関連する実験動画
Updated: Feb 21, 2026

05:26
Synthesis of Single-Crystalline Core-Shell Metal-Organic Frameworks
Published on: February 10, 2023
3.9K
コア・シェルの構造は,金属・有機構造のリガンド交換で自然に発生する
Jake A Boissonnault1, Antek G Wong-Foy1, Adam J Matzger1
1Department of Chemistry and ‡Macromolecular Science and Engineering Program, University of Michigan , 930 North University Avenue, Ann Arbor, Michigan 48109-1055, United States.
Journal of the American Chemical Society
|October 13, 2017
まとめ
メタル・オーガニック・フレームワーク (MOF) の合成後の交換は,リガンドの拡散が限られているため,コア・シェル構造を生み出します. このプロセスは,交換されたリガンドを結晶のエッジに集中させ,異なるコアシェルMOFを形成します.
科学分野:
- 材料科学
- ナノテクノロジー
- 化学工学
背景:
- メタル・オーガニック・フレームワーク (MOF) は,調節可能な構造を持つ多孔性材料です.
- 合成後の交換 (PSE) は,最初の合成後にMOFの修正を可能にします.
- PSE中のリガンド分布を理解することは,MOFの性質を制御するために不可欠です.
研究 の 目的:
- 合成後の交換 (PSE) の後のMOFの微細構造を調査する.
- PSE中にリガンドの拡散を制限する要因を決定する.
- コアシェルのMOFを作成するための方法としてPSEを確立します.
主な方法:
- PSE後のMOFの微細構造分析
- MOF-5のカーボキシラートリガンドを用いた拡散研究
- UMCM-8とUIO-66の単結晶におけるPSEの試験
主要な成果:
- MOFの交換されたリガンドは結晶の縁に濃縮され,深さと共に減少する.
- PSEの後にコア・シェルの配置が観察される.
- リンガンド拡散は,PSEプロセスの速度制限ステップとして識別されます.
- UMCM-8とUIO-66でも同様のコアシェルの傾向が見られた.
結論:
- MOFで観察されたコア・シェルの構造は,PSE中にリガンドの拡散が限られていることに起因する.
- PSEは,コアシェルのMOFの合理的な設計と合成のための実行可能な方法です.
- この研究は,合成後の改変によるMOFアーキテクチャの制御に関する洞察を提供します.
関連する概念動画
Metal-Ligand Bonds
24.6K
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
24.6K
Crystal Field Theory - Octahedral Complexes
31.1K
Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
31.1K
Complexation Equilibria: The Chelate Effect
1.4K
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...
1.4K
Valence Bond Theory
11.4K
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...
11.4K
Ionic Crystal Structures
18.5K
Ionic crystals consist of two or more different kinds of ions that usually have different sizes. The packing of these ions into a crystal structure is more complex than the packing of metal atoms that are the same size.
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
18.5K
Complexation Equilibria: Factors Influencing Stability of Complexes
876
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...
876

