posted on 2014-05-16, 00:00authored byCatherine
R. DeBlase, Ryan T. Finke, Jonathan A. Porras, Joseph M. Tanski, Jocelyn M. Nadeau
Synthesis
and characterization of two diastereomeric C-shaped molecules
containing cofacial thiophene-substituted quinoxaline rings are described.
A previously known bis-α-diketone was condensed with an excess
of 4-bromo-1,2-diaminobenzene in the presence of zinc acetate to give
a mixture of two C-shaped diastereomers with cofacial bromine-substituted
quinoxaline rings. After chromatographic separation, thiophene rings
were installed by a microwave-assisted Suzuki coupling reaction, resulting
in highly emissive diastereomeric compounds that were studied by UV–vis,
fluorescence, and NMR spectroscopy, as well as X-ray crystallography.
The unique symmetry of each diastereomer was confirmed by NMR spectroscopy.
NMR data indicated that the syn isomer has restricted
rotation about the bond connecting the thiophene and quinoxaline rings,
which was also observed in the solid state. The spectroscopic properties
of the C-shaped diastereomers were compared to a model compound containing
only a single thiophene-substituted quinoxaline ring. Ground state
intramolecular π–π interactions in solution were
detected by NMR and UV–vis spectroscopy. Red-shifted emission
bands, band broadening, and large Stokes shifts were observed, which
collectively suggest excited state π–π interactions
that produce excimer-like emissions, as well as a remarkable positive
emission solvatochromism, indicating charge-transfer character in
the excited state.