Literature DB >> 21579980

Tetra-kis(μ(2)-3,4-dimethoxy-phenyl-acetato)-κO,O':O';κO:O:O';κO:O';κO:O'-bis-[(3,4-dimethoxy-phenyl-acetato-κO,O')(1,10-phenanthroline-κN,N)thulium(III)].

Jia-Lu Liu1, Hua-Qiong Li, Guo-Liang Zhao.   

Abstract

In the title centrosymmetric dinuclear complex, [Tm(2)(C(10)H(11)O(4))(6)(C(12)H(8)N(2))(2)], the unique Tm(III) ion is coordin-ated by five 3,4-dimethoxy-phenyl-acetate (DMPA) ligands and and a bis-chelating 1,10-phenanthroline (phen) ligand via seven O atoms and two N atoms, forming a distorted tricapped trigonal-prismatic environment. The DMPA ligands coordin-ate in the bis-chelate, bridging and bridging tridentate modes.

Entities:  

Year:  2009        PMID: 21579980      PMCID: PMC2979998          DOI: 10.1107/S1600536809051435

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


Related literature

For background to the importance of coordination in magnetism, see: Yao et al. (2008 ▶); Fang & Zhang (2006 ▶); Li et al. 2008 ▶); Wang & Sevov (2008 ▶). For a related structure, see: Wang et al. (2008 ▶).

Experimental

Crystal data

[Tm2(C10H11O4)6(C12H8N2)2] M = 1869.40 Triclinic, a = 12.3025 (1) Å b = 12.3483 (2) Å c = 14.5883 (2) Å α = 91.457 (1)° β = 103.403 (1)° γ = 114.406 (1)° V = 1944.71 (4) Å3 Z = 1 Mo Kα radiation μ = 2.35 mm−1 T = 296 K 0.35 × 0.11 × 0.10 mm

Data collection

Bruker SMART APEX diffractometer Absorption correction: multi-scan (SADABS; Sheldrick, 1996 ▶) T min = 0.747, T max = 0.798 32353 measured reflections 6861 independent reflections 5961 reflections with I > 2σ(I) R int = 0.038

