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

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Bis(μ-2-methyl-8-oxidoquinolin-1-ium-κ2O:O)bis­­[(acetato-κ2O,O′)(2-methyl-8-oxidoquinolin-1-ium-κO)bis­­(nitrato-κ2O,O′)lanthanum(III)]

aDepartment of Chemistry, General Campus, Shahid Beheshti University, Tehran 1983963113, Iran, and bDepartment of Chemistry, University of Malaya, 50603 Kuala Lumpur, Malaysia
*Correspondence e-mail: seikweng@um.edu.my

(Received 17 December 2009; accepted 30 December 2009; online 16 January 2010)

The N-heterocycles in the centrosymmetric title compound, [La2(C10H9NO)4(CH3COO)2(NO3)4], exist in the zwitterionic form. One heterocycle binds to a metal center whereas the other bridges two metal centers. Each La atom is chelated by an acetate and two nitrate groups and is surrounded by nine O atoms in a distorted tricapped trigonal-prismatic coordination environment. The N—H groups form intra­molecular N—H⋯O hydrogen bonds. One of the nitrate ions is disordered over two positions in a 0.80 (3):0.20 (3) occupancy ratio.

Related literature

For bis­(μ-2-methyl­quinolin-1-ium-8-olato)bis­[(2-methyl­quin­o­lin-1-ium-8-olato-)tris­(nitrato)lanthanum(III)], see: Faza­eli et al. (2009[Fazaeli, Y., Najafi, E., Amini, M. M. & Ng, S. W. (2009). Acta Cryst. E65, m711.]).

[Scheme 1]

Experimental

Crystal data
  • [La2(C10H9NO)4(C2H3O2)2(NO3)4]

  • Mr = 1280.68

  • Monoclinic, P 21 /n

  • a = 11.3686 (8) Å

  • b = 17.5807 (12) Å

  • c = 13.0265 (10) Å

  • β = 104.820 (1)°

  • V = 2517.0 (3) Å3

  • Z = 2

  • Mo Kα radiation

  • μ = 1.76 mm−1

  • T = 295 K

  • 0.35 × 0.15 × 0.05 mm

Data collection
  • Bruker SMART APEX diffractometer

  • Absorption correction: multi-scan (SADABS; Sheldrick, 1996[Sheldrick, G. M. (1996). SADABS. University of Göttingen, Germany.]) Tmin = 0.578, Tmax = 0.917

  • 15685 measured reflections

  • 5769 independent reflections

  • 4544 reflections with I > 2σ(I)

  • Rint = 0.030

Refinement
  • R[F2 > 2σ(F2)] = 0.032

  • wR(F2) = 0.112

  • S = 1.11

  • 5769 reflections

  • 358 parameters

  • 58 restraints

  • H atoms treated by a mixture of independent and constrained refinement

  • Δρmax = 0.84 e Å−3

  • Δρmin = −0.77 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A DA D—H⋯A
N1—H1⋯O3 0.86 (1) 2.06 (1) 2.910 (5) 173 (5)
N2—H2⋯O4 0.86 (1) 2.20 (3) 2.926 (5) 143 (5)

Data collection: APEX2 (Bruker, 2008[Bruker (2008). APEX2 and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA.]); cell refinement: SAINT (Bruker, 2008[Bruker (2008). APEX2 and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA.]); data reduction: SAINT; 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: X-SEED (Barbour, 2001[Barbour, L. J. (2001). J. Supramol. Chem. 1, 189-191.]); software used to prepare material for publication: publCIF (Westrip, 2010[Westrip, S. P. (2010). publCIF. In preparation.]).

Supporting information


Related literature top

For bis(µ-2-methylquinolin-1-ium-8-olato)bis[(2-methylquinolin-1-ium-8-olato-)tris(nitrato)lanthanum(III)], see: Fazaeli et al. (2009).

Experimental top

2-Methyl-8-hydroxyquinoline (0.16 g, 1 mmol) and sodium acetate (0.08, 1 mmol) were added reacted with lanthanum nitrate hexahydrate (0.43 g, 1 mmol) in methanol (10 ml). The mixture was stirred two hours. Slow evaporation of the solution gave deep orange color crystals that are stable when heated up to 573 K.

Refinement top

Carbon-bound H-atoms were placed in calculated positions (C–H 0.93–0.96 Å) and were included in the refinement in the riding model approximation, with U(H) set to 1.2–1.5U(C).

The nitrogen-bound H atoms were located in a difference Fourier map, and were refined with a distance restraint of N–H 0.86±0.01 Å; the displacement parameters of these H atoms were refined.

One of the nitrate ions is disordered over two positions; the occupancy of the major occupied site refined to 0.80 (3). The N–O distances as well as the O···O distances were restrained to be equal within 0.01 Å of each other. The four-atom unit was restrained to be planar. The isotropic displacement parameters of the primed atoms were set to the equivalent isotropic temperature factors of the unprimed ones, and the anisotropic temperature factors of these unprimed atoms were restrained to be nearly isotropic.

