Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807023902/bt2367sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536807023902/bt2367Isup2.hkl |
CCDC reference: 650576
5-Nitro-2-hydroxybenzaldehyde (0.2 mmol, 33.5 mg), N,N-dimethylpropane-1,3-diamine (0.2 mmol, 20.5 mg), NaN3 (0.2 mmol, 6.5 mg), and Cu(CH3COO)2.H2O (0.2 mmol, 40.0 mg) were mixed in a methanol solution. The mixture was stirred at 325 K for 30 min to give a transparent blue solution. Blue crystals were obtained by slow evaporation of the solution in air.
H atoms were positioned geometrically and refined as riding atoms, with C–H distances in the range 0.93–0.97Å and Uiso(H) set at 1.2Ueq(C) and 1.5Ueq(methyl C).
Many azide-bridged polynuclear complexes have been reported previously (Zhao et al., 2003; Cai et al., 2007; Yu et al., 2006; Zhang et al., 2006; Zhu et al., 2004; Li et al., 2007). These complexes have interesting structures. We report herein the new copper(II) complex, (I), derived from the Schiff base ligand 4-nitro-2-[(3-dimethylaminopropylimino)methyl]phenol with azide bridges.
Complex (I) is an azide-bridged dinuclear copper(II) complex (Fig. 1). There is a crystallographic inversion centre at the midpoint of the two copper atoms in the complex. Each Cu atom is coordinated by one O and two N atoms of one Schiff base ligand and two briding N atoms from two azide ligands, forming a trigonal-bipyramidal geometry. The Cu···Cu distance is 3.327 (2) Å.
For related literature, see: Cai et al. (2007); Li et al. (2007); Yu et al. (2006); Zhang et al. (2006); Zhao et al. (2003); Zhu et al. (2004).
Data collection: SMART (Bruker, 2000); cell refinement: SAINT (Bruker, 2000); data reduction: SAINT; program(s) used to solve structure: SHELXTL (Bruker, 2000); program(s) used to refine structure: SHELXTL; molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL.
Fig. 1. The molecular structure of (I), with anisotropic displacement ellipsoids drawn at the 30% probability level. |
[Cu2(N3)2(C12H16N3O3)2] | F(000) = 732 |
Mr = 711.70 | Dx = 1.584 Mg m−3 |
Monoclinic, P21/n | Mo Kα radiation, λ = 0.71073 Å |
a = 8.7410 (17) Å | Cell parameters from 3793 reflections |
b = 14.846 (3) Å | θ = 2.2–27.3° |
c = 11.775 (2) Å | µ = 1.49 mm−1 |
β = 102.43 (3)° | T = 293 K |
V = 1492.2 (5) Å3 | Block, blue |
Z = 2 | 0.40 × 0.38 × 0.35 mm |
Bruker SMART APEX CCD area-detector diffractometer | 3239 independent reflections |
Radiation source: fine-focus sealed tube | 2706 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.036 |
ω scans | θmax = 27.0°, θmin = 2.2° |
Absorption correction: multi-scan (SADABS; Bruker, 2000) | h = −11→11 |
Tmin = 0.588, Tmax = 0.624 | k = −18→18 |
12293 measured reflections | l = −15→15 |
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)] = 0.031 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.074 | H-atom parameters constrained |
S = 1.04 | w = 1/[σ2(Fo2) + (0.0349P)2 + 0.1139P] where P = (Fo2 + 2Fc2)/3 |
3239 reflections | (Δ/σ)max < 0.001 |
201 parameters | Δρmax = 0.35 e Å−3 |
0 restraints | Δρmin = −0.25 e Å−3 |
[Cu2(N3)2(C12H16N3O3)2] | V = 1492.2 (5) Å3 |
Mr = 711.70 | Z = 2 |
Monoclinic, P21/n | Mo Kα radiation |
a = 8.7410 (17) Å | µ = 1.49 mm−1 |
b = 14.846 (3) Å | T = 293 K |
c = 11.775 (2) Å | 0.40 × 0.38 × 0.35 mm |
β = 102.43 (3)° |
Bruker SMART APEX CCD area-detector diffractometer | 3239 independent reflections |
Absorption correction: multi-scan (SADABS; Bruker, 2000) | 2706 reflections with I > 2σ(I) |
Tmin = 0.588, Tmax = 0.624 | Rint = 0.036 |
12293 measured reflections |
R[F2 > 2σ(F2)] = 0.031 | 0 restraints |
wR(F2) = 0.074 | H-atom parameters constrained |
S = 1.04 | Δρmax = 0.35 e Å−3 |
3239 reflections | Δρmin = −0.25 e Å−3 |
201 parameters |
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 | ||
Cu1 | 0.94961 (3) | 0.106755 (14) | 0.014558 (19) | 0.02791 (9) | |
O1 | 1.14184 (17) | 0.17565 (9) | 0.07071 (14) | 0.0480 (4) | |
O2 | 1.42356 (19) | 0.55892 (11) | 0.08461 (15) | 0.0562 (5) | |
O3 | 1.2338 (2) | 0.57421 (11) | −0.06657 (16) | 0.0573 (4) | |
N1 | 0.85117 (18) | 0.21807 (10) | −0.07976 (14) | 0.0312 (4) | |
N2 | 0.7638 (2) | 0.10303 (11) | 0.10393 (15) | 0.0374 (4) | |
N3 | 0.90672 (19) | 0.00703 (11) | −0.10862 (15) | 0.0371 (4) | |
N4 | 0.7826 (2) | −0.00746 (11) | −0.17324 (15) | 0.0359 (4) | |
N5 | 0.6652 (2) | −0.02203 (14) | −0.23562 (18) | 0.0557 (6) | |
N6 | 1.3106 (2) | 0.52861 (12) | 0.01293 (17) | 0.0416 (4) | |
C1 | 1.1769 (2) | 0.25787 (13) | 0.05229 (17) | 0.0328 (4) | |
C2 | 1.3234 (2) | 0.29231 (14) | 0.11226 (18) | 0.0371 (5) | |
H2 | 1.3917 | 0.2542 | 0.1616 | 0.044* | |
C3 | 1.3673 (2) | 0.37865 (14) | 0.10029 (19) | 0.0388 (5) | |
H3 | 1.4635 | 0.3996 | 0.1417 | 0.047* | |
C4 | 1.2658 (2) | 0.43592 (13) | 0.02469 (18) | 0.0343 (5) | |
C5 | 1.1238 (2) | 0.40603 (12) | −0.03678 (18) | 0.0333 (5) | |
H5 | 1.0589 | 0.4448 | −0.0875 | 0.040* | |
C6 | 1.0759 (2) | 0.31767 (13) | −0.02370 (16) | 0.0295 (4) | |
C7 | 0.9186 (2) | 0.29377 (13) | −0.08454 (17) | 0.0314 (4) | |
H7 | 0.8614 | 0.3379 | −0.1315 | 0.038* | |
C8 | 0.6851 (2) | 0.21132 (14) | −0.13842 (18) | 0.0376 (5) | |
H8A | 0.6699 | 0.1597 | −0.1902 | 0.045* | |
H8B | 0.6540 | 0.2650 | −0.1846 | 0.045* | |
C9 | 0.5848 (2) | 0.20112 (15) | −0.0484 (2) | 0.0428 (5) | |
H9A | 0.6061 | 0.2516 | 0.0049 | 0.051* | |
H9B | 0.4755 | 0.2048 | −0.0880 | 0.051* | |
C10 | 0.6085 (2) | 0.11484 (14) | 0.0218 (2) | 0.0401 (5) | |
H10A | 0.5274 | 0.1113 | 0.0664 | 0.048* | |
H10B | 0.5931 | 0.0645 | −0.0320 | 0.048* | |
C11 | 0.7889 (3) | 0.17461 (19) | 0.1933 (2) | 0.0604 (7) | |
H11A | 0.7017 | 0.1761 | 0.2309 | 0.091* | |
H11B | 0.7979 | 0.2318 | 0.1571 | 0.091* | |
H11C | 0.8834 | 0.1625 | 0.2499 | 0.091* | |
C12 | 0.7584 (3) | 0.01507 (18) | 0.1626 (2) | 0.0590 (7) | |
H12A | 0.8537 | 0.0065 | 0.2197 | 0.089* | |
H12B | 0.7470 | −0.0325 | 0.1061 | 0.089* | |
H12C | 0.6710 | 0.0142 | 0.1999 | 0.089* |
U11 | U22 | U33 | U12 | U13 | U23 | |
Cu1 | 0.02889 (14) | 0.01925 (13) | 0.03410 (15) | −0.00229 (9) | 0.00353 (10) | −0.00002 (9) |
O1 | 0.0389 (8) | 0.0283 (8) | 0.0686 (11) | −0.0054 (6) | −0.0064 (7) | 0.0129 (7) |
O2 | 0.0549 (10) | 0.0413 (10) | 0.0700 (12) | −0.0213 (8) | 0.0078 (9) | −0.0117 (8) |
O3 | 0.0655 (11) | 0.0321 (8) | 0.0720 (12) | −0.0070 (8) | 0.0100 (9) | 0.0082 (9) |
N1 | 0.0303 (9) | 0.0265 (9) | 0.0352 (9) | −0.0001 (7) | 0.0035 (7) | 0.0009 (7) |
N2 | 0.0352 (9) | 0.0385 (10) | 0.0377 (10) | −0.0022 (7) | 0.0059 (8) | 0.0036 (8) |
N3 | 0.0367 (9) | 0.0283 (9) | 0.0412 (10) | 0.0004 (8) | −0.0031 (8) | −0.0044 (7) |
N4 | 0.0454 (10) | 0.0247 (9) | 0.0349 (10) | 0.0028 (8) | 0.0028 (8) | −0.0036 (7) |
N5 | 0.0479 (11) | 0.0508 (12) | 0.0565 (13) | 0.0010 (10) | −0.0150 (10) | −0.0132 (10) |
N6 | 0.0439 (10) | 0.0312 (10) | 0.0536 (12) | −0.0073 (8) | 0.0188 (9) | −0.0064 (9) |
C1 | 0.0366 (11) | 0.0255 (10) | 0.0366 (11) | −0.0018 (8) | 0.0086 (9) | 0.0002 (8) |
C2 | 0.0310 (11) | 0.0369 (12) | 0.0414 (12) | 0.0006 (9) | 0.0034 (9) | 0.0050 (9) |
C3 | 0.0310 (11) | 0.0420 (13) | 0.0428 (12) | −0.0065 (9) | 0.0064 (9) | −0.0032 (10) |
C4 | 0.0380 (11) | 0.0272 (10) | 0.0407 (12) | −0.0075 (9) | 0.0153 (9) | −0.0035 (9) |
C5 | 0.0376 (11) | 0.0267 (10) | 0.0365 (11) | 0.0007 (8) | 0.0099 (9) | 0.0016 (8) |
C6 | 0.0302 (10) | 0.0260 (10) | 0.0330 (11) | −0.0019 (8) | 0.0081 (8) | −0.0006 (8) |
C7 | 0.0356 (11) | 0.0260 (10) | 0.0316 (10) | 0.0006 (8) | 0.0053 (8) | 0.0036 (8) |
C8 | 0.0338 (11) | 0.0327 (11) | 0.0421 (12) | −0.0024 (9) | −0.0010 (9) | 0.0047 (9) |
C9 | 0.0306 (11) | 0.0411 (13) | 0.0546 (14) | 0.0049 (9) | 0.0042 (10) | 0.0054 (10) |
C10 | 0.0309 (11) | 0.0422 (13) | 0.0468 (13) | −0.0029 (9) | 0.0072 (9) | 0.0018 (10) |
C11 | 0.0541 (15) | 0.0777 (19) | 0.0489 (15) | −0.0052 (13) | 0.0101 (12) | −0.0190 (14) |
C12 | 0.0505 (14) | 0.0621 (17) | 0.0653 (17) | −0.0008 (12) | 0.0145 (13) | 0.0314 (14) |
Cu1—O1 | 1.9567 (14) | C3—C4 | 1.401 (3) |
Cu1—N3 | 2.0498 (17) | C3—H3 | 0.9300 |
Cu1—N1 | 2.0720 (16) | C4—C5 | 1.369 (3) |
Cu1—N2 | 2.1178 (18) | C5—C6 | 1.396 (3) |
Cu1—N3i | 2.2492 (17) | C5—H5 | 0.9300 |
O1—C1 | 1.288 (2) | C6—C7 | 1.451 (2) |
O2—N6 | 1.237 (2) | C7—H7 | 0.9300 |
O3—N6 | 1.231 (2) | C8—C9 | 1.522 (3) |
N1—C7 | 1.276 (2) | C8—H8A | 0.9700 |
N1—C8 | 1.470 (2) | C8—H8B | 0.9700 |
N2—C11 | 1.478 (3) | C9—C10 | 1.514 (3) |
N2—C12 | 1.483 (3) | C9—H9A | 0.9700 |
N2—C10 | 1.498 (3) | C9—H9B | 0.9700 |
N3—N4 | 1.203 (2) | C10—H10A | 0.9700 |
N3—Cu1i | 2.2492 (17) | C10—H10B | 0.9700 |
N4—N5 | 1.147 (2) | C11—H11A | 0.9600 |
N6—C4 | 1.445 (3) | C11—H11B | 0.9600 |
C1—C2 | 1.417 (3) | C11—H11C | 0.9600 |
C1—C6 | 1.424 (3) | C12—H12A | 0.9600 |
C2—C3 | 1.354 (3) | C12—H12B | 0.9600 |
C2—H2 | 0.9300 | C12—H12C | 0.9600 |
O1—Cu1—N3 | 129.02 (7) | C4—C5—C6 | 120.39 (19) |
O1—Cu1—N1 | 89.52 (6) | C4—C5—H5 | 119.8 |
N3—Cu1—N1 | 101.84 (7) | C6—C5—H5 | 119.8 |
O1—Cu1—N2 | 122.72 (7) | C5—C6—C1 | 119.65 (18) |
N3—Cu1—N2 | 106.84 (7) | C5—C6—C7 | 116.77 (17) |
N1—Cu1—N2 | 90.73 (6) | C1—C6—C7 | 123.47 (18) |
O1—Cu1—N3i | 83.01 (6) | N1—C7—C6 | 126.24 (18) |
N3—Cu1—N3i | 78.68 (7) | N1—C7—H7 | 116.9 |
N1—Cu1—N3i | 170.54 (6) | C6—C7—H7 | 116.9 |
N2—Cu1—N3i | 98.18 (6) | N1—C8—C9 | 109.78 (17) |
C1—O1—Cu1 | 131.04 (13) | N1—C8—H8A | 109.7 |
C7—N1—C8 | 117.25 (16) | C9—C8—H8A | 109.7 |
C7—N1—Cu1 | 125.72 (14) | N1—C8—H8B | 109.7 |
C8—N1—Cu1 | 116.84 (12) | C9—C8—H8B | 109.7 |
C11—N2—C12 | 108.4 (2) | H8A—C8—H8B | 108.2 |
C11—N2—C10 | 110.51 (17) | C10—C9—C8 | 115.64 (18) |
C12—N2—C10 | 106.79 (16) | C10—C9—H9A | 108.4 |
C11—N2—Cu1 | 108.82 (14) | C8—C9—H9A | 108.4 |
C12—N2—Cu1 | 111.05 (14) | C10—C9—H9B | 108.4 |
C10—N2—Cu1 | 111.20 (13) | C8—C9—H9B | 108.4 |
N4—N3—Cu1 | 125.42 (14) | H9A—C9—H9B | 107.4 |
N4—N3—Cu1i | 120.61 (13) | N2—C10—C9 | 116.75 (17) |
Cu1—N3—Cu1i | 101.32 (7) | N2—C10—H10A | 108.1 |
N5—N4—N3 | 179.1 (2) | C9—C10—H10A | 108.1 |
O3—N6—O2 | 122.90 (19) | N2—C10—H10B | 108.1 |
O3—N6—C4 | 118.82 (18) | C9—C10—H10B | 108.1 |
O2—N6—C4 | 118.27 (19) | H10A—C10—H10B | 107.3 |
O1—C1—C2 | 118.69 (18) | N2—C11—H11A | 109.5 |
O1—C1—C6 | 123.94 (18) | N2—C11—H11B | 109.5 |
C2—C1—C6 | 117.36 (18) | H11A—C11—H11B | 109.5 |
C3—C2—C1 | 122.37 (19) | N2—C11—H11C | 109.5 |
C3—C2—H2 | 118.8 | H11A—C11—H11C | 109.5 |
C1—C2—H2 | 118.8 | H11B—C11—H11C | 109.5 |
C2—C3—C4 | 119.07 (19) | N2—C12—H12A | 109.5 |
C2—C3—H3 | 120.5 | N2—C12—H12B | 109.5 |
C4—C3—H3 | 120.5 | H12A—C12—H12B | 109.5 |
C5—C4—C3 | 121.14 (19) | N2—C12—H12C | 109.5 |
C5—C4—N6 | 119.42 (19) | H12A—C12—H12C | 109.5 |
C3—C4—N6 | 119.43 (19) | H12B—C12—H12C | 109.5 |
Symmetry code: (i) −x+2, −y, −z. |
Experimental details
Crystal data | |
Chemical formula | [Cu2(N3)2(C12H16N3O3)2] |
Mr | 711.70 |
Crystal system, space group | Monoclinic, P21/n |
Temperature (K) | 293 |
a, b, c (Å) | 8.7410 (17), 14.846 (3), 11.775 (2) |
β (°) | 102.43 (3) |
V (Å3) | 1492.2 (5) |
Z | 2 |
Radiation type | Mo Kα |
µ (mm−1) | 1.49 |
Crystal size (mm) | 0.40 × 0.38 × 0.35 |
Data collection | |
Diffractometer | Bruker SMART APEX CCD area-detector diffractometer |
Absorption correction | Multi-scan (SADABS; Bruker, 2000) |
Tmin, Tmax | 0.588, 0.624 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 12293, 3239, 2706 |
Rint | 0.036 |
(sin θ/λ)max (Å−1) | 0.639 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.031, 0.074, 1.04 |
No. of reflections | 3239 |
No. of parameters | 201 |
H-atom treatment | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 0.35, −0.25 |
Computer programs: SMART (Bruker, 2000), SAINT (Bruker, 2000), SAINT, SHELXTL (Bruker, 2000), SHELXTL.
Many azide-bridged polynuclear complexes have been reported previously (Zhao et al., 2003; Cai et al., 2007; Yu et al., 2006; Zhang et al., 2006; Zhu et al., 2004; Li et al., 2007). These complexes have interesting structures. We report herein the new copper(II) complex, (I), derived from the Schiff base ligand 4-nitro-2-[(3-dimethylaminopropylimino)methyl]phenol with azide bridges.
Complex (I) is an azide-bridged dinuclear copper(II) complex (Fig. 1). There is a crystallographic inversion centre at the midpoint of the two copper atoms in the complex. Each Cu atom is coordinated by one O and two N atoms of one Schiff base ligand and two briding N atoms from two azide ligands, forming a trigonal-bipyramidal geometry. The Cu···Cu distance is 3.327 (2) Å.