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Synthesis of Green/Blue Light Emitting Quinolines by Aza-D-A Reaction Using InCl3 Catalyst.


ABSTRACT: An efficient InCl3-catalyzed sequential reaction of aromatic amines, aromatic aldehydes and functionalized alkynes leading to the formation of new quinoline derivatives exhibiting significant fluorescence activities is described. The photophysical investigations of quinolines were carried out by absorption and photoluminescence measurements. One particular compound 4 h having maximum intensity, emitting green colour (??=?0.78) with average life time of 6.20 ns was the best amongst the tested compounds. The presence of the amino group at the 4-aryl substituent of the quinoline backbone played an important role in executing the Povarov cyclization successfully and enhancing the flourescence properties of the newly synthesized quinolines.

SUBMITTER: Singh RR 

PROVIDER: S-EPMC7679117 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature

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Synthesis of Green/Blue Light Emitting Quinolines by Aza-D-A Reaction Using InCl<sub>3</sub> Catalyst.

Singh Rajkumar Romeshkumar RR   Singh Thokchom Prasanta TP   Singh Ningthoujam Premananda NP   Naorem Shanta Singh SS   Singh Okram Mukherjee OM  

Journal of fluorescence 20201120 1


An efficient InCl<sub>3</sub>-catalyzed sequential reaction of aromatic amines, aromatic aldehydes and functionalized alkynes leading to the formation of new quinoline derivatives exhibiting significant fluorescence activities is described. The photophysical investigations of quinolines were carried out by absorption and photoluminescence measurements. One particular compound 4 h having maximum intensity, emitting green colour (Φ = 0.78) with average life time of 6.20 ns was the best amongst the  ...[more]

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