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Inside Back Cover: All‐Fullerene Electron Donor–Acceptor Conjugates (Angew. Chem. Int. Ed. 21/2019)
Author(s) -
Izquierdo Marta,
Platzer Benedikt,
Stasyuk Anton J.,
Stasyuk Olga A.,
Voityuk Alexander A.,
Cuesta Sergio,
Solà Miquel,
Guldi Dirk M.,
Martín Nazario
Publication year - 2019
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201904693
Subject(s) - fullerene , dumbbell , conjugate , electron acceptor , acceptor , cover (algebra) , electron donor , charge (physics) , electron transfer , photoinduced electron transfer , electron , int , chemistry , materials science , crystallography , photochemistry , physics , catalysis , organic chemistry , condensed matter physics , medicine , mechanical engineering , mathematical analysis , mathematics , quantum mechanics , engineering , physical therapy , computer science , operating system
An all‐fullerene electron donor–acceptor conjugate was designed, synthesized, and characterized. In their Communication on page 6932, M. Solà, D. M. Guldi, N. Martín et al. describe the C 60 ‐Lu 3 N@I h ‐C 80 dumbbell and demonstrate that photoinduced electron transfer leads to the formation of a long‐lived charge‐separated triplet state.