B | 0.9900 | C74—H74B | 0.9900 |
C82—H82A | 0.9800 | C84—H84A | 0.9800 |
C82—H82B | 0.9800 | C84—H84B | 0.9800 |
C82—H82C | 0.9800 | C84—H84C | 0.9800 |
C92—H92A | 0.9800 | C94—H94A | 0.9800 |
C92—H92B | 0.9800 | C94—H94B | 0.9800 |
C92—H92C | 0.9800 | C94—H94C | 0.9800 |
C102—H10C | 0.9900 | C104—H10G | 0.9900 |
C102—H10D | 0.9900 | C104—H10H | 0.9900 |
C112—H11D | 0.9800 | C114—H11J | 0.9800 |
C112—H11E | 0.9800 | C114—H11K | 0.9800 |
C112—H11F | 0.9800 | C114—H11L | 0.9800 |
C122—H12D | 0.9800 | C124—H12J | 0.9800 |
C122—H12E | 0.9800 | C124—H12K | 0.9800 |
C122—H12F | 0.9800 | C124—H12L | 0.9800 |
C132—H13D | 0.9800 | C134—H13J | 0.9800 |
C132—H13E | 0.9800 | C134—H13K | 0.9800 |
C132—H13F | 0.9800 | C134—H13L | 0.9800 |
C142—H14D | 0.9800 | C144—H14J | 0.9800 |
C142—H14E | 0.9800 | C144—H14K | 0.9800 |
C142—H14F | 0.9800 | C144—H14L | 0.9800 |
C152—H15D | 0.9800 | C154—H15J | 0.9800 |
C152—H15E | 0.9800 | C154—H15K | 0.9800 |
C152—H15F | 0.9800 | C154—H15L | 0.9800 |
C141—Si1—C131 | 110.51 (13) | C133—Si3—C143 | 110.14 (13) |
C141—Si1—C151 | 108.98 (14) | C133—Si3—C153 | 101.98 (13) |
C131—Si1—C151 | 102.26 (13) | C143—Si3—C153 | 109.89 (14) |
C141—Si1—C11 | 110.41 (11) | C133—Si3—C13 | 114.45 (11) |
C131—Si1—C11 | 114.12 (13) | C143—Si3—C13 | 110.70 (11) |
C151—Si1—C11 | 110.20 (12) | C153—Si3—C13 | 109.31 (12) |
C81—N11—C91 | 109.6 (2) | C93—N13—C83 | 109.5 (2) |
C81—N11—C71 | 111.9 (2) | C93—N13—C73 | 109.59 (19) |
C91—N11—C71 | 109.5 (2) | C83—N13—C73 | 111.7 (2) |
C111—N21—C121 | 110.0 (2) | C113—N23—C103 | 111.6 (2) |
C111—N21—C101 | 111.4 (2) | C113—N23—C123 | 110.3 (2) |
C121—N21—C101 | 111.3 (2) | C103—N23—C123 | 110.7 (2) |
O11—N31—O21 | 123.6 (2) | O13—N33—O23 | 123.3 (2) |
O11—N31—C41 | 118.4 (2) | O13—N33—C43 | 118.6 (2) |
O21—N31—C41 | 118.0 (2) | O23—N33—C43 | 118.1 (2) |
C61—C11—C21 | 117.0 (2) | C63—C13—C23 | 117.0 (2) |
C61—C11—Si1 | 120.90 (18) | C63—C13—Si3 | 120.53 (17) |
C21—C11—Si1 | 122.10 (18) | C23—C13—Si3 | 122.38 (17) |
C31—C21—C11 | 120.9 (2) | C33—C23—C13 | 121.0 (2) |
C31—C21—C71 | 116.4 (2) | C33—C23—C73 | 116.1 (2) |
C11—C21—C71 | 122.5 (2) | C13—C23—C73 | 122.7 (2) |
C41—C31—C21 | 119.6 (2) | C43—C33—C23 | 119.1 (2) |
