metal-organic compounds\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890

Bis(2,6-dihy­dr­oxy­benzoato-κ2O1,O1′)(nitrato-κ2O,O′)bis­­(1,10-phenanthroline-κ2N,N′)dysprosium(III)

aCollege of Materials Science and Engineering, China Jiliang University, Hangzhou 310018, People's Republic of China
*Correspondence e-mail: jin_hongxiao@yahoo.com.cn

(Received 11 November 2010; accepted 19 November 2010; online 24 November 2010)

In the mononuclear title complex, [Dy(C7H5O4)2(NO3)(C12H8N2)2], the DyIII atom is in a distorted bicapped square-anti­prismatic geometry formed by four N atoms from two chelating 1,10-phenanthroline (phen) ligands, four O atoms from two 2,6-dihy­droxy­benzoate (DHB) ligands and two O atoms from a nitrate anion. Inter­molecular ππ stacking inter­actions between the phen and DHB ligands [centroid–centroid distances = 3.542 (4) and 3.879 (4) Å] and between the pyridine and benzene rings of adjacent phen ligands [centroid–centroid distance = 3.751 (4) Å] stabilize the crystal structure. Intra­molecular O–H⋯O hydrogen bonds are observed in the DHB ligands.

Related literature

For a related structure, see: Zheng et al. (2010[Zheng, J., Jin, H. & Ge, H. (2010). Acta Cryst. E66, m1469-m1470.]).

[Scheme 1]

Experimental

Crystal data
  • [Dy(C7H5O4)2(NO3)(C12H8N2)2]

  • Mr = 891.14

  • Monoclinic, P 21 /c

  • a = 11.1268 (3) Å

  • b = 26.7587 (4) Å

  • c = 14.2703 (5) Å

  • β = 127.280 (2)°

  • V = 3380.72 (18) Å3

  • Z = 4

  • Cu Kα radiation

  • μ = 12.46 mm−1

  • T = 298 K

  • 0.35 × 0.32 × 0.30 mm

Data collection
  • Oxford Diffraction Gemini S Ultra CCD diffractometer

  • Absorption correction: multi-scan (CrysAlis PRO; Oxford Diffraction, 2006[Oxford Diffraction (2006). CrysAlis PRO. Oxford Diffraction Ltd, Abingdon, England.]) Tmin = 0.097, Tmax = 0.118

  • 11595 measured reflections

  • 5923 independent reflections

  • 4674 reflections with I > 2σ(I)

  • Rint = 0.043

Refinement
  • R[F2 > 2σ(F2)] = 0.051

  • wR(F2) = 0.137

  • S = 1.00

  • 5923 reflections

  • 496 parameters

  • H-atom parameters constrained

  • Δρmax = 1.68 e Å−3

  • Δρmin = −1.16 e Å−3

Table 1
Selected bond lengths (Å)

Dy1—N1 2.597 (5)
Dy1—N2 2.556 (4)
Dy1—N3 2.545 (5)
Dy1—N4 2.515 (5)
Dy1—O1 2.442 (4)
Dy1—O2 2.557 (4)
Dy1—O5 2.458 (4)
Dy1—O6 2.444 (5)
Dy1—O9 2.604 (5)
Dy1—O10 2.482 (5)

Table 2
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A DA D—H⋯A
O3—H27⋯O1 0.82 1.86 2.577 (7) 146
O4—H31⋯O2 0.82 1.86 2.588 (6) 148
O7—H34⋯O5 0.82 1.91 2.592 (7) 139
O8—H38⋯O6 0.82 1.84 2.570 (7) 148

Data collection: CrysAlis PRO (Oxford Diffraction, 2006[Oxford Diffraction (2006). CrysAlis PRO. Oxford Diffraction Ltd, Abingdon, England.]); cell refinement: CrysAlis PRO; data reduction: CrysAlis PRO; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); molecular graphics: DIAMOND (Brandenburg & Berndt, 1999[Brandenburg, K. & Berndt, M. (1999). DIAMOND. Crystal Impact GbR, Bonn, Germany.]); software used to prepare material for publication: SHELXL97.

Supporting information


Comment top

The description of the structure of the title compound is part of a series of papers on mononuclear complexes of the type [Ln(DHB)2(NO3)(phen)2] [Ln = Ce, Pr, Sm, Eu and Dy (this publication); DHB = 2,6-dihydroxybenzoate; phen = 1,10-phenanthroline]. All five compounds are isostructural to the previously reported Nd complex (Zheng et al. 2010).

Related literature top

For a related structure, see: Zheng et al. (2010).

Experimental top

All reagents are commercially available and of analytical grade. Dy(NO3)3.6H2O (0.229 g, 0.5 mmol), 2,6-dihydroxybenzoic acid (0.074 g, 0.5 mmol), 1,10-phenanthroline (0.090 g, 0.5 mmol) and NaHCO3 (0.042 g, 0.5 mmol) were dissolved in a water–ethanol solution (10 ml, v/v 1:1). The solution was refluxed for 4 h and filtered after cooling to room temperature. Yellow single crystals were obtained from the filtrate in 4 days.

Refinement top

H atoms were positioned geometrically and refined as riding atoms, with C—H = 0.93 and O—H = 0.82 Å and Uiso(H) = 1.2Ueq(C) and 1.5Ueq(O). The highest residual electron density was found 0.90 Å from Dy1 and the deepest hole 1.61 Å from O1.

Structure description top

The description of the structure of the title compound is part of a series of papers on mononuclear complexes of the type [Ln(DHB)2(NO3)(phen)2] [Ln = Ce, Pr, Sm, Eu and Dy (this publication); DHB = 2,6-dihydroxybenzoate; phen = 1,10-phenanthroline]. All five compounds are isostructural to the previously reported Nd complex (Zheng et al. 2010).

For a related structure, see: Zheng et al. (2010).

Computing details top

Data collection: CrysAlis PRO (Oxford Diffraction, 2006); cell refinement: CrysAlis PRO (Oxford Diffraction, 2006); data reduction: CrysAlis PRO (Oxford Diffraction, 2006); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: DIAMOND (Brandenburg & Berndt, 1999); software used to prepare material for publication: SHELXL97 (Sheldrick, 2008).

