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The title compound, C
26H
30N
4O
6, was synthesized by the reaction of methyl (2-{[3-(3,5-dimethoxyphenyl)-1,2,4-oxadiazol-5-yl]methoxy}phenyl)acetate and
N,
N-dimethylformamide dimethyl acetal. In the molecular structure, there are intramolecular C—H
O and C—H
N hydrogen bonds, and also intermolecular C—H
π and C—H
O interactions.
Supporting information
CCDC reference: 255918
Key indicators
- Single-crystal X-ray study
- T = 293 K
- Mean (C-C) = 0.007 Å
- R factor = 0.072
- wR factor = 0.261
- Data-to-parameter ratio = 15.5
checkCIF/PLATON results
No syntax errors found
Alert level C
RFACR01_ALERT_3_C The value of the weighted R factor is > 0.25
Weighted R factor given 0.261
PLAT026_ALERT_3_C Ratio Observed / Unique Reflections too Low .... 46 Perc.
PLAT084_ALERT_2_C High R2 Value .................................. 0.26
PLAT125_ALERT_4_C No _symmetry_space_group_name_Hall Given ....... ?
PLAT152_ALERT_1_C Supplied and Calc Volume s.u. Inconsistent ..... ?
PLAT220_ALERT_2_C Large Non-Solvent C Ueq(max)/Ueq(min) ... 2.97 Ratio
PLAT222_ALERT_3_C Large Non-Solvent H Ueq(max)/Ueq(min) ... 3.54 Ratio
PLAT340_ALERT_3_C Low Bond Precision on C-C bonds (x 1000) Ang ... 7
PLAT480_ALERT_4_C Long H...A H-Bond Reported H20B .. CG1 .. 2.98 Ang.
PLAT480_ALERT_4_C Long H...A H-Bond Reported H26C .. CG2 .. 2.91 Ang.
PLAT481_ALERT_4_C Long D...A H-Bond Reported C20 .. CG1 .. 3.92 Ang.
PLAT601_ALERT_2_C Structure Contains Solvent Accessible VOIDS of . 34.00 A 3
0 ALERT level A = In general: serious problem
0 ALERT level B = Potentially serious problem
12 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
3 ALERT type 2 Indicator that the structure model may be wrong or deficient
4 ALERT type 3 Indicator that the structure quality may be low
4 ALERT type 4 Improvement, methodology, query or suggestion
Data collection: CAD-4 Software (Enraf–Nonius, 1989); cell refinement: CAD-4 Software; data reduction: XCAD4 (Harms & Wocadlo,1995); program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: SHELXTL (Siemens,1996); software used to prepare material for publication: SHELXL97.
Methyl 2-(2-{1-[3-(3,5-dimethoxyphenyl)-1,2,4-oxadiazol-5-yl]-2-
(dimethylamino)vinyloxy}phenyl)-3-(dimethylamino)acrylate
top
Crystal data top
C26H30N4O6 | Z = 2 |
Mr = 494.54 | F(000) = 524 |
Triclinic, P1 | Dx = 1.280 Mg m−3 |
a = 8.6500 (17) Å | Mo Kα radiation, λ = 0.71073 Å |
