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Synthesis 2014; 46(21): 2976-2982
DOI: 10.1055/s-0034-1378894
DOI: 10.1055/s-0034-1378894
paper
Synthesis of Symmetrically Functionalized Oligo(het)arylenes Containing Phenylene, Thiophene, Benzthiophene, Furan, Benzofuran, Pyridine, and/or Pyrimidine Groups
Further Information
Publication History
Received: 09 July 2014
Accepted after revision: 18 July 2014
Publication Date:
13 August 2014 (online)
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Abstract
Rod-like oligomers consisting of thiophene and phenylene rings have proven to be highly interesting building blocks for the preparation of self-assembled, well-defined nanoaggregates via vapor deposition on solid supports. Changing the molecules’ chain length and substitution pattern allows to tailor the aggregates’ optical properties and morphologies. Thus, there is an ongoing demand for the synthesis of functionalized oligo(het)arylenes. Here, we describe an efficient and general approach for a broad spectrum of such molecules using a Suzuki cross-coupling strategy as the key reaction step.
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The synthesis of this compound has been described before, however, using different synthetic approaches: