Electron‐Rich EDOT Linkers in Tetracationic bis‐Triarylborane Chromophores: Influence on Water Stability, Biomacromolecule Sensing, and Photoinduced Cytotoxicity. Issue 48 (4th July 2022)
- Record Type:
- Journal Article
- Title:
- Electron‐Rich EDOT Linkers in Tetracationic bis‐Triarylborane Chromophores: Influence on Water Stability, Biomacromolecule Sensing, and Photoinduced Cytotoxicity. Issue 48 (4th July 2022)
- Main Title:
- Electron‐Rich EDOT Linkers in Tetracationic bis‐Triarylborane Chromophores: Influence on Water Stability, Biomacromolecule Sensing, and Photoinduced Cytotoxicity
- Authors:
- Ferger, Matthias
Roger, Chantal
Köster, Eva
Rauch, Florian
Lorenzen, Sabine
Krummenacher, Ivo
Friedrich, Alexandra
Košćak, Marta
Nestić, Davor
Braunschweig, Holger
Lambert, Christoph
Piantanida, Ivo
Marder, Todd B. - Abstract:
- Abstract: Three novel tetracationic bis‐triarylboranes with 3, 4‐ethylenedioxythiophene (EDOT) linkers, and their neutral precursors, showed significant red‐shifted absorption and emission compared to their thiophene‐containing analogues, with one of the EDOT‐derivatives emitting in the NIR region. Only the EDOT‐linked trixylylborane tetracation was stable in aqueous solution, indicating that direct attachment of a thiophene or even 3‐methylthiophene to the boron atom is insufficient to provide hydrolytic stability in aqueous solution. Further comparative analysis of the EDOT‐linked trixylylborane tetracation and its bis‐thiophene analogue revealed efficient photo‐induced singlet oxygen production, with the consequent biological implications. Thus, both analogues bind strongly to ds‐DNA and BSA, very efficiently enter living human cells, accumulate in several different cytoplasmic organelles with no toxic effect but, under intense visible light irradiation, they exhibit almost instantaneous and very strong cytotoxic effects, presumably attributed to singlet oxygen production. Thus, both compounds are intriguing theranostic agents, whose intracellular and probably intra‐tissue location can be monitored by strong fluorescence, allowing switching on of the strong bioactivity by well‐focused visible light. Abstract : Tetracationic bis‐triarylboranes with EDOT linkers, show red‐shifted absorption and emission compared to their thiophene‐linked analogues, with one derivativeAbstract: Three novel tetracationic bis‐triarylboranes with 3, 4‐ethylenedioxythiophene (EDOT) linkers, and their neutral precursors, showed significant red‐shifted absorption and emission compared to their thiophene‐containing analogues, with one of the EDOT‐derivatives emitting in the NIR region. Only the EDOT‐linked trixylylborane tetracation was stable in aqueous solution, indicating that direct attachment of a thiophene or even 3‐methylthiophene to the boron atom is insufficient to provide hydrolytic stability in aqueous solution. Further comparative analysis of the EDOT‐linked trixylylborane tetracation and its bis‐thiophene analogue revealed efficient photo‐induced singlet oxygen production, with the consequent biological implications. Thus, both analogues bind strongly to ds‐DNA and BSA, very efficiently enter living human cells, accumulate in several different cytoplasmic organelles with no toxic effect but, under intense visible light irradiation, they exhibit almost instantaneous and very strong cytotoxic effects, presumably attributed to singlet oxygen production. Thus, both compounds are intriguing theranostic agents, whose intracellular and probably intra‐tissue location can be monitored by strong fluorescence, allowing switching on of the strong bioactivity by well‐focused visible light. Abstract : Tetracationic bis‐triarylboranes with EDOT linkers, show red‐shifted absorption and emission compared to their thiophene‐linked analogues, with one derivative emitting in the NIR. A water‐stable EDOT‐linked tetracation and its bis‐thiophene analogue efficiently photo‐induce 1 O2 production. Both bind to ds‐DNA and BSA, enter living human cells, accumulate in several different cytoplasmic organelles with no toxic effect but, under visible light irradiation, exhibit rapid, strong cytotoxic effects. … (more)
- Is Part Of:
- Chemistry. Volume 28:Issue 48(2022)
- Journal:
- Chemistry
- Issue:
- Volume 28:Issue 48(2022)
- Issue Display:
- Volume 28, Issue 48 (2022)
- Year:
- 2022
- Volume:
- 28
- Issue:
- 48
- Issue Sort Value:
- 2022-0028-0048-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-07-04
- Subjects:
- boranes -- DNA/RNA sensors -- fluorescent probes -- singlet oxygen -- theranostics
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.202201130 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 23197.xml