相关实验视频
Updated: Dec 30, 2025
![Solid-phase Synthesis of [4.4] Spirocyclic Oximes](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F58508.jpg&w=3840&q=50)
05:15
Solid-phase Synthesis of [4.4] Spirocyclic Oximes
Published on: February 6, 2019
7.2K
网状化学中的模块化总合成
Liang Feng1, Kun-Yu Wang1, Xiu-Liang Lv1,2
1Department of Chemistry , Texas A&M University , College Station , Texas 77843-3255 , United States.
Journal of the American Chemical Society
|January 24, 2020
概括
本研究引入了一个模块化合成策略,通过将金属有机框架 (MOF) 和共价有机框架 (COF) 连接起来,来创建复杂的等级框架材料. 这种方法可以控制先进材料的调整和调整性.
科学领域:
- 材料科学
- 化学学
- 纳米技术
背景情况:
- 有机合成的模块化使得通过各种构建块和序列来构建多样化的自然产品.
- 目前的模块化合成主要局限于共价键分子化合物.
- 网状化学提供了一个通过可预测的结合相互作用组装材料的框架.
研究的目的:
- 将模块化合成概念扩展到层次框架材料.
- 以层次的方式将金属有机框架 (MOF) 和共价有机框架 (COF) 连接起来.
- 在多组件框架材料中实现可控对齐和调整性.
主要方法:
- 开发一个模块化合成策略,以逐步组装构件.
- 通过序列定义的反应将MOF和COF等级连接起来.
- 使用协调或共价键强度来指导组装序列.
主要成果:
- 成功合成具有复杂架构的等级COF-on-MOF结构.
- 在复合材料中展示受控的共价有机框架 (COF) 调整.
- 在空间分配,构成和框架材料的功能方面管理可调性.
结论:
- 这项研究首次综合了COF@MOF复合材料和受控的COF对齐.
- 可通用的模块化策略加速了多组件框架材料的发现.
- 这种方法为智能材料提供了可预测的途径,
相关概念视频
Synthesis and Decomposition Reactions
37.9K
Synthesis and decomposition are two types of redox reactions. Synthesis means to make something, whereas decomposition means to break something. The reactions are accompanied by chemical and energy changes.
37.9K
Cycloaddition Reactions: Overview
3.3K
Cycloadditions are one of the most valuable and effective synthesis routes to form cyclic compounds. These are concerted pericyclic reactions between two unsaturated compounds resulting in a cyclic product with two new σ bonds formed at the expense of π bonds. The [4 + 2] cycloaddition, known as the Diels–Alder reaction, is the most common. The other example is a [2 + 2] cycloaddition.
3.3K
Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation
2.7K
Robinson annulation is a base-catalyzed reaction for the synthesis of 2-cyclohexenone derivatives from 1,3-dicarbonyl donors (such as cyclic diketones, β-ketoesters, or β-diketones) and α,β-unsaturated carbonyl acceptors. Named after Sir Robert Robinson, who discovered it, this reaction yields a six-membered ring with three new C–C bonds (two σ bonds and one π bond).
2.7K
Limitations of Friedel–Crafts Reactions
6.6K
Several restrictions limit the use of Friedel–Crafts reactions. First, the halogen in the alkyl halide must be attached to an sp3-hybridized carbon for the Friedel–Crafts reactions to occur. Vinyl or aryl halides do not react since the carbocations formed are unstable under the reaction conditions. Second, Friedel–Crafts alkylation is susceptible to carbocation rearrangement, and the major products obtained have a rearranged carbon skeleton. In contrast, the acylium ion is...
6.6K
Cycloaddition Reactions: MO Requirements for Photochemical Activation
2.5K
Some cycloaddition reactions are activated by heat, while others are initiated by light. For example, a [2 + 2] cycloaddition between two ethylene molecules occurs only in the presence of light. It is photochemically allowed but thermally forbidden.
2.5K
Olefin Metathesis Polymerization: Overview
2.5K
Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
2.5K

