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101.
《Electroanalysis》2018,30(8):1865-1869
In this paper, a method based on chromatographic separation of analytes and their quantification using on‐line cyclic voltammetry is reported. The method based on high performance liquid chromatography on reverse phase column was optimized using free nucleobases‐guanine, adenine, thymine, and cytosine. The optimal separation of nucleobases was detected when using 0.05 M borate buffer (pH 9.0) as the mobile phase, at isocratic flow rate 1 mL min−1, and at separation column temperature of 30 °C. The accurate timing of the cyclic voltammetry enabled us to quantify the concentrations of individual nucleobases by oxidation on glassy carbon electrode. 相似文献
102.
Araki Y Mukaisyo K Sugihara H Fujiyama Y Hattori T 《Journal of separation science》2008,31(15):2827-2830
In the present study, we developed a novel, simple, and specific detection method using an RP-HPLC at UV 285 nm for the separation and quantification of N-nitroso-bile acids. First, we found that N-nitroso-bile acids have a specific spectrophotometric absorbance at 285 nm. Using this 285 nm detection system, we could especially measure N-nitroso-bile acids, even in co-existence of non-N-nitroso-bile acids. Next, we observed the decomposition of N-nitroso-glychocholate under alkaline, acidic, and neutral conditions. N-nitroso-glychocholate rapidly decomposed under alkaline conditions (pH 9) (t(1/2) = 0.96 h), but remained fairly stable under acidic (pH 2) (t(1/2) = 12.8 h) and neutral (pH 7) (t(1/2) = 7.8 h) conditions. This study is the first report, which simply and specifically analyzes N-nitroso-bile acids using an RP-HPLC system. 相似文献
103.
104.
Reverse flow injection spectrophotometric determination of iron(III) using chlortetracycline reagent
Ruengsitagoon W 《Talanta》2008,74(5):1236-1241
A simple reversed flow injection colourimetric procedure for determining iron(III) was proposed. It is based on the reaction between iron(III) with chlortetracycline, resulting in an intense yellow complex with a suitable absorption at 435 nm. A 200 μl chlortetracycline reagent solution was injected into the phosphate buffer stream (flow rate 2.0 ml min−1) which was then merged with iron(III) standard or sample in dilute nitric acid stream (flow rate 1.5 ml min−1). Optimum conditions for determining iron(III) were investigated by univariate method. Under the optimum conditions, a linear calibration graph was obtained over the range 0.5–20.0 μg ml−1. The detection limit (3σ) and the quantification limit (10σ) were 0.10 and 0.82 μg ml−1, respectively. The relatives standard deviation of the proposed method calculated from 12 replicate injections of 2.0 and 10.0 μg ml−1 iron(III) were 0.43 and 0.59%, respectively. The sample throughput was 60 h−1. The proposed method has been satisfactorily applied to the determination of iron(III) in natural waters. 相似文献
105.
The growth kinetics for AgI nanoparticles formed in the solutions of water/AOT reverse micelles in n-hexane, n-octane, n-decane, and n-dodecane were investigated. In small micelles, the rate of nanoparticles growth was found to be independent of the type of solvent, while in large micelles the growth rate grew with increasing length of solvent molecules. The effect was explained by a different amount of free water in the micelle pools of the same size. 相似文献
106.
Jianbo Yu Aidaer Muhetaer Xiaowen Gao Zhenzhen Zhang Yuying Yang Prof. Qi Li Prof. Langxing Chen Prof. Haichao Liu Prof. Dongsheng Xu 《Angewandte Chemie (International ed. in English)》2023,62(28):e202303135
Photo-assisted reverse water gas shift (RWGS) reaction is regarded green and promising in controlling the reaction gas ratio in Fischer Tropsch synthesis. But it is inclined to produce more byproducts in high H2 concentration condition. Herein, LaInO3 loaded with Ni-nanoparticles (Ni NPs) was designed to obtain an efficient photothermal RWGS reaction rate, where LaInO3 was enriched with oxygen vacancies to roundly adsorbing CO2 and the strong interaction with Ni NPs endowed the catalysts with powerful H2 activity. The optimized catalyst performed a large CO yield rate (1314 mmol gNi−1 h−1) and ≈100 % selectivity. In situ characterizations demonstrated a COOH* pathway of the reaction and photoinduced charge transfer process for reducing the RWGS reaction active energy. Our work provides valuable insights on the construction of catalysts concerning products selectivity and photoelectronic activating mechanism on CO2 hydrogenation. 相似文献
107.
