Low band gap donor-acceptor-donor compounds containing carbazole and naphthalene diimide units: Synthesis, electropolymerization and spectroelectrochemical behaviour. (20th October 2020)
- Record Type:
- Journal Article
- Title:
- Low band gap donor-acceptor-donor compounds containing carbazole and naphthalene diimide units: Synthesis, electropolymerization and spectroelectrochemical behaviour. (20th October 2020)
- Main Title:
- Low band gap donor-acceptor-donor compounds containing carbazole and naphthalene diimide units: Synthesis, electropolymerization and spectroelectrochemical behaviour
- Authors:
- Rybakiewicz, Renata
Ganczarczyk, Roman
Charyton, Martyna
Skorka, Lukasz
Ledwon, Przemyslaw
Nowakowski, Robert
Zagorska, Malgorzata
Pron, Adam - Abstract:
- Abstract: A new DπAπD compound consisting of naphthalene diimide core-functionalized with 1, 4-phenylene-functionalized carbazole, namely 2, 6-bis[4-(9 H -carbazol-9-yl)phenyl]- N, N' -bis(2-ethylhexyl)-1, 4, 5, 8-naphthalenetetracarboxylic acid diimide (CNDI ) was synthesized. Its redox properties (reduction and oxidation potentials, electron affinities (EA) and ionization potentials (IP)) were compared with those of 4, 7-bis(4-(9 H -carbazol-9-yl)phenyl)benzo[ c ][1, 2, 5]thiadiazole (CBTD ) – a specially synthesized reference compound containing identical Dπ- units and significantly weaker acceptor (benzothiadiazole). It was demonstrated that the acceptor strength, determined as the index of the spatial extent of the charge transfer, D C T P, only weakly influenced the molecule oxidation potential and by consequence its ionization potential. To the contrary, strong effect of charge transfer, expressed by D C T P, was found for the reduction potential of CNDI and CBTD, showing significantly higher reduction potential of the former leading to much higher |EA|. CNDI could be electrochemically polymerized yielding a low band gap polymer (Eg = 1.63 eV) of ambipolar character, exhibiting low ionization potential (IP = 5.48 eV) and high electron affinity (|EA| = 3.85 eV). In its cyclic voltammograms polyCNDI shows five redox states, namely neutral, first and second reduction and first and second oxidation ones. As revealed by detailed studies of electrochromic parameters onlyAbstract: A new DπAπD compound consisting of naphthalene diimide core-functionalized with 1, 4-phenylene-functionalized carbazole, namely 2, 6-bis[4-(9 H -carbazol-9-yl)phenyl]- N, N' -bis(2-ethylhexyl)-1, 4, 5, 8-naphthalenetetracarboxylic acid diimide (CNDI ) was synthesized. Its redox properties (reduction and oxidation potentials, electron affinities (EA) and ionization potentials (IP)) were compared with those of 4, 7-bis(4-(9 H -carbazol-9-yl)phenyl)benzo[ c ][1, 2, 5]thiadiazole (CBTD ) – a specially synthesized reference compound containing identical Dπ- units and significantly weaker acceptor (benzothiadiazole). It was demonstrated that the acceptor strength, determined as the index of the spatial extent of the charge transfer, D C T P, only weakly influenced the molecule oxidation potential and by consequence its ionization potential. To the contrary, strong effect of charge transfer, expressed by D C T P, was found for the reduction potential of CNDI and CBTD, showing significantly higher reduction potential of the former leading to much higher |EA|. CNDI could be electrochemically polymerized yielding a low band gap polymer (Eg = 1.63 eV) of ambipolar character, exhibiting low ionization potential (IP = 5.48 eV) and high electron affinity (|EA| = 3.85 eV). In its cyclic voltammograms polyCNDI shows five redox states, namely neutral, first and second reduction and first and second oxidation ones. As revealed by detailed studies of electrochromic parameters only three redox states (neutral, first reduction and first oxidation) demonstrate good electrochromic performance. … (more)
- Is Part Of:
- Electrochimica acta. Volume 358(2020)
- Journal:
- Electrochimica acta
- Issue:
- Volume 358(2020)
- Issue Display:
- Volume 358, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 358
- Issue:
- 2020
- Issue Sort Value:
- 2020-0358-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-10-20
- Subjects:
- Donor-acceptor-donor compounds -- Carbazole -- Naphthalene diimide -- Electrochemical polymerization -- Electrochromism
Electrochemistry -- Periodicals
Electrochemistry, Industrial -- Periodicals
541.37 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00134686 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.electacta.2020.136922 ↗
- Languages:
- English
- ISSNs:
- 0013-4686
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3698.950000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14483.xml