b = 10.700 (2) Å | Cell parameters from 25 reflections |
c = 14.817 (3) Å | θ = 9–12° |
α = 107.66 (3)° | µ = 0.09 mm−1 |
β = 97.50 (3)° | T = 293 K |
γ = 95.15 (3)° | Block, colourless |
V = 1283.4 (4) Å3 | 0.3 × 0.2 × 0.1 mm |
Data collection top
Enraf–Nonius CAD-4 diffractometer | Rint = 0.051 |
Radiation source: fine-focus sealed tube | θmax = 26.0°, θmin = 1.5° |
Graphite monochromator | h = 0→10 |
ω/2θ scans | k = −13→13 |
5386 measured reflections | l = −18→18 |
5030 independent reflections | 3 standard reflections every 200 reflections |
2308 reflections with I > 2σ(I) | intensity decay: none |
Refinement top
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)] = 0.072 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.261 | H-atom parameters constrained |
S = 1.04 | w = 1/[σ2(Fo2) + (0.13P)2] where P = (Fo2 + 2Fc2)/3 |
5030 reflections | (Δ/σ)max = 0.001 |
325 parameters | Δρmax = 0.30 e Å−3 |
0 restraints | Δρmin = −0.31 e Å−3 |
Special details top
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. |
Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top | x | y | z | Uiso*/Ueq | |
O4 | 0.2008 (3) | 0.6477 (3) | 0.6165 (2) | 0.0422 (8) | |
O3 | 0.0547 (4) | 0.6917 (3) | 0.7668 (2) | 0.0533 (9) | |
N2 | −0.0138 (4) | 0.4823 (3) | 0.7549 (2) | 0.0428 (9) | |
C2 | −0.2751 (5) | 0.5761 (4) | 1.0384 (3) | 0.0417 (11) | |
C4 | −0.1481 (5) | 0.5243 (4) | 0.8995 (3) | 0.0395 (10) | |
O2 | −0.3198 (4) | 0.6760 (3) | 1.1086 (2) | 0.0566 (9) | |
C3 | −0.1947 (5) | 0.6176 (4) | 0.9754 (3) | 0.0404 (11) | |
H3A | −0.1719 | 0.7074 | 0.9838 | 0.048* | |
C8 | 0.0561 (5) | 0.5641 (4) | 0.7178 (3) | 0.0391 (10) | |
C7 | −0.0624 (5) | 0.5673 (4) | 0.8331 (3) | 0.0380 (10) | |
N1 | −0.0253 (5) | 0.6929 (4) | 0.8451 (3) | 0.0524 (10) | |
O1 | −0.2890 (5) | 0.2174 (3) | 0.9339 (2) | 0.0675 (10) | |
C15 | 0.3841 (5) | 0.8415 (4) | 0.6754 (3) | 0.0431 (11) | |
C10 | 0.3422 (5) | 0.7114 (4) | 0.6734 (3) | 0.0378 (10) | |
C9 | 0.1336 (5) | 0.5367 (4) | 0.6359 (3) | 0.0424 (11) | |
C19 | 0.1288 (5) | 0.4107 (5) | 0.5782 (3) | 0.0473 (11) | |
H19A | 0.0687 | 0.3481 | 0.5958 | 0.057* | |
N3 | 0.1942 (5) | 0.3598 (4) | 0.5009 (3) | 0.0594 (11) | |
C1 | −0.3073 (5) | 0.4429 (4) | 1.0282 (3) | 0.0435 (11) | |
H1B | −0.3594 | 0.4157 | 1.0715 | 0.052* | |
C5 | −0.1817 (5) | 0.3911 (4) | 0.8879 (3) | 0.0427 (11) | |
H5A | −0.1516 | 0.3280 | 0.8371 | 0.051* | |
O6 | 0.3857 (5) | 0.7909 (4) | 0.4875 (2) | 0.0736 (11) | |