Refinement

R[F 2 > 2σ(F 2)] = 0.025 wR(F 2) = 0.058 S = 1.03 6861 reflections 514 parameters H-atom parameters constrained Δρmax = 0.64 e Å−3 Δρmin = −0.32 e Å−3 Data collection: SMART (Bruker, 1997 ▶); cell refinement: SAINT (Bruker, 1999 ▶); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: PLATON (Spek, 2009 ▶); software used to prepare material for publication: SHELXL97. Crystal structure: contains datablocks I, global. DOI: 10.1107/S1600536809051435/lh2956sup1.cif Structure factors: contains datablocks I. DOI: 10.1107/S1600536809051435/lh2956Isup2.hkl Additional supplementary materials: crystallographic information; 3D view; checkCIF report
[Tm2(C10H11O4)6(C12H8N2)2]Z = 1
Mr = 1869.40F(000) = 944
Triclinic, P1Dx = 1.596 Mg m3
Hall symbol: -P 1Mo Kα radiation, λ = 0.71073 Å
a = 12.3025 (1) ÅCell parameters from 8597 reflections
b = 12.3483 (2) Åθ = 2.1–27.6°
c = 14.5883 (2) ŵ = 2.35 mm1
α = 91.457 (1)°T = 296 K
β = 103.403 (1)°Block, colourless
γ = 114.406 (1)°0.35 × 0.11 × 0.10 mm
V = 1944.71 (4) Å3
Bruker SMART APEX diffractometer6861 independent reflections
Radiation source: fine-focus sealed tube5961 reflections with I > 2σ(I)
graphiteRint = 0.038
ω scansθmax = 25.0°, θmin = 2.1°
Absorption correction: multi-scan (SADABS; Sheldrick, 1996)h = −14→14
Tmin = 0.747, Tmax = 0.798k = −14→14
32353 measured reflectionsl = −17→17
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.025Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.058H-atom parameters constrained
S = 1.03w = 1/[σ2(Fo2) + (0.0303P)2 + 0.071P] where P = (Fo2 + 2Fc2)/3
6861 reflections(Δ/σ)max = 0.004
514 parametersΔρmax = 0.64 e Å3
0 restraintsΔρmin = −0.32 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
Tm10.175028 (11)0.102013 (13)0.030650 (9)0.04097 (6)
N10.3561 (2)0.1554 (2)0.18114 (19)0.0465 (6)
O10.3698 (2)−0.4441 (2)0.30577 (16)0.0521 (6)
C10.3391 (4)−0.5686 (3)0.2846 (3)0.0632 (10)
H1A0.3974−0.58840.32830.095*
H1B0.3422−0.58480.22080.095*
H1C0.2572−0.61610.29050.095*
O20.3894 (2)−0.2368 (2)0.36761 (18)0.0685 (7)
N20.3785 (2)0.1373 (2)0.0008 (2)0.0496 (7)
C20.2942 (3)−0.4026 (3)0.2490 (2)0.0413 (7)
O30.01233 (18)−0.0982 (2)0.04225 (14)0.0462 (5)
C30.2150 (3)−0.4601 (3)0.1623 (2)0.0512 (8)
H3A0.2115−0.53180.13730.061*
O40.20449 (19)−0.0728 (2)0.08331 (16)0.0487 (5)
C40.1394 (3)−0.4117 (3)0.1114 (3)0.0581 (9)
H4A0.0872−0.45120.05190.070*
O50.2337 (3)0.5128 (3)−0.43218 (19)0.0821 (8)
C50.1398 (3)−0.3071 (3)0.1466 (2)0.0460 (8)
C60.2248 (3)−0.2465 (3)0.2326 (2)0.0451 (8)
H6A0.2297−0.17370.25650.054*
O60.1019 (2)0.5544 (3)−0.3365 (2)0.0800 (8)
O70.21737 (19)0.2421 (2)−0.08600 (15)0.0469 (5)
C70.3022 (3)−0.2915 (3)0.2833 (2)0.0435 (7)
O80.2591 (2)0.3120 (2)0.06308 (15)0.0555 (6)
C80.4180 (4)−0.1159 (4)0.3958 (3)0.0852 (14)
H8A0.4800−0.08740.45560.128*
H8B0.3447−0.10990.40220.128*
H8C0.4488−0.06820.34860.128*
C90.0460 (3)−0.2642 (3)0.0961 (3)0.0550 (9)
H9A−0.0017−0.31750.03690.066*
H9B−0.0107−0.27350.13490.066*
O9−0.2502 (3)−0.0455 (3)−0.5655 (2)0.0980 (10)
C100.0931 (3)−0.1378 (3)0.0735 (2)0.0416 (7)
O10−0.1572 (3)0.1810 (3)−0.5085 (2)0.0848 (9)
O110.11190 (19)−0.0205 (2)−0.11245 (15)0.0470 (5)
C110.3103 (5)0.5021 (5)−0.4862 (3)0.1033 (16)
H11C0.28310.5165−0.54990.155*
H11D0.30600.4226−0.48750.155*
H11A0.39420.5598−0.45810.155*
C120.2587 (3)0.4949 (3)−0.3385 (2)0.0576 (9)
O12−0.09479 (19)−0.1233 (2)−0.15456 (15)0.0523 (6)
C130.3461 (3)0.4592 (3)−0.2948 (3)0.0625 (10)
H13A0.39350.4427−0.32940.075*
C140.3652 (3)0.4470 (3)−0.1987 (3)0.0633 (10)
H14A0.42530.4227−0.16930.076*
C150.2951 (3)0.4710 (3)−0.1466 (2)0.0534 (9)
C160.2053 (3)0.5051 (3)−0.1922 (3)0.0569 (9)