Structure description top

For bis(µ-2-methylquinolin-1-ium-8-olato)bis[(2-methylquinolin-1-ium-8-olato-)tris(nitrato)lanthanum(III)], see: Fazaeli et al. (2009).

Computing details top

Data collection: APEX2 (Bruker, 2008); cell refinement: SAINT (Bruker, 2008); data reduction: SAINT (Bruker, 2008); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: X-SEED (Barbour, 2001); software used to prepare material for publication: publCIF (Westrip, 2010).

Figures top
[Figure 1] Fig. 1. Anisotropic displacement ellipsoid plot (Barbour, 2001) of the title compound; ellipsoids are drawn at the 50% probability level and H atoms of arbitrary radius. The minor occupied site of the disorder nitrate ion is not shown.
Bis(µ-2-methyl-8-oxidoquinolin-1-ium-κ2O:O)bis[(acetato- κ2O,O')(2-methyl-8-oxidoquinolin-1-ium- κO)bis(nitrato-κ2O,O')lanthanum(III)] top
Crystal data top
[La2(C10H9NO)4(C2H3O2)2(NO3)4]F(000) = 1272
Mr = 1280.68Dx = 1.690 Mg m3
Monoclinic, P21/nMo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ynCell parameters from 7894 reflections
a = 11.3686 (8) Åθ = 2.2–27.8°
b = 17.5807 (12) ŵ = 1.76 mm1
c = 13.0265 (10) ÅT = 295 K
β = 104.820 (1)°Block, orange
V = 2517.0 (3) Å30.35 × 0.15 × 0.05 mm
Z = 2
Data collection top
Bruker SMART APEX
diffractometer
5769 independent reflections
Radiation source: fine-focus sealed tube4544 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.030
ω scansθmax = 27.5°, θmin = 2.0°
Absorption correction: multi-scan
(SADABS; Sheldrick, 1996)
h = 1412
Tmin = 0.578, Tmax = 0.917k = 1722
15685 measured reflectionsl = 1616
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)] = 0.032Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.112H atoms treated by a mixture of independent and constrained refinement
S = 1.11 w = 1/[σ2(Fo2) + (0.0493P)2 + 4.7409P]
where P = (Fo2 + 2Fc2)/3
5769 reflections(Δ/σ)max = 0.001
358 parametersΔρmax = 0.84 e Å3
58 restraintsΔρmin = 0.77 e Å3
Crystal data top
[La2(C10H9NO)4(C2H3O2)2(NO3)4]V = 2517.0 (3) Å3
Mr = 1280.68Z = 2
Monoclinic, P21/nMo Kα radiation
a = 11.3686 (8) ŵ = 1.76 mm1
b = 17.5807 (12) ÅT = 295 K
c = 13.0265 (10) Å0.35 × 0.15 × 0.05 mm
β = 104.820 (1)°
Data collection top
Bruker SMART APEX
diffractometer
5769 independent reflections
Absorption correction: multi-scan
(SADABS; Sheldrick, 1996)
4544 reflections with I > 2σ(I)
Tmin = 0.578, Tmax = 0.917Rint = 0.030
15685 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.03258 restraints
wR(F2) = 0.112H atoms treated by a mixture of independent and constrained refinement
S = 1.11Δρmax = 0.84 e Å3
5769 reflectionsΔρmin = 0.77 e Å3
358 parameters
Special details top

