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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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Cleij, Thomas J.
Maastricht University
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (22/22 displayed)
- 2024Electrochemical Detection of Pseudomonas aeruginosa Quorum Sensing Molecule (S)-N-Butyryl Homoserine Lactone Using Molecularly Imprinted Polymerscitations
- 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
- 2015Strategy for Enhancing the Dielectric Constant of Organic Semiconductors Without Sacrificing Charge Carrier Mobility and Solubilitycitations
- 2011Phase behavior of PCBM blends with different conjugated polymerscitations
- 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
- 2011Tetra-alkoxy substituted PPV derivatives: a new class of highly soluble liquid crystalline conjugated polymerscitations
- 2010Alkyl-Chain-Length-Independent Hole Mobility via Morphological Control with Poly(3-alkylthiophene) Nanofiberscitations
- 2010MIP-based sensor platforms for the detection of histamine in the nano- and micromolar range in aqueous mediacitations
- 2009Exploring the Dithiocarbamate Precursor Route: Observation of a Base Induced Regioregularity Excess in Poly[(2-methoxy-5-(3 ',7 '-dimethyloctyloxy))-1,4-phenylenevinylene] (MDMO-PPV)citations
- 2009Controlling the morphology of nanofiber-P3HT:PCBM blends for organic bulk heterojunction solar cellscitations
- 2008Effect of temperature on the morphological and photovoltaic stability of bulk heterojunction polymer: fullerene solar cellscitations
- 2008Charge dissociation in polymer:fullerene bulk heterojunction solar cells with enhanced permittivitycitations
- 2008NMR study of the nanomorphology in thin films of polymer blends used in organic PV devices: MDMO-PPV/PCBMcitations
- 2007The synthesis of regio-regular poly(3-alkyl-2,5-thienylene vinylene) derivatives using lithium bis(trimethylsilyl)amide (LHMDS) in the dithiocarbamate precursorcitations
- 20072,5-substituted PPV-derivatives with different polarities: The effect of side chain polarity on solubility, optical and electronic propertiescitations
- 2007The synthesis of poly(thienylene vinylene) derivatives via the dithiocarbamate route: low band gap p-type conjugated polymers for photovoltaicscitations
- 2000Occurrence of radical cation localization in chemically modified poly(methylphenylsilane): Poly(methylphenyl-co-4-dimethylaminophenylmethylsilane)s and poly (methylphenyl-co-4-bromophenylmethylsilane)scitations
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.