Figures top
[Figure 1] Fig. 1. The molecular structure of the title compound. Displacement ellipsoids are drawn at the 30% probablility level. H atoms have been omitted for clarity. Dashed orange lines denote intramolecular hydrogen bonds.
Bis(2,6-dihydroxybenzoato-κ2O1,O1')(nitrato- κ2O,O')bis(1,10-phenanthroline- κ2N,N')dysprosium(III) top
Crystal data top
[Dy(C7H5O4)2(NO3)(C12H8N2)2]F(000) = 1772
Mr = 891.14Dx = 1.751 Mg m3
Monoclinic, P21/cCu Kα radiation, λ = 1.54184 Å
Hall symbol: -P 2ybcCell parameters from 5391 reflections
a = 11.1268 (3) Åθ = 3.3–67.5°
b = 26.7587 (4) ŵ = 12.46 mm1
c = 14.2703 (5) ÅT = 298 K
β = 127.280 (2)°Prism, yellow
V = 3380.72 (18) Å30.35 × 0.32 × 0.30 mm
Z = 4
Data collection top
Oxford Diffraction Gemini S Ultra CCD
diffractometer
5923 independent reflections
Radiation source: Enhance (Cu) X-ray Source4674 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.043
Detector resolution: 15.9149 pixels mm-1θmax = 67.1°, θmin = 3.3°
ω scansh = 1113
Absorption correction: multi-scan
(CrysAlis PRO; Oxford Diffraction, 2006)
k = 3131
Tmin = 0.097, Tmax = 0.118l = 1617
11595 measured reflections
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.051Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.137H-atom parameters constrained
S = 1.00 w = 1/[σ2(Fo2) + (0.0774P)2]
where P = (Fo2 + 2Fc2)/3
5923 reflections(Δ/σ)max < 0.001
496 parametersΔρmax = 1.68 e Å3
0 restraintsΔρmin = 1.16 e Å3
Crystal data top
[Dy(C7H5O4)2(NO3)(C12H8N2)2]V = 3380.72 (18) Å3
Mr = 891.14Z = 4
Monoclinic, P21/cCu Kα radiation
a = 11.1268 (3) ŵ = 12.46 mm1
b = 26.7587 (4) ÅT = 298 K
c = 14.2703 (5) Å0.35 × 0.32 × 0.30 mm
β = 127.280 (2)°
Data collection top
Oxford Diffraction Gemini S Ultra CCD
diffractometer
5923 independent reflections
Absorption correction: multi-scan
(CrysAlis PRO; Oxford Diffraction, 2006)
4674 reflections with I > 2σ(I)
Tmin = 0.097, Tmax = 0.118Rint = 0.043
11595 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0510 restraints
wR(F2) = 0.137H-atom parameters constrained
S = 1.00Δρmax = 1.68 e Å3
5923 reflectionsΔρmin = 1.16 e Å3
496 parameters
Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
Dy10.92866 (4)0.862990 (11)0.22227 (3)0.03846 (13)
O10.8450 (5)0.83886 (15)0.0261 (4)0.0522 (11)
O20.8884 (5)0.91905 (15)0.0604 (4)0.0499 (10)
O30.7499 (6)0.80195 (16)0.1748 (4)0.0702 (15)
H270.79120.80150.10390.105*
O40.8352 (8)0.97830 (17)0.1043 (5)0.087 (2)
H310.85780.97020.04000.131*
O50.6975 (5)0.81369 (15)0.1368 (4)0.0505 (10)
O60.6691 (5)0.89410 (16)0.1017 (4)0.0584 (12)
O70.4806 (6)0.76073 (17)0.1052 (4)0.0624 (12)
H340.57060.76710.14140.094*
O80.4205 (7)0.93749 (19)0.0292 (6)0.0822 (17)
H380.50480.93440.04610.123*
O90.9472 (5)0.80198 (15)0.3727 (4)0.0583 (12)
