N,N′-Bis(4-chloro­benzyl­idene)-2,2-dimethyl­propane-1,3-diamine

Fun, H.-K.; Kargar, H.; Kia, R.

doi:10.1107/S1600536808035307

organic compounds

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ISSN: 2056-9890

Volume 64| Part 12| December 2008| Page o2273

doi:10.1107/S1600536808035307

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N,N′-Bis(4-chlorobenzylidene)-2,2-dimethylpropane-1,3-diamine

Hoong-Kun Fun,^a ^* Hadi Kargar ^b ‡ and Reza Kia ^a

^aX-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, 11800 USM, Penang, Malaysia, and ^bDepartment of Chemistry, School of Science, Payame Noor University, Ardakan, Yazd, Iran
^*Correspondence e-mail: hkfun@usm.my

(Received 28 October 2008; accepted 29 October 2008; online 8 November 2008)

The title compound, C₁₉H₂₀Cl₂N₂, is a potential bidentate Schiff base ligand. Intramolecular C—H⋯N hydrogen bonds form five-membered rings, generating S(5) ring motifs. Each imino functional group is coplanar with its adjacent benzene ring; the two benzene rings form a dihedral angle of 51.30 (4)°. An interesting feature of the crystal structure is weak intermolecular Cl⋯Cl [3.4752 (4) Å] and Cl⋯N [3.2927 (9) Å] interactions. Intermolecular Cl⋯N interactions link molecules into dimers with R₂²(22) ring motifs. The crystal structure is further stabilized by weak π–π [centroid–centroid distances = 3.6970 (6)–3.8560 (6) Å] interactions.

Related literature

For hydrogen-bond motifs, see Bernstein et al. (1995 ). For related structures see, for example: Li et al. (2005 ); Bomfim et al. (2005 ); Glidewell et al. (2005 , 2006 ); Sun et al. (2004 ); Fun et al. (2008 ).

Experimental

Crystal data

C₁₉H₂₀Cl₂N₂
M_r = 347.27
Monoclinic, P 2₁ /c
a = 19.6392 (3) Å
b = 9.3275 (2) Å
c = 9.7841 (2) Å
β = 92.213 (1)°
V = 1790.96 (6) Å³
Z = 4
Mo Kα radiation
μ = 0.36 mm⁻¹
T = 100 (1) K
0.51 × 0.35 × 0.10 mm

Data collection

Bruker SMART APEXII CCD area-detector diffractometer
Absorption correction: multi-scan (SADABS; Bruker, 2005 ) T_min = 0.836, T_max = 0.966
21670 measured reflections
6419 independent reflections
5273 reflections with I > 2σ(I)
R_int = 0.028

Refinement

R[F² > 2σ(F²)] = 0.036
wR(F²) = 0.095
S = 1.03
6419 reflections
208 parameters
H-atom parameters constrained
Δρ_max = 0.38 e Å⁻³
Δρ_min = −0.32 e Å⁻³

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
C18—H18B⋯N1	0.96	2.60	2.9346 (15)	101
C19—H19C⋯N2	0.96	2.61	2.9416 (15)	101

Data collection: APEX2 (Bruker, 2005); cell refinement: APEX2 and SAINT (Bruker, 2005); data reduction: SAINT; program(s) used to solve structure: SHELXTL (Sheldrick, 2008 ); program(s) used to refine structure: SHELXTL; molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL and PLATON (Spek, 2003 ).

Supporting information

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536808035307/tk2319sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536808035307/tk2319Isup2.hkl

checkCIF report

Comment top

Schiff bases are one of most prevalent mixed-donor ligands in the field of coordination chemistry. They play an important role in the development of coordination chemistry related to catalysis and enzymatic reactions, magnetism, and supramolecular architectures. Structures of Schiff-base compounds derived from substituted benzaldehydes and closely related to the title compound, (I), have been reported previously (Li et al., 2005; Bomfim et al., 2005; Glidewell et al., 2005, 2006; Sun et al., 2004; Fun et al., 2008).

