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Self-Assembly of Ch...
Self-Assembly of Chiro-Optical Materials from Nonchiral Oligothiophene-Porphyrin Derivatives and Random Coil Synthetic Peptides
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- Arja, Katriann (författare)
- Linköpings universitet,Kemi,Tekniska fakulteten
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- Selegård, Robert (författare)
- Linköpings universitet,Biofysik och bioteknik,Tekniska fakulteten
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- Paloncyova, Marketa (författare)
- KTH,Teoretisk kemi och biologi,KTH Royal Inst Technol, Sweden; Palacky Univ Olomouc, Czech Republic
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- Linares, Mathieu (författare)
- Linköpings universitet,Laboratoriet för organisk elektronik,Tekniska fakulteten
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- Lindgren, M. (författare)
- Norwegian Univ Sci & Technol, Norway
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- Norman, Patrick (författare)
- KTH,Teoretisk kemi och biologi,KTH Royal Inst Technol, Sweden
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- Aili, Daniel (författare)
- Linköpings universitet,Biofysik och bioteknik,Tekniska fakulteten
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- Nilsson, Peter (författare)
- Linköpings universitet,Kemi,Tekniska fakulteten
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(creator_code:org_t)
- 2022-09-29
- 2023
- Engelska.
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Ingår i: ChemPlusChem. - : Wiley. - 2192-6506. ; 88:1
- Relaterad länk:
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https://doi.org/10.1...
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https://liu.diva-por... (primary) (Raw object)
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https://urn.kb.se/re...
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https://doi.org/10.1...
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https://urn.kb.se/re...
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Abstract
Ämnesord
Stäng
- Biomimetic chiral optoelectronic materials can be utilized in electronic devices, biosensors and artificial enzymes. Herein, this work reports the chiro-optical properties and architectural arrangement of optoelectronic materials generated from self-assembly of initially nonchiral oligothiophene−porphyrin derivatives and random coil synthetic peptides. The photo-physical- and structural properties of the materials were assessed by absorption-, fluorescence- and circular dichroism spectroscopy, as well as dynamic light scattering, scanning electron microscopy and theoretical calculations. The materials display a three-dimensional ordered helical structure and optical activity that are observed due to an induced chirality of the optoelectronic element upon interaction with the peptide. Both these properties are influenced by the chemical composition of the oligothiophene−porphyrin derivative, as well as the peptide sequence. We foresee that our findings will aid in developing self-assembled optoelectronic materials with dynamic architectonical accuracies, as well as offer the possibility to generate the next generation of materials for a variety of bioelectronic applications.
Ämnesord
- NATURVETENSKAP -- Kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences (hsv//eng)
- NATURVETENSKAP -- Kemi -- Annan kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Other Chemistry Topics (hsv//eng)
Nyckelord
- circular dichroism
- oligothiophene
- porphyrin
- self-assembly
- synthetic peptides
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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