C41—C31—H31 | 120.2 | C43—C33—H33 | 120.4 |
C21—C31—H31 | 120.2 | C23—C33—H33 | 120.4 |
C31—C41—C51 | 121.9 (2) | C33—C43—C53 | 122.3 (2) |
C31—C41—N31 | 119.4 (2) | C33—C43—N33 | 119.1 (2) |
C51—C41—N31 | 118.7 (2) | C53—C43—N33 | 118.6 (2) |
C41—C51—C61 | 119.0 (2) | C43—C53—C63 | 118.8 (2) |
C41—C51—H51 | 120.5 | C43—C53—H53 | 120.6 |
C61—C51—H51 | 120.5 | C63—C53—H53 | 120.6 |
C51—C61—C11 | 121.2 (2) | C53—C63—C13 | 121.3 (2) |
C51—C61—C101 | 116.1 (2) | C53—C63—C103 | 116.1 (2) |
C11—C61—C101 | 122.6 (2) | C13—C63—C103 | 122.7 (2) |
N11—C71—C21 | 111.54 (19) | N13—C73—C23 | 111.12 (19) |
N11—C71—H71A | 109.3 | N13—C73—H73A | 109.4 |
C21—C71—H71A | 109.3 | C23—C73—H73A | 109.4 |
N11—C71—H71B | 109.3 | N13—C73—H73B | 109.4 |
C21—C71—H71B | 109.3 | C23—C73—H73B | 109.4 |
H71A—C71—H71B | 108.0 | H73A—C73—H73B | 108.0 |
N11—C81—H81A | 109.5 | N13—C83—H83A | 109.5 |
N11—C81—H81B | 109.5 | N13—C83—H83B | 109.5 |
H81A—C81—H81B | 109.5 | H83A—C83—H83B | 109.5 |
N11—C81—H81C | 109.5 | N13—C83—H83C | 109.5 |
H81A—C81—H81C | 109.5 | H83A—C83—H83C | 109.5 |
H81B—C81—H81C | 109.5 | H83B—C83—H83C | 109.5 |
N11—C91—H91A | 109.5 | N13—C93—H93A | 109.5 |
N11—C91—H91B | 109.5 | N13—C93—H93B | 109.5 |
H91A—C91—H91B | 109.5 | H93A—C93—H93B | 109.5 |
N11—C91—H91C | 109.5 | N13—C93—H93C | 109.5 |
H91A—C91—H91C | 109.5 | H93A—C93—H93C | 109.5 |
H91B—C91—H91C | 109.5 | H93B—C93—H93C | 109.5 |
N21—C101—C61 | 112.40 (19) | N23—C103—C63 | 112.27 (19) |
N21—C101—H10A | 109.1 | N23—C103—H10E | 109.2 |
C61—C101—H10A | 109.1 | C63—C103—H10E | 109.2 |
N21—C101—H10B | 109.1 | N23—C103—H10F | 109.2 |
C61—C101—H10B | 109.1 | C63—C103—H10F | 109.2 |
H10A—C101—H10B | 107.9 | H10E—C103—H10F | 107.9 |
N21—C111—H11A | 109.5 | N23—C113—H11G | 109.5 |
N21—C111—H11B | 109.5 | N23—C113—H11H | 109.5 |
H11A—C111—H11B | 109.5 | H11G—C113—H11H | 109.5 |
N21—C111—H11C | 109.5 | N23—C113—H11I | 109.5 |
H11A—C111—H11C | 109.5 | H11G—C113—H11I | 109.5 |
H11B—C111—H11C | 109.5 | H11H—C113—H11I | 109.5 |
N21—C121—H12A | 109.5 | N23—C123—H12G | 109.5 |
N21—C121—H12B | 109.5 | N23—C123—H12H | 109.5 |
H12A—C121—H12B | 109.5 | H12G—C123—H12H | 109.5 |
N21—C121—H12C | 109.5 | N23—C123—H12I | 109.5 |
H12A—C121—H12C | 109.5 | H12G—C123—H12I | 109.5 |
H12B—C121—H12C | 109.5 | H12H—C123—H12I | 109.5 |
Si1—C131—H13A | 109.5 | Si3—C133—H13G | 109.5 |
Si1—C131—H13B | 109.5 | Si3—C133—H13H | 109.5 |
H13A—C131—H13B | 109.5 | H13G—C133—H13H | 109.5 |
Si1—C131—H13C | 109.5 | Si3—C133—H13I | 109.5 |
H13A—C131—H13C | 109.5 | H13G—C133—H13I | 109.5 |
H13B—C131—H13C | 109.5 | H13H—C133—H13I | 109.5 |
Si1—C141—H14A | 109.5 | Si3—C143—H14G | 109.5 |
Si1—C141—H14B | 109.5 | Si3—C143—H14H | 109.5 |
H14A—C141—H14B | 109.5 | H14G—C143—H14H | 109.5 |
Si1—C141—H14C | 109.5 | Si3—C143—H14I | 109.5 |
H14A—C141—H14C | 109.5 | H14G—C143—H14I | 109.5 |
H14B—C141—H14C | 109.5 | H14H—C143—H14I | 109.5 |
Si1—C151—H15A | 109.5 | Si3—C153—H15G | 109.5 |
Si1—C151—H15B | 109.5 | Si3—C153—H15H | 109.5 |
H15A—C151—H15B | 109.5 | H15G—C153—H15H | 109.5 |
Si1—C151—H15C | 109.5 | Si3—C153—H15I | 109.5 |
H15A—C151—H15C | 109.5 | H15G—C153—H15I | 109.5 |
H15B—C151—H15C | 109.5 | H15H—C153—H15I | 109.5 |
C132—Si2—C142 | 110.51 (13) | C134—Si4—C144 | 110.19 (13) |
C132—Si2—C152 | 102.18 (13) | C134—Si4—C154 | 102.07 (13) |
C142—Si2—C152 | 109.54 (13) | C144—Si4—C154 | 109.37 (13) |
C132—Si2—C12 | 114.17 (12) | C134—Si4—C14 | 114.69 (12) |
C142—Si2—C12 | 110.46 (11) | C144—Si4—C14 | 110.55 (11) |
C152—Si2—C12 | 109.64 (12) | C154—Si4—C14 | 109.59 (12) |
C92—N12—C82 | 109.5 (2) | C84—N14—C94 | 109.5 (2) |
C92—N12—C72 | 109.63 (19) | C84—N14—C74 | 111.80 (19) |
C82—N12—C72 | 111.9 (2) | C94—N14—C74 | 109.58 (19) |
C112—N22—C122 | 110.3 (2) | C114—N24—C104 | 110.7 (3) |
C112—N22—C102 | 111.7 (2) | C114—N24—C124 | 112.0 (3) |
C122—N22—C102 | 111.29 (19) | C104—N24—C124 | 111.5 (3) |
O12—N32—O22 | 123.7 (2) | O14—N34—O24 | 123.1 (2) |
O12—N32—C42 | 118.6 (2) | O14—N34—C44 | 118.9 (2) |
O22—N32—C42 | 117.7 (2) | O24—N34—C44 | 118.0 (2) |
C62—C12—C22 | 117.3 (2) | C64—C14—C24 | 116.9 (2) |
C62—C12—Si2 | 120.74 (16) | C64—C14—Si4 | 120.50 (17) |
C22—C12—Si2 | 121.97 (18) | C24—C14—Si4 | 122.63 (18) |
C32—C22—C12 | 120.8 (2) | C34—C24—C14 | 121.0 (2) |
C32—C22—C72 | 116.2 (2) | C34—C24—C74 | 116.3 (2) |
C12—C22—C72 | 122.8 (2) | C14—C24—C74 | 122.4 (2) |
C42—C32—C22 | 119.3 (2) | C44—C34—C24 | 119.4 (2) |
C42—C32—H32 | 120.3 | C44—C34—H34 | 120.3 |
C22—C32—H32 | 120.3 | C24—C34—H34 | 120.3 |
C52—C42—C32 | 122.2 (2) | C54—C44—C34 | 121.8 (2) |
C52—C42—N32 | 118.5 (2) | C54—C44—N34 | 118.5 (2) |
C32—C42—N32 | 119.3 (2) | C34—C44—N34 | 119.7 (2) |
C42—C52—C62 | 118.7 (2) | C44—C54—C64 | 119.1 (2) |
C42—C52—H52 | 120.6 | C44—C54—H54 | 120.5 |
C62—C52—H52 | 120.6 | C64—C54—H54 | 120.5 |
C52—C62—C12 | 121.3 (2) | C54—C64—C14 | 121.3 (2) |
C52—C62—C102 | 115.6 (2) | C54—C64—C104 | 115.8 (2) |
C12—C62—C102 | 123.16 (19) | C14—C64—C104 | 122.9 (2) |
N12—C72—C22 | 111.90 (19) | N14—C74—C24 | 111.13 (19) |
N12—C72—H72A | 109.2 | N14—C74—H74A | 109.4 |
C22—C72—H72A | 109.2 | C24—C74—H74A | 109.4 |
N12—C72—H72B | 109.2 | N14—C74—H74B | 109.4 |
C22—C72—H72B | 109.2 | C24—C74—H74B | 109.4 |
H72A—C72—H72B | 107.9 | H74A—C74—H74B | 108.0 |
N12—C82—H82A | 109.5 | N14—C84—H84A | 109.5 |
N12—C82—H82B | 109.5 | N14—C84—H84B | 109.5 |
H82A—C82—H82B | 109.5 | H84A—C84—H84B | 109.5 |
N12—C82—H82C | 109.5 | N14—C84—H84C | 109.5 |
H82A—C82—H82C | 109.5 | H84A—C84—H84C | 109.5 |
H82B—C82—H82C | 109.5 | H84B—C84—H84C | 109.5 |
N12—C92—H92A | 109.5 | N14—C94—H94A | 109.5 |
N12—C92—H92B | 109.5 | N14—C94—H94B | 109.5 |
H92A—C92—H92B | 109.5 | H94A—C94—H94B | 109.5 |
N12—C92—H92C | 109.5 | N14—C94—H94C | 109.5 |
H92A—C92—H92C | 109.5 | H94A—C94—H94C | 109.5 |
H92B—C92—H92C | 109.5 | H94B—C94—H94C | 109.5 |
N22—C102—C62 | 112.13 (18) | N24—C104—C64 | 113.0 (2) |
N22—C102—H10C | 109.2 | N24—C104—H10G | 109.0 |
C62—C102—H10C | 109.2 | C64—C104—H10G | 109.0 |
N22—C102—H10D | 109.2 | N24—C104—H10H | 109.0 |
C62—C102—H10D | 109.2 | C64—C104—H10H | 109.0 |
H10C—C102—H10D | 107.9 | H10G—C104—H10H | 107.8 |
N22—C112—H11D | 109.5 | N24—C114—H11J | 109.5 |
N22—C112—H11E | 109.5 | N24—C114—H11K | 109.5 |
H11D—C112—H11E | 109.5 | H11J—C114—H11K | 109.5 |
N22—C112—H11F | 109.5 | N24—C114—H11L | 109.5 |
H11D—C112—H11F | 109.5 | H11J—C114—H11L | 109.5 |
H11E—C112—H11F | 109.5 | H11K—C114—H11L | 109.5 |
N22—C122—H12D | 109.5 | N24—C124—H12J | 109.5 |
N22—C122—H12E | 109.5 | N24—C124—H12K | 109.5 |
H12D—C122—H12E | 109.5 | H12J—C124—H12K | 109.5 |
N22—C122—H12F | 109.5 | N24—C124—H12L | 109.5 |
