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Structural Isomerism02:34

Structural Isomerism

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Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can...
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Metallic Solids02:37

Metallic Solids

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Metallic solids such as crystals of copper, aluminum, and iron are formed by metal atoms. The structure of metallic crystals is often described as a uniform distribution of atomic nuclei within a “sea” of delocalized electrons. The atoms within such a metallic solid are held together by a unique force known as metallic bonding that gives rise to many useful and varied bulk properties.
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability....
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π Molecular Orbitals of 1,3-Butadiene01:24

π Molecular Orbitals of 1,3-Butadiene

10.1K
Conjugated dienes have lower heats of hydrogenation than cumulated and isolated dienes, making them more stable. The enhanced stabilization of conjugated systems can be understood from their π molecular orbitals.
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the number...
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Related Experiment Video

Updated: Sep 26, 2025

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
09:34

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly

Published on: February 6, 2020

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Noncovalently bound and mechanically interlocked systems using pillar[n]arenes.

Kenichi Kato1, Shixin Fa1, Shunsuke Ohtani1

  • 1Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Kyoto, 615-8510, Japan. ogoshi@sbchem.kyoto-u.ac.jp.

Chemical Society Reviews
|April 21, 2022
PubMed
Summary

Pillar[n]arenes, unique pillar-shaped molecules, enable advanced mechanically interlocked molecules (MIMs). Their versatile properties facilitate the design of dynamic and complex supramolecular structures for novel applications.

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Area of Science:

  • Supramolecular Chemistry
  • Organic Chemistry

Background:

  • Pillar[n]arenes are macrocyclic compounds with a distinct pillar shape due to methylene bridges.
  • They possess unique properties like versatile functionality, tunable solubility, and host-guest behavior.

Purpose of the Study:

  • To explore the synthesis and design of pillar[n]arene-based mechanically interlocked molecules (MIMs).
  • To investigate the dynamic conversion capabilities and structural properties of these MIMs.

Main Methods:

  • Utilizing versatile organic synthesis techniques for pillar[n]arene functionalization.
  • Employing Nuclear Magnetic Resonance (NMR) spectroscopy to study molecular motion and structure.
  • Designing and constructing complex supramolecular architectures.

Main Results:

  • High-yield synthesis and rational design of pillar[n]arene-based MIMs achieved.
  • Development of novel MIMs capable of dynamic interconversion between states.
  • Simple NMR spectra due to high symmetry aiding in motion studies and higher-order structure creation.

Conclusions:

  • Pillar[n]arenes are excellent building blocks for sophisticated MIMs.
  • Their unique structural and dynamic properties open avenues for advanced supramolecular chemistry.
  • Potential for creating polymeric MIMs and exploring diverse applications is highlighted.