Literature DB >> 22199476

Poly[tetra-kis-(μ-benzene-1,2-dicarboxyl-ato)di-μ-formato-penta-strontium(II)].

Pei-Chi Cheng, Jun-Xiang Zhan, Cheng-You Wu, Chia-Her Lin.   

Abstract

The asymmetric unit of the title complex, [Sr(5)(C(8)H(4)O(4))(4)(HCO(2))(2)](n), contains three independent Sr(II) ions, one of which is located on an inversion center. In the crystal, the Sr(II) ions (coordination numbers 8, 9 and 12) are connected by two crystallographically distinct benzene-1,2-dicarboxyl-ate ligands and one formate ligand, forming a two-dimensional polymer parallel to (001).

Entities:  

Year:  2011        PMID: 22199476      PMCID: PMC3238585          DOI: 10.1107/S1600536811044977

Source DB:  PubMed          Journal:  Acta Crystallogr Sect E Struct Rep Online        ISSN: 1600-5368


Related literature

For general background to metal coordination polymers, see: Kitagawa et al. (2004 ▶). For related structures, see: Stein & Ruschewitz (2005 ▶); Zhang et al. (2009 ▶); Wang et al. (2010 ▶).

Experimental

Crystal data

[Sr5(C8H4O4)4(HCO2)2] M = 1184.58 Triclinic, a = 7.0292 (3) Å b = 10.2892 (4) Å c = 12.5439 (5) Å α = 91.361 (2)° β = 90.407 (2)° γ = 104.998 (2)° V = 876.00 (6) Å3 Z = 1 Mo Kα radiation μ = 7.65 mm−1 T = 295 K 0.20 × 0.18 × 0.15 mm

Data collection

Bruker APEXII CCD diffractometer Absorption correction: multi-scan (SADABS; Bruker, 2010 ▶) T min = 0.310, T max = 0.393 15465 measured reflections 4295 independent reflections 3585 reflections with I > 2σ(I) R int = 0.033

