Bis(2,5-dihydroxy­benzoato-κO)bis­(1,10-phenathroline-κ2N,N′)cadmium(II) 1.25-hydrate

Zhang, B.-Y.; Nie, J.-J.; Xu, D.-J.

doi:10.1107/S1600536808018126

metal-organic compounds

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ISSN: 2056-9890

Volume 64| Part 7| July 2008| Page m937

doi:10.1107/S1600536808018126

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Bis(2,5-dihydroxybenzoato-κO)bis(1,10-phenathroline-κ²N,N′)cadmium(II) 1.25-hydrate

Bing-Yu Zhang,^a Jing-Jing Nie ^a and Duan-Jun Xu ^a ^*

^aDepartment of Chemistry, Zhejiang University, People's Republic of China
^*Correspondence e-mail: xudj@mail.hz.zj.cn

(Received 26 May 2008; accepted 15 June 2008; online 19 June 2008)

In the crystal structure of the title compound, [Cd(C₇H₅O₄)₂(C₁₂H₈N₂)₂]·1.25H₂O, the Cd²⁺ cation is coordinated by two phenanthroline (phen) molecules and two 2,5-dihydroxybenzoate (dhba) anions in a distorted octahedral geometry. The centroid–centroid distances of 3.809 (2) and 3.680 (2) Å between nearly parallel pyridine rings of the phen ligands and the benzene rings of dhba anions indicate that the dhba anions are involved in π–π stacking in the crystal structure. The face-to-face separation of 3.35 (3) Å between parallel phen ring systems also suggests π–π stacking between adjacent complex molecules. The crystal structure contains extensive O—H⋯O and C—H⋯O hydrogen bonding.

Related literature

For general background, see: Su & Xu (2004 ); Li et al. (2005 ). For a related structure, see: Huang et al. (2006 ).

Experimental

Crystal data

[Cd(C₇H₅O₄)₂(C₁₂H₈N₂)₂]·1.25H₂O
M_r = 801.55
Monoclinic, P 2₁ /n
a = 10.8992 (18) Å
b = 27.300 (2) Å
c = 11.4218 (12) Å
β = 93.700 (6)°
V = 3391.5 (7) Å³
Z = 4
Mo Kα radiation
μ = 0.71 mm⁻¹
T = 295 (2) K
0.20 × 0.16 × 0.12 mm

Data collection

Rigaku R-AXIS RAPID IP diffractometer
Absorption correction: multi-scan (ABSCOR; Higashi, 1995 ) T_min = 0.875, T_max = 0.928
25199 measured reflections
6639 independent reflections
4509 reflections with I > 2σ(I)
R_int = 0.064

Refinement

R[F² > 2σ(F²)] = 0.042
wR(F²) = 0.092
S = 1.03
6639 reflections
478 parameters
H-atom parameters constrained
Δρ_max = 0.53 e Å⁻³
Δρ_min = −0.51 e Å⁻³

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
O1W—H1A⋯O1	0.94	2.09	2.974 (6)	155
O1W—H1B⋯O6	0.92	2.03	2.892 (6)	155
O2W—H2A⋯O2	0.88	1.99	2.869 (18)	175
O2W—H2B⋯O8ⁱ	0.86	2.42	3.28 (2)	173
O3—H3A⋯O2	0.82	1.81	2.540 (3)	147
O4—H4A⋯O7ⁱⁱ	0.82	2.09	2.877 (3)	160
O7—H7A⋯O6	0.82	1.82	2.546 (3)	147
O8—H8A⋯O3ⁱⁱⁱ	0.82	2.10	2.917 (4)	171
C23—H23⋯O1W^iv	0.93	2.49	3.339 (6)	153
C25—H25⋯O6^v	0.93	2.50	3.285 (5)	143
C30—H30⋯O1	0.93	2.56	3.155 (5)	122
C33—H33⋯O5	0.93	2.50	3.105 (5)	123
C38—H38⋯O2^vi	0.93	2.36	3.182 (5)	147
C42—H42⋯O4^vii	0.93	2.58	3.231 (5)	127
Symmetry codes: (i) x, y, z-1; (ii) -x+1, -y+1, -z+1; (iii) $[x-{\script{1\over 2}}, -y+{\script{3\over 2}}, z+{\script{1\over 2}}]$ ; (iv) x-1, y, z; (v) -x, -y+1, -z+1; (vi) $[x-{\script{1\over 2}}, -y+{\script{3\over 2}}, z-{\script{1\over 2}}]$ ; (vii) -x+1, -y+1, -z.

Data collection: PROCESS-AUTO (Rigaku, 1998 ); cell refinement: PROCESS-AUTO; data reduction: CrystalStructure (Rigaku/MSC, 2002 ); program(s) used to solve structure: SIR92 (Altomare et al., 1993 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ); molecular graphics: ORTEP-3 (Farrugia, 1997 ); software used to prepare material for publication: WinGX (Farrugia, 1999 ).

