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Synthesis of Stimuli-responsive Nanogels using Aqueous One-step Crosslinking and Co-nanopolymerization
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Mechanochemical green synthesis of hyper-crosslinked cyclodextrin polymers
Alberto Rubin Pedrazzo1, Fabrizio Caldera1, Marco Zanetti1
1Dipartimento di Chimica, Università degli Studi di Torino, Via Giuria 7, Torino 10125, Italy.
Beilstein Journal of Organic Chemistry
|July 25, 2020
Summary
This study introduces a green mechanochemistry method for synthesizing cyclodextrin nanosponges (CD-NS). This solvent-free approach yields CD-NS with properties comparable to solvent-synthesized ones and allows easy functionalization.
Area of Science:
- Materials Science
- Polymer Chemistry
- Green Chemistry
Background:
- Cyclodextrin nanosponges (CD-NS) are versatile nanostructured polymers with potential biomedical applications.
- Traditional synthesis methods often rely on organic polar aprotic solvents, which can impact the final product characteristics.
Purpose of the Study:
- To develop a novel, environmentally friendly synthetic pathway for cyclodextrin nanosponges.
- To investigate the feasibility of using mechanochemistry for CD-NS synthesis.
- To demonstrate the functionalization capabilities of the synthesized CD-NS.
Main Methods:
- Utilized mechanochemistry, specifically ball milling, for the synthesis of CD-NS.
- Employed 1,1-carbonyldiimidazole as a crosslinker in a solvent-free process.
- Functionalized the resulting polymer with organic dyes (fluorescein, methyl red, rhodamine B).
Main Results:
- Successfully synthesized CD-NS using a green, solvent-free mechanochemical approach.
- The obtained polymer exhibited comparable characteristics to conventionally synthesized CD-based carbonate NS.
- Demonstrated facile post-synthesis functionalization via reaction with organic dyes.
Conclusions:
- Mechanochemistry offers a sustainable and efficient alternative for CD-NS synthesis.
- The solvent-free method yields high-quality CD-NS suitable for further modification.
- This approach broadens the scope for developing advanced functionalized nanosponges.
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