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Related Concept Videos

Acid Halides to Amides: Aminolysis01:07

Acid Halides to Amides: Aminolysis

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Aminolysis is a nucleophilic acyl substitution reaction, where ammonia or amines act as nucleophiles to give the substitution product. Acid halides react with ammonia, primary amines, and secondary amines to yield primary, secondary, and tertiary amides, respectively.
In the first step of the aminolysis mechanism, the amine attacks the carbonyl carbon of the acyl chloride to form a tetrahedral intermediate. In the second step, the carbonyl group is re-formed with the elimination of a chloride...
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Ion Exchange

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Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or...
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Fabricating Degradable Thermoresponsive Hydrogels on Multiple Length Scales via Reactive Extrusion, Microfluidics, Self-assembly, and Electrospinning
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Dissipative Acid-Fueled Reprogrammable Supramolecular Materials.

Enzo Olivieri1, Baptiste Gasch1, Guilhem Quintard2

  • 1Aix Marseille Univ, CNRS, Centrale Marseille, iSm2, 13397 Marseille, France.

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|May 17, 2022
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Summary
This summary is machine-generated.

Researchers developed novel time-controlled smart materials using trichloroacetic acid (TCA) as fuel. These materials reversibly switch between gel and solution states, enabling applications like remoldable objects and erasing ink.

Keywords:
chiralitydissipative assemblyorganogelsmart materialsupramolecular

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Area of Science:

  • Materials Science
  • Supramolecular Chemistry

Background:

  • Smart materials offer dynamic property changes in response to stimuli.
  • Reversible gel-sol-gel transitions are crucial for advanced material applications.

Purpose of the Study:

  • To introduce trichloroacetic acid (TCA) as a fuel for creating novel time-controlled smart materials.
  • To explore the reversible gel-sol-gel transition mechanism using TCA and amine organogelators.

Main Methods:

  • Utilizing neutral amines as organogelators.
  • Inducing gel-to-solution transition via TCA addition and amine protonation.
  • Achieving solution-to-gel recovery through time-dependent TCA decarboxylation.

Main Results:

  • Demonstrated reversible gel-sol-gel switching in materials triggered by TCA.
  • Showcased time-dependent property changes enabling controlled material states.
  • Confirmed TCA decarboxylation as the mechanism for gel state recovery.

Conclusions:

  • Developed innovative time-controlled materials with reversible gel-sol-gel behavior.
  • Highlighted the potential of TCA as a fuel for dynamic material systems.
  • Identified applications in remoldable objects, erasing ink, chiroptical switches, and electrical systems.