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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Diliën, Hanne
Maastricht University
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (7/7 displayed)
- 2024Electrochemical Detection of Pseudomonas aeruginosa Quorum Sensing Molecule (S)-N-Butyryl Homoserine Lactone Using Molecularly Imprinted Polymerscitations
- 2023Recent Advances in Molecularly Imprinted Polymers for Glucose Monitoring: From Fundamental Research to Commercial Applicationcitations
- 2023Dipstick Sensor Based on Molecularly Imprinted Polymer‐Coated Screen‐Printed Electrodes for the Single‐Shot Detection of Glucose in Urine Samples—From Fundamental Study toward Point‐of‐Care Applicationcitations
- 2022Polyphosphate-Based Hydrogels as Drug-Loaded Wound Dressing: An In Vitro Studycitations
- 2021Topographical Vacuum Sealing of 3D-Printed Multiplanar Microfluidic Structurescitations
- 2011Identification and Quantification of Defect Structures in Poly(2,5-thienylene vinylene) Derivatives Prepared via the Dithiocarbamate Precursor Route by Means of NMR Spectroscopy on C-13-Labeled Polymerscitations
- 2011An Efficient Acid-Induced Conversion of Dithiocarbamate Precursor Polymers into Conjugated Materialscitations
Places of action
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article
An Efficient Acid-Induced Conversion of Dithiocarbamate Precursor Polymers into Conjugated Materials
Abstract
An acid-induced conversion method for dithiocarbamate precursor poly(thienylenevinylene) (PTV) and poly(phenylenevinylene) (PPV) derivatives is presented, which has the advantage that it can be executed at moderate temperatures. The lower conversion temperature avoids possible thermal degradation of the polymer chromophore structure, and therefore conjugated polymers with a higher effective conjugation length can be obtained. This process was studied using UV-vis and FTIR spectroscopy. The obtained results indicate that trifluoroacetic acid yields a more defect-free structure as compared to benzenesulfonic acid which induces degradation after prolonged reaction times. A tentative mechanism is proposed in which the formation of an intermediate carbenium ion is part of the rate-limiting step. It also implicates a competition between elimination and substitution reactions depending on specific reaction conditions.