Refinement

R[F 2 > 2σ(F 2)] = 0.028 wR(F 2) = 0.060 S = 1.04 4295 reflections 268 parameters H-atom parameters constrained Δρmax = 0.97 e Å−3 Δρmin = −0.39 e Å−3 Data collection: APEX2 (Bruker, 2010 ▶); cell refinement: SAINT (Bruker, 2010 ▶); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: DIAMOND (Brandenburg, 2010 ▶); software used to prepare material for publication: SHELXTL (Sheldrick, 2008 ▶). Crystal structure: contains datablock(s) I, global. DOI: 10.1107/S1600536811044977/lh5360sup1.cif Structure factors: contains datablock(s) I. DOI: 10.1107/S1600536811044977/lh5360Isup2.hkl Additional supplementary materials: crystallographic information; 3D view; checkCIF report
[Sr5(C8H4O4)4(HCO2)2]Z = 1
Mr = 1184.58F(000) = 572
Triclinic, P1Dx = 2.245 Mg m3
Hall symbol: -P 1Mo Kα radiation, λ = 0.71073 Å
a = 7.0292 (3) ÅCell parameters from 8942 reflections
b = 10.2892 (4) Åθ = 2.6–28.3°
c = 12.5439 (5) ŵ = 7.65 mm1
α = 91.361 (2)°T = 295 K
β = 90.407 (2)°Lamellar, colorless
γ = 104.998 (2)°0.20 × 0.18 × 0.15 mm
V = 876.00 (6) Å3
Bruker APEXII CCD diffractometer4295 independent reflections
Radiation source: fine-focus sealed tube3585 reflections with I > 2σ(I)
graphiteRint = 0.033
Detector resolution: 8.3333 pixels mm-1θmax = 28.3°, θmin = 1.6°
φ and ω scansh = −9→9
Absorption correction: multi-scan (SADABS; Bruker, 2010)k = −13→13
Tmin = 0.310, Tmax = 0.393l = −16→16
15465 measured reflections
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.028Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.060H-atom parameters constrained
S = 1.04w = 1/[σ2(Fo2) + (0.0254P)2 + 0.4547P] where P = (Fo2 + 2Fc2)/3
4295 reflections(Δ/σ)max = 0.001
268 parametersΔρmax = 0.97 e Å3
0 restraintsΔρmin = −0.39 e Å3
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.
xyzUiso*/Ueq
Sr11.00000.00000.00000.01600 (9)
Sr20.86724 (3)−0.37889 (2)−0.11377 (2)0.01683 (7)
Sr30.57129 (3)0.21010 (2)−0.05482 (2)0.01681 (7)
O10.6246 (3)−0.05156 (18)−0.08904 (15)0.0184 (4)
O20.8372 (3)−0.14323 (19)−0.17205 (16)0.0219 (4)
O30.2714 (3)0.03708 (19)−0.14874 (16)0.0227 (4)
O40.1994 (3)−0.17952 (19)−0.11074 (16)0.0209 (4)
O50.7838 (3)−0.26762 (19)0.05581 (15)0.0215 (4)
O61.0850 (3)−0.18764 (19)0.12185 (17)0.0254 (5)
O70.5072 (3)−0.61995 (19)0.10329 (16)0.0233 (4)
O80.8151 (3)−0.54513 (18)0.05059 (15)0.0190 (4)
O90.6767 (3)−0.6166 (2)−0.19012 (17)0.0274 (5)
O100.8059 (4)−0.4615 (3)−0.30783 (19)0.0432 (6)
C10.6836 (4)−0.1025 (3)−0.1717 (2)0.0168 (6)
C20.5647 (4)−0.1157 (3)−0.2734 (2)0.0178 (6)
C30.6460 (4)−0.1431 (3)−0.3689 (2)0.0268 (7)
H3A0.7758−0.1489−0.37010.032*
C40.5356 (5)−0.1618 (3)−0.4624 (3)0.0316 (7)
H4A0.5917−0.1788−0.52650.038*
C50.3424 (5)−0.1553 (3)−0.4603 (3)0.0327 (8)
