2013Hecheng huaxueRequires access

Synthesis and Optical Properties of Novel Coumarin Derivatives

Chen Chuan-lon

Open publisher page 0 citations

Abstract

Three novel coumarin derivatives containing anthracene ring(1 ~ 3) with yield of 43% ~77%,were synthesized from 9-anthracenecarboxyli acid by chlorination and substitution. The structures were characterized by 1H NMR,13C NMR and IR. The spectra properties of 1 ~ 3 were investigated by UV-Vis and fluorescence spectroscopies. The results showed that λmax of 1 were 315 nm,347 nm,366 nm,385 nm,λmax of 2 and 3 were 317 nm,347 nm,366 nm,385 nm. The maximum emission peak of 1 ~ 3 were about 485 nm under 366 nm excitation.

About this research paper

What this paper is about

Three novel coumarin derivatives containing anthracene ring(1 ~ 3) with yield of 43% ~77%,were synthesized from 9-anthracenecarboxyli acid by chlorination and substitution. The structures were characterized by 1H NMR,13C NMR and IR. The spectra properties of 1 ~ 3 were investigated by UV-Vis and fluorescence spectroscopies. The results showed that λmax of 1 were 315 nm,347 nm,366 nm,385 nm,λmax of 2 and 3 were 317 nm,347 nm,366 nm,385 nm. The maximum emission peak of 1 ~ 3 were about 485 nm under 366 nm excitation.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Three novel coumarin derivatives containing anthracene ring(1 ~ 3) with yield of 43% ~77%,were synthesized from 9-anthracenecarboxyli acid by chlorination and substitution. The structures were characterized by 1H NMR,13C NMR and IR. The spectra properties of 1 ~ 3 were investigated by UV-Vis and fluorescence spectroscopies. The results showed that λmax of 1 were 315 nm,347 nm,366 nm,385 nm,λmax of 2 and 3 were 317 nm,347 nm,366 nm,385 nm. The maximum emission peak of 1 ~ 3 were about 485 nm under 366 nm excitation.

Key concepts: Chemistry, Coumarin, Anthracene, Fluorescence, Proton NMR, Carbon-13 NMR, Yield (engineering), Nuclear chemistry

Related papers

Back to paper searchBrowse research topicsOriginal source
Synthesis and Optical Properties of Novel Coumarin Derivatives — Research Paper | ScholarLens