Skip to main content
Acta Crystallographica Section E: Structure Reports Online logoLink to Acta Crystallographica Section E: Structure Reports Online
. 2007 Dec 18;64(Pt 1):m201. doi: 10.1107/S1600536807066263

Tetrakis[μ-3-(3-pyridyl)acrylato-κ2 O:O′]bis{(1,10-phenanthroline-κ2 N,N′)[3-(3-pyridyl)acrylato-κ2 O,O′]europium(III)} pentahydrate

Chong-Bo Liu a, Hui-Liang Wen b,*, Fang Deng a, Jun-Hui Zuo b
PMCID: PMC2915131  PMID: 21200549

Abstract

The europiumIII ion in the title compound, [Eu2(C8H6NO2)6(C12H8N2)2]·5H2O, is coordinated by seven carboxyl­ate O atoms and two N atoms from one phenanthroline mol­ecule. The carboxyl­ate groups of 3-(3-pyrid­yl)acrylate link pairs of europium(III) ions, forming centrosymmetric dinuclear units, which further assemble into a sheet parallel to the (001) plane through hydrogen-bonding inter­actions involving the uncoordinated water mol­ecules. One water molecule is disordered.

Related literature

For related literature, see: Gunning & Cahill (2005); Liu et al. (2006); Ye et al. (2005).graphic file with name e-64-0m201-scheme1.jpg

Experimental

Crystal data

  • [Eu2(C8H6NO2)6(C12H8N2)2]·5H2O

  • M r = 1643.24

  • Monoclinic, Inline graphic

  • a = 25.434 (2) Å

  • b = 12.320 (10) Å

  • c = 22.595 (19) Å

  • β = 100.330 (10)°

  • V = 6965.4 (10) Å3

  • Z = 4

  • Mo Kα radiation

  • μ = 1.86 mm−1

  • T = 293 (2) K

  • 0.32 × 0.27 × 0.13 mm

Data collection

  • Bruker SMART CCD area-detector diffractometer

  • Absorption correction: multi-scan (SADABS; Sheldrick, 1996) T min = 0.585, T max = 0.791

  • 25928 measured reflections

  • 6480 independent reflections

  • 5721 reflections with I > 2σ(I)

  • R int = 0.022

Refinement

  • R[F 2 > 2σ(F 2)] = 0.019

  • wR(F 2) = 0.044

  • S = 1.03

  • 6480 reflections

  • 460 parameters

  • H-atom parameters constrained

  • Δρmax = 0.34 e Å−3

  • Δρmin = −0.25 e Å−3

Data collection: SMART (Bruker, 1998); cell refinement: SAINT (Bruker, 1998); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: ORTEPIII (Burnett & Johnson, 1996)and ORTEP-3 for Windows (Farrugia, 1997); software used to prepare material for publication: SHELXL97.

Supplementary Material

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536807066263/dn2276sup1.cif

e-64-0m201-sup1.cif (27.5KB, cif)

Structure factors: contains datablocks I. DOI: 10.1107/S1600536807066263/dn2276Isup2.hkl

e-64-0m201-Isup2.hkl (317.2KB, hkl)

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

Table 1. Hydrogen-bond geometry (Å, °).

D—H⋯A D—H H⋯A DA D—H⋯A
O1W—H11W⋯O6 0.85 1.94 2.775 (3) 171
O1W—H12W⋯N2i 0.85 2.02 2.856 (3) 167
O2W—H21W⋯O1Wii 0.82 2.48 2.851 (4) 109
O3W—H31W⋯O2Wiii 0.82 2.20 2.655 (7) 116

Symmetry codes: (i) Inline graphic; (ii) Inline graphic; (iii) Inline graphic.

Acknowledgments

This work is supported by the National Natural Science Foundation of China (20662007) and Nanchang University of Aeronautics (EA20072195).

supplementary crystallographic information

Comment

Recently, assembly of high-dimensional supramolecular coordination polymers have attracted considerable attention by exploiting coordination bonds, hydrogen bondings, and π-π stacks [Ye et al., 2005], not only because of their intriguing sructural diversity, but also for their potential application as smart opotoelectronic, magnetic, and porous materials. 1,10-phenanthroline has been widely used to construct stable supramolecular structures via C—H···O or C—H···N hydrogen bonds and π-π stackings, and 3-pyridylacrylic acid (HTPA) is a potential multidentate ligand, (Gunning et al., 2005; Liu et al., 2006). Here, we report the synthesis and structure of a europium supramolecular complex with 3-(3-pyridyl)acrylato and 1,10-phenanthroline, [Eu2 (C8H6NO2)6 (C12H8N2)]2.(H2O)5 (I).