In (I), Fig. 1, each imino functional group is co-planar with its adjacent benzene ring. Intramolecular C—H···N hydrogen bonds form five-membered rings, Fig. 1, producing S(5) ring motifs (Bernstein et al., 1995). The two benzene rings form a dihedral angle of 51.30 (4)°. The interesting feature of the crystal structure is the presence of weak intermolecular Cl···Cl [3.4852 (3) Å; symmetry code: x, 1 - y, -1/2 + z] and Cl···N [3.2927 (9) Å; symmetry code: -x, 1 - y, 1 - z] interactions. The intermolecular Cl···N interactions link neighbouring molecules into dimers with R₂²(22) ring motifs (Bernstein et al., 1995). The crystal structure is further stabilized by weak intermolecular π–π interactions [Cg1···Cg1= 3.8560 (6) Å; symmetry code: 1 - x, 1 - y, 1 - z; Cg2···Cg2 = 3.6970 (6) Å; symmetry code: -x, 1 - y, 1 - z] (Cg1 and Cg2 are the centroids of the C1–C6 and C12–C17 rings, respectively.

Related literature top

For hydrogen-bond motifs, see Bernstein et al. (1995). For related structures see, for example: Li et al. (2005); Bomfim et al. (2005); Glidewell et al. (2005, 2006); Sun et al. (2004); Fun et al. (2008).

Experimental top

The synthetic method has been described earlier (Fun et al., 2008). Single crystals suitable for X-ray diffraction were obtained by evaporation of an ethanol solution of (I) held at room temperature.

Computing details top

Data collection: APEX2 (Bruker, 2005); cell refinement: APEX2 (Bruker, 2005) and SAINT (Bruker, 2005); data reduction: SAINT (Bruker, 2005); program(s) used to solve structure: SHELXTL (Sheldrick, 2008); program(s) used to refine structure: SHELXTL (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2003).

Figures top

Fig. 1. The molecular structure of (I) showing atom labels and 50% probability ellipsoids for non-H atoms. Intramolecular hydrogen bonds are shown as dashed lines.

N,N'-Bis(4-dichlorobenzylidene)-2,2-dimethylpropane-1,3-diamine top

Crystal data top

C₁₉H₂₀Cl₂N₂	F(000) = 728
M_r = 347.27	D_x = 1.288 Mg m⁻³
Monoclinic, P2₁/c	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ybc	Cell parameters from 8119 reflections
a = 19.6392 (3) Å	θ = 3.0–38.9°
b = 9.3275 (2) Å	µ = 0.36 mm⁻¹
c = 9.7841 (2) Å	T = 100 K
β = 92.213 (1)°	Plate, colourless
V = 1790.96 (6) Å³	0.51 × 0.35 × 0.10 mm
Z = 4

Data collection top

Bruker SMART APEXII CCD area-detector diffractometer	6419 independent reflections
Radiation source: fine-focus sealed tube	5273 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.028
ϕ and ω scans	θ_max = 32.5°, θ_min = 1.0°
Absorption correction: multi-scan (SADABS; Bruker, 2005)	h = −29→29
T_min = 0.836, T_max = 0.966	k = −14→12
21670 measured reflections	l = −14→14

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)] = 0.036	Hydrogen site location: inferred from neighbouring sites
wR(F²) = 0.095	H-atom parameters constrained
S = 1.03	w = 1/[σ²(F_o²) + (0.0434P)² + 0.5329P] where P = (F_o² + 2F_c²)/3
6419 reflections	(Δ/σ)_max = 0.001
208 parameters	Δρ_max = 0.38 e Å⁻³
0 restraints	Δρ_min = −0.32 e Å⁻³

Crystal data top

C₁₉H₂₀Cl₂N₂	V = 1790.96 (6) Å³
M_r = 347.27	Z = 4
Monoclinic, P2₁/c	Mo Kα radiation
a = 19.6392 (3) Å	µ = 0.36 mm⁻¹
b = 9.3275 (2) Å	T = 100 K
c = 9.7841 (2) Å	0.51 × 0.35 × 0.10 mm
β = 92.213 (1)°

