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

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ISSN: 2056-9890

catena-Poly[[di­aqua­strontium(II)]-bis­­[μ-2-(3-benzoyl­phen­yl)propano­ato]]

aSchool of Pharmaceutical Science, Harbin Medical University, Harbin 150081, People's Republic of China
*Correspondence e-mail: zhangzhuyan1971@163.com

(Received 18 August 2010; accepted 25 August 2010; online 4 September 2010)

In the title coordination polymer, [Sr(C16H13O3)2(H2O)2]n, the SrII cation is eight-coordinated by six O atoms from four different 2-(3-benzoyl­phen­yl)propano­ate ligands and two O atoms of two water mol­ecules in a distorted dodeca­hedral geometry. Adjacent SrII cations are bridged by two 2-(3-benzoyl­phen­yl)propano­ate ligands, forming an infinite chain along the b axis; the chains are further linked by inter­molecular O—H—O hydrogen bonds into a three-dimensional supra­molecular network.

Related literature

For the crystal structures of metal complexes of the 2-(3-benzoyl­phen­yl)propano­ate anion, see: Tahir et al. (1997[Tahir, M. N., Ülkü, D., Ali, S., Masood, T., Danish, M. & Mazhar, M. (1997). Acta Cryst. C53, 1574-1576.]); Zhang et al. (2007a[Zhang, Z.-Y., Chen, P.-G., Deng, Z.-P., Yu, N. & Liu, B.-Y. (2007a). Acta Cryst. E63, m1900-m1901.],b[Zhang, Z.-Y., Yu, N., Guo, X.-X., Pu, J. & Sun, J.-P. (2007b). Acta Cryst. E63, m2883.]).

[Scheme 1]

Experimental

Crystal data
  • [Sr(C16H13O3)2(H2O)2]

  • Mr = 630.18

  • Monoclinic, P 21 /n

  • a = 18.665 (4) Å

  • b = 8.0406 (16) Å

  • c = 19.377 (4) Å

  • β = 93.26 (3)°

  • V = 2903.4 (10) Å3

  • Z = 4

  • Mo Kα radiation

  • μ = 1.91 mm−1

  • T = 295 K

  • 0.30 × 0.25 × 0.18 mm

Data collection
  • Rigaku R-AXIS RAPID diffractometer

  • Absorption correction: multi-scan (ABSCOR; Higashi, 1995[Higashi, T. (1995). ABSCOR. Rigaku Corporation, Tokyo, Japan.]) Tmin = 0.598, Tmax = 0.725

  • 22141 measured reflections

  • 5107 independent reflections

  • 2941 reflections with I > 2σ(I)

  • Rint = 0.087

Refinement
  • R[F2 > 2σ(F2)] = 0.050

  • wR(F2) = 0.136

  • S = 1.08

  • 5107 reflections

  • 385 parameters

  • 7 restraints

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

  • Δρmax = 0.69 e Å−3

  • Δρmin = −0.96 e Å−3

Table 1
Selected bond lengths (Å)

Sr1—O5i 2.496 (3)
Sr1—O1ii 2.514 (3)
Sr1—O1W 2.529 (4)
Sr1—O2 2.557 (4)
Sr1—O2W 2.559 (4)
Sr1—O4 2.590 (4)
Sr1—O5 2.772 (3)
Sr1—O1 2.816 (3)
Symmetry codes: (i) -x+1, -y+1, -z+1; (ii) -x+1, -y+2, -z+1.

Table 2
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A DA D—H⋯A
O1W—H1W2⋯O2i 0.85 (1) 1.83 (1) 2.678 (5) 171 (6)
O2W—H2W2⋯O4ii 0.85 (1) 1.89 (2) 2.724 (5) 166 (6)
Symmetry codes: (i) -x+1, -y+1, -z+1; (ii) -x+1, -y+2, -z+1.

Data collection: RAPID-AUTO (Rigaku, 1998[Rigaku (1998). RAPID-AUTO. Rigaku Corporation, Tokyo, Japan.]); cell refinement: RAPID-AUTO; data reduction: CrystalStructure (Rigaku/MSC, 2002[Rigaku/MSC (2002). CrystalStructure. Rigaku/MSC, The Woodlands, Texas, USA.]); 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: ORTEPII (Johnson, 1976[Johnson, C. K. (1976). ORTEPII. Report ORNL-5138. Oak Ridge National Laboratory, Tennessee, USA.]); software used to prepare material for publication: SHELXL97.

Supporting information


Comment top

2-(3-Benzoylphenyl)propanoic acid is known as nonsteroidal anti-inflamatory drug. To date, some reports on the structure of its metal complexes (Tahir et al., 1997; Zhang et al., 2007a,b) have been documented. In this paper, we present a novel 1-D SrII coordination polymer, [Sr(C16H13O3)2(H2O)2]n, (I). Its crystal structure is described here. As illustrated in Fig. 1, the complex (I) consists of one SrII cation, two 2-(3-benzoylphenyl)propanoate ligands and two coordinated water molecules. The local coordination environment around the SrII cation can be described as a distort dodecahedron, involving six oxygen atoms of four different 2-(3-benzoylphenyl)propanoate ligands and two coordinated water molecules. The 2-(3-benzoylphenyl)propanoate acts as bidentate bridging ligand to link adjacent SrII cations, leading to a 1-D chain along b axis direction (Fig. 2.), with the Sr···Sr separation of 4.1548 (8) Å. A 3-D supramolecular network structure is formed through the extended hydrogen-bonding interactions between water molecules and carboxylate O atoms (Table 2).

Related literature top

For the crystal structures of metal complexes of the 2-(3-benzoylphenyl)propanoate anion, see: Tahir et al. (1997); Zhang et al. (2007a,b).

Experimental top

The title complex was prepared by the addition of strontium nitrate (2.12 g, 10 mmol) to a hot aqueous solution of 2-(3-benzoylphenyl)propanoic acid (3.65 g, 10 mmol); the pH was adjusted to 6 with 0.1M sodium hydroxide. The solution was allowed to evaporate at room temperature. Colorless prismatic crystals separated from the filtered solution after several days. CH&N analysis. Calc. for C32H30SrO8: C 60.93, H 4.76%. Found: C 60.96, H 4.83%.

Refinement top

The H atoms were placed in calculated positions [C—H = 0.93 and 0.98 Å and Uiso(H) = 1.2Ueq (C) for aromatic H atoms and methyne H atoms, C—H = 0.96 Å and Uiso(H) = 1.5Ueq (C) for methyl H atoms] and were included in the refinement in the riding-model approximation. The H atoms of water molecules were located in difference Fourier maps and refined with the O—H distance restrained to 0.85 (1) Å and Uiso(H) = 1.5Ueq(O).

Computing details top

Data collection: RAPID-AUTO (Rigaku, 1998); cell refinement: RAPID-AUTO (Rigaku, 1998); data reduction: CrystalStructure (Rigaku/MSC, 2002); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEPII (Johnson, 1976); software used to prepare material for publication: SHELXL97 (Sheldrick, 2008).

