4.5 Article

Synthetic Routes to TEG-Substituted Diketopyrrolopyrrole-Based Low Band-Gap Polymers

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2016, Issue 19, Pages 3233-3242

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201600406

Keywords

Diketopyrrolopyrroles; Low band-gap; Polymers; Cross-coupling; Oligoether chains; Donor-acceptor systems; Pi interactions

Funding

  1. Ministero dell'Istruzione, dell'Universita e della Ricerca (MIUR)
  2. Universita degli Studi di Bari Aldo Moro [prot. 2012A4Z2RY, PON02_00563_3316357, PON03PE_00004_1]

Ask authors/readers for more resources

We report herein general synthetic routes to novel TEG-functionalized DPP-based co-polymers (TEG = triethylene glycol; DPP = diketopyrrolopyrrole) that display alternating TEG-substituted DPP moieties with various functionalized donor units; donor units contain moieties such as polythiophene segments decorated with thermocleavable tertiary esters or additional TEG chains and alkoxy-substituted benzodithiophenes. The synthetic approaches are based on Stille coupling chemistry or, for the first time for TEG-substituted DPP-based polymers, on direct heteroarylation polymerizations. Spectroscopic and electrochemical characterization as well as preliminary tests in photovoltaic cells are also reported.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available