Chemical effect on the K shell fluorescence yield of Fe, Mn, Co, Cr and Cu compounds

Chemical effects on the K shell fluorescence yields of Fe, Mn, Co, Cr and Cu compounds were investigated. Samples were excited using 59.5 keV energy photons from a²⁴¹ Am radioisotope source. K X-rays emitted by samples were counted by a Si(Li) detector with a resolution 160 eV at 5.9 keV. Chemical effects on the K shell fluorescence yields (ωk) for Fe, Mn, Co, Cr and Cu compounds were observed. The values are compared with theoretical, semiempirical fit and experimental ones for the pure elements.     

Fluorescence feedback control of a diode pumped solid state laser

We implement active feedback control in a Q-switched diode-pumped Nd:YVO₄ laser by monitoring the fluorescence intensity from the laser crystal. When the initial inversion level indicated by the detected fluorescence has reached a predetermined value, Q-switching is initiated. The Q-switched pulse energy is stabler with our feedback scheme based on the fluorescence intensity than that with the conventional Q-switching when pumping source is not stable.     

Beiträge zur Chemie der Pyrrolpigmente, 84. Mitt.: Darstellung und Lumineszenz bichromophorer 5-Aryl-dipyrrinderivate

Summary 1,3- and 1,4-Bis-dipyrrin-benzenes and their various zinc and difluoroboryl chelates are prepared. Their absorption and fluorescence spectra are compared with those of the corresponding mono-dipyrrin derivatives. The conformations of these compounds are analyzed using the ring current model and absorption spectra. Dipole-dipole type transfer of excitation energy is discussed to represent a main photophysical channel in these compounds.

     

Novel fluorescent asparaginyl-N-acetyl-d-glucosamines (Asn-GlcNAc) for the resolution of oligosaccharides in glycopeptides, based on enzyme transglycosylation reaction

Several fluorescent asparaginyl-N-acetyl-d-glucosamines (Asn-GlcNAcs), i.e., DBD-Asn-GlcNAc, NBD-Asn-GlcNAc, NDA-Asn-GlcNAc, PS-Asn-GlcNAc, FITC-Asn-GlcNAc, DMEQ-Asn-GlcNAc and DBD-PZ-Boc-Asn-GlcNAc, were synthesized as the acceptors for the resolution of oligosaccharides in glycopeptides. The resolution of oligosaccharides is based on the transglycosylation reaction with end-β-N-acetylglucosaminidase (Endo-M), isolated from Mucor hiemalis. The synthesis of each fluorescent acceptor was carried out in a one-pot reaction of Asn-GlcNAc and the corresponding fluorescent tagging reagent. The transglycosylation reaction using Endo-M proceeds at RT in neutral phosphate buffer (pH 6.0) and reached maxima at around 30 min. When Fmoc-Asn-GlcNAc (acceptor) was enzymatically reacted with Disialo-Asn (donor) in the presence of Endo-M, the ratio of Disialo-Asn-Fmoc (transglycosylation product) was almost comparable with the decreasing ratio of Fmoc-Asn-GlcNAc. Therefore, the transglycosylation activity of Endo-M from Disialo-Asn (donor) and fluorescent-Asn-GlcNAc (acceptor) was calculated from the decreasing ratio of fluorescent-Asn-GlcNAc. The order was NDA-Asn-GlcNAc > DBD-Asn-GlcNAc Fmoc-Asn-GlcNAc > NBD-Asn-GlcNAc DMEQ-Asn-GlcNAc > DNS-Asn-GlcNAc > PS-Asn-GlcNAc > FITC-Asn-GlcNAc. On the other hand, the activity with a fluorescent acceptor (DBD-PZ-Boc-Asn-GlcNAc), labeled to a carboxylic acid group in the Asn residue, was the strongest among the synthesized acceptors.     