O100.8436 (6)0.87351 (16)0.3467 (4)0.0556 (11)
O110.8566 (7)0.8210 (3)0.4675 (5)0.0883 (19)
N11.1603 (6)0.87915 (17)0.4391 (4)0.0408 (11)
N20.9734 (6)0.95380 (16)0.2914 (4)0.0442 (12)
N31.1761 (6)0.86887 (16)0.2491 (4)0.0406 (11)
N41.0506 (6)0.78088 (18)0.2394 (4)0.0435 (11)
N50.8816 (6)0.8312 (2)0.3985 (5)0.0527 (13)
C11.2533 (8)0.8434 (2)0.5122 (6)0.0483 (14)
H11.23850.81120.48200.058*
C21.3706 (8)0.8506 (3)0.6301 (6)0.0560 (16)
H21.43310.82420.67680.067*
C31.3928 (8)0.8974 (3)0.6766 (6)0.0569 (17)
H31.46920.90300.75610.068*
C41.2998 (7)0.9369 (2)0.6037 (5)0.0463 (14)
C51.1836 (7)0.9259 (2)0.4851 (5)0.0400 (12)
C61.0847 (7)0.9650 (2)0.4065 (5)0.0416 (13)
C71.1054 (8)1.0142 (2)0.4516 (6)0.0478 (15)
C81.2255 (8)1.0234 (2)0.5743 (7)0.0583 (18)
H81.23881.05550.60440.070*
C91.3175 (9)0.9870 (3)0.6454 (7)0.0618 (19)
H91.39500.99430.72380.074*
C101.0063 (9)1.0512 (2)0.3732 (6)0.0554 (17)
H101.01691.08390.39910.066*
C110.8959 (9)1.0395 (2)0.2603 (7)0.0590 (18)
H110.82831.06380.20820.071*
C120.8835 (8)0.9907 (2)0.2220 (6)0.0521 (15)
H120.80780.98360.14320.063*
C131.2359 (8)0.9120 (2)0.2500 (6)0.0528 (15)
H131.17650.94060.22480.063*
C141.3846 (8)0.9163 (3)0.2873 (6)0.0563 (17)
H141.42280.94730.28750.068*
C151.4723 (8)0.8747 (3)0.3231 (6)0.0594 (18)
H151.57150.87720.34880.071*
C161.4132 (7)0.8282 (3)0.3211 (5)0.0489 (15)
C171.2625 (7)0.8270 (2)0.2827 (5)0.0429 (13)
C181.1934 (7)0.7804 (2)0.2724 (5)0.0413 (13)
C191.2765 (7)0.7358 (2)0.2975 (5)0.0475 (14)
C201.4291 (8)0.7381 (3)0.3411 (6)0.0588 (18)
H201.48460.70870.36200.071*
C211.4956 (8)0.7820 (3)0.3529 (6)0.0595 (18)
H211.59630.78260.38200.071*
C221.1985 (8)0.6906 (2)0.2765 (6)0.0545 (17)
H221.24620.66030.28790.065*
C231.0545 (8)0.6914 (2)0.2399 (6)0.0535 (17)
H231.00270.66170.22610.064*
C240.9842 (8)0.7374 (2)0.2232 (5)0.0491 (15)
H240.88570.73730.19940.059*
C250.8441 (7)0.8824 (2)0.0106 (5)0.0425 (13)
C260.7959 (7)0.8895 (2)0.1304 (5)0.0416 (13)
C270.7498 (7)0.8487 (2)0.2084 (5)0.0482 (15)
C280.7019 (8)0.8562 (3)0.3224 (6)0.0608 (19)
H280.67180.82920.37320.073*
C290.6992 (9)0.9035 (3)0.3599 (6)0.069 (2)
H290.66610.90820.43670.083*
C300.7440 (10)0.9440 (3)0.2870 (6)0.068 (2)
H300.74180.97580.31440.082*
C310.7926 (9)0.9375 (2)0.1728 (6)0.0582 (18)
C320.6131 (7)0.8522 (2)0.1013 (5)0.0474 (15)
C330.4611 (7)0.8492 (2)0.0671 (5)0.0460 (14)
C340.4014 (7)0.8037 (3)0.0719 (5)0.0504 (15)
C350.2580 (7)0.8010 (3)0.0423 (5)0.0555 (17)
H350.21990.77070.04590.067*
C360.1724 (8)0.8441 (3)0.0071 (6)0.067 (2)
H360.07540.84220.01390.080*
C370.2255 (9)0.8898 (3)0.0021 (6)0.067 (2)
H370.16580.91830.02140.081*
C380.3692 (8)0.8923 (3)0.0329 (6)0.0594 (18)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Dy10.0455 (2)0.02877 (18)0.0461 (2)0.00037 (13)0.03041 (17)0.00158 (13)