Data collection top

Bruker SMART APEXII CCD area-detector diffractometer	6419 independent reflections
Absorption correction: multi-scan (SADABS; Bruker, 2005)	5273 reflections with I > 2σ(I)
T_min = 0.836, T_max = 0.966	R_int = 0.028
21670 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.036	0 restraints
wR(F²) = 0.095	H-atom parameters constrained
S = 1.03	Δρ_max = 0.38 e Å⁻³
6419 reflections	Δρ_min = −0.32 e Å⁻³
208 parameters

Special details top

Experimental. The low-temperature data was collected with the Oxford Cyrosystem Cobra low-temperature attachment.

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	U_iso*/U_eq
Cl1	0.497643 (14)	0.49166 (3)	0.17717 (3)	0.02553 (7)
Cl2	−0.166144 (13)	0.43828 (3)	0.54241 (3)	0.02640 (7)
N1	0.28500 (4)	0.54904 (10)	0.70403 (9)	0.01950 (17)
N2	0.14528 (4)	0.37002 (10)	0.85655 (9)	0.01864 (17)
C1	0.35398 (5)	0.47808 (13)	0.45572 (11)	0.0216 (2)
H1A	0.3155	0.4238	0.4731	0.026*
C2	0.39180 (6)	0.44677 (13)	0.34258 (11)	0.0226 (2)
H2A	0.3791	0.3720	0.2842	0.027*
C3	0.44914 (5)	0.52935 (12)	0.31802 (11)	0.01962 (19)
C4	0.46927 (5)	0.64046 (12)	0.40359 (11)	0.0208 (2)
H4A	0.5080	0.6939	0.3863	0.025*
C5	0.43069 (5)	0.67111 (12)	0.51594 (11)	0.01929 (19)
H5A	0.4434	0.7466	0.5735	0.023*
C6	0.37302 (5)	0.59009 (11)	0.54371 (10)	0.01710 (18)
C7	0.33470 (5)	0.62450 (12)	0.66609 (11)	0.01815 (19)
H7A	0.3474	0.7046	0.7176	0.022*
C8	0.25179 (5)	0.59532 (12)	0.82751 (11)	0.0202 (2)
H8A	0.2046	0.6187	0.8048	0.024*
H8B	0.2740	0.6813	0.8628	0.024*
C9	0.25474 (5)	0.47832 (12)	0.93875 (11)	0.01860 (19)
C10	0.21738 (5)	0.34242 (12)	0.88813 (11)	0.01881 (19)
H10A	0.2386	0.3070	0.8068	0.023*
H10B	0.2216	0.2688	0.9579	0.023*
C11	0.12219 (5)	0.33583 (11)	0.73837 (11)	0.01765 (18)
H11A	0.1515	0.2936	0.6777	0.021*
C12	0.05057 (5)	0.36042 (11)	0.69311 (10)	0.01656 (18)
C13	0.00695 (5)	0.44318 (12)	0.77071 (11)	0.01855 (19)
H13A	0.0230	0.4832	0.8529	0.022*
C14	−0.06007 (5)	0.46587 (12)	0.72583 (11)	0.01985 (19)
H14A	−0.0891	0.5207	0.7774	0.024*
C15	−0.08314 (5)	0.40546 (12)	0.60260 (11)	0.01940 (19)
C16	−0.04087 (5)	0.32318 (12)	0.52386 (11)	0.0204 (2)
