75903-25-2

Usage

Uses

Used in Organic Electronics:
2-[2-(3,4-dimethoxyphenyl)ethenyl]quinoline is used as a component in organic electronics for its electronic properties that contribute to the development of advanced materials and devices.
Used in Optoelectronic Devices:
In the optoelectronics industry, 2-[2-(3,4-dimethoxyphenyl)ethenyl]quinoline is utilized for its optical characteristics, which are beneficial for creating innovative devices that combine electronic and optical functionalities.
It is crucial for researchers to further investigate 2-[2-(3,4-dimethoxyphenyl)ethenyl]quinoline to unlock its full potential and integrate it into the next generation of technological advancements.

Upstream product

• 91-63-4 2-methylquinoline 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 104967-55-7 2-[2-(3,4-dimethoxyphenyl)ethyl]-1-methyl-1,2,3,4-tetrahydroquinolineanol 
• 104967-54-6 2-(3,4-dimethoxy-β-phenethyl)-1,2,3,4-tetrahydroquinoline 

Relevant academic research and scientific papers

Catalytic hydrogenation with frustrated lewis pairs: Selectivity achieved by size-exclusion design of lewis acids

Catalytic hydrogenation that utilizes frustrated Lewis pair (FLP) catalysts is a subject of growing interest because such catalysts offer a unique opportunity for the development of transition-metal-free hydrogenations. The aim of our recent efforts is to further increase the functional-group tolerance and chemoselectivity of FLP catalysts by means of size-exclusion catalyst design. Given that hydrogen molecule is the smallest molecule, our modified Lewis acids feature a highly shielded boron center that still allows the cleavage of the hydrogen but avoids undesirable FLP reactivity by simple physical constraint. As a result, greater latitude in substrate scope can be achieved, as exemplified by the chemoselective reduction of α,β-unsaturated imines, ketones, and quinolines. In addition to synthetic aspects, detailed NMR spectroscopic, DFT, and 2H isotopic labeling studies were performed to gain further mechanistic insight into FLP hydrogenation. Copyright

Synthesis and structure of styryl-substituted azines

New photochromic derivatives of 2-styrylquinoline and 2-styrylquinoxaline were obtained by the condensation of the methyl derivatives of the mentioned heterocycles with substituted benzaldehydes in the presence of basic and acidic catalysts, and also unde