Water-Processable Self-Doped Conducting Polymers via Direct (Hetero)arylation Polymerization was written by Beaumont, Catherine;Turgeon, Josyane;Idir, Mael;Neusser, David;Lapointe, Rosalie;Caron, Samuel;Dupont, William;D’Astous, Dominic;Shamsuddin, Sareeha;Hamza, Sarah;Landry, Eric;Ludwigs, Sabine;Leclerc, Mario. And the article was included in Macromolecules (Washington, DC, United States) in 2021.Recommanded Product: 2-(2-Methoxyethoxy)ethanol This article mentions the following:
The synthesis of water-processable self-doped polymers has been achieved by direct (hetero)arylation polymerization (DHAP) using water as a cosolvent. The introduction of a counterion covalently attached to the backbone of the polymers enhanced their solubility and the stability of the solutions Those polymers have shown air-stable elec. conductivities up to 50 S cm-1 without the use of any post-treatment. The good water processability of these conducting polymers is promising for printed electronics in a wide range of applications. In the experiment, the researchers used many compounds, for example, 2-(2-Methoxyethoxy)ethanol (cas: 111-77-3Recommanded Product: 2-(2-Methoxyethoxy)ethanol).
2-(2-Methoxyethoxy)ethanol (cas: 111-77-3) belongs to ethers. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.Recommanded Product: 2-(2-Methoxyethoxy)ethanol
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem