Crystal structure of 4-bromo-N-(2-bromo-3-nitro­benz­yl)-2-nitro­naphthalen-1-amine

Singh, V.P.; Venkateshwaran, K.; Singh, H.B.; Butcher, R.J.

doi:10.1107/S160053681401719X

organic compounds

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ISSN: 2056-9890

Volume 70| Part 9| September 2014| Pages o960-o961

doi:10.1107/S160053681401719X

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Crystal structure of 4-bromo-N-(2-bromo-3-nitrobenzyl)-2-nitronaphthalen-1-amine

Vijay P. Singh,^a Krishnan Venkateshwaran,^a Harkesh B. Singh ^a and Ray J. Butcher ^b ^*

^aDepartment of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400 076, India, and ^bDepartment of Chemistry, Howard University, 525 College Street NW, Washington, DC 20059, USA
^*Correspondence e-mail: rbutcher99@yahoo.com

Edited by E. R. T. Tiekink, University of Malaya, Malaysia (Received 27 June 2014; accepted 25 July 2014; online 1 August 2014)

In the title compound, C₁₇H₁₁Br₂N₃O₄, the dihedral angle between the planes of the naphthalene system and the benzene ring is 52.86 (8)°. The nitro substituent and the attached naphthalene system are almost coplanar [dihedral angle = 5.6 (4)°], probably as a consequence of an intramolecular N—H⋯O hydrogen bond with the amine group. The nitro substituent attached to the benzene ring is disordered over two sets of sites with occupancies of 0.694 (3) and 0.306 (3). The major component deviates significantly from the ring plane [dihedral angle = 53.6 (2)°]. In the crystal, the molecules are linked into a three-dimensional array by extensive π–π interactions involving both the naphthalene and benzene rings [range of centroid–centroid distances = 3.5295 (16)–3.9629 (18) Å] and C—H⋯O interactions involving the methylene H atoms and the phenyl-attached nitro group.

Keywords: crystal structure; naphthalen-1-amine; π–π interactions; hydrogen bonding; arylselenium compounds; photoluminescent selenospirocyclic compounds.

CCDC reference: 1015963

1. Related literature

For the role of secondary interactions in stabilizing organoselenium compounds, see; Singh et al. (2010 , 2012 ); Mugesh & Singh (2000 ). For the isolation of novel photoluminescent selenospirocyclic compounds via intermolecular C—C bond formation, see: Singh et al. (2011 ).

2. Experimental

2.1. Crystal data

C₁₇H₁₁Br₂N₃O₄
M_r = 481.11
Triclinic, $[P \overline 1]$
a = 8.3675 (4) Å
b = 8.5812 (5) Å
c = 12.2691 (5) Å
α = 76.973 (4)°
β = 81.053 (4)°
γ = 76.302 (5)°
V = 829.00 (8) Å³
Z = 2
Mo Kα radiation
μ = 4.92 mm⁻¹
T = 123 K
0.44 × 0.32 × 0.12 mm

2.2. Data collection

Agilent Xcalibur (Ruby, Gemini) diffractometer
Absorption correction: multi-scan (CrysAlis PRO; Agilent, 2012 ) T_min = 0.345, T_max = 1.000
12164 measured reflections
6700 independent reflections
4118 reflections with I > 2σ(I)
R_int = 0.033

2.3. Refinement

R[F² > 2σ(F²)] = 0.053
wR(F²) = 0.129
S = 1.02
6700 reflections
246 parameters
1 restraint
H atoms treated by a mixture of independent and constrained refinement
Δρ_max = 1.04 e Å⁻³
Δρ_min = −0.77 e Å⁻³

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N1—H1N⋯O2	0.84 (3)	1.91 (3)	2.624 (3)	141 (3)
C12—H12B⋯O4Aⁱ	0.99	2.54	3.532 (4)	177
C12—H12B⋯O4Bⁱ	0.99	2.61	3.462 (8)	144
Symmetry code: (i) x-1, y, z.

Data collection: CrysAlis PRO (Agilent, 2012); cell refinement: CrysAlis PRO; data reduction: CrysAlis PRO; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ); program(s) used to refine structure: SHELXL2013 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: WinGX (Farrugia, 2012 ).