Figures top
[Figure 1] Fig. 1. Molecular structure of the title polymer with 30% probability ellipsoid for the non-H atoms.
[Figure 2] Fig. 2. 1-D chain structure of the title polymer (the C atoms are omitted for clarity).
catena-Poly[[diaquastrontium(II)]-bis[µ-2-(3-benzoylphenyl)propanoato]] top
Crystal data top
[Sr(C16H13O3)2(H2O)2]F(000) = 1296
Mr = 630.18Dx = 1.442 Mg m3
Monoclinic, P21/nMo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ynCell parameters from 11966 reflections
a = 18.665 (4) Åθ = 3.1–25.0°
b = 8.0406 (16) ŵ = 1.91 mm1
c = 19.377 (4) ÅT = 295 K
β = 93.26 (3)°Prism, colorless
V = 2903.4 (10) Å30.30 × 0.25 × 0.18 mm
Z = 4
Data collection top
Rigaku R-AXIS RAPID
diffractometer
5107 independent reflections
Radiation source: fine-focus sealed tube2941 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.087
Detector resolution: 10.000 pixels mm-1θmax = 25.0°, θmin = 3.1°
ω scansh = 2222
Absorption correction: multi-scan
(ABSCOR; Higashi, 1995)
k = 99
Tmin = 0.598, Tmax = 0.725l = 2319
22141 measured reflections
Refinement top
Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.050H atoms treated by a mixture of independent and constrained refinement
wR(F2) = 0.136 w = 1/[σ2(Fo2) + (0.0533P)2 + 1.5847P]
where P = (Fo2 + 2Fc2)/3
S = 1.08(Δ/σ)max < 0.001
5107 reflectionsΔρmax = 0.69 e Å3
385 parametersΔρmin = 0.96 e Å3
7 restraintsExtinction correction: SHELXL97 (Sheldrick, 2008), Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4
Primary atom site location: structure-invariant direct methodsExtinction coefficient: 0.0013 (4)
Crystal data top
[Sr(C16H13O3)2(H2O)2]V = 2903.4 (10) Å3
Mr = 630.18Z = 4
Monoclinic, P21/nMo Kα radiation
a = 18.665 (4) ŵ = 1.91 mm1
b = 8.0406 (16) ÅT = 295 K
c = 19.377 (4) Å0.30 × 0.25 × 0.18 mm
β = 93.26 (3)°
Data collection top
Rigaku R-AXIS RAPID
diffractometer
5107 independent reflections
Absorption correction: multi-scan
(ABSCOR; Higashi, 1995)
2941 reflections with I > 2σ(I)
Tmin = 0.598, Tmax = 0.725Rint = 0.087
22141 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0507 restraints
wR(F2) = 0.136H atoms treated by a mixture of independent and constrained refinement
S = 1.08Δρmax = 0.69 e Å3
5107 reflectionsΔρmin = 0.96 e Å3
385 parameters
Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
Sr10.48764 (2)0.75146 (5)0.52610 (2)0.04083 (19)
O1W0.3724 (2)0.6001 (5)0.5485 (3)0.0869 (15)
H1W10.345 (3)0.620 (7)0.581 (3)0.130*
H1W20.373 (4)0.496 (2)0.541 (3)0.130*
O10.58168 (18)0.9811 (4)0.46912 (17)0.0504 (9)
O2W0.5312 (2)0.8995 (4)0.6376 (2)0.0639 (11)
H2W10.563 (2)0.862 (6)0.667 (2)0.096*
H2W20.538 (3)1.0040 (18)0.634 (3)0.096*
O20.61427 (19)0.7219 (4)0.4837 (2)0.0614 (10)
O30.5860 (3)0.6644 (6)0.1710 (3)0.121 (2)
O40.4452 (2)0.7775 (4)0.39694 (18)0.0623 (11)
O50.47219 (19)0.5182 (4)0.42097 (18)0.0556 (10)
O60.2021 (3)0.3645 (6)0.4167 (3)0.1007 (16)
C10.6216 (3)0.8618 (6)0.4568 (3)0.0490 (13)
C20.6843 (4)0.8805 (7)0.4118 (4)0.099 (3)
H20.72510.87150.44570.119*
C30.6965 (5)1.0412 (7)0.3813 (4)0.123 (3)
H3A0.74221.04130.36100.184*
H3B0.69601.12540.41640.184*
H3C0.65931.06360.34630.184*
C40.6951 (4)0.7317 (8)0.3669 (4)0.076 (2)
C50.7489 (4)0.6203 (8)0.3800 (4)0.078 (2)
H50.78100.63730.41780.094*
C60.7570 (4)0.4815 (7)0.3384 (4)0.0743 (19)
H60.79450.40800.34900.089*
C70.7110 (4)0.4507 (7)0.2822 (3)0.0685 (17)
H70.71640.35620.25530.082*
C80.6564 (4)0.5628 (7)0.2661 (4)0.0669 (17)
C90.6493 (4)0.7039 (7)0.3090 (4)0.076 (2)
