Steric hindrance by a metal–organic framework (MOF) is shown to influence the outcome of a catalytic reaction by controlling the orientation of its intermediates. This is demonstrated using an organocatalyst, phosphine MOF LSK‐3, which is evaluated with the aid of molecular modeling and NMR spectroscopy techniques. This report is the first application of phosphine MOFs in organocatalysis and explores the potential of a framework steric hindrance to impose selectivity on a catalytic reaction. These findings expand the opportunities for control and design of the active site in the pocket of heterogeneous catalysts. 相似文献
The CuS catalyzed coupling reactions of aryl halides and diaryl diselenides were accelerated by the addition of Fe powder in only 3-12 h with good to excellent yields. SEM-EDX indicated that the in situ iron oxides as support against catalyst agglomeration accelerated the reaction. This catalyst system was also demonstrated recyclable without significant loss of catalytic activity. 相似文献
Here, a porous cobalt–organic framework with pillared layer structures, namely [Co3OBA3PTD(H2O)2 ⋅ 2 DMA ⋅ H2O]n ( 1 , H2OBA=4,4′-oxybis(benzoic acid); PTD=6-(pyridin-4-yl)-1,3,5-triazine-2,4-diamine), was fabricated by using cobalt trinuclear nodes, low-cost carboxylic linker, and accessible nitrogen heterocyclic ligands. This compound exhibited a highly efficient solvatochromism towards CH2Cl2 within one minute and can be used 200 times at least. The corresponding dropper detector was assembled as a practical sensor. Meanwhile, the porous Co3O4 was obtained by a simple but effective annealing treatment. Electrochemical measurements confirm that this Co3O4 material derived from compound 1 shows high and stable lithium storage capabilities (1081.75 mA h g−1 at 200 mA g−1 after 115 cycles) and excellent rate properties. 相似文献
Cushioning and antibacterial packaging are the requirements of the storage and transportation of fruits and vegetables, which are essential for reducing the irreversible quality loss during the process. Herein, the composite of carboxymethyl nanocellulose, glycerin, and acrylamide derivatives acted as the shell and chitosan/AgNPs were immobilized in the core by using coaxial 3D-printing technology. Thus, the 3D-printed cushioning–antibacterial dual-function packaging aerogel with a shell–core structure (CNGA/C–AgNPs) was obtained. The CNGA/C–AgNPs packaging aerogel had good cushioning and resilience performance, and the average compression resilience rate was more than 90%. Although AgNPs was slowly released, CNGA/C–AgNPs packaging aerogel had an obvious antibacterial effect on E. coli and S. aureus. Moreover, the CNGA/C–AgNPs packaging aerogel was biodegradable. Due to the customization capabilities of 3D-printing technology, the prepared packaging aerogel can be adapted to more application scenarios by accurately designing and regulating the microstructure of aerogels, which provides a new idea for the development of food intelligent packaging. 相似文献
We describe a nonenzymatic electrochemical sensor for uric acid. It is based on a carbon nanotube ionic-liquid paste electrode modified with poly(β-cyclodextrin) that was prepared in-situ by electropolymerization. The functionalized multi-walled carbon nanotubes and the surface morphology of the modified electrodes were characterized by transmission electronic microscopy and scanning electron microscopy. The electrochemical response of uric acid was studied by cyclic voltammetry and linear sweep voltammetry. The effects of scan rate, pH value, electropolymerization cycles and accumulation time were also studied. Under optimized experimental conditions and at a working voltage of 500 mV vs. Ag/AgCl (3 M KCl), response to uric acid is linear in the 0.6 to 400 μΜ and in the 0.4 to 1 mΜ concentration ranges, and the detection limit is 0.3 μΜ (at an S/N of 3). The electrode was successfully applied to the detection of uric acid in (spiked) human urine samples.
SEM images of (a) carbon ionic liquid electrode (CILE) (b) MWNT-CILE (c) β-CD/CILE (d) β-CD/ MWNT-CILE. The surfaces of carbon ionic liquid electrode (CILE) (a) and MWNT-CILE (b) were homogenous and no separated carbon layers can be observed; After β- cyclodextrin (CD) was modified on CILE and MWNT-CILE, the surfaces of β-CD modified electrodes (c and d) exhibited loose and porous morphologies.
This paper considers a new estimating method for the bent line quantile regression model. By a simple linearization technique, the proposed method can simultaneously obtain the estimates of the regression coefficients and the change-point location. Moreover, it can be readily implemented by current software. Simulation studies demonstrate that the proposed method has good finite sample performance. Two empirical applications are also presented to illustrate the method. 相似文献