(E)-2-(1,3-Diphenyl-allyl-idene)malononitrile.

The title compound, C(18)H(12)N(2), adopts an E conformation with the benzyl-idenemalononitrile and phenyl groups located on opposite sides of the C=C bond. The two phenyl rings are oriented at a dihedral angle of 62.49 (7)°.

Related literature

For background to the use of malononitrile-containing compounds as building blocks in organic synthesis, see: Erian (1993 ▶); Liu et al. (2002 ▶); Sepiol & Milart. (1985 ▶); Zhang et al. (2003 ▶). For a related structure, see: Basu Baul et al. (2009 ▶).

Experimental

Crystal data

C18H12N2

M = 256.30

Monoclinic,

a = 12.1658 (6) Å

b = 14.8852 (9) Å

c = 8.1959 (7) Å

β = 108.457 (6)°

V = 1407.85 (16) Å3

Z = 4

Mo Kα radiation

μ = 0.07 mm−1

T = 295 K

0.50 × 0.40 × 0.40 mm

Data collection

Oxford Diffraction Gemini S Ultra diffractometer

Absorption correction: none

13329 measured reflections

2880 independent reflections

1735 reflections with I > 2σ(I)

R int = 0.025

Refinement

R[F 2 > 2σ(F 2)] = 0.035

wR(F 2) = 0.082

S = 1.01

2880 reflections

181 parameters

3 restraints

H-atom parameters constrained

Δρmax = 0.11 e Å−3

Δρmin = −0.14 e Å−3

Data collection: CrysAlis Pro (Oxford Diffraction, 2009 ▶); cell refinement: CrysAlis Pro; data reduction: CrysAlis Pro; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: ORTEP-3 (Farrugia, 1997 ▶); software used to prepare material for publication: SHELXL97.

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536809048338/xu2673sup1.cif

Structure factors: contains datablocks I. DOI: 10.1107/S1600536809048338/xu2673Isup2.hkl

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

C18H12N2	F(000) = 536
Mr = 256.30	Dx = 1.209 Mg m−3
Monoclinic, P21/c	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ybc	Cell parameters from 5219 reflections
a = 12.1658 (6) Å	θ = 3.0–29.2°
b = 14.8852 (9) Å	µ = 0.07 mm−1
c = 8.1959 (7) Å	T = 295 K
β = 108.457 (6)°	Block, yellow
V = 1407.85 (16) Å3	0.50 × 0.40 × 0.40 mm
Z = 4

Oxford Diffraction Gemini S Ultra diffractometer	1735 reflections with I > 2σ(I)
Radiation source: Enhance (Mo) X-ray Source	Rint = 0.025
graphite	θmax = 26.4°, θmin = 3.0°
Detector resolution: 15.9149 pixels mm-1	h = −15→15
ω scans	k = −12→18
13329 measured reflections	l = −10→10
2880 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)] = 0.035	Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.082	H-atom parameters constrained
S = 1.01	w = 1/[σ2(Fo2) + (0.0388P)2] where P = (Fo2 + 2Fc2)/3
2880 reflections	(Δ/σ)max = 0.001
181 parameters	Δρmax = 0.11 e Å−3
3 restraints	Δρmin = −0.13 e Å−3