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.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/UeqOcc. (<1)
La10.59038 (2)0.543193 (14)0.648779 (18)0.02973 (9)
O10.4836 (3)0.53330 (19)0.7782 (3)0.0433 (8)
O20.5705 (3)0.54741 (16)0.4544 (2)0.0298 (6)
O30.6618 (3)0.4169 (2)0.7427 (3)0.0490 (9)
O40.7505 (3)0.44741 (19)0.6178 (3)0.0466 (9)
O50.3958 (7)0.6311 (4)0.5777 (6)0.0566 (18)0.80 (3)
O5'0.420 (3)0.6466 (19)0.570 (2)0.057*0.20 (3)
O60.5573 (5)0.6913 (4)0.6548 (12)0.085 (3)0.80 (3)
O6'0.567 (2)0.677 (2)0.704 (3)0.085*0.20 (3)
O70.3882 (10)0.7522 (4)0.6030 (10)0.103 (3)0.80 (3)
O7'0.428 (4)0.7585 (17)0.638 (4)0.103*0.20 (3)
O80.7936 (4)0.6159 (2)0.6401 (3)0.0556 (10)
O90.7741 (4)0.5927 (3)0.7967 (3)0.0620 (11)
O100.9344 (4)0.6514 (3)0.7766 (4)0.0782 (14)
N10.5090 (4)0.4012 (2)0.8897 (3)0.0398 (9)
N20.7810 (3)0.4997 (2)0.4128 (3)0.0360 (9)
N30.4457 (7)0.6920 (3)0.6115 (6)0.0563 (18)0.80 (3)
N3'0.472 (3)0.6941 (14)0.638 (2)0.056*0.20 (3)
N40.8361 (4)0.6214 (3)0.7390 (4)0.0470 (10)
C10.4074 (4)0.5195 (3)0.8361 (3)0.0363 (10)
C20.3143 (5)0.5680 (3)0.8457 (4)0.0474 (12)
H2A0.30380.61400.80930.057*
C30.2355 (5)0.5488 (4)0.9092 (4)0.0597 (16)
H30.17340.58220.91290.072*
C40.2472 (6)0.4829 (4)0.9653 (5)0.0618 (16)
H40.19440.47211.00740.074*
C50.3394 (5)0.4310 (3)0.9597 (4)0.0494 (13)
C60.4183 (5)0.4505 (3)0.8952 (4)0.0384 (11)
C70.3617 (6)0.3623 (4)1.0154 (4)0.0602 (16)
H70.31240.34821.05930.072*
C80.4531 (7)0.3161 (3)1.0068 (4)0.0597 (17)
H80.46520.27031.04390.072*
C90.5307 (6)0.3360 (3)0.9425 (4)0.0503 (13)
C100.6331 (7)0.2879 (4)0.9293 (5)0.0681 (18)
H10A0.69720.31980.91800.102*
H10B0.60530.25490.86920.102*
H10C0.66320.25790.99200.102*
C110.6280 (4)0.5961 (3)0.4055 (3)0.0302 (9)
C120.5900 (4)0.6680 (3)0.3746 (4)0.0396 (11)
H120.52070.68720.39080.048*
C130.6541 (5)0.7138 (3)0.3183 (4)0.0509 (13)
H130.62590.76280.29940.061*
C140.7547 (5)0.6897 (3)0.2905 (4)0.0512 (13)
H140.79320.72080.25130.061*
C150.7998 (4)0.6162 (3)0.3222 (4)0.0410 (11)
C160.7377 (4)0.5703 (3)0.3809 (3)0.0326 (9)
C170.9041 (5)0.5839 (4)0.2988 (5)0.0527 (14)
H170.94780.61210.26070.063*
C180.9410 (5)0.5128 (4)0.3310 (5)0.0586 (16)
H181.00940.49270.31410.070*
C190.8779 (4)0.4684 (3)0.3897 (4)0.0443 (12)
C200.9120 (5)0.3891 (3)0.4264 (5)0.0587 (15)
H20A0.89420.38100.49370.088*
H20B0.99740.38160.43370.088*
H20C0.86640.35370.37540.088*
C210.7278 (4)0.3996 (3)0.6821 (4)0.0436 (11)
C220.7752 (6)0.3200 (4)0.6835 (6)0.074 (2)
H22A0.82540.30850.75290.110*
H22B0.82250.31550.63230.110*
H22C0.70820.28510.66590.110*
H10.552 (4)0.410 (3)0.845 (3)0.043 (14)*
H20.748 (4)0.472 (2)0.452 (3)0.042 (15)*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
La10.03124 (15)0.03346 (15)0.02601 (13)0.00429 (11)0.01007 (9)0.00058 (10)
O10.055 (2)0.046 (2)0.0370 (17)0.0002 (16)0.0253 (16)0.0023 (14)
O20.0299 (15)0.0332 (16)0.0284 (14)0.0021 (12)0.0112 (12)0.0018 (12)
O30.053 (2)0.051 (2)0.047 (2)0.0087 (18)0.0209 (17)0.0113 (17)
O40.050 (2)0.041 (2)0.054 (2)0.0048 (16)0.0236 (17)0.0087 (16)
