An uncoordinatedly tertiary nitrogen based tricarboxylate Calcium network with Lewis acid-base dual catalytic sites for cyanosilylation of aldehydes

2020 ◽  
Author(s):  
Xian-Ming Zhang ◽  
Ying-Xia Wang ◽  
Hui-Min Wang ◽  
Pan Meng ◽  
Dong-Xia Song ◽  
...  

The design and utilization of dual sites for synergistic catalysts has been recognised as an efficient method towards high-efficiency catalysis in the cyanosilylation of aldehydes, which gives the key intermediates...

2016 ◽  
Vol 49 (2) ◽  
pp. 311-319 ◽  
Author(s):  
Jin-Wook Lee ◽  
Hui-Seon Kim ◽  
Nam-Gyu Park

2019 ◽  
Vol 48 (23) ◽  
pp. 8044-8048 ◽  
Author(s):  
Ying-Hua Zhou ◽  
Zhiyan Zhang ◽  
Margaret Patrick ◽  
Fan Yang ◽  
Rangling Wei ◽  
...  

UiO-67-bpydc-Zn with isolated multi-catalytic active sites was fabricated as a catalyst for the hydrolysis of bis(p-nitrophenyl) phosphate as a DNA model. The enhanced activity may likely be attributed to the cooperation effects between the Lewis acid from the zirconium center at the node and the zinc hydroxide Lewis base in the linkers.


2015 ◽  
Vol 51 (2) ◽  
pp. 338-341 ◽  
Author(s):  
Jiangjiang Duan ◽  
Xiaomei He ◽  
Lina Zhang

Novel magnetic cellulose–TiO2 nanocomposite microspheres were prepared successfully by in situ synthesis of TiO2 nanoparticles in the micro/nanopores of cellulose–Fe3O4 microsphere, which exhibited highly selective enrichment of trace phosphopeptides, as a result of the high-efficiency Lewis acid–base reaction.


2017 ◽  
Vol 5 (10) ◽  
pp. 5195-5203 ◽  
Author(s):  
Ngoc Duy Pham ◽  
Vincent Tiing Tiong ◽  
Peng Chen ◽  
Lianzhou Wang ◽  
Gregory J. Wilson ◽  
...  

19% perovskite solar cells with enhanced electronic properties of MAPbI3film through employing 2.5% PbCl2additive in the precursor.


2020 ◽  
Vol 17 (7) ◽  
pp. 540-547
Author(s):  
Chun-Hui Yang ◽  
Cheng Wu ◽  
Jun-Ming Zhang ◽  
Xiang-Zhang Tao ◽  
Jun Xu ◽  
...  

Background: The sulfinic esters are important and useful building blocks in organic synthesis. Objective: The aim of this study was to develop a simple and efficient method for the synthesis of sulfinic esters. Materials and Methods: Constant current electrolysis from thiols and alcohols was selected as the method for the synthesis of sulfinic esters. Results and Discussion: A novel electrochemical method for the synthesis of sulfinic esters from thiophenols and alcohols has been developed. Up to 27 examples of sulfinic esters have been synthesized using the current methods. This protocol shows good functional group tolerance as well as high efficiency. In addition, this protocol can be easily scaled up with good efficiency. Notably, heterocycle-containing substrates, including pyridine, thiophene, and benzothiazole, gave the desired products in good yields. A plausible reaction mechanism is proposed. Conclusion: This research not only provides a green and efficient method for the synthesis of sulfinic esters but also shows new applications of electrochemistry in organic synthesis. It is considered that this green and efficient synthetic protocol used to prepare sulfinic esters will have good applications in the future.


1980 ◽  
Vol 45 (2) ◽  
pp. 335-338 ◽  
Author(s):  
Adéla Kotočová ◽  
Ulrich Mayer

The solvation effect of a number of nonaqueous polar solvents was studied on the oxidation-reduction properties of the [Co(en)3]3+-[Co(en)3]2+ system. Interactions of these ions with the solvent molecules are discussed in terms of their coordination, which is accompanied by a specific interaction of the Lewis acid-base type, namely formation of a hydrogen bond between the interacting particles. This is the main controlling factor of the redox properties of the studied system.


2021 ◽  
Vol 60 (6) ◽  
pp. 3893-3901
Author(s):  
Douglas Turnbull ◽  
Praveen Chaudhary ◽  
Paul Hazendonk ◽  
Stacey D. Wetmore ◽  
Michael Gerken
Keyword(s):  

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