Issue contents
Download PDF of article
Download CIF
3D view
Navigation
Highlighting
Dictionary of Crystallography reference
IUPAC Gold Book reference
more ...
Download citation
FormatBIBTeX
EndNote
RefMan
Refer
Medline
CIF
SGML
Plain Text
share
Previous article
Next article
Previous article
Issue contents
Download PDF of article
Download CIF
3D view
Navigation
Highlighting
Dictionary of Crystallography reference
IUPAC Gold Book reference
more ...
Download citation
FormatBIBTeX
EndNote
RefMan
Refer
Medline
CIF
SGML
Plain Text
share
Next article

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

Journal logoCRYSTALLOGRAPHIC
COMMUNICATIONS
ISSN: 2056-9890
Volume 69| Part 11| November 2013| Pages m591-m592
doi:10.1107/S1600536813027323

Di-μ-acetato-κ4O:O′-bis­­[(1,10-phenanthroline-κ2N,N′)(tri­fluoro­methane­sulfonato-κO)copper(II)]

Nanthawat Wannarit,a Chaveng Pakawatchaib and Sujittra Youngmea*

aMaterials Chemistry Research Unit, Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen 40002, Thailand, and bDepartment of Chemistry, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand
*Correspondence e-mail: sujittra@kku.ac.th

(Received 30 August 2013; accepted 4 October 2013; online 12 October 2013)

The complete molecule of the title compound, [Cu2(C2H3O2)2(CF3O3S)2(C12H8N2)2], is completed by the application of a twofold rotation and comprises two CuII ions, each of which is penta­coordinated by two N atoms from a bidentate 1,10-phenanthroline (phen) ligand, two O atoms from acetate ligands and an O atom from a tri­fluoro­methane­sulfonate anion, forming a (4 + 1) distorted square-pyramidal coordination geometry. The CuII ions are connected by two acetate bridges in a syn–syn configuration. The F atoms of the tri­fluoro­methane­sulfonate ligands are disordered, with site-occupation factors of 70 and 30. The molecular structure is stabilized by intra­molecular face-to-face π–π inter­actions with centroid–centroid distances in the range 3.5654 (12)–3.8775(12) Å. The crystal structure is stabilized by C—H⋯O interactions, leading to a three-dimensional lattice structure.

CCDC reference: 964934

Related literature

For general background to this work, see: Moreira et al. (2007[Moreira, I. P. R., Costa, R., Filatov, M. & Illas, F. (2007). J. Chem. Theory Comput. 3, 764-774.]); Calvo et al. (2011[Calvo, R., Abud, J. E., Sartoris, R. P. & Santana, R. C. (2011). Phys. Rev. B, 84, 104433, 1-13.]); Reinoso et al. (2005[Reinoso, S., Vitoria, P., Felices, L. S., Lezama, L. & Gutiérrez-Zorrilla, J. M. (2005). Chem. Eur. J. 11, 1538-1548.], 2007[Reinoso, S., Vitoria, P., Gutiérrez-Zorrilla, J. M., Lezama, L., Madariaga, J. M., Felices, L. S. & Iturrospe, A. (2007). Inorg. Chem. 46, 4010-4021.]); Ritchie et al. (2006[Ritchie, C., Burkholder, E., Kögerler, P. & Cronin, L. (2006). Dalton Trans. pp. 1712-1714.]); Wang et al. (2006[Wang, J.-P., Ren, Q., Zhao, J.-W. & Niu, J.-Y. (2006). Inorg. Chem. Commun. 9, 1281-1285.]). For literature used in the synthetic procedures, see: Youngme et al. (2008[Youngme, S., Cheansirisomboon, A., Danvirutai, C., Pakawatchai, C., Chaichit, N., Engkagul, C., van Albada, G. A., Costa, J. S. & Reedijk, J. (2008). Polyhedron, 27, 1875-1882.]). For a related crystal structure, see: Tokii et al. (1990[Tokii, T., Watanabe, N., Nakashima, M., Muto, Y., Morooka, M., Ohba, S. & Saito, I. (1990). Bull. Chem. Soc. Jpn, 63, 364-369.]). For potential applications, see: Hill & Brown (1986[Hill, C. L. & Brown, R. B. (1986). J. Am. Chem. Soc. 108, 536-538.]); Mansuy et al. (1991[Mansuy, D., Bartoli, J. F., Battioni, P., Lyon, D. K. & Finke, R. G. (1991). J. Am. Chem. Soc. 113, 7222-7226.]); Hill & Zhang (1995[Hill, C. L. & Zhang, X. (1995). Nature (London), 373, 324-326.]). For an explanation of the τ parameter, see: Addison et al. (1984[Addison, A. W., Rao, T. N., Reedijk, J., van Rijn, J. & Verschoor, G. C. (1984). J. Chem. Soc. Dalton Trans. pp. 1349-1356.]). For spectroscopic properties, see: Castro et al. (1992[Castro, I., Faus, J., Julve, M., Bois, C., Real, J. A. & Lloret, F. (1992). J. Chem. Soc. Dalton Trans. pp. 47-52.]); Sletten & Julve (1999[Sletten, J. & Julve, M. (1999). Acta Chem. Scand. 53, 631-633.]).