H16A	−0.0571	0.2832	0.4418	0.024*
C17	0.02632 (5)	0.30141 (12)	0.56973 (11)	0.01898 (19)
H17A	0.0553	0.2470	0.5175	0.023*
C18	0.32900 (5)	0.43799 (14)	0.97383 (12)	0.0249 (2)
H18A	0.3534	0.5214	1.0058	0.037*
H18B	0.3497	0.4014	0.8937	0.037*
H18C	0.3304	0.3660	1.0440	0.037*
C19	0.22142 (6)	0.53832 (14)	1.06574 (12)	0.0261 (2)
H19A	0.2452	0.6231	1.0960	0.039*
H19B	0.2235	0.4678	1.1372	0.039*
H19C	0.1747	0.5616	1.0435	0.039*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Cl1	0.02940 (13)	0.02639 (15)	0.02128 (12)	0.00830 (10)	0.00692 (10)	0.00370 (10)
Cl2	0.01662 (11)	0.02663 (15)	0.03566 (15)	0.00011 (9)	−0.00260 (9)	0.00411 (11)
N1	0.0189 (4)	0.0204 (4)	0.0192 (4)	−0.0005 (3)	0.0014 (3)	0.0005 (3)
N2	0.0146 (3)	0.0200 (4)	0.0215 (4)	−0.0014 (3)	0.0025 (3)	0.0000 (3)
C1	0.0202 (4)	0.0231 (5)	0.0214 (5)	−0.0044 (4)	0.0001 (4)	−0.0006 (4)
C2	0.0251 (5)	0.0231 (5)	0.0197 (5)	−0.0028 (4)	−0.0007 (4)	−0.0026 (4)
C3	0.0221 (4)	0.0194 (5)	0.0175 (4)	0.0048 (4)	0.0024 (4)	0.0038 (4)
C4	0.0199 (4)	0.0176 (5)	0.0250 (5)	−0.0003 (4)	0.0039 (4)	0.0043 (4)
C5	0.0195 (4)	0.0154 (5)	0.0230 (5)	−0.0013 (3)	0.0012 (4)	0.0006 (4)
C6	0.0169 (4)	0.0167 (5)	0.0177 (4)	0.0001 (3)	−0.0004 (3)	0.0023 (4)
C7	0.0178 (4)	0.0174 (5)	0.0191 (4)	0.0002 (3)	−0.0002 (3)	0.0007 (4)
C8	0.0185 (4)	0.0197 (5)	0.0226 (5)	−0.0003 (4)	0.0044 (4)	−0.0008 (4)
C9	0.0162 (4)	0.0215 (5)	0.0182 (4)	−0.0019 (3)	0.0019 (3)	−0.0015 (4)
C10	0.0158 (4)	0.0191 (5)	0.0216 (5)	0.0002 (3)	0.0018 (3)	0.0000 (4)
C11	0.0165 (4)	0.0160 (5)	0.0207 (5)	0.0005 (3)	0.0049 (3)	0.0005 (4)
C12	0.0161 (4)	0.0153 (4)	0.0184 (4)	−0.0005 (3)	0.0028 (3)	0.0019 (3)
C13	0.0190 (4)	0.0185 (5)	0.0183 (5)	0.0007 (3)	0.0033 (3)	−0.0006 (4)
C14	0.0180 (4)	0.0189 (5)	0.0230 (5)	0.0017 (4)	0.0046 (4)	0.0015 (4)
C15	0.0156 (4)	0.0177 (5)	0.0249 (5)	−0.0010 (3)	0.0005 (3)	0.0049 (4)
C16	0.0215 (4)	0.0195 (5)	0.0202 (5)	−0.0020 (4)	−0.0003 (4)	−0.0008 (4)
C17	0.0194 (4)	0.0180 (5)	0.0197 (5)	0.0007 (3)	0.0029 (3)	−0.0006 (4)
C18	0.0186 (4)	0.0303 (6)	0.0255 (5)	−0.0024 (4)	−0.0025 (4)	0.0008 (4)
C19	0.0272 (5)	0.0292 (6)	0.0222 (5)	−0.0042 (4)	0.0065 (4)	−0.0055 (4)

