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関連する概念動画

Colors and Magnetism03:02

Colors and Magnetism

13.7K
Color in Coordination Complexes
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
13.7K
Valence Bond Theory02:42

Valence Bond Theory

10.9K
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
10.9K
Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

1.1K
In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
1.1K
Complexation Equilibria: Factors Influencing Stability of Complexes01:09

Complexation Equilibria: Factors Influencing Stability of Complexes

739
In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...
739
Formation of Complex Ions03:45

Formation of Complex Ions

25.5K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
25.5K
Ladder Diagrams: Complexation Equilibria01:07

Ladder Diagrams: Complexation Equilibria

572
Ladder diagrams are useful for evaluating equilibria involving metal-ligand complexes. The vertical scale of the ladder diagram represents the concentration of unreacted or free ligand, pL. The horizontal lines on the scale depict the log of stepwise formation constants for metal-ligand complexes and indicate the dominant species in all the regions.
The formation constant, K1, for the formation of Cd(NH3)2+ complex from cadmium and ammonia is 3.55 × 102. Log K1 (i.e. pNH3) is 2.55, and...
572

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関連する実験動画

Updated: Jan 2, 2026

Synthesis and Performance Evaluations of ZnCoS/ZnCdS with Twin Crystal Structure for Multifunctional Redox Photocatalysis in Energy Applications
09:22

Synthesis and Performance Evaluations of ZnCoS/ZnCdS with Twin Crystal Structure for Multifunctional Redox Photocatalysis in Energy Applications

Published on: July 25, 2025

592

ボウル型とカプセル型自己組み立て亜鉛複合体間の多刺激反応性相互変換

Kenichi Endo1, Hitoshi Ube1, Mitsuhiko Shionoya1

  • 1Department of Chemistry, Graduate School of Science , The University of Tokyo , 7-3-1 Hongo , Bunkyo-ku , Tokyo 113-0033 , Japan.

Journal of the American Chemical Society
|December 6, 2019
PubMed
まとめ

研究者らは,リガンド,酸,塩基,溶媒,ゲストなどの複数の刺激に反応して,ボウルとカプセルの形を変化させる新しい金属有機構造を開発しました.

科学分野:

  • 超分子化学
  • 協調化学
  • 材料科学

背景:

  • メタル・オーガニック・アーキテクチャは構造的な可塑性を発揮し,反応性のあるシステムでの応用を可能にします.
  • 刺激に反応する既存のシステムは 通常"つのトリガーに反応します
  • 複数の刺激に反応する金属有機構造の相互変換は非常に望ましいが,めったに達成されない.

研究 の 目的:

  • 異なる自己組み立てた亜鉛 (II) 複合体間の多刺激反応性相互変換を報告する.
  • 多機能素材の設計原理を探求する.

主な方法:

  • ポルフィリンベースのリガンドLと亜鉛 (II) イオンの合成.
  • Zn4L3X6 (ボウル形) と Zn4L4 (カプセル形) の複合体間の均衡形成の調査.
  • 外的リガンド,ブロンステッド酸/塩基,溶媒,ゲスト分子を用いて構造的相互変換を誘導する.

主要な成果:

  • ボウル形 [ZnII4L3X6] とカプセル形 [ZnII4L4] の相互変換が実証されている.
  • 構造的変異を誘発する4つの異なる外部刺激 (リンガンド,酸/塩基,溶媒,ゲスト) を特定した.
  • 均衡種に基づく相互変換の詳細なメカニズム的な洞察

さらに関連する動画

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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water

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Last Updated: Jan 2, 2026

Synthesis and Performance Evaluations of ZnCoS/ZnCdS with Twin Crystal Structure for Multifunctional Redox Photocatalysis in Energy Applications
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Synthesis and Performance Evaluations of ZnCoS/ZnCdS with Twin Crystal Structure for Multifunctional Redox Photocatalysis in Energy Applications

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592
Thermochemical Studies of NiII and ZnII Ternary Complexes Using Ion Mobility-Mass Spectrometry
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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
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結論:

  • 自己組み立ての亜鉛 (II) 複合体における多刺激反応性構造的相互変換を達成した.
  • この発見は,多機能で多反応性の 超分子システムを設計するための基礎となる.
  • この研究は,機能的な材料における複雑な分子変換の可能性を強調しています.