P
Prantik Mondal
Researcher at Indian Institute of Technology Kharagpur
Publications - 20
Citations - 344
Prantik Mondal is an academic researcher from Indian Institute of Technology Kharagpur. The author has contributed to research in topics: Click chemistry & Chain transfer. The author has an hindex of 8, co-authored 17 publications receiving 193 citations.
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Self-Healable and Ultrahydrophobic Polyurethane-POSS Hybrids by Diels–Alder “Click” Reaction: A New Class of Coating Material
TL;DR: In this paper, polyurethane functionalized with pendant furan moiety (FPU) was prepared using a novel chain extender (FA-FGE) which was obtained from the reaction between furfurylamine (FA) and fur furyl glycidyl ether (FGE).
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Self-Healable Polyurethane Elastomer Based on Dual Dynamic Covalent Chemistry Using Diels–Alder “Click” and Disulfide Metathesis Reactions
TL;DR: In this article, a dual-functional polyurethane elastomer having disulfide as well as furfuryl functionality was used for a variety of applications, including medical applications.
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A new class of self-healable hydrophobic materials based on ABA triblock copolymer via RAFT polymerization and Diels-Alder “click chemistry”
TL;DR: In this article, a tri-block copolymer (BCP) was obtained by RAFT polymerization using PDMS-CTA as macro-RAFT agent and the formation of FDF triblock copolymers was confirmed by 1 H NMR, GPC and DSC analyses.
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Polyurethane with an ionic liquid crosslinker: a new class of super shape memory-like polymers
TL;DR: In this article, a new class of ionic liquid crosslinked shape-memory polyurethane (PU-IL) based on polycaprolactone diol and 4,4′-methylenebis(phenyl isocyanate) (MDI) was synthesized.
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A healable thermo-reversible functional polymer prepared via RAFT polymerization and ultrafast 'click' chemistry using a triazolinedione derivative.
TL;DR: The preparation and characterization of a functional polymer bearing a pendant indole group via a reversible-addition fragmentation and chain transfer process followed by its modification via an Alder-ene 'click' reaction using a 1,2,4-triazoline-3,5-dione (TAD) derivative showed thermo-reversible as well as healing characteristics.