Geometric parameters (Å, º) top

Cl1—C3	1.7411 (11)	C9—C19	1.5323 (15)
Cl2—C15	1.7390 (10)	C9—C10	1.5370 (15)
N1—C7	1.2703 (13)	C10—H10A	0.9700
N1—C8	1.4602 (14)	C10—H10B	0.9700
N2—C11	1.2664 (14)	C11—C12	1.4761 (14)
N2—C10	1.4603 (13)	C11—H11A	0.9300
C1—C2	1.3876 (15)	C12—C17	1.3939 (15)
C1—C6	1.3956 (15)	C12—C13	1.3987 (14)
C1—H1A	0.9300	C13—C14	1.3876 (14)
C2—C3	1.3929 (15)	C13—H13A	0.9300
C2—H2A	0.9300	C14—C15	1.3908 (16)
C3—C4	1.3805 (16)	C14—H14A	0.9300
C4—C5	1.3886 (14)	C15—C16	1.3860 (15)
C4—H4A	0.9300	C16—C17	1.3921 (14)
C5—C6	1.3970 (14)	C16—H16A	0.9300
C5—H5A	0.9300	C17—H17A	0.9300
C6—C7	1.4741 (14)	C18—H18A	0.9600
C7—H7A	0.9300	C18—H18B	0.9600
C8—C9	1.5408 (16)	C18—H18C	0.9600
C8—H8A	0.9700	C19—H19A	0.9600
C8—H8B	0.9700	C19—H19B	0.9600
C9—C18	1.5322 (15)	C19—H19C	0.9600

C7—N1—C8	116.79 (9)	C9—C10—H10A	109.3
C11—N2—C10	117.31 (9)	N2—C10—H10B	109.3
C2—C1—C6	120.72 (10)	C9—C10—H10B	109.3
C2—C1—H1A	119.6	H10A—C10—H10B	107.9
C6—C1—H1A	119.6	N2—C11—C12	122.56 (9)
C1—C2—C3	118.84 (10)	N2—C11—H11A	118.7
C1—C2—H2A	120.6	C12—C11—H11A	118.7
C3—C2—H2A	120.6	C17—C12—C13	119.48 (9)
C4—C3—C2	121.67 (10)	C17—C12—C11	119.22 (9)
C4—C3—Cl1	118.62 (8)	C13—C12—C11	121.30 (9)
C2—C3—Cl1	119.71 (9)	C14—C13—C12	120.38 (10)
C3—C4—C5	118.84 (10)	C14—C13—H13A	119.8
C3—C4—H4A	120.6	C12—C13—H13A	119.8
C5—C4—H4A	120.6	C13—C14—C15	119.07 (10)
C4—C5—C6	120.92 (10)	C13—C14—H14A	120.5
C4—C5—H5A	119.5	C15—C14—H14A	120.5
C6—C5—H5A	119.5	C16—C15—C14	121.61 (9)
C1—C6—C5	119.00 (9)	C16—C15—Cl2	118.88 (9)
C1—C6—C7	122.08 (9)	C14—C15—Cl2	119.47 (8)
C5—C6—C7	118.91 (9)	C15—C16—C17	118.83 (10)
N1—C7—C6	122.61 (10)	C15—C16—H16A	120.6
N1—C7—H7A	118.7	C17—C16—H16A	120.6
C6—C7—H7A	118.7	C16—C17—C12	120.63 (9)
N1—C8—C9	111.67 (9)	C16—C17—H17A	119.7
N1—C8—H8A	109.3	C12—C17—H17A	119.7
C9—C8—H8A	109.3	C9—C18—H18A	109.5
N1—C8—H8B	109.3	C9—C18—H18B	109.5
C9—C8—H8B	109.3	H18A—C18—H18B	109.5
H8A—C8—H8B	107.9	C9—C18—H18C	109.5
C18—C9—C19	109.91 (9)	H18A—C18—H18C	109.5
C18—C9—C10	107.95 (9)	H18B—C18—H18C	109.5
C19—C9—C10	110.43 (8)	C9—C19—H19A	109.5
C18—C9—C8	109.97 (8)	C9—C19—H19B	109.5
C19—C9—C8	107.97 (9)	H19A—C19—H19B	109.5
C10—C9—C8	110.61 (9)	C9—C19—H19C	109.5
N2—C10—C9	111.70 (9)	H19A—C19—H19C	109.5
N2—C10—H10A	109.3	H19B—C19—H19C	109.5

