Synthesis and bioconjugation of first alkynylated poly(dithieno[3,2-b:2′,3′-d]pyrrole)s

Literature Information

Publication Date 2017-11-06
DOI 10.1039/C7PY01528C
Impact Factor 5.582
Authors

Sylvia Schmid, Jasmina Gačanin, Peter Bäuerle


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Abstract

First synthesis of an alkynylated dithieno[3,2-b:2′,3′-d]pyrrole (DTP) monomer was developed, which allows electrochemical polymerization on platinum and indium tin oxide (ITO) electrodes. The obtained DTP-based polymer (pDTP) was successfully post-modified with redox active and biological entities via bio-orthogonal 1,3-dipolar cycloaddition reactions and [2 + 2]-cycloaddition. In vitro experiments with A549-human lung carcinoma cells evidenced the general biocompatibility of the compositionally tuneable pDTP-coated electrodes.

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Polymer Chemistry

Polymer Chemistry
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