H12D—C122—H12F | 109.5 | H12J—C124—H12L | 109.5 |
H12E—C122—H12F | 109.5 | H12K—C124—H12L | 109.5 |
Si2—C132—H13D | 109.5 | Si4—C134—H13J | 109.5 |
Si2—C132—H13E | 109.5 | Si4—C134—H13K | 109.5 |
H13D—C132—H13E | 109.5 | H13J—C134—H13K | 109.5 |
Si2—C132—H13F | 109.5 | Si4—C134—H13L | 109.5 |
H13D—C132—H13F | 109.5 | H13J—C134—H13L | 109.5 |
H13E—C132—H13F | 109.5 | H13K—C134—H13L | 109.5 |
Si2—C142—H14D | 109.5 | Si4—C144—H14J | 109.5 |
Si2—C142—H14E | 109.5 | Si4—C144—H14K | 109.5 |
H14D—C142—H14E | 109.5 | H14J—C144—H14K | 109.5 |
Si2—C142—H14F | 109.5 | Si4—C144—H14L | 109.5 |
H14D—C142—H14F | 109.5 | H14J—C144—H14L | 109.5 |
H14E—C142—H14F | 109.5 | H14K—C144—H14L | 109.5 |
Si2—C152—H15D | 109.5 | Si4—C154—H15J | 109.5 |
Si2—C152—H15E | 109.5 | Si4—C154—H15K | 109.5 |
H15D—C152—H15E | 109.5 | H15J—C154—H15K | 109.5 |
Si2—C152—H15F | 109.5 | Si4—C154—H15L | 109.5 |
H15D—C152—H15F | 109.5 | H15J—C154—H15L | 109.5 |
H15E—C152—H15F | 109.5 | H15K—C154—H15L | 109.5 |
C141—Si1—C11—C61 | −83.6 (2) | C133—Si3—C13—C63 | 154.31 (18) |
C131—Si1—C11—C61 | 151.23 (18) | C143—Si3—C13—C63 | −80.5 (2) |
C151—Si1—C11—C61 | 36.9 (2) | C153—Si3—C13—C63 | 40.7 (2) |
C141—Si1—C11—C21 | 98.4 (2) | C133—Si3—C13—C23 | −23.4 (2) |
C131—Si1—C11—C21 | −26.8 (2) | C143—Si3—C13—C23 | 101.8 (2) |
C151—Si1—C11—C21 | −141.15 (19) | C153—Si3—C13—C23 | −137.0 (2) |
C61—C11—C21—C31 | −6.7 (3) | C63—C13—C23—C33 | −7.7 (3) |
Si1—C11—C21—C31 | 171.41 (16) | Si3—C13—C23—C33 | 170.06 (18) |
C61—C11—C21—C71 | 168.3 (2) | C63—C13—C23—C73 | 166.5 (2) |
Si1—C11—C21—C71 | −13.6 (3) | Si3—C13—C23—C73 | −15.8 (3) |
C11—C21—C31—C41 | 2.0 (3) | C13—C23—C33—C43 | 3.3 (3) |
C71—C21—C31—C41 | −173.2 (2) | C73—C23—C33—C43 | −171.3 (2) |
C21—C31—C41—C51 | 3.3 (3) | C23—C33—C43—C53 | 2.8 (4) |
C21—C31—C41—N31 | −179.59 (19) | C23—C33—C43—N33 | −179.6 (2) |
O11—N31—C41—C31 | −178.5 (2) | O13—N33—C43—C33 | −173.9 (2) |
O21—N31—C41—C31 | 1.2 (3) | O23—N33—C43—C33 | 5.5 (3) |
O11—N31—C41—C51 | −1.3 (3) | O13—N33—C43—C53 | 3.8 (3) |
O21—N31—C41—C51 | 178.4 (2) | O23—N33—C43—C53 | −176.8 (2) |
C31—C41—C51—C61 | −3.7 (3) | C33—C43—C53—C63 | −4.1 (4) |
N31—C41—C51—C61 | 179.23 (19) | N33—C43—C53—C63 | 178.3 (2) |
