Related Experiment Video
Updated: Mar 31, 2026

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of PhosphorusI
Published on: November 22, 2016
Dipyrrolyphenol as a precursor of π-electronic anion that forms ion pairs with cations
Hiromitsu Maeda1, Ayaka Fukui1, Ryohei Yamakado1
1College of Pharmaceutical Sciences, Ritsumeikan University, Kusatsu 525-8577, Japan. maedahir@ph.ritsumei.ac.jp.
Abstract:
A nitro-substituted dipyrrolylphenol was synthesized as a precursor of a π-electronic anion, whose phenolate (phenoxide) moiety upon deprotonation was stabilized by the hydrogen-bond-donating pyrrole NH, thus forming solid-state ion pairs with various cationic species.
More Related Videos
14:11Synthesis of pH Dependent Pyrazole, Imidazole, and Isoindolone Dipyrrinone Fluorophores using a Claisen-Schmidt Condensation Approach
Published on: June 10, 2021
06:561,3,5-Triphenylbenzene and Corannulene as Electron Receptors for Lithium Solvated Electron Solutions
Published on: October 10, 2016
Related Concept Videos
π Molecular Orbitals of the Allyl Cation and Anion
Ion Exchange
Cationic Chain-Growth Polymerization: Mechanism
Ionic Association
Aromatic Hydrocarbon Anions: Structural Overview
Due to the absence of continuous...
Metal-Ligand Bonds
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...