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Back Cover: Stereocontrolled Synthesis of Chiral Heteroaromatic Propellers with Small Optical Bandgaps (Angew. Chem. Int. Ed. 15/2019)
Author(s) -
Navakouski Maksim,
Zhylitskaya Halina,
Chmielewski Piotr J.,
Lis Tadeusz,
Cybińska Joanna,
Stępień Marcin
Publication year - 2019
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201902135
Subject(s) - stereospecificity , chromophore , cover (algebra) , int , reagent , chemistry , stereochemistry , chirality (physics) , redox , optically active , combinatorial chemistry , chiral symmetry , organic chemistry , physics , catalysis , computer science , quantum mechanics , engineering , mechanical engineering , nambu–jona lasinio model , operating system , quark
A simple reagent , N ‐bromosuccinimide, is the oxidant of choice in the stereospecific synthesis of azacoronene propellers. This new family of chiral chromophores features small electronic bandgaps, rich redox chemistry, and large chiroptical responses, as discussed by M. Stępień and co‐workers in their Communication on page 4929.