Literature DB >> 21754774

N,N-Dihexyl-4-[2-(4-nitro-phen-yl)vin-yl]aniline.

Dieter Schollmeyer1, Heiner Detert.   

Abstract

The title compound, C(26)H(36)N(2)O(2), was prepared by Horner olefination of p-dihexyl-amino-benzaldehyde and diethyl p-nitro-benzyl-phospho-nate. It crystallizes with two independent mol-ecules in the asymmetric unit. Both have similar geometries of the π-systems but the conformations of all hexyl chains are different. Whereas one hexyl chain of the first mol-ecule shows the typical all-anti conformation, the second is arranged in a gauche-anti-gauche-anti conformation with N-C-C-C, C-C-C-C, C-C-C-C and C-C-C-C torsion angles of -65.1 (4), 167.3 (3), 63.3 (4), and 179.4 (3)°. One of the hexyl chains in the other mol-ecule has an anti-anti-gauche-anti conformation [N-C-C-C, C-C-C-C, C-C-C-C and C-C-C-C torsion angles = 179.6 (3), -179.8 (3), -68.7 (5) and -178.8 (4)°], the other starts with an anti-gauche-gauche sequence. Molecules A and B are composed of five planar subunits. The angle sums around the N atoms are in the range 356 (2)-360.0 (2)°. Torsion angles between these segments do not exceed 4.9 (4)°, except for one of the alkyl chains each [molecule A = 26.2 (4)°; molecule B = -6.0 (4)°]. The high planarity of the molecules and the short aniline C-N bonds [1.385 (3) Å in molecule A and 1.378 (3) Å in molecule B] indicate a strong electronic coupling through the stilbene unit. One methylene group is disordered over two positions with an occupancy ratio of 0.72:0.28.

Entities:  

Year:  2011        PMID: 21754774      PMCID: PMC3120587          DOI: 10.1107/S1600536811016709

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


Related literature

For chromophores and fluoro­phores based on quadrupolar donor–acceptor-substituted stilbenoid systems, see: Detert & Sugiono (2005 ▶); Strehmel et al. (2003 ▶); Nemkovich et al. (2010 ▶). Similar amino­nitro­stilbenes had been prepared earlier, see: Pfeiffer et al. (1915 ▶); Chardonnens & Heinrich (1939 ▶); Meier et al. (2004 ▶). The optical properties of these dyes are strongly dependent on charge transfer and torsion angles, see: Baumann et al. (1977 ▶); Goerner (1998 ▶); Dekhtyar & Rettig (2007 ▶). Conjugated oligomers with basic sites are sensing materials for polarity and cations, see: Wilson & Bunz (2005 ▶); Zucchero et al. (2009 ▶). For a comparable compound, see: Fischer et al. (2011 ▶).

Experimental

Crystal data

C26H36N2O2 M = 408.57 Triclinic, a = 9.6574 (9) Å b = 11.4153 (10) Å c = 23.604 (2) Å α = 93.297 (3)° β = 94.834 (3)° γ = 112.696 (3)° V = 2380.6 (4) Å3 Z = 4 Mo Kα radiation μ = 0.07 mm−1 T = 173 K 0.54 × 0.37 × 0.06 mm

Data collection

Bruker SMART APEXII diffractometer Absorption correction: multi-scan (PLATON; Spek, 2009 ▶) T min = 0.936, T max = 0.996 90478 measured reflections 11464 independent reflections 7228 reflections with I > 2σ(I) R int = 0.062

Refinement

R[F 2 > 2σ(F 2)] = 0.082 wR(F 2) = 0.239 S = 1.02 11464 reflections 553 parameters H-atom parameters constrained Δρmax = 0.76 e Å−3 Δρmin = −0.46 e Å−3 Data collection: APEX2 (Bruker, 2006 ▶); cell refinement: SAINT (Bruker, 2006 ▶); data reduction: SAINT; program(s) used to solve structure: SIR97 (Altomare et al., 1999 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: PLATON (Spek, 2009 ▶); software used to prepare material for publication: PLATON. Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536811016709/bt5539sup1.cif Structure factors: contains datablocks I. DOI: 10.1107/S1600536811016709/bt5539Isup2.hkl Supplementary material file. DOI: 10.1107/S1600536811016709/bt5539Isup3.cml Additional supplementary materials: crystallographic information; 3D view; checkCIF report
C26H36N2O2Z = 4
Mr = 408.57F(000) = 888
Triclinic, P1Dx = 1.140 Mg m3
Hall symbol: -P 1Melting point: 351 K
a = 9.6574 (9) ÅMo Kα radiation, λ = 0.71073 Å
b = 11.4153 (10) ÅCell parameters from 9897 reflections
c = 23.604 (2) Åθ = 2.2–27°
α = 93.297 (3)°µ = 0.07 mm1
β = 94.834 (3)°T = 173 K
γ = 112.696 (3)°Plate, red
V = 2380.6 (4) Å30.54 × 0.37 × 0.06 mm
Bruker SMART APEXII diffractometer11464 independent reflections
Radiation source: sealed Tube7228 reflections with I > 2σ(I)
graphiteRint = 0.062
CCD scanθmax = 28.0°, θmin = 1.7°
Absorption correction: multi-scan (PLATON; Spek, 2009)h = −12→12
Tmin = 0.936, Tmax = 0.996k = −15→15
90478 measured reflectionsl = −31→31
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.082Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.239H-atom parameters constrained
S = 1.02w = 1/[σ2(Fo2) + (0.0941P)2 + 2.795P] where P = (Fo2 + 2Fc2)/3
11464 reflections(Δ/σ)max < 0.001
553 parametersΔρmax = 0.76 e Å3
0 restraintsΔρmin = −0.46 e Å3
Experimental. 1H-NMR (CDCl3): δ = 8.13 ("d", J = 8.4 Hz, 2 H, 3-H, 5-H, Ph-NO2); 7.52 ("d", J = 8.4 Hz, 2 H, 2-H, 6-H, Ph-NO2); 7.39 ("d", J = 8.3 Hz, 2 H, 3-H, 5-H Ph-NHex2); 7.17 (d, J = 16.5 Hz, 1 H, vin); 6.87 (d, J = 16.5 Hz, 1 H, vin); 6.62 ("d", J = 8.1 Hz, 2 H, 2-H, 6-H PhNHex2); 3.23 ("t", 4 H, NCH2); 1.60 (m, 4 H, CH2); 1.27 (m, 12 H, CH2); 0.90 ("t", 6 H, CH3). 13C-NMR (CDCl3): δ = 148.7, 145.6, 145.2, 133.8, 128.6, 125.9, 124.1, 123.1, 120.7, 111.5, 51.1, 31.7, 27.3, 26.8, 22.7, 14.1.
Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes.
Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger.
xyzUiso*/UeqOcc. (<1)
C1A0.7433 (2)0.6361 (2)0.55422 (10)0.0267 (5)
C2A0.6830 (3)0.5037 (2)0.55662 (11)0.0292 (5)
H2A0.63120.44940.52300.035*
C3A0.6969 (3)0.4498 (2)0.60700 (11)0.0299 (5)
H3A0.65650.35980.60780.036*
C4A0.7708 (3)0.5296 (2)0.65599 (11)0.0286 (5)
C5A0.8300 (3)0.6620 (3)0.65598 (11)0.0333 (5)
H5A0.87840.71540.69020.040*
C6A0.8169 (3)0.7144 (2)0.60510 (11)0.0316 (5)
H6A0.85820.80450.60460.038*
C7A0.7272 (3)0.6856 (2)0.49919 (11)0.0289 (5)
H7A0.68000.62400.46730.035*
C8A0.7720 (3)0.8085 (2)0.48902 (11)0.0280 (5)
H8A0.82200.87020.52060.034*
C9A0.7519 (2)0.8571 (2)0.43441 (10)0.0253 (5)
C10A0.6745 (3)0.7776 (2)0.38404 (11)0.0285 (5)
H10A0.63910.68770.38460.034*
C11A0.6488 (3)0.8271 (2)0.33405 (11)0.0296 (5)
H11A0.59530.77040.30130.036*
C12A0.7001 (3)0.9604 (2)0.33048 (11)0.0288 (5)
C13A0.7832 (3)1.0403 (2)0.38008 (11)0.0301 (5)
H13A0.82321.13030.37920.036*
C14A0.8068 (3)0.9889 (2)0.42997 (11)0.0285 (5)
H14A0.86251.04540.46260.034*
N15A0.6672 (3)1.0079 (2)0.28070 (9)0.0358 (5)
C16A0.5310 (3)0.9287 (3)0.24208 (12)0.0367 (6)
H16A0.47980.98400.22870.044*
H16B0.46120.86500.26410.044*
C17A0.5583 (3)0.8580 (3)0.18967 (11)0.0365 (6)
H17A0.61240.92100.16370.044*
H17B0.62380.81350.20220.044*
C18A0.4126 (3)0.7616 (3)0.15729 (12)0.0426 (7)
