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Isatin Super-acid-catalyzed polymerization 


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Superacid-catalyzed polymerization of isatin has been studied in several papers. The polymerization reactions involve the use of superacid catalysts, such as trifluoromethanesulfonic acid, to promote the condensation of isatin with other monomers. The resulting polymers have been characterized by various techniques, including gel permeation chromatography, nuclear magnetic resonance, and diffusion-ordered spectroscopy . The polymers obtained from the polymerization reactions have shown high molecular weights and ultra-high molecular weights, depending on the stoichiometry of the monomers used . The isatin-based polymers have been explored for various applications, including fuel cells, energy storage batteries, and membrane separation . Mathematical models have also been developed to predict the kinetics and molecular weight development of superacid-catalyzed polymerization reactions involving isatin and other monomers . The resulting polymers have exhibited excellent thermal stability and optical properties, making them suitable for optoelectronic devices and proton exchange membrane fuel cells . Spiro poly(isatin-ethersulfone) polymers have been synthesized using superacid-catalyzed polyhydroxyalkylation reactions, and their morphology has been studied to understand their proton conductivity and ion exchange capacity .

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The paper mentions that spiro poly(isatin-ethersulfone) polymers were prepared from isatin by super acid catalyzed polyhydroxyalkylation reactions.
The paper discusses the superacid-catalyzed step-growth polymerization of isatin and biphenyl or terphenyl monomers, but it does not specifically mention the polymerization of isatin alone.
The paper mentions that the isatin aromatic hydrocarbon copolymer is synthesized through a super acid catalyzed hydroxyalkylation polycondensation reaction.
The paper discusses the super acid-catalyzed polymerization of phenothiazine and modified isatin, but it does not specifically mention isatin super-acid-catalyzed polymerization.
The paper discusses the superacid-catalyzed polyhydroxyalkylation of biphenyl and 1-propyl isatin, but it does not specifically mention isatin super-acid-catalyzed polymerization.

Related Questions

What is the degree of polymerization?5 answersThe degree of polymerization (DP) is a crucial parameter in characterizing polymers. It represents the number of monomeric units in a polymer chain. The DP is directly related to the size of macromolecules and influences their properties, such as electronic circular dichroism spectra. Different types of interactions, like p-p, charge-transfer, and van der Waals interactions, can affect the self-assembly of monomers into supramolecular polymers with high DP. In the polymerization process, the degree of conversion (DC) is also significant, representing the extent of monomer conversion into polymers. Understanding and controlling the DP and DC are essential for tailoring the properties of polymers for various applications.
What is in situ polymerization?4 answersIn situ polymerization refers to the process of polymer formation that occurs directly within a specific environment or system, without the need for isolating intermediates. This technique has been explored in various scenarios, such as the polymerization of solvophobic monomers within solvophilic polymers to create network structures, and the in-situ polymerization of diacetylene-containing lipidated peptide amphiphiles inside living cells for potential biomedical applications. Additionally, in the realm of supramolecular polymers, in situ chemical reactions have been achieved within π-conjugated molecules to create dynamic materials with spatiotemporal properties. The concept of in situ polymerization offers a versatile approach for creating tailored polymers with specific functionalities directly within the desired system or environment.
What are the effects of catalytic coating activity on polymeric?5 answersCatalytic coating activity on polymeric materials has been shown to have significant effects on their performance. For example, cationic polyelectrolyte coatings have been found to increase the catalytic activity of gold nanoislands (Au NIs) towards transfer hydrogenation and oxidation reactions. Coating fluorocarbonsulfonic acid polymers onto a support greatly improves their catalytic efficiency and maintains a high level of activity over time. In the case of nitrogen-doped carbon shell-coated catalysts, the durability and activity of platinum and platinum-nickel alloy catalysts were increased, leading to improved performance in fuel cells. These findings highlight the potential of catalytic coatings to enhance the activity and durability of polymeric materials in various applications.
What are the potential applications of poly isatin-based anion and proton exchange membrane fuel cells (AEMFCs and PEMFCs)?5 answersPoly isatin-based anion and proton exchange membrane fuel cells (AEMFCs and PEMFCs) have potential applications in various fields. PEMFCs are considered suitable for transportation and portable energy frameworks, with commercialized products already in use worldwide. AEMFCs, on the other hand, face challenges related to the performance of their key component, the anion exchange membrane. However, recent research has shown that AEMs functionalized with organometallic cations have excellent stability and comprehensive performance, making them potential candidates for fuel cell applications. Additionally, poly isatin-based AEMs have been synthesized and investigated, showing promising results in terms of mechanical properties, ion exchange capacity, dimensional stability, and conductivity. These AEMs have the potential to be used in fuel cells, such as direct borohydride fuel cells, demonstrating high OH− conductivity and power density. Overall, both AEMFCs and PEMFCs have potential applications in various fields, including transportation, portable energy, and stationary power plants.
How can poly isatin be used to improve the performance of proton exchange membrane fuel cells?3 answersPoly isatin can be used to improve the performance of proton exchange membrane fuel cells (PEMFCs) in several ways. Firstly, the incorporation of ether-bond free and piperidinium cationic groups in anion exchange membranes (AEMs) based on poly(isatin-piperidium-terphenyl) promotes chemical stability and enhances the mechanical properties of the membranes. Secondly, the design of bifunctional poly(p-terphenyl-co-isatin piperidinium) copolymers with tethered phosphonic acid (t-PA) and intrinsic tertiary amine base groups provides a well-designed platform for rapid proton transport, resulting in improved electrochemical performance and service lifetime of high temperature PEMs. Thirdly, poly(alkyl–fluorene isatin)-based PEMs with pendant sulfonate groups exhibit excellent physical and chemical properties, high proton conductivity, and good mechanical stability, making them suitable for PEMFCs. Additionally, aliphatic chain-containing poly(isatin diphenyl-co-terphenyl) copolymers with side-chain sulfonic acid groups show excellent proton conductivity and oxidative stability, making them promising for application in fuel cells. Lastly, poly(isatin biphenylene) membranes functionalized with organometallic cations demonstrate excellent stability, hydroxide conductivity, dimensional stability, and mechanical properties, making them potential candidates for anion exchange membranes in fuel cells.
What are the mechanisms by which IA improves the properties of urea formol resins?5 answersThe mechanisms by which IA improves the properties of urea-formaldehyde (UF) resins include increasing the molecular branching coefficient and molecular weight of the resin, which leads to an increased curing cross-linking density and improved bonding strength. IA also reduces the formaldehyde release amount of the bonded products, making the resin adhesive low-toxicity. Additionally, IA can greatly improve the bonding strength and lower the formaldehyde release amount of amine resin adhesives, without changing the existing process conditions. Modified UF resins with IA show lower free formaldehyde content and higher boiling-water resistance compared to unmodified resins, resulting in improved water resistance properties. Melamine, a type of IA, improves the resistance against attack by humidity and water, especially at elevated temperatures. Overall, IA enhances the performance of UF resins by improving water resistance, reducing formaldehyde emissions, and increasing bonding strength.

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