The solvothermal reaction of zinc acetate dihydrate with a mixture of benzene-1,4-dicarboxylic acid (H(2)BDC) and benzene-1,3,5-tricarboxylic acid (H(3)BTC) in a solution containing N,N'-dimethylformamide (DMF), absolute ethanol, and chlorobenzene gave rise to a metal-organic polymer, Zn(3).BDC.2BTC.2NH(CH(3))(2).2NH(2)(CH(3))(2). The structure of this polymer possesses a unique three-dimensional framework with tri-zinc clusters, and BDC and BTC units colinking the clusters. Moreover, this metal-organic polymer exhibits strong photoluminescence at room temperature, and the main emission band is at about 430 nm (lambda(ex) = 325 nm). Crystal data for this compound (C(17)H(20)N(2)O(8)Zn(1.5)): monoclinic, space group P2(1)/n, cell dimensions a = 11.6171(3) A, b = 14.2456(4) A, c = 12.6426(3) A, beta = 107.030(2) degrees, V = 2000.51(9) A(3), and Z = 4.

Four new rare-earth compounds, [Eu(NDC)1.5(DMF)2] (1), [Nd2(NDC)3(DMF)4].H2O (2), [La2(NDC)3(DMF)4].0.5H2O (3), and [Eu(BTC)(H2O)] (4), where NDC = 1,4-naphthalenedicarboxylate, BTC = 1,3,5-benzenetricarboxylate, and DMF = N,N-dimethylformamide, have been synthesized through preheating and cooling-down crystallization. Compounds 1-3 possess similar 2D structures, in which the NDC ligands link M(III) (M = La, Nd, and Eu) ions of two adjacent double chains constructed by NDC ligands and dinuclear M(III) building units. In compound 4, the Eu(III) ion is seven-coordinated by O atoms from six BTC ligands and one terminal water molecule in a distorted pentagonal-bipyramidal coordination environment. If the BTC ligand and the Eu(III) ion are regarded as six-connected nodes, respectively, the structure of compound 4 can be well described as a 3D six-connected net. Furthermore, compounds 1 and 4 exhibit strong red luminescence upon 355-nm excitation. Compound 2 displays interesting emissions in the near-IR region, and yellow (580 nm) pumping of this compound results in UV and intense blue emissions through an up-conversion process. The magnetic properties of compounds 1, 2, and 4 have been studied through measurement of their magnetic susceptibilities over the temperature range of 4-300 K.

A series of Pb(II) coordination polymers [Pb(ndc)(dpp)] (1), [Pb(ndc)(ptcp)].0.5 H2O (2), [Pb(ndc)(dppz)] (3), [Pb(ndc)(tcpn)(2)] (4), [Pb2(ndc)2(tcpp)] (5), [Pb(Hndc)2].H2O (6), [Pb(ndc)(dma)] (7), [Pb(bdc)(dma)] (8), [Pb(trans-chdc)(H2O)] (9), and [Pb2(cis-chdc)2].NH(CH3)2 (10), where ndc=1,4-naphthalenedicarboxylate, dpp=4,7-diphenyl-1,10-phenanthroline, ptcp=2-phenyl-1H-1,3,7,8-tetraazacyclopenta[l]phenanthrene, dppz=dipyrido[3,2-a:2',3'-c]phenazine, tcpn=2-(1H-1,3,7,8-tetraazacyclopenta[l]phenanthren-2-yl)naphthol, tcpp=4-(1H-1,3,7,8-tetraazacyclopenta[l]phenanthren-2-yl)phenol, dma=N,N-dimethylacetamide, bdc=1,4-benzenedicarboxylate, and chdc=1,4-cyclohexanedicarboxylate, have been synthesized from a hydrothermal or solvothermal reaction system by varying the ligands or the solvents. Compounds 1-5 crystallize with an N-donor chelating ligand and an aromatic dicarboxylate linker. Compounds 1-4 are 1D polymers with different pi-pi stacking interactions, whereas compound 5 consists of 2D layers. The structures of compounds 7, 8, and 10 are 3D frameworks formed by connection of the Pb(II) centers by organic acid ligands. Compound 7 is chiral although the ndc ligand is achiral, while the framework of 8 is a typical 3D (3,4)-connected net. Compound 10 is the first example of Pb(II) wheel cluster [Pb(8)O(8)] units bridged by carboxylate groups. Compound 6 contains 1D chains which are further extended to a 3D structure by pi-pi interactions. Compound 9 consists of a 2D network constructed by Pb(II) centers and trans-chdc ligands. The structural differences between 7 and 8 and between 9 and 10 indicate the importance of solvents for framework formation of the coordination polymers. By varying the solvent the cis and trans conformations of H(2)chdc in 9 and 10 were separated completely. The photoluminescence and nonlinear optical properties of the coordination polymers have also been investigated.

Three new 3d-4f heterometallic coordination polymers, [Ln(2)(H(2)O)(4)M(2)(H(2)O)(2)(QA)(5)].nH(2)O (H(2)QA = quinolinic acid; Ln = Gd, M = Ni, n = 7 (1); Ln = Gd, M = Co, n = 6.5 (2); Ln = Dy, M = Co, n = 6.5 (3)), have been synthesized through hydrothermal pretreatment and cooling-down crystallization. These compounds possess the isostructural 3D frameworks with 1D chairlike channels along the c axis, which are occupied by noncoordinating water molecules. Crystal data: for 1, C(35)H(41)Gd(2)Ni(2)N(5)O(33), orthorhombic, space group Pna2(1), with a = 28.567(6) A, b = 14.498(3) A, c = 12.250(2) A, and Z = 4; for 2, C(35)H(40)Gd(2)Co(2)N(5)O(32.5), orthorhombic, space group Pna2(1), with a = 28.843(3) A, b = 14.4325(13) A, c = 12.2275(9) A, and Z = 4; for 3, C(35)H(40)Dy(2)Co(2)N(5)O(32.5), orthorhombic, space group Pna2(1), with a = 28.8471(14) A, b = 14.4534(10) A, c = 12.2520(7) A, and Z = 4. The magnetic behaviors for the three compounds have been investigated.

Four homochiral porous lanthanide phosphonates, [Ln(H2L)3].2H2O, (H3L = (S)-HO3PCH2-NHC4H7-CO2H, Ln = Tb (1), Dy (2), Eu (3), Gd (4)), have been synthesized under hydrothermal conditions. These compounds are isostructural, and they possess a 3D supramolecular framework built up from 1D triple-strand helical chains. Each of the helical chain consists of phosphonate groups bridging adjacent Ln(III) ions. The helical chains are stacked through hydrogen bonds to form 1D tubular channels along the c axis. Moreover, helical water chains are located in the 1D channels, and after removal of these water chains, the compounds exhibit selective adsorption capacities for N2, H2O, and CH3OH molecules. Compounds 1 and 3 show strong green and red fluorescent emissions, respectively, in the solid state at room temperature. Crystal data for 1: TbP3O17N3C18H37, tetragonal (No.76), space group P4(1), a = 12.4643(3) Angstrom, b = 12.4643(3) Angstrom, c = 18.7577(5) Angstrom, V = 2914.17(13) Angstrom(3), and Z = 4. For 2: DyP3O17N3C18H37, a = 12.4486(3) Angstrom, b = 12.4486(3) Angstrom, c = 18.7626(5) Angstrom, V = 2907.60(13) Angstrom(3), and Z = 4. For 3, EuP3O17N3C18H37, a = 12.4799(3) Angstrom, b = 12.4799(3) Angstrom, c = 18.8239(5) Angstrom, V = 2931.78(13) Angstrom(3), and Z = 4. For 4: GdP3O17N3C18H37, a = 12.4877(18) Angstrom, b = 12.4877(18) Angstrom, c = 18.824(4) Angstrom, V = 2935.5(8) Angstrom(3), and Z = 4.

We have proposed a dual-quenching electrochemiluminescence (ECL) strategy which is based on tris(2,2′-bipyridyl)ruthenium(II) [Ru(bpy) 3 2+ ] as chromophores caged in three-dimensional (3D) zinc oxalate metal−organic frameworks [Ru(bpy) 3 2+ /zinc oxalate MOFs] for ultrasensitive detection of amyloid-β (Aβ). The threedimensional chromophore connectivity in zinc oxalate MOFs provided a network for rapid excited-state energy transfer migration among Ru(bpy) 3 2+ units which shielded the chromophores from solvent molecules and led to a high-energy Ru emission efficiency. In addition, we found that both Au nanoparticles and NiFe-based nanocube MOFs could contribute to the reduction of the ECL intensity of the chromophore. The ECL emission spectra of 3D Ru(bpy) 3 2+ /zinc oxalate MOFs overlapped appropriately with the ultraviolet−visible (UV−vis) absorption spectra of Au@NiFe MOFs composites, which could trigger the resonance energy transfer (RET) behavior between Ru(bpy) 3 2+ /zinc oxalate MOFs (donor) and Au@NiFe MOFs (acceptor), achieving the dual-quenching effect of Ru(bpy) 3 2+ encapsulated in 3D zinc oxalate MOFs and significantly boosting the sensitivity of the Aβ detection immunosensor. In order to examine the clinical practicability, we have applied it to verify the content of Aβ solution ranging from 100 fg mL −1 to 50 ng mL −1 and obtained the calibration curve with high correlation coefficient, along with the low limit of detection of 13.8 fg mL −1 . Above all, this work demonstrated an approach of constructing dual-quenching effect ECL immunosensors in whole 3D MOF systems and its application in ECL detection methodology.

A unique metal-organic polymer MnؒPDBؒH 2 O (H 2 PDB ‫؍‬ pyridine-3,4-dicarboxylic acid), with weak antiferromagnetic interactions both between the manganese(II) centers of an infinite Mn-O-C chain and between the adjacent chains, has been synthesized by the hydrothermal reaction of Mn(CH 3 COO) 2 ؒ4H 2 O with H 2 PDB; X-ray diffraction shows that the polymer possesses a one-dimensional rectangular channel built up from pyridine rings and pseudo-layers formed by infinite straight Mn-O-C chain building units.

Here, a dual-mode quenched electrochemiluminescence (ECL) immunosensor based on PtPd@PDA was proposed. Among them, nitrogen-doped hydrazide conjugated carbon dots (NHCDs), as an ECL emitter and a donor of resonance energy transfer, were quenched by PtPd@PDA (receptor). At the same time, PDA in PtPd@PDA, as an oxygen radical scavenger, completed the further quenching of the ECL signal by consuming O 2•− generated by the decomposition of co-reactant H 2 O 2 . The dual-mode quenching from the above two channels was achieved. In addition, compared with the traditional carbon quantum dots, NHCDs as ECL emitters had lower excitation potential. Moreover, a large number of amino groups provided by aminated MWCNTs could capture more antibodies while connecting with NHCDs. Under the optimum experimental conditions, taking aflatoxin B1 as the target, the proposed sensor with good specificity, stability, and reproducibility had good linearity when the concentration of AFB1 was 0.01−100 ng/mL, with the detection limit of 2.63 pg/ mL (S/N = 3). This strategy provided more possibilities for the application of dopamine metal nanocomposites in electrochemiluminescence analysis and offered a new approach to detect AFB1.