H90.61290.78010.29810.092*
C100.6085 (4)0.5418 (8)0.2023 (4)0.077 (2)
C110.5888 (3)0.3725 (8)0.1769 (4)0.0702 (17)
C120.5806 (4)0.3459 (10)0.1070 (5)0.095 (2)
H120.58830.43290.07670.114*
C130.5614 (5)0.1937 (13)0.0815 (5)0.114 (3)
H130.55820.17600.03400.137*
C140.5467 (4)0.0669 (11)0.1253 (6)0.110 (3)
H140.53200.03570.10750.133*
C150.5536 (4)0.0905 (10)0.1952 (5)0.098 (2)
H150.54360.00430.22510.117*
C160.5757 (4)0.2436 (8)0.2210 (4)0.0779 (18)
H160.58180.25940.26860.093*
C170.4514 (3)0.6286 (6)0.3793 (3)0.0474 (13)
C180.4340 (3)0.5796 (6)0.3037 (3)0.0538 (14)
H180.47910.54120.28550.065*
C190.4084 (4)0.7250 (7)0.2587 (3)0.084 (2)
H19A0.40050.68840.21180.126*
H19B0.44400.81120.26110.126*
H19C0.36430.76740.27500.126*
C200.3822 (3)0.4346 (6)0.2974 (3)0.0484 (13)
C210.3833 (3)0.3290 (7)0.2406 (3)0.0553 (14)
H210.41580.34940.20700.066*
C220.3376 (3)0.1952 (7)0.2326 (3)0.0620 (16)
H220.33910.12720.19390.074*
C230.2894 (3)0.1624 (7)0.2824 (3)0.0607 (15)
H230.26020.06890.27840.073*
C240.2845 (3)0.2682 (6)0.3384 (3)0.0547 (14)
C250.3314 (3)0.4039 (6)0.3452 (3)0.0535 (14)
H250.32840.47510.38270.064*
C260.2298 (3)0.2443 (7)0.3910 (3)0.0646 (15)
C270.2095 (3)0.0740 (7)0.4110 (3)0.0587 (15)
C280.2581 (4)0.0550 (7)0.4146 (3)0.0701 (17)
H280.30450.03820.40100.084*
C290.2382 (5)0.2089 (8)0.4383 (4)0.089 (2)
H290.27180.29430.44170.107*
C300.1708 (6)0.2376 (10)0.4565 (4)0.104 (3)
H300.15800.34280.47150.125*
C310.1211 (4)0.1121 (11)0.4530 (4)0.096 (2)
H310.07460.13250.46570.115*
C320.1397 (3)0.0456 (8)0.4305 (3)0.0731 (18)
H320.10610.13110.42860.088*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Sr10.0499 (3)0.0273 (3)0.0458 (3)0.0009 (2)0.0062 (2)0.0017 (2)
O1W0.069 (3)0.039 (2)0.158 (5)0.001 (2)0.052 (3)0.004 (3)
O10.054 (2)0.0337 (19)0.064 (2)0.0082 (17)0.0082 (18)0.0007 (17)
O2W0.095 (3)0.042 (2)0.053 (3)0.003 (2)0.017 (2)0.0068 (18)
O20.064 (2)0.035 (2)0.089 (3)0.0039 (17)0.029 (2)0.0076 (18)
O30.170 (6)0.065 (3)0.127 (5)0.017 (3)0.008 (4)0.032 (3)
O40.097 (3)0.035 (2)0.053 (2)0.0004 (19)0.015 (2)0.0016 (16)
O50.076 (3)0.0331 (19)0.057 (2)0.0020 (18)0.0084 (19)0.0084 (17)
O60.103 (4)0.059 (3)0.145 (5)0.002 (3)0.047 (3)0.016 (3)
C10.055 (3)0.035 (3)0.058 (4)0.004 (3)0.009 (3)0.006 (3)
C20.132 (6)0.045 (4)0.130 (6)0.018 (4)0.091 (5)0.021 (4)
C30.195 (9)0.053 (4)0.131 (7)0.034 (5)0.100 (6)0.019 (4)
C40.086 (5)0.050 (4)0.096 (5)0.023 (4)0.052 (4)0.013 (4)
C50.076 (4)0.060 (4)0.103 (5)0.009 (4)0.043 (4)0.014 (4)
C60.071 (4)0.048 (4)0.106 (6)0.002 (3)0.030 (4)0.011 (4)
C70.081 (5)0.051 (4)0.076 (5)0.001 (3)0.033 (4)0.009 (3)
C80.077 (4)0.043 (3)0.083 (5)0.001 (3)0.027 (4)0.010 (3)
C90.085 (5)0.036 (3)0.114 (6)0.008 (3)0.056 (5)0.015 (3)
C100.090 (5)0.047 (4)0.099 (6)0.011 (4)0.037 (4)0.019 (4)
C110.072 (4)0.063 (4)0.076 (5)0.009 (3)0.012 (4)0.016 (4)
C120.095 (6)0.081 (6)0.108 (7)0.006 (4)0.006 (5)0.012 (5)
C130.121 (7)0.108 (7)0.111 (7)0.015 (6)0.008 (6)0.002 (6)
C140.100 (6)0.079 (6)0.149 (9)0.006 (5)0.030 (6)0.016 (6)
C150.087 (5)0.070 (5)0.135 (8)0.002 (4)0.003 (5)0.020 (5)
C160.082 (4)0.059 (4)0.095 (5)0.005 (4)0.019 (4)0.016 (4)
C170.054 (3)0.036 (3)0.051 (3)0.009 (3)0.003 (3)0.002 (3)
C180.066 (4)0.046 (3)0.048 (3)0.010 (3)0.006 (3)0.001 (2)
C190.121 (6)0.066 (4)0.062 (4)0.029 (4)0.026 (4)0.021 (3)
C200.058 (3)0.040 (3)0.046 (3)0.003 (3)0.006 (3)0.003 (2)
C210.072 (4)0.048 (3)0.045 (3)0.002 (3)0.007 (3)0.003 (3)
C220.077 (4)0.047 (3)0.060 (4)0.002 (3)0.008 (3)0.009 (3)