C11 | 0.4389 (5) | 0.6536 (5) | 0.7256 (3) | 0.0468 (11) | |
H11A | 0.4096 | 0.5672 | 0.7244 | 0.056* | |
N4 | 0.1334 (5) | 1.0292 (4) | 0.7408 (3) | 0.0630 (12) | |
C6 | −0.2608 (5) | 0.3519 (4) | 0.9529 (3) | 0.0442 (11) | |
C16 | 0.2789 (6) | 0.9039 (4) | 0.6189 (3) | 0.0474 (12) | |
C12 | 0.5788 (6) | 0.7238 (6) | 0.7794 (3) | 0.0593 (14) | |
H12A | 0.6438 | 0.6846 | 0.8147 | 0.071* | |
O5 | 0.1883 (6) | 0.9031 (4) | 0.4601 (3) | 0.0987 (15) | |
C22 | 0.1727 (6) | 0.9867 (4) | 0.6552 (3) | 0.0537 (13) | |
H22A | 0.1185 | 1.0187 | 0.6103 | 0.064* | |
C26 | −0.3762 (6) | 0.6448 (5) | 1.1859 (3) | 0.0597 (14) | |
H26A | −0.4031 | 0.7232 | 1.2295 | 0.090* | |
H26B | −0.2959 | 0.6107 | 1.2190 | 0.090* | |
H26C | −0.4678 | 0.5793 | 1.1614 | 0.090* | |
C17 | 0.2756 (7) | 0.8715 (5) | 0.5172 (4) | 0.0642 (15) | |
C14 | 0.5273 (6) | 0.9081 (5) | 0.7291 (4) | 0.0624 (14) | |
H14A | 0.5593 | 0.9938 | 0.7297 | 0.075* | |
C25 | −0.3652 (7) | 0.1707 (5) | 0.9979 (4) | 0.0706 (16) | |
H25A | −0.3779 | 0.0757 | 0.9767 | 0.106* | |
H25B | −0.4667 | 0.2002 | 0.9996 | 0.106* | |
H25C | −0.3032 | 0.2044 | 1.0609 | 0.106* | |
C24 | 0.2012 (7) | 1.0022 (5) | 0.8251 (4) | 0.0754 (17) | |
H24A | 0.2821 | 0.9471 | 0.8100 | 0.113* | |
H24B | 0.1211 | 0.9575 | 0.8479 | 0.113* | |
H24C | 0.2460 | 1.0840 | 0.8740 | 0.113* | |
C23 | 0.0081 (7) | 1.1133 (6) | 0.7554 (4) | 0.0797 (18) | |
H23A | −0.0321 | 1.1263 | 0.6958 | 0.119* | |
H23B | 0.0496 | 1.1974 | 0.8025 | 0.119* | |
H23C | −0.0753 | 1.0713 | 0.7774 | 0.119* | |
C13 | 0.6233 (6) | 0.8502 (6) | 0.7816 (4) | 0.0681 (15) | |
H13A | 0.7181 | 0.8972 | 0.8184 | 0.082* | |
C18 | 0.3929 (10) | 0.7522 (8) | 0.3874 (4) | 0.114 (3) | |
H18A | 0.4736 | 0.6965 | 0.3741 | 0.170* | |
H18B | 0.4165 | 0.8296 | 0.3691 | 0.170* | |
H18C | 0.2933 | 0.7044 | 0.3517 | 0.170* | |
C20 | 0.2816 (6) | 0.4390 (6) | 0.4553 (4) | 0.0762 (18) | |
H20A | 0.2928 | 0.5307 | 0.4930 | 0.114* | |
H20B | 0.2258 | 0.4267 | 0.3922 | 0.114* | |
H20C | 0.3838 | 0.4118 | 0.4506 | 0.114* | |
C21 | 0.1713 (7) | 0.2199 (5) | 0.4517 (4) | 0.0819 (19) | |
H21A | 0.1133 | 0.1751 | 0.4865 | 0.123* | |
H21B | 0.2718 | 0.1890 | 0.4475 | 0.123* | |
H21C | 0.1136 | 0.2020 | 0.3882 | 0.123* | |
Atomic displacement parameters (Å2) top | U11 | U22 | U33 | U12 | U13 | U23 |
O4 | 0.0405 (18) | 0.0456 (18) | 0.0432 (17) | 0.0009 (14) | 0.0045 (14) | 0.0207 (14) |
O3 | 0.062 (2) | 0.0453 (19) | 0.060 (2) | 0.0128 (16) | 0.0294 (18) | 0.0173 (16) |
