3,4-ethylene dioxythiophene, also known as 3,4-ethylenedioxythiophene, referred to as EDOT, colorless to pale yellow liquid, melting point of 10.5 ℃. Slightly soluble in water, 20 ℃ under the conditions of water solubility of 2.1g / L, a slight unpleasant odor.
Monomers, such as hydroxymethyl-3,4-ethylenedioxythiophene (HM), can be electropolymerized into a conducting polymer that is capable of a high rate of electron transfer, and can increase the flow of current on the electrode surface. HM-EDOT is a suitable monomer for this project because it has a hydroxyl functional group, which allows for increased solubility in aqueous environments. The monomer HM can be functionalized and synthesized into carboxylic acid-3,4-ethylenedioxythiophene (COOH).
BeiLi Brand CAS 126213-50-1 99.9% 3,4-Ethylenedioxythiophene EDOT is using technology patents developed by the company with reliable quality assurance.Our patented technology makes it easy to obtain the target-3,4-Ethylenedioxythiophene EDOT with a short route, high product yield, mild reaction conditions, recyclable materials such as raw materials and solvents, which greatly reduces production costs, reducing the emission of waste, less pollution, with good prospects for industrial applications.
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Thiophene, also known as thiofuran, is a cyclic compound containing four carbon atoms and one sulphur atom in a ring. It is a toxic, flammable, highly reactive, colorless liquid insoluble in water (soluble in alcohol and ether) and melts at 38 C, boils at 84 C. It is used as a solvent and chemical intermediate. Its derivatives are widely used in manufacturing dyes, aroma compounds and pharmaceuticals. They are used as monomers to make condensation copolymers.
Due to extended pi-electron cloud overlaps, organometallic molecules or aromatic oligometers such as anthracene exhibit semiconductor properties. Conductive polymers have extended delocalized bonds that creates electrical conductivity when charge carriers generated make positive charges (holes) and negative charges (electrons) move to opposite electrodes. Doping is the intentional impurities in a pure semiconductor to generate charge carriers. The transportation of charges is responsible for fluorescence and electrical energy. These can form well-ordered thin crystalline films. Organic semiconductors have some merits of self radiation, flexibility, light weight, easy fabrication, and low cost. Organic electroluminescence materials have lead to the rapid development of photovoltaic and display devices such as organic solar cells, biosensitizers, OLED(Organic Light Emiting Diode), OTFT(Organic Thin Film Transistor), Wearable Display, and e-Paper. Some examples of organic electroluminescence materials are:
Oligomer Electro Luminescence Materials
Penyl substituent cyclopentadiene derivatives
Polymer Electro Luminescence Materials
3,4-Ethylenedioxythiophene is a monomer for the manufacture of conjugated polymer [ poly(3,4-ethylenedioxythiophene)] for the applications of redox activity, electroactivity, and conductivity.
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