Synthesis, structure and luminescent properties of two three-dimensional d10 metal complexes constructed from pyridine-3,4-dicarboxylic acid with new network topologies

2006 ◽  
Vol 796 (1-3) ◽  
pp. 172-178 ◽  
Author(s):  
Xinlong Wang ◽  
Chao Qin ◽  
Enbo Wang ◽  
Lin Xu ◽  
Zhongmin Su
2014 ◽  
Vol 1068 ◽  
pp. 182-188 ◽  
Author(s):  
Lian-Ke Wang ◽  
Yan-Fang Shen ◽  
Hui-Juan Li ◽  
Xiao-Yu Zhao ◽  
Zheng Zheng ◽  
...  

2013 ◽  
Vol 750-752 ◽  
pp. 1708-1711
Author(s):  
Rui Ping Zheng ◽  
Hui Yuan Chen ◽  
Jun Jie He ◽  
He Ping Zeng

Two new Ce(III) coordination polymers formulated as Ce(bpdc)(Hbpdc)(DMF)2 (1) and [Ce2(bpdc)3(DMF)2(H2O)4]·2DMF (2) (H2bpdc = 2,2'-bipyridine-4,4'-dicarboxylic acid, DMF = N,N-Dimethyl formamide) have been synthesized under solvothermal condition and characterized by single-crystal X-ray diffraction. Compound 1 crystallizes in monoclinic, space group C2/c with a = 2.2520(2), b = 1.17787(12), c = 1.16128(11) nm, α = 90, β = 95.5600(10), γ = 90°, V = 3.0658(5) nm3, Z = 4, Mr = 771.70, Dc = 1.672×10-9 g/cm3. Compound 2 crystallizes in triclinic, space group Pwith a = 1.00610(10), b = 1.17219(11), c = 1.36891(14) nm, α = 66.9340(10), β = 87.182(2), γ = 76.2570(10) °, V = 1.4411(2) nm3, Z = 1, Mr = 1371.25, Dc = 1.580×10-9 g/cm3. Both compounds exhibit 3D Ce(III)–organic frameworks. Furthermore, thermal stability and luminescent properties were also investigated. CCDC:(1)913670, (2)909563.


ChemInform ◽  
2010 ◽  
Vol 30 (49) ◽  
pp. no-no
Author(s):  
Vivian Wing-Wah Yam ◽  
Kenneth Kam-Wing Lo
Keyword(s):  

2008 ◽  
Vol 77 (3) ◽  
pp. 578-583 ◽  
Author(s):  
Chaofan Zhong ◽  
Hualiang Huang ◽  
Aihong He ◽  
Hailiang Zhang

Crystals ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 372
Author(s):  
Mei-An Zhu ◽  
Shuai-Shuai Han ◽  
Feng Deng ◽  
Jia-Le Li ◽  
Shui-Sheng Chen

The coordination polymer, namely, [Cd(H2L)(nobda)]n (1) was prepared by the reaction of Cd(NO3)2·4H2O with 4-amino-1,2-benzenedicarboxylic acid (H2nobda) and 1,4-di(1H-imidazol-4-yl)benzene (H2L), and characterized by single-crystal X-ray diffraction, elemental analysis, infrared (IR) spectroscopy, thermogravimetric analysis, and powder X-ray diffraction (PXRD). The carboxylic acid of H2nobda ligands was completely deprotonated to be nobda2− anions, which act as tridentate ligand to connect the Cd2+ to form two-dimensional (2D) network, while the neutral H2L ligands serve as a linear didentate bridge to connect two adjacent Cd2+ ions upper and down the 2D layer. The adjacent 2D layers were further linked into the three-dimensional (3D) supramolecular polymer by the weak interactions such as hydrogen bonds and π−π stacking interactions. The ultraviolet-visible (UV-vis) absorption spectra and luminescent properties in the solid state at room temperature have been investigated.


2018 ◽  
Vol 74 (12) ◽  
pp. 1719-1724 ◽  
Author(s):  
Yimin Mao ◽  
Peter Y. Zavalij

Two ZnII-based coordination polymers (CPs) were synthesized by the hydrothermal method, using Zn(NO3)2·6H2O and furan-2,5-dicarboxylic acid (FDCA) in dimethylformamide (DMF) solvent, at 95 °C. Poly[tetrakis(dimethylazanium) [tetrakis(μ2-furan-2,5-dicarboxylato-κ2 O 2:O 5)dizinc(II)]], {(C2H8N)4[Zn2(C6H2O5)4]} n or {[DMA]4[ZnII 2(FDC)4]} n (DMA = dimethylazanium and FDC = furan-2,5-dicarboxylate), (1), was obtained with a 1:1 molar ratio of ZnII and FDCA. It crystallized in the monoclinic space group C2/c. Coordinated by ZnII ions, FDC2− ligands form 21 double-stranded helices propagating along the b axis. The helices are interconnected and extend laterally in the a direction, forming a two-dimensional (2D) sheet-like network. The 2D sheets are stacked along the c direction without interconnections. DMA cations are cocrystallized in (1) and are hydrogen bonded with carboxylate O atoms of the FDC2− ligands. The hydrogen-bonding pattern consists of R 2 2(4) and R 2 2(10) motifs alternating in a chain. Poly[bis(dimethylazanium) [bis(μ4-furan-2,5-dicarboxylato-κO 2:κO 2′:κO 5:κO 5)bis(μ3-furan-2,5-dicarboxylato-κO 2:κO 2′:κO 5)dizinc(II)] dimethylformamide 3.08-solvate], {(C2H8N)2[Zn2(C6H2O5)4]·3.08C3H7NO} n or {[DMA]2[ZnII 3(FDC)4]·3.08DMF} n , (2), was obtained with a 1:2 molar ratio of ZnII and FDCA. It crystallized in the monoclinic space group P21/c, forming a three-dimensional network. The pores are filled with DMA cations and DMF solvent molecules.


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