H5A0.2678−0.1684−0.52310.039*
C60.2587 (4)−0.1293 (3)−0.3652 (3)0.0292 (7)
H6A0.1279−0.1256−0.36430.035*
C70.3690 (4)−0.1087 (3)−0.2717 (2)0.0184 (6)
C80.2747 (4)−0.0818 (3)−0.1693 (2)0.0172 (6)
C90.9131 (4)−0.2604 (3)0.1291 (2)0.0166 (6)
C100.8555 (4)−0.3394 (3)0.2271 (2)0.0183 (6)
C110.9164 (4)−0.2784 (3)0.3253 (3)0.0280 (7)
H11A0.9963−0.19090.32870.034*
C120.8602 (5)−0.3458 (3)0.4187 (3)0.0336 (8)
H12A0.9028−0.30420.48430.040*
C130.7407 (5)−0.4750 (3)0.4136 (3)0.0343 (8)
H13A0.7023−0.52080.47600.041*
C140.6777 (4)−0.5367 (3)0.3161 (3)0.0275 (7)
H14A0.5956−0.62360.31360.033*
C150.7349 (4)−0.4711 (3)0.2222 (2)0.0180 (6)
C160.6787 (4)−0.5489 (3)0.1181 (2)0.0159 (6)
C170.7073 (5)−0.5772 (4)−0.2845 (3)0.0377 (8)
H17A0.6537−0.6374−0.34000.045*
U11U22U33U12U13U23
Sr10.01285 (16)0.01455 (18)0.0203 (2)0.00311 (13)−0.00091 (13)0.00027 (15)
Sr20.01502 (12)0.01474 (13)0.02072 (15)0.00390 (10)0.00023 (10)0.00003 (10)
Sr30.01324 (12)0.01526 (13)0.02143 (15)0.00273 (9)0.00058 (10)0.00130 (10)
O10.0151 (9)0.0180 (10)0.0201 (11)0.0006 (8)−0.0004 (8)−0.0016 (8)
O20.0151 (9)0.0235 (11)0.0280 (12)0.0065 (8)−0.0020 (8)0.0008 (9)
O30.0229 (10)0.0179 (10)0.0287 (12)0.0080 (8)−0.0001 (9)−0.0042 (9)
O40.0140 (9)0.0210 (10)0.0263 (12)0.0015 (8)0.0003 (8)0.0058 (9)
O50.0269 (10)0.0175 (10)0.0216 (11)0.0086 (8)−0.0045 (8)−0.0001 (8)
O60.0189 (10)0.0213 (11)0.0352 (13)0.0027 (8)0.0041 (9)0.0083 (9)
O70.0153 (9)0.0236 (11)0.0287 (12)0.0013 (8)−0.0013 (8)−0.0036 (9)
O80.0186 (9)0.0184 (10)0.0213 (11)0.0065 (8)0.0053 (8)0.0022 (8)
O90.0330 (12)0.0234 (11)0.0267 (13)0.0084 (9)−0.0005 (9)0.0044 (10)
O100.0558 (16)0.0426 (15)0.0303 (14)0.0106 (13)0.0049 (12)0.0044 (12)
C10.0116 (12)0.0135 (13)0.0230 (16)−0.0008 (10)0.0000 (11)0.0018 (12)
C20.0172 (13)0.0157 (13)0.0198 (15)0.0031 (11)−0.0012 (11)−0.0003 (11)
C30.0213 (14)0.0315 (17)0.0276 (18)0.0070 (13)0.0027 (13)−0.0010 (14)
C40.0345 (18)0.041 (2)0.0199 (17)0.0101 (15)0.0023 (13)−0.0011 (15)
C50.0356 (18)0.043 (2)0.0197 (17)0.0106 (15)−0.0081 (14)−0.0037 (15)
C60.0212 (14)0.0410 (19)0.0272 (18)0.0119 (13)−0.0062 (12)−0.0037 (15)
C70.0169 (13)0.0144 (13)0.0238 (16)0.0038 (11)0.0010 (11)0.0003 (12)
C80.0085 (11)0.0192 (14)0.0243 (16)0.0046 (10)−0.0050 (10)−0.0009 (12)
C90.0193 (13)0.0128 (13)0.0194 (15)0.0072 (11)0.0027 (11)−0.0014 (11)
C100.0169 (13)0.0180 (14)0.0193 (15)0.0035 (11)−0.0010 (11)−0.0004 (12)
C110.0282 (16)0.0227 (16)0.0287 (18)−0.0007 (13)−0.0039 (13)−0.0041 (14)
C120.0386 (19)0.038 (2)0.0212 (18)0.0048 (15)−0.0021 (14)−0.0069 (15)
C130.0440 (19)0.0368 (19)0.0199 (18)0.0057 (16)0.0035 (15)0.0068 (15)
C140.0295 (16)0.0211 (15)0.0293 (18)0.0019 (13)0.0020 (13)0.0021 (14)
C150.0144 (12)0.0196 (14)0.0199 (15)0.0043 (11)0.0018 (11)−0.0003 (12)