O10.065 (3)0.039 (2)0.050 (2)0.0029 (19)0.033 (2)0.0047 (18)
O20.066 (3)0.040 (2)0.050 (2)0.0004 (19)0.038 (2)0.0041 (18)
O30.083 (4)0.044 (2)0.057 (3)0.004 (2)0.028 (3)0.008 (2)
O40.154 (6)0.043 (2)0.066 (3)0.019 (3)0.067 (4)0.005 (2)
O50.046 (2)0.041 (2)0.064 (3)0.0088 (18)0.033 (2)0.0041 (19)
O60.060 (3)0.044 (2)0.075 (3)0.002 (2)0.043 (3)0.009 (2)
O70.059 (3)0.052 (2)0.075 (3)0.002 (2)0.041 (3)0.010 (2)
O80.076 (4)0.053 (3)0.110 (4)0.019 (3)0.053 (3)0.017 (3)
O90.066 (3)0.040 (2)0.069 (3)0.000 (2)0.040 (3)0.000 (2)
O100.067 (3)0.049 (2)0.070 (3)0.004 (2)0.052 (3)0.002 (2)
O110.097 (4)0.129 (5)0.066 (3)0.013 (4)0.063 (3)0.010 (3)
N10.053 (3)0.033 (2)0.046 (3)0.002 (2)0.035 (2)0.0000 (19)
N20.063 (3)0.029 (2)0.046 (3)0.003 (2)0.035 (3)0.0012 (19)
N30.043 (3)0.037 (2)0.050 (3)0.006 (2)0.033 (2)0.004 (2)
N40.051 (3)0.038 (2)0.043 (2)0.005 (2)0.029 (2)0.001 (2)
N50.050 (3)0.060 (3)0.052 (3)0.006 (3)0.033 (3)0.005 (3)
C10.061 (4)0.041 (3)0.055 (4)0.006 (3)0.042 (3)0.004 (3)
C20.053 (4)0.063 (4)0.051 (4)0.009 (3)0.031 (3)0.007 (3)
C30.047 (3)0.072 (4)0.051 (3)0.006 (3)0.029 (3)0.006 (3)
C40.043 (3)0.049 (3)0.053 (3)0.007 (3)0.032 (3)0.008 (3)
C50.045 (3)0.039 (3)0.049 (3)0.005 (2)0.035 (3)0.005 (2)
C60.052 (3)0.033 (3)0.053 (3)0.006 (2)0.039 (3)0.003 (2)
C70.064 (4)0.036 (3)0.072 (4)0.015 (3)0.056 (4)0.013 (3)
C80.074 (5)0.044 (3)0.083 (5)0.021 (3)0.061 (4)0.022 (3)
C90.063 (4)0.062 (4)0.068 (4)0.023 (4)0.043 (4)0.026 (4)
C100.086 (5)0.029 (3)0.081 (5)0.004 (3)0.067 (4)0.003 (3)
C110.084 (5)0.034 (3)0.079 (5)0.012 (3)0.060 (4)0.014 (3)
C120.068 (4)0.037 (3)0.059 (4)0.004 (3)0.042 (3)0.002 (3)
C130.061 (4)0.045 (3)0.060 (4)0.005 (3)0.041 (3)0.005 (3)
C140.059 (4)0.060 (4)0.064 (4)0.023 (3)0.044 (4)0.012 (3)
C150.053 (4)0.077 (5)0.055 (4)0.019 (4)0.036 (3)0.010 (3)
C160.041 (3)0.067 (4)0.040 (3)0.006 (3)0.026 (3)0.006 (3)
C170.045 (3)0.046 (3)0.038 (3)0.003 (3)0.026 (3)0.007 (2)
C180.048 (3)0.045 (3)0.034 (3)0.000 (3)0.027 (3)0.002 (2)
C190.056 (4)0.051 (3)0.040 (3)0.012 (3)0.032 (3)0.004 (3)
C200.059 (4)0.064 (4)0.049 (4)0.016 (3)0.030 (3)0.005 (3)
C210.047 (4)0.084 (5)0.050 (4)0.007 (4)0.031 (3)0.000 (3)
C220.073 (5)0.039 (3)0.052 (4)0.012 (3)0.039 (3)0.002 (3)
C230.073 (5)0.032 (3)0.055 (4)0.000 (3)0.039 (3)0.003 (3)
C240.051 (3)0.038 (3)0.056 (4)0.009 (3)0.031 (3)0.006 (3)
C250.045 (3)0.041 (3)0.046 (3)0.001 (2)0.030 (3)0.001 (2)
C260.044 (3)0.040 (3)0.041 (3)0.002 (2)0.026 (3)0.001 (2)
C270.040 (3)0.048 (3)0.047 (3)0.005 (3)0.021 (3)0.005 (3)
C280.055 (4)0.072 (5)0.049 (4)0.000 (3)0.028 (3)0.017 (3)
C290.078 (5)0.084 (5)0.048 (4)0.010 (4)0.039 (4)0.005 (4)
C300.094 (6)0.063 (4)0.059 (4)0.010 (4)0.052 (4)0.007 (3)
C310.078 (5)0.047 (3)0.052 (4)0.010 (3)0.040 (4)0.000 (3)
