Issue 39, 2019

Synthesis and chiroptical properties of stereogenic cyclic dimers based on 2,2′-biselenophene and [2.2]paracyclophane

Abstract

Stereogenic cyclic dimers based on 2,2′-biselenophene linked with [2.2]paracyclophane have been synthesized to investigate their chiroptical properties. Embedding selenophene led to the formation of intramolecular Se⋯π interactions between the two biselenophene strands. The resulting rigid cyclic system exhibits enhanced chiroptical properties when compared with its precursor. In addition, the electrochemical properties were also investigated.

Graphical abstract: Synthesis and chiroptical properties of stereogenic cyclic dimers based on 2,2′-biselenophene and [2.2]paracyclophane

Supplementary files

Article information

Article type
Communication
Submitted
31 Aug 2019
Accepted
23 Sep 2019
First published
24 Sep 2019

Org. Biomol. Chem., 2019,17, 8822-8826

Synthesis and chiroptical properties of stereogenic cyclic dimers based on 2,2′-biselenophene and [2.2]paracyclophane

M. Hasegawa, K. Kobayakawa, Y. Nojima and Y. Mazaki, Org. Biomol. Chem., 2019, 17, 8822 DOI: 10.1039/C9OB01907C

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