C160.0172 (13)0.0129 (13)0.0194 (15)0.0071 (10)−0.0019 (11)0.0023 (11)
C170.0385 (19)0.037 (2)0.039 (2)0.0135 (16)0.0002 (16)−0.0016 (17)
Sr1—O3i2.641 (2)O6—C91.251 (3)
Sr1—O3ii2.641 (2)O6—Sr3iii2.6281 (19)
Sr1—O2iii2.661 (2)O7—C161.248 (3)
Sr1—O22.661 (2)O7—Sr2iv2.6335 (18)
Sr1—O6iii2.6729 (19)O7—Sr3viii2.729 (2)
Sr1—O62.6729 (19)O8—C161.277 (3)
Sr1—O12.7742 (17)O8—Sr2v2.6710 (18)
Sr1—O1iii2.7742 (17)O8—Sr3viii2.9331 (19)
Sr1—O5iii2.8848 (19)O9—C171.262 (4)
Sr1—O52.8848 (19)O9—Sr3viii2.467 (2)
Sr1—O4i2.9242 (19)O10—C171.256 (4)
Sr1—O4ii2.9242 (19)C1—C21.504 (4)
Sr2—O52.536 (2)C2—C31.384 (4)
Sr2—O102.556 (2)C2—C71.396 (4)
Sr2—O22.6087 (19)C3—C41.384 (4)
Sr2—O92.620 (2)C3—H3A0.9300
Sr2—O7iv2.6335 (18)C4—C51.378 (4)
Sr2—O8v2.6710 (18)C4—H4A0.9300
Sr2—O82.6766 (18)C5—C61.384 (5)
Sr2—O4ii2.6789 (18)C5—H5A0.9300
Sr3—O9vi2.467 (2)C6—C71.383 (4)
Sr3—O1i2.6128 (19)C6—H6A0.9300
Sr3—O6iii2.6281 (19)C7—C81.502 (4)
Sr3—O32.6314 (19)C8—Sr1vii3.125 (3)
Sr3—O4i2.6938 (19)C8—Sr3i3.420 (3)
Sr3—O5i2.7104 (18)C9—C101.490 (4)
Sr3—O7vi2.729 (2)C10—C111.383 (4)
Sr3—O12.8361 (19)C10—C151.400 (4)
Sr3—O8vi2.9332 (19)C11—C121.382 (4)
O1—C11.271 (3)C11—H11A0.9300
O1—Sr3i2.6129 (19)C12—C131.376 (5)
O2—C11.255 (3)C12—H12A0.9300
O3—C81.250 (3)C13—C141.380 (4)
O3—Sr1vii2.641 (2)C13—H13A0.9300
O4—C81.264 (3)C14—C151.382 (4)
O4—Sr2vii2.6789 (18)C14—H14A0.9300
O4—Sr3i2.6938 (19)C15—C161.510 (4)
O4—Sr1vii2.9242 (19)C16—Sr3viii3.190 (3)
O5—C91.275 (3)C17—H17A0.9300
O5—Sr3i2.7104 (18)
O3i—Sr1—O3ii180.00 (9)O3—Sr3—O165.33 (5)
O3i—Sr1—O2iii72.69 (6)O4i—Sr3—O176.04 (6)
O3ii—Sr1—O2iii107.31 (6)O5i—Sr3—O1124.22 (5)
O3i—Sr1—O2107.31 (6)O7vi—Sr3—O1141.68 (6)
O3ii—Sr1—O272.69 (6)O9vi—Sr3—O8vi71.45 (6)
O2iii—Sr1—O2180.0O1i—Sr3—O8vi109.25 (5)
O3i—Sr1—O6iii103.66 (6)O6iii—Sr3—O8vi82.40 (6)
O3ii—Sr1—O6iii76.34 (6)O3—Sr3—O8vi161.74 (5)
O2iii—Sr1—O6iii102.22 (6)O4i—Sr3—O8vi62.49 (5)
O2—Sr1—O6iii77.78 (6)O5i—Sr3—O8vi100.39 (5)
O3i—Sr1—O676.34 (6)O7vi—Sr3—O8vi45.82 (5)
O3ii—Sr1—O6103.66 (6)O1—Sr3—O8vi132.73 (5)
O2iii—Sr1—O677.78 (6)O9vi—Sr3—C16vi86.49 (7)
O2—Sr1—O6102.22 (6)O1i—Sr3—C16vi89.85 (6)
O6iii—Sr1—O6180.0O6iii—Sr3—C16vi104.15 (6)
O3i—Sr1—O168.69 (6)O3—Sr3—C16vi142.52 (6)
O3ii—Sr1—O1111.31 (6)O4i—Sr3—C16vi63.56 (6)
O2iii—Sr1—O1131.93 (5)O5i—Sr3—C16vi83.02 (6)
O2—Sr1—O148.07 (5)O7vi—Sr3—C16vi22.65 (6)
O6iii—Sr1—O161.89 (6)O1—Sr3—C16vi139.48 (6)
O6—Sr1—O1118.11 (6)O8vi—Sr3—C16vi23.60 (6)
O3i—Sr1—O1iii111.31 (6)O9vi—Sr3—C8i143.07 (7)
O3ii—Sr1—O1iii68.69 (6)O1i—Sr3—C8i48.65 (6)
O2iii—Sr1—O1iii48.07 (5)O6iii—Sr3—C8i81.07 (6)
O2—Sr1—O1iii131.93 (5)O3—Sr3—C8i111.74 (6)
O6iii—Sr1—O1iii118.11 (6)O4i—Sr3—C8i19.62 (6)
O6—Sr1—O1iii61.89 (6)O5i—Sr3—C8i119.24 (6)