C230.069 (4)0.043 (3)0.068 (4)0.004 (3)0.009 (3)0.008 (3)
C240.056 (3)0.047 (3)0.060 (3)0.002 (3)0.002 (3)0.002 (3)
C250.060 (4)0.041 (3)0.059 (4)0.003 (3)0.009 (3)0.005 (3)
C260.065 (4)0.049 (3)0.078 (4)0.004 (3)0.000 (3)0.009 (3)
C270.062 (4)0.057 (4)0.056 (4)0.004 (3)0.003 (3)0.006 (3)
C280.082 (5)0.057 (4)0.070 (4)0.006 (4)0.001 (3)0.002 (3)
C290.134 (7)0.062 (5)0.073 (5)0.009 (5)0.007 (5)0.002 (3)
C300.173 (9)0.061 (5)0.082 (5)0.023 (6)0.028 (6)0.002 (4)
C310.106 (6)0.100 (6)0.085 (5)0.038 (5)0.026 (5)0.014 (5)
C320.076 (5)0.074 (4)0.070 (4)0.008 (4)0.008 (4)0.013 (3)
Geometric parameters (Å, º) top
Sr1—O5i2.496 (3)C11—C121.370 (9)
Sr1—O1ii2.514 (3)C11—C161.375 (8)
Sr1—O1W2.529 (4)C12—C131.361 (11)
Sr1—O22.557 (4)C12—H120.9300
Sr1—O2W2.559 (4)C13—C141.363 (11)
Sr1—O42.590 (4)C13—H130.9300
Sr1—O52.772 (3)C14—C151.367 (11)
Sr1—O12.816 (3)C14—H140.9300
Sr1—C13.037 (5)C15—C161.383 (9)
Sr1—C173.050 (5)C15—H150.9300
O1W—H1W10.85 (6)C16—H160.9300
O1W—H1W20.852 (10)C17—C181.535 (7)
O1—C11.246 (5)C18—C191.519 (7)
O1—Sr1ii2.514 (3)C18—C201.515 (7)
O2W—H2W10.85 (4)C18—H180.9800
O2W—H2W20.852 (10)C19—H19A0.9600
O2—C11.251 (6)C19—H19B0.9600
O3—C101.220 (7)C19—H19C0.9600
O4—C171.252 (6)C20—C251.384 (7)
O5—C171.246 (5)C20—C211.392 (7)
O5—Sr1i2.496 (3)C21—C221.377 (7)
O6—C261.217 (6)C21—H210.9300
C1—C21.505 (7)C22—C231.381 (8)
C2—C31.445 (6)C22—H220.9300
C2—C41.500 (8)C23—C241.386 (7)
C2—H20.9800C23—H230.9300
C3—H3A0.9600C24—C251.400 (7)
C3—H3B0.9600C24—C261.494 (8)
C3—H3C0.9600C25—H250.9300
C4—C51.358 (9)C26—C271.479 (8)
C4—C91.389 (10)C27—C281.378 (8)
C5—C61.389 (8)C27—C321.395 (8)
C5—H50.9300C28—C291.378 (8)
C6—C71.372 (8)C28—H280.9300
C6—H60.9300C29—C301.345 (11)
C7—C81.382 (8)C29—H290.9300
C7—H70.9300C30—C311.369 (10)
C8—C91.417 (8)C30—H300.9300
C8—C101.494 (9)C31—C321.391 (9)
C9—H90.9300C31—H310.9300
C10—C111.487 (9)C32—H320.9300
O5i—Sr1—O1ii150.60 (11)H3B—C3—H3C109.5
O5i—Sr1—O1W75.52 (13)C5—C4—C9117.3 (6)
O1ii—Sr1—O1W87.76 (11)C5—C4—C2122.7 (8)
O5i—Sr1—O277.86 (11)C9—C4—C2120.0 (7)
O1ii—Sr1—O2125.34 (10)C4—C5—C6121.7 (7)
O1W—Sr1—O2145.14 (12)C4—C5—H5119.1
O5i—Sr1—O2W89.06 (11)C6—C5—H5119.1
O1ii—Sr1—O2W73.17 (12)C7—C6—C5121.4 (6)
O1W—Sr1—O2W108.15 (16)C7—C6—H6119.3
O2—Sr1—O2W93.41 (14)C5—C6—H6119.3
O5i—Sr1—O4122.37 (11)C6—C7—C8118.8 (6)
O1ii—Sr1—O480.61 (11)C6—C7—H7120.6
O1W—Sr1—O489.33 (16)C8—C7—H7120.6
O2—Sr1—O486.23 (13)C7—C8—C9118.9 (7)
O2W—Sr1—O4147.50 (11)C7—C8—C10120.7 (6)
O5i—Sr1—O574.36 (12)C9—C8—C10120.3 (6)
O1ii—Sr1—O5125.00 (11)C4—C9—C8121.9 (7)
O1W—Sr1—O575.31 (14)C4—C9—H9119.1
O2—Sr1—O576.14 (12)C8—C9—H9119.1
O2W—Sr1—O5161.83 (11)O3—C10—C11120.2 (7)
O4—Sr1—O548.03 (10)O3—C10—C8119.5 (6)
O5i—Sr1—O1123.47 (11)C11—C10—C8120.3 (6)
O1ii—Sr1—O177.71 (11)C12—C11—C16118.9 (7)
O1W—Sr1—O1159.64 (14)C12—C11—C10118.8 (6)
O2—Sr1—O147.69 (10)C16—C11—C10122.2 (7)
O2W—Sr1—O181.43 (12)C13—C12—C11120.7 (8)
O4—Sr1—O174.41 (11)C13—C12—H12119.6
O5—Sr1—O1101.34 (10)C11—C12—H12119.6
O5i—Sr1—C1101.54 (13)C12—C13—C14120.3 (9)
O1ii—Sr1—C1101.82 (13)C12—C13—H13119.8
O1W—Sr1—C1160.99 (16)C14—C13—H13119.8
O2—Sr1—C123.92 (11)C13—C14—C15120.1 (9)
O2W—Sr1—C190.44 (14)C13—C14—H14119.9
O4—Sr1—C176.29 (14)C15—C14—H14119.9
O5—Sr1—C185.78 (12)C14—C15—C16119.5 (8)
O1—Sr1—C124.20 (10)C14—C15—H15120.3
O5i—Sr1—C1798.46 (13)C16—C15—H15120.3
O1ii—Sr1—C17102.95 (13)C11—C16—C15120.4 (8)
O1W—Sr1—C1781.86 (16)C11—C16—H16119.8
O2—Sr1—C1780.23 (13)C15—C16—H16119.8
