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81.
This study presents electrostatically self‐assembled nanoparticles from linear flexible polyelectrolytes (poly(diallyldimethylammonium chloride or quarternized poly(4‐vinylpyridine)) and an ionic photo‐isomerizable azo dye (Acid Yellow 38) that can change their size upon UV‐light irradiation. Assemblies with narrow size distribution are stable in aqueous solution. For samples with under‐stoichiometric dye load, UV‐light exposure triggers a size decrease, e.g. from a hydrodynamic radius of Rh = 94 nm to Rh = 62 nm for an Ay38‐PDADMAC sample with a charge ratio of lcharge = 0.7. Size changes are caused by trans‐cis isomerization of the dye, accompanied by a change in hydrophilicity, binding enthalpy and entropy. Assemblies are characterized by static and dynamic light scattering, atomic force microscopy, UV–vis spectroscopy and isothermal titration calorimetry. Zeta potential measurements give insight into the electrostatic stabilization and size‐control of the ionic nano‐assemblies, revealing a master curve of effective surface charge density versus hydrodynamic radius. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys., 2013 相似文献
82.
通过水热方法,采用H3CAM(H3CAM=4-hydroxy-pyridine-2,6-dicarboxylic acid)与Cd(NO3)2.4H2O反应,合成了1个镉配位聚合物[Cd4(HCAM)4(H2O)8]n(1),并对其结构和荧光性质进行了研究。结构分析结果表明该配合物属于单斜晶系,C2/c空间群。四个HCAM2-配体桥联4个镉离子形成了1个四核镉单元。这些孤立的单元通过氢键作用形成了1个三维配位框架。研究表明,该配合物在室温下能发出兰色荧光。 相似文献
83.
Nandhagopal RajaRengan Ramesh 《Tetrahedron letters》2012,53(35):4770-4774
A convenient and general method of synthesis of binuclear ruthenium(II) pyridazine complex was reported. The synthesized complex was characterized by analytical and spectral methods. The structure of the complex was confirmed by X-ray diffraction technique and was found to be an efficient catalyst for the transfer hydrogenation of ketones with excellent conversions in the presence of isopropanol/KOH at 82 °C. The effect of solvents, bases, and different catalyst/substrate ratio for the reaction was also investigated. 相似文献
84.
《Analytical letters》2012,45(1):57-61
Abstract A new method for the determination of the titre of ascorbic acid standard solutions employing potassium dichromate as a primary standard has been developed. In a pyrophosphate medium, the pyrophosphate complex of divalent manganese is oxidized by dichromate to the pyrophosphate complex of tervalent manganese; the latter oxidizes o-tolidine reversibly with formation of the corresponding quinonediimine, which is visually titrated by the ascorbic acid standard solution. 相似文献
85.
Abstract. A novel germanate compound, |[Ni(dien)2]3(H2O)3|[Ge7O13F5]2(designated JU‐85, dien = diethylenetriamine), was solvothermally synthesized. The structure of JU‐85 was determined by single‐crystal X‐ray diffraction and further characterized by powder X‐ray diffraction, inductively coupled plasma, infrared spectroscopy, elemental analysis, and thermogravimetric analysis. JU‐85 has dissymmetric chains constructed from diagonally linked Ge7 building units and various Ni(dien)22+ complexes formed in situ during the synthesis. Compared with its structural analogue, FJ‐6, JU‐85 contains less complex cations and different host‐guest assembly. Besides the diagonal linkage in JU‐85, other dissymmetric linkages of Ge7 building units were enumerated, which could be used as the stereogenic centers for the design of novel chiral germanate compounds. 相似文献
86.
《Journal of Coordination Chemistry》2012,65(4):393-402
The reaction of CuCl2 with 2-amino-5-cyanopyridine and HCl in 1-propanol gave bis(2-amino-5-cyanopyridinium) diaquadichlorocopper(II) dichloride (1). Crystal data for 1 are: monoclinic, space group: P21/c, a = 8.461(3) Å, b=14.665(5) Å, c=7.883(3) Å, g =96.105(4)°, V=972.6(6) Å 3 , Z=2, Dcalc =1.645 Mg/m3, w =1.691 mm?1, F(OOO)=486, MoK f( u =0.71073 Å), R1=0.0431 for [∣I∣ S 2 σ (I)] and R1=0.0680 for all 1944 unique reflections and 130 parameters. The structure exists as square planar Cu(H2O)2Cl2 units with long semi-coordinate bonds to the cyano nitrogens of the 2-amino-5-cyanopyridinium ions. Hydrogen bonding from the water molecules and N―H hydrogens to the chloride irons stablises the lattice. 相似文献
87.
《Journal of Coordination Chemistry》2012,65(7):1212-1220
A tetranuclear Zn(ΙΙ) complex, [Zn4L2(OAc)2(CH3OH)2] with an unsymmetric Salen-type bisoxime (H3L?=?6-hydroxy-4′,6′-dibromo-2,2′-[ethylenediyldioxybis(nitrilomethylidyne)]diphenol), has been synthesized and structurally characterized. There are two kinds of coordination geometry (trigonal bipyramidal and square pyramidal) in the Zn(ΙΙ) complex. The molecule has serious distortion probably from the asymmetry. The complex exhibits blue emission with the maximum emission wavelength λ max?=?423?nm when excited with 340?nm. 相似文献
88.
《Journal of Coordination Chemistry》2012,65(7):1266-1277
Two new rhenium(I) complexes chelated by a substituted 2,2′-bipyridine with general formula Re(CO)3LCl, where L?=?6?-(2″-methoxyphenyl)-2,2′-bipyridine (L1 ) and 6?-(4″-diphenylaminophenyl)-2,2′-bipyridine (L2 ), are synthesized and characterized by IR, NMR, and elemental analysis. Structure of 1 was determined by single-crystal X-ray crystallography, revealing that rhenium is six-coordinate octahedral. The electrochemical, photophysical, and thermal properties of the two rhenium(I) complexes were investigated. Electroluminescent devices were fabricated by doping 1 in polymer blend host of poly(vinylcarbazole) and 2-tert-butylphenyl-5-biphenyl-1,3,4-oxadiazole using simple solution spin-coating technique. The device exhibits a maximum current efficiency of 2.97?cd?A?1 and peak brightness in excess of 2390?cd?m?2. 相似文献
89.
《Journal of Coordination Chemistry》2012,65(10):1812-1820
A Fe(III) complex with Cl counter ion based on a branched Schiff base has been synthesized and studied. The compound was produced by the reaction of the Schiff base with FeCl3 at room temperature in benzene–ethanol. The complex is symmetric, i.e., bis-chelate, with an octahedral coordination of Fe. The compound revealed phase transitions of the “solid–solid” type. The complex displayed a temperature-induced spin transition (S?=?1/2???5/2) which was detected by EPR. 相似文献
90.
《Journal of Coordination Chemistry》2012,65(22):3914-3922
Two octacyanometallate-based NiII–MIV [M?=?Mo(1), W(2)] bimetallic assemblies chelated with tetradentate macrocyclic ligands have been synthesized by slow diffusion and characterized structurally. In both complexes, M and Ni centers acting as linker and connector, respectively, are connected by M–CN–Ni–NC–M linkages to form a 3-D diamond-type topological network. Magnetic behaviors of both complexes show a very weak antiferromagnetic interaction between NiII ions mediated by the diamagnetic [M(CN)8]4? bridges. 相似文献