Affiliation:
1. Faculty of Chemistry and Pharmacy Institute of Organic Chemistry University Regensburg 93040 Regensburg Germany
2. Faculty of Chemistry and Pharmacy Institute of Physical and Theoretical Chemistry University Regensburg 93040 Regensburg Germany
Abstract
AbstractThe amino alcohol meglumine solubilizes organic compounds in water and enforces the formation of electron donor acceptor (EDA) complexes of haloarenes with indoles, anilines, anisoles or thiols, which are not observed in organic solvents. UV‐A photoinduced electron transfer within the EDA complexes induces the mesolytic cleavage of the halide ion and radical recombination of the arenes leading, after rearomatization and proton loss to C−C or C−S coupling products. Depending on the substitution pattern selective and unique cross‐couplings are observed. UV and NMR measurements reveal the importance of the assembly for the photoinduced reaction. Enforced EDA aggregate formation in water allows new activation modes for organic photochemical synthesis.
Funder
Deutsche Forschungsgemeinschaft
Fonds der Chemischen Industrie
Cited by
1 articles.
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