Dialdehyde Polysaccharides as Templates for Green Synthesis of Polypyrrole-Based Materials without Oxidative Polymerization
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081707%3A_____%2F25%3A00636643" target="_blank" >RIV/68081707:_____/25:00636643 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/70883521:28110/25:63596079 RIV/70883521:28610/25:63596079
Výsledek na webu
<a href="https://pubs.acs.org/doi/10.1021/acssuschemeng.5c02711" target="_blank" >https://pubs.acs.org/doi/10.1021/acssuschemeng.5c02711</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acssuschemeng.5c02711" target="_blank" >10.1021/acssuschemeng.5c02711</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Dialdehyde Polysaccharides as Templates for Green Synthesis of Polypyrrole-Based Materials without Oxidative Polymerization
Popis výsledku v původním jazyce
Polypyrrole (PPy) is one of the most promising conductive polymers, with potential applications in energy storage, flexible electronics, and biomedicine. Broader use of PPy-based materials is, however, limited by harmful reactants used in their preparation and by the absence of strong interactions between relatively chemically inert PPy and the used matrices. Here, an innovative and green method is introduced based on a spontaneous condensation reaction between dialdehyde polysaccharides (DAPs) and pyrrole. The unique structure of DAPs spontaneously facilitates the chaining of pyrrole cycles into PPy copolymers without any added oxidizing agent or catalysts. This presents a new approach for preparing PPy-based materials with low cytotoxicity and strong antioxidative, anti-inflammatory, and immunomodulatory effects, ideal for biomedical applications. Moreover, this method can be combined with traditional oxidative polymerization to prepare covalently linked PPy composites with greatly improved resistance toward wear and loss of conductivity.
Název v anglickém jazyce
Dialdehyde Polysaccharides as Templates for Green Synthesis of Polypyrrole-Based Materials without Oxidative Polymerization
Popis výsledku anglicky
Polypyrrole (PPy) is one of the most promising conductive polymers, with potential applications in energy storage, flexible electronics, and biomedicine. Broader use of PPy-based materials is, however, limited by harmful reactants used in their preparation and by the absence of strong interactions between relatively chemically inert PPy and the used matrices. Here, an innovative and green method is introduced based on a spontaneous condensation reaction between dialdehyde polysaccharides (DAPs) and pyrrole. The unique structure of DAPs spontaneously facilitates the chaining of pyrrole cycles into PPy copolymers without any added oxidizing agent or catalysts. This presents a new approach for preparing PPy-based materials with low cytotoxicity and strong antioxidative, anti-inflammatory, and immunomodulatory effects, ideal for biomedical applications. Moreover, this method can be combined with traditional oxidative polymerization to prepare covalently linked PPy composites with greatly improved resistance toward wear and loss of conductivity.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10404 - Polymer science
Návaznosti výsledku
Projekt
<a href="/cs/project/GA24-11534S" target="_blank" >GA24-11534S: Vodivé (bio)polymerní kompozity s kovalentně vázaným polypyrrolem pro biomedicínské aplikace</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2025
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
ACS Sustainable Chemistry & Engineering
ISSN
2168-0485
e-ISSN
2168-0485
Svazek periodika
13
Číslo periodika v rámci svazku
22
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
12
Strana od-do
8435-8446
Kód UT WoS článku
001498874600001
EID výsledku v databázi Scopus
2-s2.0-105006908655