[Scheme 1]

Experimental

Crystal data

  • [Cu2(C2H3O2)2(CF3O3S)2(C12H8N2)2]

  • Mr = 903.72

  • Monoclinic, C 2/c

  • a = 13.1198 (5) Å

  • b = 16.1282 (6) Å

  • c = 16.3659 (6) Å

  • β = 95.507 (1)°

  • V = 3447.0 (2) Å3

  • Z = 4

  • Mo Kα radiation

  • μ = 1.45 mm−1

  • T = 293 K

  • 0.24 × 0.21 × 0.18 mm
Data collection

  • Bruker SMART APEX CCD diffractometer

  • Absorption correction: multi-scan (SADABS; Sheldrick, 2000[Sheldrick, G. M. (2000). SADABS. University of Göttingen, Germany.]) Tmin = 0.872, Tmax = 1.000

  • 23313 measured reflections

  • 4178 independent reflections

  • 3491 reflections with I > 2σ(I)

  • Rint = 0.022
Refinement

  • R[F2 > 2σ(F2)] = 0.034

  • wR(F2) = 0.102

  • S = 1.04

  • 4178 reflections

  • 272 parameters

  • H-atom parameters constrained

  • Δρmax = 0.37 e Å−3

  • Δρmin = −0.32 e Å−3

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A D⋯A D—H⋯A
C1—H1⋯O5i 0.93 2.43 3.229 (3) 144
C3—H3⋯O4ii 0.93 2.34 3.213 (3) 157
C8—H8⋯O3iii 0.93 2.56 3.421 (3) 154
Symmetry codes: (i) -x+1, -y+2, -z+1; (ii) [x-{\script{1\over 2}}, y-{\script{1\over 2}}, z]; (iii) [-x+{\script{3\over 2}}, y-{\script{1\over 2}}, -z+{\script{3\over 2}}].

Data collection: SMART (Bruker, 2000[Bruker (2000). SMART and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA.]); cell refinement: SMART; data reduction: SAINT (Bruker, 2000[Bruker (2000). SMART and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA.]) and SHELXTL (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); program(s) used to solve structure: SHELXTL; program(s) used to refine structure: SHELXL97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); molecular graphics: ORTEP-3 for Windows (Farrugia, 2012[Farrugia, L. J. (2012). J. Appl. Cryst. 45, 849-854.]) and Mercury (Macrae et al., 2006[Macrae, C. F., Edgington, P. R., McCabe, P., Pidcock, E., Shields, G. P., Taylor, R., Towler, M. & van de Streek, J. (2006). J. Appl. Cryst. 39, 453-457.]); software used to prepare material for publication: PLATON (Spek, 2009[Spek, A. L. (2009). Acta Cryst. D65, 148-155.]) and pubCIF (Westrip, 2010[Westrip, S. P. (2010). J. Appl. Cryst. 43, 920-925.]).

Supporting information

CCDC reference: 964934

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536813027323/im2439sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S1600536813027323/im2439Isup2.hkl

checkCIF report


Comment top

The synthesis and characterization of polycarboxylato-bridged dinuclear copper(II) compounds namely dinuclear tetracarboxylato-bridged CuII compounds (paddlewheel-like structure) (e.g. Moreira et al., 2007; Youngme et al., 2008) and also dinuclear CuII compounds containing dicarboxylato-bridges (Tokii et al., 1990; Reinoso et al., 2005; Ritchie et al., 2006) have attacted much attention in several years. These compounds have been prepared with the aim of studying their intramolecular magnetic properties which are determined predominantly by strong antiferromagnetic interactions. In addition, the dicarboxylato-bridged dinuclear CuII compounds have been frequently used as the models for the basic understanding of their magneto-structural correlations in theoretical studies (Moreira et al., 2007; Calvo et al., 2011). Copper(II) compounds containing doubly acetato-bridged dinuclear units, [Cu(phen)(µ-OOCCH3)2Cu(phen)]2+ (where phen = 1,10-phenanthroline), have also been shown to exhibit antiferromagnetic behavior (Tokii et al., 1990). Furthermore, this type of dinuclear unit was used as the secondary building block in functionalized polyoxometalate (POMs) materials (Wang et al., 2006; Reinoso et al., 2007; Calvo et al., 2011) to extend the dimensionality of structures leading to new hybrid materials and more selective applications, for example catalytic properties in organic oxidations (Hill & Brown, 1986; Mansuy et al., 1991; Hill, & Zhang, 1995).