H16A0.15640.5194−0.15800.068*
C170.1865 (3)0.5185 (3)−0.2867 (3)0.0564 (9)
C180.0160 (4)0.5660 (4)−0.2907 (4)0.0914 (14)
H18A−0.03790.5918−0.33340.137*
H18B0.06020.6242−0.23470.137*
H18C−0.03220.4899−0.27330.137*
C190.3135 (4)0.4569 (3)−0.0425 (3)0.0640 (10)
H19A0.27600.4999−0.01440.077*
H19B0.40150.4944−0.01150.077*
C200.2600 (3)0.3284 (3)−0.0220 (2)0.0456 (8)
C21−0.2939 (5)−0.1633 (5)−0.6054 (3)0.1053 (17)
H21A−0.3540−0.1780−0.66520.158*
H21B−0.3319−0.2160−0.56330.158*
H21C−0.2263−0.1776−0.61550.158*
C22−0.1625 (3)−0.0060 (4)−0.4787 (3)0.0617 (10)
C23−0.1222 (3)−0.0781 (3)−0.4219 (3)0.0585 (9)
H23A−0.1556−0.1601−0.44220.070*
C24−0.0336 (3)−0.0302 (3)−0.3362 (2)0.0488 (8)
C250.0151 (3)0.0914 (3)−0.3078 (2)0.0594 (9)
H25A0.07510.1250−0.25010.071*
C26−0.0237 (4)0.1647 (4)−0.3637 (3)0.0667 (10)
H26A0.01070.2468−0.34370.080*
C27−0.1136 (3)0.1156 (4)−0.4491 (2)0.0602 (10)
C28−0.1058 (5)0.3062 (5)−0.4796 (4)0.1056 (17)
H28A−0.14330.3422−0.52670.158*
H28B−0.01810.3405−0.47260.158*
H28C−0.12100.3206−0.41990.158*
C290.0109 (3)−0.1085 (3)−0.2735 (2)0.0544 (9)
H29A−0.0424−0.1925−0.29750.065*
H29B0.0943−0.0927−0.27550.065*
C300.0095 (3)−0.0830 (3)−0.1716 (2)0.0459 (8)
C310.3467 (3)0.1640 (3)0.2691 (2)0.0534 (9)
H31A0.27280.16000.27790.064*
C320.4414 (3)0.1785 (3)0.3499 (3)0.0617 (10)
H32A0.43110.18600.41050.074*
C330.5489 (3)0.1816 (3)0.3375 (3)0.0645 (10)
H33A0.61290.19060.39010.077*
C340.5632 (3)0.1712 (3)0.2472 (3)0.0549 (9)
C350.6728 (3)0.1718 (3)0.2281 (4)0.0746 (12)
H35A0.73710.17610.27860.089*
C360.6844 (3)0.1663 (4)0.1397 (4)0.0761 (13)
H36A0.75700.16730.13020.091*
C370.5883 (3)0.1588 (3)0.0593 (3)0.0592 (10)
C380.5985 (3)0.1566 (3)−0.0335 (3)0.0713 (12)
H38A0.67120.1615−0.04570.086*
C390.5023 (4)0.1473 (4)−0.1062 (3)0.0726 (12)
H39A0.50900.1484−0.16840.087*
C400.3922 (3)0.1361 (3)−0.0859 (3)0.0600 (10)
H40A0.32580.1273−0.13630.072*
C410.4763 (3)0.1515 (3)0.0748 (3)0.0485 (8)
C420.4642 (3)0.1595 (3)0.1689 (2)0.0442 (8)
U11U22U33U12U13U23
Tm10.04263 (9)0.06291 (11)0.03925 (9)0.03882 (7)0.01862 (6)0.02181 (7)
N10.0437 (14)0.0538 (17)0.0553 (18)0.0325 (13)0.0142 (12)0.0189 (14)
O10.0606 (14)0.0536 (14)0.0516 (14)0.0386 (12)0.0048 (11)0.0131 (11)
C10.085 (3)0.066 (2)0.058 (2)0.055 (2)0.0112 (19)0.0174 (19)
O20.0852 (18)0.0539 (16)0.0568 (16)0.0380 (14)−0.0132 (13)0.0011 (13)
N20.0496 (15)0.0606 (18)0.0589 (18)0.0355 (14)0.0275 (14)0.0227 (14)
C20.0425 (16)0.052 (2)0.0419 (18)0.0303 (15)0.0132 (14)0.0166 (15)
O30.0473 (12)0.0716 (15)0.0467 (13)0.0461 (11)0.0211 (10)0.0259 (11)
C30.062 (2)0.057 (2)0.048 (2)0.0425 (18)0.0064 (16)0.0029 (17)
O40.0422 (12)0.0622 (14)0.0601 (14)0.0369 (11)0.0178 (10)0.0243 (12)
C40.058 (2)0.064 (2)0.053 (2)0.0375 (19)−0.0061 (16)0.0000 (18)
O50.093 (2)0.117 (2)0.0538 (16)0.0547 (18)0.0318 (15)0.0371 (16)
C50.0411 (17)0.049 (2)0.055 (2)0.0275 (15)0.0089 (15)0.0168 (16)
C60.0489 (18)0.0406 (18)0.054 (2)0.0255 (15)0.0155 (15)0.0158 (16)
O60.0758 (18)0.102 (2)0.086 (2)0.0550 (17)0.0296 (15)0.0426 (17)
O70.0538 (13)0.0596 (15)0.0419 (13)0.0341 (12)0.0197 (10)0.0159 (12)
C70.0472 (17)0.0441 (19)0.0422 (18)0.0235 (15)0.0095 (14)0.0116 (15)
O80.0776 (16)0.0684 (16)0.0387 (13)0.0454 (13)0.0210 (11)0.0209 (12)
C80.097 (3)0.060 (3)0.080 (3)0.039 (2)−0.015 (2)−0.010 (2)
C90.0455 (18)0.055 (2)0.070 (2)0.0310 (17)0.0078 (16)0.0166 (18)
O90.101 (2)0.092 (2)0.078 (2)0.0443 (19)−0.0206 (18)−0.0066 (18)
C100.0466 (18)0.063 (2)0.0347 (17)0.0405 (17)0.0144 (13)0.0146 (15)
O100.101 (2)0.086 (2)0.0683 (19)0.0523 (18)0.0012 (16)0.0217 (16)
O110.0476 (13)0.0688 (15)0.0452 (13)0.0393 (12)0.0220 (11)0.0189 (11)