C320.050 (4)0.049 (3)0.040 (3)0.003 (3)0.026 (3)0.002 (3)
C330.041 (3)0.058 (3)0.040 (3)0.004 (3)0.025 (3)0.002 (3)
C340.045 (3)0.067 (4)0.042 (3)0.001 (3)0.028 (3)0.000 (3)
C350.047 (4)0.079 (5)0.044 (3)0.002 (3)0.029 (3)0.000 (3)
C360.048 (4)0.105 (6)0.049 (4)0.007 (4)0.031 (3)0.001 (4)
C370.057 (4)0.085 (5)0.060 (4)0.029 (4)0.035 (4)0.008 (4)
C380.058 (4)0.066 (4)0.053 (4)0.015 (3)0.033 (3)0.006 (3)
Geometric parameters (Å, º) top
Dy1—N12.597 (5)C9—H90.9300
Dy1—N22.556 (4)C10—C111.344 (10)
Dy1—N32.545 (5)C10—H100.9300
Dy1—N42.515 (5)C11—C121.389 (9)
Dy1—O12.442 (4)C11—H110.9300
Dy1—O22.557 (4)C12—H120.9300
Dy1—O52.458 (4)C13—C141.403 (9)
Dy1—O62.444 (5)C13—H130.9300
Dy1—O92.604 (5)C14—C151.360 (11)
Dy1—O102.482 (5)C14—H140.9300
O1—C251.274 (7)C15—C161.401 (10)
O2—C251.275 (7)C15—H150.9300
O3—C271.340 (8)C16—C171.414 (8)
O3—H270.8196C16—C211.439 (10)
O4—C311.345 (8)C17—C181.425 (8)
O4—H310.8201C18—C191.417 (8)
O5—C321.275 (7)C19—C221.410 (10)
O6—C321.281 (8)C19—C201.413 (10)
O7—C341.348 (8)C20—C211.344 (11)
O7—H340.8198C20—H200.9300
O8—C381.352 (9)C21—H210.9300
O8—H380.8190C22—C231.352 (10)
O9—N51.267 (7)C22—H220.9300
O10—N51.277 (7)C23—C241.398 (9)
O11—N51.205 (7)C23—H230.9300
N1—C11.330 (8)C24—H240.9300
N1—C51.363 (7)C25—C261.462 (8)
N2—C121.326 (8)C26—C311.411 (9)
N2—C61.363 (8)C26—C271.415 (8)
N3—C131.328 (8)C27—C281.386 (10)
N3—C171.360 (8)C28—C291.365 (11)
N4—C241.322 (8)C28—H280.9300
N4—C181.356 (8)C29—C301.371 (11)
C1—C21.382 (9)C29—H290.9300
C1—H10.9300C30—C311.383 (10)
C2—C31.367 (10)C30—H300.9300
C2—H20.9300C32—C331.452 (9)
C3—C41.402 (10)C33—C341.407 (9)
C3—H30.9300C33—C381.418 (9)
C4—C51.404 (8)C34—C351.383 (9)
C4—C91.433 (9)C35—C361.384 (11)
C5—C61.439 (8)C35—H350.9300
C6—C71.420 (8)C36—C371.379 (12)
C7—C101.398 (9)C36—H360.9300
C7—C81.442 (10)C37—C381.380 (10)
C8—C91.329 (11)C37—H370.9300
C8—H80.9300
O1—Dy1—O679.39 (17)C9—C8—H8119.4
O1—Dy1—O574.42 (15)C7—C8—H8119.4
O6—Dy1—O553.02 (13)C8—C9—C4121.4 (6)
O1—Dy1—O10143.53 (17)C8—C9—H9119.3
O6—Dy1—O1070.42 (17)C4—C9—H9119.3
O5—Dy1—O1071.23 (16)C11—C10—C7120.0 (6)
O1—Dy1—N471.90 (15)C11—C10—H10120.0
O6—Dy1—N4134.73 (16)C7—C10—H10120.0
O5—Dy1—N485.41 (15)C10—C11—C12119.4 (6)
O10—Dy1—N4116.50 (15)C10—C11—H11120.3
O1—Dy1—N379.34 (16)C12—C11—H11120.3
O6—Dy1—N3142.59 (16)N2—C12—C11123.8 (6)
O5—Dy1—N3145.01 (14)N2—C12—H12118.1
O10—Dy1—N3137.05 (16)C11—C12—H12118.1
N4—Dy1—N364.45 (15)N3—C13—C14122.9 (6)
O1—Dy1—N2122.95 (14)N3—C13—H13118.5
O6—Dy1—N279.54 (16)C14—C13—H13118.5
O5—Dy1—N2127.03 (16)C15—C14—C13119.2 (6)
O10—Dy1—N271.66 (16)C15—C14—H14120.4
N4—Dy1—N2145.66 (16)C13—C14—H14120.4
N3—Dy1—N286.76 (16)C14—C15—C16119.9 (7)
O1—Dy1—O251.87 (12)C14—C15—H15120.0
O6—Dy1—O271.26 (16)C16—C15—H15120.0