顺序式X射线荧光光谱仪常见故障的诊断方法

介绍顺序式X射线荧光光谱仪5种常见故障的诊断及处理方法。故障部位包括X射线装置、样品室和光谱室的真空、探测器、晶体和测角仪。     

Fluorescent determination of graphene quantum dots in water samples

This work presents a simple, fast and sensitive method for the preconcentration and quantification of graphene quantum dots (GQDs) in aqueous samples. GQDs are considered an object of analysis (analyte) not an analytical tool which is the most frequent situation in Analytical Nanoscience and Nanotechnology. This approach is based on the preconcentration of graphene quantum dots on an anion exchange sorbent by solid phase extraction and their subsequent elution prior fluorimetric analysis of the solution containing graphene quantum dots. Parameters of the extraction procedure such as sample volume, type of solvent, sample pH, sample flow rate and elution conditions were investigated in order to achieve extraction efficiency. The limits of detection and quantification were 7.5 μg L⁻¹ and 25 μg L⁻¹, respectively. The precision for 200 μg L⁻¹, expressed as %RSD, was 2.8%. Recoveries percentages between 86.9 and 103.9% were obtained for two different concentration levels. Interferences from other nanoparticles were studied and no significant changes were observed at the concentration levels tested. Consequently, the optimized procedure has great potential to be applied to the determination of graphene quantum dots at trace levels in drinking and environmental waters.     

A novel chemosensor based on Fe(III)-complexation for selective recognition and rapid detection of fluoride anions in aqueous media

A novel fluorogenic receptor 1 was prepared by the reaction of thiosemicarbazide with 1-naphthaldehyde. Based on in situ-formed 1-Fe(III) complexes having the specific binding affinity for F⁻ anions, this sensory system allows rapid recognition and quantitative detection of fluoride in neutral aqueous media in an ‘off-on’ fashion. The fluoride measurement method not only exhibits a low detection limit but also has strong anti-interference ability to common coexisting ions, as evidenced by competitive experiments.     

Tetrapyridyl tetraphenylethylenes: supramolecular building blocks with aggregation-induced emission properties

Two tetrapyridyl-substituted tetraphenylethylenes have been prepared via Suzuki coupling between tetrabromo tetraphenylethylene and 3- or 4-pyridine boronic acid. Both compounds exhibit aggregation-induced emission as determined by solid state fluorescence spectroscopy and solution phase fluorescence measurements performed in aqueous/organic solvent mixtures. Solution phase fluorescence was also found to be switchable as a function of pH. 3-Pyridyl-substituted tetraphenylethylene has been structurally characterized by X-ray crystallography.     

A coumarin-based fluorescent PET sensor utilizing supramolecular pKa shifts

A new coumarin derivative containing benzothiazole and piperazine substituents was synthesized. Preferential inclusion of the benzothiazole group, over the coumarin and piperazine groups, inside the cavity of the molecular container cucurbit[7]uril (CB7) was evidenced by using optical and NMR techniques. The binding constant of the new complex with CB7 is higher in its protonated forms (e.g., K = 2.8 × 10⁶ M⁻¹) than in its neutral forms, which led to an increase in the pK_a value associated with protonation of the aza nitrogen on the benzothiazole ring of ca. 2.5 units. Such CB7-induced protonation disabled the photoinduced electron transfer (PET) in the included molecule, enhancing its coumarin fluorescence up to ca. 45-fold (pH 3.5, 410 nm). The results are discussed in the context of designing sensitive analytical tools for reversible monitoring of optically inactive analytes by competitive displacement experiments.     

A new class of fluorescent dyes based on 1,3-benzodioxole and [1,3]-dioxolo[4.5-f]benzodioxole

We report on synthesis and photophysical properties of a new class of fluorescent dyes. They are characterized by large Stokes-shifts, long fluorescence lifetimes in organic solvents and a pronounced dependency of the fluorescence lifetime on the solvent polarity. Also worthy of note is the high bleaching stability. To provide access to biochemical and medical applications a series of derivatives were prepared, which exhibit specific reactivity towards different biologically relevant functional groups (carboxylic acids, amines, maleimides, N-hydroxysuccinimide esters). Furthermore, two alkynes were prepared, which could be used in ‘Click’ chemistry.