H18A0.34630.80610.14570.051*
H18B0.35980.69790.18320.051*
C19A0.4365 (3)0.6919 (3)0.10420 (13)0.0492 (7)
H19A0.48560.75530.07760.059*
H19B0.50610.65030.11560.059*
C20A0.2913 (4)0.5916 (4)0.07301 (16)0.0611 (9)
H20A0.22110.63280.06180.073*
H20B0.24260.52750.09940.073*
C21A0.3172 (6)0.5242 (5)0.0199 (2)0.0898 (14)
H21A0.35590.5857−0.00800.135*
H21B0.22160.45620.00320.135*
H21C0.39090.48710.03040.135*
C22A0.7282 (4)1.1465 (3)0.27664 (12)0.0441 (7)
H22A0.82411.18640.30230.053*
H22B0.65621.18090.29050.053*
C23A0.7578 (3)1.1851 (3)0.21672 (13)0.0458 (7)
H23A0.66261.14280.19080.055*
H23B0.78651.27830.21740.055*
C24A0.8803 (3)1.1523 (3)0.19208 (13)0.0414 (6)
H24A0.86471.06350.19870.050*
H24B0.98021.20940.21210.050*
C25A0.8794 (4)1.1664 (4)0.12703 (16)0.0613 (9)
H25A0.95471.13660.11250.074*
H25B0.77881.10960.10760.074*
C26A0.9133 (5)1.2980 (4)0.11120 (16)0.0713 (11)
H26A1.01381.35570.13050.086*
H26B0.83741.32800.12490.086*
C27A0.9124 (7)1.3054 (6)0.04722 (19)0.1085 (18)
H27A0.99061.27960.03370.163*
H27B0.93261.39320.03870.163*
H27C0.81331.24820.02790.163*
N28A0.7893 (2)0.4731 (2)0.70886 (10)0.0372 (5)
O29A0.8486 (3)0.5447 (2)0.75293 (9)0.0525 (6)
O30A0.7460 (3)0.3564 (2)0.70650 (10)0.0582 (6)
C1B0.7306 (3)0.1556 (2)0.55379 (10)0.0259 (5)
C2B0.8781 (3)0.1709 (2)0.57579 (11)0.0295 (5)
H2B0.96210.22480.55850.035*
C3B0.9028 (3)0.1091 (2)0.62198 (11)0.0299 (5)
H3B1.00250.11980.63610.036*
C4B0.7792 (3)0.0308 (2)0.64740 (10)0.0284 (5)
C5B0.6329 (3)0.0132 (2)0.62734 (11)0.0324 (5)
H5B0.5497−0.04040.64510.039*
C6B0.6098 (3)0.0750 (2)0.58092 (11)0.0311 (5)
H6B0.50950.06260.56690.037*
C7B0.6979 (3)0.2171 (2)0.50471 (10)0.0283 (5)
H7B0.59430.19470.49180.034*
C8B0.7989 (3)0.3022 (2)0.47587 (10)0.0281 (5)
H8B0.90250.32540.48910.034*
C9B0.7659 (3)0.3625 (2)0.42645 (10)0.0267 (5)
C10B0.8844 (3)0.4518 (2)0.40158 (11)0.0328 (5)
H10B0.98530.47350.41820.039*
C11B0.8600 (3)0.5092 (3)0.35394 (11)0.0352 (6)
H11B0.94410.56970.33910.042*
C12B0.7125 (3)0.4798 (2)0.32682 (11)0.0306 (5)
C13B0.5924 (3)0.3903 (2)0.35199 (11)0.0320 (5)
H13B0.49140.36760.33530.038*
C14B0.6190 (3)0.3355 (2)0.40022 (11)0.0301 (5)
H14B0.53520.27750.41620.036*
N15B0.6857 (3)0.5360 (2)0.27927 (10)0.0399 (5)
C16B0.8077 (4)0.6393 (3)0.25697 (14)0.0484 (7)
H16C0.88250.69120.28930.058*
H16D0.76510.69530.23820.058*
C17B0.8870 (4)0.5911 (3)0.21473 (15)0.0531 (8)
H17C0.81400.54160.18150.064*
H17D0.92910.53410.23290.064*
C18B1.0185 (4)0.7074 (4)0.19407 (18)0.0707 (11)
H18C1.08460.75910.22840.085*
H18D1.07960.67280.17210.085*
C19B0.9767 (6)0.7943 (5)0.1586 (2)0.0883 (15)
H19C0.91550.82960.18010.106*0.72
H19D1.07020.86660.15230.106*0.72
H19E0.86620.76580.15900.106*0.28
H19F1.02180.87810.18170.106*0.28
C20B0.8959 (6)0.7375 (5)0.1057 (3)0.0666 (14)0.72
H20C0.79420.67600.11170.080*0.72
H20D0.94810.68930.08680.080*0.72
C20C1.0014 (17)0.8248 (15)0.0996 (6)0.068 (4)0.28
H20E1.02290.75580.07990.081*0.28
H20F1.09350.90410.10120.081*0.28
C21B0.8777 (7)0.8424 (5)0.0632 (2)0.1038 (18)
H21D0.81360.88180.07910.156*0.72
H21E0.83120.79900.02530.156*0.72
H21F0.97750.90850.06020.156*0.72
H21G0.82650.88250.08700.156*0.28
H21H0.80490.75920.04560.156*0.28
H21I0.92070.89710.03330.156*0.28
C22B0.5380 (3)0.4863 (3)0.24494 (12)0.0399 (6)
H22C0.53260.55150.22000.048*
H22D0.45850.47120.27080.048*
C23B0.5053 (3)0.3612 (3)0.20748 (14)0.0473 (7)
H23C0.58470.37660.18160.057*
H23D0.51160.29630.23250.057*
C24B0.3527 (4)0.3085 (4)0.17207 (16)0.0614 (9)
H24C0.34620.37270.14670.074*
H24D0.27290.29280.19780.074*
C25B0.3234 (5)0.1819 (4)0.13500 (18)0.0762 (12)
H25C0.34020.12140.16040.091*
H25D0.21570.14420.11890.091*
C26B0.4170 (5)0.1923 (5)0.0872 (2)0.0840 (13)
H26C0.52510.22680.10260.101*
H26D0.40190.25270.06130.101*
C27B0.3756 (7)0.0624 (5)0.0532 (2)0.1055 (18)
H27D0.39010.00240.07880.158*
H27E0.44060.07210.02260.158*
H27F0.26970.02970.03660.158*
N28B0.8047 (3)−0.0349 (2)0.69623 (10)0.0383 (5)
O29B0.9345 (3)−0.0210 (2)0.71236 (10)0.0575 (6)
O30B0.6945 (3)−0.1038 (2)0.71804 (10)0.0596 (6)
U11U22U33U12U13U23
C1A0.0187 (10)0.0273 (12)0.0363 (13)0.0110 (9)0.0049 (9)0.0032 (10)
C2A0.0235 (11)0.0274 (12)0.0366 (13)0.0103 (10)0.0048 (9)−0.0006 (10)
C3A0.0227 (11)0.0271 (12)0.0420 (14)0.0112 (10)0.0078 (10)0.0051 (10)
C4A0.0209 (11)0.0343 (13)0.0363 (13)0.0157 (10)0.0081 (9)0.0057 (10)
C5A0.0281 (12)0.0386 (14)0.0339 (13)0.0151 (11)0.0007 (10)−0.0012 (11)
C6A0.0284 (12)0.0262 (12)0.0402 (14)0.0114 (10)0.0028 (10)0.0016 (10)
C7A0.0228 (11)0.0276 (12)0.0358 (13)0.0100 (10)0.0020 (9)0.0010 (10)
C8A0.0197 (11)0.0283 (12)0.0359 (13)0.0096 (9)0.0038 (9)0.0011 (10)
C9A0.0170 (10)0.0252 (11)0.0365 (13)0.0103 (9)0.0077 (9)0.0046 (9)
C10A0.0229 (11)0.0223 (11)0.0405 (13)0.0083 (9)0.0069 (10)0.0036 (10)
C11A0.0280 (12)0.0280 (12)0.0327 (12)0.0105 (10)0.0058 (10)0.0015 (10)
C12A0.0249 (11)0.0306 (12)0.0357 (13)0.0139 (10)0.0111 (10)0.0070 (10)
C13A0.0278 (12)0.0228 (11)0.0410 (14)0.0101 (10)0.0098 (10)0.0027 (10)
C14A0.0222 (11)0.0256 (12)0.0381 (13)0.0097 (9)0.0058 (9)0.0010 (10)
N15A0.0406 (12)0.0324 (11)0.0357 (12)0.0147 (10)0.0066 (9)0.0077 (9)
C16A0.0326 (13)0.0430 (15)0.0418 (15)0.0208 (12)0.0088 (11)0.0118 (12)
C17A0.0317 (13)0.0415 (15)0.0393 (14)0.0165 (12)0.0062 (11)0.0076 (11)
C18A0.0302 (14)0.0505 (17)0.0442 (16)0.0120 (12)0.0047 (11)0.0087 (13)
C19A0.0385 (16)0.0561 (19)0.0482 (17)0.0134 (14)0.0042 (13)0.0054 (14)
C20A0.054 (2)0.060 (2)0.060 (2)0.0147 (17)−0.0010 (16)−0.0039 (17)
C21A0.085 (3)0.087 (3)0.084 (3)0.026 (3)0.005 (2)−0.026 (3)
C22A0.0618 (19)0.0332 (14)0.0434 (16)0.0226 (14)0.0147 (14)0.0107 (12)
C23A0.0422 (16)0.0447 (16)0.0552 (18)0.0197 (13)0.0109 (13)0.0155 (14)
C24A0.0304 (14)0.0432 (16)0.0539 (17)0.0160 (12)0.0098 (12)0.0130 (13)
C25A0.0460 (19)0.070 (2)0.071 (2)0.0246 (17)0.0136 (16)0.0029 (19)
C26A0.063 (2)0.080 (3)0.063 (2)0.015 (2)0.0167 (19)0.021 (2)
C27A0.129 (5)0.131 (5)0.060 (3)0.040 (4)0.014 (3)0.036 (3)
N28A0.0298 (11)0.0476 (14)0.0411 (13)0.0211 (10)0.0074 (9)0.0115 (11)
O29A0.0680 (15)0.0632 (14)0.0372 (11)0.0392 (12)−0.0007 (10)0.0037 (10)
O30A0.0649 (15)0.0431 (12)0.0606 (14)0.0135 (11)0.0012 (11)0.0210 (11)
C1B0.0266 (12)0.0211 (11)0.0322 (12)0.0114 (9)0.0067 (9)0.0009 (9)
C2B0.0210 (11)0.0297 (12)0.0373 (13)0.0083 (10)0.0081 (9)0.0035 (10)
C3B0.0225 (11)0.0302 (12)0.0366 (13)0.0104 (10)0.0031 (9)0.0012 (10)
C4B0.0304 (12)0.0261 (12)0.0326 (12)0.0142 (10)0.0072 (10)0.0049 (9)
C5B0.0252 (12)0.0308 (13)0.0426 (14)0.0104 (10)0.0120 (10)0.0074 (11)
C6B0.0203 (11)0.0304 (12)0.0448 (14)0.0111 (10)0.0076 (10)0.0064 (11)
C7B0.0250 (11)0.0267 (12)0.0361 (13)0.0132 (10)0.0048 (9)0.0010 (10)
C8B0.0244 (11)0.0279 (12)0.0345 (13)0.0130 (10)0.0041 (9)0.0006 (10)
C9B0.0251 (11)0.0252 (11)0.0332 (12)0.0128 (9)0.0075 (9)0.0018 (9)
C10B0.0232 (12)0.0349 (13)0.0393 (14)0.0098 (10)0.0051 (10)0.0044 (11)
C11B0.0258 (12)0.0352 (14)0.0424 (15)0.0081 (11)0.0083 (11)0.0095 (11)
C12B0.0304 (13)0.0292 (12)0.0369 (13)0.0154 (10)0.0084 (10)0.0072 (10)
C13B0.0246 (12)0.0351 (13)0.0404 (14)0.0154 (10)0.0065 (10)0.0059 (11)
C14B0.0258 (12)0.0282 (12)0.0376 (13)0.0101 (10)0.0106 (10)0.0070 (10)
N15B0.0327 (12)0.0424 (13)0.0471 (13)0.0154 (10)0.0067 (10)0.0167 (11)
C16B0.0522 (18)0.0490 (18)0.0496 (17)0.0233 (15)0.0124 (14)0.0159 (14)
C17B0.0476 (18)0.058 (2)0.063 (2)0.0310 (16)0.0076 (15)0.0102 (16)
C18B0.051 (2)0.092 (3)0.076 (3)0.028 (2)0.0311 (19)0.031 (2)
C19B0.101 (4)0.085 (3)0.100 (4)0.047 (3)0.053 (3)0.036 (3)
