{6,6'-Dimeth-oxy-2,2'-[ethane-1,2-diylbis(nitrilo-methyl-idyne)]diphenolato-1κO,O,O,O:2κO,N,N',O}(ethanol-1κO)-μ-nitrato-1:2κO:O'-dinitrato-1κO,O'-samarium(III)zinc(II).

In the title heteronuclear Zn(II)-Sm(III) complex, [SmZn(C(18)H(18)N(2)O(4))(NO(3))(3)(CH(3)CH(2)OH)], with the hexa-dentate Schiff base compartmental ligand N,N'-bis-(3-methoxy-salicyl-idene)ethyl-enediamine (H(2)L), the Sm(III) and Zn(II) ions are triply bridged by two phenolate O atoms from the Schiff base ligand and one nitrate anion. The five-coordinate Zn(II) ion is in a square-pyramidal geometry formed by the donor centers of two imine N atoms, two phenolate O atoms and one of the bridging nitrate O atoms. The Sm(III) center is in a ten-fold coordination of O atoms, involving the phenolate O atoms, two meth-oxy O atoms, one ethanol O atom, and two O atoms from two nitrate anions and one from the bridging nitrate anion. In the crystal, inter-molecular O-H⋯O and C-H⋯O inter-actions generate a layer structure extending parallel to (101).

Related literature

For the preparation, magnetic and optical properties of 3d-4f hetorometallic dinuclear complexes, see: Baggio et al. (2000 ▶); Caravan et al. (1999 ▶); Edder et al. (2000 ▶); Knoer et al. (2005 ▶).

Experimental

Crystal data

[SmZn(C18H18N2O4)(NO3)3(C2H6O)]

M = 774.16

Monoclinic,

a = 9.975 (3) Å

b = 13.780 (4) Å

c = 19.889 (6) Å

β = 91.745 (4)°

V = 2732.4 (13) Å3

Z = 4

Mo Kα radiation

μ = 3.08 mm−1

T = 293 K

0.26 × 0.23 × 0.19 mm

Data collection

Bruker APEXII area-detector diffractometer

Absorption correction: multi-scan (SADABS; Bruker, 2004 ▶) T min = 0.501, T max = 0.592

16112 measured reflections

4741 independent reflections

4175 reflections with I > 2σ(I)

R int = 0.021

Refinement

R[F 2 > 2σ(F 2)] = 0.027

wR(F 2) = 0.079

S = 1.08

4741 reflections

377 parameters

3 restraints

H atoms treated by a mixture of independent and constrained refinement

Δρmax = 0.67 e Å−3

Δρmin = −0.70 e Å−3

Data collection: APEX2 (Bruker, 2004 ▶); cell refinement: SAINT (Bruker, 2004 ▶); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: SHELXL97; software used to prepare material for publication: SHELXL97 and publCIF (Westrip, 2009 ▶).

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536809033558/at2862sup1.cif

Structure factors: contains datablocks I. DOI: 10.1107/S1600536809033558/at2862Isup2.hkl

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

[SmZn(C18H18N2O4)(NO3)3(C2H6O)]	F(000) = 1532
Mr = 774.16	Dx = 1.882 Mg m−3
Monoclinic, P21/n	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2yn	Cell parameters from 5725 reflections
a = 9.975 (3) Å	θ = 2.5–28.2°
b = 13.780 (4) Å	µ = 3.08 mm−1
c = 19.889 (6) Å	T = 293 K
β = 91.745 (4)°	Block, yellow
V = 2732.4 (13) Å3	0.26 × 0.23 × 0.19 mm
Z = 4

Bruker APEXII area-detector diffractometer	4741 independent reflections
Radiation source: fine-focus sealed tube	4175 reflections with I > 2σ(I)
graphite	Rint = 0.021
φ and ω scans	θmax = 25.0°, θmin = 1.8°
Absorption correction: multi-scan (SADABS; Bruker, 2004)	h = −11→11
Tmin = 0.501, Tmax = 0.592	k = −15→16
16112 measured reflections	l = −23→23