C41—C51—C61—C11 | −1.4 (3) | C43—C53—C63—C13 | −0.7 (3) |
C41—C51—C61—C101 | 178.7 (2) | C43—C53—C63—C103 | 178.7 (2) |
C21—C11—C61—C51 | 6.3 (3) | C23—C13—C63—C53 | 6.4 (3) |
Si1—C11—C61—C51 | −171.78 (16) | Si3—C13—C63—C53 | −171.39 (17) |
C21—C11—C61—C101 | −173.7 (2) | C23—C13—C63—C103 | −173.0 (2) |
Si1—C11—C61—C101 | 8.1 (3) | Si3—C13—C63—C103 | 9.2 (3) |
C81—N11—C71—C21 | −56.6 (3) | C93—N13—C73—C23 | −178.9 (2) |
C91—N11—C71—C21 | −178.4 (2) | C83—N13—C73—C23 | −57.4 (3) |
C31—C21—C71—N11 | 123.5 (2) | C33—C23—C73—N13 | 121.9 (2) |
C11—C21—C71—N11 | −51.7 (3) | C13—C23—C73—N13 | −52.6 (3) |
C111—N21—C101—C61 | −74.6 (2) | C113—N23—C103—C63 | −70.9 (3) |
C121—N21—C101—C61 | 162.2 (2) | C123—N23—C103—C63 | 165.9 (2) |
C51—C61—C101—N21 | −24.5 (3) | C53—C63—C103—N23 | −28.8 (3) |
C11—C61—C101—N21 | 155.5 (2) | C13—C63—C103—N23 | 150.6 (2) |
C132—Si2—C12—C62 | 152.50 (18) | C134—Si4—C14—C64 | 154.47 (18) |
C142—Si2—C12—C62 | −82.2 (2) | C144—Si4—C14—C64 | −80.2 (2) |
C152—Si2—C12—C62 | 38.6 (2) | C154—Si4—C14—C64 | 40.4 (2) |
C132—Si2—C12—C22 | −25.5 (2) | C134—Si4—C14—C24 | −24.0 (2) |
C142—Si2—C12—C22 | 99.8 (2) | C144—Si4—C14—C24 | 101.3 (2) |
C152—Si2—C12—C22 | −139.4 (2) | C154—Si4—C14—C24 | −138.05 (19) |
C62—C12—C22—C32 | −7.3 (3) | C64—C14—C24—C34 | −7.9 (3) |
Si2—C12—C22—C32 | 170.74 (17) | Si4—C14—C24—C34 | 170.62 (17) |
C62—C12—C22—C72 | 166.6 (2) | C64—C14—C24—C74 | 166.5 (2) |
Si2—C12—C22—C72 | −15.3 (3) | Si4—C14—C24—C74 | −15.0 (3) |
C12—C22—C32—C42 | 2.4 (3) | C14—C24—C34—C44 | 3.2 (3) |
C72—C22—C32—C42 | −171.9 (2) | C74—C24—C34—C44 | −171.5 (2) |
C22—C32—C42—C52 | 3.3 (4) | C24—C34—C44—C54 | 3.1 (3) |
C22—C32—C42—N32 | −179.6 (2) | C24—C34—C44—N34 | −179.5 (2) |
O12—N32—C42—C52 | 0.1 (3) | O14—N34—C44—C54 | 1.9 (3) |
O22—N32—C42—C52 | −179.9 (2) | O24—N34—C44—C54 | −178.3 (2) |
O12—N32—C42—C32 | −177.1 (2) | O14—N34—C44—C34 | −175.5 (2) |
O22—N32—C42—C32 | 2.8 (3) | O24—N34—C44—C34 | 4.2 (3) |
C32—C42—C52—C62 | −3.7 (4) | C34—C44—C54—C64 | −4.3 (3) |
N32—C42—C52—C62 | 179.2 (2) | N34—C44—C54—C64 | 178.29 (19) |
C42—C52—C62—C12 | −1.6 (3) | C44—C54—C64—C14 | −0.8 (3) |
C42—C52—C62—C102 | 178.0 (2) | C44—C54—C64—C104 | 179.3 (2) |