O50.052 (3)0.039 (3)0.076 (3)0.006 (2)0.011 (3)0.003 (3)
O60.073 (4)0.033 (3)0.127 (7)0.005 (3)0.013 (4)0.011 (3)
O70.116 (6)0.073 (4)0.119 (6)0.053 (4)0.026 (5)0.015 (4)
O80.061 (2)0.065 (3)0.044 (2)0.026 (2)0.0209 (18)0.0052 (18)
O90.055 (2)0.093 (3)0.0380 (19)0.027 (2)0.0114 (17)0.002 (2)
O100.045 (2)0.105 (4)0.081 (3)0.033 (2)0.010 (2)0.011 (3)
N10.053 (3)0.039 (2)0.0288 (19)0.0081 (19)0.0135 (18)0.0017 (16)
N20.034 (2)0.045 (2)0.0330 (19)0.0017 (18)0.0151 (16)0.0014 (17)
N30.062 (4)0.055 (4)0.053 (4)0.019 (3)0.019 (3)0.006 (3)
N40.039 (2)0.051 (3)0.050 (2)0.011 (2)0.0106 (19)0.008 (2)
C10.043 (3)0.041 (3)0.026 (2)0.008 (2)0.0112 (19)0.0061 (18)
C20.057 (3)0.052 (3)0.035 (2)0.001 (3)0.016 (2)0.002 (2)
C30.043 (3)0.096 (5)0.043 (3)0.000 (3)0.017 (2)0.010 (3)
C40.059 (4)0.089 (5)0.047 (3)0.020 (3)0.030 (3)0.006 (3)
C50.054 (3)0.065 (4)0.031 (2)0.021 (3)0.014 (2)0.006 (2)
C60.048 (3)0.042 (3)0.026 (2)0.013 (2)0.0116 (19)0.0040 (19)
C70.083 (4)0.064 (4)0.042 (3)0.025 (3)0.032 (3)0.002 (3)
C80.104 (5)0.035 (3)0.044 (3)0.033 (3)0.026 (3)0.002 (2)
C90.077 (4)0.039 (3)0.035 (2)0.009 (3)0.014 (2)0.002 (2)
C100.101 (5)0.054 (4)0.050 (3)0.007 (4)0.021 (3)0.008 (3)
C110.027 (2)0.039 (2)0.0233 (18)0.0047 (18)0.0037 (16)0.0001 (17)
C120.038 (3)0.038 (3)0.044 (3)0.000 (2)0.012 (2)0.002 (2)
C130.052 (3)0.047 (3)0.052 (3)0.011 (3)0.010 (2)0.003 (2)
C140.060 (3)0.053 (3)0.043 (3)0.014 (3)0.017 (2)0.013 (2)
C150.032 (2)0.061 (3)0.030 (2)0.014 (2)0.0090 (18)0.006 (2)
C160.029 (2)0.043 (3)0.0243 (19)0.0067 (19)0.0034 (16)0.0024 (18)
C170.045 (3)0.065 (4)0.054 (3)0.019 (3)0.023 (2)0.007 (3)
C180.039 (3)0.079 (4)0.069 (4)0.007 (3)0.035 (3)0.020 (3)
C190.033 (2)0.057 (3)0.042 (3)0.001 (2)0.008 (2)0.013 (2)
C200.050 (3)0.064 (4)0.062 (4)0.012 (3)0.013 (3)0.010 (3)
C210.035 (3)0.045 (3)0.049 (3)0.004 (2)0.008 (2)0.011 (2)
C220.075 (4)0.049 (4)0.105 (6)0.025 (3)0.038 (4)0.019 (4)
Geometric parameters (Å, º) top
La1—O12.322 (3)C3—C41.358 (9)
La1—O22.485 (3)C3—H30.9300
La1—O6'2.49 (3)C4—C51.405 (9)
La1—O2i2.536 (3)C4—H40.9300
La1—O32.564 (4)C5—C71.399 (8)
La1—O42.586 (3)C5—C61.418 (7)
La1—O92.603 (4)C7—C81.346 (9)
La1—O5'2.66 (3)C7—H70.9300
La1—O62.635 (6)C8—C91.408 (8)
La1—O52.663 (7)C8—H80.9300
La1—O82.668 (4)C9—C101.484 (9)
La1—C212.942 (5)C10—H10A0.9600
O1—C11.309 (5)C10—H10B0.9600
O2—C111.334 (5)C10—H10C0.9600
O2—La1i2.536 (3)C11—C121.363 (6)
O3—C211.257 (6)C11—C161.438 (6)
O4—C211.260 (6)C12—C131.410 (7)
O5—N31.239 (6)C12—H120.9300
O5'—N3'1.241 (7)C13—C141.353 (8)
O6—N31.250 (6)C13—H130.9300
O6'—N3'1.241 (7)C14—C151.412 (8)
O7—N31.233 (5)C14—H140.9300
O7'—N3'1.240 (7)C15—C171.416 (7)
O8—N41.258 (6)C15—C161.417 (6)
O9—N41.260 (5)C17—C181.351 (9)
O10—N41.219 (5)C17—H170.9300
N1—C91.327 (7)C18—C191.410 (8)
N1—C61.362 (7)C18—H180.9300
N1—H10.859 (10)C19—C201.492 (8)
N2—C191.333 (6)C20—H20A0.9600
N2—C161.362 (6)C20—H20B0.9600
N2—H20.861 (10)C20—H20C0.9600
C1—C21.389 (7)C21—C221.498 (8)
C1—C61.426 (7)C22—H22A0.9600
