1,4-Dihex-yloxy-2,5-bis-(2-nitro-phen-yl)benzene.

The title compound, C(30)H(36)N(2)O(6), was prepared via twofold Suzuki coupling of a diboronic acid with bromo-nitro-benzene. The mol-ecule is located on a crystallographic inversion centre. The lateral benzene ring and the central ring make a dihedral angle of 48.75 (14)° and the nitro group is twisted by 41.47 (13)° out of the plane of the benzene ring. The nitro and hex-yloxy groups are in close proximity and the hex-yloxy chain adopts an all-anti conformation.

Related literature

For the synthesis of carbazoles and heteroanalogous carbazoles, see: Letessier et al. (2011 ▶); Dassonneville et al. (2011 ▶); Nissen & Detert (2011 ▶); Letessier & Detert (2012 ▶). For the Cadogan reaction, see: Cadogan (1962 ▶). For Suzuki cross-couplings see Miyaura & Suzuki (1995 ▶). For π-systems for optoelectronic applications, see: Nemkovich et al. (2009 ▶). For structures of substituted p-terphenyls, see: Jones et al. (2005 ▶), Moschel et al. (2011 ▶). For torsion in biphenyls, see: Miao et al. (2009 ▶); Fischer et al. (2007 ▶).

Experimental

Crystal data

C30H36N2O6

M = 520.61

Monoclinic,

a = 7.9314 (4) Å

b = 19.2029 (17) Å

c = 9.1247 (5) Å

β = 96.368 (5)°

V = 1381.17 (16) Å3

Z = 2

Mo Kα radiation

μ = 0.09 mm−1

T = 193 K

0.44 × 0.30 × 0.20 mm

Data collection

Stoe IPDS 2T diffractometer

8154 measured reflections

3331 independent reflections

2610 reflections with I > 2σ(I)

R int = 0.026

Refinement

R[F 2 > 2σ(F 2)] = 0.044

wR(F 2) = 0.120

S = 1.07

3331 reflections

173 parameters

H-atom parameters constrained

Δρmax = 0.31 e Å−3

Δρmin = −0.27 e Å−3

Data collection: X-AREA (Stoe & Cie, 2011 ▶); cell refinement: X-AREA; data reduction: X-RED (Stoe & Cie, 2011 ▶); 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 datablock(s) I, global. DOI: 10.1107/S1600536812009944/bt5839sup1.cif

Structure factors: contains datablock(s) I. DOI: 10.1107/S1600536812009944/bt5839Isup2.hkl

Supplementary material file. DOI: 10.1107/S1600536812009944/bt5839Isup3.cml

Additional supplementary materials: crystallographic information; 3D view; checkCIF report

C30H36N2O6	F(000) = 556
Mr = 520.61	Dx = 1.252 Mg m−3
Monoclinic, P21/n	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2yn	Cell parameters from 7928 reflections
a = 7.9314 (4) Å	θ = 3.2–29.1°
b = 19.2029 (17) Å	µ = 0.09 mm−1
c = 9.1247 (5) Å	T = 193 K
β = 96.368 (5)°	Block, yellow
V = 1381.17 (16) Å3	0.44 × 0.30 × 0.20 mm
Z = 2

Stoe IPDS 2T diffractometer	2610 reflections with I > 2σ(I)
Radiation source: sealed X-ray tube, 12 x 0.4 mm long-fine focus	Rint = 0.026
Plane graphite monochromator	θmax = 28.0°, θmin = 3.2°
Detector resolution: 6.67 pixels mm-1	h = −10→10
ω scan	k = −25→22
8154 measured reflections	l = −12→10
3331 independent reflections

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)] = 0.044	Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.120	H-atom parameters constrained
S = 1.07	w = 1/[σ2(Fo2) + (0.0562P)2 + 0.4038P] where P = (Fo2 + 2Fc2)/3
3331 reflections	(Δ/σ)max < 0.001
173 parameters	Δρmax = 0.31 e Å−3
0 restraints	Δρmin = −0.27 e Å−3

Experimental. 1H-NMR (400 MHz, CDCl3): δ = 7.95 (dd, 3J = 8.5 Hz, 4J= 1.2 Hz, 2 H, 3-H); 7.64 (dt, 3J = 7.5 Hz, 4J = 1.4 Hz, 2 H, 4-H); 7.49 - 7.45 (m, 4 H); 6.83 (s, 2 H, 2-H); 3.81 (bs (t), 4 H, O—CH2); 1.59 - 1.54 (m, 4 H); 1.25 - 1.18 (m, 12 H); 0.80 (t, 3J = 6.9 Hz, 6 H, CH3).13C-NMR (75 MHz, CDCl3): δ = 149.7 (s, 2-C), 149.5 (s), 132.9 (s), 132.6 (d), 132.5 (d), 128.1 (d), 127.8 (s), 123.9 (d), 113.4 (d), 69.1 (t), 31.3 (t), 28.8 (t), 25.4 (t), 22.5 (t), 13.8 (q).IR (ATR): ν = 3734, 3585, 3070, 2944, 2869, 2855, 2363, 2334, 1608, 1573, 1530, 1510, 1469, 1441, 1387, 1358, 1290, 1255, 1209, 1165, 1144, 1025, 997, 870, 860.MS (EI): m/z = 520 (100%, M+.).

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
C1	0.46215 (15)	0.52525 (7)	0.35512 (14)	0.0240 (3)
C2	0.35820 (15)	0.54228 (7)	0.46442 (14)	0.0252 (3)
C3	0.60362 (16)	0.48321 (8)	0.39358 (14)	0.0264 (3)
H3	0.6756	0.4717	0.3206	0.032*
C4	0.43305 (15)	0.55452 (7)	0.20336 (14)	0.0232 (3)
C5	0.57076 (16)	0.58310 (8)	0.14150 (15)	0.0299 (3)
H5	0.6801	0.5811	0.1956	0.036*
C6	0.55321 (18)	0.61424 (8)	0.00394 (16)	0.0338 (3)
H6	0.6502	0.6318	−0.0362	0.041*
C7	0.39481 (18)	0.61991 (8)	−0.07522 (16)	0.0309 (3)
H7	0.3820	0.6432	−0.1676	0.037*
C8	0.25493 (17)	0.59149 (7)	−0.01925 (15)	0.0273 (3)
H8	0.1456	0.5945	−0.0732	0.033*
C9	0.27660 (15)	0.55862 (7)	0.11640 (14)	0.0225 (3)
N10	0.12608 (13)	0.52343 (6)	0.16019 (12)	0.0271 (3)
O11	−0.01207 (12)	0.55180 (6)	0.13048 (12)	0.0381 (3)
O12	0.14470 (14)	0.46637 (6)	0.21901 (12)	0.0380 (3)
O13	0.22425 (12)	0.58564 (6)	0.42244 (10)	0.0314 (2)
C14	0.11269 (18)	0.60345 (9)	0.52871 (16)	0.0330 (3)
H14A	0.1748	0.6300	0.6106	0.040*
H14B	0.0665	0.5607	0.5699	0.040*
C15	−0.02962 (17)	0.64694 (9)	0.45359 (16)	0.0330 (3)
H15A	0.0189	0.6874	0.4055	0.040*
H15B	−0.0946	0.6188	0.3758	0.040*
C16	−0.1481 (2)	0.67270 (12)	0.5597 (2)	0.0560 (6)
H16A	−0.1793	0.6328	0.6201	0.067*
H16B	−0.0862	0.7067	0.6274	0.067*
C17	−0.30865 (18)	0.70652 (8)	0.49024 (18)	0.0344 (3)
H17A	−0.2781	0.7465	0.4299	0.041*
H17B	−0.3715	0.6726	0.4231	0.041*
C18	−0.4239 (3)	0.73189 (14)	0.5993 (3)	0.0670 (7)
H18A	−0.4492	0.6924	0.6631	0.080*
H18B	−0.3626	0.7675	0.6632	0.080*
C19	−0.5889 (2)	0.76264 (11)	0.5319 (3)	0.0602 (6)
H19A	−0.5662	0.8048	0.4767	0.090*
H19B	−0.6592	0.7745	0.6101	0.090*
H19C	−0.6488	0.7287	0.4650	0.090*

	U11	U22	U33	U12	U13	U23
C1	0.0190 (5)	0.0341 (7)	0.0187 (6)	0.0020 (5)	0.0005 (4)	−0.0030 (5)
C2	0.0172 (5)	0.0358 (7)	0.0218 (6)	0.0056 (5)	−0.0005 (4)	−0.0031 (5)
C3	0.0204 (6)	0.0391 (7)	0.0199 (6)	0.0049 (5)	0.0027 (5)	−0.0037 (5)
C4	0.0202 (5)	0.0296 (6)	0.0198 (6)	0.0027 (5)	0.0023 (4)	−0.0032 (5)
C5	0.0189 (6)	0.0436 (8)	0.0271 (7)	−0.0031 (5)	0.0017 (5)	−0.0039 (6)
C6	0.0302 (7)	0.0441 (8)	0.0285 (7)	−0.0111 (6)	0.0094 (6)	−0.0021 (6)
C7	0.0375 (7)	0.0326 (7)	0.0229 (6)	−0.0045 (6)	0.0040 (5)	0.0024 (5)
C8	0.0260 (6)	0.0322 (7)	0.0228 (6)	0.0003 (5)	−0.0010 (5)	0.0010 (5)
C9	0.0186 (5)	0.0268 (6)	0.0219 (6)	−0.0002 (5)	0.0020 (4)	−0.0012 (5)
N10	0.0210 (5)	0.0398 (7)	0.0201 (5)	−0.0036 (5)	0.0009 (4)	−0.0006 (5)
O11	0.0178 (4)	0.0605 (7)	0.0353 (6)	0.0027 (4)	0.0006 (4)	−0.0021 (5)
O12	0.0358 (5)	0.0425 (6)	0.0351 (6)	−0.0098 (5)	0.0014 (4)	0.0114 (5)
O13	0.0239 (4)	0.0492 (6)	0.0213 (5)	0.0155 (4)	0.0029 (4)	0.0003 (4)
C14	0.0277 (6)	0.0471 (9)	0.0254 (7)	0.0141 (6)	0.0078 (5)	0.0025 (6)
C15	0.0248 (6)	0.0453 (8)	0.0288 (7)	0.0118 (6)	0.0030 (5)	0.0009 (6)
C16	0.0502 (10)	0.0811 (14)	0.0402 (9)	0.0427 (10)	0.0203 (8)	0.0197 (9)
C17	0.0254 (6)	0.0330 (7)	0.0459 (9)	0.0059 (6)	0.0090 (6)	0.0019 (6)
C18	0.0543 (11)	0.0902 (16)	0.0615 (13)	0.0435 (11)	0.0297 (10)	0.0211 (12)
C19	0.0324 (8)	0.0556 (12)	0.0951 (17)	0.0150 (8)	0.0188 (10)	0.0009 (11)

C1—C3	1.3952 (18)	O13—C14	1.4250 (15)
C1—C2	1.4014 (17)	C14—C15	1.5065 (19)
C1—C4	1.4886 (18)	C14—H14A	0.9900
C2—O13	1.3705 (15)	C14—H14B	0.9900
C2—C3i	1.3867 (19)	C15—C16	1.506 (2)
C3—C2i	1.3867 (19)	C15—H15A	0.9900
C3—H3	0.9500	C15—H15B	0.9900
C4—C5	1.3963 (18)	C16—C17	1.505 (2)
C4—C9	1.3990 (17)	C16—H16A	0.9900
C5—C6	1.383 (2)	C16—H16B	0.9900
C5—H5	0.9500	C17—C18	1.505 (2)
C6—C7	1.382 (2)	C17—H17A	0.9900
C6—H6	0.9500	C17—H17B	0.9900
C7—C8	1.3838 (19)	C18—C19	1.503 (3)
C7—H7	0.9500	C18—H18A	0.9900
C8—C9	1.3831 (18)	C18—H18B	0.9900
C8—H8	0.9500	C19—H19A	0.9800
C9—N10	1.4655 (16)	C19—H19B	0.9800
N10—O12	1.2218 (16)	C19—H19C	0.9800
N10—O11	1.2268 (15)
C3—C1—C2	118.44 (12)	O13—C14—H14B	110.0
C3—C1—C4	119.33 (11)	C15—C14—H14B	110.0
C2—C1—C4	122.08 (11)	H14A—C14—H14B	108.4
O13—C2—C3i	123.90 (11)	C16—C15—C14	112.27 (12)
O13—C2—C1	116.22 (11)	C16—C15—H15A	109.2
C3i—C2—C1	119.85 (12)	C14—C15—H15A	109.2
C2i—C3—C1	121.70 (11)	C16—C15—H15B	109.2
C2i—C3—H3	119.2	C14—C15—H15B	109.2
C1—C3—H3	119.2	H15A—C15—H15B	107.9
C5—C4—C9	115.65 (12)	C17—C16—C15	115.45 (14)
C5—C4—C1	118.49 (11)	C17—C16—H16A	108.4
C9—C4—C1	125.82 (11)	C15—C16—H16A	108.4
C6—C5—C4	122.16 (12)	C17—C16—H16B	108.4
C6—C5—H5	118.9	C15—C16—H16B	108.4
C4—C5—H5	118.9	H16A—C16—H16B	107.5
C7—C6—C5	120.15 (12)	C18—C17—C16	114.11 (15)
C7—C6—H6	119.9	C18—C17—H17A	108.7
C5—C6—H6	119.9	C16—C17—H17A	108.7
C6—C7—C8	119.71 (13)	C18—C17—H17B	108.7
C6—C7—H7	120.1	C16—C17—H17B	108.7
C8—C7—H7	120.1	H17A—C17—H17B	107.6
C9—C8—C7	119.02 (12)	C19—C18—C17	114.93 (19)
C9—C8—H8	120.5	C19—C18—H18A	108.5
C7—C8—H8	120.5	C17—C18—H18A	108.5
C8—C9—C4	123.21 (12)	C19—C18—H18B	108.5
C8—C9—N10	115.49 (11)	C17—C18—H18B	108.5
C4—C9—N10	121.17 (11)	H18A—C18—H18B	107.5
O12—N10—O11	123.84 (12)	C18—C19—H19A	109.5
O12—N10—C9	118.09 (11)	C18—C19—H19B	109.5
O11—N10—C9	118.01 (12)	H19A—C19—H19B	109.5
C2—O13—C14	118.44 (10)	C18—C19—H19C	109.5
O13—C14—C15	108.30 (11)	H19A—C19—H19C	109.5
O13—C14—H14A	110.0	H19B—C19—H19C	109.5
C15—C14—H14A	110.0
C3—C1—C2—O13	177.82 (12)	C7—C8—C9—N10	−173.60 (12)
C4—C1—C2—O13	2.17 (19)	C5—C4—C9—C8	−3.0 (2)
C3—C1—C2—C3i	−0.7 (2)	C1—C4—C9—C8	174.57 (13)
C4—C1—C2—C3i	−176.30 (13)	C5—C4—C9—N10	172.61 (12)
C2—C1—C3—C2i	0.7 (2)	C1—C4—C9—N10	−9.8 (2)
C4—C1—C3—C2i	176.44 (13)	C8—C9—N10—O12	138.53 (13)
C3—C1—C4—C5	−44.37 (18)	C4—C9—N10—O12	−37.39 (18)
C2—C1—C4—C5	131.25 (14)	C8—C9—N10—O11	−38.71 (17)
C3—C1—C4—C9	138.15 (14)	C4—C9—N10—O11	145.37 (13)
C2—C1—C4—C9	−46.2 (2)	C3i—C2—O13—C14	−2.8 (2)
C9—C4—C5—C6	0.8 (2)	C1—C2—O13—C14	178.78 (13)
C1—C4—C5—C6	−176.95 (13)	C2—O13—C14—C15	−176.02 (12)
C4—C5—C6—C7	2.1 (2)	O13—C14—C15—C16	−175.95 (16)
C5—C6—C7—C8	−2.9 (2)	C14—C15—C16—C17	−170.43 (16)
C6—C7—C8—C9	0.8 (2)	C15—C16—C17—C18	−179.81 (19)
C7—C8—C9—C4	2.2 (2)	C16—C17—C18—C19	−177.1 (2)