(E)-2-Chloro-N'-(2-hydr-oxy-1-naphthyl-methyl-ene)benzohydrazide.

In the structue of the title compound, C(18)H(13)ClN(2)O(2), a new Schiff base, the dihedral angle between the benzene and naphthyl ring system mean planes is 22.5 (2)°. The mol-ecule has an E configuration about the C=N bond, and an intra-molecular hydrogen bond involving the hydoxyl substituent on the naphthyl ring and the N' atom of the hydrazide. The crystal structure is stabilized by inter-molecular N-H⋯O hydrogen bonds, forming one-dimensional chains running parallel to the a axis.

Related literature

For background on Schiff base compounds, hydrazone compounds and their biological properties, see: Kucukguzel et al. (2006 ▶); Khattab (2005 ▶); Karthikeyan et al. (2006 ▶); Okabe et al. (1993 ▶). For bond distances, see: Allen et al. (1987 ▶). For related structures, see: Shan et al. (2008 ▶); Fun et al. (2008 ▶); Yang (2008 ▶); Ma et al. (2008 ▶); Diao, Huang et al. (2008 ▶); Diao, Zhen et al. (2008 ▶); Ejsmont et al. (2008 ▶).

Experimental

Crystal data

C18H13ClN2O2

M = 324.75

Monoclinic,

a = 7.2797 (14) Å

b = 29.148 (6) Å

c = 7.6889 (16) Å

β = 112.130 (3)°

V = 1511.3 (5) Å3

Z = 4

Mo Kα radiation

μ = 0.26 mm−1

T = 298 (2) K

0.32 × 0.27 × 0.26 mm

Data collection

Bruker SMART CCD area-detector diffractometer

Absorption correction: multi-scan (SADABS; Bruker, 2001 ▶) T min = 0.920, T max = 0.934

8693 measured reflections

3255 independent reflections

2320 reflections with I > 2σ(I)

R int = 0.036

Refinement

R[F 2 > 2σ(F 2)] = 0.044

wR(F 2) = 0.105

S = 1.03

3255 reflections

213 parameters

1 restraint

H atoms treated by a mixture of independent and constrained refinement

Δρmax = 0.21 e Å−3

Δρmin = −0.20 e Å−3

Data collection: SMART (Bruker, 2007 ▶); cell refinement: SAINT (Bruker, 2007 ▶); 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.

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536808031371/su2067sup1.cif

Structure factors: contains datablocks I. DOI: 10.1107/S1600536808031371/su2067Isup2.hkl

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

C18H13ClN2O2	F(000) = 672
Mr = 324.75	Dx = 1.427 Mg m−3
Monoclinic, P21/n	Mo Kα radiation, λ = 0.71073 Å
a = 7.2797 (14) Å	Cell parameters from 2129 reflections
b = 29.148 (6) Å	θ = 2.5–25.3°
c = 7.6889 (16) Å	µ = 0.26 mm−1
β = 112.130 (3)°	T = 298 K
V = 1511.3 (5) Å3	Block, colourless
Z = 4	0.32 × 0.27 × 0.26 mm

Bruker SMART CCD area-detector diffractometer	3255 independent reflections
Radiation source: fine-focus sealed tube	2320 reflections with I > 2σ(I)
graphite	Rint = 0.036
ω scans	θmax = 27.0°, θmin = 2.8°
Absorption correction: multi-scan (SADABS; Bruker, 2001)	h = −9→9
Tmin = 0.920, Tmax = 0.935	k = −31→37
8693 measured reflections	l = −9→6

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) = 0.105	H atoms treated by a mixture of independent and constrained refinement
S = 1.03	w = 1/[σ2(Fo2) + (0.0421P)2 + 0.2242P] where P = (Fo2 + 2Fc2)/3
3255 reflections	(Δ/σ)max < 0.001
213 parameters	Δρmax = 0.21 e Å−3
1 restraint	Δρmin = −0.20 e Å−3

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds 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 > 2sigma(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
Cl1	0.90066 (8)	0.109541 (17)	0.58158 (8)	0.05120 (18)
N1	0.9283 (2)	0.28478 (5)	0.6687 (2)	0.0368 (4)
N2	0.8931 (2)	0.25535 (5)	0.5185 (2)	0.0368 (4)
O1	0.9748 (2)	0.30053 (5)	1.0131 (2)	0.0538 (4)
H1	0.9791	0.2855	0.9244	0.081*
O2	1.10008 (19)	0.20185 (4)	0.70363 (18)	0.0444 (4)
C1	0.8785 (2)	0.35871 (6)	0.7742 (3)	0.0344 (4)
C2	0.9227 (3)	0.34426 (6)	0.9575 (3)	0.0393 (5)
C3	0.9128 (3)	0.37438 (7)	1.0959 (3)	0.0474 (5)
H3	0.9382	0.3637	1.2167	0.057*
C4	0.8661 (3)	0.41905 (8)	1.0537 (3)	0.0513 (6)
H4	0.8594	0.4386	1.1467	0.062*
C5	0.8273 (3)	0.43664 (7)	0.8724 (3)	0.0451 (5)
C6	0.7811 (4)	0.48343 (8)	0.8286 (4)	0.0652 (7)
H6	0.7739	0.5032	0.9210	0.078*
C7	0.7473 (4)	0.49996 (8)	0.6555 (5)	0.0782 (9)
H7	0.7179	0.5309	0.6294	0.094*
C8	0.7564 (4)	0.47067 (8)	0.5156 (4)	0.0739 (8)
H8	0.7334	0.4823	0.3966	0.089*
C9	0.7988 (3)	0.42509 (7)	0.5512 (3)	0.0542 (6)
H9	0.8043	0.4061	0.4561	0.065*
C10	0.8341 (3)	0.40654 (6)	0.7300 (3)	0.0388 (5)
C11	0.8664 (3)	0.32609 (6)	0.6287 (3)	0.0355 (4)
H11	0.8127	0.3352	0.5037	0.043*
C12	0.9814 (3)	0.21388 (6)	0.5489 (3)	0.0329 (4)
C13	0.9258 (2)	0.18457 (6)	0.3775 (3)	0.0317 (4)
C14	0.8905 (3)	0.13760 (6)	0.3788 (3)	0.0348 (4)
C15	0.8421 (3)	0.11196 (7)	0.2176 (3)	0.0471 (5)
H15	0.8181	0.0807	0.2204	0.057*
C16	0.8291 (3)	0.13237 (8)	0.0521 (3)	0.0529 (6)
H16	0.7964	0.1148	−0.0565	0.064*
C17	0.8642 (3)	0.17866 (7)	0.0464 (3)	0.0501 (5)
H17	0.8559	0.1924	−0.0654	0.060*
C18	0.9117 (3)	0.20441 (6)	0.2079 (3)	0.0396 (5)
H18	0.9349	0.2357	0.2037	0.048*
H2	0.799 (2)	0.2634 (6)	0.4086 (18)	0.047 (6)*

	U11	U22	U33	U12	U13	U23
Cl1	0.0587 (3)	0.0436 (3)	0.0540 (4)	−0.0002 (2)	0.0242 (3)	0.0116 (2)
N1	0.0399 (9)	0.0341 (8)	0.0326 (9)	0.0012 (7)	0.0095 (7)	−0.0065 (7)
N2	0.0402 (9)	0.0344 (8)	0.0278 (9)	0.0059 (7)	0.0039 (7)	−0.0035 (7)
O1	0.0788 (11)	0.0439 (8)	0.0389 (9)	0.0039 (8)	0.0224 (8)	0.0056 (7)
O2	0.0500 (8)	0.0404 (7)	0.0294 (8)	0.0053 (6)	−0.0006 (6)	0.0002 (6)
C1	0.0308 (9)	0.0349 (10)	0.0356 (11)	−0.0021 (8)	0.0105 (8)	−0.0039 (8)
C2	0.0366 (10)	0.0419 (11)	0.0401 (12)	−0.0046 (9)	0.0154 (9)	−0.0041 (9)
C3	0.0508 (12)	0.0563 (13)	0.0383 (12)	−0.0091 (10)	0.0205 (10)	−0.0107 (10)
C4	0.0491 (12)	0.0551 (13)	0.0530 (15)	−0.0102 (10)	0.0228 (11)	−0.0247 (11)
C5	0.0374 (11)	0.0402 (11)	0.0547 (14)	−0.0054 (9)	0.0141 (10)	−0.0149 (10)
C6	0.0664 (16)	0.0421 (13)	0.079 (2)	0.0021 (11)	0.0187 (14)	−0.0185 (13)
C7	0.092 (2)	0.0353 (13)	0.094 (2)	0.0088 (12)	0.0198 (18)	0.0016 (14)
C8	0.096 (2)	0.0482 (14)	0.0684 (19)	0.0107 (13)	0.0212 (15)	0.0119 (13)
C9	0.0691 (15)	0.0403 (12)	0.0506 (14)	0.0050 (10)	0.0196 (12)	0.0016 (10)
C10	0.0328 (10)	0.0354 (10)	0.0457 (12)	−0.0023 (8)	0.0120 (9)	−0.0045 (9)
C11	0.0353 (10)	0.0362 (10)	0.0318 (10)	−0.0013 (8)	0.0089 (8)	−0.0015 (8)
C12	0.0338 (10)	0.0324 (9)	0.0301 (10)	−0.0017 (8)	0.0093 (8)	0.0010 (8)
C13	0.0293 (9)	0.0341 (9)	0.0285 (10)	0.0028 (8)	0.0074 (8)	−0.0017 (8)
C14	0.0318 (9)	0.0339 (10)	0.0361 (11)	0.0023 (8)	0.0097 (8)	0.0005 (8)
C15	0.0470 (12)	0.0372 (11)	0.0528 (14)	−0.0003 (9)	0.0139 (10)	−0.0097 (10)
C16	0.0553 (13)	0.0575 (14)	0.0384 (13)	0.0062 (11)	0.0091 (10)	−0.0156 (11)
C17	0.0575 (13)	0.0597 (14)	0.0326 (12)	0.0077 (11)	0.0163 (10)	0.0002 (10)
C18	0.0434 (11)	0.0378 (10)	0.0355 (11)	0.0037 (9)	0.0124 (9)	0.0013 (9)