C2—C31.408 (8)C22—H22B0.9600
C2—H2A0.9300C22—H22C0.9600
O1—La1—O2144.47 (11)O5'—N3'—O6'119.9 (7)
O1—La1—O6'75.4 (9)O7'—N3'—La1176.0 (13)
O2—La1—O6'106.1 (9)O5'—N3'—La163.9 (12)
O1—La1—O2i84.12 (11)O6'—N3'—La156.0 (12)
O2—La1—O2i67.27 (11)O10—N4—O8121.1 (5)
O6'—La1—O2i129.1 (6)O10—N4—O9121.9 (5)
O1—La1—O375.49 (11)O8—N4—O9117.0 (4)
O2—La1—O3116.55 (11)O10—N4—La1178.6 (4)
O6'—La1—O3136.3 (9)O8—N4—La160.0 (2)
O2i—La1—O378.84 (11)O9—N4—La157.0 (2)
O1—La1—O4125.74 (11)O1—C1—C2124.7 (5)
O2—La1—O475.19 (11)O1—C1—C6119.3 (4)
O6'—La1—O4142.2 (6)C2—C1—C6115.9 (4)
O2i—La1—O487.10 (11)C1—C2—C3121.3 (5)
O3—La1—O450.30 (11)C1—C2—H2A119.4
O1—La1—O987.53 (12)C3—C2—H2A119.4
O2—La1—O9126.22 (10)C4—C3—C2122.1 (6)
O6'—La1—O966.1 (6)C4—C3—H3118.9
O2i—La1—O9159.37 (12)C2—C3—H3118.9
O3—La1—O980.82 (13)C3—C4—C5119.9 (5)
O4—La1—O982.54 (14)C3—C4—H4120.1
O1—La1—O5'82.3 (8)C5—C4—H4120.1
O2—La1—O5'73.8 (6)C7—C5—C4124.9 (5)
O6'—La1—O5'49.1 (5)C7—C5—C6117.3 (6)
O2i—La1—O5'82.6 (7)C4—C5—C6117.9 (5)
O3—La1—O5'152.3 (8)N1—C6—C5118.7 (5)
O4—La1—O5'148.9 (7)N1—C6—C1118.4 (4)
O9—La1—O5'115.0 (6)C5—C6—C1123.0 (5)
O1—La1—O687.0 (3)C8—C7—C5121.2 (5)
O2—La1—O691.4 (3)C8—C7—H7119.4
O6'—La1—O614.7 (7)C5—C7—H7119.4
O2i—La1—O6123.18 (19)C7—C8—C9121.0 (5)
O3—La1—O6150.6 (3)C7—C8—H8119.5
O4—La1—O6139.4 (2)C9—C8—H8119.5
O9—La1—O675.0 (2)N1—C9—C8117.4 (6)
O5'—La1—O640.6 (6)N1—C9—C10118.7 (5)
O1—La1—O575.8 (2)C8—C9—C10123.9 (5)
O2—La1—O577.14 (18)C9—C10—H10A109.5
O6'—La1—O554.1 (6)C9—C10—H10B109.5
O2i—La1—O575.98 (17)H10A—C10—H10B109.5
O3—La1—O5143.3 (2)C9—C10—H10C109.5
O4—La1—O5151.49 (17)H10A—C10—H10C109.5
O9—La1—O5120.07 (17)H10B—C10—H10C109.5
O5'—La1—O59.0 (7)O2—C11—C12125.4 (4)
O6—La1—O547.51 (16)O2—C11—C16117.6 (4)
O1—La1—O8133.29 (12)C12—C11—C16117.0 (4)
O2—La1—O878.27 (10)C11—C12—C13121.1 (5)
O6'—La1—O873.6 (7)C11—C12—H12119.5
O2i—La1—O8142.52 (10)C13—C12—H12119.5
O3—La1—O8105.23 (13)C14—C13—C12123.0 (5)
O4—La1—O869.72 (12)C14—C13—H13118.5
O9—La1—O848.04 (11)C12—C13—H13118.5
O5'—La1—O8102.1 (8)C13—C14—C15118.5 (5)
O6—La1—O870.12 (18)C13—C14—H14120.8
O5—La1—O8111.0 (2)C15—C14—H14120.8
O1—La1—C21100.66 (13)C14—C15—C17124.4 (5)
O2—La1—C2194.73 (12)C14—C15—C16119.0 (5)
O6'—La1—C21149.1 (7)C17—C15—C16116.6 (5)
O2i—La1—C2179.82 (12)N2—C16—C15119.6 (4)
O3—La1—C2125.22 (12)N2—C16—C11119.1 (4)
O4—La1—C2125.30 (12)C15—C16—C11121.4 (4)
O9—La1—C2183.26 (15)C18—C17—C15121.0 (5)
O5'—La1—C21161.7 (6)C18—C17—H17119.5
O6—La1—C21156.65 (18)C15—C17—H17119.5
O5—La1—C21155.77 (18)C17—C18—C19121.3 (5)
O8—La1—C2189.09 (13)C17—C18—H18119.4
C1—O1—La1168.0 (3)C19—C18—H18119.4
C11—O2—La1125.3 (2)N2—C19—C18117.3 (5)
C11—O2—La1i121.7 (2)N2—C19—C20118.3 (5)
La1—O2—La1i112.73 (10)C18—C19—C20124.3 (5)
C21—O3—La194.4 (3)C19—C20—H20A109.5
C21—O4—La193.3 (3)C19—C20—H20B109.5
N3—O5—La196.5 (4)H20A—C20—H20B109.5
N3'—O5'—La191.4 (12)C19—C20—H20C109.5
N3—O6—La197.6 (4)H20A—C20—H20C109.5
N3'—O6'—La199.6 (13)H20B—C20—H20C109.5
N4—O8—La195.9 (3)O3—C21—O4120.8 (5)