N2 | 0.045 (2) | 0.044 (2) | 0.043 (2) | 0.0071 (18) | 0.0135 (17) | 0.0153 (18) |
C2 | 0.042 (3) | 0.049 (3) | 0.033 (2) | 0.010 (2) | 0.007 (2) | 0.011 (2) |
C4 | 0.036 (2) | 0.051 (3) | 0.036 (2) | 0.014 (2) | 0.0085 (19) | 0.016 (2) |
O2 | 0.076 (2) | 0.0520 (19) | 0.0471 (19) | 0.0157 (17) | 0.0273 (18) | 0.0149 (16) |
C3 | 0.049 (3) | 0.036 (2) | 0.038 (2) | 0.004 (2) | 0.009 (2) | 0.015 (2) |
C8 | 0.035 (2) | 0.040 (2) | 0.045 (3) | 0.005 (2) | 0.007 (2) | 0.017 (2) |
C7 | 0.025 (2) | 0.046 (3) | 0.046 (3) | 0.0088 (19) | 0.0052 (19) | 0.016 (2) |
N1 | 0.055 (3) | 0.050 (2) | 0.058 (3) | 0.010 (2) | 0.027 (2) | 0.017 (2) |
O1 | 0.098 (3) | 0.045 (2) | 0.071 (2) | 0.0123 (19) | 0.038 (2) | 0.0230 (18) |
C15 | 0.046 (3) | 0.048 (3) | 0.039 (2) | 0.006 (2) | 0.009 (2) | 0.017 (2) |
C10 | 0.035 (2) | 0.047 (3) | 0.035 (2) | 0.006 (2) | 0.0103 (19) | 0.015 (2) |
C9 | 0.043 (3) | 0.043 (3) | 0.044 (3) | 0.001 (2) | 0.012 (2) | 0.018 (2) |
C19 | 0.038 (3) | 0.055 (3) | 0.049 (3) | 0.001 (2) | 0.010 (2) | 0.017 (2) |
N3 | 0.060 (3) | 0.060 (3) | 0.055 (3) | 0.004 (2) | 0.023 (2) | 0.009 (2) |
C1 | 0.041 (3) | 0.051 (3) | 0.042 (3) | 0.006 (2) | 0.007 (2) | 0.020 (2) |
C5 | 0.044 (3) | 0.046 (3) | 0.040 (2) | 0.015 (2) | 0.012 (2) | 0.011 (2) |
O6 | 0.080 (3) | 0.099 (3) | 0.050 (2) | 0.016 (2) | 0.018 (2) | 0.031 (2) |
C11 | 0.048 (3) | 0.056 (3) | 0.046 (3) | 0.018 (2) | 0.014 (2) | 0.025 (2) |
N4 | 0.071 (3) | 0.050 (2) | 0.062 (3) | 0.019 (2) | 0.002 (2) | 0.009 (2) |
C6 | 0.044 (3) | 0.043 (3) | 0.049 (3) | 0.008 (2) | 0.011 (2) | 0.018 (2) |
C16 | 0.058 (3) | 0.041 (3) | 0.045 (3) | 0.004 (2) | 0.000 (2) | 0.021 (2) |
C12 | 0.042 (3) | 0.096 (4) | 0.050 (3) | 0.021 (3) | 0.005 (2) | 0.034 (3) |
O5 | 0.142 (4) | 0.108 (3) | 0.061 (2) | 0.049 (3) | 0.008 (3) | 0.043 (2) |
C22 | 0.068 (3) | 0.037 (3) | 0.050 (3) | 0.005 (2) | −0.005 (3) | 0.013 (2) |
C26 | 0.074 (4) | 0.067 (3) | 0.048 (3) | 0.021 (3) | 0.032 (3) | 0.019 (2) |
C17 | 0.079 (4) | 0.062 (3) | 0.060 (3) | 0.016 (3) | 0.005 (3) | 0.033 (3) |
C14 | 0.058 (3) | 0.057 (3) | 0.066 (3) | −0.008 (3) | −0.004 (3) | 0.020 (3) |
C25 | 0.098 (5) | 0.044 (3) | 0.072 (4) | −0.003 (3) | 0.023 (3) | 0.021 (3) |
C24 | 0.094 (5) | 0.066 (4) | 0.074 (4) | 0.034 (3) | 0.019 (3) | 0.025 (3) |
C23 | 0.069 (4) | 0.072 (4) | 0.088 (4) | 0.027 (3) | 0.008 (3) | 0.008 (3) |
C13 | 0.051 (3) | 0.084 (4) | 0.061 (3) | 0.002 (3) | −0.004 (3) | 0.018 (3) |
C18 | 0.152 (7) | 0.147 (7) | 0.066 (4) | 0.042 (6) | 0.050 (5) | 0.051 (4) |