A new doubly acetato-bridged dinuclear CuII compound containing additional trifluoromethanesulfonate anions has been synthesized and its structural features are reported here. Compound I, bis((µ-acetato)(trifluoromethanesulfonato)(1,10-phenanthroline))dicopper(II) crystallized in the space group C2/c with an asymmetric unit containing one half of the dinuclear unit (Fig.1). This dinuclear unit has C2 symmetry around the b axis with Cu···Cu distance of 3.0309 (4) Å. Structurally, compound I consists of two [Cu(phen)(OSO2CF3)]+ cations connected together by two bridging acetato ligands in a syn-syn configuration. Both CuII atoms exhibit five coordination of CuN2O2O' chromophore, with the basal plane consisting of two phen N atoms [Cu—N = 2.0153 (18) and 1.9980 (18) Å] and two O atoms from acetate ligands [Cu—O = 1.9387 (17) and 1.9377 (18)]. Due to symmetry both square planes are parallel to one another. The apical position at CuII is occupied by an O atom from trifluoromethanesulfonate anion [Cu—O = 2.261 (2)], leading to the (4 + 1) square-pyramidal geometry. The square base of CuII chromophore is not perfectly planar, with the tetrahedral twist of 16.52 (7)° and CuII is situated above the basal plane by 0.14 (1) Å pointing towards the O atom of the trifluoromethanesulfonate anion. The distortion of a square pyramid can be best described by the structural parameter τ (τ = 0 for a square pyramid and τ =1 for a trigonal bipyramid (Addison et al., 1984)), with τ = 0.23 for the title compound. The molecular structure of I reveals intramolecular face-to-face π-π interaction between aromatic rings of phen ligands (Fig. 1). Phenanthroline molecules are parallel with an average contact and angle of phen planes of 3.63 (3) Å and 5.96 (3)°, respectively. In general, the ligands are featureless: neither of phen group departs significantly from planarity [maximum deviations: 0.082 Å for C11 and 0.099 Å for C10 of Cg3 ring(N2, C6, C9, C10, C11, C12)] and the C—O bonds in the acetato bridging ligands display an almost perfect resonance [C13≐ O1 = 1.257 (3) Å and C13≐O2 = 1.250 (3) Å]. The crystal structure of compound I is determined by intermolecular hydrogen bonding interactions between methyl groups of acetato ligands (H14A) or phen ligands (H7 as hydrogen bond donor sites and H10) and oxygen/fluoride accepetors at trifluoromethanesulfonate anions (O3, O5 and F3) (see Table 1), generating two-dimensional layers parallel to the ab plane (Fig. 2). Moreover, these two-dimensional sheets are interconnected by hydrogen bond interactions between C—H of phen ligands and oxygen atoms of trifluoromethanesulfonate anions [C1—H1···O5i; symetry code (i) = -x+1, -y+2, -z+1] (see Table 2) in direction of crystallographic c axis, leading to three-dimensional lattice structure (Fig. 3). Although containing the same [(phen)Cu(µ-OOCCH3)2Cu(phen)]2+ unit, the structural topology of I is distinct from that of the related compound [Cu(phen)(µ-O2CCH3)(H2O)]2(NO3)2.4H2O (Tokii et al., 1990) in which the apical position is occupied by water molecule. The dinuclear unit of this related compound also crystallized in C2/c space group and has C2 symmetry around the b axis with Cu···Cu distance of 3.063 Å, but its crystal lattice is mainly stabilized by intra- and intermolecular π-π interactions, generating a one-dimensional chain-like sructure. It is clear that the difference of the structural topology between compound I and the related compound caused by the effect of coordinated trifluoromethanesulfonate anions whereas nitrate anions are not coordinated to Cu in the other structure.

The diffuse reflectance spectrum of I displays a broad band at 15400 cm-1 and a lower energy shoulder at 14300 cm-1. This feature corresponds to a dominantly distorted square pyramidal geometry of CuII ions and is consistent with the observed structural parameters. The transitions may be assigned as dxy, dyz, dxz→ dx2-y2 and dz2→ dx2-y2. The IR spectrum of I, in addition to the phen vibrations shows the broad and intense bands of the stretching of the ionic CF3SO3- at 1276 νas(S–O), 1158 νas(C–F) and 1031 νs(S–O) cm-1 (Castro et al., 1992). The IR spectrum also shows two broad and intense bands at 1567 and 1385 cm-1, corresponding to the νas(COO-) and νs(COO-) vibrations of acetate bridging ligands. The latter spectral properties completely disappear for related mononuclear compounds as [Cu(phen)3](CF3SO3)2.H2O (Sletten & Julve, 1999).

Related literature top

For general background to this work, see: Moreira et al. (2007); Calvo et al. (2011); Reinoso et al. (2005); Ritchie et al. (2006); Wang et al. (2006). For literature used in the synthetic procedures, see: Youngme et al. (2008). For a related crystal structure, see: Tokii et al. (1990). For potential applications, see: Hill & Brown (1986); Mansuy et al. (1991); Hill & Zhang (1995). For an explanation of the τ parameter, see: Addison et al. (1984). For additional related literature, see: Castro et al. (1992); Reinoso et al. (2007); Sletten & Julve (1999).

Experimental top

A warm ethanolic solution (25 ml) of phen (0.198 g, 1.0 mmol) was added to a warm aqueous solution (15 ml) of Cu(CF3SO3)2 (0.370 g, 1.0 mmol). Then NaO2CCH3 solid (0.124 g, 1.0 mmol) was added to the mixture, yielding a clear dark blue solution. After a week, the blue rectangle-shaped crystals of compound I were obtained. The crystals were filtered off, washed with mother liquor and air-dried. Yield: ca 45%. Anal. Calc. for Cu2C30H24N4O10F6S2: C, 39.78; H, 2.67; N, 6.19%. Found: C, 39.12; H, 2.51; N, 6.36%.

Refinement top

All H atoms were constrained to ideal positions, with C—H = 0.93 Å and Uiso(H) =1.2Ueq(C) for H atoms at phen and C—H = 0.96 Å and Uiso(H) =1.2Ueq(C) for H atoms of acetate groups. Fluorine atoms of the trifluoromethanesulfonato ligands are disordered with site occupation factors of 70:30%.

Computing details top

Data collection: SMART (Bruker, 2000); cell refinement: SMART (Bruker, 2000); data reduction: SAINT (Bruker, 2000) and SHELXTL (Sheldrick, 2008); program(s) used to solve structure: SHELXTL (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 2012) and Mercury (Macrae et al., 2006); software used to prepare material for publication: PLATON (Spek, 2009) and pubCIF (Westrip, 2010).

Figures top
[Figure 1] Fig. 1. Molecular structure and atomic numbering scheme with thermal ellipsoids shown at 50% probability level.
[Figure 2] Fig. 2. The crystal packing. View of two-dimensional layer constructed by intermolecular hydrogen bonding and view of the intramolecular face-to-face π-π interactions between aromatic rings of phen ligands.
[Figure 3] Fig. 3. The crystal packing. View of three-dimensional framework (side view) constructued by intermolecular hydrogen bonding interactions between two-dimensional layers (C1—H1···O5i, symmetry code: (i) = -x+1, -y+2, -z+1).
Di-µ-acetato-κ4O:O'-bis[(1,10-phenanthroline-κ2N,N')(trifluoromethanesulfonato-κO)copper(II)] top
Crystal data top
[Cu2(C2H3O2)2(CF3O3S)2(C12H8N2)2]F(000) = 1816
Mr = 903.72Dx = 1.741 Mg m−3
Monoclinic, C2/cMo Kα radiation, λ = 0.71073 Å
Hall symbol: -C 2ycCell parameters from 8485 reflections
a = 13.1198 (5) Åθ = 2.3–26.4°
b = 16.1282 (6) ŵ = 1.45 mm−1
c = 16.3659 (6) ÅT = 293 K
β = 95.507 (1)°Block, blue
V = 3447.0 (2) Å30.24 × 0.21 × 0.18 mm
Z = 4
Data collection top
Bruker SMART APEX CCD
diffractometer		4178 independent reflections
Radiation source: fine-focus sealed tube3491 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.022
phi and ω scansθmax = 28.1°, θmin = 2.0°
Absorption correction: multi-scan
(SADABS; Sheldrick, 2000)		h = −17→17
Tmin = 0.872, Tmax = 1.000k = −21→21
23313 measured reflectionsl = −21→21
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)] = 0.034Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.102H-atom parameters constrained
S = 1.04 w = 1/[σ2(Fo2) + (0.0624P)2 + 1.5014P]
where P = (Fo2 + 2Fc2)/3
4178 reflections(Δ/σ)max = 0.001
272 parametersΔρmax = 0.37 e Å−3
0 restraintsΔρmin = −0.32 e Å−3
Crystal data top
[Cu2(C2H3O2)2(CF3O3S)2(C12H8N2)2]V = 3447.0 (2) Å3
Mr = 903.72Z = 4
Monoclinic, C2/cMo Kα radiation
a = 13.1198 (5) ŵ = 1.45 mm−1
b = 16.1282 (6) ÅT = 293 K
c = 16.3659 (6) Å0.24 × 0.21 × 0.18 mm
β = 95.507 (1)°
Data collection top
Bruker SMART APEX CCD
diffractometer		4178 independent reflections
Absorption correction: multi-scan
(SADABS; Sheldrick, 2000)		3491 reflections with I > 2σ(I)
Tmin = 0.872, Tmax = 1.000Rint = 0.022
23313 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0340 restraints
wR(F2) = 0.102H-atom parameters constrained
S = 1.04Δρmax = 0.37 e Å−3
4178 reflectionsΔρmin = −0.32 e Å−3
272 parameters
Special details top

Geometry. Bond distances, angles etc. have been calculated using the rounded fractional coordinates. All e.s.d.'s are estimated from the variances of the (full) variance-covariance matrix. The cell e.s.d.'s are taken into account in the estimation of distances, angles and torsion angles

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/UeqOcc. (<1)
Cu10.59608 (2)0.99743 (1)0.70547 (2)0.0458 (1)
S10.78035 (4)1.01647 (3)0.56674 (3)0.0539 (2)
F10.8335 (6)0.8733 (4)0.6161 (4)0.176 (4)0.700
F20.9340 (5)0.9174 (4)0.5429 (4)0.137 (2)0.700
F30.9359 (6)0.9687 (6)0.6618 (6)0.199 (4)0.700
O10.63242 (11)1.07473 (9)0.79413 (10)0.0626 (5)
O20.51246 (12)1.08054 (9)0.64547 (10)0.0608 (5)
O30.73435 (13)1.03226 (11)0.64052 (11)0.0712 (6)
O40.8331 (2)1.08491 (14)0.53822 (17)0.1123 (10)
O50.7149 (2)0.97542 (18)0.50650 (17)0.1224 (11)
N10.53445 (12)0.90229 (9)0.63975 (10)0.0449 (5)
N20.68014 (12)0.90588 (10)0.76211 (9)0.0472 (5)
C10.46043 (16)0.90316 (14)0.57797 (12)0.0556 (7)
C20.41990 (18)0.83081 (17)0.54255 (14)0.0640 (8)
C30.45639 (18)0.75590 (15)0.56951 (15)0.0633 (8)
C40.53672 (15)0.75244 (12)0.63350 (13)0.0509 (6)
C50.57234 (13)0.82808 (11)0.66659 (11)0.0423 (5)
C60.65295 (13)0.82997 (11)0.73215 (11)0.0430 (5)
C70.58190 (18)0.67773 (13)0.66651 (17)0.0649 (8)
C80.65946 (18)0.67936 (13)0.72685 (16)0.0642 (8)
C90.69878 (15)0.75606 (13)0.76071 (13)0.0526 (6)
C100.78116 (18)0.76280 (16)0.82166 (15)0.0664 (8)
C110.81020 (18)0.83952 (18)0.85040 (15)0.0701 (8)
C120.75733 (17)0.91011 (15)0.82085 (13)0.0605 (7)
C130.57629 (16)1.10508 (11)0.84421 (13)0.0514 (6)
C140.6188 (2)1.17618 (14)0.89565 (17)0.0706 (8)
C150.8783 (3)0.9414 (2)0.5977 (2)0.0953 (14)
F3A0.9596 (9)0.9817 (7)0.6337 (13)0.153 (7)0.300
F1A0.8515 (8)0.8809 (8)0.6463 (7)0.083 (3)0.300
F2A0.9048 (15)0.9173 (13)0.5189 (12)0.193 (8)0.300
H10.435200.953900.558000.0670*
H20.367500.833600.500100.0770*
H30.428800.707300.546100.0760*
H70.557400.627000.646000.0780*
H120.776600.961600.842900.0730*
H14A0.689701.183800.887600.1060*
H14B0.612401.164600.952500.1060*
H14C0.581401.225700.879900.1060*
H80.688000.629700.746800.0770*
H100.815500.715700.842200.0800*
H110.865600.844800.890000.0840*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Cu10.0501 (2)0.0364 (1)0.0522 (2)0.0032 (1)0.0111 (1)−0.0044 (1)
S10.0583 (3)0.0503 (3)0.0537 (3)0.0031 (2)0.0083 (2)0.0036 (2)
F10.280 (8)0.069 (3)0.194 (7)0.081 (4)0.099 (6)0.051 (4)
F20.115 (3)0.157 (5)0.152 (4)0.072 (3)0.077 (4)0.039 (4)
F30.128 (6)0.280 (9)0.172 (5)0.051 (5)−0.073 (5)0.031 (5)
O10.0620 (9)0.0553 (8)0.0732 (10)−0.0075 (7)0.0200 (7)−0.0240 (7)
O20.0659 (9)0.0482 (7)0.0716 (9)0.0163 (7)0.0235 (7)0.0118 (7)
O30.0704 (10)0.0658 (10)0.0820 (11)0.0007 (8)0.0305 (9)−0.0070 (9)
O40.135 (2)0.0787 (14)0.1311 (19)−0.0137 (13)0.0530 (16)0.0345 (13)
O50.127 (2)0.131 (2)0.0992 (18)0.0116 (17)−0.0404 (16)−0.0369 (16)
N10.0464 (8)0.0425 (8)0.0464 (8)0.0047 (6)0.0076 (6)−0.0021 (6)
N20.0475 (8)0.0505 (9)0.0444 (8)0.0024 (7)0.0084 (6)−0.0017 (6)
C10.0570 (11)0.0594 (12)0.0500 (11)0.0093 (9)0.0027 (9)−0.0019 (9)
C20.0589 (12)0.0782 (16)0.0539 (12)−0.0017 (10)−0.0005 (9)−0.0116 (10)
C30.0647 (13)0.0629 (13)0.0634 (13)−0.0117 (10)0.0125 (10)−0.0195 (10)
C40.0527 (10)0.0442 (9)0.0586 (11)−0.0023 (8)0.0194 (9)−0.0061 (8)
C50.0433 (8)0.0400 (8)0.0458 (9)0.0023 (7)0.0154 (7)−0.0022 (7)
C60.0423 (8)0.0433 (9)0.0456 (9)0.0042 (7)0.0154 (7)0.0017 (7)
C70.0725 (14)0.0384 (10)0.0869 (16)−0.0017 (9)0.0240 (13)−0.0038 (10)
C80.0719 (14)0.0399 (10)0.0845 (16)0.0131 (9)0.0271 (12)0.0100 (10)
C90.0505 (10)0.0547 (11)0.0554 (11)0.0112 (8)0.0189 (9)0.0101 (9)
C100.0628 (13)0.0766 (15)0.0608 (13)0.0211 (11)0.0104 (10)0.0149 (11)
C110.0553 (12)0.1009 (19)0.0528 (12)0.0110 (12)−0.0016 (10)0.0062 (12)
C120.0567 (11)0.0728 (14)0.0515 (11)−0.0018 (10)0.0028 (9)−0.0072 (10)
C130.0623 (11)0.0364 (8)0.0575 (11)−0.0067 (8)0.0154 (9)−0.0053 (8)
C140.0791 (15)0.0531 (12)0.0838 (16)−0.0205 (11)0.0291 (13)−0.0256 (11)
C150.083 (2)0.098 (2)0.109 (3)0.0357 (18)0.0305 (19)0.0181 (19)
F3A0.046 (3)0.082 (5)0.32 (2)0.000 (3)−0.039 (7)0.004 (8)
F1A0.093 (4)0.075 (5)0.087 (5)0.038 (3)0.042 (3)0.038 (4)
F2A0.165 (14)0.234 (16)0.185 (14)0.086 (10)0.037 (10)−0.120 (12)
Geometric parameters (Å, º) top
Cu1—O11.9376 (16)C3—C41.414 (3)
Cu1—O21.9385 (16)C4—C51.397 (3)
Cu1—O32.2597 (18)C4—C71.426 (3)
Cu1—N11.9995 (15)C5—C61.433 (2)
Cu1—N22.0148 (16)C6—C91.395 (3)
S1—O31.4237 (18)C7—C81.349 (4)
S1—O41.406 (2)C8—C91.431 (3)
S1—O51.409 (3)C9—C101.403 (3)
S1—C151.803 (4)C10—C111.365 (4)
F1—C151.295 (8)C11—C121.395 (4)
F1A—C151.327 (13)C13—C141.498 (3)
F2—C151.270 (7)C1—H10.9302
F2A—C151.42 (2)C2—H20.9304
F3—C151.309 (10)C3—H30.9304
F3A—C151.337 (15)C7—H70.9299
O1—C131.253 (3)C8—H80.9300
O2—C13i1.256 (3)C10—H100.9295
N1—C11.333 (3)C11—H110.9301
N1—C51.353 (2)C12—H120.9307
N2—C121.329 (3)C14—H14A0.9598
N2—C61.354 (2)C14—H14B0.9605
C1—C21.386 (3)C14—H14C0.9596
C2—C31.358 (4)
Cu1···O53.760 (3)O4···H3iv2.3363
Cu1···O1i3.2474 (15)O4···H11v2.7477
Cu1···O2i3.2315 (16)O5···H14Bv2.7315
Cu1···N1i3.5407 (16)O5···H1vi2.4275
Cu1···N2i3.9955 (16)N1···Cu1i3.5407 (16)
Cu1···C1i3.991 (2)N2···F1A3.103 (11)
Cu1···C5i4.1970 (18)N2···Cu1i3.9955 (16)
Cu1···H8ii3.5723N2···C1i3.344 (3)
F1···O32.920 (7)C1···C12i3.439 (3)
F1···O52.796 (7)C1···O5vi3.229 (3)
F1···C63.251 (8)C1···N2i3.344 (3)
F1···C14iii3.249 (7)C1···C13i3.546 (3)
F1A···N23.103 (11)C1···Cu1i3.991 (2)
F1A···C63.184 (11)C3···O4vii3.213 (3)
F1A···C123.254 (11)C3···C9i3.599 (3)
F1A···O53.160 (12)C5···C6i3.525 (2)
F1A···O32.881 (12)C5···Cu1i4.1970 (18)
F2···O53.027 (7)C5···C5i3.472 (2)
F2···O43.006 (7)C6···C5i3.525 (2)
F2A···O42.89 (2)C6···F1A3.184 (11)
F2A···O52.65 (2)C6···F13.251 (8)
F3···O42.983 (10)C8···O1iii3.256 (3)
F3···O32.826 (8)C9···C3i3.599 (3)
F3A···O42.733 (16)C11···O4viii3.293 (4)
F3A···O33.078 (12)C12···C1i3.439 (3)
F1···H14Ciii2.6275C12···F1A3.254 (11)
F1A···H14Ciii2.7013C13···C13i3.512 (3)
F3A···H7iv2.6700C13···C1i3.546 (3)
O1···C8ii3.256 (3)C13···O5viii3.335 (3)
O1···Cu1i3.2474 (15)C14···O5viii3.228 (4)
O2···Cu1i3.2315 (16)C14···F1ii3.249 (7)
O3···F32.826 (8)C2···H14Bv3.0447
O3···F12.920 (7)C8···H14Aiii2.8533
O3···F3A3.078 (12)C13···H1i2.9284
O3···F1A2.881 (12)H1···C13i2.9284
O4···F32.983 (10)H1···O5vi2.4275
O4···C3iv3.213 (3)H1···O22.6401
O4···F23.006 (7)H3···H72.5822
O4···C11v3.293 (4)H3···O4vii2.3363
O4···F2A2.89 (2)H7···F3Avii2.6700
O4···F3A2.733 (16)H7···H32.5822
O5···Cu13.760 (3)H8···H102.5804
O5···F2A2.65 (2)H8···Cu1iii3.5723
O5···C13v3.335 (3)H8···O1iii2.6624
O5···C14v3.228 (4)H8···O3iii2.5589
O5···F23.027 (7)H10···H82.5804
O5···F1A3.160 (12)H11···O4viii2.7477
O5···F12.796 (7)H12···O12.6934
O5···C1vi3.229 (3)H14A···C8ii2.8533
O1···H122.6934H14B···C2viii3.0447
O1···H8ii2.6624H14B···O5viii2.7315
O2···H12.6401H14C···F1ii2.6275
O3···H8ii2.5589H14C···F1Aii2.7013
O1—Cu1—O291.21 (6)C8—C9—C10124.5 (2)
O1—Cu1—O392.37 (6)C9—C10—C11119.1 (2)
O1—Cu1—N1162.62 (7)C10—C11—C12120.5 (2)
O1—Cu1—N292.44 (6)N2—C12—C11121.8 (2)
O2—Cu1—O391.76 (7)O1—C13—C14117.14 (19)
O2—Cu1—N194.48 (6)O1—C13—O2i125.13 (18)
O2—Cu1—N2176.35 (6)O2i—C13—C14117.73 (19)
O3—Cu1—N1103.84 (7)S1—C15—F1107.9 (4)
O3—Cu1—N288.28 (6)S1—C15—F2116.7 (4)
N1—Cu1—N281.97 (6)S1—C15—F3109.9 (5)
O3—S1—O4113.79 (13)S1—C15—F1A116.1 (5)
O3—S1—O5113.45 (13)S1—C15—F2A99.1 (8)
O3—S1—C15103.33 (13)S1—C15—F3A108.3 (5)
O4—S1—O5115.02 (16)F1—C15—F2102.1 (5)
O4—S1—C15105.09 (16)F1—C15—F3109.8 (6)
O5—S1—C15104.55 (16)F2—C15—F3110.0 (6)
Cu1—O1—C13128.57 (14)F1A—C15—F2A116.4 (10)
Cu1—O2—C13i129.53 (14)F1A—C15—F3A109.8 (9)
Cu1—O3—S1141.19 (11)F2A—C15—F3A106.2 (12)
Cu1—N1—C1128.86 (14)N1—C1—H1118.98
Cu1—N1—C5112.78 (12)C2—C1—H1118.97
C1—N1—C5118.28 (16)C1—C2—H2119.86
Cu1—N2—C6112.49 (12)C3—C2—H2119.87
Cu1—N2—C12129.82 (15)C2—C3—H3120.32
C6—N2—C12117.66 (17)C4—C3—H3120.31
N1—C1—C2122.0 (2)C4—C7—H7119.34
C1—C2—C3120.3 (2)C8—C7—H7119.47
C2—C3—C4119.4 (2)C7—C8—H8119.37
C3—C4—C5116.78 (18)C9—C8—H8119.37
C3—C4—C7124.6 (2)C9—C10—H10120.49
C5—C4—C7118.66 (19)C11—C10—H10120.44
N1—C5—C4123.22 (17)C10—C11—H11119.78
N1—C5—C6116.49 (16)C12—C11—H11119.74
C4—C5—C6120.29 (17)N2—C12—H12119.07
N2—C6—C5116.13 (16)C11—C12—H12119.09
N2—C6—C9124.13 (17)C13—C14—H14A109.53
C5—C6—C9119.74 (17)C13—C14—H14B109.45
C4—C7—C8121.2 (2)C13—C14—H14C109.45
C7—C8—C9121.3 (2)H14A—C14—H14B109.50
C6—C9—C8118.75 (19)H14A—C14—H14C109.50
C6—C9—C10116.73 (19)H14B—C14—H14C109.39
O2—Cu1—O1—C1368.10 (18)Cu1—N1—C1—C2−174.67 (16)
O3—Cu1—O1—C13159.91 (17)C5—N1—C1—C21.8 (3)
N2—Cu1—O1—C13−111.71 (17)Cu1—N1—C5—C4176.12 (15)
O1—Cu1—O2—C13i−78.62 (18)Cu1—N1—C5—C6−4.0 (2)
O3—Cu1—O2—C13i−171.03 (18)C1—N1—C5—C4−0.9 (3)
N1—Cu1—O2—C13i84.94 (18)C1—N1—C5—C6178.99 (17)
O1—Cu1—O3—S1−175.37 (18)Cu1—N2—C6—C50.7 (2)
O2—Cu1—O3—S1−84.09 (18)Cu1—N2—C6—C9−179.80 (15)
N1—Cu1—O3—S110.96 (19)C12—N2—C6—C5−177.49 (17)
N2—Cu1—O3—S192.26 (18)C12—N2—C6—C92.0 (3)
O2—Cu1—N1—C1−0.85 (18)Cu1—N2—C12—C11−176.94 (16)
O2—Cu1—N1—C5−177.49 (13)C6—N2—C12—C110.9 (3)
O3—Cu1—N1—C1−93.78 (17)N1—C1—C2—C3−1.1 (3)
O3—Cu1—N1—C589.58 (13)C1—C2—C3—C4−0.6 (3)
N2—Cu1—N1—C1−180.00 (18)C2—C3—C4—C51.4 (3)
N2—Cu1—N1—C53.37 (13)C2—C3—C4—C7−179.5 (2)
O1—Cu1—N2—C6161.25 (13)C3—C4—C7—C8179.0 (2)
O1—Cu1—N2—C12−20.80 (18)C5—C4—C7—C8−1.9 (3)
O3—Cu1—N2—C6−106.45 (13)C7—C4—C5—C60.2 (3)
O3—Cu1—N2—C1271.50 (18)C3—C4—C5—N1−0.7 (3)
N1—Cu1—N2—C6−2.21 (12)C3—C4—C5—C6179.43 (18)
N1—Cu1—N2—C12175.74 (18)C7—C4—C5—N1−179.86 (19)
O4—S1—O3—Cu1146.81 (18)C4—C5—C6—C92.6 (3)
O5—S1—O3—Cu112.8 (2)N1—C5—C6—N22.2 (2)
C15—S1—O3—Cu1−99.8 (2)N1—C5—C6—C9−177.30 (17)
O3—S1—C15—F167.4 (4)C4—C5—C6—N2−177.90 (17)
O3—S1—C15—F2−178.4 (4)N2—C6—C9—C10−3.1 (3)
O3—S1—C15—F3−52.3 (5)C5—C6—C9—C8−3.8 (3)
O4—S1—C15—F1−173.0 (4)C5—C6—C9—C10176.37 (18)
O4—S1—C15—F2−58.8 (4)N2—C6—C9—C8176.76 (19)
O4—S1—C15—F367.2 (5)C4—C7—C8—C90.6 (4)
O5—S1—C15—F1−51.5 (4)C7—C8—C9—C62.2 (3)
O5—S1—C15—F262.7 (4)C7—C8—C9—C10−178.0 (2)
O5—S1—C15—F3−171.3 (5)C8—C9—C10—C11−178.5 (2)
Cu1—O1—C13—C14−167.96 (15)C6—C9—C10—C111.3 (3)
Cu1—O1—C13—O2i12.1 (3)C9—C10—C11—C121.4 (4)
Cu1—O2—C13i—O1i−5.3 (3)C10—C11—C12—N2−2.6 (4)
Cu1—O2—C13i—C14i174.68 (15)
Symmetry codes: (i) −x+1, y, −z+3/2; (ii) −x+3/2, y+1/2, −z+3/2; (iii) −x+3/2, y−1/2, −z+3/2; (iv) x+1/2, y+1/2, z; (v) x, −y+2, z−1/2; (vi) −x+1, −y+2, −z+1; (vii) x−1/2, y−1/2, z; (viii) x, −y+2, z+1/2.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
C1—H1···O5vi0.932.433.229 (3)144
C3—H3···O4vii0.932.343.213 (3)157
C8—H8···O3iii0.932.563.421 (3)154
Symmetry codes: (iii) −x+3/2, y−1/2, −z+3/2; (vi) −x+1, −y+2, −z+1; (vii) x−1/2, y−1/2, z.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
C1—H1···O5i0.93002.43003.229 (3)144.00
C3—H3···O4ii0.93002.34003.213 (3)157.00
C8—H8···O3iii0.93002.56003.421 (3)154.00
Symmetry codes: (i) −x+1, −y+2, −z+1; (ii) x−1/2, y−1/2, z; (iii) −x+3/2, y−1/2, −z+3/2.
 

Acknowledgements

The authors gratefully acknowledge financial support from the Thailand Research Fund, the Higher Education Research Promotion and National Research University Project of Thailand, Office of the Higher Education Commission, through the Advanced Functional Materials Cluster of Khon Kaen University and the Center of Excellence for Innovation in Chemistry (PERCH–CIC), Commission on Higher Education, Ministry of Education, Thailand.

References

First citationAddison, A. W., Rao, T. N., Reedijk, J., van Rijn, J. & Verschoor, G. C. (1984). J. Chem. Soc. Dalton Trans. pp. 1349–1356.  CSD CrossRef Web of Science Google Scholar
 First citationBruker (2000). SMART and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA.  Google Scholar
 First citationCalvo, R., Abud, J. E., Sartoris, R. P. & Santana, R. C. (2011). Phys. Rev. B, 84, 104433, 1–13.  Google Scholar
 First citationCastro, I., Faus, J., Julve, M., Bois, C., Real, J. A. & Lloret, F. (1992). J. Chem. Soc. Dalton Trans. pp. 47–52.  CSD CrossRef Web of Science Google Scholar
 First citationFarrugia, L. J. (2012). J. Appl. Cryst. 45, 849–854.  Web of Science CrossRef CAS IUCr Journals Google Scholar
 First citationHill, C. L. & Brown, R. B. (1986). J. Am. Chem. Soc. 108, 536–538.  CrossRef CAS PubMed Web of Science Google Scholar
 First citationHill, C. L. & Zhang, X. (1995). Nature (London), 373, 324–326.  CrossRef CAS Web of Science Google Scholar
 First citationMacrae, C. F., Edgington, P. R., McCabe, P., Pidcock, E., Shields, G. P., Taylor, R., Towler, M. & van de Streek, J. (2006). J. Appl. Cryst. 39, 453–457.  Web of Science CrossRef CAS IUCr Journals Google Scholar
 First citationMansuy, D., Bartoli, J. F., Battioni, P., Lyon, D. K. & Finke, R. G. (1991). J. Am. Chem. Soc. 113, 7222–7226.  CrossRef CAS Web of Science Google Scholar
 First citationMoreira, I. P. R., Costa, R., Filatov, M. & Illas, F. (2007). J. Chem. Theory Comput. 3, 764–774.  Web of Science CrossRef Google Scholar
 First citationReinoso, S., Vitoria, P., Felices, L. S., Lezama, L. & Gutiérrez-Zorrilla, J. M. (2005). Chem. Eur. J. 11, 1538–1548.  Web of Science CSD CrossRef PubMed CAS Google Scholar
 First citationReinoso, S., Vitoria, P., Gutiérrez-Zorrilla, J. M., Lezama, L., Madariaga, J. M., Felices, L. S. & Iturrospe, A. (2007). Inorg. Chem. 46, 4010–4021.  Web of Science CSD CrossRef PubMed CAS Google Scholar
 First citationRitchie, C., Burkholder, E., Kögerler, P. & Cronin, L. (2006). Dalton Trans. pp. 1712–1714.  Web of Science CSD CrossRef PubMed Google Scholar
 First citationSheldrick, G. M. (2000). 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 citationSletten, J. & Julve, M. (1999). Acta Chem. Scand. 53, 631–633.  Web of Science CrossRef CAS Google Scholar
 First citationSpek, A. L. (2009). Acta Cryst. D65, 148–155.  Web of Science CrossRef CAS IUCr Journals Google Scholar
 First citationTokii, T., Watanabe, N., Nakashima, M., Muto, Y., Morooka, M., Ohba, S. & Saito, I. (1990). Bull. Chem. Soc. Jpn, 63, 364–369.  CrossRef CAS Web of Science Google Scholar
 First citationWang, J.-P., Ren, Q., Zhao, J.-W. & Niu, J.-Y. (2006). Inorg. Chem. Commun. 9, 1281–1285.  Web of Science CSD CrossRef CAS Google Scholar
 First citationWestrip, S. P. (2010). J. Appl. Cryst. 43, 920–925.  Web of Science CrossRef CAS IUCr Journals Google Scholar
 First citationYoungme, S., Cheansirisomboon, A., Danvirutai, C., Pakawatchai, C., Chaichit, N., Engkagul, C., van Albada, G. A., Costa, J. S. & Reedijk, J. (2008). Polyhedron, 27, 1875–1882.  Web of Science CSD CrossRef CAS 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
Volume 69| Part 11| November 2013| Pages m591-m592
doi:10.1107/S1600536813027323
Follow Acta Cryst. E
Sign up for e-alerts
E-alerts
Follow Acta Cryst. on Twitter
Twitter
Follow us on facebook
Facebook
Sign up for RSS feeds
RSS