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
C8	1.02337 (9)	0.42702 (8)	0.80790 (16)	0.0520 (3)
H8	0.9756	0.4731	0.7487	0.062*
C9	1.14221 (9)	0.42886 (8)	0.80802 (15)	0.0468 (3)
C16	1.17980 (10)	0.50107 (7)	0.73655 (16)	0.0492 (3)
C10	1.22053 (10)	0.35243 (7)	0.87880 (15)	0.0466 (3)
C7	0.97483 (10)	0.36634 (8)	0.88354 (15)	0.0492 (3)
H7	1.0225	0.3211	0.9464	0.059*
C4	0.76990 (10)	0.41976 (8)	0.76497 (17)	0.0578 (3)
H4	0.7914	0.4586	0.6915	0.069*
C6	0.81719 (11)	0.30629 (8)	0.98007 (17)	0.0564 (3)
H6	0.8706	0.2677	1.0531	0.068*
C5	0.85340 (9)	0.36488 (7)	0.87593 (15)	0.0461 (3)
C1	0.70315 (12)	0.30433 (9)	0.97724 (19)	0.0679 (4)
H1	0.6804	0.2649	1.0484	0.081*
C2	0.62347 (11)	0.36058 (9)	0.86948 (19)	0.0679 (4)
H2	0.5470	0.3601	0.8692	0.082*
C11	1.32866 (10)	0.36506 (8)	0.99982 (17)	0.0572 (3)
H11	1.3530	0.4227	1.0384	0.069*
C3	0.65660 (11)	0.41749 (9)	0.76217 (18)	0.0651 (4)
H3	0.6021	0.4547	0.6873	0.078*
C17	1.29300 (11)	0.50807 (8)	0.71970 (17)	0.0578 (3)
C14	1.25937 (13)	0.19431 (9)	0.8861 (2)	0.0751 (4)
H14	1.2363	0.1364	0.8474	0.090*
C15	1.18644 (11)	0.26573 (8)	0.82240 (18)	0.0604 (4)
H15	1.1142	0.2559	0.7414	0.073*
C13	1.36577 (13)	0.20804 (10)	1.0064 (2)	0.0778 (5)
H13	1.4144	0.1595	1.0492	0.093*
C12	1.40048 (12)	0.29275 (10)	1.06346 (19)	0.0707 (4)
H12	1.4726	0.3018	1.1453	0.085*
C18	1.10284 (11)	0.57361 (9)	0.66242 (17)	0.0544 (3)
N2	1.03886 (10)	0.62944 (8)	0.60031 (16)	0.0742 (4)
N1	1.38156 (11)	0.51654 (8)	0.70138 (18)	0.0851 (4)

	U11	U22	U33	U12	U13	U23
C8	0.0442 (7)	0.0488 (7)	0.0631 (8)	0.0040 (5)	0.0171 (6)	0.0015 (6)
C9	0.0427 (7)	0.0482 (7)	0.0495 (8)	−0.0006 (5)	0.0144 (5)	−0.0057 (6)
C16	0.0458 (6)	0.0452 (7)	0.0570 (8)	−0.0010 (5)	0.0169 (6)	−0.0030 (6)
C10	0.0433 (7)	0.0475 (7)	0.0530 (8)	0.0017 (5)	0.0208 (6)	0.0013 (6)
C7	0.0462 (7)	0.0503 (7)	0.0505 (8)	0.0049 (5)	0.0146 (6)	0.0000 (6)
C4	0.0474 (7)	0.0592 (8)	0.0668 (9)	0.0011 (6)	0.0178 (6)	0.0085 (7)
C6	0.0566 (8)	0.0565 (7)	0.0588 (9)	0.0020 (6)	0.0222 (7)	0.0023 (7)
C5	0.0440 (7)	0.0458 (7)	0.0508 (8)	0.0001 (5)	0.0182 (6)	−0.0039 (6)
C1	0.0608 (9)	0.0757 (9)	0.0755 (11)	−0.0076 (7)	0.0335 (8)	0.0056 (8)
C2	0.0465 (8)	0.0847 (10)	0.0779 (10)	−0.0075 (7)	0.0272 (7)	−0.0097 (9)
C11	0.0486 (7)	0.0614 (8)	0.0613 (9)	−0.0012 (6)	0.0168 (6)	0.0034 (7)
C3	0.0436 (8)	0.0732 (9)	0.0757 (10)	0.0054 (6)	0.0149 (7)	0.0012 (8)
C17	0.0549 (7)	0.0536 (8)	0.0690 (9)	−0.0005 (6)	0.0253 (7)	0.0041 (7)
C14	0.0774 (11)	0.0503 (8)	0.1059 (13)	0.0079 (7)	0.0408 (10)	0.0020 (8)
C15	0.0530 (8)	0.0548 (8)	0.0753 (10)	0.0018 (6)	0.0229 (7)	−0.0052 (7)
C13	0.0682 (10)	0.0724 (11)	0.0999 (13)	0.0228 (8)	0.0365 (10)	0.0281 (9)
C12	0.0509 (8)	0.0846 (11)	0.0754 (11)	0.0103 (7)	0.0181 (7)	0.0199 (9)
C18	0.0528 (7)	0.0489 (7)	0.0626 (9)	−0.0029 (5)	0.0199 (6)	0.0020 (6)
N2	0.0721 (8)	0.0606 (7)	0.0865 (10)	0.0055 (6)	0.0202 (7)	0.0097 (7)
N1	0.0661 (8)	0.0863 (9)	0.1148 (11)	0.0025 (6)	0.0457 (8)	0.0183 (8)

