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Indenofluorene-Exte...
Indenofluorene-Extended Tetrathiafulvalene Scaffolds for Dye-Sensitized Solar Cells
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- Mogensen, Josefine (författare)
- Univ Copenhagen, Dept Chem, Univ Pk 5, DK-2100 Copenhagen Ø, Denmark
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- Michaels, Hannes (författare)
- Uppsala universitet,Fysikalisk kemi
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- Roy, Rajarshi (författare)
- Uppsala universitet,Institutionen för kemi - Ångström
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- Broløs, Line (författare)
- Univ Copenhagen, Dept Chem, Univ Pk 5, DK-2100 Copenhagen Ø, Denmark
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- Drøhse Kilde, Martin (författare)
- Univ Copenhagen, Dept Chem, Univ Pk 5, DK-2100 Copenhagen Ø, Denmark
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- Freitag, Marina (författare)
- Uppsala universitet,Fysikalisk kemi,Newcastle Univ, Sch Nat & Environm Sci, Bedson Bldg, Newcastle Upon Tyne NE1 7RY, Tyne & Wear, England
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- Brøndsted Nielsen, Mogens (författare)
- Uppsala universitet,Institutionen för kemi - Ångström,Univ Copenhagen, Dept Chem, Univ Pk 5, DK-2100 Copenhagen Ø, Denmark
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(creator_code:org_t)
- 2020-09-10
- 2020
- Engelska.
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Ingår i: European Journal of Organic Chemistry. - : Wiley. - 1434-193X .- 1099-0690. ; 2020:38, s. 6127-6134
- Relaterad länk:
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https://urn.kb.se/re...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- Indenofluorene‐extended tetrathiafulvalenes (IF‐TTFs) comprise a class of π‐conjugated sensitizers that exhibit strong absorptions in the visible region and two reversible one‐electron oxidations. Herein we present the synthesis and optical as well as redox properties of novel IF‐TTF donor‐acceptor scaffolds that were integrated in dye‐sensitized solar cells (DSCs) via anchoring of a carboxylic acid end‐group on the scaffolds to TiO2. Synthetically, the scaffolds were constructed by Sonogashira coupling reactions between an iodo‐functionalized IF‐TTF and an acceptor moeity containing a terminal alkyne. These very first IF‐TTF based candidates for DSCs exhibited high performances, in particular a dye incorporating a benzothiadiazole acceptor moiety, showing a conversion efficiency of 6.4 %. This result signals that IF‐TTF derivatives present a promising class of compounds for further structural modifications. Such modifications will benefit from the readiness of the iodo‐funcitonalized IF‐TTF building block to undergo Pd‐catalyzed coupling reactions.
Ämnesord
- NATURVETENSKAP -- Kemi -- Organisk kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Organic Chemistry (hsv//eng)
- NATURVETENSKAP -- Kemi -- Fysikalisk kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Physical Chemistry (hsv//eng)
Nyckelord
- Conjugation
- Cross-coupling
- Dyes
- Redox chemistry
- Sulfur heterocycles
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- ref (ämneskategori)
- art (ämneskategori)
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