Each EuIII centre is coordinated by seven carboxylate oxygen atoms and two nitrogen atoms from one phenanthroline molecule; the carboxylate groups of 3-(3-pyridyl)acrylato adopt bridging bidentate, chelating and bridging-chlelating tridentate modes respectively (Fig. 1). the dihedral angles between them are 59.229 (73), 84.724 (65) and 72.190 (56) ° respectively. The carboxylate groups of 3-(3-pyridyl)acrylato link pairs of europium(III) ions to form dinuclear units, which further build up a sheet parallel to the (0 0 1) plane through hydrogen bondings involving the uncoordinated water molecules (Table 1).

Experimental

A mixture of EuCl3.6H2O (0.1 mmol), 3-pyridylacrylic acid (0.1 mmol), 1,10-phenanthroline (0.1 mmol), H2O (10 ml), and 0.65 M NaOH aqueous solution (0.1 mmol) was sealed in a 25 ml Teflon-lined stainless reactor and heated at 393 K for 72 h under autogenous pressure, then cooled to room temperature, when a few colourless crystals were obtained. Analysis: found C 52.33, H 3.96, N 8.73%; C72H62Eu2N10O17 requires C 52.01, H 3.85, N 8.43%.

Refinement

All H atoms attached to C atoms were fixed geometrically and treated as riding with C—H = 0.93 Å with Uiso(H) = 1.2Ueq(C). H atoms of water molecule were located in difference Fourier maps and included in the subsequent refinement using restraints (O—H= 0.82 (1)Å and H···H= 1.39 (2) Å) with Uiso(H) = 1.5Ueq(O). In the last stage of refinement they were treated as riding on their parent O atoms.

Figures

Fig. 1.

Fig. 1.

: The molecular structure of complex (I), showing the atom-labelling scheme. Displacement ellipsoids are drawn at the 30% probability level and H atoms are represented as small spheres of arbitrary radius. [Symmetry code: (i) 1 - x, 1 - y, 1 - z.]

Crystal data

[Eu2(C8H6NO2)6(C12H8N2)2]·5H2O F000 = 3304
Mr = 1643.24 Dx = 1.567 Mg m3
Monoclinic, C2/c Mo Kα radiation λ = 0.71073 Å
Hall symbol: -C 2yc Cell parameters from 7048 reflections
a = 25.434 (2) Å θ = 2.7–28.1º
b = 12.320 (10) Å µ = 1.86 mm1
c = 22.595 (19) Å T = 293 (2) K
β = 100.330 (10)º Block, colorless
V = 6965.4 (10) Å3 0.32 × 0.27 × 0.13 mm
Z = 4

Data collection

Bruker SMART CCD area-detector diffractometer 6480 independent reflections
Radiation source: fine-focus sealed tube 5721 reflections with I > 2σ(I)
Monochromator: graphite Rint = 0.022
T = 293(2) K θmax = 25.5º
φ and ω scans θmin = 2.5º
Absorption correction: multi-scan(SADABS; Sheldrick, 1996) h = −30→30
Tmin = 0.585, Tmax = 0.791 k = −14→14
25928 measured reflections l = −27→27

Refinement

Refinement on F2 Secondary atom site location: difference Fourier map
Least-squares matrix: full Hydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.019 H-atom parameters constrained
wR(F2) = 0.044   w = 1/[σ2(Fo2) + (0.0183P)2 + 8.1685P] where P = (Fo2 + 2Fc2)/3
S = 1.03 (Δ/σ)max = 0.006
6480 reflections Δρmax = 0.34 e Å3
460 parameters Δρmin = −0.25 e Å3
Primary atom site location: structure-invariant direct methods Extinction correction: none

Special details

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.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2)