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)] = 0.027	Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.079	H atoms treated by a mixture of independent and constrained refinement
S = 1.08	w = 1/[σ2(Fo2) + (0.045P)2 + 4.1668P] where P = (Fo2 + 2Fc2)/3
4741 reflections	(Δ/σ)max < 0.001
377 parameters	Δρmax = 0.67 e Å−3
3 restraints	Δρmin = −0.70 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
C1	0.5387 (4)	0.1513 (4)	0.1046 (2)	0.0435 (11)
H1A	0.6226	0.1846	0.1108	0.065*
H1B	0.5050	0.1609	0.0594	0.065*
H1C	0.5517	0.0832	0.1126	0.065*
C2	0.4878 (4)	0.1904 (3)	0.21745 (19)	0.0287 (8)
C3	0.4091 (4)	0.2491 (3)	0.25846 (18)	0.0248 (8)
C4	0.4475 (4)	0.2570 (3)	0.32728 (19)	0.0309 (9)
C5	0.5626 (4)	0.2059 (3)	0.3513 (2)	0.0405 (11)
H5	0.5894	0.2119	0.3963	0.049*
C6	0.6343 (5)	0.1489 (4)	0.3106 (2)	0.0468 (12)
H6	0.7083	0.1151	0.3280	0.056*
C7	0.5978 (4)	0.1404 (3)	0.2430 (2)	0.0416 (10)
H7	0.6473	0.1011	0.2150	0.050*
C8	0.3727 (4)	0.3097 (3)	0.37649 (19)	0.0325 (9)
H8	0.4042	0.3070	0.4209	0.039*
C9	0.1883 (5)	0.4013 (3)	0.4187 (2)	0.0419 (11)
H9A	0.1913	0.4716	0.4174	0.050*
H9B	0.2236	0.3797	0.4621	0.050*
C10	0.0444 (5)	0.3652 (4)	0.4069 (2)	0.0432 (11)
H10A	0.0380	0.2976	0.4201	0.052*
H10B	−0.0162	0.4027	0.4340	0.052*
C11	−0.1155 (4)	0.3718 (3)	0.3160 (2)	0.0376 (10)
H11	−0.1793	0.3652	0.3488	0.045*
C12	−0.1630 (4)	0.3768 (3)	0.2471 (2)	0.0337 (9)
C13	−0.3008 (4)	0.3975 (3)	0.2340 (3)	0.0454 (11)
H13	−0.3576	0.4041	0.2700	0.054*
C14	−0.3520 (4)	0.4080 (3)	0.1702 (3)	0.0482 (12)
H14	−0.4427	0.4212	0.1631	0.058*
C15	−0.2698 (4)	0.3991 (3)	0.1159 (2)	0.0419 (11)
H15	−0.3044	0.4081	0.0724	0.050*
C16	−0.1355 (4)	0.3769 (3)	0.1268 (2)	0.0327 (9)
C17	−0.0801 (4)	0.3635 (3)	0.1915 (2)	0.0291 (8)
C18	−0.0918 (5)	0.3868 (4)	0.0095 (2)	0.0523 (13)
H18A	−0.1594	0.3406	−0.0040	0.078*
H18B	−0.0188	0.3835	−0.0207	0.078*
H18C	−0.1295	0.4509	0.0085	0.078*
C19	0.0334 (4)	0.0595 (3)	0.1448 (3)	0.0453 (11)
H19A	0.0360	0.0054	0.1761	0.054*
H19B	0.0421	0.0337	0.0998	0.054*
C20	−0.0964 (5)	0.1103 (4)	0.1492 (3)	0.0640 (15)
H20A	−0.1040	0.1376	0.1934	0.096*
H20B	−0.1683	0.0651	0.1409	0.096*
H20C	−0.1014	0.1612	0.1163	0.096*
H14S	0.189 (4)	0.093 (3)	0.1907 (18)	0.045 (14)*
N1	0.2671 (4)	0.3598 (3)	0.36409 (16)	0.0334 (8)
N2	0.0069 (4)	0.3757 (3)	0.33567 (17)	0.0365 (8)
N3	0.2742 (4)	0.5201 (3)	0.18223 (18)	0.0429 (8)
N4	0.3575 (4)	0.3693 (3)	−0.00107 (19)	0.0461 (10)
N5	0.1636 (4)	0.1430 (3)	−0.00124 (17)	0.0380 (8)
O1	0.3020 (3)	0.29131 (19)	0.22943 (13)	0.0285 (6)
O2	0.0480 (2)	0.3360 (2)	0.19722 (13)	0.0310 (6)
O3	0.4443 (3)	0.1886 (2)	0.15072 (13)	0.0340 (6)
O4	−0.0437 (3)	0.3650 (2)	0.07643 (14)	0.0378 (7)
O5	0.2537 (3)	0.4574 (2)	0.13814 (15)	0.0460 (8)
O6	0.2370 (3)	0.5111 (2)	0.24316 (13)	0.0334 (6)
O7	0.3498 (5)	0.6110 (3)	0.1638 (3)	0.0920 (15)
O8	0.4194 (3)	0.3382 (2)	0.05096 (16)	0.0441 (7)
O9	0.2306 (3)	0.3687 (2)	−0.00015 (14)	0.0422 (7)
O10	0.4160 (5)	0.3958 (4)	−0.0499 (2)	0.0997 (17)
O11	0.0688 (3)	0.1928 (2)	0.02181 (14)	0.0383 (7)
O12	0.2775 (3)	0.1549 (2)	0.02628 (15)	0.0408 (7)
O13	0.1458 (4)	0.0871 (3)	−0.04800 (19)	0.0694 (11)
O14	0.1442 (3)	0.1242 (2)	0.16021 (15)	0.0361 (7)
Sm1	0.209482 (19)	0.287372 (15)	0.113944 (9)	0.02816 (9)
Zn1	0.17006 (4)	0.38157 (3)	0.27338 (2)	0.02711 (12)

	U11	U22	U33	U12	U13	U23
C1	0.035 (2)	0.060 (3)	0.036 (2)	0.016 (2)	0.0029 (18)	−0.011 (2)
C2	0.0245 (19)	0.034 (2)	0.027 (2)	−0.0018 (16)	−0.0040 (15)	0.0050 (16)
C3	0.0228 (19)	0.028 (2)	0.0233 (19)	−0.0031 (15)	−0.0020 (14)	0.0067 (15)
C4	0.028 (2)	0.038 (2)	0.027 (2)	−0.0031 (17)	−0.0074 (16)	0.0051 (17)
C5	0.035 (2)	0.058 (3)	0.028 (2)	0.001 (2)	−0.0093 (18)	0.0101 (19)
C6	0.036 (2)	0.058 (3)	0.046 (3)	0.012 (2)	−0.012 (2)	0.015 (2)
C7	0.036 (2)	0.045 (3)	0.044 (3)	0.0095 (19)	0.0013 (19)	0.007 (2)
C8	0.036 (2)	0.041 (2)	0.0203 (19)	−0.0063 (18)	−0.0052 (16)	0.0038 (17)
C9	0.056 (3)	0.049 (3)	0.021 (2)	0.003 (2)	0.0044 (18)	−0.0073 (19)
C10	0.052 (3)	0.053 (3)	0.026 (2)	0.004 (2)	0.0140 (19)	−0.0007 (19)
C11	0.035 (2)	0.036 (2)	0.043 (3)	−0.0011 (18)	0.0172 (19)	−0.0053 (19)
C12	0.026 (2)	0.031 (2)	0.045 (2)	−0.0022 (16)	0.0072 (17)	−0.0053 (18)
C13	0.028 (2)	0.041 (3)	0.068 (3)	−0.0012 (19)	0.015 (2)	−0.008 (2)
C14	0.022 (2)	0.049 (3)	0.074 (4)	0.0056 (19)	−0.004 (2)	−0.007 (2)
C15	0.029 (2)	0.038 (3)	0.057 (3)	0.0059 (18)	−0.010 (2)	−0.005 (2)
C16	0.029 (2)	0.027 (2)	0.042 (2)	0.0032 (16)	−0.0028 (17)	−0.0083 (17)
C17	0.025 (2)	0.024 (2)	0.038 (2)	0.0009 (15)	0.0006 (16)	−0.0061 (16)
C18	0.051 (3)	0.066 (3)	0.039 (3)	0.017 (2)	−0.013 (2)	−0.001 (2)
C19	0.038 (3)	0.038 (3)	0.060 (3)	−0.002 (2)	−0.002 (2)	0.006 (2)
C20	0.036 (3)	0.059 (3)	0.097 (5)	−0.002 (2)	0.009 (3)	−0.003 (3)
N1	0.043 (2)	0.0359 (19)	0.0215 (16)	−0.0051 (16)	0.0014 (14)	−0.0033 (14)
N2	0.040 (2)	0.041 (2)	0.0291 (18)	−0.0007 (16)	0.0111 (15)	0.0003 (15)
N3	0.058 (2)	0.038 (2)	0.0329 (14)	0.0040 (17)	0.0048 (15)	−0.0028 (12)
N4	0.053 (3)	0.048 (2)	0.038 (2)	0.0035 (18)	0.0141 (18)	0.0109 (18)
N5	0.047 (2)	0.038 (2)	0.0287 (18)	−0.0019 (17)	−0.0023 (16)	−0.0059 (16)
O1	0.0244 (14)	0.0385 (16)	0.0221 (14)	0.0051 (11)	−0.0042 (10)	−0.0010 (11)
O2	0.0226 (13)	0.0421 (16)	0.0282 (14)	0.0061 (12)	−0.0005 (11)	−0.0067 (12)
O3	0.0251 (14)	0.0489 (17)	0.0279 (15)	0.0091 (12)	−0.0016 (11)	−0.0054 (12)
O4	0.0317 (15)	0.0516 (18)	0.0298 (15)	0.0093 (13)	−0.0054 (12)	−0.0056 (13)
O5	0.071 (2)	0.0360 (17)	0.0308 (15)	−0.0057 (15)	0.0056 (15)	−0.0015 (11)
O6	0.0410 (16)	0.0288 (15)	0.0303 (12)	−0.0026 (12)	0.0015 (11)	−0.0031 (11)
O7	0.114 (4)	0.069 (3)	0.095 (4)	−0.018 (3)	0.033 (3)	−0.002 (2)
O8	0.0332 (16)	0.053 (2)	0.0460 (19)	−0.0035 (14)	−0.0014 (13)	0.0090 (15)
O9	0.0420 (18)	0.054 (2)	0.0309 (16)	0.0052 (14)	−0.0023 (13)	0.0070 (14)
O10	0.085 (3)	0.143 (5)	0.074 (3)	0.015 (3)	0.042 (3)	0.058 (3)
O11	0.0355 (16)	0.0480 (18)	0.0310 (16)	0.0025 (13)	−0.0073 (12)	−0.0040 (13)
O12	0.0341 (17)	0.0488 (19)	0.0393 (17)	0.0041 (13)	−0.0037 (13)	−0.0085 (14)
O13	0.082 (3)	0.069 (3)	0.056 (2)	−0.001 (2)	−0.013 (2)	−0.036 (2)
O14	0.0323 (16)	0.0368 (17)	0.0386 (17)	−0.0058 (12)	−0.0078 (13)	0.0112 (13)
Sm1	0.02985 (13)	0.03342 (14)	0.02110 (13)	0.00080 (8)	−0.00085 (8)	−0.00187 (8)
Zn1	0.0286 (2)	0.0328 (3)	0.0200 (2)	−0.00050 (18)	0.00205 (17)	−0.00135 (17)

