Synfacts 2017; 13(09): 0923
DOI: 10.1055/s-0036-1591205
Synthesis of Materials and Unnatural Products
© Georg Thieme Verlag Stuttgart · New York

Utilizing Cyclopentadiene for the Design of New Polyenyne Motifs

Contributor(s): Timothy M. Swager, Kosuke Yoshinaga
Rahman MM. Zhao X. Harrell J. Chen L. Pietrangelo A. * Rutgers University, Newark, USA
Poly(cyclopentadienylene Ethynylene)s: Breaking Conventional Polyenyne Motifs.

ACS Macro Lett. 2017;
6: 632-636
Further Information

Publication History

Publication Date:
18 August 2017 (online)

 
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Significance

Conjugated polyenynes are a unique class of polymers with backbones consisting entirely of sp- and nonaromatic sp2-hybridized carbon atoms. Despite its attractive electronic properties and potential application in materials science, the discovery of new polyenyne motifs remains challenging because of the dearth of suitable precursors and preparatory methods. Herein, Pietrangelo and co-workers report the synthesis of poly(cyclopentadienylene ethynylene)s (PCEs) and poly(p-phenylene ethynylene)/poly(cyclopentadienylene ethynylene) copolymers (PPECEs), in which a cyclopentadiene motif is incorporated into their monomeric structures.


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Comment

Interestingly, the authors’ results suggest that the solubilizing group structure of the PCEs has an effect on the polymer molecular weight and optical absorption profiles. In contrast, the solubilizing group structure of copolymer PPECEs has little effect on their optical absorption. Taken together, these results indicate that the cyclopentadiene constituents are responsible for the low-energy electronic transitions of PCEs. Evaluation of PPEs as semiconductors in organic electronic devices is under way.


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