ChemInform Abstract: Iridium-Catalyzed ortho-Selective C-H Silylation of Aromatic Compounds Directed Toward the Synthesis of π-Conjugated Molecules with Lewis Acid-Base Interaction.

ChemInform ◽  
2015 ◽  
Vol 46 (34) ◽  
pp. no-no
Author(s):  
Takayuki Wakaki ◽  
Motomu Kanai ◽  
Yoichiro Kuninobu
Keyword(s):  
Lewis Acid ◽  
Aromatic Compounds ◽  
Acid Base ◽  
Base Interaction ◽  
Conjugated Molecules ◽  
Acid Base Interaction

Development of Novel C–H Bond Transformations and Their Application to the Synthesis of Organic Functional Molecules

Synlett ◽  
2018 ◽  
Vol 29 (16) ◽  
pp. 2093-2107 ◽  
Author(s):  
Yoichiro Kuninobu
Keyword(s):  
Hydrogen Bonding ◽  
Lewis Acid ◽  
Functional Materials ◽  
Personal Account ◽  
Acid Base ◽  
Base Interaction ◽  
Conjugated Molecules ◽  
Heteroaromatic Compounds ◽  
Acid Unit ◽  
Acid Base Interaction

This personal account summarizes our recent progress in the development of C–H transformations. We achieved ortho-selective C–H borylations and silylations by using Lewis acid–base interaction between two substrates and we achieved meta- and ortho-selective C–H borylations by using hydrogen bonding or Lewis acid–base interaction between a hydrogen donor or Lewis acid unit of a ligand and a functional group of a substrate. Regioselective C–H trifluoromethylations and related reactions of six-membered heteroaromatic compounds were realized at their 2- and 4-positions and at their benzylic positions. In addition, we developed C–H transformations directed towards the synthesis of organic functional materials, such as highly soluble polyimides or π-conjugated molecules containing either heteroatom(s) or a Lewis acid–base interaction.1 Introduction2 Regioselective C–H Transformations Controlled by Noncovalent Bond Interactions2.1 Regioselective C–H Transformations Controlled by Lewis Acid–Base Interaction between Two Substrates2.2 Regioselective C–H Transformation Controlled by Hydrogen Bonding between Ligand and Substrate2.3 Regioselective C–H Transformations Controlled by Lewis Acid–Base Interactions between Ligands and Substrates3 Trifluoromethylation and Related Transformations of Six-Membered Heteroaromatic Compounds3.1 2-Position-Selective C–H Trifluoromethylation of Six-Membered Heteroaromatic Compounds3.2 4-Position-Selective C–H Trifluoromethylation of Six-Membered Heteroaromatic Compounds3.3 Benzyl Position-Selective C–H Trifluoromethylation of Six-Membered Heteroaromatic Compounds4 C–H Transformations Leading to the Synthesis of Organic Functional Materials4.1 Heteroatom-Containing π-Conjugated Molecules4.2 π-Conjugated Molecules Containing a Lewis Acid–Base Interaction4.3 Soluble Polyimide Derivatives5 Conclusions

Lewis acids in situ modulate pyridazine-imine Ni catalysed ethylene (co)polymerisation

2019 ◽  
Vol 43 (34) ◽  
pp. 13630-13634 ◽  
Author(s):  
Guohong Wang ◽  
Min Li ◽  
Wenmin Pang ◽  
Min Chen ◽  
Chen Tan
Keyword(s):  
Electron Density ◽  
Lewis Acid ◽  
Lewis Acids ◽  
Acid Base ◽  
Base Interaction ◽  
Acid Base Interaction

The Lewis acid-base interaction between B(iii) Lewis acids and the pyridazine moiety reduced the electron density from the Ni center and in situ modulated the pyridazine-imine nickel catalyzed ethylene (co)polymerisation.

scholarly journals An all solid-state Li ion battery composed of low molecular weight crystalline electrolyte

RSC Advances ◽  
2020 ◽  
Vol 10 (15) ◽  
pp. 8780-8789 ◽  
Author(s):  
Prerna Joshi ◽  
Raman Vedarajan ◽  
Anjaiah Sheelam ◽  
Kothandaraman Ramanujam ◽  
Bernard Malaman ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Solid State ◽  
Lewis Acid ◽  
Low Molecular Weight ◽  
Li Ion Battery ◽  
Acid Base ◽  
Base Interaction ◽  
Li Ion ◽  
Acid Base Interaction

A non-polymer crystalline organoboron electrolyte results in the formation of nano-channels for directional conduction of Li ions, owing to presence of boron, allowing Lewis acid–base interaction.

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