The mono(pyridine-N-oxide) analog of the H4dota macrocylic ligand, H3do3a-pyNO, is capable of forming thermodynamically stable and kinetically inert Ln(III) complexes. Its Eu(III) and Tb(III) complexes display a strong long-lived fluorescence as a result of the antenna effect of the pyridine-N-oxide fluorophore in the reagent. It is shown that H3do3a-pyNO can be used as a fluorogenic reagent for the determination of Eu(III) and Tb(III) at pH 6.5 and cL=1 mM. At an excitation wavelength of 286 nm, the emission maxima are 615 nm (Eu(III)-complex), and 547 nm (Tb(III)complex). Detection limits are at concentrations around 1.0 μM and linearity of the method spans over 2 orders of magnitude. The method was applied to artificial and real samples (spiked mineral waters, extracts from cathode ray tube luminophore dust) and gave satisfactory results. The method is simple, rapid, and hardly interfered by other metal ions. 相似文献
The reaction of Os3 (CO)10(NCCH3)2 and triethylamine provides H2 Os3 (CO)10 and HOs3 (CO)10(CHCHNEt2) in equimolar amounts. The structure of the latter compound has been shown to involve an iminium ion center anchored to the Os3 framework by a bridging (substituted) methylene moiety. 相似文献
The natural flavonoid compounds quercetin (3,3′,4′,5,7-pentahydroxyflavone) and luteolin (3′,4′,5,7-tetrahydroxyflavone) are
important bioactive compounds with antioxidative, anti-allergic, and anti-inflammatory properties. However, both are unstable
when exposed to atmospheric oxygen, which causes degradation and complicates their analytical determinations. The oxidative
change of these flavonoids was observed and followed by UV–visible spectrophotometry, both in aqueous and ethanolic solutions.
The distribution of the degradation products in aqueous media was monitored by LC–MS and LC–DAD analysis. The amounts of oxidative
reaction products increase with the exposure time. The oxidative degradation reduces the pharmacological efficiency of these
antioxidants and renders analytical determination inaccurate. The oxidative changes in flavonoid test solutions can explain
the inconsistent dissociation constants reported in the literature. Dissociation constants of quercetin and luteolin were
determined both by alkalimetric titration and by UV–visible spectrophotometry under deaerated conditions. The values pK1 = 5.87 ± 0.14 and pK2 = 8.48 ± 0.09 for quercetin, and pK1 = 5.99 ± 0.32 and pK2 = 8.40 ± 0.42 for luteolin were found. 相似文献
A new co-crystal of tetraaqua acrylato cobalt (II) complex and melamine, [Co(acr)2(H2O)4]·4MA·2DMF (acr = acrylate, MA = melamine, DMF = dimethylformamide), has been synthesized and characterized using IR, UV-Vis, thermogravimetric analysis, and single-crystal X-ray diffraction. The complex contains discrete unities of [Co(acr)2(H2O)4], melamine, and DMF linked by hydrogen bonds. Investigations evidenced that Co(II) has an octahedral stereochemistry and both acrylate ions present unidentate coordination mode. Thermal decomposition occurs in four steps and denotes that melamine is lost at high temperatures, and this indicates a greater stability that may be associated with the presence of hydrogen bonds network.
A series of new 4‐aryloctahydropyrido[1,2‐c]pyrimidine‐1,3‐diones 6a,b,d‐h and j were synthesized by intramolecular cyclization of α‐aryl‐α‐(1‐ethoxycarbonyl‐2‐piperidyl)‐acetamide derivatives 5a,b,d‐h and j . The structures of compounds were determined by 1H and 13C nmr spectroscopy. Nmr and X‐ray diffraction data indicate that the configuration at the C4, C4a stereocenters constitute RR and SS pair. 相似文献
We have designed and synthesised a new organometallic molecule containing three ferrocene groups for use as a highly sensitive electrochemical marker in biological assays. This trisferrocene derivative was conjugated to different PNA monomers, and the electrochemical activities of the conjugates were extensively investigated in organic solvents, in view of their potential diagnostic applications. The results showed that the introduction of a trisferrocene unit on the PNA monomer triples the current signal in comparison with the monoferrocene-labelled one. Despite their greater molecular complexity, trisferrocene-conjugated PNA monomers are even more electrochemically active than the reference ferrocene. By using differential pulse voltammetry (DPV), the detection limit can reach 10(-8) M in acetonitrile solution. These results are a good premise for the use of the trisferrocene unit as an effective electrochemical probe for biomolecules. 相似文献
The magnetic properties of lead selenide (PbSe) and indium-doped lead telluride (PbTe:In) composites have been studied by using the electron paramagnetic resonance (EPR) technique. The samples were obtained by using the pulsed laser deposition method (PLD). Temperature dependences of the EPR spectra were obtained. The analysis of the temperature dependencies of the integral intensity of the EPR spectra was performed using the Curie–Weiss law. In these materials, the paramagnetic centers of Pb1+ and Pb3+ ions were identified. The results are discussed. 相似文献
An extended viologen dication 1, containing one viologen subunit, was used as a model for the inclusion complex formation between cyclodextrin (CD) molecules and molecular wires comprising several subunits. UV–Vis and fluorescence spectroscopic measurements confirmed the formation of two types of the inclusion complexes 1:1 and 2:1 between αCD and 1 in the aqueous solution containing 20% of ethanol. The complex formation constants were obtained from the fluorescence spectral changes: Ka = 25 ± 3 mM?1 for [αCD–1] complex and Ka = 0.21 ± 0.07 mM?2 for [(αCD)2–1] complex, respectively. Cyclodextrins βCD and γCD do not form the inclusion complexes with 1 in these aqueous solutions. The time-dependent differential capacitance measurements confirmed the adsorption of 1 in the form of a complex at the electrode/electrolyte interface. These studies were conducted with the aim to find the most suitable CD cavity that would separate individual molecular wires from each other on the electrode/electrolyte interface. 相似文献