Related Experiment Video

Updated: Feb 18, 2026

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
09:22

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

Published on: February 7, 2017

8.3K

Stimuli-Responsive Supramolecular Assemblies between Twisted Cucurbit[14]uril and Hemicyanine Dyes and Their Analysis

Jing Zhang1, Qing Tang1, Zhong-Zheng Gao1

  • 1The Engineering and Research Center for Southwest Bio-Pharmaceutical Resources of National Education Ministry of China, ‡Key Laboratory of Macrocyclic and Supramolecular Chemistry of Guizhou Province, and §College of Tobacco of Guizhou University, Guizhou University , Guiyang 550025, China.

The Journal of Physical Chemistry. B
|November 23, 2017
PubMed

More Related Videos

Synthesis of Wavelength-shifting DNA Hybridization Probes by Using Photostable Cyanine Dyes07:44

Synthesis of Wavelength-shifting DNA Hybridization Probes by Using Photostable Cyanine Dyes

Published on: July 6, 2016

11.6K
Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores09:46

Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores

Published on: August 19, 2013

16.0K

Related Concept Videos

Aryldiazonium Salts to Azo Dyes: Diazo Coupling01:11

Aryldiazonium Salts to Azo Dyes: Diazo Coupling

The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para...
3.7K