x y z Uiso*/Ueq Occ. (<1)
Eu1 0.528205 (4) 0.611291 (8) 0.562535 (4) 0.02456 (4)
O5 0.58593 (7) 0.57165 (15) 0.66055 (7) 0.0457 (4)
O6 0.62759 (6) 0.62061 (13) 0.58772 (7) 0.0417 (4)
N3 0.82161 (9) 0.3750 (2) 0.77152 (12) 0.0627 (7)
N4 0.55055 (7) 0.81740 (14) 0.56748 (8) 0.0312 (4)
N5 0.48983 (7) 0.72683 (15) 0.64279 (8) 0.0311 (4)
C17 0.62845 (9) 0.58151 (19) 0.63974 (11) 0.0375 (6)
C18 0.68033 (10) 0.5427 (2) 0.67463 (12) 0.0442 (6)
H18 0.7110 0.5515 0.6581 0.053*
C19 0.68467 (10) 0.4966 (2) 0.72778 (11) 0.0430 (6)
H19 0.6538 0.4954 0.7444 0.052*
C20 0.73241 (10) 0.4467 (2) 0.76421 (11) 0.0415 (6)
C21 0.73315 (12) 0.4186 (3) 0.82349 (13) 0.0589 (8)
H21 0.7035 0.4319 0.8412 0.071*
C22 0.77820 (14) 0.3705 (3) 0.85628 (14) 0.0729 (10)
H22 0.7796 0.3521 0.8964 0.087*
C23 0.82070 (13) 0.3506 (3) 0.82849 (15) 0.0664 (9)
H23 0.8508 0.3179 0.8509 0.080*
C24 0.77778 (10) 0.4222 (2) 0.74091 (12) 0.0500 (7)
H24 0.7777 0.4400 0.7009 0.060*
C25 0.58064 (10) 0.8617 (2) 0.53183 (11) 0.0418 (6)
H25 0.5997 0.8160 0.5106 0.050*
C26 0.58516 (12) 0.9740 (2) 0.52446 (12) 0.0531 (7)
H26 0.6067 1.0017 0.4988 0.064*
C27 0.55780 (12) 1.0418 (2) 0.55515 (13) 0.0562 (7)
H27 0.5599 1.1165 0.5501 0.067*
C28 0.52609 (10) 0.99896 (19) 0.59464 (12) 0.0450 (6)
C29 0.49626 (13) 1.0650 (2) 0.62910 (15) 0.0629 (8)
H29 0.4973 1.1401 0.6255 0.076*
C30 0.46693 (12) 1.0205 (2) 0.66633 (15) 0.0611 (8)
H30 0.4485 1.0655 0.6886 0.073*
C31 0.46320 (10) 0.9054 (2) 0.67276 (12) 0.0435 (6)
C32 0.43288 (10) 0.8555 (2) 0.71132 (12) 0.0505 (7)
H32 0.4134 0.8978 0.7338 0.061*
C33 0.43197 (10) 0.7457 (2) 0.71572 (11) 0.0472 (6)
H33 0.4124 0.7120 0.7415 0.057*
C34 0.46102 (9) 0.6843 (2) 0.68077 (10) 0.0395 (6)
H34 0.4602 0.6091 0.6842 0.047*
C35 0.49140 (8) 0.83702 (18) 0.63913 (10) 0.0318 (5)
C36 0.52348 (9) 0.88490 (17) 0.59938 (10) 0.0331 (5)
O1 0.44766 (7) 0.35404 (12) 0.53195 (7) 0.0375 (4)
O2 0.47138 (6) 0.48567 (12) 0.60014 (7) 0.0389 (4)
O3 0.44546 (6) 0.55841 (12) 0.47089 (7) 0.0367 (4)
O4 0.44788 (6) 0.71259 (12) 0.51991 (7) 0.0382 (4)
N1 0.40521 (14) 0.2529 (3) 0.83252 (12) 0.0830 (9)
N2 0.21675 (9) 0.92111 (19) 0.44666 (11) 0.0541 (6)
C1 0.44874 (9) 0.39752 (17) 0.58251 (10) 0.0328 (5)
C2 0.42104 (10) 0.33633 (19) 0.62482 (10) 0.0395 (5)
H2 0.3976 0.2814 0.6090 0.047*
C3 0.42757 (10) 0.35487 (19) 0.68318 (11) 0.0390 (6)
H3 0.4495 0.4129 0.6979 0.047*
C4 0.40369 (11) 0.2931 (2) 0.72740 (11) 0.0428 (6)
C5 0.36142 (13) 0.2224 (2) 0.71075 (14) 0.0632 (8)
H5 0.3466 0.2118 0.6704 0.076*
C6 0.34154 (17) 0.1676 (3) 0.75602 (19) 0.0866 (12)
H6 0.3129 0.1199 0.7466 0.104*
C7 0.36502 (18) 0.1855 (3) 0.81466 (18) 0.0882 (12)
H7 0.3516 0.1473 0.8442 0.106*
C8 0.42271 (12) 0.3066 (3) 0.78849 (12) 0.0584 (8)
H8 0.4498 0.3571 0.7997 0.070*
C9 0.42372 (9) 0.64675 (17) 0.48230 (9) 0.0295 (5)
C10 0.36825 (9) 0.67176 (18) 0.45216 (10) 0.0336 (5)
H10 0.3514 0.6266 0.4216 0.040*
C11 0.34228 (9) 0.75715 (18) 0.46803 (10) 0.0346 (5)
H11 0.3607 0.7998 0.4989 0.041*
C12 0.28771 (9) 0.79227 (19) 0.44256 (11) 0.0392 (6)
C13 0.25486 (11) 0.7384 (3) 0.39657 (14) 0.0658 (9)
H13 0.2674 0.6777 0.3789 0.079*
C14 0.20331 (12) 0.7750 (3) 0.37698 (17) 0.0795 (11)
H14 0.1807 0.7390 0.3464 0.095*
C15 0.18612 (11) 0.8654 (3) 0.40342 (15) 0.0651 (9)
H15 0.1512 0.8888 0.3904 0.078*
C16 0.26665 (10) 0.8837 (2) 0.46531 (12) 0.0457 (6)
H16 0.2886 0.9220 0.4956 0.055*
O1W 0.69847 (9) 0.61683 (17) 0.50760 (12) 0.0848 (8)
H11W 0.6788 0.6122 0.5340 0.127*
H12W 0.6986 0.5565 0.4895 0.127*
O2W 0.30658 (11) 0.1792 (3) 0.55009 (14) 0.1219 (11)
H21W 0.2805 0.2095 0.5594 0.183*
H22W 0.2973 0.1433 0.5193 0.183*
O3W 0.3341 (3) 0.9915 (5) 0.6047 (3) 0.133 (2) 0.50
H32W 0.3035 1.0082 0.6078 0.199* 0.50
H31W 0.3521 1.0410 0.5944 0.199* 0.50

Atomic displacement parameters (Å2)

U11 U22 U33 U12 U13 U23
Eu1 0.02668 (6) 0.02120 (6) 0.02471 (6) −0.00104 (4) 0.00168 (4) −0.00081 (4)
O5 0.0382 (10) 0.0595 (11) 0.0366 (9) 0.0112 (8) −0.0010 (8) 0.0015 (8)
O6 0.0356 (9) 0.0442 (10) 0.0416 (10) −0.0015 (7) −0.0026 (7) 0.0035 (8)
N3 0.0460 (14) 0.0697 (17) 0.0676 (17) 0.0169 (12) −0.0031 (12) 0.0009 (13)
N4 0.0331 (10) 0.0262 (10) 0.0332 (10) −0.0044 (8) 0.0026 (8) −0.0031 (8)
N5 0.0327 (10) 0.0322 (10) 0.0270 (9) −0.0002 (8) 0.0018 (8) −0.0025 (8)
C17 0.0348 (13) 0.0324 (13) 0.0411 (14) 0.0016 (10) −0.0045 (11) −0.0092 (10)
C18 0.0327 (13) 0.0459 (15) 0.0499 (15) 0.0015 (11) −0.0033 (11) −0.0014 (12)
C19 0.0366 (13) 0.0420 (14) 0.0471 (15) 0.0007 (11) −0.0016 (11) −0.0039 (12)
C20 0.0400 (14) 0.0367 (13) 0.0431 (14) 0.0008 (11) −0.0057 (11) −0.0026 (11)
C21 0.0577 (18) 0.068 (2) 0.0492 (17) 0.0100 (15) 0.0041 (14) 0.0027 (14)
C22 0.079 (2) 0.084 (2) 0.0483 (18) 0.0120 (19) −0.0102 (17) 0.0169 (16)
C23 0.0566 (19) 0.0612 (19) 0.070 (2) 0.0155 (15) −0.0192 (16) 0.0079 (16)
C24 0.0455 (15) 0.0541 (16) 0.0469 (15) 0.0046 (13) −0.0013 (12) 0.0001 (12)
C25 0.0464 (15) 0.0380 (14) 0.0418 (14) −0.0111 (11) 0.0102 (11) −0.0053 (11)
C26 0.0648 (18) 0.0425 (15) 0.0533 (17) −0.0208 (14) 0.0140 (14) 0.0019 (13)
C27 0.0678 (19) 0.0272 (14) 0.072 (2) −0.0109 (13) 0.0082 (16) 0.0033 (13)
C28 0.0483 (15) 0.0273 (12) 0.0564 (16) −0.0001 (11) 0.0012 (12) −0.0037 (11)
C29 0.070 (2) 0.0292 (14) 0.090 (2) 0.0054 (14) 0.0161 (18) −0.0103 (15)
C30 0.0621 (19) 0.0410 (16) 0.082 (2) 0.0117 (14) 0.0170 (17) −0.0203 (15)
C31 0.0387 (14) 0.0424 (15) 0.0483 (15) 0.0069 (11) 0.0048 (11) −0.0116 (11)
C32 0.0383 (14) 0.0632 (18) 0.0511 (16) 0.0081 (13) 0.0110 (12) −0.0178 (14)
C33 0.0389 (14) 0.0665 (19) 0.0373 (14) −0.0032 (13) 0.0099 (11) −0.0062 (13)
C34 0.0429 (14) 0.0412 (14) 0.0346 (13) −0.0038 (11) 0.0077 (11) −0.0019 (10)
C35 0.0298 (11) 0.0306 (12) 0.0322 (12) 0.0016 (9) −0.0025 (9) −0.0049 (10)
C36 0.0326 (12) 0.0288 (12) 0.0348 (12) 0.0001 (10) −0.0024 (9) −0.0040 (10)
O1 0.0497 (10) 0.0332 (8) 0.0308 (8) −0.0102 (7) 0.0099 (7) −0.0043 (7)
O2 0.0511 (10) 0.0324 (9) 0.0353 (9) −0.0135 (8) 0.0136 (8) −0.0048 (7)
O3 0.0388 (9) 0.0252 (8) 0.0454 (9) 0.0047 (7) 0.0059 (7) −0.0021 (7)
O4 0.0359 (9) 0.0310 (8) 0.0426 (9) 0.0043 (7) −0.0074 (7) −0.0062 (7)
N1 0.102 (2) 0.097 (2) 0.0588 (17) 0.014 (2) 0.0373 (17) 0.0253 (17)
N2 0.0400 (13) 0.0515 (14) 0.0725 (16) 0.0131 (11) 0.0148 (12) 0.0069 (12)
C1 0.0365 (12) 0.0291 (12) 0.0329 (12) −0.0023 (10) 0.0064 (10) 0.0012 (10)
C2 0.0475 (14) 0.0341 (13) 0.0392 (13) −0.0128 (11) 0.0136 (11) −0.0034 (11)
C3 0.0453 (14) 0.0330 (13) 0.0413 (14) −0.0038 (11) 0.0145 (11) 0.0005 (10)
C4 0.0541 (16) 0.0347 (13) 0.0443 (15) 0.0045 (11) 0.0215 (12) 0.0046 (11)
C5 0.085 (2) 0.0511 (18) 0.0599 (19) −0.0153 (16) 0.0310 (17) 0.0009 (14)
C6 0.110 (3) 0.063 (2) 0.099 (3) −0.032 (2) 0.053 (3) 0.003 (2)
C7 0.121 (3) 0.080 (3) 0.079 (3) 0.008 (2) 0.060 (3) 0.028 (2)
C8 0.0684 (19) 0.068 (2) 0.0432 (16) 0.0044 (15) 0.0209 (14) 0.0110 (14)
C9 0.0330 (12) 0.0250 (11) 0.0299 (11) 0.0008 (9) 0.0038 (9) 0.0039 (9)
C10 0.0329 (12) 0.0299 (12) 0.0354 (12) −0.0021 (10) −0.0011 (10) −0.0044 (10)
C11 0.0327 (12) 0.0337 (12) 0.0354 (12) −0.0028 (10) 0.0009 (10) −0.0018 (10)
C12 0.0321 (13) 0.0388 (13) 0.0456 (14) 0.0026 (10) 0.0045 (11) 0.0012 (11)
C13 0.0437 (16) 0.065 (2) 0.080 (2) 0.0141 (14) −0.0149 (15) −0.0226 (17)
C14 0.0462 (18) 0.082 (2) 0.098 (3) 0.0138 (17) −0.0224 (17) −0.025 (2)
C15 0.0340 (15) 0.072 (2) 0.085 (2) 0.0112 (14) −0.0021 (15) 0.0104 (18)
C16 0.0371 (13) 0.0432 (14) 0.0565 (16) 0.0046 (12) 0.0078 (12) 0.0001 (12)
O1W 0.0709 (15) 0.0684 (15) 0.128 (2) −0.0128 (12) 0.0522 (15) −0.0190 (14)
O2W 0.093 (2) 0.123 (3) 0.140 (3) −0.0135 (19) −0.0045 (19) 0.010 (2)
O3W 0.139 (5) 0.103 (5) 0.133 (5) −0.017 (4) −0.036 (4) 0.009 (4)

Geometric parameters (Å, °)

Eu1—O3i 2.3604 (15) C32—H32 0.9300
Eu1—O1i 2.3638 (15) C33—C34 1.397 (3)
Eu1—O2 2.3763 (15) C33—H33 0.9300
Eu1—O4 2.4400 (15) C34—H34 0.9300
Eu1—O5 2.4765 (16) C35—C36 1.443 (3)
Eu1—O6 2.4922 (16) O1—C1 1.258 (3)
Eu1—N4 2.6001 (18) O1—Eu1i 2.3638 (15)
Eu1—N5 2.6272 (18) O2—C1 1.260 (3)
Eu1—O3 2.7530 (16) O3—C9 1.268 (3)
Eu1—C17 2.843 (2) O3—Eu1i 2.3604 (15)
Eu1—C9 2.969 (2) O4—C9 1.253 (3)
Eu1—Eu1i 4.0137 (3) N1—C7 1.322 (5)
O5—C17 1.260 (3) N1—C8 1.336 (4)
O6—C17 1.267 (3) N2—C15 1.327 (4)
N3—C23 1.326 (4) N2—C16 1.345 (3)
N3—C24 1.335 (3) C1—C2 1.490 (3)
N4—C25 1.324 (3) C2—C3 1.319 (3)
N4—C36 1.365 (3) C2—H2 0.9300
N5—C34 1.332 (3) C3—C4 1.471 (3)
N5—C35 1.361 (3) C3—H3 0.9300
C17—C18 1.489 (3) C4—C5 1.382 (4)
C18—C19 1.315 (3) C4—C8 1.388 (4)
C18—H18 0.9300 C5—C6 1.394 (4)
C19—C20 1.474 (3) C5—H5 0.9300
C19—H19 0.9300 C6—C7 1.370 (5)
C20—C21 1.380 (4) C6—H6 0.9300
C20—C24 1.385 (4) C7—H7 0.9300
C21—C22 1.381 (4) C8—H8 0.9300
C21—H21 0.9300 C9—C10 1.485 (3)
C22—C23 1.366 (5) C10—C11 1.325 (3)
C22—H22 0.9300 C10—H10 0.9300
C23—H23 0.9300 C11—C12 1.469 (3)
C24—H24 0.9300 C11—H11 0.9300
C25—C26 1.400 (3) C12—C13 1.381 (4)
C25—H25 0.9300 C12—C16 1.385 (3)
C26—C27 1.355 (4) C13—C14 1.382 (4)
C26—H26 0.9300 C13—H13 0.9300
C27—C28 1.408 (4) C14—C15 1.371 (4)
C27—H27 0.9300 C14—H14 0.9300
C28—C36 1.412 (3) C15—H15 0.9300
C28—C29 1.434 (4) C16—H16 0.9300
C29—C30 1.338 (4) O1W—H11W 0.8462
C29—H29 0.9300 O1W—H12W 0.8481
C30—C31 1.431 (4) O2W—H21W 0.8204
C30—H30 0.9300 O2W—H22W 0.8227
C31—C32 1.404 (4) O3W—H32W 0.8204
C31—C35 1.413 (3) O3W—H31W 0.8198
C32—C33 1.357 (4)
O3i—Eu1—O1i 74.72 (5) N3—C24—H24 117.5
O3i—Eu1—O2 76.31 (5) C20—C24—H24 117.5
O1i—Eu1—O2 135.54 (5) N4—C25—C26 123.3 (2)
O3i—Eu1—O4 126.32 (5) N4—C25—H25 118.4
O1i—Eu1—O4 83.44 (6) C26—C25—H25 118.4
O2—Eu1—O4 87.38 (6) C27—C26—C25 119.2 (3)
O3i—Eu1—O5 87.40 (6) C27—C26—H26 120.4
O1i—Eu1—O5 129.42 (6) C25—C26—H26 120.4
O2—Eu1—O5 81.54 (6) C26—C27—C28 119.9 (2)
O4—Eu1—O5 140.72 (5) C26—C27—H27 120.1
O3i—Eu1—O6 77.26 (5) C28—C27—H27 120.1
O1i—Eu1—O6 77.34 (6) C27—C28—C36 117.5 (2)
O2—Eu1—O6 127.26 (6) C27—C28—C29 123.4 (2)
O4—Eu1—O6 144.08 (5) C36—C28—C29 119.1 (3)
O5—Eu1—O6 52.45 (6) C30—C29—C28 121.2 (3)
O3i—Eu1—N4 143.74 (6) C30—C29—H29 119.4
O1i—Eu1—N4 76.83 (5) C28—C29—H29 119.4
O2—Eu1—N4 139.73 (5) C29—C30—C31 121.6 (3)
O4—Eu1—N4 71.25 (5) C29—C30—H30 119.2
O5—Eu1—N4 93.68 (6) C31—C30—H30 119.2
O6—Eu1—N4 74.94 (6) C32—C31—C35 117.5 (2)
O3i—Eu1—N5 149.61 (6) C32—C31—C30 123.4 (2)
O1i—Eu1—N5 135.59 (5) C35—C31—C30 119.1 (3)
O2—Eu1—N5 77.35 (5) C33—C32—C31 120.0 (2)
O4—Eu1—N5 66.85 (5) C33—C32—H32 120.0
O5—Eu1—N5 73.95 (6) C31—C32—H32 120.0
O6—Eu1—N5 107.73 (5) C32—C33—C34 118.8 (2)
N4—Eu1—N5 63.04 (6) C32—C33—H33 120.6
O3i—Eu1—O3 76.84 (5) C34—C33—H33 120.6
O1i—Eu1—O3 69.55 (5) N5—C34—C33 124.0 (2)