O5—Dy1—O2107.97 (14)C15—C16—C17117.4 (6)
O10—Dy1—O2130.24 (14)C15—C16—C21123.7 (7)
N4—Dy1—O2112.92 (15)C17—C16—C21118.9 (6)
N3—Dy1—O271.39 (15)N3—C17—C16122.5 (6)
N2—Dy1—O271.20 (14)N3—C17—C18117.6 (5)
O1—Dy1—N1145.48 (16)C16—C17—C18119.9 (6)
O6—Dy1—N1132.75 (16)N4—C18—C19122.9 (6)
O5—Dy1—N1131.74 (15)N4—C18—C17118.2 (5)
O10—Dy1—N170.26 (16)C19—C18—C17118.8 (6)
N4—Dy1—N186.66 (15)C22—C19—C20123.5 (6)
N3—Dy1—N166.91 (16)C22—C19—C18116.4 (6)
N2—Dy1—N163.96 (15)C20—C19—C18120.1 (6)
O2—Dy1—N1118.90 (14)C21—C20—C19121.2 (6)
O1—Dy1—O9124.35 (14)C21—C20—H20119.4
O6—Dy1—O9105.28 (16)C19—C20—H20119.4
O5—Dy1—O967.00 (15)C20—C21—C16120.9 (7)
O10—Dy1—O949.88 (15)C20—C21—H21119.5
N4—Dy1—O966.62 (16)C16—C21—H21119.5
N3—Dy1—O9112.12 (16)C23—C22—C19120.2 (6)
N2—Dy1—O9112.21 (15)C23—C22—H22119.9
O2—Dy1—O9174.91 (14)C19—C22—H22119.9
N1—Dy1—O966.19 (15)C22—C23—C24119.2 (6)
C25—O1—Dy197.6 (4)C22—C23—H23120.4
C25—O2—Dy192.2 (3)C24—C23—H23120.4
C27—O3—H27109.5N4—C24—C23123.4 (7)
C31—O4—H31109.4N4—C24—H24118.3
C32—O5—Dy193.5 (4)C23—C24—H24118.3
C32—O6—Dy194.0 (4)O1—C25—O2118.3 (5)
C34—O7—H34109.5O1—C25—C26120.4 (5)
C38—O8—H38109.5O2—C25—C26121.3 (5)
N5—O9—Dy194.6 (3)C31—C26—C27117.5 (6)
N5—O10—Dy1100.3 (4)C31—C26—C25121.1 (5)
C1—N1—C5116.9 (5)C27—C26—C25121.4 (5)
C1—N1—Dy1123.6 (4)O3—C27—C28118.1 (6)
C5—N1—Dy1119.2 (4)O3—C27—C26121.2 (6)
C12—N2—C6117.3 (5)C28—C27—C26120.7 (6)
C12—N2—Dy1122.6 (4)C29—C28—C27119.7 (6)
C6—N2—Dy1119.8 (3)C29—C28—H28120.2
C13—N3—C17118.1 (6)C27—C28—H28120.2
C13—N3—Dy1123.0 (4)C28—C29—C30121.6 (7)
C17—N3—Dy1118.1 (4)C28—C29—H29119.2
C24—N4—C18117.7 (5)C30—C29—H29119.2
C24—N4—Dy1122.8 (4)C29—C30—C31119.8 (7)
C18—N4—Dy1119.4 (4)C29—C30—H30120.1
O11—N5—O9123.8 (6)C31—C30—H30120.1
O11—N5—O10121.0 (6)O4—C31—C30117.9 (6)
O9—N5—O10115.2 (5)O4—C31—C26121.4 (6)
N1—C1—C2124.5 (6)C30—C31—C26120.7 (6)
N1—C1—H1117.8O5—C32—O6117.8 (6)
C2—C1—H1117.8O5—C32—C33121.1 (6)
C3—C2—C1118.6 (6)O6—C32—C33121.0 (6)
C3—C2—H2120.7C34—C33—C38117.3 (6)
C1—C2—H2120.7C34—C33—C32121.3 (6)
C2—C3—C4119.6 (6)C38—C33—C32121.3 (6)
C2—C3—H3120.2O7—C34—C35116.8 (6)
C4—C3—H3120.2O7—C34—C33121.8 (6)
C3—C4—C5117.7 (6)C35—C34—C33121.4 (6)
C3—C4—C9123.0 (6)C34—C35—C36118.7 (7)
C5—C4—C9119.4 (6)C34—C35—H35120.6
N1—C5—C4122.7 (5)C36—C35—H35120.6
N1—C5—C6117.4 (5)C37—C36—C35122.4 (7)
C4—C5—C6119.9 (5)C37—C36—H36118.8
N2—C6—C7122.0 (5)C35—C36—H36118.8
N2—C6—C5119.1 (5)C36—C37—C38118.5 (7)
C7—C6—C5118.9 (5)C36—C37—H37120.8
C10—C7—C6117.5 (6)C38—C37—H37120.8
C10—C7—C8123.5 (6)O8—C38—C37117.8 (7)
C6—C7—C8119.1 (6)O8—C38—C33120.6 (7)
C9—C8—C7121.3 (6)C37—C38—C33121.7 (7)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O3—H27···O10.821.862.577 (7)146
O4—H31···O20.821.862.588 (6)148
O7—H34···O50.821.912.592 (7)139
O8—H38···O60.821.842.570 (7)148

