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31.
1H NMR method showed that in systems based on triisobutylaluminum (TIBA) and triphenylcyclopropenylium [Ph3C3]+[B(C6F5)4]–(CPB) or triphenylmethylium [Ph3C]+[B(C6F5)4]–(TB) perfluorophenylborates in a toluene–dichloromethane mixture the Friedel–Crafts process occurs with the formation of ditolylmethane (DTM) accompanied by the complete decomposition of TIBA to form isobutane. 19F NMR spectroscopy showed that the [B(C6F5)4]–anion decomposes in the systems to form B(C6F5)3 and HC6F5. The short-living [AlBu2 i]+ cation formed in the reaction of perfluorophenylborates with TIBA is assumed to be the species initiating the process. It has been shown that CPB is less reactive than TB. The addition of a stoichiometric amount of Ph2CCpFluHfMe2 exerts no effect on the process with the CPB-containing system but inhibits the reaction in the case of TB.  相似文献   
32.
A reaction of organic dichalcogenides R2Y2 (R = Ph, Bn, Pr; Y = S, Se) with 1,4-dichlorobut-2-yne in the system hydrazine hydrate–KOH leads to four principal products: 1,4-bis(organylchalcogenyl)but-2-ynes, 1-organylchalcogenylbut-1-en-3-ynes, 4-organylchalcogenylbut-1-en-3-ynes, and 3(5)-methylpyrazole. The selectivity of the formation of individual products is determined by the ratio of the substrates used and the reaction temperature. A plausible mechanism of chalcogenation considered in the work agrees with the effect of the nature of chalcogene atoms and organic substituents R on stability of intermediates and products. The stabilization of carbanions by α chalcogene-containing groups corresponds to the following order: PhS > PhSe > BnS > BnSe > PrS.  相似文献   
33.
Nickel nanoparticles were deposited on the surface of highly oriented pyrolytical graphite by laser electrodispersion and precipitation from a solution of reverse micelles. The particles were studied using scanning tunneling microscopy and spectroscopy as well as Auger spectroscopy. The elemental composition of the nanoparticles and specific features of the electronic structure of their surface were determined. Adsorption of molecular hydrogen was also studied.  相似文献   
34.
35.
The synthesis of an octavalent bolaamphiphile with D-glucose moiety as branching unit has been designed and accomplished via 1,3-dipolar cycloaddition of bis(tetra-O-propargylglucoside) and 8 equiv of 2-azidoethyl β-D-lactoside.  相似文献   
36.
The structures of the O‐glycosyltransferase LanGT2 and the engineered, C? C bond‐forming variant LanGT2S8Ac show how the replacement of a single loop can change the functionality of the enzyme. Crystal structures of the enzymes in complex with a nonhydrolyzable nucleotide‐sugar analogue revealed that there is a conformational transition to create the binding sites for the aglycon substrate. This induced‐fit transition was explored by molecular docking experiments with various aglycon substrates.  相似文献   
37.
The group 6 molybdenum(II) cyclopentadienyl amidinate (CPAM) bis(carbonyl) complex [Cp*Mo{N(iPr)C(Ph)N(iPr)}(CO)2] (Cp*=η5‐C5Me5) serves as a precatalyst for the high‐yielding photocatalytic production of COS from CO and S8 under near‐ambient conditions (e.g., 10 psi, 25 °C). Further documented is the isolation and structural characterization of several key transition‐metal intermediates which collectively support a novel molybdenum(IV)‐based catalytic cycle as being operative. Finally, in the presence of an excess amount of a primary amine, it is demonstrated that this catalytic system can be successfully used for the “on‐demand” generation and utilization of COS as a chemical reagent for the synthesis of ureas.  相似文献   
38.
This study proposes changes to the design and evaluation of the CO2 headspace test, which is used as a simple method for assessment of the complete biodegradability of surfactants. It presents a modified equation for the calculation of biodegradation. It is proposed that the solution of 7 mol L?1 sodium hydroxide commonly used in the process involving alkalinisation of the vial contents be replaced with 15 mol L?1 sodium hydroxide. The use of the higher hydroxide concentration leads to a significant reduction in the value of the blank CO2 headspace test.  相似文献   
39.
The target of the present investigation is synthesis and characterization of an amphiphilic diblock copolymer with antibacterial property. Ring opening polymerization (ROP) of ε-caprolactone (CL) and tetrahydrofuran (THF) was carried out under inert atmosphere by using L-cysteine as a bridging agent in the presence of stannous octoate (SO) as a catalyst. The nano silver end capped diblock copolymer was synthesized by in situ method. Thus obtained nano silver end capped L-cysteine bridged diblock copolymer was characterized by various analytical methods like Fourier transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, circular dichroism (CD), fluorescence spectroscopy, gel permeation chromatography (GPC), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), field emission scanning electron microscopy (FESEM), high resolution transmission electron microscopy (HRTEM) and zeta potential. The antimicrobial property of the nano silver end capped diblock copolymer against e-coli was tested.  相似文献   
40.
Plasma Chemistry and Plasma Processing - Two dielectric barrier discharge reactors, based on L-shaped electrodes, were designed and fabricated for in-line surface treatment of polyimide (PI)...  相似文献   
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