C20B0.052 (3)0.050 (3)0.098 (4)0.025 (2)−0.002 (3)−0.010 (3)
C20C0.072 (9)0.079 (10)0.060 (8)0.034 (8)0.011 (7)0.029 (7)
C21B0.128 (5)0.109 (4)0.095 (4)0.077 (4)−0.021 (3)−0.002 (3)
C22B0.0383 (15)0.0479 (16)0.0432 (15)0.0257 (13)0.0066 (12)0.0127 (13)
C23B0.0376 (16)0.0514 (18)0.0565 (19)0.0209 (14)0.0056 (13)0.0078 (14)
C24B0.0423 (18)0.075 (2)0.071 (2)0.0289 (17)0.0038 (16)−0.0003 (19)
C25B0.053 (2)0.089 (3)0.074 (3)0.020 (2)−0.0077 (19)−0.009 (2)
C26B0.074 (3)0.094 (3)0.080 (3)0.031 (3)−0.003 (2)0.007 (3)
C27B0.145 (5)0.113 (4)0.078 (3)0.078 (4)0.000 (3)−0.013 (3)
N28B0.0439 (13)0.0387 (13)0.0393 (12)0.0223 (11)0.0091 (10)0.0095 (10)
O29B0.0466 (13)0.0743 (16)0.0606 (14)0.0321 (12)0.0014 (10)0.0250 (12)
O30B0.0543 (14)0.0668 (15)0.0651 (15)0.0247 (12)0.0219 (11)0.0365 (12)
C1A—C2A1.401 (3)C3B—C4B1.394 (3)
C1A—C6A1.411 (3)C3B—H3B0.9500
C1A—C7A1.466 (3)C4B—C5B1.385 (3)
C2A—C3A1.390 (3)C4B—N28B1.465 (3)
C2A—H2A0.9500C5B—C6B1.384 (4)
C3A—C4A1.384 (4)C5B—H5B0.9500
C3A—H3A0.9500C6B—H6B0.9500
C4A—C5A1.394 (4)C7B—C8B1.347 (3)
C4A—N28A1.466 (3)C7B—H7B0.9500
C5A—C6A1.390 (4)C8B—C9B1.461 (3)
C5A—H5A0.9500C8B—H8B0.9500
C6A—H6A0.9500C9B—C10B1.406 (3)
C7A—C8A1.342 (3)C9B—C14B1.408 (3)
C7A—H7A0.9500C10B—C11B1.381 (4)
C8A—C9A1.460 (3)C10B—H10B0.9500
C8A—H8A0.9500C11B—C12B1.416 (4)
C9A—C14A1.403 (3)C11B—H11B0.9500
C9A—C10A1.414 (3)C12B—N15B1.378 (3)
C10A—C11A1.382 (3)C12B—C13B1.419 (3)
C10A—H10A0.9500C13B—C14B1.382 (3)
C11A—C12A1.417 (3)C13B—H13B0.9500
C11A—H11A0.9500C14B—H14B0.9500
C12A—N15A1.385 (3)N15B—C22B1.463 (4)
C12A—C13A1.414 (4)N15B—C16B1.469 (4)
C13A—C14A1.386 (3)C16B—C17B1.508 (4)
C13A—H13A0.9500C16B—H16C0.9900
C14A—H14A0.9500C16B—H16D0.9900
N15A—C16A1.471 (3)C17B—C18B1.578 (5)
N15A—C22A1.471 (3)C17B—H17C0.9900
C16A—C17A1.535 (4)C17B—H17D0.9900
C16A—H16A0.9900C18B—C19B1.482 (6)
C16A—H16B0.9900C18B—H18C0.9900
C17A—C18A1.518 (4)C18B—H18D0.9900
C17A—H17A0.9900C19B—C20B1.393 (7)
C17A—H17B0.9900C19B—C20C1.472 (13)
C18A—C19A1.527 (4)C19B—H19C0.9900
C18A—H18A0.9900C19B—H19D0.9900
C18A—H18B0.9900C19B—H19E0.9900
C19A—C20A1.520 (4)C19B—H19F0.9900
C19A—H19A0.9900C20B—C21B1.655 (7)
C19A—H19B0.9900C20B—H20C0.9900
C20A—C21A1.523 (5)C20B—H20D0.9900
C20A—H20A0.9900C20C—C21B1.495 (14)
C20A—H20B0.9900C20C—H20E0.9900
C21A—H21A0.9800C20C—H20F0.9900
C21A—H21B0.9800C21B—H21D0.9800
C21A—H21C0.9800C21B—H21E0.9800
C22A—C23A1.523 (4)C21B—H21F0.9800
C22A—H22A0.9900C21B—H21G0.9800
C22A—H22B0.9900C21B—H21H0.9800
C23A—C24A1.520 (4)C21B—H21I0.9800
C23A—H23A0.9900C22B—C23B1.543 (4)
C23A—H23B0.9900C22B—H22C0.9900
C24A—C25A1.553 (5)C22B—H22D0.9900
C24A—H24A0.9900C23B—C24B1.511 (4)
C24A—H24B0.9900C23B—H23C0.9900
C25A—C26A1.487 (5)C23B—H23D0.9900
C25A—H25A0.9900C24B—C25B1.559 (5)
C25A—H25B0.9900C24B—H24C0.9900
C26A—C27A1.517 (5)C24B—H24D0.9900
C26A—H26A0.9900C25B—C26B1.487 (6)
C26A—H26B0.9900C25B—H25C0.9900
C27A—H27A0.9800C25B—H25D0.9900
C27A—H27B0.9800C26B—C27B1.534 (6)
C27A—H27C0.9800C26B—H26C0.9900
N28A—O30A1.229 (3)C26B—H26D0.9900
N28A—O29A1.232 (3)C27B—H27D0.9800
C1B—C6B1.408 (3)C27B—H27E0.9800
C1B—C2B1.415 (3)C27B—H27F0.9800
C1B—C7B1.462 (3)N28B—O29B1.225 (3)
C2B—C3B1.385 (3)N28B—O30B1.229 (3)
C2B—H2B0.9500
C2A—C1A—C6A117.9 (2)C6B—C5B—H5B120.6
C2A—C1A—C7A118.5 (2)C4B—C5B—H5B120.6
C6A—C1A—C7A123.6 (2)C5B—C6B—C1B122.0 (2)
C3A—C2A—C1A121.6 (2)C5B—C6B—H6B119.0
C3A—C2A—H2A119.2C1B—C6B—H6B119.0
C1A—C2A—H2A119.2C8B—C7B—C1B127.0 (2)
C4A—C3A—C2A118.8 (2)C8B—C7B—H7B116.5
C4A—C3A—H3A120.6C1B—C7B—H7B116.5
C2A—C3A—H3A120.6C7B—C8B—C9B126.9 (2)
C3A—C4A—C5A121.6 (2)C7B—C8B—H8B116.6
C3A—C4A—N28A119.0 (2)C9B—C8B—H8B116.6
C5A—C4A—N28A119.4 (2)C10B—C9B—C14B115.9 (2)
C6A—C5A—C4A118.9 (2)C10B—C9B—C8B120.1 (2)
C6A—C5A—H5A120.5C14B—C9B—C8B123.9 (2)
C4A—C5A—H5A120.5C11B—C10B—C9B122.6 (2)
C5A—C6A—C1A121.0 (2)C11B—C10B—H10B118.7
C5A—C6A—H6A119.5C9B—C10B—H10B118.7
C1A—C6A—H6A119.5C10B—C11B—C12B121.4 (2)
C8A—C7A—C1A127.0 (2)C10B—C11B—H11B119.3
C8A—C7A—H7A116.5C12B—C11B—H11B119.3
C1A—C7A—H7A116.5N15B—C12B—C11B122.4 (2)
C7A—C8A—C9A126.7 (2)N15B—C12B—C13B121.5 (2)
C7A—C8A—H8A116.6C11B—C12B—C13B116.1 (2)
C9A—C8A—H8A116.6C14B—C13B—C12B121.6 (2)
C14A—C9A—C10A116.1 (2)C14B—C13B—H13B119.2
C14A—C9A—C8A120.4 (2)C12B—C13B—H13B119.2
C10A—C9A—C8A123.4 (2)C13B—C14B—C9B122.3 (2)
C11A—C10A—C9A121.8 (2)C13B—C14B—H14B118.8
C11A—C10A—H10A119.1C9B—C14B—H14B118.8
C9A—C10A—H10A119.1C12B—N15B—C22B121.4 (2)
C10A—C11A—C12A121.7 (2)C12B—N15B—C16B121.7 (2)
C10A—C11A—H11A119.2C22B—N15B—C16B116.6 (2)
C12A—C11A—H11A119.2N15B—C16B—C17B113.0 (3)
N15A—C12A—C13A122.6 (2)N15B—C16B—H16C109.0
N15A—C12A—C11A120.7 (2)C17B—C16B—H16C109.0
C13A—C12A—C11A116.7 (2)N15B—C16B—H16D109.0
C14A—C13A—C12A120.8 (2)C17B—C16B—H16D109.0
C14A—C13A—H13A119.6H16C—C16B—H16D107.8
C12A—C13A—H13A119.6C16B—C17B—C18B109.8 (3)
C13A—C14A—C9A122.8 (2)C16B—C17B—H17C109.7
C13A—C14A—H14A118.6C18B—C17B—H17C109.7
C9A—C14A—H14A118.6C16B—C17B—H17D109.7
C12A—N15A—C16A118.6 (2)C18B—C17B—H17D109.7
C12A—N15A—C22A120.0 (2)H17C—C17B—H17D108.2
C16A—N15A—C22A117.4 (2)C19B—C18B—C17B118.0 (3)
N15A—C16A—C17A115.4 (2)C19B—C18B—H18C107.8
N15A—C16A—H16A108.4C17B—C18B—H18C107.8
C17A—C16A—H16A108.4C19B—C18B—H18D107.8
N15A—C16A—H16B108.4C17B—C18B—H18D107.8
C17A—C16A—H16B108.4H18C—C18B—H18D107.1
H16A—C16A—H16B107.5C20B—C19B—C18B114.5 (5)
C18A—C17A—C16A112.6 (2)C20C—C19B—C18B131.5 (7)
C18A—C17A—H17A109.1C20B—C19B—H19C108.6
C16A—C17A—H17A109.1C20C—C19B—H19C119.7
C18A—C17A—H17B109.1C18B—C19B—H19C108.6
C16A—C17A—H17B109.1C20B—C19B—H19D108.6
H17A—C17A—H17B107.8C18B—C19B—H19D108.6
C17A—C18A—C19A113.6 (2)H19C—C19B—H19D107.6
C17A—C18A—H18A108.8C20C—C19B—H19E104.4
C19A—C18A—H18A108.8C18B—C19B—H19E104.4
C17A—C18A—H18B108.8C20C—C19B—H19F104.4
C19A—C18A—H18B108.8C18B—C19B—H19F104.4
H18A—C18A—H18B107.7H19E—C19B—H19F105.6
C20A—C19A—C18A113.7 (3)C19B—C20B—C21B112.8 (4)
C20A—C19A—H19A108.8C19B—C20B—H20C109.0
C18A—C19A—H19A108.8C21B—C20B—H20C109.0
C20A—C19A—H19B108.8C19B—C20B—H20D109.0
C18A—C19A—H19B108.8C21B—C20B—H20D109.0
H19A—C19A—H19B107.7H20C—C20B—H20D107.8
C19A—C20A—C21A112.9 (3)C19B—C20C—C21B117.9 (10)
C19A—C20A—H20A109.0C19B—C20C—H20E107.8
C21A—C20A—H20A109.0C21B—C20C—H20E107.8
C19A—C20A—H20B109.0C19B—C20C—H20F107.8
C21A—C20A—H20B109.0C21B—C20C—H20F107.8
H20A—C20A—H20B107.8H20E—C20C—H20F107.2
C20A—C21A—H21A109.5C20C—C21B—H21D121.9
C20A—C21A—H21B109.5C20B—C21B—H21D109.5
H21A—C21A—H21B109.5C20C—C21B—H21E126.7
C20A—C21A—H21C109.5C20B—C21B—H21E109.5
H21A—C21A—H21C109.5H21D—C21B—H21E109.5
H21B—C21A—H21C109.5C20B—C21B—H21F109.5
N15A—C22A—C23A114.5 (2)H21D—C21B—H21F109.5
N15A—C22A—H22A108.6H21E—C21B—H21F109.5
C23A—C22A—H22A108.6C20C—C21B—H21G109.5
N15A—C22A—H22B108.6C20B—C21B—H21G100.2
C23A—C22A—H22B108.6H21E—C21B—H21G121.3
H22A—C22A—H22B107.6H21F—C21B—H21G106.3
C24A—C23A—C22A114.9 (2)C20C—C21B—H21H109.5
C24A—C23A—H23A108.5H21D—C21B—H21H103.3
C22A—C23A—H23A108.5H21G—C21B—H21H109.5
C24A—C23A—H23B108.5C20C—C21B—H21I109.5
C22A—C23A—H23B108.5H21D—C21B—H21I102.6
H23A—C23A—H23B107.5H21G—C21B—H21I109.5
C23A—C24A—C25A111.7 (2)H21H—C21B—H21I109.5
C23A—C24A—H24A109.3N15B—C22B—C23B113.5 (2)
C25A—C24A—H24A109.3N15B—C22B—H22C108.9
C23A—C24A—H24B109.3C23B—C22B—H22C108.9
C25A—C24A—H24B109.3N15B—C22B—H22D108.9
H24A—C24A—H24B107.9C23B—C22B—H22D108.9
C26A—C25A—C24A115.0 (3)H22C—C22B—H22D107.7
C26A—C25A—H25A108.5C24B—C23B—C22B113.9 (3)
C24A—C25A—H25A108.5C24B—C23B—H23C108.8
C26A—C25A—H25B108.5C22B—C23B—H23C108.8
C24A—C25A—H25B108.5C24B—C23B—H23D108.8
H25A—C25A—H25B107.5C22B—C23B—H23D108.8