C6—C1—C2—C3	−0.13 (17)	C11—N2—C10—C9	125.72 (10)
C1—C2—C3—C4	0.35 (17)	C18—C9—C10—N2	178.07 (9)
C1—C2—C3—Cl1	179.70 (9)	C19—C9—C10—N2	57.90 (12)
C2—C3—C4—C5	−0.74 (17)	C8—C9—C10—N2	−61.57 (11)
Cl1—C3—C4—C5	179.89 (8)	C10—N2—C11—C12	−178.94 (9)
C3—C4—C5—C6	0.93 (16)	N2—C11—C12—C17	−170.66 (10)
C2—C1—C6—C5	0.31 (17)	N2—C11—C12—C13	10.16 (16)
C2—C1—C6—C7	−178.88 (10)	C17—C12—C13—C14	0.35 (16)
C4—C5—C6—C1	−0.72 (16)	C11—C12—C13—C14	179.52 (10)
C4—C5—C6—C7	178.50 (10)	C12—C13—C14—C15	−0.14 (16)
C8—N1—C7—C6	179.80 (9)	C13—C14—C15—C16	0.08 (16)
C1—C6—C7—N1	4.79 (16)	C13—C14—C15—Cl2	−177.78 (8)
C5—C6—C7—N1	−174.40 (10)	C14—C15—C16—C17	−0.23 (16)
C7—N1—C8—C9	−120.74 (10)	Cl2—C15—C16—C17	177.64 (8)
N1—C8—C9—C18	57.83 (12)	C15—C16—C17—C12	0.44 (16)
N1—C8—C9—C19	177.75 (8)	C13—C12—C17—C16	−0.51 (16)
N1—C8—C9—C10	−61.31 (11)	C11—C12—C17—C16	−179.70 (10)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
C18—H18B···N1	0.96	2.60	2.9346 (15)	101
C19—H19C···N2	0.96	2.61	2.9416 (15)	101

Experimental details

Crystal data
Chemical formula	C₁₉H₂₀Cl₂N₂
M_r	347.27
Crystal system, space group	Monoclinic, P2₁/c
Temperature (K)	100
a, b, c (Å)	19.6392 (3), 9.3275 (2), 9.7841 (2)
β (°)	92.213 (1)
V (Å³)	1790.96 (6)
Z	4
Radiation type	Mo Kα
µ (mm⁻¹)	0.36
Crystal size (mm)	0.51 × 0.35 × 0.10

Data collection
Diffractometer	Bruker SMART APEXII CCD area-detector diffractometer
Absorption correction	Multi-scan (SADABS; Bruker, 2005)
T_min, T_max	0.836, 0.966
No. of measured, independent and observed [I > 2σ(I)] reflections	21670, 6419, 5273
R_int	0.028
(sin θ/λ)_max (Å⁻¹)	0.756

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.036, 0.095, 1.03
No. of reflections	6419
No. of parameters	208
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.38, −0.32

Computer programs: , APEX2 (Bruker, 2005) and SAINT (Bruker, 2005), SAINT (Bruker, 2005), SHELXTL (Sheldrick, 2008) and PLATON (Spek, 2003).

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
C18—H18B···N1	0.96	2.60	2.9346 (15)	101
C19—H19C···N2	0.96	2.61	2.9416 (15)	101

Footnotes

‡Additional correspondence author, e-mail: hkargar@pnu.ac.ir.

Acknowledgements

HKF and RK thank the Malaysian Government and Universiti Sains Malaysia for Science Fund grant No. 305/PFIZIK/613312. RK thanks Universiti Sains Malaysia for a post-doctoral research fellowship. HK thanks Payame Noor University for financial support.

References

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