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Related Concept Videos

Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the generated carbocation,...
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael acceptor.
Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...

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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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Solid-to-solid formation at the solid-liquid interface leading to a chiral coordination polymer from an achiral

Sabbani Supriya1, Samar K Das

  • 1School of Chemistry, University of Hyderabad, Hyderabad-500 046, India.

Chemical Communications (Cambridge, England)
|January 6, 2011
PubMed
Summary

A copper complex crystal transforms from achiral to chiral. This solid-liquid interface reaction replaces sulfate with azide anions, creating a novel coordination polymer.

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Published on: November 2, 2011

Area of Science:

  • Solid-state chemistry
  • Coordination chemistry
  • Crystallography

Background:

  • Copper(II) complexes are versatile in materials science.
  • Solid-liquid interface reactions offer unique pathways for crystal transformation.
  • Chirality in coordination polymers is crucial for advanced applications.

Purpose of the Study:

  • To investigate the transformation of an achiral copper complex crystal into a chiral coordination polymer.
  • To demonstrate anion exchange at the solid-liquid interface.
  • To synthesize and characterize the resulting chiral coordination polymer.

Main Methods:

  • Single crystal X-ray diffraction was used to determine the structures of the achiral precursor and the chiral product.
  • Solid-liquid interface reaction by dipping the achiral crystal into an aqueous azide solution.
  • Chemical analysis to confirm anion exchange.

Main Results:

  • An achiral copper(II) sulfate complex crystal [Cu(II)(C(6)H(8)N(2))(2)SO(4)]·H(2)O (1) was successfully synthesized.
  • The achiral crystal transformed into a chiral coordination polymer [Cu(II)(C(6)H(8)N(2))(N(3))(2)](n) (2) upon exposure to an aqueous azide solution.
  • The transformation involved the replacement of sulfate anions by azide anions at the solid-liquid interface, inducing chirality.

Conclusions:

  • Solid-liquid interface reactions can be a powerful tool for generating chiral coordination polymers from achiral precursors.
  • Anion exchange at the interface is a viable mechanism for inducing structural changes and chirality.
  • The study presents a novel method for synthesizing chiral coordination polymers with potential applications in enantioselective catalysis or chiral recognition.