C25A—C26A—C27A112.3 (4)H23C—C23B—H23D107.7
C25A—C26A—H26A109.1C23B—C24B—C25B112.5 (3)
C27A—C26A—H26A109.1C23B—C24B—H24C109.1
C25A—C26A—H26B109.1C25B—C24B—H24C109.1
C27A—C26A—H26B109.1C23B—C24B—H24D109.1
H26A—C26A—H26B107.9C25B—C24B—H24D109.1
C26A—C27A—H27A109.5H24C—C24B—H24D107.8
C26A—C27A—H27B109.5C26B—C25B—C24B116.3 (4)
H27A—C27A—H27B109.5C26B—C25B—H25C108.2
C26A—C27A—H27C109.5C24B—C25B—H25C108.2
H27A—C27A—H27C109.5C26B—C25B—H25D108.2
H27B—C27A—H27C109.5C24B—C25B—H25D108.2
O30A—N28A—O29A123.6 (2)H25C—C25B—H25D107.4
O30A—N28A—C4A117.8 (2)C25B—C26B—C27B111.4 (4)
O29A—N28A—C4A118.5 (2)C25B—C26B—H26C109.3
C6B—C1B—C2B117.2 (2)C27B—C26B—H26C109.3
C6B—C1B—C7B119.1 (2)C25B—C26B—H26D109.3
C2B—C1B—C7B123.7 (2)C27B—C26B—H26D109.3
C3B—C2B—C1B121.5 (2)H26C—C26B—H26D108.0
C3B—C2B—H2B119.3C26B—C27B—H27D109.5
C1B—C2B—H2B119.3C26B—C27B—H27E109.5
C2B—C3B—C4B119.0 (2)H27D—C27B—H27E109.5
C2B—C3B—H3B120.5C26B—C27B—H27F109.5
C4B—C3B—H3B120.5H27D—C27B—H27F109.5
C5B—C4B—C3B121.6 (2)H27E—C27B—H27F109.5
C5B—C4B—N28B119.3 (2)O29B—N28B—O30B123.2 (2)
C3B—C4B—N28B119.2 (2)O29B—N28B—C4B118.4 (2)
C6B—C5B—C4B118.9 (2)O30B—N28B—C4B118.4 (2)
C6A—C1A—C2A—C3A−1.3 (3)C2B—C3B—C4B—C5B0.4 (4)
C7A—C1A—C2A—C3A178.5 (2)C2B—C3B—C4B—N28B179.9 (2)
C1A—C2A—C3A—C4A0.8 (3)C3B—C4B—C5B—C6B0.0 (4)
C2A—C3A—C4A—C5A0.5 (3)N28B—C4B—C5B—C6B−179.5 (2)
C2A—C3A—C4A—N28A−178.4 (2)C4B—C5B—C6B—C1B−0.4 (4)
C3A—C4A—C5A—C6A−1.4 (3)C2B—C1B—C6B—C5B0.3 (4)
N28A—C4A—C5A—C6A177.5 (2)C7B—C1B—C6B—C5B179.6 (2)
C4A—C5A—C6A—C1A0.9 (4)C6B—C1B—C7B—C8B175.9 (2)
C2A—C1A—C6A—C5A0.4 (3)C2B—C1B—C7B—C8B−4.8 (4)
C7A—C1A—C6A—C5A−179.4 (2)C1B—C7B—C8B—C9B179.3 (2)
C2A—C1A—C7A—C8A177.2 (2)C7B—C8B—C9B—C10B178.8 (2)
C6A—C1A—C7A—C8A−3.0 (4)C7B—C8B—C9B—C14B−2.4 (4)
C1A—C7A—C8A—C9A−178.2 (2)C14B—C9B—C10B—C11B−0.7 (4)
C7A—C8A—C9A—C14A−179.1 (2)C8B—C9B—C10B—C11B178.3 (2)
C7A—C8A—C9A—C10A2.7 (4)C9B—C10B—C11B—C12B−0.7 (4)
C14A—C9A—C10A—C11A−2.7 (3)C10B—C11B—C12B—N15B180.0 (2)
C8A—C9A—C10A—C11A175.6 (2)C10B—C11B—C12B—C13B1.1 (4)
C9A—C10A—C11A—C12A0.7 (4)N15B—C12B—C13B—C14B−178.9 (2)
C10A—C11A—C12A—N15A−177.1 (2)C11B—C12B—C13B—C14B0.0 (4)
C10A—C11A—C12A—C13A1.9 (3)C12B—C13B—C14B—C9B−1.5 (4)
N15A—C12A—C13A—C14A176.5 (2)C10B—C9B—C14B—C13B1.8 (4)
C11A—C12A—C13A—C14A−2.5 (3)C8B—C9B—C14B—C13B−177.1 (2)
C12A—C13A—C14A—C9A0.4 (4)C11B—C12B—N15B—C22B167.1 (2)
C10A—C9A—C14A—C13A2.1 (3)C13B—C12B—N15B—C22B−14.0 (4)
C8A—C9A—C14A—C13A−176.1 (2)C11B—C12B—N15B—C16B−6.0 (4)
C13A—C12A—N15A—C16A−152.7 (2)C13B—C12B—N15B—C16B172.9 (3)
C11A—C12A—N15A—C16A26.2 (3)C12B—N15B—C16B—C17B88.2 (3)
C13A—C12A—N15A—C22A4.3 (4)C22B—N15B—C16B—C17B−85.2 (3)
C11A—C12A—N15A—C22A−176.7 (2)N15B—C16B—C17B—C18B−178.6 (3)
C12A—N15A—C16A—C17A−100.9 (3)C16B—C17B—C18B—C19B−67.8 (5)
C22A—N15A—C16A—C17A101.5 (3)C17B—C18B—C19B—C20B−63.9 (6)
N15A—C16A—C17A—C18A170.3 (2)C17B—C18B—C19B—C20C−117.3 (10)
C16A—C17A—C18A—C19A178.8 (2)C20C—C19B—C20B—C21B−45.2 (9)
C17A—C18A—C19A—C20A177.7 (3)C18B—C19B—C20B—C21B−170.0 (4)
C18A—C19A—C20A—C21A179.5 (3)C20B—C19B—C20C—C21B55.2 (10)
C12A—N15A—C22A—C23A149.4 (2)C18B—C19B—C20C—C21B141.3 (8)
C16A—N15A—C22A—C23A−53.3 (3)C19B—C20C—C21B—C20B−48.7 (8)
N15A—C22A—C23A—C24A−65.1 (4)C19B—C20B—C21B—C20C49.5 (9)
C22A—C23A—C24A—C25A167.3 (3)C12B—N15B—C22B—C23B−74.1 (3)
C23A—C24A—C25A—C26A63.3 (4)C16B—N15B—C22B—C23B99.4 (3)
C24A—C25A—C26A—C27A179.4 (3)N15B—C22B—C23B—C24B179.6 (3)
C3A—C4A—N28A—O30A4.3 (3)C22B—C23B—C24B—C25B−179.8 (3)
C5A—C4A—N28A—O30A−174.7 (2)C23B—C24B—C25B—C26B−68.7 (5)
C3A—C4A—N28A—O29A−176.5 (2)C24B—C25B—C26B—C27B−178.8 (4)
C5A—C4A—N28A—O29A4.6 (3)C5B—C4B—N28B—O29B178.0 (2)
C6B—C1B—C2B—C3B0.1 (3)C3B—C4B—N28B—O29B−1.6 (4)
C7B—C1B—C2B—C3B−179.1 (2)C5B—C4B—N28B—O30B−0.2 (4)
C1B—C2B—C3B—C4B−0.4 (4)C3B—C4B—N28B—O30B−179.8 (2)
  8 in total