O2—Eu1—O3 71.51 (5) N5—C34—H34 118.0
O4—Eu1—O3 49.54 (5) C33—C34—H34 118.0
O5—Eu1—O3 151.25 (6) N5—C35—C31 122.6 (2)
O6—Eu1—O3 142.18 (5) N5—C35—C36 118.14 (19)
N4—Eu1—O3 113.28 (5) C31—C35—C36 119.3 (2)
N5—Eu1—O3 108.60 (5) N4—C36—C28 122.1 (2)
O3i—Eu1—C17 78.89 (6) N4—C36—C35 118.33 (19)
O1i—Eu1—C17 103.18 (7) C28—C36—C35 119.6 (2)
O2—Eu1—C17 103.45 (7) C1—O1—Eu1i 140.95 (14)
O4—Eu1—C17 154.62 (6) C1—O2—Eu1 136.14 (14)
O5—Eu1—C17 26.26 (6) C9—O3—Eu1i 169.88 (14)
O6—Eu1—C17 26.44 (6) C9—O3—Eu1 86.92 (12)
N4—Eu1—C17 86.25 (6) Eu1i—O3—Eu1 103.16 (5)
N5—Eu1—C17 92.85 (6) C9—O4—Eu1 102.16 (13)
O3—Eu1—C17 155.71 (6) C7—N1—C8 115.2 (3)
O3i—Eu1—C9 102.08 (6) C15—N2—C16 116.7 (2)
O1i—Eu1—C9 76.75 (6) O1—C1—O2 126.1 (2)
O2—Eu1—C9 77.23 (6) O1—C1—C2 115.56 (19)
O4—Eu1—C9 24.37 (5) O2—C1—C2 118.4 (2)
O5—Eu1—C9 153.82 (6) C3—C2—C1 124.4 (2)
O6—Eu1—C9 153.25 (6) C3—C2—H2 117.8
N4—Eu1—C9 92.72 (6) C1—C2—H2 117.8
N5—Eu1—C9 86.51 (6) C2—C3—C4 126.6 (2)
O3—Eu1—C9 25.25 (5) C2—C3—H3 116.7
C17—Eu1—C9 178.95 (6) C4—C3—H3 116.7
O3i—Eu1—Eu1i 41.90 (4) C5—C4—C8 117.5 (2)
O1i—Eu1—Eu1i 66.76 (4) C5—C4—C3 122.5 (2)
O2—Eu1—Eu1i 69.10 (4) C8—C4—C3 120.0 (2)
O4—Eu1—Eu1i 84.45 (4) C4—C5—C6 118.2 (3)
O5—Eu1—Eu1i 125.08 (4) C4—C5—H5 120.9
O6—Eu1—Eu1i 114.34 (4) C6—C5—H5 120.9
N4—Eu1—Eu1i 138.18 (4) C7—C6—C5 118.6 (3)
N5—Eu1—Eu1i 136.55 (4) C7—C6—H6 120.7
O3—Eu1—Eu1i 34.93 (3) C5—C6—H6 120.7
C17—Eu1—Eu1i 120.79 (5) N1—C7—C6 125.1 (3)
C9—Eu1—Eu1i 60.18 (4) N1—C7—H7 117.4
C17—O5—Eu1 93.33 (14) C6—C7—H7 117.4
C17—O6—Eu1 92.42 (14) N1—C8—C4 125.3 (3)
C23—N3—C24 116.3 (3) N1—C8—H8 117.4
C25—N4—C36 118.12 (19) C4—C8—H8 117.4
C25—N4—Eu1 121.48 (15) O4—C9—O3 120.99 (19)
C36—N4—Eu1 119.38 (14) O4—C9—C10 119.13 (19)
C34—N5—C35 117.2 (2) O3—C9—C10 119.86 (19)
C34—N5—Eu1 123.15 (15) O4—C9—Eu1 53.47 (10)
C35—N5—Eu1 118.67 (14) O3—C9—Eu1 67.83 (11)
O5—C17—O6 120.7 (2) C10—C9—Eu1 169.61 (15)
O5—C17—C18 120.6 (2) C11—C10—C9 121.3 (2)
O6—C17—C18 118.6 (2) C11—C10—H10 119.4
O5—C17—Eu1 60.41 (12) C9—C10—H10 119.4
O6—C17—Eu1 61.14 (12) C10—C11—C12 127.6 (2)
C18—C17—Eu1 168.00 (16) C10—C11—H11 116.2
C19—C18—C17 122.9 (2) C12—C11—H11 116.2
C19—C18—H18 118.5 C13—C12—C16 116.6 (2)
C17—C18—H18 118.5 C13—C12—C11 123.7 (2)
C18—C19—C20 128.0 (3) C16—C12—C11 119.7 (2)
C18—C19—H19 116.0 C12—C13—C14 119.7 (3)
C20—C19—H19 116.0 C12—C13—H13 120.2
C21—C20—C24 116.6 (2) C14—C13—H13 120.2
C21—C20—C19 120.9 (2) C15—C14—C13 119.0 (3)
C24—C20—C19 122.5 (2) C15—C14—H14 120.5
C20—C21—C22 119.6 (3) C13—C14—H14 120.5
C20—C21—H21 120.2 N2—C15—C14 123.4 (3)
C22—C21—H21 120.2 N2—C15—H15 118.3
C23—C22—C21 118.6 (3) C14—C15—H15 118.3
C23—C22—H22 120.7 N2—C16—C12 124.6 (3)
C21—C22—H22 120.7 N2—C16—H16 117.7
N3—C23—C22 123.9 (3) C12—C16—H16 117.7
N3—C23—H23 118.0 H11W—O1W—H12W 109.4
C22—C23—H23 118.0 H21W—O2W—H22W 109.8
N3—C24—C20 125.0 (3) H32W—O3W—H31W 115.1