Supporting information

CCDC reference: 1015963

Crystal structure: contains datablock I. DOI: 10.1107/S160053681401719X/tk5325sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S160053681401719X/tk5325Isup2.hkl

Supporting information file. DOI: 10.1107/S160053681401719X/tk5325Isup3.cml

checkCIF report

Comment top

Arylselenium compounds having one ortho-coordinating group have been widely studied as reagents in organic synthesis, glutathione peroxidase mimics, and precursors for the synthesis of macrocycles (Singh et al., 2012; Mugesh & Singh, 2000). Introduction of a second ortho-coordinating group towards selenium leads to interesting reactivity of the selenium derivatives and isolation of unusual species (Singh et al., 2010). Recently, we reported the isolation of novel photoluminescent selenospirocyclic compounds via intermolecular C—C bond formation (Singh et al., 2011). In continuation of this research, we attempted the synthesis of naphthylamine based spirocyclic compounds. However, the reaction led to the isolation of 4-bromo-N-(2-bromo-3-nitrobenzyl)-2-nitronaphthalen-1-amine (2) instead of the desired spiro-compound (3) (Fig. 1).

In the structure of the title compound, Fig. 2, the naphthyl nitro substituent is almost coplanar with the naphthyl ring (dihedral angle = 5.6 (4)°) probably as a consequence of an intramolecular hydrogen bond with the N—H moiety. However, the nitro substituent attached to the benzene deviates significantly from the ring plane (dihedral angle = 53.6 (2)° for the major component); this is disordered with occupancies of 0.694 (3) and 0.306 (3). The dihedral angle between the two ring systems is 52.86 (8)°. The molecules are linked into a three-dimensional array, Fig. 3, by extensive π–π interactions involving both the naphthyl ring (Cg1; C1, C2, C3, C4, C5, C10: Cg2; C5, C6, C7, C8, C9, C10) and benzene ring (Cg3; C13, C14, C15, C16, C17, C18), see Table 1, and, in addition, there are weak intermolecular C—H···O interactions involving the methylene H atoms and the benzenenitro group, Table 2.

Experimental top

Referring to Fig. 1, to a stirred solution of selenide 1 (0.400 g 1 mmol in 3 mL CHCl₃) at 0° C, was added bromine (0.05 ml in 1 mL CHCl₃). After 30 mins a yellow precipitate was formed. Stirring was continued for further 30 mins, Et₃N (0.140 ml) added and the stirring continued for an additional 6 h. After completion of the reaction, the reaction mixture was poured into water and extracted with CHCl₃ (2 × 30 mL). The combined organic layers were dried over sodium sulfate and evaporated on a rotary evaporator to get a brown solid. Yield: 0.230 g (49 %); ¹H NMR (CDCl₃): δ [ppm] = 7.57-7.83 (m, 6H), 8.12 (s, CH, 1H), 8.29-8.32 (d, J = 8.43 Hz, 1H), 8.55-8.58 (dd, J = 0.73, 7.33 Hz, 1H), 8.66-8.69 (dd, J = 0.73, 8.06 Hz, 1H). ¹³C NMR (CDCl₃): δ [ppm] = 122.7, 123.8, 125.3, 128.1, 128.2, 128.3, 128.5, 129.2, 130.0, 132.2, 132.4, 133.2, 133.4, 135.8, 138.2, 142.5, 164.9. IR (KBr): 3455, 2924, 1666, 1510, 1374, 1296, 768, 734 cm^-1.

Refinement top

C-bound H atoms were placed in geometrically idealized positions and constrained to ride on their parent atoms with C—H distances of 0.95–0.99 Å, and with U_iso(H) = 1.2–1.5U_eq(C). The N-bound H atom was refined freely. One of the nitro groups was disordered over two conformations with occupancies of 0.694 (3) and 0.306 (4). The two conformers were constrained to have similar metrical parameters. Highest residual electron density peak; 1.02 e/Å³ is 0.74 A from Br2, and the deepest hole of -0.81 e/Å³ is 0.65 A from Br1. Twelve reflections were removed from the final refinement owing to poor agreement.

Related literature top

For the role of secondary interactions in stabilizing organoselenium compounds, see; Singh et al. (2010, 2012); Mugesh & Singh (2000). For the isolation of novel photoluminescent selenospirocyclic compounds via intermolecular C—C bond formation, see: Singh et al. (2011).

Computing details top

Data collection: CrysAlis PRO (Agilent, 2012); cell refinement: CrysAlis PRO (Agilent, 2012); data reduction: CrysAlis PRO (Agilent, 2012); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL2013 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: WinGX (Farrugia, 2012).

Figures top

	Fig. 1. The reaction scheme.
	Fig. 2. The molecular structure of C₁₇H₁₁Br₂N₃O₄ showing the numbering scheme and 30% probability displacement ellipsoids and the intramolecular N—H···O hydrogen bond (shown as a dashed bond).
	Fig. 3. The molecular packing for C₁₇H₁₁Br₂N₃O₄ viewed along the c axis showing the linking of the molecules into a three-dimensional array by π–π interactions as well as a network of C—H···O interactions (shown as dashed bonds).

4-Bromo-N-(2-bromo-3-nitrobenzyl)-2-nitronaphthalen-1-amine top

Crystal data top

C₁₇H₁₁Br₂N₃O₄	Z = 2
M_r = 481.11	F(000) = 472
Triclinic, P1	D_x = 1.927 Mg m⁻³
a = 8.3675 (4) Å	Mo Kα radiation, λ = 0.71073 Å
b = 8.5812 (5) Å	Cell parameters from 3926 reflections
c = 12.2691 (5) Å	θ = 5.0–34.9°
α = 76.973 (4)°	µ = 4.92 mm⁻¹
β = 81.053 (4)°	T = 123 K
γ = 76.302 (5)°	Plate, orange
V = 829.00 (8) Å³	0.44 × 0.32 × 0.12 mm

Data collection top

Agilent Xcalibur (Ruby, Gemini) diffractometer	4118 reflections with I > 2σ(I)
Detector resolution: 10.5081 pixels mm^-1	R_int = 0.033
ω scans	θ_max = 35.0°, θ_min = 5.0°
Absorption correction: multi-scan (CrysAlis PRO; Agilent, 2012)	h = −13→13
T_min = 0.345, T_max = 1.000	k = −12→13
12164 measured reflections	l = −19→19
6700 independent reflections

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)] = 0.053	Hydrogen site location: mixed
wR(F²) = 0.129	H atoms treated by a mixture of independent and constrained refinement
S = 1.02	w = 1/[σ²(F_o²) + (0.0498P)² + 0.3384P] where P = (F_o² + 2F_c²)/3
6700 reflections	(Δ/σ)_max = 0.001
246 parameters	Δρ_max = 1.04 e Å⁻³
1 restraint	Δρ_min = −0.77 e Å⁻³

Crystal data top

C₁₇H₁₁Br₂N₃O₄	γ = 76.302 (5)°
M_r = 481.11	V = 829.00 (8) Å³
Triclinic, P1	Z = 2
a = 8.3675 (4) Å	Mo Kα radiation
b = 8.5812 (5) Å	µ = 4.92 mm⁻¹
c = 12.2691 (5) Å	T = 123 K
α = 76.973 (4)°	0.44 × 0.32 × 0.12 mm
β = 81.053 (4)°

Data collection top

Agilent Xcalibur (Ruby, Gemini) diffractometer	6700 independent reflections
Absorption correction: multi-scan (CrysAlis PRO; Agilent, 2012)	4118 reflections with I > 2σ(I)
T_min = 0.345, T_max = 1.000	R_int = 0.033
12164 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.053	1 restraint
wR(F²) = 0.129	H atoms treated by a mixture of independent and constrained refinement
S = 1.02	Δρ_max = 1.04 e Å⁻³
6700 reflections	Δρ_min = −0.77 e Å⁻³
246 parameters

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.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å²) top

	x	y	z	U_iso*/U_eq	Occ. (<1)
Br1	0.52119 (4)	0.68126 (4)	0.76444 (2)	0.03410 (10)
Br2	0.98711 (4)	0.82225 (4)	0.23405 (3)	0.03346 (10)
O1	0.9351 (3)	0.3484 (3)	0.5032 (2)	0.0374 (6)
O2	0.8810 (3)	0.4048 (3)	0.3315 (2)	0.0346 (5)
O3A	1.3573 (4)	0.6322 (4)	0.0114 (3)	0.0334 (7)	0.694 (3)
O4A	1.2701 (4)	0.8769 (5)	0.0461 (4)	0.0480 (10)	0.694 (3)
O3B	1.3147 (8)	0.8513 (9)	−0.0408 (7)	0.0334 (7)	0.306 (3)
O4B	1.3038 (10)	0.6768 (10)	0.1138 (8)	0.0480 (10)	0.306 (3)
N1	0.6518 (3)	0.6613 (3)	0.2639 (2)	0.0230 (5)
H1N	0.724 (4)	0.577 (4)	0.254 (3)	0.027 (9)*
N2	0.8518 (3)	0.4286 (3)	0.4272 (2)	0.0240 (5)
N3	1.2471 (3)	0.7536 (3)	0.0266 (2)	0.0276 (6)
C1	0.6183 (3)	0.6659 (3)	0.3756 (2)	0.0171 (5)
C2	0.7114 (3)	0.5555 (3)	0.4567 (2)	0.0196 (5)
C3	0.6804 (3)	0.5624 (3)	0.5728 (2)	0.0211 (5)
H3A	0.7467	0.4854	0.6252	0.025*
C4	0.5575 (3)	0.6778 (4)	0.6087 (2)	0.0216 (5)
C5	0.4516 (3)	0.7931 (3)	0.5332 (2)	0.0183 (5)
C6	0.3170 (3)	0.9116 (4)	0.5696 (3)	0.0264 (6)
H6A	0.2998	0.9217	0.6463	0.032*
C7	0.2119 (3)	1.0113 (4)	0.4962 (3)	0.0292 (7)
H7A	0.1240	1.0917	0.5220	0.035*
C8	0.2318 (3)	0.9967 (4)	0.3842 (3)	0.0267 (6)
H8A	0.1552	1.0642	0.3346	0.032*
C9	0.3622 (3)	0.8845 (3)	0.3448 (2)	0.0216 (5)
H9A	0.3741	0.8749	0.2682	0.026*
C10	0.4788 (3)	0.7832 (3)	0.4170 (2)	0.0171 (5)
C12	0.6425 (3)	0.8012 (4)	0.1692 (2)	0.0224 (6)
H12A	0.6430	0.9014	0.1961	0.027*
H12B	0.5383	0.8185	0.1351	0.027*
C13	0.7896 (3)	0.7678 (3)	0.0821 (2)	0.0196 (5)
C14	0.9489 (3)	0.7762 (3)	0.0981 (2)	0.0197 (5)
C15	1.0768 (3)	0.7462 (4)	0.0142 (2)	0.0220 (6)
C16	1.0535 (3)	0.7066 (4)	−0.0846 (2)	0.0265 (6)
H16A	1.1437	0.6861	−0.1406	0.032*
C17	0.8958 (4)	0.6977 (4)	−0.1002 (2)	0.0286 (6)
H17A	0.8765	0.6709	−0.1674	0.034*
C18	0.7659 (3)	0.7280 (4)	−0.0171 (2)	0.0251 (6)
H18A	0.6581	0.7213	−0.0284	0.030*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Br1	0.03423 (17)	0.0569 (2)	0.01698 (15)	−0.01906 (15)	0.00074 (12)	−0.01145 (14)
Br2	0.03155 (17)	0.0494 (2)	0.02682 (17)	−0.01218 (14)	−0.00825 (13)	−0.01525 (14)
O1	0.0319 (11)	0.0295 (13)	0.0449 (15)	0.0057 (9)	−0.0109 (11)	−0.0035 (11)
O2	0.0336 (12)	0.0256 (12)	0.0354 (13)	0.0041 (9)	0.0090 (10)	−0.0068 (10)
O3A	0.0187 (13)	0.0379 (18)	0.0399 (18)	−0.0008 (12)	−0.0021 (12)	−0.0062 (14)
O4A	0.0293 (16)	0.042 (2)	0.077 (3)	−0.0142 (15)	−0.0194 (17)	−0.0033 (19)
O3B	0.0187 (13)	0.0379 (18)	0.0399 (18)	−0.0008 (12)	−0.0021 (12)	−0.0062 (14)
O4B	0.0293 (16)	0.042 (2)	0.077 (3)	−0.0142 (15)	−0.0194 (17)	−0.0033 (19)
N1	0.0283 (12)	0.0210 (13)	0.0178 (11)	−0.0034 (10)	0.0014 (9)	−0.0045 (9)
N2	0.0187 (10)	0.0158 (12)	0.0353 (14)	−0.0023 (9)	−0.0050 (10)	−0.0002 (10)
N3	0.0184 (11)	0.0345 (16)	0.0282 (13)	−0.0085 (11)	−0.0050 (10)	0.0023 (11)
C1	0.0144 (10)	0.0196 (13)	0.0179 (12)	−0.0063 (9)	0.0009 (9)	−0.0039 (10)
C2	0.0168 (11)	0.0173 (13)	0.0237 (13)	−0.0033 (10)	−0.0009 (10)	−0.0032 (10)
C3	0.0202 (12)	0.0237 (14)	0.0189 (13)	−0.0079 (10)	−0.0044 (10)	0.0020 (10)
C4	0.0213 (12)	0.0310 (15)	0.0162 (12)	−0.0127 (11)	−0.0005 (10)	−0.0056 (11)
C5	0.0145 (10)	0.0204 (13)	0.0220 (13)	−0.0078 (9)	0.0028 (9)	−0.0075 (10)
C6	0.0230 (13)	0.0292 (16)	0.0311 (16)	−0.0082 (11)	0.0046 (12)	−0.0163 (12)
C7	0.0185 (12)	0.0239 (16)	0.046 (2)	−0.0037 (11)	0.0035 (12)	−0.0147 (14)
C8	0.0173 (12)	0.0191 (14)	0.0401 (18)	−0.0009 (10)	−0.0033 (12)	−0.0016 (12)
C9	0.0164 (11)	0.0251 (15)	0.0229 (13)	−0.0046 (10)	−0.0052 (10)	−0.0018 (11)
C10	0.0148 (10)	0.0152 (12)	0.0206 (13)	−0.0032 (9)	−0.0023 (9)	−0.0021 (9)
C12	0.0187 (11)	0.0292 (15)	0.0179 (13)	−0.0031 (10)	−0.0026 (10)	−0.0033 (11)
C13	0.0185 (11)	0.0246 (14)	0.0149 (12)	−0.0050 (10)	−0.0023 (9)	−0.0010 (10)
C14	0.0221 (12)	0.0208 (14)	0.0167 (12)	−0.0060 (10)	−0.0062 (10)	−0.0002 (10)
C15	0.0141 (11)	0.0264 (15)	0.0244 (14)	−0.0056 (10)	−0.0039 (10)	−0.0003 (11)
C16	0.0183 (12)	0.0381 (18)	0.0205 (14)	−0.0055 (12)	0.0021 (10)	−0.0036 (12)
C17	0.0287 (14)	0.0424 (19)	0.0159 (13)	−0.0087 (13)	−0.0025 (11)	−0.0066 (12)
C18	0.0205 (12)	0.0385 (18)	0.0185 (14)	−0.0105 (12)	−0.0042 (10)	−0.0039 (12)

Geometric parameters (Å, º) top

Br1—C4	1.893 (3)	C6—C7	1.364 (5)
Br2—C14	1.887 (3)	C6—H6A	0.9500
O1—N2	1.231 (3)	C7—C8	1.388 (5)
O2—N2	1.214 (3)	C7—H7A	0.9500
O3A—N3	1.245 (4)	C8—C9	1.378 (4)
O4A—N3	1.199 (4)	C8—H8A	0.9500
O3B—N3	1.214 (7)	C9—C10	1.419 (4)
O4B—N3	1.224 (9)	C9—H9A	0.9500
N1—C1	1.363 (3)	C12—C13	1.517 (4)
N1—C12	1.467 (4)	C12—H12A	0.9900
N1—H1N	0.85 (3)	C12—H12B	0.9900
N2—C2	1.461 (3)	C13—C18	1.390 (4)
N3—C15	1.474 (3)	C13—C14	1.398 (4)
C1—C2	1.400 (4)	C14—C15	1.386 (4)
C1—C10	1.457 (4)	C15—C16	1.383 (4)
C2—C3	1.420 (4)	C16—C17	1.385 (4)
C3—C4	1.344 (4)	C16—H16A	0.9500
C3—H3A	0.9500	C17—C18	1.388 (4)
C4—C5	1.432 (4)	C17—H17A	0.9500
C5—C6	1.417 (4)	C18—H18A	0.9500
C5—C10	1.426 (4)