O2W—Sr1—C17168.83 (13)O5—C17—O4122.3 (5)
O4—Sr1—C1723.91 (11)O5—C17—C18118.5 (5)
O5—Sr1—C1724.12 (11)O4—C17—C18119.2 (4)
O1—Sr1—C1787.53 (12)O5—C17—Sr165.3 (3)
C1—Sr1—C1780.01 (13)O4—C17—Sr157.0 (3)
O5i—Sr1—Sr1ii154.28 (8)C18—C17—Sr1175.9 (3)
O1ii—Sr1—Sr1ii41.47 (7)C19—C18—C20111.6 (4)
O1W—Sr1—Sr1ii127.72 (10)C19—C18—C17113.1 (5)
O2—Sr1—Sr1ii83.90 (7)C20—C18—C17111.9 (4)
O2W—Sr1—Sr1ii73.97 (8)C19—C18—H18106.6
O4—Sr1—Sr1ii73.69 (7)C20—C18—H18106.6
O5—Sr1—Sr1ii118.70 (7)C17—C18—H18106.6
O1—Sr1—Sr1ii36.24 (7)C18—C19—H19A109.5
C1—Sr1—Sr1ii60.37 (10)C18—C19—H19B109.5
C17—Sr1—Sr1ii96.11 (10)H19A—C19—H19B109.5
O5i—Sr1—Sr1i39.46 (8)C18—C19—H19C109.5
O1ii—Sr1—Sr1i153.66 (8)H19A—C19—H19C109.5
O1W—Sr1—Sr1i71.59 (9)H19B—C19—H19C109.5
O2—Sr1—Sr1i73.55 (7)C25—C20—C21117.4 (5)
O2W—Sr1—Sr1i128.12 (8)C25—C20—C18122.9 (5)
O4—Sr1—Sr1i82.92 (7)C21—C20—C18119.7 (5)
O5—Sr1—Sr1i34.90 (7)C22—C21—C20122.0 (5)
O1—Sr1—Sr1i117.22 (7)C22—C21—H21119.0
C1—Sr1—Sr1i94.03 (10)C20—C21—H21119.0
C17—Sr1—Sr1i59.01 (10)C21—C22—C23119.6 (5)
Sr1ii—Sr1—Sr1i148.45 (2)C21—C22—H22120.2
Sr1—O1W—H1W1126 (5)C23—C22—H22120.2
Sr1—O1W—H1W2115 (4)C22—C23—C24120.4 (5)
H1W1—O1W—H1W2109 (6)C22—C23—H23119.8
C1—O1—Sr1ii168.6 (3)C24—C23—H23119.8
C1—O1—Sr187.9 (3)C23—C24—C25118.8 (5)
Sr1ii—O1—Sr1102.29 (11)C23—C24—C26122.2 (5)
Sr1—O2W—H2W1125 (4)C25—C24—C26118.9 (5)
Sr1—O2W—H2W2115 (4)C20—C25—C24121.7 (5)
H2W1—O2W—H2W2108 (5)C20—C25—H25119.1
C1—O2—Sr1100.1 (3)C24—C25—H25119.1
C17—O4—Sr199.1 (3)O6—C26—C27120.4 (6)
C17—O5—Sr1i163.7 (3)O6—C26—C24120.0 (5)
C17—O5—Sr190.5 (3)C27—C26—C24119.6 (5)
Sr1i—O5—Sr1105.64 (12)C28—C27—C32119.0 (6)
O1—C1—O2122.1 (5)C28—C27—C26122.1 (6)
O1—C1—C2121.8 (5)C32—C27—C26118.7 (6)
O2—C1—C2116.0 (5)C29—C28—C27120.2 (7)
O1—C1—Sr167.9 (3)C29—C28—H28119.9
O2—C1—Sr156.0 (3)C27—C28—H28119.9
C2—C1—Sr1166.3 (4)C30—C29—C28121.0 (8)
C3—C2—C4116.5 (6)C30—C29—H29119.5
C3—C2—C1118.2 (5)C28—C29—H29119.5
C4—C2—C1113.0 (5)C29—C30—C31120.1 (7)
C3—C2—H2101.8C29—C30—H30120.0
C4—C2—H2101.8C31—C30—H30120.0
C1—C2—H2101.8C30—C31—C32120.5 (7)
C2—C3—H3A109.5C30—C31—H31119.8
C2—C3—H3B109.5C32—C31—H31119.8
H3A—C3—H3B109.5C31—C32—C27119.2 (6)
C2—C3—H3C109.5C31—C32—H32120.4
H3A—C3—H3C109.5C27—C32—H32120.4
O5i—Sr1—O1—C127.6 (3)O1—C1—C2—C31.5 (10)
O1ii—Sr1—O1—C1174.7 (3)O2—C1—C2—C3178.0 (7)
O1W—Sr1—O1—C1129.3 (4)Sr1—C1—C2—C3131.0 (16)
O2—Sr1—O1—C18.1 (3)O1—C1—C2—C4142.6 (6)
O2W—Sr1—O1—C1110.8 (3)O2—C1—C2—C441.0 (9)
O4—Sr1—O1—C191.2 (3)Sr1—C1—C2—C410 (2)
O5—Sr1—O1—C151.0 (3)C3—C2—C4—C5112.9 (9)
C17—Sr1—O1—C170.9 (3)C1—C2—C4—C5105.4 (7)
Sr1ii—Sr1—O1—C1174.7 (3)C3—C2—C4—C966.8 (9)
Sr1i—Sr1—O1—C117.9 (3)C1—C2—C4—C974.9 (8)
O5i—Sr1—O1—Sr1ii157.66 (11)C9—C4—C5—C61.6 (8)
O1ii—Sr1—O1—Sr1ii0.0C2—C4—C5—C6178.7 (5)
O1W—Sr1—O1—Sr1ii45.4 (4)C4—C5—C6—C70.0 (9)
O2—Sr1—O1—Sr1ii177.2 (2)C5—C6—C7—C81.4 (9)
O2W—Sr1—O1—Sr1ii74.52 (13)C6—C7—C8—C91.0 (8)
O4—Sr1—O1—Sr1ii83.54 (13)C6—C7—C8—C10175.2 (5)
O5—Sr1—O1—Sr1ii123.71 (12)C5—C4—C9—C81.9 (9)
C1—Sr1—O1—Sr1ii174.7 (3)C2—C4—C9—C8178.4 (5)
C17—Sr1—O1—Sr1ii103.83 (14)C7—C8—C9—C40.6 (8)
Sr1i—Sr1—O1—Sr1ii156.83 (7)C10—C8—C9—C4176.9 (5)
O5i—Sr1—O2—C1171.7 (3)C7—C8—C10—O3145.4 (6)
O1ii—Sr1—O2—C111.6 (4)C9—C8—C10—O330.8 (9)
O1W—Sr1—O2—C1147.5 (4)C7—C8—C10—C1134.2 (8)
O2W—Sr1—O2—C183.4 (3)C9—C8—C10—C11149.6 (6)
O4—Sr1—O2—C164.1 (3)O3—C10—C11—C1234.6 (10)
O5—Sr1—O2—C1111.7 (3)C8—C10—C11—C12145.0 (6)
O1—Sr1—O2—C18.2 (3)O3—C10—C11—C16142.9 (7)
C17—Sr1—O2—C187.4 (3)C8—C10—C11—C1637.5 (9)
Sr1ii—Sr1—O2—C19.9 (3)C16—C11—C12—C131.3 (11)
Sr1i—Sr1—O2—C1147.8 (3)C10—C11—C12—C13178.9 (7)
O5i—Sr1—O4—C171.2 (4)C11—C12—C13—C143.0 (13)
O1ii—Sr1—O4—C17159.0 (3)C12—C13—C14—C152.2 (13)
O1W—Sr1—O4—C1771.1 (3)C13—C14—C15—C160.1 (13)
O2—Sr1—O4—C1774.3 (3)C12—C11—C16—C151.1 (10)
O2W—Sr1—O4—C17164.7 (3)C10—C11—C16—C15176.4 (6)
O5—Sr1—O4—C170.4 (3)C14—C15—C16—C111.8 (11)
O1—Sr1—O4—C17121.3 (3)Sr1i—O5—C17—O4174.3 (9)
C1—Sr1—O4—C1796.3 (3)Sr1—O5—C17—O40.8 (5)
Sr1ii—Sr1—O4—C17159.0 (3)Sr1i—O5—C17—C184.7 (15)
Sr1i—Sr1—O4—C170.4 (3)Sr1—O5—C17—C18178.2 (4)
O5i—Sr1—O5—C17178.1 (4)Sr1i—O5—C17—Sr1173.5 (13)
O1ii—Sr1—O5—C1726.6 (3)Sr1—O4—C17—O50.9 (6)
O1W—Sr1—O5—C17103.1 (3)Sr1—O4—C17—C18178.2 (4)
O2—Sr1—O5—C1797.1 (3)O5i—Sr1—C17—O51.8 (4)
O2W—Sr1—O5—C17153.3 (4)O1ii—Sr1—C17—O5157.9 (3)
O4—Sr1—O5—C170.4 (3)O1W—Sr1—C17—O572.1 (3)
O1—Sr1—O5—C1756.3 (3)O2—Sr1—C17—O577.9 (3)
C1—Sr1—O5—C1774.9 (3)O2W—Sr1—C17—O5133.8 (6)
Sr1ii—Sr1—O5—C1722.2 (3)O4—Sr1—C17—O5179.2 (5)
Sr1i—Sr1—O5—C17178.1 (4)O1—Sr1—C17—O5125.3 (3)
O5i—Sr1—O5—Sr1i0.0C1—Sr1—C17—O5102.2 (3)
O1ii—Sr1—O5—Sr1i155.29 (11)Sr1ii—Sr1—C17—O5160.6 (3)
O1W—Sr1—O5—Sr1i78.75 (16)Sr1i—Sr1—C17—O51.3 (2)
O2—Sr1—O5—Sr1i81.03 (14)O5i—Sr1—C17—O4179.0 (3)
O2W—Sr1—O5—Sr1i24.8 (4)O1ii—Sr1—C17—O421.3 (3)
O4—Sr1—O5—Sr1i178.6 (2)O1W—Sr1—C17—O4107.1 (3)
O1—Sr1—O5—Sr1i121.86 (12)O2—Sr1—C17—O4103.0 (3)
C1—Sr1—O5—Sr1i103.23 (15)O2W—Sr1—C17—O447.1 (9)
C17—Sr1—O5—Sr1i178.1 (4)O5—Sr1—C17—O4179.2 (5)
Sr1ii—Sr1—O5—Sr1i155.97 (8)O1—Sr1—C17—O455.5 (3)
Sr1ii—O1—C1—O2167.6 (13)C1—Sr1—C17—O478.7 (3)
Sr1—O1—C1—O214.6 (5)Sr1ii—Sr1—C17—O420.2 (3)
Sr1ii—O1—C1—C216 (2)Sr1i—Sr1—C17—O4179.6 (4)
Sr1—O1—C1—C2169.1 (6)O5—C17—C18—C19179.2 (5)
Sr1ii—O1—C1—Sr1153.0 (17)O4—C17—C18—C191.7 (7)
Sr1—O2—C1—O116.4 (6)O5—C17—C18—C2052.1 (7)
Sr1—O2—C1—C2167.2 (5)O4—C17—C18—C20128.8 (5)
O5i—Sr1—C1—O1156.7 (3)C19—C18—C20—C2598.5 (6)
O1ii—Sr1—C1—O15.3 (3)C17—C18—C20—C2529.4 (7)
O1W—Sr1—C1—O1124.3 (4)C19—C18—C20—C2179.5 (7)
O2—Sr1—C1—O1165.1 (5)C17—C18—C20—C21152.6 (5)
O2W—Sr1—C1—O167.6 (3)C25—C20—C21—C222.2 (8)
O4—Sr1—C1—O182.4 (3)C18—C20—C21—C22179.8 (5)
O5—Sr1—C1—O1130.2 (3)C20—C21—C22—C230.7 (8)
C17—Sr1—C1—O1106.6 (3)C21—C22—C23—C243.3 (9)
Sr1ii—Sr1—C1—O13.6 (2)C22—C23—C24—C253.0 (8)
Sr1i—Sr1—C1—O1164.1 (3)C22—C23—C24—C26175.8 (5)
O5i—Sr1—C1—O28.3 (3)C21—C20—C25—C242.4 (8)
O1ii—Sr1—C1—O2170.3 (3)C18—C20—C25—C24179.6 (5)
O1W—Sr1—C1—O270.7 (6)C23—C24—C25—C200.1 (8)
O2W—Sr1—C1—O297.4 (3)C26—C24—C25—C20178.7 (5)
O4—Sr1—C1—O2112.5 (3)C23—C24—C26—O6143.7 (6)
O5—Sr1—C1—O264.8 (3)C25—C24—C26—O635.1 (8)
O1—Sr1—C1—O2165.1 (5)C23—C24—C26—C2735.8 (8)
C17—Sr1—C1—O288.4 (3)C25—C24—C26—C27145.4 (5)
Sr1ii—Sr1—C1—O2168.6 (4)O6—C26—C27—C28145.7 (6)
Sr1i—Sr1—C1—O230.8 (3)C24—C26—C27—C2834.8 (8)
O5i—Sr1—C1—C265.8 (19)O6—C26—C27—C3230.7 (9)
O1ii—Sr1—C1—C2132.2 (19)C24—C26—C27—C32148.8 (5)
O1W—Sr1—C1—C213 (2)C32—C27—C28—C291.1 (9)
O2—Sr1—C1—C257.5 (18)C26—C27—C28—C29175.3 (6)
O2W—Sr1—C1—C2154.9 (19)C27—C28—C29—C301.8 (10)
O4—Sr1—C1—C255.1 (19)C28—C29—C30—C311.3 (12)
O5—Sr1—C1—C27.3 (19)C29—C30—C31—C320.1 (12)
O1—Sr1—C1—C2137 (2)C30—C31—C32—C270.6 (10)
C17—Sr1—C1—C230.9 (19)C28—C27—C32—C310.1 (9)
Sr1ii—Sr1—C1—C2133.9 (19)C26—C27—C32—C31176.6 (6)
Sr1i—Sr1—C1—C226.6 (19)
Symmetry codes: (i) x+1, y+1, z+1; (ii) x+1, y+2, z+1.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O1W—H1W2···O2i0.85 (1)1.83 (1)2.678 (5)171 (6)
O2W—H2W2···O4ii0.85 (1)1.89 (2)2.724 (5)166 (6)
Symmetry codes: (i) x+1, y+1, z+1; (ii) x+1, y+2, z+1.