C110.141 (4)0.134 (4)0.055 (3)0.067 (4)0.046 (3)0.034 (3)
C120.064 (2)0.066 (2)0.047 (2)0.0271 (19)0.0227 (17)0.0229 (18)
O120.0468 (12)0.0839 (17)0.0425 (13)0.0401 (12)0.0180 (10)0.0170 (12)
C130.067 (2)0.073 (3)0.063 (2)0.035 (2)0.0336 (19)0.019 (2)
C140.069 (2)0.074 (3)0.059 (2)0.042 (2)0.0185 (19)0.027 (2)
C150.066 (2)0.048 (2)0.048 (2)0.0207 (17)0.0237 (17)0.0157 (17)
C160.066 (2)0.055 (2)0.060 (2)0.0282 (18)0.0294 (18)0.0185 (18)
C170.061 (2)0.055 (2)0.060 (2)0.0288 (18)0.0206 (18)0.0229 (18)
C180.075 (3)0.101 (4)0.121 (4)0.053 (3)0.036 (3)0.033 (3)
C190.077 (3)0.064 (2)0.048 (2)0.025 (2)0.0199 (18)0.0160 (19)
C200.0430 (17)0.065 (2)0.043 (2)0.0352 (17)0.0141 (14)0.0178 (18)
C210.091 (3)0.126 (5)0.073 (3)0.040 (3)−0.008 (3)−0.024 (3)
C220.060 (2)0.076 (3)0.048 (2)0.032 (2)0.0076 (17)0.013 (2)
C230.058 (2)0.064 (2)0.054 (2)0.0277 (19)0.0145 (17)0.0062 (19)
C240.0536 (19)0.071 (3)0.0369 (18)0.0351 (18)0.0225 (15)0.0174 (17)
C250.070 (2)0.066 (3)0.041 (2)0.033 (2)0.0074 (17)0.0117 (18)
C260.082 (3)0.063 (2)0.052 (2)0.032 (2)0.011 (2)0.0130 (19)
C270.067 (2)0.073 (3)0.044 (2)0.035 (2)0.0110 (17)0.019 (2)
C280.132 (4)0.086 (4)0.097 (4)0.053 (3)0.013 (3)0.040 (3)
C290.066 (2)0.075 (2)0.046 (2)0.046 (2)0.0266 (16)0.0155 (18)
C300.054 (2)0.066 (2)0.0426 (18)0.0442 (18)0.0218 (16)0.0221 (17)
C310.054 (2)0.064 (2)0.054 (2)0.0370 (18)0.0136 (16)0.0200 (18)
C320.065 (2)0.067 (2)0.054 (2)0.035 (2)0.0039 (18)0.0174 (19)
C330.057 (2)0.057 (2)0.068 (3)0.0271 (19)−0.0076 (19)0.009 (2)
C340.0394 (18)0.0397 (19)0.081 (3)0.0204 (15)0.0012 (17)0.0059 (18)
C350.0370 (19)0.060 (3)0.114 (4)0.0225 (18)−0.004 (2)−0.005 (3)
C360.0330 (19)0.065 (3)0.131 (4)0.0257 (18)0.016 (2)−0.002 (3)
C370.0403 (18)0.047 (2)0.104 (3)0.0265 (16)0.0279 (19)0.010 (2)
C380.049 (2)0.063 (2)0.120 (4)0.0294 (19)0.046 (2)0.010 (2)
C390.073 (3)0.076 (3)0.097 (3)0.041 (2)0.055 (2)0.023 (2)
C400.059 (2)0.074 (3)0.071 (3)0.042 (2)0.0354 (19)0.024 (2)
C410.0388 (17)0.0427 (19)0.074 (2)0.0238 (15)0.0208 (16)0.0148 (17)
C420.0380 (16)0.0388 (18)0.065 (2)0.0244 (14)0.0142 (15)0.0163 (16)
Tm1—O3i2.2840 (18)C12—C171.399 (5)
Tm1—O12i2.308 (2)O12—C301.258 (4)
Tm1—O112.317 (2)O12—Tm1i2.308 (2)
Tm1—O82.348 (2)C13—C141.389 (5)
Tm1—O72.444 (2)C13—H13A0.9300
Tm1—O42.4459 (19)C14—C151.382 (5)
Tm1—O32.497 (2)C14—H14A0.9300
Tm1—N22.502 (2)C15—C161.378 (5)
Tm1—N12.581 (2)C15—C191.508 (5)
Tm1—C202.750 (3)C16—C171.371 (5)
Tm1—C102.846 (3)C16—H16A0.9300
Tm1—Tm1i3.8506 (3)C18—H18A0.9600
N1—C311.321 (4)C18—H18B0.9600
N1—C421.363 (4)C18—H18C0.9600
O1—C21.367 (3)C19—C201.514 (5)
O1—C11.430 (4)C19—H19A0.9700
C1—H1A0.9600C19—H19B0.9700
C1—H1B0.9600C21—H21A0.9600
C1—H1C0.9600C21—H21B0.9600
O2—C71.367 (4)C21—H21C0.9600
O2—C81.410 (4)C22—C271.379 (5)
N2—C401.314 (4)C22—C231.392 (5)
N2—C411.363 (4)C23—C241.378 (5)
C2—C31.365 (4)C23—H23A0.9300
C2—C71.404 (4)C24—C251.377 (5)
O3—C101.280 (3)C24—C291.523 (4)
O3—Tm1i2.2840 (18)C25—C261.388 (5)
C3—C41.390 (4)C25—H25A0.9300
C3—H3A0.9300C26—C271.383 (5)
O4—C101.240 (4)C26—H26A0.9300
C4—C51.375 (4)C28—H28A0.9600
C4—H4A0.9300C28—H28B0.9600
O5—C121.374 (4)C28—H28C0.9600
O5—C111.403 (5)C29—C301.517 (4)
C5—C61.387 (4)C29—H29A0.9700
C5—C91.511 (4)C29—H29B0.9700
C6—C71.376 (4)C31—C321.398 (4)
C6—H6A0.9300C31—H31A0.9300
O6—C171.362 (4)C32—C331.361 (5)
O6—C181.425 (5)C32—H32A0.9300
O7—C201.242 (4)C33—C341.378 (5)
O8—C201.264 (4)C33—H33A0.9300
C8—H8A0.9600C34—C421.418 (4)
C8—H8B0.9600C34—C351.436 (5)
C8—H8C0.9600C35—C361.333 (6)
C9—C101.500 (5)C35—H35A0.9300
C9—H9A0.9700C36—C371.430 (6)
C9—H9B0.9700C36—H36A0.9300
O9—C221.380 (4)C37—C381.388 (6)
O9—C211.381 (5)C37—C411.414 (4)
O10—C271.367 (4)C38—C391.356 (6)
