<div>
<div>
<div>
<p>Organic electronic materials have advantages over inorganics in terms of versatility, cost and
processability. Recent advancements in organic materials for light emitting diodes (OLED), field
effect transistors (OFET), and photovoltaics have engendered extensive innovation potential on
this field. In this research, we focus on synthesizing SQ (silsesquioxane) based oligomers cross-
linked by di-bromo-aromatic linkers and explore how the cross-linker and oligomer length
influence their photophysical properties. Bis-tri-alkoxy silyl (linker) model compounds were
synthesized to compare non-cage photophysical properties with the oligomers. Several techniques
such as UV/Vis, fluorescence, FTIR, thermal gravimetric analysis (TGA) have been used to
characterize the systems. Time-resolved fluorescence and femtosecond transient absorption
spectroscopy are used to understand the excited state dynamics of these materials. Studies are
carried out to understand the differences between monomers and oligomers and potential energy
transfer and charge transfer between the cages and cross-linking chromophores. Transient
absorption showed lower energy absorption from the excited states, suggesting short range
communication between moieties. Single photon counting studies have shown distinct lifetime
differences between most linkers and cages showing possible excitation energy transfer through
these materials. Transient absorption anisotropy measurements have shown signatures for
excitation energy transfer between linker chromophores for oligomeric compounds. The
silsesquioxane (SQ) backbone of the oligomers gives substantial thermal stability as well as
solution processability, giving better flexibility for achieving energy transfer between linking
chromophores.
</p>
</div>
</div>
</div>