The development and widespread application of organic electronic devices require the availability of simple and cost-effective suitable materials. In this study, the preparation of a new class of conjugated compounds on the basis of a dithienocyclohexanone (DTCH) core is reported. Several synthetic strategies for the preparation of dialkyl DTCH derivatives are explored, with special emphasis on the establishment of a sustainable synthetic access. Two successful synthetic pathways, both consisting of five steps, are identified: the first one featuring readily available 3-thiophenecarboxaldeyde and the second one 3-ethynylthiophene as the starting materials. Both procedures are characterized by reasonably high overall yields (over 30%) and remarkably low factors (<400). Preliminary evidences of the use of such building blocks in the micellar Suzuki-Miyaura cross-coupling reactions leading to promising molecular semiconductors are also given. Moreover, on a small molecule containing DTCH moiety, solar cell performance was investigated.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641726 | PMC |
http://dx.doi.org/10.1021/acsomega.7b00987 | DOI Listing |
ACS Omega
August 2017
Renewable Energies & Environmental R&D Center - Istituto Guido Donegani, Eni S.p.A., Via Giacomo Fauser 4, 28100 Novara, Italy.
The development and widespread application of organic electronic devices require the availability of simple and cost-effective suitable materials. In this study, the preparation of a new class of conjugated compounds on the basis of a dithienocyclohexanone (DTCH) core is reported. Several synthetic strategies for the preparation of dialkyl DTCH derivatives are explored, with special emphasis on the establishment of a sustainable synthetic access.
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