C1—O3	1.430 (5)	C17—O2	1.334 (5)
C1—H1A	0.9600	C18—O4	1.433 (5)
C1—H1B	0.9600	C18—H18A	0.9600
C1—H1C	0.9600	C18—H18B	0.9600
C2—C7	1.379 (6)	C18—H18C	0.9600
C2—O3	1.384 (5)	C19—O14	1.446 (5)
C2—C3	1.406 (6)	C19—C20	1.477 (7)
C3—O1	1.333 (4)	C19—H19A	0.9700
C3—C4	1.414 (5)	C19—H19B	0.9700
C4—C5	1.418 (6)	C20—H20A	0.9600
C4—C8	1.444 (6)	C20—H20B	0.9600
C5—C6	1.348 (7)	C20—H20C	0.9600
C5—H5	0.9300	N1—Zn1	2.043 (3)
C6—C7	1.387 (6)	N2—Zn1	2.077 (3)
C6—H6	0.9300	N3—O5	1.244 (5)
C7—H7	0.9300	N3—O6	1.284 (4)
C8—N1	1.277 (5)	N3—O7	1.512 (6)
C8—H8	0.9300	N4—O10	1.205 (5)
C9—N1	1.474 (5)	N4—O8	1.264 (5)
C9—C10	1.530 (7)	N4—O9	1.267 (5)
C9—H9A	0.9700	N5—O13	1.217 (5)
C9—H9B	0.9700	N5—O12	1.257 (4)
C10—N2	1.462 (5)	N5—O11	1.265 (5)
C10—H10A	0.9700	O1—Zn1	2.028 (3)
C10—H10B	0.9700	O1—Sm1	2.450 (3)
C11—N2	1.272 (6)	O2—Zn1	2.014 (3)
C11—C12	1.438 (6)	O2—Sm1	2.439 (3)
C11—H11	0.9300	O3—Sm1	2.787 (3)
C12—C17	1.413 (6)	O4—Sm1	2.822 (3)
C12—C13	1.420 (6)	O5—Sm1	2.429 (3)
C13—C14	1.362 (7)	O6—Zn1	2.004 (3)
C13—H13	0.9300	O8—Sm1	2.570 (3)
C14—C15	1.380 (7)	O9—Sm1	2.545 (3)
C14—H14	0.9300	O11—Sm1	2.621 (3)
C15—C16	1.385 (6)	O12—Sm1	2.627 (3)
C15—H15	0.9300	O14—Sm1	2.523 (3)
C16—O4	1.387 (5)	O14—H14S	0.855 (19)
C16—C17	1.398 (6)
O3—C1—H1A	109.5	O5—N3—O7	118.5 (4)
O3—C1—H1B	109.5	O6—N3—O7	118.0 (3)
H1A—C1—H1B	109.5	O10—N4—O8	121.8 (4)
O3—C1—H1C	109.5	O10—N4—O9	121.5 (4)
H1A—C1—H1C	109.5	O8—N4—O9	116.7 (3)
H1B—C1—H1C	109.5	O13—N5—O12	121.7 (4)
C7—C2—O3	124.6 (4)	O13—N5—O11	121.8 (4)
C7—C2—C3	121.7 (4)	O12—N5—O11	116.6 (3)
O3—C2—C3	113.7 (3)	C3—O1—Zn1	127.1 (2)
O1—C3—C2	117.0 (3)	C3—O1—Sm1	132.1 (2)
O1—C3—C4	125.1 (3)	Zn1—O1—Sm1	100.77 (10)
C2—C3—C4	117.8 (3)	C17—O2—Zn1	122.1 (2)