C8—C7	1.3344 (15)	C1—C2	1.3706 (19)
C8—C9	1.4457 (14)	C1—H1	0.9300
C8—H8	0.9300	C2—C3	1.3703 (18)
C9—C16	1.3701 (15)	C2—H2	0.9300
C9—C10	1.4795 (15)	C11—C12	1.3804 (17)
C16—C17	1.4308 (16)	C11—H11	0.9300
C16—C18	1.4323 (18)	C3—H3	0.9300
C10—C11	1.3869 (16)	C17—N1	1.1409 (14)
C10—C15	1.3892 (16)	C14—C13	1.372 (2)
C7—C5	1.4590 (15)	C14—C15	1.3773 (18)
C7—H7	0.9300	C14—H14	0.9300
C4—C3	1.3718 (16)	C15—H15	0.9300
C4—C5	1.3932 (16)	C13—C12	1.364 (2)
C4—H4	0.9300	C13—H13	0.9300
C6—C1	1.3805 (16)	C12—H12	0.9300
C6—C5	1.3861 (15)	C18—N2	1.1423 (15)
C6—H6	0.9300
C7—C8—C9	127.01 (11)	C2—C1—H1	120.0
C7—C8—H8	116.5	C6—C1—H1	120.0
C9—C8—H8	116.5	C3—C2—C1	119.97 (12)
C16—C9—C8	118.92 (10)	C3—C2—H2	120.0
C16—C9—C10	120.68 (10)	C1—C2—H2	120.0
C8—C9—C10	120.36 (10)	C12—C11—C10	120.54 (12)
C9—C16—C17	124.07 (10)	C12—C11—H11	119.7
C9—C16—C18	120.73 (10)	C10—C11—H11	119.7
C17—C16—C18	115.09 (10)	C2—C3—C4	120.18 (12)
C11—C10—C15	118.66 (11)	C2—C3—H3	119.9
C11—C10—C9	121.57 (11)	C4—C3—H3	119.9
C15—C10—C9	119.77 (11)	N1—C17—C16	177.09 (14)
C8—C7—C5	125.53 (11)	C13—C14—C15	120.38 (13)
C8—C7—H7	117.2	C13—C14—H14	119.8
C5—C7—H7	117.2	C15—C14—H14	119.8
C3—C4—C5	121.17 (12)	C14—C15—C10	120.15 (13)
C3—C4—H4	119.4	C14—C15—H15	119.9
C5—C4—H4	119.4	C10—C15—H15	119.9
C1—C6—C5	121.10 (12)	C12—C13—C14	120.22 (13)
C1—C6—H6	119.5	C12—C13—H13	119.9
C5—C6—H6	119.5	C14—C13—H13	119.9
C6—C5—C4	117.56 (10)	C13—C12—C11	120.06 (14)
C6—C5—C7	119.86 (11)	C13—C12—H12	120.0
C4—C5—C7	122.57 (11)	C11—C12—H12	120.0
C2—C1—C6	119.99 (12)	N2—C18—C16	177.74 (14)
C7—C8—C9—C16	−174.10 (11)	C8—C7—C5—C6	−170.60 (11)
C7—C8—C9—C10	8.02 (18)	C8—C7—C5—C4	10.37 (18)
C8—C9—C16—C17	−176.08 (12)	C5—C6—C1—C2	0.38 (19)
C10—C9—C16—C17	1.80 (17)	C6—C1—C2—C3	1.3 (2)
C8—C9—C16—C18	−0.14 (17)	C15—C10—C11—C12	−0.38 (18)
C10—C9—C16—C18	177.74 (12)	C9—C10—C11—C12	−179.70 (11)
C16—C9—C10—C11	53.38 (16)	C1—C2—C3—C4	−1.44 (19)
C8—C9—C10—C11	−128.77 (12)	C5—C4—C3—C2	−0.05 (19)
C16—C9—C10—C15	−125.93 (12)	C13—C14—C15—C10	0.4 (2)
C8—C9—C10—C15	51.92 (15)	C11—C10—C15—C14	−0.09 (18)
C9—C8—C7—C5	−177.82 (12)	C9—C10—C15—C14	179.25 (11)
C1—C6—C5—C4	−1.80 (17)	C15—C14—C13—C12	−0.3 (2)
C1—C6—C5—C7	179.11 (12)	C14—C13—C12—C11	−0.2 (2)
C3—C4—C5—C6	1.64 (17)	C10—C11—C12—C13	0.5 (2)
C3—C4—C5—C7	−179.30 (12)