C20 | 0.062 (4) | 0.104 (5) | 0.053 (3) | −0.014 (3) | 0.026 (3) | 0.010 (3) |
C21 | 0.090 (5) | 0.060 (4) | 0.081 (4) | 0.001 (3) | 0.034 (4) | −0.005 (3) |
Geometric parameters (Å, º) top
O4—C10 | 1.380 (5) | C11—H11A | 0.9300 |
O4—C9 | 1.400 (5) | N4—C22 | 1.312 (6) |
O3—C8 | 1.340 (5) | N4—C24 | 1.430 (6) |
O3—N1 | 1.423 (4) | N4—C23 | 1.466 (6) |
N2—C8 | 1.311 (5) | C16—C22 | 1.380 (7) |
N2—C7 | 1.380 (5) | C16—C17 | 1.436 (7) |
C2—O2 | 1.371 (5) | C12—C13 | 1.362 (7) |
C2—C1 | 1.385 (6) | C12—H12A | 0.9300 |
C2—C3 | 1.385 (6) | O5—C17 | 1.206 (6) |
C4—C5 | 1.382 (6) | C22—H22A | 0.9300 |
C4—C3 | 1.391 (6) | C26—H26A | 0.9600 |
C4—C7 | 1.460 (6) | C26—H26B | 0.9600 |
O2—C26 | 1.417 (5) | C26—H26C | 0.9600 |
C3—H3A | 0.9300 | C14—C13 | 1.377 (7) |
C8—C9 | 1.427 (6) | C14—H14A | 0.9300 |
C7—N1 | 1.305 (5) | C25—H25A | 0.9600 |
O1—C6 | 1.372 (5) | C25—H25B | 0.9600 |
O1—C25 | 1.405 (6) | C25—H25C | 0.9600 |
C15—C14 | 1.385 (6) | C24—H24A | 0.9600 |
C15—C10 | 1.397 (6) | C24—H24B | 0.9600 |
C15—C16 | 1.491 (6) | C24—H24C | 0.9600 |
C10—C11 | 1.376 (6) | C23—H23A | 0.9600 |
C9—C19 | 1.353 (6) | C23—H23B | 0.9600 |
C19—N3 | 1.333 (5) | C23—H23C | 0.9600 |
C19—H19A | 0.9300 | C13—H13A | 0.9300 |
N3—C21 | 1.435 (6) | C18—H18A | 0.9600 |
N3—C20 | 1.453 (6) | C18—H18B | 0.9600 |
C1—C6 | 1.373 (6) | C18—H18C | 0.9600 |
C1—H1B | 0.9300 | C20—H20A | 0.9600 |
C5—C6 | 1.391 (6) | C20—H20B | 0.9600 |
C5—H5A | 0.9300 | C20—H20C | 0.9600 |
O6—C17 | 1.367 (6) | C21—H21A | 0.9600 |
O6—C18 | 1.424 (6) | C21—H21B | 0.9600 |
C11—C12 | 1.373 (7) | C21—H21C | 0.9600 |
| | | |
C10—O4—C9 | 116.1 (3) | C13—C12—H12A | 119.6 |
C8—O3—N1 | 106.4 (3) | C11—C12—H12A | 119.6 |
C8—N2—C7 | 102.4 (3) | N4—C22—C16 | 132.4 (5) |
O2—C2—C1 | 124.2 (4) | N4—C22—H22A | 113.8 |
O2—C2—C3 | 114.8 (4) | C16—C22—H22A | 113.8 |
C1—C2—C3 | 121.1 (4) | O2—C26—H26A | 109.5 |
C5—C4—C3 | 119.7 (4) | O2—C26—H26B | 109.5 |
C5—C4—C7 | 120.3 (4) | H26A—C26—H26B | 109.5 |
C3—C4—C7 | 120.0 (4) | O2—C26—H26C | 109.5 |
C2—O2—C26 | 118.1 (4) | H26A—C26—H26C | 109.5 |
C2—C3—C4 | 119.6 (4) | H26B—C26—H26C | 109.5 |
C2—C3—H3A | 120.2 | O5—C17—O6 | 120.6 (5) |
C4—C3—H3A | 120.2 | O5—C17—C16 | 128.2 (6) |
N2—C8—O3 | 113.2 (4) | O6—C17—C16 | 111.2 (4) |
N2—C8—C9 | 129.7 (4) | C13—C14—C15 | 121.3 (5) |
O3—C8—C9 | 117.1 (4) | C13—C14—H14A | 119.3 |
N1—C7—N2 | 114.9 (4) | C15—C14—H14A | 119.3 |
N1—C7—C4 | 120.9 (4) | O1—C25—H25A | 109.5 |