Cl1—C14	1.737 (2)	C6—H6	0.9300
N1—C11	1.282 (2)	C7—C8	1.394 (4)
N1—N2	1.383 (2)	C7—H7	0.9300
N2—C12	1.347 (2)	C8—C9	1.368 (3)
N2—H2	0.896 (9)	C8—H8	0.9300
O1—C2	1.353 (2)	C9—C10	1.408 (3)
O1—H1	0.8200	C9—H9	0.9300
O2—C12	1.229 (2)	C11—H11	0.9300
C1—C2	1.388 (3)	C12—C13	1.493 (2)
C1—C10	1.443 (3)	C13—C14	1.394 (2)
C1—C11	1.445 (3)	C13—C18	1.395 (3)
C2—C3	1.402 (3)	C14—C15	1.375 (3)
C3—C4	1.354 (3)	C15—C16	1.375 (3)
C3—H3	0.9300	C15—H15	0.9300
C4—C5	1.411 (3)	C16—C17	1.377 (3)
C4—H4	0.9300	C16—H16	0.9300
C5—C6	1.415 (3)	C17—C18	1.379 (3)
C5—C10	1.418 (3)	C17—H17	0.9300
C6—C7	1.348 (4)	C18—H18	0.9300
C11—N1—N2	116.37 (16)	C8—C9—H9	119.6
C12—N2—N1	119.02 (15)	C10—C9—H9	119.6
C12—N2—H2	123.0 (13)	C9—C10—C5	118.02 (18)
N1—N2—H2	117.4 (13)	C9—C10—C1	122.90 (18)
C2—O1—H1	109.5	C5—C10—C1	119.08 (19)
C2—C1—C10	118.55 (17)	N1—C11—C1	121.25 (18)
C2—C1—C11	120.65 (17)	N1—C11—H11	119.4
C10—C1—C11	120.71 (17)	C1—C11—H11	119.4
O1—C2—C1	122.49 (17)	O2—C12—N2	122.65 (17)
O1—C2—C3	116.01 (18)	O2—C12—C13	123.31 (16)
C1—C2—C3	121.50 (19)	N2—C12—C13	114.02 (15)
C4—C3—C2	120.0 (2)	C14—C13—C18	117.70 (17)
C4—C3—H3	120.0	C14—C13—C12	123.07 (17)
C2—C3—H3	120.0	C18—C13—C12	119.22 (16)
C3—C4—C5	121.66 (19)	C15—C14—C13	120.87 (19)
C3—C4—H4	119.2	C15—C14—Cl1	117.58 (15)
C5—C4—H4	119.2	C13—C14—Cl1	121.53 (14)
C4—C5—C6	121.8 (2)	C16—C15—C14	120.25 (19)
C4—C5—C10	119.08 (19)	C16—C15—H15	119.9
C6—C5—C10	119.1 (2)	C14—C15—H15	119.9
C7—C6—C5	121.2 (2)	C15—C16—C17	120.3 (2)
C7—C6—H6	119.4	C15—C16—H16	119.8
C5—C6—H6	119.4	C17—C16—H16	119.8
C6—C7—C8	119.9 (2)	C16—C17—C18	119.4 (2)
C6—C7—H7	120.0	C16—C17—H17	120.3
C8—C7—H7	120.0	C18—C17—H17	120.3
C9—C8—C7	120.9 (3)	C17—C18—C13	121.45 (18)
C9—C8—H8	119.6	C17—C18—H18	119.3
C7—C8—H8	119.6	C13—C18—H18	119.3
C8—C9—C10	120.8 (2)

D—H···A	D—H	H···A	D···A	D—H···A
N2—H2···O2i	0.90 (1)	1.97 (1)	2.842 (2)	164 (2)
O1—H1···N1	0.82	1.86	2.581 (2)	146

Table 1

Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N2—H2⋯O2i	0.896 (9)	1.972 (11)	2.842 (2)	163.5 (18)
O1—H1⋯N1	0.82	1.86	2.581 (2)	146

Symmetry code: (i) .