N4—O9—La199.0 (3)O3—C21—C22119.3 (5)
C9—N1—C6124.4 (4)O4—C21—C22119.8 (5)
C9—N1—H1116 (4)O3—C21—La160.3 (3)
C6—N1—H1119 (4)O4—C21—La161.4 (3)
C19—N2—C16124.2 (4)C22—C21—La1168.3 (4)
C19—N2—H2114 (3)C21—C22—H22A109.5
C16—N2—H2122 (3)C21—C22—H22B109.5
O7—N3—O5121.7 (5)H22A—C22—H22B109.5
O7—N3—O6120.1 (5)C21—C22—H22C109.5
O5—N3—O6118.1 (5)H22A—C22—H22C109.5
O7'—N3'—O5'120.2 (7)H22B—C22—H22C109.5
O7'—N3'—O6'120.0 (7)
O2—La1—O1—C129.7 (17)La1—O6—N3—O54.4 (5)
O6'—La1—O1—C1127.1 (18)La1—O5'—N3'—O7'179.9 (17)
O2i—La1—O1—C15.9 (16)La1—O5'—N3'—O6'0.1 (17)
O3—La1—O1—C185.8 (16)La1—O6'—N3'—O7'179.9 (19)
O4—La1—O1—C188.0 (16)La1—O6'—N3'—O5'0.1 (19)
O9—La1—O1—C1167.0 (16)O1—La1—N3'—O5'98.4 (18)
O5'—La1—O1—C177.4 (17)O2—La1—N3'—O5'48.0 (18)
O6—La1—O1—C1117.9 (16)O6'—La1—N3'—O5'179.9 (18)
O5—La1—O1—C171.1 (16)O2i—La1—N3'—O5'18.3 (19)
O8—La1—O1—C1176.7 (16)O3—La1—N3'—O5'115 (2)
C21—La1—O1—C184.3 (16)O4—La1—N3'—O5'101.2 (18)
O1—La1—O2—C11135.0 (3)O9—La1—N3'—O5'174.2 (18)
O6'—La1—O2—C1147.8 (7)O6—La1—N3'—O5'142 (2)
O2i—La1—O2—C11174.0 (4)O5—La1—N3'—O5'15.6 (18)
O3—La1—O2—C11122.4 (3)O8—La1—N3'—O5'126.3 (18)
O4—La1—O2—C1192.9 (3)O1—La1—N3'—O6'81.7 (19)
O9—La1—O2—C1124.1 (4)O4—La1—N3'—O6'78.7 (19)
O5'—La1—O2—C1185.4 (8)O5'—La1—N3'—O6'179.9 (18)
O6—La1—O2—C1148.3 (3)O5—La1—N3'—O6'164.5 (19)
O5—La1—O2—C1194.0 (4)La1—O8—N4—O10179.0 (5)
O8—La1—O2—C1121.1 (3)La1—O8—N4—O90.9 (5)
C21—La1—O2—C11109.2 (3)La1—O9—N4—O10179.0 (5)
O1—La1—O2—La1i38.9 (2)La1—O9—N4—O81.0 (5)
O6'—La1—O2—La1i126.2 (7)O1—La1—N4—O8163.4 (3)
O2i—La1—O2—La1i0.0O2—La1—N4—O82.7 (3)
O3—La1—O2—La1i63.64 (15)O6'—La1—N4—O899.8 (11)
O4—La1—O2—La1i93.10 (13)O2i—La1—N4—O856.4 (5)
O9—La1—O2—La1i161.98 (14)O3—La1—N4—O8120.8 (3)
O5'—La1—O2—La1i88.6 (8)O4—La1—N4—O873.5 (3)
O6—La1—O2—La1i125.68 (16)O9—La1—N4—O8179.0 (5)
O5—La1—O2—La1i80.0 (2)O5'—La1—N4—O874.3 (8)
O8—La1—O2—La1i164.96 (15)O6—La1—N4—O884.4 (5)
C21—La1—O2—La1i76.88 (14)O5—La1—N4—O879.1 (4)
O1—La1—O3—C21176.5 (3)C21—La1—N4—O896.7 (3)
O2—La1—O3—C2132.4 (3)O1—La1—N4—O917.6 (4)
O6'—La1—O3—C21133.9 (10)O2—La1—N4—O9176.3 (3)
O2i—La1—O3—C2189.8 (3)O6'—La1—N4—O981.2 (11)
O4—La1—O3—C215.8 (3)O2i—La1—N4—O9122.6 (4)
O9—La1—O3—C2193.7 (3)O3—La1—N4—O958.2 (3)
O5'—La1—O3—C21138.6 (12)O4—La1—N4—O9105.5 (3)
O6—La1—O3—C21128.3 (4)O5'—La1—N4—O9106.7 (8)
O5—La1—O3—C21137.1 (3)O6—La1—N4—O996.6 (5)
O8—La1—O3—C2151.9 (3)O5—La1—N4—O9101.9 (4)
O1—La1—O4—C218.5 (4)O8—La1—N4—O9179.0 (5)
O2—La1—O4—C21139.4 (3)C21—La1—N4—O982.3 (3)
O6'—La1—O4—C21123.4 (15)La1—O1—C1—C294.4 (16)
O2i—La1—O4—C2172.1 (3)La1—O1—C1—C685.9 (16)
O3—La1—O4—C215.8 (3)O1—C1—C2—C3179.6 (5)
O9—La1—O4—C2190.0 (3)C6—C1—C2—C30.7 (7)
O5'—La1—O4—C21142.6 (15)C1—C2—C3—C40.9 (9)
O6—La1—O4—C21146.3 (5)C2—C3—C4—C50.9 (9)
O5—La1—O4—C21125.1 (5)C3—C4—C5—C7178.6 (6)
O8—La1—O4—C21137.9 (3)C3—C4—C5—C60.6 (8)
O1—La1—O5—N396.7 (6)C9—N1—C6—C51.3 (7)
O2—La1—O5—N3106.5 (6)C9—N1—C6—C1178.5 (4)
O6'—La1—O5—N314.5 (10)C7—C5—C6—N11.1 (7)
O2i—La1—O5—N3176.0 (6)C4—C5—C6—N1179.3 (5)
O3—La1—O5—N3136.0 (5)C7—C5—C6—C1178.6 (5)