O10—C281.415 (5)C38—H38A0.9300
O11—C301.259 (4)C39—C401.404 (5)
C11—H11C0.9600C39—H39A0.9300
C11—H11D0.9600C40—H40A0.9300
C11—H11A0.9600C41—C421.419 (5)
C12—C131.359 (5)
O3i—Tm1—O12i75.69 (7)O3—C10—Tm161.27 (16)
O3i—Tm1—O1176.05 (7)C9—C10—Tm1178.2 (2)
O12i—Tm1—O11138.51 (8)C27—O10—C28117.0 (3)
O3i—Tm1—O889.39 (8)C30—O11—Tm1135.28 (19)
O12i—Tm1—O879.23 (8)O5—C11—H11C109.5
O11—Tm1—O8129.97 (7)O5—C11—H11D109.5
O3i—Tm1—O774.97 (7)H11C—C11—H11D109.5
O12i—Tm1—O7124.10 (7)O5—C11—H11A109.5
O11—Tm1—O775.85 (8)H11C—C11—H11A109.5
O8—Tm1—O754.12 (8)H11D—C11—H11A109.5
O3i—Tm1—O4124.40 (7)C13—C12—O5125.5 (3)
O12i—Tm1—O493.43 (7)C13—C12—C17119.9 (3)
O11—Tm1—O478.36 (7)O5—C12—C17114.6 (3)
O8—Tm1—O4142.79 (8)C30—O12—Tm1i137.4 (2)
O7—Tm1—O4142.18 (7)C12—C13—C14120.4 (3)
O3i—Tm1—O372.78 (7)C12—C13—H13A119.8
O12i—Tm1—O371.47 (8)C14—C13—H13A119.8
O11—Tm1—O371.52 (7)C15—C14—C13120.3 (3)
O8—Tm1—O3148.56 (7)C15—C14—H14A119.9
O7—Tm1—O3138.45 (7)C13—C14—H14A119.9
O4—Tm1—O352.42 (6)C16—C15—C14118.7 (3)
O3i—Tm1—N2141.43 (8)C16—C15—C19120.3 (3)
O12i—Tm1—N2139.68 (8)C14—C15—C19121.0 (3)
O11—Tm1—N278.56 (8)C17—C16—C15121.5 (3)
O8—Tm1—N285.13 (8)C17—C16—H16A119.2
O7—Tm1—N270.97 (7)C15—C16—H16A119.2
O4—Tm1—N277.18 (8)O6—C17—C16125.2 (3)
O3—Tm1—N2124.89 (7)O6—C17—C12115.6 (3)
O3i—Tm1—N1149.64 (8)C16—C17—C12119.2 (3)
O12i—Tm1—N175.49 (8)O6—C18—H18A109.5
O11—Tm1—N1133.46 (7)O6—C18—H18B109.5
O8—Tm1—N176.06 (8)H18A—C18—H18B109.5
O7—Tm1—N1114.57 (8)O6—C18—H18C109.5
O4—Tm1—N166.81 (8)H18A—C18—H18C109.5
O3—Tm1—N1106.50 (7)H18B—C18—H18C109.5
N2—Tm1—N164.71 (9)C15—C19—C20114.9 (3)
O3i—Tm1—C2081.95 (8)C15—C19—H19A108.5
O12i—Tm1—C20102.70 (9)C20—C19—H19A108.5
O11—Tm1—C20102.70 (9)C15—C19—H19B108.5
O8—Tm1—C2027.28 (9)C20—C19—H19B108.5
O7—Tm1—C2026.86 (8)H19A—C19—H19B107.5
O4—Tm1—C20152.20 (8)O7—C20—O8121.0 (3)
O3—Tm1—C20154.73 (7)O7—C20—C19121.7 (3)
N2—Tm1—C2075.87 (8)O8—C20—C19117.3 (3)
N1—Tm1—C2095.26 (9)O7—C20—Tm162.72 (17)
O3i—Tm1—C1099.16 (8)O8—C20—Tm158.36 (17)
O12i—Tm1—C1081.72 (8)C19—C20—Tm1175.2 (3)
O11—Tm1—C1073.53 (8)O9—C21—H21A109.5
O8—Tm1—C10156.48 (8)O9—C21—H21B109.5
O7—Tm1—C10149.32 (8)H21A—C21—H21B109.5
O4—Tm1—C1025.70 (7)O9—C21—H21C109.5
O3—Tm1—C1026.72 (7)H21A—C21—H21C109.5
N2—Tm1—C10100.89 (8)H21B—C21—H21C109.5
N1—Tm1—C1085.93 (8)C27—C22—O9114.8 (3)
C20—Tm1—C10175.58 (9)C27—C22—C23119.8 (3)
O3i—Tm1—Tm1i38.27 (5)O9—C22—C23125.4 (4)
O12i—Tm1—Tm1i69.35 (5)C24—C23—C22121.2 (4)
O11—Tm1—Tm1i69.60 (5)C24—C23—H23A119.4
O8—Tm1—Tm1i123.15 (6)C22—C23—H23A119.4
O7—Tm1—Tm1i109.36 (5)C25—C24—C23118.5 (3)
O4—Tm1—Tm1i86.54 (5)C25—C24—C29120.0 (3)
O3—Tm1—Tm1i34.51 (4)C23—C24—C29121.5 (3)
N2—Tm1—Tm1i146.58 (7)C24—C25—C26121.1 (3)
N1—Tm1—Tm1i134.10 (6)C24—C25—H25A119.4
C20—Tm1—Tm1i120.22 (6)C26—C25—H25A119.4
C10—Tm1—Tm1i61.01 (6)C27—C26—C25119.9 (4)
C31—N1—C42117.6 (3)C27—C26—H26A120.0
C31—N1—Tm1124.5 (2)C25—C26—H26A120.0
C42—N1—Tm1117.2 (2)O10—C27—C22116.6 (3)
C2—O1—C1116.1 (2)O10—C27—C26123.9 (4)
O1—C1—H1A109.5C22—C27—C26119.5 (3)
O1—C1—H1B109.5O10—C28—H28A109.5
H1A—C1—H1B109.5O10—C28—H28B109.5
O1—C1—H1C109.5H28A—C28—H28B109.5
H1A—C1—H1C109.5O10—C28—H28C109.5
H1B—C1—H1C109.5H28A—C28—H28C109.5
C7—O2—C8117.0 (3)H28B—C28—H28C109.5
C40—N2—C41118.4 (3)C30—C29—C24110.6 (3)
C40—N2—Tm1121.5 (2)C30—C29—H29A109.5
C41—N2—Tm1120.0 (2)C24—C29—H29A109.5
C3—C2—O1124.8 (3)C30—C29—H29B109.5
C3—C2—C7118.9 (3)C24—C29—H29B109.5
O1—C2—C7116.4 (3)H29A—C29—H29B108.1
C10—O3—Tm1i158.6 (2)O12—C30—O11125.8 (3)
C10—O3—Tm192.01 (18)O12—C30—C29116.7 (3)
Tm1i—O3—Tm1107.22 (7)O11—C30—C29117.4 (3)
C2—C3—C4120.2 (3)N1—C31—C32123.9 (3)
C2—C3—H3A119.9N1—C31—H31A118.0
C4—C3—H3A119.9C32—C31—H31A118.0
