Novel mixed ligand complexes of Co(II), Ni(II), Cu(II), and Zn(II) with 1,10-phenanthroline and acesulfame. Synthesis,structural analysis and hydrogen adsorption study

Four novel metal organic framework (MOF) structures containing acesulfame (ace) and 1,10-phenanthroline (phen) ligands of Co²⁺, Ni²⁺, Cu²⁺ and Zn²⁺ metal cations were synthesized. The crystal structure analysis of three compounds (1, 2, and 3) was also performed. The structural formula for complex 4 is proposed based on spectroscopic and thermal analysis data. It has been determined that structures 1, 2, and 4 are in a distorted octahedral geometry. It has been suggested that the charge balance of the coordination sphere with 2+ is provided by two monoanionic ace ligands located outside the coordination sphere as counter-ion. In structure 3, there are two Cu^II metal cations, two phen ligands coordinated as bidentate to each metal cation and ace ligand that provides monoanionic-monodentate coordination. The Cu²⁺ cation has distorted bipyramidal geometry. The maximum hydrogen gas adsorption has been found 1.4575 mL/g (0.046 wt%) for the Ni complex.     

Synthesis of functionalized polymeric adsorbent selective to cobalt

Amino derivative of chloromethylated polystyrene resin was synthesized and functionalized by 1,10‐phenanthroline (1,10‐Phen) to yield a novel adsorbent, namely 4‐methylamino‐[N,N‐bis(2,2^′)‐1,10‐phenanthroline] polystyrene ( 4‐MABPPS ). The complete development of novel adsorbent along with its characterization is described in detail. The adsorption ability and selectivity of 4‐MABPPS were investigated for cobalt and zirconium ions so as to efficiently separate cobalt ion impurities from zircalloy cladding material of nuclear reactors. The experimental results showed selective uptake of cobalt by the adsorbent in the presence of zirconium. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Synthesis, characterization and DNA binding of the complexes of rare earth with phenanthroline and demethylcantharate

Three novel rare earth complexes, [Ln2(DCA)2(phen)2](NO3)2·6H2O (Ln(III)=Sm(III)(1), Er(III)(2), Yb(III)(3); DCA2-=de-methylcantharate, 7-oxabicyclo[2.2.1] heptane-2,3-dicarboxylate, C8H8O52-; phen=1,10-phenanthroline, C12H8N2) were synthesized. The structures were characterized by elemental analysis, molar conductance, IR and TGA. The results suggested that the structural features of the complexes were: in each DCA2-, one carboxylate group, as bidentate bridging group, connected two rare earth ions; the other carboxylate group, as bidentate chelate group took part in the coordination with rare earth ion. And cyclic ether oxygen of DCA2- and nitrogen atoms of phen took part in the coordination. The probable coordination number was seven. The interaction of the complexes with DNA was studied by UV-spectra, fluorescence spectra and viscosity measurements. Following increasing the concentration of DNA, the UV absorption bands nearby 265 nm of the three complexes appeared hypochromism and red-shift phenomena. And the values of binding constants Kb were 1.89×105 L/mol (1), 3.54×104 L/mol (2) and 3.83×104 L/mol (3). The complexes could quench the fluorescence of EB-DNA system, and the values of equilibrium constants Ksq were 1.72(1), 0.56(2) and 1.09(3). The relative viscosity of DNA steadily decreased with increasing the concentration of complexes. So, we could infer that the complexes may partially insert into DNA. The study of agarose gel electrophoresis showed that the complexes could cleave plasmid DNA, and the process of the reaction was through unclassical redox mechanism.     

Photophysical properties of a new ternary europium complex with 2-thenoyltrifluoroacetone and 5-nitro-1,10-phenanthroline

A ligand, 5-nitro-1,10-phenanthroline (phenNO2), was synthesized. Its Eu(III) complex with 2-thenoyltrifluoroacetone (HTTA) was prepared and characterized by elemental analysis, IR and 1H NMR spectra. The photophysical properties of the complex were studied in detail by using UV, luminescence spectra, luminescence lifetime and quantum yield. The complex exhibited nearly monochromatic red emission at 612 nm, a remarkable luminescence quantum yield at room temperature (36.0%) upon ligand excitation and a long 5D0 lifetime (458 μs), which indicated that the ligand phenNO2 could sensitize the luminescence of Eu(III) ion efficiently.     

