Related Experiment Video

Updated: Jun 17, 2026

Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology
07:07

Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology

Published on: March 12, 2015

Novel optical/electrochemical selective 1,2,3-triazole ring-appended chemosensor for the Al3+ ion

Sang Hoon Kim1, Hong Seok Choi, Joohoon Kim

  • 1Department of Chemistry, Korea University, Seoul 136-701, Korea.

Organic Letters
|January 2, 2010
PubMed

More Related Videos

An Aptamer-based Sensor for Unchelated Gadolinium(III)05:15

An Aptamer-based Sensor for Unchelated Gadolinium(III)

Published on: January 9, 2017

A Polyaniline-based Sensor of Nucleic Acids07:58

A Polyaniline-based Sensor of Nucleic Acids

Published on: November 1, 2016

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 position.