C22—C12—C62—C52 | 6.9 (3) | C24—C14—C64—C54 | 6.7 (3) |
Si2—C12—C62—C52 | −171.13 (17) | Si4—C14—C64—C54 | −171.87 (17) |
C22—C12—C62—C102 | −172.7 (2) | C24—C14—C64—C104 | −173.4 (2) |
Si2—C12—C62—C102 | 9.2 (3) | Si4—C14—C64—C104 | 8.0 (3) |
C92—N12—C72—C22 | −177.6 (2) | C84—N14—C74—C24 | −58.2 (3) |
C82—N12—C72—C22 | −55.9 (3) | C94—N14—C74—C24 | −179.8 (2) |
C32—C22—C72—N12 | 122.9 (2) | C34—C24—C74—N14 | 122.5 (2) |
C12—C22—C72—N12 | −51.3 (3) | C14—C24—C74—N14 | −52.2 (3) |
C112—N22—C102—C62 | −72.7 (2) | C114—N24—C104—C64 | −76.1 (3) |
C122—N22—C102—C62 | 163.5 (2) | C124—N24—C104—C64 | 158.5 (3) |
C52—C62—C102—N22 | −28.1 (3) | C54—C64—C104—N24 | −28.9 (3) |
C12—C62—C102—N22 | 151.5 (2) | C14—C64—C104—N24 | 151.2 (2) |
D—H···A | D—H | H···A | D···A | D—H···A |
C101—H10A···O24 | 0.99 | 2.66 | 3.411 (3) | 133 |
C102—H10C···O23 | 0.99 | 2.70 | 3.452 (3) | 133 |
C103—H10E···O22 | 0.99 | 2.63 | 3.402 (3) | 135 |
C104—H10G···O21 | 0.99 | 2.59 | 3.390 (3) | 138 |
C51—H51···N21 | 0.95 | 2.39 | 2.753 (3) | 102 |
C52—H52···N22 | 0.95 | 2.41 | 2.754 (3) | 101 |
C53—H53···N23 | 0.95 | 2.43 | 2.764 (3) | 101 |
C54—H54···N24 | 0.95 | 2.42 | 2.755 (4) | 101 |
Experimental details
Crystal data | |
Chemical formula | C15H27N3O2Si |
Mr | 309.49 |
Crystal system, space group | Triclinic, P1 |
Temperature (K) | 150 |
a, b, c (Å) | 14.2353 (2), 16.1402 (2), 17.1387 (3) |
α, β, γ (°) | 75.0826 (7), 73.6940 (8), 73.5679 (9) |
V (Å3) | 3556.63 (9) |
Z | 8 |
Radiation type | Mo Kα |
µ (mm−1) | 0.14 |
Crystal size (mm) | 0.38 × 0.20 × 0.10 |
Data collection | |
Diffractometer | Nonius KappaCCD |
Absorption correction | – |
No. of measured, independent and observed [I > 2σ(I)] reflections | 37090, 13201, 9550 |
Rint | 0.042 |
(sin θ/λ)max (Å−1) | 0.606 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.054, 0.148, 1.04 |
No. of reflections | 13201 |
No. of parameters | 785 |
No. of restraints | 12 |
H-atom treatment | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 1.23, −0.49 |
Computer programs: COLLECT (Nonius, 1999), DENZO (Otwinowski & Minor, 1997), DENZO, SHELXS97 (Sheldrick, 1997), PLATON (Spek, 2003), manual editing of SHELXL97 (Sheldrick, 1997) output.