Supporting information

Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536808018126/rk2092sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536808018126/rk2092Isup2.hkl

checkCIF report

Comment top

As part of investigation on the nature of π-π stacking between aromatic rings (Su & Xu, 2004; Li et al., 2005), the title complex recently has been prepared and its crystal structure is reported here.

The molecular structure of the title compound is shown on Fig. 1. The Cd²⁺ cation is coordinated by two phenanthroline (phen) ligands and two 2,5-dihydroxybenzoate (dhba) anions with a distorted octahedral geometry. The centroid-to-centroid distance of 3.809 (2)Å between nearly parallel N1-pyridine and C2ⁱ-benzene rings (dihedral angle 4.89 (17)°; symmetry code: (i) x-1, y, z) and the centroid-to-centroid distance of 3.680 (2)Å between nearly parallel N4-pyridine and C12ⁱⁱ-benzene rings (dihedral angle 5.33 (11)°; symmetry code: (ii) x, y, z-1) indicate that dhba anions are involved in π-π stacking in the crystal structure (Fig. 2), which agrees with the situation found in the 3,5-dihydroxybenzoate complex of Cu²⁺ (Huang et al., 2006). The face-to-face separation of 3.35 (3)Å suggests the existence of π-π stacking between parallel C31-phen and C31ⁱⁱⁱ-phen ring systems (Fig. 3) (symmetry code: (iii) -x, 1-y, 1-z). The crystal structure contains extensive O–H···O and C–H···O hydrogen bonding (Table 1).

Related literature top

For general background, see: Su & Xu (2004); Li et al. (2005). For a related structure, see: Huang et al. (2006).

Experimental top

Cd(NO₃)₂^.4H₂O (0.31 g, 1 mmol), dhba (0.31 g, 2 mmol), phen (0.36 g, 2 mmol) and Na₂CO₃ (0.10 g, 1 mmol) were dissolved in a water-ethanol mixture (20 ml, 2:1). The solution was refluxed for 2 h. After cooling to room temperature the solution was filtered. Single crystals of the title compound were obtained from the filtrate after 4 weeks.

Computing details top

Data collection: PROCESS-AUTO (Rigaku, 1998); cell refinement: PROCESS-AUTO (Rigaku, 1998; data reduction: CrystalStructure (Rigaku/MSC, 2002); program(s) used to solve structure: SIR92 (Altomare et al., 1993); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 (Farrugia, 1997); software used to prepare material for publication: WinGX (Farrugia, 1999).

Figures top

	Fig. 1. The molecular structure of the title compound with the numbering scheme. The displacement ellipsoids are drawn at 40% probability level. H atoms are presented as a small spheres of arbitrary radius. Dashed lines indicate hydrogen bonding.
	Fig. 2. A diagram showing π-π stacking between phen and dhba (symmetry codes: (i) x-1, y, z; (ii) x, y, z-1).
	Fig. 3. A diagram showing π-π stacking between phen ligands (symmetry code: (iii) -x, 1-y, 1-z).

Bis(2,5-dihydroxybenzoato-κO)bis(1,10-phenathroline- κ²N,N')cadmium(II) 1.25-hydrate top

Crystal data top

[Cd(C₇H₅O₄)₂(C₁₂H₈N₂)₂]·1.25H₂O	F(000) = 1626
M_r = 801.55	D_x = 1.570 Mg m⁻³
Monoclinic, P2₁/n	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2yn	Cell parameters from 6929 reflections
a = 10.8992 (18) Å	θ = 2.2–25.5°
b = 27.300 (2) Å	µ = 0.71 mm⁻¹
c = 11.4218 (12) Å	T = 295 K
β = 93.700 (6)°	Prism, colourless
V = 3391.5 (7) Å³	0.20 × 0.16 × 0.12 mm
Z = 4

Data collection top

Rigaku R-AXIS RAPID IP diffractometer	6639 independent reflections
Radiation source: Fine-focus sealed tube	4509 reflections with I > 2σ(I)
Graphite monochromator	R_int = 0.064
Detector resolution: 10.0 pixels mm^-1	θ_max = 26.0°, θ_min = 1.5°
ω scans	h = −13→13
Absorption correction: multi-scan (ABSCOR; Higashi, 1995)	k = −33→31
T_min = 0.875, T_max = 0.928	l = −8→14
25199 measured reflections

Refinement top

Refinement on F²	Primary atom site location: Direct
Least-squares matrix: Full	Secondary atom site location: Difmap
R[F² > 2σ(F²)] = 0.042	Hydrogen site location: Geom
wR(F²) = 0.092	H-atom parameters constrained
S = 1.03	w = 1/[σ²(F_o²) + (0.0349P)²] where P = (F_o² + 2F_c²)/3
6639 reflections	(Δ/σ)_max = 0.001
478 parameters	Δρ_max = 0.53 e Å⁻³
0 restraints	Δρ_min = −0.51 e Å⁻³

Crystal data top

[Cd(C₇H₅O₄)₂(C₁₂H₈N₂)₂]·1.25H₂O	V = 3391.5 (7) Å³
M_r = 801.55	Z = 4
Monoclinic, P2₁/n	Mo Kα radiation
a = 10.8992 (18) Å	µ = 0.71 mm⁻¹
b = 27.300 (2) Å	T = 295 K
c = 11.4218 (12) Å	0.20 × 0.16 × 0.12 mm
β = 93.700 (6)°

Data collection top

Rigaku R-AXIS RAPID IP diffractometer	6639 independent reflections
Absorption correction: multi-scan (ABSCOR; Higashi, 1995)	4509 reflections with I > 2σ(I)
T_min = 0.875, T_max = 0.928	R_int = 0.064
25199 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.042	0 restraints
wR(F²) = 0.092	H-atom parameters constrained
S = 1.03	Δρ_max = 0.53 e Å⁻³
6639 reflections	Δρ_min = −0.51 e Å⁻³
478 parameters

Special details top

Geometry. All s.u.'s (except the s.u. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell s.u.'s are taken into account individually in the estimation of s.u.'s in distances, angles and torsion angles; correlations between s.u.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell s.u.'s is used for estimating s.u.'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	Occ. (<1)
Cd	0.27239 (2)	0.627675 (9)	0.32033 (2)	0.03808 (10)
N1	0.0736 (3)	0.61272 (10)	0.3827 (3)	0.0437 (8)
N2	0.2176 (3)	0.54243 (10)	0.2903 (3)	0.0426 (7)
N3	0.2325 (3)	0.71386 (10)	0.2909 (3)	0.0409 (7)
N4	0.1908 (2)	0.64287 (10)	0.1245 (3)	0.0373 (7)
O1	0.4520 (2)	0.60327 (9)	0.2586 (2)	0.0554 (7)
O2	0.5248 (2)	0.67858 (9)	0.2365 (2)	0.0590 (8)
O3	0.7449 (2)	0.69059 (9)	0.1815 (2)	0.0618 (8)
H3A	0.6784	0.6982	0.2059	0.093*
O4	0.7610 (2)	0.49241 (8)	0.0835 (2)	0.0627 (8)
H4A	0.7009	0.4782	0.1067	0.094*
O5	0.3253 (2)	0.65203 (10)	0.5037 (2)	0.0559 (7)
O6	0.3497 (3)	0.57527 (10)	0.5661 (2)	0.0674 (8)
O7	0.4132 (2)	0.55776 (9)	0.7805 (2)	0.0625 (8)
H7A	0.3931	0.5512	0.7119	0.094*
O8	0.3815 (3)	0.75593 (9)	0.8687 (3)	0.0688 (8)
H8A	0.3502	0.7709	0.8122	0.103*
O1W	0.5601 (4)	0.53969 (17)	0.4499 (5)	0.164 (2)
H1A	0.5263	0.5510	0.3770	0.246*
H1B	0.5107	0.5518	0.5061	0.246*
O2W	0.4794 (19)	0.7748 (7)	0.1426 (18)	0.175 (8)	0.25
H2A	0.4951	0.7462	0.1748	0.262*	0.25
H2B	0.4471	0.7692	0.0728	0.262*	0.25
C1	0.5335 (3)	0.63324 (14)	0.2289 (3)	0.0428 (9)
C2	0.6459 (3)	0.61142 (12)	0.1815 (3)	0.0374 (8)
C3	0.7463 (3)	0.64152 (13)	0.1592 (3)	0.0438 (9)
C4	0.8490 (3)	0.62084 (14)	0.1130 (3)	0.0527 (10)
H4	0.9160	0.6405	0.0985	0.063*
C5	0.8524 (3)	0.57144 (14)	0.0885 (3)	0.0532 (11)
H5	0.9217	0.5581	0.0573	0.064*
C6	0.7541 (3)	0.54164 (13)	0.1099 (3)	0.0451 (9)
C7	0.6515 (3)	0.56179 (12)	0.1553 (3)	0.0410 (9)
H7	0.5848	0.5418	0.1687	0.049*
C11	0.3464 (3)	0.62091 (14)	0.5830 (4)	0.0452 (10)
C12	0.3709 (3)	0.63929 (12)	0.7055 (3)	0.0379 (9)
C13	0.4065 (3)	0.60753 (13)	0.7972 (4)	0.0440 (9)
C14	0.4356 (3)	0.62616 (15)	0.9088 (4)	0.0543 (10)
H14	0.4607	0.6050	0.9695	0.065*
C15	0.4274 (3)	0.67550 (15)	0.9302 (4)	0.0535 (10)
H15	0.4482	0.6876	1.0049	0.064*
C16	0.3888 (3)	0.70707 (13)	0.8417 (4)	0.0441 (9)
C17	0.3611 (3)	0.68917 (12)	0.7302 (3)	0.0417 (9)
H17	0.3354	0.7107	0.6705	0.050*
C21	0.0050 (3)	0.64614 (15)	0.4309 (4)	0.0552 (11)
H21	0.0377	0.6773	0.4431	0.066*
C22	−0.1138 (4)	0.63710 (16)	0.4643 (4)	0.0647 (12)
H22	−0.1592	0.6619	0.4968	0.078*
C23	−0.1624 (4)	0.59145 (16)	0.4486 (4)	0.0614 (12)
H23	−0.2415	0.5848	0.4702	0.074*
C24	−0.0925 (3)	0.55470 (14)	0.3999 (3)	0.0490 (10)
C25	−0.1337 (4)	0.50485 (16)	0.3857 (4)	0.0598 (12)
H25	−0.2114	0.4964	0.4080	0.072*
C26	−0.0631 (4)	0.47059 (16)	0.3413 (4)	0.0586 (11)
H26	−0.0931	0.4388	0.3329	0.070*
C27	0.0583 (4)	0.48147 (14)	0.3058 (3)	0.0491 (10)
C28	0.1355 (4)	0.44647 (14)	0.2590 (4)	0.0626 (12)
H28	0.1086	0.4144	0.2484	0.075*
C29	0.2502 (4)	0.45961 (14)	0.2292 (4)	0.0617 (12)
H29	0.3022	0.4368	0.1978	0.074*
C30	0.2876 (4)	0.50804 (13)	0.2466 (4)	0.0552 (11)
H30	0.3660	0.5167	0.2266	0.066*
C31	0.1027 (3)	0.52963 (13)	0.3183 (3)	0.0421 (9)
C32	0.0266 (3)	0.56682 (13)	0.3680 (3)	0.0417 (9)
C33	0.2558 (3)	0.74832 (14)	0.3709 (4)	0.0526 (10)
H33	0.2890	0.7391	0.4446	0.063*
C34	0.2328 (4)	0.79784 (15)	0.3495 (5)	0.0650 (13)
H34	0.2506	0.8211	0.4076	0.078*
C35	0.1838 (4)	0.81149 (14)	0.2419 (5)	0.0616 (12)
H35	0.1677	0.8444	0.2261	0.074*
C36	0.1574 (3)	0.77631 (13)	0.1546 (4)	0.0465 (10)
C37	0.1035 (4)	0.78818 (15)	0.0403 (4)	0.0587 (12)
H37	0.0841	0.8206	0.0220	0.070*
C38	0.0809 (3)	0.75324 (16)	−0.0406 (4)	0.0614 (12)
H38	0.0451	0.7617	−0.1139	0.074*
C39	0.1107 (3)	0.70333 (14)	−0.0161 (4)	0.0455 (10)
C40	0.0917 (3)	0.66543 (17)	−0.0998 (4)	0.0591 (11)
H40	0.0586	0.6725	−0.1750	0.071*
C41	0.1219 (3)	0.61860 (15)	−0.0698 (4)	0.0549 (11)
H41	0.1090	0.5933	−0.1236	0.066*
C42	0.1721 (3)	0.60929 (15)	0.0422 (4)	0.0496 (10)
H42	0.1942	0.5772	0.0608	0.060*
C43	0.1612 (3)	0.69012 (13)	0.0952 (3)	0.0386 (9)
C44	0.1847 (3)	0.72736 (13)	0.1834 (3)	0.0386 (9)

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Cd	0.04016 (15)	0.03730 (16)	0.03675 (18)	−0.00085 (12)	0.00215 (11)	−0.00014 (13)
N1	0.0454 (17)	0.0433 (18)	0.043 (2)	−0.0004 (14)	0.0040 (15)	0.0050 (15)
N2	0.0491 (18)	0.0400 (17)	0.038 (2)	−0.0047 (14)	0.0013 (15)	0.0008 (15)
N3	0.0441 (17)	0.0397 (18)	0.039 (2)	−0.0014 (13)	0.0033 (15)	−0.0020 (16)
N4	0.0418 (16)	0.0407 (17)	0.0295 (18)	0.0013 (13)	0.0030 (14)	−0.0008 (15)
O1	0.0436 (15)	0.0530 (16)	0.071 (2)	0.0009 (12)	0.0142 (14)	0.0005 (14)
O2	0.0641 (17)	0.0426 (16)	0.071 (2)	0.0051 (13)	0.0099 (15)	−0.0185 (14)
O3	0.0644 (18)	0.0385 (15)	0.083 (2)	−0.0101 (12)	0.0099 (16)	−0.0104 (14)
O4	0.0762 (19)	0.0411 (16)	0.073 (2)	0.0051 (13)	0.0205 (16)	−0.0073 (14)
O5	0.0759 (19)	0.0534 (17)	0.0372 (17)	−0.0074 (14)	−0.0060 (14)	0.0017 (14)
O6	0.101 (2)	0.0471 (17)	0.055 (2)	−0.0132 (15)	0.0091 (17)	−0.0127 (15)
O7	0.083 (2)	0.0428 (16)	0.062 (2)	0.0002 (14)	0.0042 (16)	0.0066 (14)
O8	0.092 (2)	0.0461 (17)	0.067 (2)	−0.0010 (15)	−0.0033 (17)	−0.0163 (15)
O1W	0.106 (3)	0.200 (5)	0.191 (5)	0.021 (3)	0.043 (3)	0.052 (4)
O2W	0.22 (2)	0.158 (17)	0.144 (19)	0.026 (15)	−0.026 (16)	0.012 (14)
C1	0.042 (2)	0.049 (2)	0.037 (2)	0.0022 (18)	−0.0025 (17)	−0.0046 (19)
C2	0.0400 (19)	0.037 (2)	0.035 (2)	0.0011 (15)	0.0003 (17)	0.0003 (17)
C3	0.050 (2)	0.041 (2)	0.040 (3)	−0.0044 (16)	0.0013 (19)	0.0014 (17)
C4	0.047 (2)	0.054 (3)	0.058 (3)	−0.0085 (18)	0.012 (2)	0.009 (2)
C5	0.049 (2)	0.060 (3)	0.052 (3)	0.0049 (19)	0.014 (2)	0.001 (2)
C6	0.058 (2)	0.040 (2)	0.037 (2)	0.0063 (18)	0.0031 (19)	−0.0011 (18)
C7	0.042 (2)	0.039 (2)	0.042 (2)	−0.0003 (16)	0.0018 (18)	0.0032 (17)
C11	0.043 (2)	0.049 (3)	0.044 (3)	−0.0119 (17)	0.0054 (18)	−0.008 (2)
C12	0.0353 (19)	0.043 (2)	0.036 (2)	−0.0043 (15)	0.0035 (16)	0.0005 (17)
C13	0.048 (2)	0.039 (2)	0.046 (3)	−0.0022 (17)	0.0075 (19)	0.005 (2)
C14	0.057 (2)	0.060 (3)	0.046 (3)	−0.005 (2)	−0.003 (2)	0.014 (2)
C15	0.057 (2)	0.067 (3)	0.036 (3)	−0.009 (2)	0.002 (2)	−0.005 (2)
C16	0.048 (2)	0.045 (2)	0.039 (3)	−0.0036 (17)	0.0025 (19)	−0.005 (2)
C17	0.044 (2)	0.037 (2)	0.043 (3)	0.0012 (16)	0.0008 (18)	0.0035 (18)
C21	0.053 (2)	0.052 (2)	0.061 (3)	0.0064 (19)	0.010 (2)	0.006 (2)
C22	0.058 (3)	0.065 (3)	0.073 (3)	0.017 (2)	0.017 (2)	0.014 (2)
C23	0.045 (2)	0.083 (3)	0.057 (3)	0.010 (2)	0.012 (2)	0.024 (3)
C24	0.043 (2)	0.066 (3)	0.038 (2)	−0.0071 (19)	−0.0060 (19)	0.017 (2)
C25	0.049 (2)	0.080 (3)	0.049 (3)	−0.023 (2)	−0.007 (2)	0.020 (2)
C26	0.066 (3)	0.059 (3)	0.050 (3)	−0.027 (2)	−0.008 (2)	0.010 (2)
C27	0.063 (3)	0.046 (2)	0.036 (2)	−0.0118 (19)	−0.008 (2)	0.0047 (19)
C28	0.087 (3)	0.043 (2)	0.057 (3)	−0.012 (2)	−0.006 (3)	−0.001 (2)
C29	0.073 (3)	0.042 (2)	0.070 (3)	0.001 (2)	0.006 (2)	−0.007 (2)
C30	0.058 (2)	0.046 (2)	0.062 (3)	−0.0027 (19)	0.010 (2)	0.000 (2)
C31	0.049 (2)	0.044 (2)	0.032 (2)	−0.0084 (17)	−0.0033 (18)	0.0103 (18)
C32	0.042 (2)	0.054 (2)	0.029 (2)	−0.0024 (17)	−0.0011 (17)	0.0100 (18)
C33	0.055 (2)	0.048 (2)	0.055 (3)	−0.0009 (19)	0.001 (2)	−0.010 (2)
C34	0.069 (3)	0.045 (3)	0.081 (4)	0.000 (2)	0.005 (3)	−0.019 (3)
C35	0.054 (3)	0.036 (2)	0.095 (4)	0.0041 (18)	0.009 (3)	0.001 (3)
C36	0.036 (2)	0.043 (2)	0.061 (3)	0.0022 (17)	0.011 (2)	0.004 (2)
C37	0.050 (2)	0.049 (3)	0.078 (4)	0.0118 (19)	0.011 (2)	0.021 (3)
C38	0.051 (2)	0.076 (3)	0.058 (3)	0.010 (2)	0.006 (2)	0.030 (3)
C39	0.038 (2)	0.058 (3)	0.041 (3)	0.0046 (17)	0.0042 (18)	0.012 (2)
C40	0.051 (2)	0.088 (3)	0.039 (3)	−0.001 (2)	0.000 (2)	0.002 (3)
C41	0.054 (2)	0.070 (3)	0.041 (3)	−0.002 (2)	0.003 (2)	−0.010 (2)
C42	0.047 (2)	0.059 (3)	0.044 (3)	0.0043 (19)	0.006 (2)	−0.002 (2)
C43	0.0302 (18)	0.045 (2)	0.041 (2)	0.0007 (15)	0.0055 (17)	0.0082 (19)
C44	0.0310 (18)	0.043 (2)	0.043 (3)	0.0016 (15)	0.0098 (17)	0.0058 (19)

Geometric parameters (Å, º) top

Cd—O1	2.225 (2)	C14—H14	0.9300
Cd—O5	2.237 (3)	C15—C16	1.374 (5)
Cd—N1	2.360 (3)	C15—H15	0.9300
Cd—N4	2.389 (3)	C16—C17	1.379 (5)
Cd—N3	2.412 (3)	C17—H17	0.9300
Cd—N2	2.422 (3)	C21—C22	1.396 (5)
N1—C21	1.322 (4)	C21—H21	0.9300
N1—C32	1.360 (4)	C22—C23	1.361 (5)
N2—C30	1.327 (4)	C22—H22	0.9300
N2—C31	1.358 (4)	C23—C24	1.397 (5)
N3—C33	1.325 (4)	C23—H23	0.9300
N3—C44	1.353 (4)	C24—C32	1.410 (5)
N4—C42	1.319 (4)	C24—C25	1.439 (5)
N4—C43	1.366 (4)	C25—C26	1.332 (5)
O1—C1	1.270 (4)	C25—H25	0.9300
O2—C1	1.245 (4)	C26—C27	1.440 (5)
O3—C3	1.364 (4)	C26—H26	0.9300
O3—H3A	0.8200	C27—C28	1.402 (5)
O4—C6	1.380 (4)	C27—C31	1.405 (5)
O4—H4A	0.8200	C28—C29	1.364 (5)
O5—C11	1.252 (4)	C28—H28	0.9300
O6—C11	1.262 (4)	C29—C30	1.394 (5)
O7—C13	1.375 (4)	C29—H29	0.9300
O7—H7A	0.8200	C30—H30	0.9300
O8—C16	1.373 (4)	C31—C32	1.450 (5)
O8—H8A	0.8200	C33—C34	1.394 (5)
O1W—H1A	0.9410	C33—H33	0.9300
O1W—H1B	0.9244	C34—C35	1.360 (6)
O2W—H2A	0.8772	C34—H34	0.9300
O2W—H2B	0.8639	C35—C36	1.400 (5)
C1—C2	1.495 (5)	C35—H35	0.9300
C2—C7	1.390 (4)	C36—C44	1.404 (5)
C2—C3	1.405 (5)	C36—C37	1.434 (6)
C3—C4	1.387 (5)	C37—C38	1.339 (6)
C4—C5	1.378 (5)	C37—H37	0.9300
C4—H4	0.9300	C38—C39	1.424 (5)
C5—C6	1.380 (5)	C38—H38	0.9300
C5—H5	0.9300	C39—C43	1.399 (5)
C6—C7	1.377 (5)	C39—C40	1.414 (5)
C7—H7	0.9300	C40—C41	1.358 (5)
C11—C12	1.494 (5)	C40—H40	0.9300
C12—C17	1.396 (4)	C41—C42	1.383 (5)
C12—C13	1.395 (5)	C41—H41	0.9300
C13—C14	1.390 (5)	C42—H42	0.9300
C14—C15	1.373 (5)	C43—C44	1.443 (5)

O1—Cd—O5	101.93 (10)	C16—C17—H17	119.4
O1—Cd—N1	152.57 (10)	C12—C17—H17	119.4
O5—Cd—N1	87.41 (10)	N1—C21—C22	123.5 (4)
O1—Cd—N4	92.14 (10)	N1—C21—H21	118.3
O5—Cd—N4	151.96 (10)	C22—C21—H21	118.3
N1—Cd—N4	91.11 (10)	C23—C22—C21	119.0 (4)
O1—Cd—N3	113.72 (9)	C23—C22—H22	120.5
O5—Cd—N3	82.76 (10)	C21—C22—H22	120.5
N1—Cd—N3	92.88 (9)	C22—C23—C24	119.5 (4)
N4—Cd—N3	69.34 (10)	C22—C23—H23	120.2
O1—Cd—N2	83.18 (9)	C24—C23—H23	120.2
O5—Cd—N2	117.68 (10)	C23—C24—C32	118.0 (4)
N1—Cd—N2	69.74 (10)	C23—C24—C25	123.4 (4)
N4—Cd—N2	87.76 (10)	C32—C24—C25	118.6 (4)
N3—Cd—N2	151.29 (10)	C26—C25—C24	121.6 (4)
C21—N1—C32	118.0 (3)	C26—C25—H25	119.2
C21—N1—Cd	124.1 (3)	C24—C25—H25	119.2
C32—N1—Cd	117.9 (2)	C25—C26—C27	121.7 (4)
C30—N2—C31	117.9 (3)	C25—C26—H26	119.1
C30—N2—Cd	126.2 (2)	C27—C26—H26	119.1
C31—N2—Cd	115.9 (2)	C28—C27—C31	117.7 (4)
C33—N3—C44	118.5 (3)	C28—C27—C26	123.5 (4)
C33—N3—Cd	124.9 (3)	C31—C27—C26	118.8 (4)
C44—N3—Cd	116.6 (2)	C29—C28—C27	119.9 (4)
C42—N4—C43	117.3 (3)	C29—C28—H28	120.1
C42—N4—Cd	125.3 (3)	C27—C28—H28	120.1
C43—N4—Cd	117.5 (2)	C28—C29—C30	118.5 (4)
C1—O1—Cd	122.5 (2)	C28—C29—H29	120.7
C3—O3—H3A	109.5	C30—C29—H29	120.7
C6—O4—H4A	109.5	N2—C30—C29	123.7 (4)
C11—O5—Cd	120.0 (2)	N2—C30—H30	118.2
C13—O7—H7A	109.5	C29—C30—H30	118.2
C16—O8—H8A	109.5	N2—C31—C27	122.3 (3)
H1A—O1W—H1B	106.5	N2—C31—C32	118.1 (3)
H2A—O2W—H2B	106.5	C27—C31—C32	119.5 (3)
O2—C1—O1	124.3 (3)	N1—C32—C24	122.0 (3)
O2—C1—C2	119.3 (3)	N1—C32—C31	118.3 (3)
O1—C1—C2	116.3 (3)	C24—C32—C31	119.8 (3)
C7—C2—C3	119.0 (3)	N3—C33—C34	122.9 (4)
C7—C2—C1	121.0 (3)	N3—C33—H33	118.5
C3—C2—C1	119.9 (3)	C34—C33—H33	118.5
O3—C3—C4	119.3 (3)	C35—C34—C33	118.7 (4)
O3—C3—C2	121.5 (3)	C35—C34—H34	120.7
C4—C3—C2	119.2 (3)	C33—C34—H34	120.7
C5—C4—C3	120.6 (3)	C34—C35—C36	120.4 (4)
C5—C4—H4	119.7	C34—C35—H35	119.8
C3—C4—H4	119.7	C36—C35—H35	119.8
C4—C5—C6	120.6 (3)	C35—C36—C44	117.1 (4)
C4—C5—H5	119.7	C35—C36—C37	123.1 (4)
C6—C5—H5	119.7	C44—C36—C37	119.8 (4)
C7—C6—C5	119.3 (3)	C38—C37—C36	120.9 (4)
C7—C6—O4	121.9 (3)	C38—C37—H37	119.6
C5—C6—O4	118.8 (3)	C36—C37—H37	119.6
C6—C7—C2	121.2 (3)	C37—C38—C39	121.1 (4)
C6—C7—H7	119.4	C37—C38—H38	119.4
C2—C7—H7	119.4	C39—C38—H38	119.4
O5—C11—O6	124.4 (4)	C43—C39—C40	117.2 (4)
O5—C11—C12	117.6 (3)	C43—C39—C38	119.7 (4)
O6—C11—C12	118.0 (4)	C40—C39—C38	123.1 (4)
C17—C12—C13	118.4 (3)	C41—C40—C39	119.7 (4)
C17—C12—C11	120.4 (3)	C41—C40—H40	120.2
C13—C12—C11	121.2 (3)	C39—C40—H40	120.2
O7—C13—C14	118.5 (4)	C40—C41—C42	118.8 (4)
O7—C13—C12	121.7 (4)	C40—C41—H41	120.6
C14—C13—C12	119.8 (3)	C42—C41—H41	120.6
C15—C14—C13	120.6 (4)	N4—C42—C41	124.4 (4)
C15—C14—H14	119.7	N4—C42—H42	117.8
C13—C14—H14	119.7	C41—C42—H42	117.8
C14—C15—C16	120.3 (4)	N4—C43—C39	122.6 (3)
C14—C15—H15	119.8	N4—C43—C44	117.7 (3)
C16—C15—H15	119.8	C39—C43—C44	119.7 (3)
C15—C16—O8	117.6 (4)	N3—C44—C36	122.4 (3)
C15—C16—C17	119.7 (4)	N3—C44—C43	118.8 (3)
O8—C16—C17	122.7 (4)	C36—C44—C43	118.8 (4)
C16—C17—C12	121.2 (3)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O1W—H1A···O1	0.94	2.09	2.974 (6)	155
O1W—H1B···O6	0.92	2.03	2.892 (6)	155
O2W—H2A···O2	0.88	1.99	2.869 (18)	175
O2W—H2B···O8ⁱ	0.86	2.42	3.28 (2)	173
O3—H3A···O2	0.82	1.81	2.540 (3)	147
O4—H4A···O7ⁱⁱ	0.82	2.09	2.877 (3)	160
O7—H7A···O6	0.82	1.82	2.546 (3)	147
O8—H8A···O3ⁱⁱⁱ	0.82	2.10	2.917 (4)	171
C23—H23···O1W^iv	0.93	2.49	3.339 (6)	153
C25—H25···O6^v	0.93	2.50	3.285 (5)	143
C30—H30···O1	0.93	2.56	3.155 (5)	122
C33—H33···O5	0.93	2.50	3.105 (5)	123
C38—H38···O2^vi	0.93	2.36	3.182 (5)	147
C42—H42···O4^vii	0.93	2.58	3.231 (5)	127

