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991.
A novel hyperbranched conjugated chemosensor with bipyridyl groups as periphery groups(BPY-HPV) was synthesized.BPY-HPV was highly sensitive to metal ions(Cu2+,Ni2+) for the strong coordination interaction(Ksv at the order of 107 mol-1 L) monitored by fluorescence spectroscopy.Moreover,by hydrogen bonds and charge transfer interaction,BPY-HPV shows strong interaction with 1,1,2,2-tetrachloroethane whatever in CH2Cl2(Ksv~106 mol-1 L) or film. 相似文献
992.
A novel fluorescent Zn2+ probe based on 6-methoxyquinolin was synthesized in four steps from inexpensive starting materials.It exhibits very strong fluorescence responses and has a remarkably high selectivity to Zn2+ than other physiological relevant metal ions.This new compound could be used as low-priced yet high-quality Zn2+ probe. 相似文献
993.
Hai Guang Zhang Xu Tang Tao Kao Shan Chen Chun Xue Yuan Shi Na Yan Min Hua Jiang 《中国化学快报》2011,22(6):647-650
A new acid-base fluorescent switch containing both imidazo[4,5-f][1,10]-phenanthroline and triphenylamine groups has been synthesized.Its fluorescence emissions and absorptions can be reversibiy changed through protonation/deprotonation of imidazole and amine moiety by controlling the intramolecular charge transfer(ICT) process,leading to off-on-off fluorescent molecular switching. 相似文献
994.
995.
996.
Health or environmental issue caused by abnormal level of metal ions like Zn2+ or Cd2+ is a worldwide concern. Developing an inexpensive and facile detection method for Zn2+ and Cd2+ is in urgent demand. Due to their super optical properties, fluorescent quantum dots (QDs) have been developed as a promising alternative for organic dyes in fluorescence analysis. In this study, a CdTe QDs-based sensitive and selective probe for Zn2+ and Cd2+ in aqueous media was reported. The proposed probe worked in fluorescence “turn-on” mode. The initial bright fluorescence of CdTe QDs was effectively quenched by sulfur anions (S2−). The presence of Zn2+ (or Cd2+) can “turn-on” the weak fluorescence of QDs quenched by S2− due to the formation of ZnS (or CdS) passivation shell. Under optimal conditions, a good linear relationship between the fluorescence response and concentration of Zn2+ (or Cd2+) could be obtained in the range from 1.6 to 35 μM (1.3–25 μM for Cd2+). The limit of detection (LOD) for Zn2+ and Cd2+ were found to be 1.2 and 0.5 μM, respectively. Furthermore, the present probe exhibited a high selectivity for Zn2+ and Cd2+ over other metal ions and was successfully used in the detection of Zn2+ or Cd2+ in real water samples. 相似文献
997.
Angela Cardelli Lucia Ricci Giacomo Ruggeri Silvia Borsacchi Marco Geppi 《European Polymer Journal》2011,(8):1589-1600
A micrometric silica modified with perylene derivative (SiO2–TES) has been prepared by hydrolysis–condensation reactions between silica and N,N’-bis-(3-triethoxysilylpropyl)-perylene-tetracarboxyldiimide (P-TES) and utilized as filler in LLDPE films together with a compatibilizer. Spectroscopic analyses on SiO2–TES confirmed the grafting of P-TES on silica, while its amount was determined by thermogravimetric analysis. Solid state NMR provided information about the structure of silicon atoms involved in the condensation of SiO2 and P-TES that resulted mainly in silicon atoms grafted with bi-dentate anchorages.UV–Vis and fluorescence analyses carried out on P-TES showed the ability of the dye to generate J-type aggregates in apolar solvents. The same analyses on SiO2–TES revealed the presence of both isolated and aggregated dye molecules grafted on silica surface, while on polymeric dispersions of SiO2–TES, they have shown only the presence of P-TES aggregates grafted to silica.Thanks to the direct correlation between optical properties (obtained both by UV–Vis and by fluorescence analyses) and the chemical environment of composites, the luminescent silica SiO2–TES could be used to estimate the filler dispersion extent in different microcomposite polymer materials. 相似文献
998.