C10—O4—Tm195.47 (17)C33—C32—C31118.4 (4)
C5—C4—C3121.8 (3)C33—C32—H32A120.8
C5—C4—H4A119.1C31—C32—H32A120.8
C3—C4—H4A119.1C32—C33—C34120.3 (3)
C12—O5—C11117.8 (3)C32—C33—H33A119.9
C4—C5—C6117.4 (3)C34—C33—H33A119.9
C4—C5—C9121.0 (3)C33—C34—C42118.1 (3)
C6—C5—C9121.5 (3)C33—C34—C35123.7 (4)
C7—C6—C5121.7 (3)C42—C34—C35118.2 (4)
C7—C6—H6A119.2C36—C35—C34121.5 (4)
C5—C6—H6A119.2C36—C35—H35A119.2
C17—O6—C18118.0 (3)C34—C35—H35A119.2
C20—O7—Tm190.42 (18)C35—C36—C37121.8 (3)
O2—C7—C6125.3 (3)C35—C36—H36A119.1
O2—C7—C2114.9 (3)C37—C36—H36A119.1
C6—C7—C2119.8 (3)C38—C37—C41118.3 (3)
C20—O8—Tm194.4 (2)C38—C37—C36123.4 (3)
O2—C8—H8A109.5C41—C37—C36118.3 (4)
O2—C8—H8B109.5C39—C38—C37119.8 (3)
H8A—C8—H8B109.5C39—C38—H38A120.1
O2—C8—H8C109.5C37—C38—H38A120.1
H8A—C8—H8C109.5C38—C39—C40118.9 (4)
H8B—C8—H8C109.5C38—C39—H39A120.6
C10—C9—C5118.0 (3)C40—C39—H39A120.6
C10—C9—H9A107.8N2—C40—C39123.2 (4)
C5—C9—H9A107.8N2—C40—H40A118.4
C10—C9—H9B107.8C39—C40—H40A118.4
C5—C9—H9B107.8N2—C41—C37121.3 (3)
H9A—C9—H9B107.1N2—C41—C42118.6 (3)
C22—O9—C21118.6 (4)C37—C41—C42120.1 (3)
O4—C10—O3120.1 (3)N1—C42—C34121.7 (3)
O4—C10—C9122.9 (3)N1—C42—C41118.4 (3)
O3—C10—C9117.0 (3)C34—C42—C41119.9 (3)
O4—C10—Tm158.82 (15)
O3i—Tm1—N1—C3125.7 (3)N2—Tm1—C10—O423.0 (2)
O12i—Tm1—N1—C316.9 (2)N1—Tm1—C10—O4−40.31 (18)
O11—Tm1—N1—C31−138.2 (2)Tm1i—Tm1—C10—O4172.9 (2)
O8—Tm1—N1—C3189.2 (3)O3i—Tm1—C10—O3−9.1 (2)
O7—Tm1—N1—C31128.1 (2)O12i—Tm1—C10—O364.85 (16)
O4—Tm1—N1—C31−93.3 (3)O11—Tm1—C10—O3−81.50 (16)
O3—Tm1—N1—C31−58.3 (3)O8—Tm1—C10—O3101.0 (2)
N2—Tm1—N1—C31−179.6 (3)O7—Tm1—C10—O3−85.0 (2)
C20—Tm1—N1—C31108.7 (3)O4—Tm1—C10—O3−178.9 (3)
C10—Tm1—N1—C31−75.6 (3)N2—Tm1—C10—O3−155.98 (16)
Tm1i—Tm1—N1—C31−33.8 (3)N1—Tm1—C10—O3140.75 (17)
O3i—Tm1—N1—C42−163.31 (18)Tm1i—Tm1—C10—O3−6.08 (13)
O12i—Tm1—N1—C42178.0 (2)O3i—Tm1—O11—C30−22.7 (3)
O11—Tm1—N1—C4232.8 (2)O12i—Tm1—O11—C3025.6 (3)
O8—Tm1—N1—C42−99.8 (2)O8—Tm1—O11—C30−99.8 (3)
O7—Tm1—N1—C42−60.8 (2)O7—Tm1—O11—C30−100.4 (3)
O4—Tm1—N1—C4277.7 (2)O4—Tm1—O11—C30107.5 (3)
O3—Tm1—N1—C42112.7 (2)O3—Tm1—O11—C3053.5 (3)
N2—Tm1—N1—C42−8.6 (2)N2—Tm1—O11—C30−173.4 (3)
C20—Tm1—N1—C42−80.3 (2)N1—Tm1—O11—C30149.0 (3)
C10—Tm1—N1—C4295.5 (2)C20—Tm1—O11—C30−100.9 (3)
Tm1i—Tm1—N1—C42137.26 (18)C10—Tm1—O11—C3081.5 (3)
O3i—Tm1—N2—C40−16.0 (3)Tm1i—Tm1—O11—C3016.9 (3)
O12i—Tm1—N2—C40−165.9 (2)C11—O5—C12—C13−5.0 (6)
O11—Tm1—N2—C4033.5 (3)C11—O5—C12—C17174.0 (4)
O8—Tm1—N2—C40−98.9 (3)O5—C12—C13—C14178.4 (4)
O7—Tm1—N2—C40−45.3 (3)C17—C12—C13—C14−0.7 (6)
O4—Tm1—N2—C40114.0 (3)C12—C13—C14—C150.1 (6)
O3—Tm1—N2—C4091.2 (3)C13—C14—C15—C161.0 (6)
N1—Tm1—N2—C40−175.8 (3)C13—C14—C15—C19179.3 (3)
C20—Tm1—N2—C40−72.9 (3)C14—C15—C16—C17−1.6 (5)
C10—Tm1—N2—C40104.1 (3)C19—C15—C16—C17−179.9 (3)
Tm1i—Tm1—N2—C4051.3 (3)C18—O6—C17—C16−7.7 (6)
O3i—Tm1—N2—C41167.8 (2)C18—O6—C17—C12172.8 (4)
O12i—Tm1—N2—C4117.9 (3)C15—C16—C17—O6−178.4 (3)
O11—Tm1—N2—C41−142.6 (2)C15—C16—C17—C121.1 (5)
O8—Tm1—N2—C4184.9 (2)C13—C12—C17—O6179.7 (3)
O7—Tm1—N2—C41138.5 (2)O5—C12—C17—O60.5 (5)
O4—Tm1—N2—C41−62.1 (2)C13—C12—C17—C160.1 (6)
O3—Tm1—N2—C41−85.0 (2)O5—C12—C17—C16−179.1 (3)
N1—Tm1—N2—C418.0 (2)C16—C15—C19—C20102.8 (4)
C20—Tm1—N2—C41111.0 (2)C14—C15—C19—C20−75.4 (4)
C10—Tm1—N2—C41−72.1 (2)Tm1—O7—C20—O8−3.0 (3)
Tm1i—Tm1—N2—C41−124.9 (2)Tm1—O7—C20—C19177.8 (3)
C1—O1—C2—C3−17.4 (4)Tm1—O8—C20—O73.1 (3)
C1—O1—C2—C7163.7 (3)Tm1—O8—C20—C19−177.6 (2)
O3i—Tm1—O3—C10170.6 (2)C15—C19—C20—O8−171.4 (3)
O12i—Tm1—O3—C10−109.14 (17)O3i—Tm1—C20—O7−72.51 (16)
O11—Tm1—O3—C1089.95 (17)O12i—Tm1—C20—O7−145.79 (16)
O8—Tm1—O3—C10−131.31 (18)O11—Tm1—C20—O71.14 (17)
O7—Tm1—O3—C10129.97 (17)O8—Tm1—C20—O7−177.0 (3)
