相关实验视频

Updated: Jul 6, 2026

Synthesis and Characterization of Functionalized Metal-organic Frameworks
11:27

Synthesis and Characterization of Functionalized Metal-organic Frameworks

Published on: September 5, 2014

和的金属芳香复合物的循环添加反应:一个机械 DFT 调查

Mark A Iron1, Jan M L Martin, Milko E van der Boom

  • 1Department of Organic Chemistry, Weizmann Institute of Science, 76100 Rehovot, Israel.

Journal of the American Chemical Society
|September 18, 2003
PubMed
概括

密度函数理论 (DFT) 揭示了金属芳香复合物的独特反应机制. 化复合物经历协同反应,而化和化复合物表现出阶段性机制.

更多相关视频

Synthesis of a Water-soluble Metal–Organic Complex Array06:40

Synthesis of a Water-soluble Metal–Organic Complex Array

Published on: October 8, 2016

Discovery and Synthesis Optimization of Isoreticular Al(III) Phosphonate-Based Metal-Organic Framework Compounds Using High-Throughput Methods07:20

Discovery and Synthesis Optimization of Isoreticular Al(III) Phosphonate-Based Metal-Organic Framework Compounds Using High-Throughput Methods

Published on: October 6, 2023

相关概念视频

[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.
Diels–Alder Reaction Forming Cyclic Products: Stereochemistry01:28

Diels–Alder Reaction Forming Cyclic Products: Stereochemistry

The Diels–Alder reaction is one of the robust methods for synthesizing unsaturated six-membered rings. The reaction involves a concerted cyclic movement of six π electrons: four π electrons from the diene and two π electrons from the dienophile.