Visible‐Light‐Induced Di‐\(\pi\)‐Methane Rearrangement of Dibenzobarrelene Derivatives

Please always quote using this URN: urn:nbn:de:bvb:20-opus-212633
  • It is demonstrated that the di‐\(\pi\)‐methane (DPM) rearrangement of carbonyl‐substituted dibenzobarrelene (9,10‐dihydro‐9,10‐ethenoanthracene) derivatives is induced by visible‐light‐induced triplet photosensitization with Ir(ppy)\(_{3}\), Ir(dFppy)\(_{3}\) or 1‐butyl‐7,8‐dimethoxy‐3‐methylalloxazine as catalysts, whereas derivatives that lack carbonyl substituents are photoinert under these conditions. Notably, the products are formed almost quantitatively.

Download full text files

Export metadata

Additional Services

Share in Twitter Search Google Scholar Statistics
Metadaten
Author: Julika Schlosser, Radek Cibulka, Philipp Groß, Heiko Ihmels, Christian J. Mohrschladt
URN:urn:nbn:de:bvb:20-opus-212633
Document Type:Journal article
Faculties:Fakultät für Chemie und Pharmazie / Institut für Organische Chemie
Language:English
Parent Title (English):ChemPhotoChem
Year of Completion:2020
Volume:4
Issue:2
First Page:132
Last Page:137
Source:ChemPhotoChem 2020, 4(2):132-137. DOI: 10.1002/cptc.201900221
DOI:https://doi.org/10.1002/cptc.201900221
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 54 Chemie / 547 Organische Chemie
Tag:di-\(\pi\)-methane rearrangement; dibenzosemibullvalenes; ethenoanthracenes; photocatalysis; photosensitization
Release Date:2021/04/15
Licence (German):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International