z-logo
Premium
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.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom