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関連する概念動画

Chair Conformation of Cyclohexane02:02

Chair Conformation of Cyclohexane

The chair conformation is the most stable form of cyclohexane due to the absence of angle and torsional strain. The absence of angle strain is a result of cyclohexane’s bond angle being very close to the ideal tetrahedral bond angle of 109.5° in its chair conformer. Similarly, the torsional strain is also absent owing to the perfectly staggered arrangement of bonds.
The hydrogen atoms linked to carbons are arranged in two different axial and equatorial orientations to achieve this staggered...
Conformations of Cyclohexane02:11

Conformations of Cyclohexane

Cyclohexane does not exist in a planar form due to the high angle and torsional strain it would experience in the planar structure. Instead, it adopts non-planar chair and boat conformations.
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal tetrahedral value,...
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)

Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
Thermal Electrocyclic Reactions: Stereochemistry01:17

Thermal Electrocyclic Reactions: Stereochemistry

The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Aromatic Hydrocarbon Cations: Structural Overview01:18

Aromatic Hydrocarbon Cations: Structural Overview

Cycloheptatriene is a neutral monocyclic unsaturated hydrocarbon that consists of an odd number of carbon atoms and an intervening sp3 carbon in the ring. The three double bonds in the ring correspond to 6 π electrons, which is a Huckel number, and therefore satisfies the criteria of 4n + 2 π electrons. However, the intervening sp3 carbon disrupts the continuous overlap of p orbitals. As a result, cycloheptatriene is not aromatic.
Removing one hydrogen from the intervening CH2 group with both...
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction01:16

[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

The Diels–Alder reaction is an example of a thermal pericyclic reaction between a conjugated diene and an alkene or alkyne, commonly referred to as a dienophile. The reaction involves a concerted movement of six π electrons, four from the diene and two from the dienophile, forming an unsaturated six-membered ring. As a result, these reactions are classified as [4+2] cycloadditions.

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関連する実験動画

Updated: May 25, 2026

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
09:35

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units

Published on: September 18, 2016

銅で組み立てられた[3]ロタキサン,その2つのリングは翼を振る翼のように作用する.

Antoine Joosten1, Yann Trolez, Jean-Paul Collin

  • 1Laboratoire de Chimie Organo-Minérale, Institut de Chimie, Université de Strasbourg-CNRS/UMR7177, 4 rue Blaise Pascal, 67070 Strasbourg Cedex, France.

Journal of the American Chemical Society
|January 13, 2012
PubMed
まとめ

研究者らは,クリック化学を用いて,新しい銅複合体 [3]ロタキサンを開発した. この分子機械は,金属の調整変化によって引き起こされるユニークな"翼を叩く"動きを示し,新しい機能的な分子機械の道を開く.

さらに関連する動画

[(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
09:12

[(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst

Published on: May 21, 2019

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
09:22

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

Published on: February 7, 2017

関連する実験動画

Last Updated: May 25, 2026

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
09:35

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units

Published on: September 18, 2016

[(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
09:12

[(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst

Published on: May 21, 2019

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
09:22

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

Published on: February 7, 2017

科学分野:

  • 超分子化学 超分子化学
  • 協調化化学について
  • マテリアルサイエンス 材料科学

背景:

  • ロタキサンは,分子機械における潜在的応用を持つ機械的に相互に絡み合っている分子である.
  • 金属中心の組み込みは,ロタキサンシステムにダイナミックで反応的な行動を導入することができます.
  • クリック化学は,複雑な分子構造を構築するための効率的で信頼できる方法を提供します.

研究 の 目的:

  • スイッチ可能な調整環境を持つ新しい銅複合体 [3] ロタキサンを合成する.
  • ロタキサンの幾何学とダイナミクスに金属の調整が及ぼす影響を調査する.
  • 機能的な分子機械としてのこのシステムの可能性を探求する.

主な方法:

  • ストッパーリングのためのクリック化学を用いた[3]ロタキサンの合成.
  • 異なる金属イオン (Cu(I),Cu(II),Zn(2+)) と複合する.
  • 協調モードと幾何学を決定するためのスペクトロスコピーと構造分析.

主要な成果:

  • 新しい銅複合体 [3]ロタキサンが成功して合成されました.
  • ロタキサン内のトリアゾール群は,金属の協調球に協調するか,金属の協調球の外に留まることもできます.
  • 金属交換 (Cu(I) / Zn(2+)) またはリドックスプロセス (Cu(II) / Cu(I)) は,重要な幾何学的な変化を誘導し, "翼を叩く"運動につながります.

結論:

  • 合成されたロタキサンは,金属の協調に基づいた制御可能なダイナミックな行動を示します.
  • 観測された"翼をたたむ"運動は,速くて定量的なものです.
  • このシステムは,高度な分子機械や反応性のある材料の開発に期待を寄せている.