Publications by authors named "Joseph A Paquette"

We report the synthesis of novel polycatenar dibenzopentacenequinones and that are designed to form columnar liquid crystalline phases. The mesomorphic properties of these compounds were investigated by polarized optical microscopy, differential scanning calorimetry, and powder X-ray diffraction. While compound exhibits two distinct columnar mesophases between 148 and 177 °C, fluorinated exhibits a columnar mesophase from 121 to 336 °C.

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The electronic structure of 1,3,5-triphenyl-6-oxoverdazyl, a heteroatom-rich stable organic radical, and its diamagnetic 1,3,5-triphenyl-6-oxotetrazane precursor are probed using X-ray absorption near-edge structure (XANES) spectroscopy. The N K-edge XANES spectra of the 6-oxoverdazyl radical contain strong N 1s → π* resonances for each set of equivalent nitrogen atoms. The fact that these resonances are absent from the analogous spectra of the 6-oxotetrazane, whereas the O K-edge and C K-edge XANES spectra of both species are very similar, demonstrates that the unpaired electron of the radical is localized primarily on the N atoms of the 6-oxoverdazyl heterocycle.

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The synthesis and characterization of a new class of nickel-containing polymers is described. The optimized copolymerization of alkyne-bearing nickel(II) complexes of Goedken's macrocycle (4,11-dihydro-5,7,12,14-tetramethyldibenzo[b,i][1,4,8,11]tetraazacyclotetradecine) and brominated 9,9-dihexylfluorene produced polymers with potential application as functional redox-active materials. The title polymers exhibit electrochemically reversible, ligand-centered oxidation events at 0.

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We report the synthesis and characterization of a series of novel hexaalkoxydibenz[a,c]anthracenes. While the parent compound is not mesomorphic, the introduction of substituents in the 10- and 13-positions yields compounds with columnar liquid crystalline phases over very broad temperature ranges.

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