Experimental details

Crystal data
Chemical formula[Sr(C16H13O3)2(H2O)2]
Mr630.18
Crystal system, space groupMonoclinic, P21/n
Temperature (K)295
a, b, c (Å)18.665 (4), 8.0406 (16), 19.377 (4)
β (°) 93.26 (3)
V3)2903.4 (10)
Z4
Radiation typeMo Kα
µ (mm1)1.91
Crystal size (mm)0.30 × 0.25 × 0.18
Data collection
DiffractometerRigaku R-AXIS RAPID
diffractometer
Absorption correctionMulti-scan
(ABSCOR; Higashi, 1995)
Tmin, Tmax0.598, 0.725
No. of measured, independent and
observed [I > 2σ(I)] reflections
22141, 5107, 2941
Rint0.087
(sin θ/λ)max1)0.595
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.050, 0.136, 1.08
No. of reflections5107
No. of parameters385
No. of restraints7
H-atom treatmentH atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å3)0.69, 0.96

Computer programs: RAPID-AUTO (Rigaku, 1998), CrystalStructure (Rigaku/MSC, 2002), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEPII (Johnson, 1976).

Selected geometric parameters (Å, º) top
Sr1—O5i2.496 (3)Sr1—O2W2.559 (4)
Sr1—O1ii2.514 (3)Sr1—O42.590 (4)
Sr1—O1W2.529 (4)Sr1—O52.772 (3)
Sr1—O22.557 (4)Sr1—O12.816 (3)
O5i—Sr1—O1ii150.60 (11)O2W—Sr1—O4147.50 (11)
O5i—Sr1—O1W75.52 (13)O5i—Sr1—O574.36 (12)
O1ii—Sr1—O1W87.76 (11)O1ii—Sr1—O5125.00 (11)
O5i—Sr1—O277.86 (11)O1W—Sr1—O575.31 (14)
O1ii—Sr1—O2125.34 (10)O2—Sr1—O576.14 (12)
O1W—Sr1—O2145.14 (12)O2W—Sr1—O5161.83 (11)
O5i—Sr1—O2W89.06 (11)O4—Sr1—O548.03 (10)
O1ii—Sr1—O2W73.17 (12)O5i—Sr1—O1123.47 (11)
O1W—Sr1—O2W108.15 (16)O1ii—Sr1—O177.71 (11)
O2—Sr1—O2W93.41 (14)O1W—Sr1—O1159.64 (14)
O5i—Sr1—O4122.37 (11)O2—Sr1—O147.69 (10)
O1ii—Sr1—O480.61 (11)O2W—Sr1—O181.43 (12)
O1W—Sr1—O489.33 (16)O4—Sr1—O174.41 (11)
O2—Sr1—O486.23 (13)O5—Sr1—O1101.34 (10)
Symmetry codes: (i) x+1, y+1, z+1; (ii) x+1, y+2, z+1.
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O1W—H1W2···O2i0.852 (10)1.833 (13)2.678 (5)171 (6)
O2W—H2W2···O4ii0.852 (10)1.889 (17)2.724 (5)166 (6)
Symmetry codes: (i) x+1, y+1, z+1; (ii) x+1, y+2, z+1.
 

Acknowledgements

The authors thank the Project of Heilongjiang Provincial Health Office (No. 2009–246) and Harbin Medical University for supporting this work.

References

First citationHigashi, T. (1995). ABSCOR. Rigaku Corporation, Tokyo, Japan.  Google Scholar
First citationJohnson, C. K. (1976). ORTEPII. Report ORNL-5138. Oak Ridge National Laboratory, Tennessee, USA.  Google Scholar
First citationRigaku (1998). RAPID-AUTO. Rigaku Corporation, Tokyo, Japan.  Google Scholar
First citationRigaku/MSC (2002). CrystalStructure. Rigaku/MSC, The Woodlands, Texas, USA.  Google Scholar
First citationSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.  Web of Science CrossRef CAS IUCr Journals Google Scholar
First citationTahir, M. N., Ülkü, D., Ali, S., Masood, T., Danish, M. & Mazhar, M. (1997). Acta Cryst. C53, 1574–1576.  CSD CrossRef CAS Web of Science IUCr Journals Google Scholar
First citationZhang, Z.-Y., Chen, P.-G., Deng, Z.-P., Yu, N. & Liu, B.-Y. (2007a). Acta Cryst. E63, m1900–m1901.  Web of Science CSD CrossRef IUCr Journals Google Scholar
First citationZhang, Z.-Y., Yu, N., Guo, X.-X., Pu, J. & Sun, J.-P. (2007b). Acta Cryst. E63, m2883.  Web of Science CSD CrossRef IUCr Journals Google Scholar

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