Publication detail

Diphenylamine end-capped diketopyrrolopyrroles with phenylene–vinylene conjugation extension

FREBORT, Š. VALA, M. LUŇÁK, S. HONOVÁ, J. MIKYSEK, T. ELIÁŠ, Z. LYČKA, A.

Original Title

Diphenylamine end-capped diketopyrrolopyrroles with phenylene–vinylene conjugation extension

Type

journal article in Web of Science

Language

English

Original Abstract

Two pyrrolo[3,4-c]pyrrole-1,4-diones (diketopyrrolopyrroles, DPP) with 4''-diphenylamino-stilben-4'-yl substituents at the 3- and 3,6-positions of the DPP heterocycle are synthesized. The 1H and 13C NMR spectra of their soluble derivatives, N(2) and N(5)-dialkylated by 2-ethylhexyl bromoacetate, were completely assigned. Soluble DPPs show photovoltaic activity in bulk heterojunction solar cells. Their electrochemistry and absorption and fluorescence spectra were studied.

Keywords

Diketopyrrolopyrrole, Alkylation, NMR, Organic photovoltaics

Authors

FREBORT, Š.; VALA, M.; LUŇÁK, S.; HONOVÁ, J.; MIKYSEK, T.; ELIÁŠ, Z.; LYČKA, A.

RIV year

2014

Released

23. 4. 2014

Publisher

Elsevier

ISBN

0040-4039

Periodical

TETRAHEDRON LETTERS

Year of study

2014

Number

55

State

United Kingdom of Great Britain and Northern Ireland

Pages from

2829

Pages to

2834

Pages count

6

URL

BibTex

@article{BUT107085,
  author="FREBORT, Š. and VALA, M. and LUŇÁK, S. and HONOVÁ, J. and MIKYSEK, T. and ELIÁŠ, Z. and LYČKA, A.",
  title="Diphenylamine end-capped diketopyrrolopyrroles with phenylene–vinylene conjugation extension",
  journal="TETRAHEDRON LETTERS",
  year="2014",
  volume="2014",
  number="55",
  pages="2829--2834",
  doi="10.1016/j.tetlet.2014.03.080",
  issn="0040-4039",
  url="https://www.sciencedirect.com/science/article/pii/S0040403914005012"
}