C1—N1—C12	127.2 (2)	C9—C8—C7	120.2 (3)
C1—N1—H1N	111 (2)	C9—C8—H8A	119.9
C12—N1—H1N	116 (2)	C7—C8—H8A	119.9
O2—N2—O1	122.8 (3)	C8—C9—C10	121.0 (3)
O2—N2—C2	120.1 (2)	C8—C9—H9A	119.5
O1—N2—C2	117.1 (3)	C10—C9—H9A	119.5
O3B—N3—O4B	122.8 (5)	C9—C10—C5	118.2 (2)
O4A—N3—O3A	125.1 (3)	C9—C10—C1	121.3 (2)
O4A—N3—C15	118.2 (3)	C5—C10—C1	120.5 (2)
O3B—N3—C15	119.2 (4)	N1—C12—C13	109.3 (2)
O4B—N3—C15	117.1 (4)	N1—C12—H12A	109.8
O3A—N3—C15	116.7 (3)	C13—C12—H12A	109.8
N1—C1—C2	122.2 (2)	N1—C12—H12B	109.8
N1—C1—C10	121.2 (2)	C13—C12—H12B	109.8
C2—C1—C10	116.6 (2)	H12A—C12—H12B	108.3
C1—C2—C3	122.5 (2)	C18—C13—C14	118.7 (2)
C1—C2—N2	122.3 (3)	C18—C13—C12	119.2 (2)
C3—C2—N2	115.1 (3)	C14—C13—C12	122.1 (3)
C4—C3—C2	120.1 (3)	C15—C14—C13	118.8 (3)
C4—C3—H3A	120.0	C15—C14—Br2	121.3 (2)
C2—C3—H3A	120.0	C13—C14—Br2	119.9 (2)
C3—C4—C5	121.8 (3)	C16—C15—C14	122.6 (2)
C3—C4—Br1	118.3 (2)	C16—C15—N3	116.3 (2)
C5—C4—Br1	119.9 (2)	C14—C15—N3	121.1 (3)
C6—C5—C10	118.8 (3)	C15—C16—C17	118.5 (3)
C6—C5—C4	122.8 (3)	C15—C16—H16A	120.7
C10—C5—C4	118.4 (2)	C17—C16—H16A	120.7
C7—C6—C5	121.0 (3)	C16—C17—C18	119.7 (3)
C7—C6—H6A	119.5	C16—C17—H17A	120.2
C5—C6—H6A	119.5	C18—C17—H17A	120.2
C6—C7—C8	120.8 (3)	C17—C18—C13	121.7 (3)
C6—C7—H7A	119.6	C17—C18—H18A	119.2
C8—C7—H7A	119.6	C13—C18—H18A	119.2

C12—N1—C1—C2	−141.9 (3)	N1—C1—C10—C9	7.0 (4)
C12—N1—C1—C10	40.5 (4)	C2—C1—C10—C9	−170.8 (2)
N1—C1—C2—C3	178.1 (2)	N1—C1—C10—C5	−176.1 (2)
C10—C1—C2—C3	−4.1 (4)	C2—C1—C10—C5	6.2 (3)
N1—C1—C2—N2	0.6 (4)	C1—N1—C12—C13	138.6 (3)
C10—C1—C2—N2	178.3 (2)	N1—C12—C13—C18	105.6 (3)
O2—N2—C2—C1	−7.7 (4)	N1—C12—C13—C14	−74.5 (3)
O1—N2—C2—C1	173.1 (2)	C18—C13—C14—C15	0.6 (4)
O2—N2—C2—C3	174.6 (2)	C12—C13—C14—C15	−179.2 (3)
O1—N2—C2—C3	−4.6 (3)	C18—C13—C14—Br2	−177.7 (2)
C1—C2—C3—C4	0.2 (4)	C12—C13—C14—Br2	2.4 (4)
N2—C2—C3—C4	177.9 (2)	C13—C14—C15—C16	−0.6 (4)
C2—C3—C4—C5	1.9 (4)	Br2—C14—C15—C16	177.7 (2)
C2—C3—C4—Br1	179.86 (19)	C13—C14—C15—N3	179.9 (3)
C3—C4—C5—C6	177.4 (3)	Br2—C14—C15—N3	−1.7 (4)
Br1—C4—C5—C6	−0.6 (3)	O4A—N3—C15—C16	125.2 (4)
C3—C4—C5—C10	0.2 (4)	O3B—N3—C15—C16	60.9 (6)
Br1—C4—C5—C10	−177.74 (18)	O4B—N3—C15—C16	−129.3 (6)
C10—C5—C6—C7	2.0 (4)	O3A—N3—C15—C16	−52.1 (4)
C4—C5—C6—C7	−175.2 (3)	O4A—N3—C15—C14	−55.3 (4)
C5—C6—C7—C8	1.5 (4)	O3B—N3—C15—C14	−119.6 (6)
C6—C7—C8—C9	−2.3 (4)	O4B—N3—C15—C14	50.2 (6)
C7—C8—C9—C10	−0.5 (4)	O3A—N3—C15—C14	127.4 (3)
C8—C9—C10—C5	3.9 (4)	C14—C15—C16—C17	0.4 (5)
C8—C9—C10—C1	−179.1 (2)	N3—C15—C16—C17	179.8 (3)
C6—C5—C10—C9	−4.6 (4)	C15—C16—C17—C18	−0.1 (5)
C4—C5—C10—C9	172.7 (2)	C16—C17—C18—C13	0.2 (5)
C6—C5—C10—C1	178.4 (2)	C14—C13—C18—C17	−0.4 (4)
C4—C5—C10—C1	−4.3 (4)	C12—C13—C18—C17	179.4 (3)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1N···O2	0.84 (3)	1.91 (3)	2.624 (3)	141 (3)
C12—H12A···O3Bⁱ	0.99	2.57	3.117 (8)	115
C12—H12B···O4Aⁱⁱ	0.99	2.54	3.532 (4)	177
C12—H12B···O4Bⁱⁱ	0.99	2.61	3.462 (8)	144

Symmetry codes: (i) −x+2, −y+2, −z; (ii) x−1, y, z.

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1N···O2	0.84 (3)	1.91 (3)	2.624 (3)	141 (3)
C12—H12A···O3Bⁱ	0.99	2.57	3.117 (8)	115
C12—H12B···O4Aⁱⁱ	0.99	2.54	3.532 (4)	177
C12—H12B···O4Bⁱⁱ	0.99	2.61	3.462 (8)	144

Symmetry codes: (i) −x+2, −y+2, −z; (ii) x−1, y, z.

π–π interactions (Å) top

Ring 1	Ring 2	Distance	Perpedicular distance	Slippage	Symmetry
Cg1	Cg1	3.5295 (16)	3.3867 (11)	0.94	1-x,1-y,1-z
Cg2	Cg2	3.8868 (15)	3.3859 (12)	1.91	1-x,-y,1-z
Cg3	Cg3	3.9629 (18)	3.5873 (12)	1.68	-x,1-y,2-z

Acknowledgements

RJB acknowledges the NSF MRI program (grant No. CHE-0619278) for funds to purchase an X-ray diffractometer.

References

Agilent (2012). CrysAlis PRO and CrysAlis RED. Agilent Technologies, Yarnton, England. Google Scholar
Farrugia, L. J. (2012). J. Appl. Cryst. 45, 849–854. Web of Science CrossRef CAS IUCr Journals Google Scholar
Mugesh, G. & Singh, H. B. (2000). Chem. Soc. Rev. 29, 347–357. Web of Science CrossRef CAS Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Singh, V. P., Singh, H. B. & Butcher, R. J. (2010). Eur. J. Inorg. Chem. pp. 637–647. Web of Science CSD CrossRef Google Scholar
Singh, V. P., Singh, H. B. & Butcher, R. J. (2011). Chem. Commun. 47, 7221–7223. Web of Science CSD CrossRef CAS Google Scholar
Singh, V. P., Singh, P., Singh, H. B. & Butcher, R. J. (2012). Tetrahedron Lett. 53, 4591–4594. Web of Science CSD CrossRef CAS Google Scholar

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Volume 70| Part 9| September 2014| Pages o960-o961

doi:10.1107/S160053681401719X

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organic compounds\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Crystal structure of 4-bromo-N-(2-bromo-3-nitro­benz­yl)-2-nitro­naphthalen-1-amine

1. Related literature

2. Experimental

2.1. Crystal data

2.2. Data collection

2.3. Refinement

Supporting information

Acknowledgements

References

organic compounds

Crystal structure of 4-bromo-N-(2-bromo-3-nitrobenzyl)-2-nitronaphthalen-1-amine