D—H···A | D—H | H···A | D···A | D—H···A |
C101—H10A···O24 | 0.99 | 2.66 | 3.411 (3) | 132.5 |
C102—H10C···O23 | 0.99 | 2.70 | 3.452 (3) | 132.9 |
C103—H10E···O22 | 0.99 | 2.63 | 3.402 (3) | 134.5 |
C104—H10G···O21 | 0.99 | 2.59 | 3.390 (3) | 137.7 |
C51—H51···N21 | 0.95 | 2.39 | 2.753 (3) | 102.0 |
C52—H52···N22 | 0.95 | 2.41 | 2.754 (3) | 101.0 |
C53—H53···N23 | 0.95 | 2.43 | 2.764 (3) | 100.6 |
C54—H54···N24 | 0.95 | 2.42 | 2.755 (4) | 100.5 |
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Organometallic transition metal complexes based on the NCN pincer ligand (NCN = 2,6-bis[(dimethylamino)methyl]phenyl) are found in numerous applications, e.g. in catalysis. Variations of the para substituent of the NCN pincer ligand have drawn interest for several reasons. The electronic properties can be fine-tuned by choosing the appropriate substituent and result in a variation of the catalytic, spectroscopic and diagnostic properties. Therefore we report here the structure of the title compound, (I), which is a nitro functionilized NCN pincer ligand in the para position. The asymmetric unit of (I) consist of four independent C15H27N3O2Si molecules (Fig. 1). All four molecules have essentially the same geometry as can be seen in Fig. 2 in a quaternion fit (Mackay, 1984).
The coordination geometries of the Si atoms are slightly distorted tetrahedral, with the largest deviation for the angles C13X-SiX-C15X (X = 1, 2, 3 and 4) of 7° from the ideal value of 109°. The Si distances to the methyl groups vary between 1.864 (3) and 1.887 (3) Å, while the Si—C distances to the aromatic ring are longer [1.916 (2) - 1.922 (2) Å]. Similar geometric parameters were found in [(Me3Si)2{C6(CH2NMe2)4}] reported by Steenwinkel et al. (1997). The deviation of the Si atom of the SiMe3 group with respect to the plane of the aromatic ring varies between 0.264 (1) and 0.288 (1) Å.
The nitro groups are coplanar with the phenyl ring with torsion angles between -1.3 (3) and 5.5 (3) °. The N—O distances range of the nitro group is 1.216 (3) to 1.234 (3) Å, the O—N—O angles vary between 123.1 (2) to 123.7 (2)° and the C—N—O angles lay between 117.7 (2) and 118.9 (2)°. These geometric parameters agree well with those found in m-nitro-N,N-dimethylaniline (Delugeard & Messager, 1975). The N atoms of the nitro group are in the plane of the aromatic ring, with a deviation of 0.057 (3) to 0.073 (2) Å.
The torsion angles C9X—N1X—C7X—C2X (-179.8 (2) - -177.6 (2)°) and C12X—N2X—C10X—C6X (158.5 (3) - 165.9 (2)°) of the N(CH3)2 groups result in a non crystallographic CS symmetry, with N atoms mutually trans. The N atoms of the N(CH3)2 groups show the largest difference with respect to the plane of the aromatic ring, N1X with 1.388 (3) to 1.469 (2) and N2X with 0.712 (2) to 0.816 (2) Å.
The molecules have acute intramolecular C—H···N contacts with H···N distances between 2.39 and 2.43 Å. The geometry of the involved N2X atoms are tetrahedral, the C—N—C angles vary between 110.0 (2) and 111.4 (2)°. The free electron pairs of the N atoms are pointing in the direction of the H atoms and therefore we assume the presence of C—H···N hydrogen bonds. Intermolecular C—H···O contacts occur between H10Y (Y = A, C, E and G) and O2X with a range of 2.63 and 2.70Å and connect two molecules into dimeric structures (Fig. 2), respectively (Table 1).
Despite the presence of four independent molecules there is no pseudo- translational symmetry present. The corresponding <|E2-1|> value of 0.985 is close to the expected value of 0.968 for a centrosymmetric structure (SHELXS97, Sheldrick, 1997). An additional test on pseudo-translational symmetry as implemented in the program SIR97 (Altomare et al., 1999) also did not give an indication for pseudo-translational symmetry. The analyses of the normal probability distribution of equivalent bond distances shows that all distances are distributed normally, except three outliers. These outliers belong to the substituents of N24. The corresponding C atoms (C104, C114 and C124) also show rather high anisotropic displacement parameters, which are the reason for the anomalous C—N bonds.