制造自扩张的金属有机,使用环可打开的连接体
Ami Nishijima1, Yuto Osugi1, Takashi Uemura1
1Department of Applied Chemistry, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, 113-8656, Tokyo, Japan.
Angewandte Chemie (International ed. in English)
|March 7, 2024
概括
研究人员开发了具有可调节腔体大小的自扩展金属有机 (MOCs). 这一突破使得能够创建功能性MOC来增强分子捕获,克服以前的合成限制.
科学领域:
- 超分子化学 超分子化学
- 材料科学 材料科学 材料科学
背景情况:
- 金属有机 (MOCs) 是通过协调驱动组装合成的,为各种应用提供可访问的分子腔.
- 定制MOC腔的大小,形状和化学环境对于先进的分子结合至关重要.
- 对MOC结构的精确控制是由金属协调和连接体配置决定的.
研究的目的:
- 报告自我扩展的MOC,在子尺寸和灵活性方面具有可调节的结构变化.
- 展示一种创新的方法,用于创建具有扩大腔的功能MOC.
- 为了克服与受不利的扩展MOC结构相关的合成挑战.
主要方法:
- 设计了一种循环连接体,其 oligomeric 链连接着 stilbene 的环.
- 使用设计的配体和Rh.II) 离子组装的母MOCs.
- 诱导MOC扩张通过选择性断裂的stilbene双键.
主要成果:
- 成功合成了自我膨胀的MOC,在保持拓的同时,在子大小和灵活性方面表现出显著的变化.
- 证明扩展的MOCs有效地因其扩大的腔隙而捕获多牙型N-捐赠分子.
- 展示了由于热因素导致扩大MOC的直接合成的不切实际性.
结论:
- 使用环开放性联体的自我扩张为MOCs的精密工程提供了一个可行的策略.
- 这种方法可以生产具有不可访问的扩大腔的功能MOC.
- 开发的方法允许通过定制的MOC结构进行适应性分子结合.
相关概念视频
Metal-Ligand Bonds
20.8K
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...
20.8K
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
2.6K
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...
2.6K
Complexation Equilibria: The Chelate Effect
514
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...
514
Properties of Organometallic Compounds
994
Organometallic compounds are compounds that contain a carbon–metal bond. Carbon belongs to an organyl group like alkyl, aryl, allyl, or benzyl groups. The metal can be from Group I or Group II of the periodic table, a transition metal, or a semimetal.
994
Ziegler–Natta Chain-Growth Polymerization: Overview
3.3K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
3.3K
Complexation Equilibria: Factors Influencing Stability of Complexes
369
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...
369


