Premium
Fulleretic Well‐Defined Scaffolds: Donor–Fullerene Alignment Through Metal Coordination and Its Effect on Photophysics
Author(s) -
Williams Derek E.,
Dolgopolova Ekaterina A.,
Godfrey Danielle C.,
Ermolaeva Evgeniya D.,
Pellechia Perry J.,
Greytak Andrew B.,
Smith Mark D.,
Avdoshenko Stanislav M.,
Popov Alexey A.,
Shustova Natalia B.
Publication year - 2016
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.201603584
Subject(s) - fullerene , photoluminescence , acceptor , magic angle spinning , spectroscopy , materials science , organic solar cell , chemistry , photochemistry , chemical physics , nanotechnology , nuclear magnetic resonance spectroscopy , optoelectronics , stereochemistry , organic chemistry , physics , polymer , quantum mechanics , condensed matter physics
Herein, we report the first example of a crystalline metal–donor–fullerene framework, in which control of the donor–fullerene mutual orientation was achieved through chemical bond formation, in particular, by metal coordination. The 13 C cross‐polarization magic‐angle spinning NMR spectroscopy, X‐ray diffraction, and time‐resolved fluorescence spectroscopy were performed for comprehensive structural analysis and energy‐transfer (ET) studies of the fulleretic donor–acceptor scaffold. Furthermore, in combination with photoluminescence measurements, the theoretical calculations of the spectral overlap function, Förster radius, excitation energies, and band structure were employed to elucidate the photophysical and ET processes in the prepared fulleretic material. We envision that the well‐defined fulleretic donor–acceptor materials could contribute not only to the basic science of fullerene chemistry but would also be used towards effective development of organic photovoltaics and molecular electronics.