1.  The influence of sigma and pi acceptors on two-photon absorption and solvatochromism of dipolar and quadrupolar unsaturated organic compounds.

Authors:  Bernd Strehmel; Ananda M Sarker; Heiner Detert
Journal:  Chemphyschem       Date:  2003-03-17       Impact factor: 3.102

2.  Charge-transfer transitions in twisted stilbenoids: interchangeable features and generic distinctions of single- and double-bond twists.

Authors:  M Dekhtyar; W Rettig
Journal:  J Phys Chem A       Date:  2007-02-28       Impact factor: 2.781

3.  A short history of SHELX.

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

4.  Switching of intramolecular charge transfer in cruciforms: metal ion sensing.

Authors:  James N Wilson; Uwe H F Bunz
Journal:  J Am Chem Soc       Date:  2005-03-30       Impact factor: 15.419

5.  Extension of conjugation leading to bathochromic or hypsochromic effects in OPV series.

Authors:  Herbert Meier; Jürgen Gerold; Heinz Kolshorn; Bastian Mühling
Journal:  Chemistry       Date:  2004-01-23       Impact factor: 5.236

6.  Bis(4'-dibutylaminostyryl)benzene: spectroscopic behavior upon protonation or methylation.

Authors:  Anthony J Zucchero; Juan Tolosa; Laren M Tolbert; Uwe H F Bunz
Journal:  Chemistry       Date:  2009-12-07       Impact factor: 5.236

7.  Monoclinic polymorph of 2,5-bis[4-(dimethyl-amino)-styr-yl]-3,6-dimethyl-pyrazine.

Authors:  Janina Fischer; Volker Schmitt; Dieter Schollmeyer; Heiner Detert
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-03-12

8.  Structure validation in chemical crystallography.

Authors:  Anthony L Spek
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2009-01-20
  8 in total
  2 in total

1.  (E)-N,N-Diethyl-2,6-diisopropyl-4-[2-(4-nitro-phen-yl)ethen-yl]aniline.

Authors:  Christoph Wink; Dieter Schollmeyer; Heiner Detert
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-11-20

2.  {2-[(9,9-Dihexyl-fluoren-2-yl)carbon-yl]phen-yl}(4-meth-oxy-phen-yl)methanone.

Authors:  P Narayanan; K Sethusankar; Meganathan Nandakumar; Arasambattu K Mohanakrishnan
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-06-20
  2 in total

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