Related Experiment Video
Updated: Oct 22, 2025

Synthesis of pH Dependent Pyrazole, Imidazole, and Isoindolone Dipyrrinone Fluorophores using a Claisen-Schmidt Condensation Approach
Published on: June 10, 2021
Access to Highly Luminescent N-Doped Diazaborepins with Penta-, Hexa-, and Heptagon Substructures
Chenglong Li1, Yafei Shi1, Pengfei Li1
1Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, Key Laboratory of Cluster Science of the Ministry of Education, School of Chemistry and Chemical Engineering, Beijing Institute of Technology of China, Beijing 102488, People's Republic of China.
Abstract:
Two diazaborepins (BNN1 and BNN2) have been accomplished via a highly efficient pathway in the step-economic transformation. Oxidative dimerization of carbazole derivatives followed by borylation reaction gave heterocyclic diazaborepin as the key building block. Replacement of carbon moiety in traditional borepins with N-N functionality led to a significant red shift of their emissions up to 585 nm with strong red color as solids. This work offered an approach to diazaborepin-based materials for applications in light-emitting field.
More Related Videos
08:51Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
12:07Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
Related Concept Videos
Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions
Diazonium Group Substitution: –OH and –H
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
Variables Affecting Phosphorescence and Fluorescence
Photoluminescence: Applications
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...