O4—La1—O5—N3120.6 (4)C4—C5—C6—C10.4 (7)
O9—La1—O5—N318.1 (7)O1—C1—C6—N10.4 (6)
O5'—La1—O5—N339 (4)C2—C1—C6—N1179.3 (4)
O6—La1—O5—N32.5 (3)O1—C1—C6—C5179.8 (4)
O8—La1—O5—N334.7 (6)C2—C1—C6—C50.5 (7)
C21—La1—O5—N3179.0 (4)C4—C5—C7—C8179.0 (6)
O1—La1—O5'—N3'77.3 (16)C6—C5—C7—C81.0 (8)
O2—La1—O5'—N3'129.3 (18)C5—C7—C8—C91.0 (9)
O6'—La1—O5'—N3'0.1 (10)C6—N1—C9—C81.2 (7)
O2i—La1—O5'—N3'162.3 (18)C6—N1—C9—C10179.8 (5)
O3—La1—O5'—N3'114.1 (18)C7—C8—C9—N11.0 (8)
O4—La1—O5'—N3'126.1 (12)C7—C8—C9—C10180.0 (6)
O9—La1—O5'—N3'6 (2)La1—O2—C11—C1284.2 (5)
O6—La1—O5'—N3'17.1 (10)La1i—O2—C11—C1289.2 (5)
O5—La1—O5'—N3'120 (5)La1—O2—C11—C1697.3 (4)
O8—La1—O5'—N3'55.5 (17)La1i—O2—C11—C1689.2 (4)
C21—La1—O5'—N3'178.0 (13)O2—C11—C12—C13176.7 (4)
O1—La1—O6—N371.0 (6)C16—C11—C12—C131.8 (7)
O2—La1—O6—N373.5 (6)C11—C12—C13—C140.9 (8)
O6'—La1—O6—N3108 (3)C12—C13—C14—C152.1 (8)
O2i—La1—O6—N310.0 (8)C13—C14—C15—C17179.9 (5)
O3—La1—O6—N3123.7 (4)C13—C14—C15—C160.6 (7)
O4—La1—O6—N3142.1 (3)C19—N2—C16—C152.2 (7)
O9—La1—O6—N3159.2 (6)C19—N2—C16—C11176.3 (4)
O5'—La1—O6—N310.7 (11)C14—C15—C16—N2179.4 (4)
O5—La1—O6—N32.5 (3)C17—C15—C16—N21.0 (6)
O8—La1—O6—N3150.5 (7)C14—C15—C16—C112.1 (6)
C21—La1—O6—N3178.9 (4)C17—C15—C16—C11177.5 (4)
O1—La1—O6'—N3'92.4 (17)O2—C11—C16—N23.2 (6)
O2—La1—O6'—N3'50.8 (19)C12—C11—C16—N2178.2 (4)
O2i—La1—O6'—N3'23 (2)O2—C11—C16—C15175.3 (4)
O3—La1—O6'—N3'142.0 (14)C12—C11—C16—C153.3 (6)
O4—La1—O6'—N3'137.2 (11)C14—C15—C17—C18179.3 (5)
O9—La1—O6'—N3'174 (2)C16—C15—C17—C180.3 (7)
O5'—La1—O6'—N3'0.1 (10)C15—C17—C18—C190.5 (9)
O6—La1—O6'—N3'49 (2)C16—N2—C19—C182.0 (7)
O5—La1—O6'—N3'9.5 (12)C16—N2—C19—C20177.6 (4)
O8—La1—O6'—N3'123 (2)C17—C18—C19—N20.5 (8)
C21—La1—O6'—N3'178.7 (9)C17—C18—C19—C20179.0 (5)
O1—La1—O8—N421.5 (4)La1—O3—C21—O410.7 (5)
O2—La1—O8—N4177.3 (3)La1—O3—C21—C22166.5 (5)
O6'—La1—O8—N471.8 (9)La1—O4—C21—O310.6 (5)
O2i—La1—O8—N4154.2 (3)La1—O4—C21—C22166.6 (5)
O3—La1—O8—N462.7 (3)O1—La1—C21—O33.4 (3)
O4—La1—O8—N498.9 (3)O2—La1—C21—O3151.3 (3)
O9—La1—O8—N40.5 (3)O6'—La1—C21—O375.9 (18)
O5'—La1—O8—N4112.3 (7)O2i—La1—C21—O385.4 (3)
O6—La1—O8—N486.9 (5)O4—La1—C21—O3169.6 (5)
O5—La1—O8—N4111.6 (3)O9—La1—C21—O382.8 (3)
C21—La1—O8—N482.3 (3)O5'—La1—C21—O3101 (3)
O1—La1—O9—N4163.5 (3)O6—La1—C21—O3104.1 (9)
O2—La1—O9—N44.5 (4)O5—La1—C21—O382.4 (6)
O6'—La1—O9—N488.4 (11)O8—La1—C21—O3130.6 (3)
O2i—La1—O9—N4130.4 (3)O1—La1—C21—O4173.0 (3)
O3—La1—O9—N4120.8 (3)O2—La1—C21—O439.2 (3)
O4—La1—O9—N469.9 (3)O6'—La1—C21—O493.6 (18)
O5'—La1—O9—N483.2 (9)O2i—La1—C21—O4105.0 (3)
O6—La1—O9—N476.0 (4)O3—La1—C21—O4169.6 (5)
O5—La1—O9—N491.6 (4)O9—La1—C21—O486.8 (3)
O8—La1—O9—N40.6 (3)O5'—La1—C21—O489 (3)
C21—La1—O9—N495.4 (3)O6—La1—C21—O465.5 (9)
La1—O5—N3—O7175.8 (4)O5—La1—C21—O4108.1 (6)
La1—O5—N3—O64.4 (5)O8—La1—C21—O439.0 (3)
La1—O6—N3—O7175.7 (4)
Symmetry code: (i) x+1, y+1, z+1.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N1—H1···O30.86 (1)2.06 (1)2.910 (5)173 (5)
N2—H2···O40.86 (1)2.20 (3)2.926 (5)143 (5)