C3—C4—C5	118.7 (4)	C17—O2—Sm1	132.1 (2)
C3—C4—C8	124.4 (4)	Zn1—O2—Sm1	101.52 (10)
C5—C4—C8	116.8 (4)	C2—O3—C1	115.4 (3)
C6—C5—C4	121.8 (4)	C2—O3—Sm1	118.7 (2)
C6—C5—H5	119.1	C1—O3—Sm1	124.9 (2)
C4—C5—H5	119.1	C16—O4—C18	115.8 (3)
C5—C6—C7	120.1 (4)	C16—O4—Sm1	117.3 (2)
C5—C6—H6	119.9	C18—O4—Sm1	126.7 (3)
C7—C6—H6	119.9	N3—O5—Sm1	146.6 (3)
C2—C7—C6	119.9 (4)	N3—O6—Zn1	118.6 (2)
C2—C7—H7	120.1	N4—O8—Sm1	96.1 (2)
C6—C7—H7	120.1	N4—O9—Sm1	97.2 (2)
N1—C8—C4	125.5 (4)	N5—O11—Sm1	97.6 (2)
N1—C8—H8	117.3	N5—O12—Sm1	97.6 (2)
C4—C8—H8	117.3	C19—O14—Sm1	132.6 (2)
N1—C9—C10	106.2 (3)	C19—O14—H14S	103 (3)
N1—C9—H9A	110.5	Sm1—O14—H14S	125 (3)
C10—C9—H9A	110.5	O5—Sm1—O2	73.74 (10)
N1—C9—H9B	110.5	O5—Sm1—O1	74.45 (10)
C10—C9—H9B	110.5	O2—Sm1—O1	66.10 (9)
H9A—C9—H9B	108.7	O5—Sm1—O14	146.58 (10)
N2—C10—C9	109.1 (3)	O2—Sm1—O14	79.28 (10)
N2—C10—H10A	109.9	O1—Sm1—O14	76.81 (9)
C9—C10—H10A	109.9	O5—Sm1—O9	74.48 (10)
N2—C10—H10B	109.9	O2—Sm1—O9	123.96 (10)
C9—C10—H10B	109.9	O1—Sm1—O9	141.92 (10)
H10A—C10—H10B	108.3	O14—Sm1—O9	138.33 (10)
N2—C11—C12	125.3 (4)	O5—Sm1—O8	71.83 (11)
N2—C11—H11	117.4	O2—Sm1—O8	145.17 (10)
C12—C11—H11	117.4	O1—Sm1—O8	99.31 (9)
C17—C12—C13	118.0 (4)	O14—Sm1—O8	130.09 (10)
C17—C12—C11	123.7 (4)	O9—Sm1—O8	49.82 (10)
C13—C12—C11	118.2 (4)	O5—Sm1—O11	135.09 (10)
C14—C13—C12	121.6 (4)	O2—Sm1—O11	105.13 (9)
C14—C13—H13	119.2	O1—Sm1—O11	147.66 (9)
C12—C13—H13	119.2	O14—Sm1—O11	70.91 (9)
C13—C14—C15	120.4 (4)	O9—Sm1—O11	69.69 (10)
C13—C14—H14	119.8	O8—Sm1—O11	102.80 (10)
C15—C14—H14	119.8	O5—Sm1—O12	138.80 (10)
C14—C15—C16	119.5 (4)	O2—Sm1—O12	146.17 (9)
C14—C15—H15	120.3	O1—Sm1—O12	122.69 (9)
C16—C15—H15	120.3	O14—Sm1—O12	72.40 (10)