O4—Tm1—O3—C100.58 (16)O4—Tm1—C20—O790.2 (2)
N2—Tm1—O3—C1029.2 (2)O3—Tm1—C20—O7−72.4 (3)
N1—Tm1—O3—C10−41.16 (17)N2—Tm1—C20—O775.68 (17)
C20—Tm1—O3—C10170.5 (2)N1—Tm1—C20—O7137.93 (16)
Tm1i—Tm1—O3—C10170.6 (2)Tm1i—Tm1—C20—O7−72.47 (17)
O3i—Tm1—O3—Tm1i0.0O3i—Tm1—C20—O8104.51 (17)
O12i—Tm1—O3—Tm1i80.27 (8)O12i—Tm1—C20—O831.24 (18)
O11—Tm1—O3—Tm1i−80.64 (8)O11—Tm1—C20—O8178.16 (16)
O8—Tm1—O3—Tm1i58.10 (16)O7—Tm1—C20—O8177.0 (3)
O7—Tm1—O3—Tm1i−40.62 (13)O4—Tm1—C20—O8−92.7 (2)
O4—Tm1—O3—Tm1i−170.01 (13)O3—Tm1—C20—O8104.6 (2)
N2—Tm1—O3—Tm1i−141.43 (9)N2—Tm1—C20—O8−107.29 (18)
N1—Tm1—O3—Tm1i148.25 (9)N1—Tm1—C20—O8−45.04 (18)
C20—Tm1—O3—Tm1i−0.1 (2)Tm1i—Tm1—C20—O8104.56 (17)
C10—Tm1—O3—Tm1i−170.6 (2)C21—O9—C22—C27173.0 (4)
O1—C2—C3—C4178.1 (3)C21—O9—C22—C23−7.0 (6)
C7—C2—C3—C4−3.1 (5)C27—C22—C23—C24−0.2 (6)
O3i—Tm1—O4—C10−12.2 (2)O9—C22—C23—C24179.8 (4)
O12i—Tm1—O4—C1062.79 (19)C22—C23—C24—C25−0.3 (5)
O11—Tm1—O4—C10−76.13 (18)C22—C23—C24—C29179.9 (3)
O8—Tm1—O4—C10139.46 (18)C23—C24—C25—C260.1 (5)
O7—Tm1—O4—C10−123.88 (19)C29—C24—C25—C26179.9 (3)
O3—Tm1—O4—C10−0.60 (16)C24—C25—C26—C270.6 (6)
N2—Tm1—O4—C10−156.9 (2)C28—O10—C27—C22−178.8 (4)
N1—Tm1—O4—C10135.4 (2)C28—O10—C27—C260.1 (6)
C20—Tm1—O4—C10−171.3 (2)O9—C22—C27—O10−0.2 (5)
Tm1i—Tm1—O4—C10−6.26 (18)C23—C22—C27—O10179.8 (3)
C2—C3—C4—C5−1.3 (5)O9—C22—C27—C26−179.1 (4)
C3—C4—C5—C64.3 (5)C23—C22—C27—C260.9 (6)
C3—C4—C5—C9−172.3 (3)C25—C26—C27—O10−179.9 (4)
C4—C5—C6—C7−3.0 (5)C25—C26—C27—C22−1.1 (6)
C9—C5—C6—C7173.6 (3)C25—C24—C29—C3048.9 (4)
O3i—Tm1—O7—C20102.08 (17)C23—C24—C29—C30−131.3 (3)
O12i—Tm1—O7—C2041.48 (19)Tm1i—O12—C30—O118.3 (5)
O11—Tm1—O7—C20−178.85 (17)Tm1i—O12—C30—C29−169.3 (2)
O8—Tm1—O7—C201.68 (16)Tm1—O11—C30—O12−22.4 (5)
O4—Tm1—O7—C20−130.47 (17)Tm1—O11—C30—C29155.2 (2)
O3—Tm1—O7—C20142.17 (16)C24—C29—C30—O1274.1 (4)
N2—Tm1—O7—C20−96.29 (18)C24—C29—C30—O11−103.7 (3)
N1—Tm1—O7—C20−47.19 (18)C42—N1—C31—C320.9 (5)
C10—Tm1—O7—C20−175.35 (16)Tm1—N1—C31—C32171.9 (3)
Tm1i—Tm1—O7—C20119.15 (16)N1—C31—C32—C33−1.5 (6)
C8—O2—C7—C6−12.4 (5)C31—C32—C33—C340.4 (5)
C8—O2—C7—C2168.0 (3)C32—C33—C34—C421.0 (5)
C5—C6—C7—O2179.1 (3)C32—C33—C34—C35−179.0 (3)
C5—C6—C7—C2−1.2 (5)C33—C34—C35—C36−177.3 (4)
C3—C2—C7—O2−176.0 (3)C42—C34—C35—C362.7 (6)
O1—C2—C7—O22.9 (4)C34—C35—C36—C37−0.4 (6)
C3—C2—C7—C64.3 (4)C35—C36—C37—C38178.0 (4)
O1—C2—C7—C6−176.8 (3)C35—C36—C37—C41−3.0 (6)
O3i—Tm1—O8—C20−73.46 (17)C41—C37—C38—C39−0.1 (5)
O12i—Tm1—O8—C20−149.01 (18)C36—C37—C38—C39178.8 (4)
O11—Tm1—O8—C20−2.3 (2)C37—C38—C39—C40−2.1 (6)
O7—Tm1—O8—C20−1.66 (16)C41—N2—C40—C390.7 (5)
O4—Tm1—O8—C20129.61 (17)Tm1—N2—C40—C39−175.5 (3)
O3—Tm1—O8—C20−127.64 (18)C38—C39—C40—N21.9 (6)
N2—Tm1—O8—C2068.32 (18)C40—N2—C41—C37−3.0 (5)
N1—Tm1—O8—C20133.45 (18)Tm1—N2—C41—C37173.2 (2)
C10—Tm1—O8—C20174.55 (18)C40—N2—C41—C42176.6 (3)
Tm1i—Tm1—O8—C20−92.58 (17)Tm1—N2—C41—C42−7.1 (4)
C4—C5—C9—C10−128.0 (4)C38—C37—C41—N22.8 (5)
C6—C5—C9—C1055.6 (5)C36—C37—C41—N2−176.2 (3)
Tm1—O4—C10—O31.1 (3)C38—C37—C41—C42−176.8 (3)
Tm1—O4—C10—C9−179.4 (3)C36—C37—C41—C424.1 (5)
Tm1i—O3—C10—O4153.6 (4)C31—N1—C42—C340.6 (4)
Tm1—O3—C10—O4−1.1 (3)Tm1—N1—C42—C34−171.0 (2)
Tm1i—O3—C10—C9−26.0 (7)C31—N1—C42—C41−179.5 (3)
Tm1—O3—C10—C9179.4 (3)Tm1—N1—C42—C418.9 (4)
Tm1i—O3—C10—Tm1154.6 (5)C33—C34—C42—N1−1.6 (5)
C5—C9—C10—O49.4 (5)C35—C34—C42—N1178.4 (3)
C5—C9—C10—O3−171.1 (3)C33—C34—C42—C41178.5 (3)
O3i—Tm1—C10—O4169.83 (18)C35—C34—C42—C41−1.5 (5)
O12i—Tm1—C10—O4−116.22 (19)N2—C41—C42—N1−1.5 (4)
O11—Tm1—C10—O497.43 (18)C37—C41—C42—N1178.2 (3)
O8—Tm1—C10—O4−80.1 (3)N2—C41—C42—C34178.4 (3)
O7—Tm1—C10—O493.9 (2)C37—C41—C42—C34−1.9 (5)
O3—Tm1—C10—O4178.9 (3)
  6 in total