S-nitrosylated proteins are biomarkers of oxidative damage in aging and Alzheimer's disease (AD). Here, we report a new method for detecting and quantifying nitrosylated proteins by capillary gel electrophoresis with laser induced fluorescence detection (CGE-LIF). Dylight 488 maleimide was used to specifically label thiol group (SH) after switching the S-nitrosothiol (S-NO) to SH in cysteine using the "fluorescence switch" assay. In vitro nitrosylation model-BSA subjected to S-nitrosoglutathione (GSNO) optimized the labeling reactions and characterized the response of the LIF detector. The method proves to be highly sensitive, detecting 1.3 picomolar (pM) concentration of nitrosothiols in nanograms of proteins, which is the lowest limit of detection of nitrosothiols reported to date. We further demonstrated the direct application of this method in monitoring protein nitrosylation damage in MQ mediated human colon adenocarcinoma cells. The nitrosothiol amounts in MQ treated and untreated cells are 14.8±0.2 and 10.4±0.5 pmol/mg of proteins, respectively. We also depicted nitrosylated protein electrophoretic profiles of brain cerebrum of 5-month-old AD transgenic (Tg) mice model. In Tg mice brain, 15.5±0.4 pmol of nitrosothiols/mg of proteins was quantified while wild type contained 11.7±0.3 pmol/mg proteins. The methodology is validated to quantify low levels of S-nitrosylated protein in complex protein mixtures from both physiological and pathological conditions. 相似文献
999.
Hydrophilic-interaction liquid chromatography (HILIC), reversed-phase chromatography (RPC) and porous graphitic carbon (PGC) chromatography are typically applied for liquid chromatographic separations of protein N-glycans. Hence the performances of these chromatography modes for the separation of fluorescently labeled standard glycan samples (monoclonal antibody, fetuin, ribonuclease-B) covering high-mannose and a broad range of complex type glycans were investigated. In RPC the retention of sialylated glycans was enhanced by adding an ion-pairing agent to the mobile phase, resulting in improved peak shapes for sialylated glycans compared to methods recently reported in literature. For ion pairing RPC (IP-RPC) and HILIC ultra-high performance stationary phases were utilized to maximize the peak capacity and thus the resolution. But due to the shallow gradient in RPC the peak capacity was lower than on PGC. Retention times in HILIC and IP-RPC could be correlated to the monosaccharide compositions of the glycans by multiple linear regression, whereas no adequate model was obtained for PGC chromatography, indicating the significance of the three-dimensional structure of the analytes for retention in this method. Generally low correlations were observed between the chromatography methods, indicating their orthogonality. The high selectivities, as well as the commercial availability of ultra-high performance stationary phases render HILIC the chromatography method of choice for the analysis of glycans. Even though for complete characterization of complex glycan samples a combination of chromatography methods may be necessary. 相似文献
1000.
Zhang LN Wu FY Liu AH 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2011,79(1):97-103
A new compound, 2,5-di-[2-(4-hydroxy-phenyl)ethylene]-terephthalonitrile (DHPEPN), was synthesized. The interaction between bovine serum albumin (BSA) and DHPEPN in Tris-HCl buffer solution (pH 7.4) was investigated using fluorescence and UV-vis absorption spectroscopy. The mechanism of BSA fluorescence quenched by DHPEPN is discussed according to the Stern-Volmer equation. The binding constant and the thermodynamic parameters ΔH, ΔS, ΔG at different temperatures were calculated. The results indicate that the van der Waals interaction and hydrogen bonding play major roles in the binding process. The distance between BSA and DHPEPN is estimated to be 3.59 nm based on the F?rster resonance energy transfer theory. The spectral changes of synchronous fluorescence and three-dimensional fluorescence suggest that both of the microenvironment of DHPEPN and the conformation of BSA are changed during binding between DHPEPN and BSA. 相似文献