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881.
由香茅醛合成羟基香茅醛的研究   总被引:2,自引:0,他引:2  
羟基香茅醛具有玲兰样香气,是一种传统的合成香料,主要用于调配各种花系列香精、食品香精、化妆品香精等。我们对它的合成方法进行了改进研究,用二乙醇胺与香茅醛缩合生成噁唑烷衍生物,将醛基保护,再用硫酸加助催化剂将其双键水合,进而将缩合物水解得握基香茅醛。  相似文献   
882.
Jin  Jie  Tian  Xu  Tao  Yi  Kou  Xianli  Mi  Yuanhao  Xu  Xiaokang  Yang  Huifeng 《Journal of Solid State Electrochemistry》2023,27(9):2309-2321
Journal of Solid State Electrochemistry - CrMoCN coatings with different carbon contents are prepared on 316L stainless steel substrates by closed-field unbalanced magnetron sputtering. The...  相似文献   
883.
Metal organic framework (MOF) glasses are a coordination network of metal nodes and organic ligands as an undercooled frozen-in liquid, and have therefore broadened the potential of MOF materials in the fundamental research and application scenarios. On the road to deploying MOF glasses as electrocatalysts, it remains several basic scientific hurdles although MOF glasses not only inherit the structural merits of MOFs but also endow with active catalytic features including concentrated defects, metal centers and disorder structure etc. The research on the ionic conductivity, catalytic stability and reactivity of MOF glasses has yielded scientific insights towards its electrocatalytic applications. Here, we first comb the history, definition and basic properties of MOF glasses. Then, we identify the main synthetic methods and characterization techniques. Finally, we advance the potentials and challenges of MOF glasses as electrocatalysts in furthering the understanding of these themes.  相似文献   
884.
Chemoselective terpolymerization can produce polymer materials with diverse compositions and sequential structures, and thus have attracted considerable attention in the field of polymer synthesis. However, the intrinsic complexity of three-component system also brings great chanllenge, in regard to the reactivity and selectivity of different monomers. Herein, we report the terpolymerization of CO2/epoxide/anhydride by a binary organocatalytic C3N3-Py-P3/TEB (triethylborane) system. Both the activity and chemoselectivity were highly dependent upon the molar ratio of C3N3-Py-P3 to TEB, and sequence-controlled poly(ester-carbonate) copolymers were readily synthesized through one-pot/one-step methodology by tuning the stoichiometric ratio of phosphazene/TEB. In particular, C3N3-Py-P3/TEB with a molar ratio of 1/0.5 exhibited an unprecedentedly high chemoselectivity for ring-opening alternating copolymerization (ROAC) of cyclohexene oxide (CHO) and phthalic anhydride (PA) first and then ROAC of CO2/CHO. Thus, well-defined triblock polycarbonate-b-polyester-b-polycarbonate copolymers can be produced from the mixture of CO2, CHO and PA using a bifunctional initiator. With C3N3-Py-P3/TEB=1/1, tapered copolymers were obtained, while random copolymers with high content of polycarbonate (PC) were synthesized with further increasing the amount of TEB. The mechanism of the unexpected chemoselectivity was further investigated by DFT calculations.  相似文献   
885.
Herein, we report an ATP-responsive nanoparticle (GroELNP) whose surface is fully covered with the biomolecular machine “chaperonin protein GroEL”. GroELNP was synthesized by DNA hybridization between a gold NP with DNA strands on its surface and GroEL carrying complementary DNA strands at its apical domains. The unique structure of GroELNP was visualized by transmission electron microscopy including under cryogenic conditions. The immobilized GroEL units retain their machine-like function and enable GroELNP to capture denatured green fluorescent protein and release it in response to ATP. Interestingly, the ATPase activity of GroELNP per GroEL was 4.8 and 4.0 times greater than those of precursor cysGroEL and its DNA-functionalized analogue, respectively. Finally, we confirmed that GroELNP could be iteratively extended to double-layered NP.  相似文献   
886.
Optical force probes that can release force-dependent and visualized signals with minimal changes in the polymer main chains under mechanical load are highly sought after but currently limited. In this study, we introduce a flex-activated mechanophore (FA) based on the Diels–Alder adduct of anthracene and dimethyl acetylenedicarboxylatea that exhibits turn-on mechanofluorescence. We demonstrate that when FA is incorporated into polymer networks or in its crystalline state, it can release fluorescent anthracenes through a retro-Diels–Alder mechanochemical reaction under compression or hydrostatic high pressure, respectively. The flex-activated mechanism of FA is successfully confirmed. Furthermore, we systematically modulate the force delivered to the mechanophore by varying the crosslinking density of the networks and the applied macroscopic pressures. This modulation leads to incremental increases in mechanophore activation, successive release of anthracenes, and quantitative enhancement of fluorescence intensity. The exceptional potential of FA as a sensitive force probe in different bulk states is highlighted, benefiting from its unique flex-activated mode with highly emissive fluorophore releasing. Overall, this report enriches our understanding of the structures and functions of flex-activated mechanophores and polymeric materials.  相似文献   
887.
Journal of Solid State Electrochemistry - Electrochemical magnetorheological finishing (EC–MRF) is an ultrasmooth planarization method that etches a workpiece surface with a controllable...  相似文献   
888.
Journal of Solid State Electrochemistry - A magnetorheological electro-Fenton composite polishing technology was proposed that enables chemical and mechanical “double enhancement” of...  相似文献   
889.
The European Physical Journal A - Initially, yields (or abundances) and branching ratios of β-delayed neutrons (βdn) from fission products (Pn-values) have had their main importance in...  相似文献   
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