Experimental details

Crystal data
Chemical formula[La2(C10H9NO)4(C2H3O2)2(NO3)4]
Mr1280.68
Crystal system, space groupMonoclinic, P21/n
Temperature (K)295
a, b, c (Å)11.3686 (8), 17.5807 (12), 13.0265 (10)
β (°) 104.820 (1)
V3)2517.0 (3)
Z2
Radiation typeMo Kα
µ (mm1)1.76
Crystal size (mm)0.35 × 0.15 × 0.05
Data collection
DiffractometerBruker SMART APEX
diffractometer
Absorption correctionMulti-scan
(SADABS; Sheldrick, 1996)
Tmin, Tmax0.578, 0.917
No. of measured, independent and
observed [I > 2σ(I)] reflections
15685, 5769, 4544
Rint0.030
(sin θ/λ)max1)0.650
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.032, 0.112, 1.11
No. of reflections5769
No. of parameters358
No. of restraints58
H-atom treatmentH atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å3)0.84, 0.77

Computer programs: APEX2 (Bruker, 2008), SAINT (Bruker, 2008), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), X-SEED (Barbour, 2001), publCIF (Westrip, 2010).

Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N1—H1···O30.86 (1)2.06 (1)2.910 (5)173 (5)
N2—H2···O40.86 (1)2.20 (3)2.926 (5)143 (5)
 

Acknowledgements

We thank Shahid Beheshti University and the University of Malaya for supporting this study.

References

First citationBarbour, L. J. (2001). J. Supramol. Chem. 1, 189–191.  CrossRef CAS Google Scholar
First citationBruker (2008). APEX2 and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA.  Google Scholar
First citationFazaeli, Y., Najafi, E., Amini, M. M. & Ng, S. W. (2009). Acta Cryst. E65, m711.  Web of Science CSD CrossRef IUCr Journals Google Scholar
First citationSheldrick, G. M. (1996). SADABS. University of Göttingen, Germany.  Google Scholar
First citationSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.  Web of Science CrossRef CAS IUCr Journals Google Scholar
First citationWestrip, S. P. (2010). publCIF. In preparation.  Google Scholar

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