Facile syntheses of quater-, penta-, and sexipyrroles |
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Authors: | Sessler Jonathan L Aguilar Apolonio Sanchez-Garcia David Seidel Daniel Köhler Thomas Arp Forrest Lynch Vincent M |
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Affiliation: | Department of Chemistry and Biochemistry, Institute for Cellular and Molecular Biology, The University of Texas, Austin, 78712-0165, USA. sessler@mail.utexas.edu |
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Abstract: | alpha,alpha-Linked oligopyrroles are attractive precursors for both expanded porphyrin and conducting polymer chemistry. We demonstrate facile methods for synthesizing quater-, penta-, and sexipyrroles from more readily available bi- and terpyrrole intermediates. These products demonstrate stability in their brightly colored oxidized forms, while reduction using borohydride reagents gives the corresponding all-pyrrole oligomers, which oxidize readily in air. The oxidized quater- and sexipyrroles were characterized by single-crystal X-ray diffraction analysis. |
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