ChemInform Abstract: A New Type of Lewis Acid-Base Bifunctional M(salphen) (M: Zn, Cu and Ni) Catalysts for CO2Fixation.

ChemInform ◽  
2015 ◽  
Vol 46 (40) ◽  
pp. no-no
Author(s):  
Yanwei Ren ◽  
Jungui Chen ◽  
Chaorong Qi ◽  
Huanfeng Jiang
Keyword(s):  
ChemCatChem ◽  
2015 ◽  
Vol 7 (10) ◽  
pp. 1535-1538 ◽  
Author(s):  
Yanwei Ren ◽  
Jungui Chen ◽  
Chaorong Qi ◽  
Huanfeng Jiang
Keyword(s):  

2012 ◽  
Vol 84 (11) ◽  
pp. 2219-2231 ◽  
Author(s):  
Henrik Gulyás ◽  
Amadeu Bonet ◽  
Cristina Pubill-Ulldemolins ◽  
Cristina Solé ◽  
Jessica Cid ◽  
...  

It has been demonstrated that the interaction of a simple Lewis base with tetraalkoxydiboranes generates an unusual nucleophilic character in one of the boryl moieties. The interaction of amines, N-heterocyclic carbenes (NHCs), and alkoxides with a diboron reagent results in the formation of a Lewis acid–base adduct, in which the formally intact sp2 boryl moiety becomes nucleophilic. We describe in this work the application of this new type of nucleophilic boron synthon in the selective preparation of organoboranes through β-boration and diboration reactions.


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):  

2021 ◽  
Vol 27 (1) ◽  
pp. 17-23
Author(s):  
Guniganti Balakishan ◽  
Gullapalli Kumaraswamy ◽  
Vykunthapu Narayanarao ◽  
Pagilla Shankaraiah

Abstract A Cu(II)-catalyzed Csp2-Se and Csp2-Sulfur bond formation was achieved with moderate to good yields without the aid of Lewis acid and base. The reaction is compatible with a wide range of heterocycles such as benzothiazole, thiazole, and imidazole. Also, this typical protocol is found to be active in thio-selenation via S-H activation. Additionally, we proposed a plausible mechanistic pathway involving Cu(III) putative intermediate.


Author(s):  
Shotaro Tada ◽  
Norifumi Asakuma ◽  
Shiori Ando ◽  
Toru Asaka ◽  
Yusuke Daiko ◽  
...  

This paper reports on the relationship between the H2 chemisorption properties and reversible structural reorientation of the possible active site around Al formed in-situ within polymer-derived ceramics (PDCs) based on...


Author(s):  
Shan Peng ◽  
Zhongqiu Chen ◽  
Qing Huang ◽  
Xiaohong Xia ◽  
Zhuo Wang ◽  
...  

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