A novel technique of immobilizing indicator dyes by electrostatic adsorption and covalent bonding to fabricate optical sensors was developed.3-Amino-9-ethylcarbazole(AEC)was attached to the outmost surface of quartz g...A novel technique of immobilizing indicator dyes by electrostatic adsorption and covalent bonding to fabricate optical sensors was developed.3-Amino-9-ethylcarbazole(AEC)was attached to the outmost surface of quartz glass slide via aminosilanizing the slide,crosslinking chitosan,adsorbing Au nanoparticle,self-assembling HS(CH2)11OH,and coupling AEC.Thus, an AEC-immobilized optical sensor was obtained.The sensor exhibits a wide linear response range from 7.0×10- 7to 1.0×10 -4 mol/L and a correlation coefficient of 0.995 9 for the detection of 2-nitrophenol.The detection limit and response time of the sensor are 1.0×10- 7mol/L and less than 10 s,respectively.The fluorescence intensity of the used sensor can be restored to the blank value by simply rinsing with blank buffer.A very effective matrix for immobilizing indicator dye is provided by the proposed technique, which is adaptable to other indicator dyes with amino groups besides AEC.展开更多
3-Amino-9-ethylcarbazole （AEC） was employed for monosaccharide derivatization. The derivatives can be analyzed by high-performance liquid chromatography （HPLC） with an ultraviolet detection （wavelength： 254 nm）...3-Amino-9-ethylcarbazole （AEC） was employed for monosaccharide derivatization. The derivatives can be analyzed by high-performance liquid chromatography （HPLC） with an ultraviolet detection （wavelength： 254 nm）. Monosaccharides were quantitatively derivatized with 3-amino-9-ethylcarbazole （AEC） at 70 ℃ for 60 min. The method was linear for all samples over the concentration range tested （r〉0.999）, the precision was found to be satisfactory （R.S.D. 〈 3%）, and the recovery ratios were 〉98.62%. The stability analysis showed R.S.D. was between 1.81%-3.16%. Detection limits for the samples （D-glucose, L-xylose, D-mannose, L-arabinose, and L-rhamnose） ranged from 0.06 to 1.97 ng/mL （S/N=3）. Under the optimized derivatization and HPLC conditions, five monosaccharides were well separated using a narrow bore C18 column （250 mm×4.6 mm） with 0.1 mol/L ammonium acetate containing 25% acetonitrile at a flow rate of 0.5 mL/min. As an application, the method has been successfully applied to the determination of monosaccharide compositions of three polysaccharides SPPA-1, SPPB-1 and SPPC- 1 of Spirulina platensis. This method also has potential application to oligosaccharide or glycan analyses.展开更多
Agreen regioselective synthesis of some new and known 9-aryl-5,9-dihydropyrimido[4,5-d][l,2,4]triazolo[1,5-a]pyrimidine-6,8（4H,7H）-diones has been described via the microwave-assisted one-pot reaction of 3-amino-1H-...Agreen regioselective synthesis of some new and known 9-aryl-5,9-dihydropyrimido[4,5-d][l,2,4]triazolo[1,5-a]pyrimidine-6,8（4H,7H）-diones has been described via the microwave-assisted one-pot reaction of 3-amino-1H-1,2,4-triazoles,aromatic aldehydes and barbituric acids under solvent- and catalyst-free conditions.This operationally simple procedure is less laborious and provides a better scope than previously reported procedures.展开更多
基金Project(20775010)supported by the National Natural Science Foundation of ChinaProject(208095)supported by the Key Project ofMinistry of Education,China+1 种基金Project(07A006)supported by the Scientific Research Fund of Hunan Provincial Education Department,ChinaProject(07JJ3020)supported by Hunan Provincial Natural Science Foundation of China
文摘A novel technique of immobilizing indicator dyes by electrostatic adsorption and covalent bonding to fabricate optical sensors was developed.3-Amino-9-ethylcarbazole(AEC)was attached to the outmost surface of quartz glass slide via aminosilanizing the slide,crosslinking chitosan,adsorbing Au nanoparticle,self-assembling HS(CH2)11OH,and coupling AEC.Thus, an AEC-immobilized optical sensor was obtained.The sensor exhibits a wide linear response range from 7.0×10- 7to 1.0×10 -4 mol/L and a correlation coefficient of 0.995 9 for the detection of 2-nitrophenol.The detection limit and response time of the sensor are 1.0×10- 7mol/L and less than 10 s,respectively.The fluorescence intensity of the used sensor can be restored to the blank value by simply rinsing with blank buffer.A very effective matrix for immobilizing indicator dye is provided by the proposed technique, which is adaptable to other indicator dyes with amino groups besides AEC.
基金Project supported by the Hi-Tech Research and Development program of China （No. 2006AA02Z146）, the Natural Science Foundation of Shaanxi Province （No. 2005C131） and the Science and Technology Key Program of Ministry of Education of China （No. 206147）.
文摘3-Amino-9-ethylcarbazole （AEC） was employed for monosaccharide derivatization. The derivatives can be analyzed by high-performance liquid chromatography （HPLC） with an ultraviolet detection （wavelength： 254 nm）. Monosaccharides were quantitatively derivatized with 3-amino-9-ethylcarbazole （AEC） at 70 ℃ for 60 min. The method was linear for all samples over the concentration range tested （r〉0.999）, the precision was found to be satisfactory （R.S.D. 〈 3%）, and the recovery ratios were 〉98.62%. The stability analysis showed R.S.D. was between 1.81%-3.16%. Detection limits for the samples （D-glucose, L-xylose, D-mannose, L-arabinose, and L-rhamnose） ranged from 0.06 to 1.97 ng/mL （S/N=3）. Under the optimized derivatization and HPLC conditions, five monosaccharides were well separated using a narrow bore C18 column （250 mm×4.6 mm） with 0.1 mol/L ammonium acetate containing 25% acetonitrile at a flow rate of 0.5 mL/min. As an application, the method has been successfully applied to the determination of monosaccharide compositions of three polysaccharides SPPA-1, SPPB-1 and SPPC- 1 of Spirulina platensis. This method also has potential application to oligosaccharide or glycan analyses.
文摘Agreen regioselective synthesis of some new and known 9-aryl-5,9-dihydropyrimido[4,5-d][l,2,4]triazolo[1,5-a]pyrimidine-6,8（4H,7H）-diones has been described via the microwave-assisted one-pot reaction of 3-amino-1H-1,2,4-triazoles,aromatic aldehydes and barbituric acids under solvent- and catalyst-free conditions.This operationally simple procedure is less laborious and provides a better scope than previously reported procedures.
