Adjusting the energy levels and bandgaps of conjugated polymers via Lewis acid–base reactions

2018 ◽  
Vol 42 (23) ◽  
pp. 18961-18968 ◽  
Author(s):  
Yongchun Li ◽  
Huifeng Meng ◽  
Yuqing Li ◽  
Bo Pang ◽  
Genggeng Luo ◽  
...  
Keyword(s):  
Conjugated Polymers ◽  
Lewis Acid ◽  
Energy Levels ◽  
Optoelectronic Properties ◽  
Acid Base

Stoichiometry of the Lewis acid–base coordination between polymers and BCF and the effects on the optoelectronic properties.

Solvation and redox properties of [Co(en)3]3+-[Co(en)3]2+ system

1980 ◽  
Vol 45 (2) ◽  
pp. 335-338 ◽  
Author(s):  
Adéla Kotočová ◽  
Ulrich Mayer
Keyword(s):  
Hydrogen Bond ◽  
Lewis Acid ◽  
Specific Interaction ◽  
Redox Properties ◽  
Solvation Effect ◽  
Interacting Particles ◽  
Acid Base ◽  
Polar Solvents ◽  
Oxidation Reduction ◽  
Solvent Molecules

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.

Chalcogen versus Dative Bonding in [SF3]+ Lewis Acid–Base Adducts: [SF3(NCCH3)2]+, [SF3(NC5H5)2]+, and [SF3(phen)]+ (phen = 1,10-phenanthroline)

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

scholarly journals Lewis acid / Base-free Strategy for the Synthesis of 2-Arylthio and Selenyl Benzothiazole / Thiazole and Imidazole

2021 ◽  
Vol 27 (1) ◽  
pp. 17-23
Author(s):  
Guniganti Balakishan ◽  
Gullapalli Kumaraswamy ◽  
Vykunthapu Narayanarao ◽  
Pagilla Shankaraiah
Keyword(s):  
Lewis Acid ◽  
Bond Formation ◽  
Acid Base ◽  
Mechanistic Pathway ◽  
Wide Range ◽  
Acid And Base ◽  
Lewis Acid And Base ◽  
Sulfur Bond

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.

scholarly journals Novel hydrogen chemisorption properties of amorphous ceramic compounds consisting of p-block elements: exploring Lewis acid-base Al–N pair site formed in-situ within polymer-derived silicon-aluminum-nitrogen-based system

2021 ◽  
Author(s):  
Shotaro Tada ◽  
Norifumi Asakuma ◽  
Shiori Ando ◽  
Toru Asaka ◽  
Yusuke Daiko ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Active Site ◽  
Hydrogen Chemisorption ◽  
Acid Base ◽  
Polymer Derived Ceramics ◽  
System P ◽  
Ceramic Compounds ◽  
The Relationship

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...

Manipulation of Lewis acid–base complexation in the Zr-centered quaternary system for monodisperse spherical zircons

2020 ◽  
Author(s):  
Shan Peng ◽  
Zhongqiu Chen ◽  
Qing Huang ◽  
Xiaohong Xia ◽  
Zhuo Wang ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Quaternary System ◽  
Acid Base

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 ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Efficient Method ◽  
High Efficiency ◽  
Acid Base ◽  
Catalytic Sites ◽  
Tertiary Nitrogen

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...

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