Arnab Dutta, Krzysztof Dzieszkowski, Marco Farinone, Łukasz Orzeł, Krzysztof Kruczała, Monika Kijewska, Miłosz Pawlicki
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Folding of a Dynamic Macrocyclic System to Stabilize its Cation Radical State
A precise design of unsaturated systems remains an important factor that determines the quality of formed products based on a specific spatial orientation, but also defining the available -electron density open for postsynthetic modulation via a redox change. Three strictly defined reagents showing a different degree of flexibility, but also introducing two mutual orientations of reacting ends (parallel and obtuse) determine the quality of formed products obtained via an intramolecular or an intermolecular reaction. The redox activated transformation of mono- and double-looped systems results in a dissimilar oxidation state of a strongly pi-conjugated dication (2 electron process) or a cation-radical (1 electron process) derived from the difference in dynamic of the skeleton documented for monomer and dimer, respectively.
期刊介绍:
Organic Chemistry Frontiers is an esteemed journal that publishes high-quality research across the field of organic chemistry. It places a significant emphasis on studies that contribute substantially to the field by introducing new or significantly improved protocols and methodologies. The journal covers a wide array of topics which include, but are not limited to, organic synthesis, the development of synthetic methodologies, catalysis, natural products, functional organic materials, supramolecular and macromolecular chemistry, as well as physical and computational organic chemistry.