Symmetry codes: (i) x, y, z−1; (ii) −x+1, −y+1, −z+1; (iii) x−1/2, −y+3/2, z+1/2; (iv) x−1, y, z; (v) −x, −y+1, −z+1; (vi) x−1/2, −y+3/2, z−1/2; (vii) −x+1, −y+1, −z.

Experimental details

Crystal data
Chemical formula	[Cd(C₇H₅O₄)₂(C₁₂H₈N₂)₂]·1.25H₂O
M_r	801.55
Crystal system, space group	Monoclinic, P2₁/n
Temperature (K)	295
a, b, c (Å)	10.8992 (18), 27.300 (2), 11.4218 (12)
β (°)	93.700 (6)
V (Å³)	3391.5 (7)
Z	4
Radiation type	Mo Kα
µ (mm⁻¹)	0.71
Crystal size (mm)	0.20 × 0.16 × 0.12

Data collection
Diffractometer	Rigaku R-AXIS RAPID IP diffractometer
Absorption correction	Multi-scan (ABSCOR; Higashi, 1995)
T_min, T_max	0.875, 0.928
No. of measured, independent and observed [I > 2σ(I)] reflections	25199, 6639, 4509
R_int	0.064
(sin θ/λ)_max (Å⁻¹)	0.617

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.042, 0.092, 1.03
No. of reflections	6639
No. of parameters	478
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.53, −0.51

Computer programs: PROCESS-AUTO (Rigaku, 1998), PROCESS-AUTO (Rigaku, 1998, CrystalStructure (Rigaku/MSC, 2002), SIR92 (Altomare et al., 1993), SHELXL97 (Sheldrick, 2008), ORTEP-3 (Farrugia, 1997), WinGX (Farrugia, 1999).

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
O1W—H1A···O1	0.94	2.09	2.974 (6)	155
O1W—H1B···O6	0.92	2.03	2.892 (6)	155
O2W—H2A···O2	0.88	1.99	2.869 (18)	175
O2W—H2B···O8ⁱ	0.86	2.42	3.28 (2)	173
O3—H3A···O2	0.82	1.81	2.540 (3)	147
O4—H4A···O7ⁱⁱ	0.82	2.09	2.877 (3)	160
O7—H7A···O6	0.82	1.82	2.546 (3)	147
O8—H8A···O3ⁱⁱⁱ	0.82	2.10	2.917 (4)	171
C23—H23···O1W^iv	0.93	2.49	3.339 (6)	153
C25—H25···O6^v	0.93	2.50	3.285 (5)	143
C30—H30···O1	0.93	2.56	3.155 (5)	122
C33—H33···O5	0.93	2.50	3.105 (5)	123
C38—H38···O2^vi	0.93	2.36	3.182 (5)	147
C42—H42···O4^vii	0.93	2.58	3.231 (5)	127

Symmetry codes: (i) x, y, z−1; (ii) −x+1, −y+1, −z+1; (iii) x−1/2, −y+3/2, z+1/2; (iv) x−1, y, z; (v) −x, −y+1, −z+1; (vi) x−1/2, −y+3/2, z−1/2; (vii) −x+1, −y+1, −z.

Acknowledgements

The work was supported by the ZIJIN project of Zhejiang University, China.

References

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