O1—Sr1—O1iii180.0O7vi—Sr3—C8i77.15 (6)
O3i—Sr1—O5iii120.83 (6)O1—Sr3—C8i66.95 (6)
O3ii—Sr1—O5iii59.17 (6)O8vi—Sr3—C8i78.75 (6)
O2iii—Sr1—O5iii68.95 (6)C16vi—Sr3—C8i73.62 (6)
O2—Sr1—O5iii111.05 (6)O9vi—Sr3—Sr1vii125.58 (5)
O6iii—Sr1—O5iii46.67 (5)O1i—Sr3—Sr1vii41.76 (4)
O6—Sr1—O5iii133.33 (5)O6iii—Sr3—Sr1vii144.06 (4)
O1—Sr1—O5iii108.47 (5)O3—Sr3—Sr1vii38.86 (4)
O1iii—Sr1—O5iii71.53 (5)O4i—Sr3—Sr1vii109.12 (4)
O3i—Sr1—O559.17 (6)O5i—Sr3—Sr1vii44.41 (4)
O3ii—Sr1—O5120.83 (6)O7vi—Sr3—Sr1vii84.43 (4)
O2iii—Sr1—O5111.05 (6)O1—Sr3—Sr1vii82.91 (4)
O2—Sr1—O568.95 (6)O8vi—Sr3—Sr1vii130.22 (4)
O6iii—Sr1—O5133.33 (5)C16vi—Sr3—Sr1vii106.72 (5)
O6—Sr1—O546.67 (5)C8i—Sr3—Sr1vii90.35 (4)
O1—Sr1—O571.53 (5)C1—O1—Sr3i119.45 (16)
O1iii—Sr1—O5108.47 (5)C1—O1—Sr189.98 (14)
O5iii—Sr1—O5180.0Sr3i—O1—Sr199.39 (6)
O3i—Sr1—O4i46.64 (5)C1—O1—Sr3129.32 (16)
O3ii—Sr1—O4i133.36 (5)Sr3i—O1—Sr3108.81 (6)
O2iii—Sr1—O4i59.32 (5)Sr1—O1—Sr396.94 (5)
O2—Sr1—O4i120.68 (5)C1—O2—Sr2126.39 (17)
O6iii—Sr1—O4i65.35 (6)C1—O2—Sr195.62 (17)
O6—Sr1—O4i114.65 (6)Sr2—O2—Sr198.51 (6)
O1—Sr1—O4i73.41 (5)C8—O3—Sr3121.66 (16)
O1iii—Sr1—O4i106.59 (5)C8—O3—Sr1vii100.71 (17)
O5iii—Sr1—O4i75.06 (5)Sr3—O3—Sr1vii102.43 (7)
O5—Sr1—O4i104.94 (5)C8—O4—Sr2vii135.86 (16)
O3i—Sr1—O4ii133.36 (5)C8—O4—Sr3i114.66 (15)
O3ii—Sr1—O4ii46.64 (5)Sr2vii—O4—Sr3i109.39 (6)
O2iii—Sr1—O4ii120.68 (5)C8—O4—Sr1vii87.01 (16)
O2—Sr1—O4ii59.32 (5)Sr2vii—O4—Sr1vii90.77 (5)
O6iii—Sr1—O4ii114.65 (6)Sr3i—O4—Sr1vii96.68 (6)
O6—Sr1—O4ii65.35 (6)C9—O5—Sr2112.02 (16)
O1—Sr1—O4ii106.59 (5)C9—O5—Sr3i132.22 (17)
O1iii—Sr1—O4ii73.41 (5)Sr2—O5—Sr3i115.44 (7)
O5iii—Sr1—O4ii104.94 (5)C9—O5—Sr186.87 (15)
O5—Sr1—O4ii75.06 (5)Sr2—O5—Sr194.66 (6)
O4i—Sr1—O4ii180.00 (5)Sr3i—O5—Sr194.48 (5)
O5—Sr2—O10153.40 (7)C9—O6—Sr3iii138.19 (17)
O5—Sr2—O275.35 (6)C9—O6—Sr197.19 (16)
O10—Sr2—O288.68 (7)Sr3iii—O6—Sr1104.80 (7)
O5—Sr2—O9125.53 (6)C16—O7—Sr2iv143.91 (17)
O10—Sr2—O950.80 (7)C16—O7—Sr3viii99.92 (17)
O2—Sr2—O9128.29 (6)Sr2iv—O7—Sr3viii111.61 (7)
O5—Sr2—O7iv66.86 (6)C16—O8—Sr2v118.00 (16)
O10—Sr2—O7iv88.28 (7)C16—O8—Sr2121.54 (15)
O2—Sr2—O7iv72.55 (6)Sr2v—O8—Sr2115.75 (6)
O9—Sr2—O7iv75.32 (6)C16—O8—Sr3viii89.57 (15)
O5—Sr2—O8v101.16 (6)Sr2v—O8—Sr3viii102.86 (6)
O10—Sr2—O8v105.39 (7)Sr2—O8—Sr3viii99.56 (6)
O2—Sr2—O8v129.55 (6)C17—O9—Sr3viii153.6 (2)
O9—Sr2—O8v95.28 (6)C17—O9—Sr291.1 (2)
O7iv—Sr2—O8v153.14 (6)Sr3viii—O9—Sr2114.79 (8)
O5—Sr2—O868.06 (6)C17—O10—Sr294.3 (2)
O10—Sr2—O8123.11 (7)O2—C1—O1122.6 (3)
O2—Sr2—O8143.15 (6)O2—C1—C2118.3 (3)
O9—Sr2—O873.66 (6)O1—C1—C2119.0 (2)
O7iv—Sr2—O888.90 (6)O2—C1—Sr160.21 (14)
O8v—Sr2—O864.25 (6)O1—C1—Sr165.40 (14)
O5—Sr2—O4ii85.44 (6)C2—C1—Sr1162.29 (18)
O10—Sr2—O4ii106.46 (7)C3—C2—C7119.5 (3)
O2—Sr2—O4ii63.25 (6)C3—C2—C1119.7 (2)
