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Polyvinylcarbazole (PVK) is a temperature-resistant [2] thermoplastic polymer produced by radical polymerization from the monomer N-vinylcarbazole. It is a photoconductive polymer and thus the basis for photorefractive polymers and organic light-emitting diodes .
Piezospectroscopy (also known as photoluminescence piezospectroscopy) is an analytical technique that reveals internal stresses in alumina-containing materials, particularly thermal barrier coatings (TBCs).
Upon exposure to γ-irradiation, N-vinylcarbazole undergoes solid-state polymerisation. [ 5 ] It is produced by the vinylation of carbazole with acetylene in the presence of base.
Living cationic polymerization is a living polymerization technique involving cationic propagating species. [1] [2] It enables the synthesis of very well defined polymers (low molar mass distribution) and of polymers with unusual architecture such as star polymers and block copolymers and living cationic polymerization is therefore as such of commercial and academic interest.
Photoluminescence (abbreviated as PL) is light emission from any form of matter after the absorption of photons (electromagnetic radiation). [1] It is one of many forms of luminescence (light emission) and is initiated by photoexcitation (i.e. photons that excite electrons to a higher energy level in an atom), hence the prefix photo- . [ 2 ]
In physics and physical chemistry, time-resolved spectroscopy is the study of dynamic processes in materials or chemical compounds by means of spectroscopic techniques.Most often, processes are studied after the illumination of a material occurs, but in principle, the technique can be applied to any process that leads to a change in properties of a material.
Electrochemiluminescence or electrogenerated chemiluminescence (ECL) is a kind of luminescence produced during electrochemical reactions in solutions. In electrogenerated chemiluminescence, electrochemically generated intermediates undergo a highly exergonic reaction to produce an electronically excited state that then emits light upon relaxation to a lower-level state.
In one modification, both steps are rolled into one by carrying out the reaction in acetic acid. [9] In the third step, this compound is oxidized by red lead to carbazole itself. Another classic is the Bucherer carbazole synthesis, which uses a naphthol and an aryl hydrazine. [10] Bucherer carbazole synthesis