Hongmin Wang Shuting Fu Bo Shang Sungho Jeon Yiren Zhong Nia J. Harmon Chungseok Choi Eric A. Stach Hailiang Wang 《Angewandte Chemie (International ed. in English)》2023,62(30):e202305251
Photothermal CO2 reduction is one of the most promising routes to efficiently utilize solar energy for fuel production at high rates. However, this reaction is currently limited by underdeveloped catalysts with low photothermal conversion efficiency, insufficient exposure of active sites, low active material loading, and high material cost. Herein, we report a potassium-modified carbon-supported cobalt (K+−Co−C) catalyst mimicking the structure of a lotus pod that addresses these challenges. As a result of the designed lotus-pod structure which features an efficient photothermal C substrate with hierarchical pores, an intimate Co/C interface with covalent bonding, and exposed Co catalytic sites with optimized CO binding strength, the K+−Co−C catalyst shows a record-high photothermal CO2 hydrogenation rate of 758 mmol gcat−1 h−1 (2871 mmol gCo−1 h−1) with a 99.8 % selectivity for CO, three orders of magnitude higher than typical photochemical CO2 reduction reactions. We further demonstrate with this catalyst effective CO2 conversion under natural sunlight one hour before sunset during the winter season, putting forward an important step towards practical solar fuel production. 相似文献
108.
Hongmin Liu Chunxiu Liu Liying Jiang Jian Liu Qingde Yang Zonghui Guo Xinxia Cai 《Electroanalysis》2008,20(2):170-177
An osmium redox hydrogel mediated biosensor for continuous monitoring of glucose extracted from subcutaneous solution by reverse iontophoresis has been developed. For the measurement of low concentration glucose, osmium‐poly(vinylpyridine) wiring horseradish peroxidase was introduced to modify the smooth Au electrodes, and the developed glucose biosensor exhibited a high sensitivity of 11.45 nA μM?1 cm?2 and a low detection limit of 2 μM, as well as a high operational stability of more than 97% of its initial activity over a test period of 13.5 h in stirred glucose solution at low applied potential (?0.1 V vs. Ag|AgCl), efficiently inhibiting the electroactive interferences. Permeability of the hydrogels was studied and a diffusion coefficient of 2.4×10?5 cm2/s for H2O2 was obtained. In addition, the effects, such as temperature and the variation happening on Ag|AgCl counter electrode, on determination of glucose were also considered. The proof‐of‐feasibility of the biosensors for the monitoring of the glucose extracted from the subcutaneous solution was tested in vitro, and the responses of the sensors were analyzed. A linear response to current produced by extracted glucose in the concentration range of subcutaneous glucose from 1.0 to 12 mM was obtained with a correlation coefficient up to 0.989. These results testify the feasibility of the developed sensors for measuring the low concentration glucose and have significance for the development of noninvasive glucose monitoring system for the control of diabetes. 相似文献
109.
Nan Zhang Ying Li Dr. Sanyang Han Dr. Ying Wei Huan Hu Ran Huo Dr. Chunbo Duan Dr. Jing Zhang Dr. Chunmiao Han Prof. Guohua Xie Prof. Hui Xu 《Angewandte Chemie (International ed. in English)》2023,62(27):e202305018
Clusters combine the advantages of organic molecules and inorganic nanomaterials, which are promising alternatives for optoelectronic applications. Nonetheless, recently emerged cluster light-emitting diodes require further excited state optimization of cluster emitters, especially to reduce population of the cluster-centered triplet quenching state (3CC). Here we report that redox-active ligands enhance reverse intersystem crossing (RISC) of Cu4I4 cluster for triplet-to-singlet conversion, and thermally activated delayed fluorescence (TADF) host can provide an external RISC channel. It indicates that the complementarity between TADF host and cluster in RISC transitions gives rise to 100 % triplet conversion efficiency and complete singlet exciton convergence, rendering 100-fold increased singlet radiation rate constant and tenfold decreased triplet non-radiation rate constant. We achieve a photoluminescence quantum yield of 99 % and a record external quantum efficiency of 29.4 %. 相似文献
110.
Sai Luo Junjie Wang Dr. Nengquan Li Dr. Xiu-Fang Song Xintong Wan Prof. Dr. Kai Li Prof. Dr. Chuluo Yang 《Angewandte Chemie (International ed. in English)》2023,62(49):e202310943
B- and N-embedded multiple resonance (MR) type thermally activated delayed fluorescence (TADF) emitters usually suffer from slow reverse intersystem crossing (RISC) process and aggregation-caused emission quenching. Here, we report the design of a sandwich structure by placing the B−N MR core between two electron-donating moieties, inducing through-space charge transfer (TSCT) states. The proper adjusting of the energy levels brings about a 10-fold higher RISC rate in comparison with the parent B−N molecule. In the meantime, a high photoluminescence quantum yield of 91 % and a good color purity were maintained. Organic light-emitting diodes based on the new MR emitter achieved a maximum external quantum efficiency of 31.7 % and small roll-offs at high brightness. High device efficiencies were also obtained for a wide range of doping concentrations of up to 20 wt % thanks to the steric shielding of the B−N core. A good operational stability with LT95 of 85.2 h has also been revealed. The dual steric and electronic effects resulting from the introduction of a TSCT state offer an effective molecular design to address the critical challenges of MR-TADF emitters. 相似文献