O9—Sr2—O4ii147.58 (6)C7—C2—C1120.6 (3)
O7iv—Sr2—O4ii132.53 (6)C2—C3—C4120.5 (3)
O8v—Sr2—O4ii66.31 (6)C2—C3—H3A119.7
O8—Sr2—O4ii116.43 (6)C4—C3—H3A119.7
O5—Sr2—C17144.39 (8)C5—C4—C3119.8 (3)
O10—Sr2—C1725.29 (8)C5—C4—H4A120.1
O2—Sr2—C17108.87 (8)C3—C4—H4A120.1
O9—Sr2—C1725.52 (8)C4—C5—C6120.3 (3)
O7iv—Sr2—C1780.49 (8)C4—C5—H5A119.9
O8v—Sr2—C17101.96 (8)C6—C5—H5A119.9
O8—Sr2—C1798.66 (8)C7—C6—C5120.2 (3)
O4ii—Sr2—C17128.81 (8)C7—C6—H6A119.9
O5—Sr2—C921.42 (6)C5—C6—H6A119.9
O10—Sr2—C9174.73 (7)C6—C7—C2119.7 (3)
O2—Sr2—C987.44 (6)C6—C7—C8119.3 (2)
O9—Sr2—C9130.15 (7)C2—C7—C8121.0 (3)
O7iv—Sr2—C987.16 (6)O3—C8—O4123.9 (3)
O8v—Sr2—C979.84 (6)O3—C8—C7117.3 (2)
O8—Sr2—C959.46 (6)O4—C8—C7118.8 (2)
O4ii—Sr2—C974.88 (6)O3—C8—Sr1vii56.14 (14)
C17—Sr2—C9155.22 (9)O4—C8—Sr1vii69.17 (15)
O5—Sr2—Sr146.07 (4)C7—C8—Sr1vii164.05 (18)
O10—Sr2—Sr1127.95 (6)O3—C8—Sr3i108.26 (18)
O2—Sr2—Sr141.23 (4)O4—C8—Sr3i45.72 (12)
O9—Sr2—Sr1163.24 (5)C7—C8—Sr3i115.95 (16)
O7iv—Sr2—Sr188.05 (4)Sr1vii—C8—Sr3i79.71 (6)
O8v—Sr2—Sr1100.66 (4)O6—C9—O5122.1 (3)
O8—Sr2—Sr1108.71 (4)O6—C9—C10119.3 (2)
O4ii—Sr2—Sr147.09 (4)O5—C9—C10118.6 (2)
C17—Sr2—Sr1150.09 (7)O6—C9—Sr159.12 (13)
C9—Sr2—Sr149.25 (5)O5—C9—Sr168.79 (14)
O5—Sr2—Sr3viii99.78 (4)C10—C9—Sr1153.70 (18)
O10—Sr2—Sr3viii82.14 (6)O6—C9—Sr297.14 (17)
O2—Sr2—Sr3viii147.27 (4)O5—C9—Sr246.56 (13)
O9—Sr2—Sr3viii31.50 (5)C10—C9—Sr2126.17 (17)
O7iv—Sr2—Sr3viii75.82 (4)Sr1—C9—Sr278.21 (6)
O8v—Sr2—Sr3viii83.16 (4)C11—C10—C15119.4 (3)
O8—Sr2—Sr3viii42.44 (4)C11—C10—C9118.8 (3)
O4ii—Sr2—Sr3viii149.44 (4)C15—C10—C9121.7 (2)
C17—Sr2—Sr3viii56.95 (7)C12—C11—C10121.0 (3)
C9—Sr2—Sr3viii99.28 (5)C12—C11—H11A119.5
Sr1—Sr2—Sr3viii145.840 (8)C10—C11—H11A119.5
O9vi—Sr3—O1i164.51 (6)C13—C12—C11119.4 (3)
O9vi—Sr3—O6iii73.93 (6)C13—C12—H12A120.3
O1i—Sr3—O6iii121.54 (6)C11—C12—H12A120.3
O9vi—Sr3—O3103.04 (7)C12—C13—C14120.3 (3)
O1i—Sr3—O371.31 (6)C12—C13—H13A119.9
O6iii—Sr3—O3113.33 (6)C14—C13—H13A119.9
O9vi—Sr3—O4i123.48 (6)C13—C14—C15120.9 (3)
O1i—Sr3—O4i67.42 (6)C13—C14—H14A119.6
O6iii—Sr3—O4i69.37 (6)C15—C14—H14A119.6
O3—Sr3—O4i130.36 (6)C14—C15—C10119.0 (3)
O9vi—Sr3—O5i87.78 (6)C14—C15—C16118.4 (2)
O1i—Sr3—O5i76.83 (6)C10—C15—C16122.4 (2)
O6iii—Sr3—O5i159.68 (6)O7—C16—O8122.4 (3)
O3—Sr3—O5i61.60 (6)O7—C16—C15120.0 (2)
O4i—Sr3—O5i129.85 (6)O8—C16—C15117.5 (2)
O9vi—Sr3—O7vi96.29 (6)O7—C16—Sr3viii57.43 (14)
O1i—Sr3—O7vi75.32 (6)O8—C16—Sr3viii66.83 (14)
O6iii—Sr3—O7vi126.54 (6)C15—C16—Sr3viii161.68 (17)
O3—Sr3—O7vi120.04 (6)O10—C17—O9123.8 (3)
O4i—Sr3—O7vi74.30 (6)O10—C17—Sr260.42 (19)
O5i—Sr3—O7vi63.16 (6)O9—C17—Sr263.39 (18)
O9vi—Sr3—O1120.34 (6)O10—C17—H17A118.1
O1i—Sr3—O171.19 (6)O9—C17—H17A118.1
O6iii—Sr3—O161.57 (5)Sr2—C17—H17A177.4
  3 in total

