Unveiling stereoselective ladders <i>via</i> photo-oligomerization of a diazaanthracene macrocycle
Stereoselective oligomers are synthesized from a photoresponsive macrocycle via [4 + 4] cycloaddition. Oligomers up to octamer were isolated and characterized. They retain reactivity, thus further oligomerizing independently or with fresh monomers.
Authors
- Yann Ferrand (ORCID: https://orcid.org/0000-0002-6552-6914)
- Bappaditya Gole (ORCID: https://orcid.org/0000-0002-0001-6569)
- Ivan Huc (ORCID: https://orcid.org/0000-0001-7036-9696)
- J. Kumar (ORCID: https://orcid.org/0009-0003-3744-4297)
Institutions
- Centre National de la Recherche Scientifique (FR)
- Université de Bordeaux (FR)
- Shiv Nadar University (IN)
- Chimie et Biologie des Membranes et des Nanoobjects (FR)
- Institut Européen de Chimie et Biologie (FR)
- Institut Polytechnique de Bordeaux (FR)
- Ludwig-Maximilians-Universität München (DE)
Publication Details
- Journal
- Organic Chemistry Frontiers
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5qo00159e
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Arthritis National Research Foundation
- National Research Foundation
- Department of Science and Technology, Ministry of Science and Technology, India