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Doubly N‐Confused [36]Octaphyrin(1.1.1.1.1.1.1.1): Isomerization, Bis‐Metal Coordination, and Topological Chirality
Ist Teil von
Angewandte Chemie International Edition, 2017-11, Vol.56 (45), p.14252-14256
Auflage
International ed. in English
Ort / Verlag
Germany: Wiley Subscription Services, Inc
Erscheinungsjahr
2017
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
A novel [36]octaphyrin analogue embedding two N‐confused pyrrole units demonstrated unique prototropy‐coupled isomerization between the Figure‐of‐eight and dumbbell conformers. Upon bis‐metal coordination, fixation of fully π‐conjugated Figure‐of‐eight structures was achieved as referred from the X‐ray crystal structure. Chirogenesis of the helical enantiomers was proved by intense circular dichroism (CD) response in the near infrared (NIR) region.
Eight‐figured chirality: A novel [36]octaphyrin analogue embedding two N‐confused pyrrole units demonstrates unique prototropy‐coupled isomerization. Upon bis‐metal complexation, fully π‐conjugated, helical Figure‐of‐eight structures are realized. Distinct CD response in the NIR region confirms chirogenesis of the helical enantiomers.