1.  Functional porous coordination polymers.

Authors:  Susumu Kitagawa; Ryo Kitaura; Shin-ichiro Noro
Journal:  Angew Chem Int Ed Engl       Date:  2004-04-26       Impact factor: 15.336

2.  A short history of SHELX.

Authors:  George M Sheldrick
Journal:  Acta Crystallogr A       Date:  2007-12-21       Impact factor: 2.290

3.  Synthesis, structure, and luminescent properties of hybrid inorganic-organic framework materials formed by lead aromatic carboxylates: inorganic connectivity variation from 0D to 3D.

Authors:  Lei Zhang; Zhao-Ji Li; Qi-Pu Lin; Ye-Yan Qin; Jian Zhang; Pei-Xiu Yin; Jian-Kai Cheng; Yuan-Gen Yao
Journal:  Inorg Chem       Date:  2009-07-20       Impact factor: 5.165

  3 in total
  1 in total

1.  A series of four novel alkaline earth metal-organic frameworks constructed of Ca(ii), Sr(ii), Ba(ii) ions and tetrahedral MTB linker: structural diversity, stability study and low/high-pressure gas adsorption properties.

Authors:  Miroslav Almáši; Vladimír Zeleňák; Róbert Gyepes; Ľuboš Zauška; Sandrine Bourrelly
Journal:  RSC Adv       Date:  2020-09-01       Impact factor: 4.036

  1 in total

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