Experimental details

Crystal data
Chemical formula[Dy(C7H5O4)2(NO3)(C12H8N2)2]
Mr891.14
Crystal system, space groupMonoclinic, P21/c
Temperature (K)298
a, b, c (Å)11.1268 (3), 26.7587 (4), 14.2703 (5)
β (°) 127.280 (2)
V3)3380.72 (18)
Z4
Radiation typeCu Kα
µ (mm1)12.46
Crystal size (mm)0.35 × 0.32 × 0.30
Data collection
DiffractometerOxford Diffraction Gemini S Ultra CCD
Absorption correctionMulti-scan
(CrysAlis PRO; Oxford Diffraction, 2006)
Tmin, Tmax0.097, 0.118
No. of measured, independent and
observed [I > 2σ(I)] reflections
11595, 5923, 4674
Rint0.043
(sin θ/λ)max1)0.597
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.051, 0.137, 1.00
No. of reflections5923
No. of parameters496
H-atom treatmentH-atom parameters constrained
Δρmax, Δρmin (e Å3)1.68, 1.16

Computer programs: CrysAlis PRO (Oxford Diffraction, 2006), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), DIAMOND (Brandenburg & Berndt, 1999).

Selected bond lengths (Å) top
Dy1—N12.597 (5)Dy1—O22.557 (4)
Dy1—N22.556 (4)Dy1—O52.458 (4)
Dy1—N32.545 (5)Dy1—O62.444 (5)
Dy1—N42.515 (5)Dy1—O92.604 (5)
Dy1—O12.442 (4)Dy1—O102.482 (5)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O3—H27···O10.821.862.577 (7)146
O4—H31···O20.821.862.588 (6)148
O7—H34···O50.821.912.592 (7)139
O8—H38···O60.821.842.570 (7)148
 

Acknowledgements

The authors are grateful for financial support from the Natural Science Foundation of Zhejiang Province (project No. 2010 Y4100495).

References

First citationBrandenburg, K. & Berndt, M. (1999). DIAMOND. Crystal Impact GbR, Bonn, Germany.  Google Scholar
First citationOxford Diffraction (2006). CrysAlis PRO. Oxford Diffraction Ltd, Abingdon, England.  Google Scholar
First citationSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.  Web of Science CrossRef CAS IUCr Journals Google Scholar
First citationZheng, J., Jin, H. & Ge, H. (2010). Acta Cryst. E66, m1469–m1470.  Web of Science CSD CrossRef IUCr Journals Google Scholar

This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Follow Acta Cryst. E
Sign up for e-alerts
Follow Acta Cryst. on Twitter
Follow us on facebook
Sign up for RSS feeds