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Cover Picture: Metal Nitride Cluster Fullerene M 3 N@C 80 (M=Y, Sc) Based Dyads: Synthesis, and Electrochemical, Theoretical and Photophysical Studies (Chem. Eur. J. 4/2009)
Author(s) -
Pinzón Julio R.,
Cardona Claudia M.,
Herranz Maria Ángeles,
PlonskaBrzezinska Marta E.,
Palkar Amit,
Athans Andreas J.,
Martín Nazario,
RodríguezFortea Antonio,
Poblet Josep M.,
Bottari Giovanni,
Torres Tomás,
Gayathri S. Shankara,
Guldi Dirk M.,
Echegoyen Luis
Publication year - 2009
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.200990001
Subject(s) - chemistry , metalation , moiety , ferrocene , ligand (biochemistry) , cycloaddition , fullerene , crystallography , stereochemistry , polymer chemistry , electrochemistry , medicinal chemistry , organic chemistry , catalysis , electrode , biochemistry , receptor
Endohedral fullerene dyads… are described by L. Echegoyen et al. on page 864 ff., which have been obtained by pyrrolidine and cyclopropane derivatives of the trimetallic nitride templated (TNT) endohedral metallofullerenes I h ‐Sc 3 N@C 80 and I h ‐Y 3 N@C 80 connected to an electron‐donor unit (i.e., tetrathiafulvalene, phthalocyanine or ferrocene) through 1,3‐dipolar cycloaddition reactions of azomethine ylides and Bingel–Hirsch‐type reactions.