scholarly journals Lewis base-assisted Lewis acid-catalyzed selective alkene formation via alcohol dehydration and synthesis of 2-cinnamyl-1,3-dicarbonyl compounds from 2-aryl-3,4-dihydropyrans

2016 ◽  
Vol 37 (6) ◽  
pp. 979-986 ◽  
Author(s):  
Changhui Liu ◽  
Bin Pan ◽  
Yanlong Gu
2016 ◽  
Vol 81 (14) ◽  
pp. 6136-6141 ◽  
Author(s):  
Danbo Xie ◽  
Dan Shen ◽  
Qiliang Chen ◽  
Jiaqi Zhou ◽  
Xiaofei Zeng ◽  
...  

Author(s):  
Paul H. Kasai

In disk drives of current generation, the thickness of the disk lubricant has been reduced to the level of a sub-monomolecular film. For a mono- or a sub-monomolecular film of a perfluoropolyether terminated with a primary hydroxyl unit at both ends, each lubricant molecular chain is chemically bound to the carbon substrate at both termini, and if it has a hydrocarbon sector inserted at its center, the hydrocarbon sectors would assemble at the top of the film. They are thus poised most aptly to react as a Lewis base (an electron donor) to the Lewis acid centers on the slider thus abating the Lewis acid-catalyzed lubricant degradation.


Author(s):  
Paul H. Kasai ◽  
Ryosuke Sagata

In disk drives of current generation, the thickness of the disk lubricant has been reduced to the level of a sub-monomolecular film. For a mono- or a sub-monomolecular film of a perfluoropolyether terminated with a primary hydroxyl unit at both ends, each lubricant molecular chain is chemically bound to the carbon substrate at both termini, and if it has a hydrocarbon sector inserted at its center, the hydrocarbon sectors would assemble at the top of the film. They are thus poised most aptly to react as a Lewis base (an electron donor) to the Lewis acid centers on the slider thus abating the Lewis acid-catalyzed lubricant degradation. A TOF-SIMS study of lubricant films of various thicknesses was performed. The study substantiated the envisaged lubricant posture.


1995 ◽  
Vol 73 (1) ◽  
pp. 56-60 ◽  
Author(s):  
Angela R. Suárez ◽  
Alejandra G. Suárez ◽  
Sandra E. Martín ◽  
María R. Mazzieri

The participation of ion-paired Lewis acid/Lewis base in the dehydrohalogenations of 1,2-dibromo-1,1 -diarylalkanes catalyzed by Fe0 and by Fe(II) and Fe(III) bromides was investigated. The reactivities of the catalyst employed were correlated with their chemical hardness. The influence of para substituents on the phenyl rings of the substrates and the results obtained in Lewis-acid-catalyzed and thermal dehydrobromination of the same compounds were compared. The experimental results could not be explained in terms of a Lewis-acid-catalyzed dehydrobromination. Keywords: dehydrohalogenation, bromoalkanes, Lewis acid catalysts, ion-pair mechanism.


2019 ◽  
Vol 84 (5) ◽  
pp. 2941-2950 ◽  
Author(s):  
Wenbo Huang ◽  
Jing Xu ◽  
Changhui Liu ◽  
Zhiyan Chen ◽  
Yanlong Gu

2018 ◽  
Author(s):  
Haley Albright ◽  
Paul S. Riehl ◽  
Christopher C. McAtee ◽  
Jolene P. Reid ◽  
Jacob R. Ludwig ◽  
...  

<div>Catalytic carbonyl-olefin metathesis reactions have recently been developed as a powerful tool for carbon-carbon bond</div><div>formation. However, currently available synthetic protocols rely exclusively on aryl ketone substrates while the corresponding aliphatic analogs remain elusive. We herein report the development of Lewis acid-catalyzed carbonyl-olefin ring-closing metathesis reactions for aliphatic ketones. Mechanistic investigations are consistent with a distinct mode of activation relying on the in situ formation of a homobimetallic singly-bridged iron(III)-dimer as the active catalytic species. These “superelectrophiles” function as more powerful Lewis acid catalysts that form upon association of individual iron(III)-monomers. While this mode of Lewis acid activation has previously been postulated to exist, it has not yet been applied in a catalytic setting. The insights presented are expected to enable further advancement in Lewis acid catalysis by building upon the activation principle of “superelectrophiles” and broaden the current scope of catalytic carbonyl-olefin metathesis reactions.</div>


Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1170
Author(s):  
Yuan Zhu ◽  
Benkun Qi ◽  
Xinquan Liang ◽  
Jianquan Luo ◽  
Yinhua Wan

Herein, corn stover (CS) was pretreated by less corrosive lewis acid FeCl3 acidified solutions of neat and aqueous deep eutectic solvent (DES), aqueous ChCl and glycerol at 120 °C for 4 h with single FeCl3 pretreatment as control. It was unexpected that acidified solutions of both ChCl and glycerol were found to be more efficient at removing lignin and xylan, leading to higher enzymatic digestibility of pretreated CS than acidified DES. Comparatively, acidified ChCl solution exhibited better pretreatment performance than acidified glycerol solution. In addition, 20 wt% water in DES dramatically reduced the capability of DES for delignification and xylan removal and subsequent enzymatic cellulose saccharification of pretreated CS. Correlation analysis showed that enzymatic saccharification of pretreated CS was highly correlated to delignification and cellulose crystallinity, but lowly correlated to xylan removal. Recyclability experiments of different acidified pretreatment solutions showed progressive decrease in the pretreatment performance with increasing recycling runs. After four cycles, the smallest decrease in enzymatic cellulose conversion (22.07%) was observed from acidified neat DES pretreatment, while the largest decrease (43.80%) was from acidified ChCl pretreatment. Those findings would provide useful information for biomass processing with ChCl, glycerol and ChCl-glycerol DES.


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