C15—C16—O4	124.8 (4)	O9—Sm1—O12	71.60 (10)
C15—C16—C17	121.8 (4)	O8—Sm1—O12	68.60 (10)
O4—C16—C17	113.5 (3)	O11—Sm1—O12	48.25 (9)
O2—C17—C16	117.8 (3)	O5—Sm1—O3	105.83 (10)
O2—C17—C12	123.5 (4)	O2—Sm1—O3	121.53 (8)
C16—C17—C12	118.6 (4)	O1—Sm1—O3	58.34 (8)
O4—C18—H18A	109.5	O14—Sm1—O3	72.15 (9)
O4—C18—H18B	109.5	O9—Sm1—O3	110.93 (9)
H18A—C18—H18B	109.5	O8—Sm1—O3	64.54 (9)
O4—C18—H18C	109.5	O11—Sm1—O3	111.62 (9)
H18A—C18—H18C	109.5	O12—Sm1—O3	66.62 (8)
H18B—C18—H18C	109.5	O5—Sm1—O4	80.93 (10)
O14—C19—C20	111.1 (4)	O2—Sm1—O4	58.08 (8)
O14—C19—H19A	109.4	O1—Sm1—O4	123.23 (8)
C20—C19—H19A	109.4	O14—Sm1—O4	101.26 (9)
O14—C19—H19B	109.4	O9—Sm1—O4	72.24 (9)
C20—C19—H19B	109.4	O8—Sm1—O4	120.25 (9)
H19A—C19—H19B	108.0	O11—Sm1—O4	63.13 (9)
C19—C20—H20A	109.5	O12—Sm1—O4	109.57 (9)
C19—C20—H20B	109.5	O3—Sm1—O4	173.01 (9)
H20A—C20—H20B	109.5	O6—Zn1—O2	104.55 (12)
C19—C20—H20C	109.5	O6—Zn1—O1	100.96 (11)
H20A—C20—H20C	109.5	O2—Zn1—O1	82.54 (10)
H20B—C20—H20C	109.5	O6—Zn1—N1	104.02 (13)
C8—N1—C9	121.5 (3)	O2—Zn1—N1	151.32 (13)
C8—N1—Zn1	128.0 (3)	O1—Zn1—N1	89.69 (12)
C9—N1—Zn1	110.2 (3)	O6—Zn1—N2	119.22 (13)
C11—N2—C10	120.6 (4)	O2—Zn1—N2	88.27 (13)
C11—N2—Zn1	125.5 (3)	O1—Zn1—N2	139.80 (13)
C10—N2—Zn1	113.6 (3)	N1—Zn1—N2	79.99 (14)
O5—N3—O6	123.4 (4)

D—H···A	D—H	H···A	D···A	D—H···A
C1—H1B···O12	0.96	2.35	2.995 (5)	125
C18—H18B···O9	0.96	2.52	3.237 (6)	132
O14—H14S···O6i	0.86 (2)	1.87 (2)	2.718 (4)	171 (5)
C8—H8···O11ii	0.93	2.55	3.440 (5)	160

Table 1

Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
C18—H18B⋯O9	0.96	2.52	3.237 (6)	132
O14—H14S⋯O6i	0.855 (19)	1.87 (2)	2.718 (4)	171 (5)
C8—H8⋯O11ii	0.93	2.55	3.440 (5)	160

Symmetry codes: (i) ; (ii) .