Dimer formation of viologen derivatives and their electrochromic properties

Sung Hoon Kim, Jin Seok Bae, Seok Hwan Hwang, Tae Sun Gwon, Myung Ki Doh

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

The electrochromic properties of 1,1′-diethyl-4,4′-hipyridinium dibromide (EV), 1,1′-dipropyl-4,4′-bipyridinium dihromide (PV), 1,1′-dibutyl-4,4′-bipyridinium dibromide (BV) and 1-ethyl-1′-butyl bipyridinium dibromide (EBV) were studied using a propylenecarbonate/methanol solution with Bu4NBF4 as the supporting electrolyte. A monomer-dimer equilibrium is proposed to explain the observation that the EV and EBV cation radical solutions are violet at an applied voltage of 1.7-3.0 V, but become blue in the open-circuit condition. C 1997 Elsevier Science Ltd. All rights reserved.

Original languageEnglish
Pages (from-to)167-172
Number of pages6
JournalDyes and Pigments
Volume33
Issue number2
DOIs
StatePublished - Feb 1997

Keywords

  • Aggregation
  • Display
  • Electrochemistry
  • Electrochromism
  • ITO glass
  • Viologen

Fingerprint

Dive into the research topics of 'Dimer formation of viologen derivatives and their electrochromic properties'. Together they form a unique fingerprint.

Cite this