posted on 2021-02-12, 15:35authored byYanrong Li, Sreehari Surendran Rajasree, Ga Young Lee, Jierui Yu, Jian-Hong Tang, Ruidong Ni, Guigen Li, Kendall. N. Houk, Pravas Deria, Peter J. Stang
Two trigonal prismatic metallacages <b>1</b> and <b>2</b> bearing triphenylamine and anthracene
moieties are designed and
synthesized to fabricate artificial light-harvesting systems (LHSs).
These two cages are prepared via the coordination-driven self-assembly
of two anthracene–triphenylamine-based tripyridyl ligand <b>3</b>, three dicarboxylates, and six 90° Pt(II) acceptors.
The design of the anthracene–triphenylamine chromophore makes
possible the tunable excited-state property (like the emissive transition
energy and lifetime) as a function of the solvent polarity, temperature,
and concentration. The synergistic photophysical footprint of these
metallacages, defined by their high absorptivity and emission quantum
yield (QY) relative to the free ligand <b>3</b>, signifies them
as a superior light sensitizer component in an LHS. In the presence
of the fluorescent dye Nile Red (NR) as an energy acceptor, the metallacages
display efficient (>93%) excited energy transfer to NR through
an
apparent static quenching mechanism in viscous dimethyl sulfoxide
solvent.