1,10-邻二氮菲-苦味酸三元配合物分光光度法测定痕量铁

利用在醋酸 -醋酸钠缓冲溶液 (pH4.6)中Fe2 +与 1,10 -邻二氮菲 -苦味酸盐形成橙红色配合物的显色反应 ,建立了一种新的测定人发中痕量铁的分光光度法 ,用于正常人及患者头发中的痕量铁分析。     

长链羧酸铕四元配合物的合成及其发光性质

合成了铕与长链羧酸、二苯甲酰甲烷、邻菲啰啉形成的四元配合物,用元素分析、红外光谱、核磁共振氢谱和紫外光谱对所合成的铕四元配合物进行了表征。由于长链羧酸的引入,铕配合物在氯仿等挥发性有机溶剂中具有良好的溶解性,这为今后与高分子基体复合创造了条件。铕配合物在342nm光波激发下,发出以铕的特征发射谱线612nm左右为主的强荧光。     

Functional mesoporous carbon built from the 1,10-phenanthroline building block: A new class of catalyst support

A simple synthesis of a high surface area catalyst support composed of a nanoporous carbon architecture built from a 1,10-phenanthroline precursor is described.     

One Step Synthesis of NiO Nanoparticles via Solid-State Thermal Decomposition at Low-Temperature of Novel Aqua(2,9-dimethyl-1,10-phenanthroline)NiCl2 Complex

[NiCl₂(C₁₄H₁₂N₂)(H₂O)] complex has been synthesized from nickel chloride hexahydrate (NiCl₂·6H₂O) and 2,9-dimethyl-1,10-phenanthroline (dmphen) as N,N-bidentate ligand. The synthesized complex was characterized by elemental analysis, infrared (IR) spectroscopy, ultraviolet-visible (UV-vis) spectroscopy and differential thermal/thermogravimetric analysis (TG/DTA). The complex was further confirmed by single crystal X-ray diffraction (XRD) as triclinic with space group P-1. The desired complex, subjected to thermal decomposition at low temperature of 400 ºC in an open atmosphere, revealed a novel and facile synthesis of pure NiO nanoparticles with uniform spherical particle; the structure of the NiO nanoparticles product was elucidated on the basis of Fourier transform infrared (FT-IR), UV-vis spectroscopy, TG/DTA, XRD, scanning electron microscopy (SEM), energy-dispersive X-ray spectrometry (EDXS) and transmission electron microscopy (TEM).     

铕-苯甲酸-1,10-菲咯啉的合成及谱学性质

合成了稀土元素铕( )-苯甲酸-1,10-菲咯啉的三元配合物。通过元素分析和红外光谱确定了配合物的组成为EuL3phen(L∶苯甲酸根,phen∶1,10-菲咯啉)。通过发射光谱和激发光谱的测试表明,三元配合物在579、591、614、649、690nm处产生发射峰,分别归属于Eu3+的5D0→7F0、5D0→7F1、5D0→7F2、5D0→7F3、5D0→7F4跃迁。从发射光谱的峰强和激发光谱在200nm～380nm范围内产生宽而强的吸收峰可以得出第二配体phen的加入能显著增加Eu3+的发光强度,由此说明phen的加入更有利于配体吸收能量,也有利于配体更有效地向Eu3+传递能量。另外,对三元配合物的远红外光谱和拉曼光谱进行了分析。     

Studies on syntheses and properties of novel CeO2/polyimide nanocomposite films from Ce(Phen)3 complex

A series of cerium dioxide (CeO₂)/polyimide (PI) nanocomposites were successfully prepared from Ce(Phen)₃ and polyamic acid (PAA) via the solution direct-dispersing method, followed by a step thermal imidization process. TGA and XPS studies showed that the cerium complex decomposed to form CeO₂ during the thermal imidization process at 300 °C. SEM observation showed that the formed CeO₂ as nanoparticles was well dispersed in polyimide matrix with a size of about 50-100 nm for samples with different contents of CeO₂. Thermal analysis indicated that the introduction of CeO₂ decreased the thermal stability of nanocomposite films due to the decomposition of Ce(Phen)₃ in the imidization process, while the glass transition temperature (T_g) increased obviously, especially nanocomposite films with high loading of CeO₂ exhibited a trend of disappearance of T_g. DMTA and static tensile measurements showed that the storage modulus of nanocomposite films increased, while the elongation at break decreased with increasing CeO₂ content.