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排序方式: 共有330条查询结果,搜索用时 15 毫秒
1.
Karakuş Erman Erdemir Eda Suna Garen Liv Lokman Gunduz Simay Can Şevval Arzu 《Journal of fluorescence》2021,31(6):1617-1625
Journal of Fluorescence - We have constructed a novel fluorescein-based fluorescent chemosensor, FL-In, functionalised with an indole moiety and capable of sensing by both the optical... 相似文献
2.
The hydrothermal syntheses of the alkali metal molybdenum bronzes from starting solids (HxMoO3) with structural affinities to the desired products were investigated. Single-phase potassium blue and red bronzes were prepared by the hydrothermal treatments at around 430 K, and characterized by powder X-ray diffraction, IR spectroscopy, and SEM. The formation processes of these two bronzes during the hydrothermal treatments were found to differ. The blue bronze was formed by a structure-inheriting solid-state route from HxMoO3 with x<0.3, whereas the red bronze was formed for x>0.3 through a solution dissolution/deposition route via the formation of MoO3+MoO2. 相似文献
3.
A simple synthesis of 3,3,3-trifluoropropenyl compounds by means of the TBAF-mediated Horner reaction is described. The reagent, 2,2,2-trifluoroethyldiphenylphosphine oxide, was readily prepared either by Arbuzov reaction of ethyl diphenylphosphinite with 2,2,2-trifluoroethyl iodide or by treating chlorodiphenylphosphine with trifluoroacetic acid and water. Treatment of the phosphine oxide with aromatic aldehydes in the presence of TBAF at room temperature afforded the corresponding 3,3,3-trifluoropropenyl compounds in good yields. The present method is very convenient for preparing 3,3,3-trifluoropropenyl compounds from aromatic aldehydes in terms of availability of the reagent, operational simplicity, and good yields of the products. 相似文献
4.
Bunzo Eda Machio Iwasaki 《Journal of polymer science. Part A, Polymer chemistry》1986,24(9):2119-2129
In the γ-irradiated aromatic epoxy resin, diglycidylether of bisphenol A cured with diaminodiphenylmethane, the cyclohexadienyl-type radical is produced as one of the main radical species. Although both the resin and the hardener contain benzene rings, it is concluded that the cyclohexadienyl-type radical is formed by selective addition of the OH hydrogen to the benzene ring on the resin side. The selectivity is accounted for in terms of electron capture by the benzene ring followed by proton transfer from the OH group which is located in front of the benzene ring. This reaction scheme is further supported by the effect of the addition of an electron scavenger on the radical yield as well as by the photobleaching behavior of the radicals involved. 相似文献
5.
Samples of nominal 18 carat and 21 carat gold jewelleries from the local market were non-destructively bulk analyzed using neutron activation analysis. Neutrons of 14 MeV energy were used with a fast pneumatic sample transfer system. The actual gold contents, as well as the composition of the base metals in these samples were determined. The fast neutron activation was found to be an efficient, quick and accurate method of characterizing the precious metal objects routinely in bulk, with a large sample throughput. The results demonstrate the commercial availability of the technique for non-destructive bulk analysis of precious metal objects. 相似文献
6.
7.
We have determined the crystal structure of the title compound, which has a triclinic cell with cell parameters of , , , α=76.617°, β=84.188°, γ=74.510° and space group . The crystal structure suggests the chemical formula CoMoO4·3/4H2O. The structure consists of MoO4 tetrahedra and CoO6 octahedra, confirming the earlier X-ray absorption near-edge spectroscopic (XANES) investigation on the hydrate. The comparison of the crystal structures of the hydrate and the α-,β-, and hp-phases shows that the hydrate exhibits metal cation coordinations similar to those of the β-phase, but had arrangements of CoO6 and MoOn polyhedra similar to those of the hp-phase. 相似文献
8.
A study of structural modifications of MPB-07 was undertaken as part of a synthetic program aimed at discovering small molecules with CFTR activation potential. Solid-phase synthesis techniques were used to prepare derivatives of MPB-07 employing the Zincke reaction for the construction of aromatic, quaternary ammonium salts such as those found in 2 or 3. In this transformation, primary amines react with highly electrophilic N-2,4-dinitrophenylpyridinium (DNP) salt 4 to afford pyridinium salt 8 with release of 2,4-dinitroaniline 6. Thus, the reaction of 1-(2,4-dinitrophenyl)pyridinium salts with various polymer-bound amino ethers, followed by cleavage from the resin, delivers the desired salts in good yield and high purity. 相似文献
9.
Abstract— Time-resolved measurements were made of near-infrared emission from 5-( N -hexadecanoyl)amino-eosinlabeled L1210 leukemia cells following pulsed-laser excitation. The cells were suspended in phosphate-buffered saline made with deuterium oxide solvent. A significant fraction of the emission occuring10–80 μs after the laser pulse was due to singlet oxygen. This singlet-oxygen emission is believed to result from singlet oxygen generated near the cell-membrane surface, where 5-( N -hexadecanoyl)amino eosin is known to concentrate, and then diffusing out into the buffer. The intensity and the kinetics of the experimentally observed singlet-oxygen emission were in excellent agreement with the predictions of a theoretical one-dimensional model of singlet-oxygen diffusion and quenching.
During the10–80 μs time period studied, most of the singlet oxygen was located in the buffer. Thus, the use of water-soluble singlet-oxygen quenchers, such as histidine, provide one means of separating the singlet-oxygen emission quenchers, such as histidine, provide one means of separating the singlet-oxygen emission from other sources of light during this time interval. 相似文献
During the10–80 μs time period studied, most of the singlet oxygen was located in the buffer. Thus, the use of water-soluble singlet-oxygen quenchers, such as histidine, provide one means of separating the singlet-oxygen emission quenchers, such as histidine, provide one means of separating the singlet-oxygen emission from other sources of light during this time interval. 相似文献
10.
A. Aksoy 《Journal of Radioanalytical and Nuclear Chemistry》1993,169(2):463-469
The absolute total and full-energy peak (FEP) efficiencies of a high purity germanium (HPGe) photon detector are measured in the energy range from 40 keV to 1500 keV. The functional parameters are fitted to the calibration points from 14 long-lived standard sources (129I,241Am,109Cd,57Co,139Ce,137Cs,54Mn,65Zn,60Co,22Na,133Ba,152Eu,154Eu and166mHo) within an accuracy better than the quoted uncertainty of the calibration sources. The efficiencies in far and close geometries are compared. 相似文献