Symmetry codes: (i) −x+1, −y+1, −z+1.

Hydrogen-bond geometry (Å, °)

D—H···A D—H H···A D···A D—H···A
O1W—H11W···O6 0.85 1.94 2.775 (3) 171
O1W—H12W···N2ii 0.85 2.02 2.856 (3) 167
O2W—H21W···O1Wiii 0.82 2.48 2.851 (4) 109
O3W—H31W···O2Wiv 0.82 2.20 2.655 (7) 116

Symmetry codes: (ii) x+1/2, y−1/2, z; (iii) x−1/2, y−1/2, z; (iv) x, y+1, z.

Footnotes

Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: DN2276).

References

  1. Bruker (1998). SAINT (Version 5.10) and SMART (Version 5.0). Bruker AXS Inc., Madison, Wisconsin, USA.
  2. Burnett, M. N. & Johnson, C. K. (1996). ORTEPIII. Report ORNL-6895. Oak Ridge National Laboratory, Oak Ridge, Tennessee, USA.
  3. Farrugia, L. J. (1997). J. Appl. Cryst.30, 565.
  4. Gunning, N. S. & Cahill, C. L. (2005). J. Chem. Soc. Dalton Trans. pp. 2788–2792. [DOI] [PubMed]
  5. Liu, C.-B., Nie, X.-L., Ding, L., Xie, M.-Y. & Wen, H.-L. (2006). Acta Cryst. E62, m2319–m2320.
  6. Sheldrick, G. M. (1996). SADABS. University of Göttingen, Germany.
  7. Sheldrick, G. M. (1997). SHELXS97 and SHELXL97, University of Göttingen, Germany.
  8. Ye, B.-H., Tong, M.-L. & Chen, X.-M. (2005). Coord. Chem. Rev.249, 545–565.

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536807066263/dn2276sup1.cif

e-64-0m201-sup1.cif (27.5KB, cif)

Structure factors: contains datablocks I. DOI: 10.1107/S1600536807066263/dn2276Isup2.hkl

e-64-0m201-Isup2.hkl (317.2KB, hkl)

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


Articles from Acta Crystallographica Section E: Structure Reports Online are provided here courtesy of International Union of Crystallography

RESOURCES