N2—C7—C4 | 124.2 (4) | O1—C25—H25B | 109.5 |
C7—N1—O3 | 103.1 (3) | H25A—C25—H25B | 109.5 |
C6—O1—C25 | 117.6 (4) | O1—C25—H25C | 109.5 |
C14—C15—C10 | 117.8 (4) | H25A—C25—H25C | 109.5 |
C14—C15—C16 | 121.6 (4) | H25B—C25—H25C | 109.5 |
C10—C15—C16 | 120.6 (4) | N4—C24—H24A | 109.5 |
C11—C10—O4 | 123.7 (4) | N4—C24—H24B | 109.5 |
C11—C10—C15 | 120.7 (4) | H24A—C24—H24B | 109.5 |
O4—C10—C15 | 115.7 (4) | N4—C24—H24C | 109.5 |
C19—C9—O4 | 123.7 (4) | H24A—C24—H24C | 109.5 |
C19—C9—C8 | 120.5 (4) | H24B—C24—H24C | 109.5 |
O4—C9—C8 | 115.6 (4) | N4—C23—H23A | 109.5 |
N3—C19—C9 | 131.9 (4) | N4—C23—H23B | 109.5 |
N3—C19—H19A | 114.0 | H23A—C23—H23B | 109.5 |
C9—C19—H19A | 114.0 | N4—C23—H23C | 109.5 |
C19—N3—C21 | 121.2 (4) | H23A—C23—H23C | 109.5 |
C19—N3—C20 | 123.9 (4) | H23B—C23—H23C | 109.5 |
C21—N3—C20 | 114.8 (4) | C12—C13—C14 | 119.7 (5) |
C6—C1—C2 | 118.7 (4) | C12—C13—H13A | 120.2 |
C6—C1—H1B | 120.7 | C14—C13—H13A | 120.2 |
C2—C1—H1B | 120.7 | O6—C18—H18A | 109.5 |
C4—C5—C6 | 119.6 (4) | O6—C18—H18B | 109.5 |
C4—C5—H5A | 120.2 | H18A—C18—H18B | 109.5 |
C6—C5—H5A | 120.2 | O6—C18—H18C | 109.5 |
C17—O6—C18 | 116.0 (5) | H18A—C18—H18C | 109.5 |
C12—C11—C10 | 119.8 (5) | H18B—C18—H18C | 109.5 |
C12—C11—H11A | 120.1 | N3—C20—H20A | 109.5 |
C10—C11—H11A | 120.1 | N3—C20—H20B | 109.5 |
C22—N4—C24 | 126.6 (5) | H20A—C20—H20B | 109.5 |
C22—N4—C23 | 119.1 (5) | N3—C20—H20C | 109.5 |
C24—N4—C23 | 114.3 (5) | H20A—C20—H20C | 109.5 |
O1—C6—C1 | 124.1 (4) | H20B—C20—H20C | 109.5 |
O1—C6—C5 | 114.5 (4) | N3—C21—H21A | 109.5 |
C1—C6—C5 | 121.3 (4) | N3—C21—H21B | 109.5 |
C22—C16—C17 | 114.9 (4) | H21A—C21—H21B | 109.5 |
C22—C16—C15 | 125.2 (4) | N3—C21—H21C | 109.5 |
C17—C16—C15 | 119.8 (4) | H21A—C21—H21C | 109.5 |
C13—C12—C11 | 120.7 (5) | H21B—C21—H21C | 109.5 |
Hydrogen-bond geometry (Å, º) top
D—H···A | D—H | H···A | D···A | D—H···A |
C5—H5A···N2 | 0.93 | 2.62 | 2.933 (5) | 100 |
C19—H19A···N2 | 0.93 | 2.59 | 2.960 (5) | 104 |
C20—H20A···O4 | 0.96 | 2.17 | 2.943 (5) | 136 |
C22—H22A···O5 | 0.93 | 2.38 | 2.780 (6) | 106 |
C20—H20B···Cg1i | 0.96 | 2.98 | 3.921 (6) | 169 |
C26—H26C···Cg2ii | 0.96 | 2.91 | 3.723 (5) | 143 |
C23—H23A···O5iii | 0.96 | 2.43 | 3.362 (7) | 162 |
C23—H23B···O2iv | 0.96 | 2.56 | 3.339 (7) | 138 |
C24—H24C···O2iv | 0.96 | 2.52 | 3.305 (7) | 139 |
Symmetry codes: (i) −x, −y+1, −z+1; (ii) −x−1, −y+1, −z+2; (iii) −x, −y+2, −z+1; (iv) −x, −y+2, −z+2. |
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