1.  A short history of SHELX.

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

2.  Diversity of coordination architecture of metal 4,5-dicarboxyimidazole.

Authors:  Rui-Qin Fang; Xian-Ming Zhang
Journal:  Inorg Chem       Date:  2006-06-12       Impact factor: 5.165

3.  catena-Poly[[di-μ-chlorido-bis-{[6-methoxy-2-(4-methyl-phenyl-iminio-methyl)phenolato-κO,O']cadmium(II)}]-di-μ(2)-thio-cyanato-κN:S;κS:N].

Authors:  Hua-Qiong Li; Hui-Duo Xian; Jian-Feng Liu; Guo-Liang Zhao
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-11-22

4.  Synthesis, structures, and magnetic properties of metal-coordination polymers with benzenepentacarboxylate linkers.

Authors:  Xin-Yi Wang; Slavi C Sevov
Journal:  Inorg Chem       Date:  2007-12-21       Impact factor: 5.165

5.  Poly[diaqua-penta-kis(μ(4)-benzene-1,2-dicarboxyl-ato)(μ(3)-benzene-1,2-dicarboxyl-ato)tetra-thulium(III)].

Authors:  Guo-Ming Wang; Chun-Sheng Duan; Hui-Luan Liu; Hui Li
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-02-13

6.  Structure validation in chemical crystallography.

Authors:  Anthony L Spek
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2009-01-20
  6 in total
  12 in total

1.  Bis[μ-2-(4-hydroxyphenyl)acetato]-κO,O':O;κO:O,O'-bis{aqua(4,4'-bi-pyri-dine-κN)bis[2-(4-hydroxyphenyl)acetato-κO,O']gadolinium(III)} monohydrate.

Authors:  Jia-Lu Liu; Jian-Feng Liu; Guo-Liang Zhao
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-10-23

2.  Bis[μ-2-(4-hy-droxy-phen-yl)acetato]-κO,O':O;κO:O,O'-bis-{aqua-(4,4'-bipyridine-κN)bis-[2-(4-hy-droxy-phen-yl)acetato-κO,O']ytterbium(III)} monohydrate.

Authors:  Jia-Lu Liu; Jian-Feng Liu; Guo-Liang Zhao
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-10-31

3.  catena-Poly[[{diaqua-[2-(4-hy-droxy-phen-yl)acetato-κO,O']cerium(III)}-bis-[μ-2-(4-hy-droxy-phen-yl)acetato]-κO,O':O;κO:O,O'] 4,4'-bipyridine disolvate monohydrate].

Authors:  Jia-Lu Liu; Jian-Feng Liu; Guo-Liang Zhao
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-11-27

4.  [μ-2-(4-Hy-droxy-phen-yl)acetato]-κO:O,O';κO,O':O'-bis-{aqua-(4,4'-bi-pyridine-κN)bis-[2-(4-hy-droxy-phen-yl)acetato-κO,O']holmium(III)} mono-hydrate.

Authors:  Jia-Lu Liu; Jian-Feng Liu; Guo-Liang Zhao
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-01-15

5.  Bis[2-(4-hy-droxy-phen-yl)acetato-κO]bis-(1,10-phenanthroline-κN,N')cadmium penta-hydrate.

Authors:  Yu-Ye Yu
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-01-22

6.  Bis[μ-2-(4-hy-droxy-phen-yl)acetato]-κO,O':O;κO:O,O'-bis-{aqua-(4,4'-bipyridine-κN)bis-[2-(4-hy-droxy-phen-yl)acetato-κO,O']dysprosium(III)} monohydrate.

Authors:  Jia-Lu Liu; Jian-Feng Liu; Guo-Liang Zhao
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-11-06

7.  catena-Poly[[[diaqua-(nitrato-κO,O')cerium(III)]-bis-[μ-2-(4-hy-droxy-phen-yl)acetato]-κO,O':O;κO:O,O'] mono-hydrate].

Authors:  Hang-Ming Guo
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-11-20

8.  Tetra-kis[μ-2-(3,4-dimeth-oxy-phen-yl)acetato]-κO:O';κO,O':O;κO:O,O'-bis-{[2-(3,4-dimeth-oxy-phen-yl)acetato-κO,O'](1,10-phenanthroline-κN,N')samarium(III)}.

Authors:  Jia-Lu Liu; Hua-Qiong Li; Guo-Liang Zhao
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-10-09

9.  Bis[μ-2-(4-hy-droxy-phen-yl)acetato]-κO,O':O;κO:O,O'-bis-{aqua-(4,4'-bi-pyridine-κN)[2-(4-hy-droxy-phen-yl)acetato-κO,O']erbium(III)} monohydrate.

Authors:  Jia-Lu Liu; Jian-Feng Liu; Guo-Liang Zhao
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-11-06

10.  Bis[μ-2-(4-hy-droxy-phen-yl)acetato]-κO,O':O;κO:O,O'-bis-{aqua-(4,4'-bipyridine-κN)[2-(4-hy-droxy-phen-yl)acetato-κO,O']samarium(III)} monohydrate.

Authors:  Jia-Lu Liu; Jian-Feng Liu; Guo-Liang Zhao
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-11-06
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