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In chemistry, chain propagation (sometimes just referred to as propagation) is a process in which a reactive intermediate is continuously regenerated during the course of a chemical chain reaction. For example, in the chlorination of methane , there is a two-step propagation cycle involving as chain carriers a chlorine atom and a methyl radical ...
chain branching (a propagation step where one active particle enters the step and two or more are formed); chain transfer (a propagation step in which the active particle is a growing polymer chain which reacts to form an inactive polymer whose growth is terminated and an active small particle (such as a radical), which may then react to form a ...
In chemistry, a reaction mechanism is the step by step sequence of elementary reactions by which overall chemical reaction occurs. [1] A chemical mechanism is a theoretical conjecture that tries to describe in detail what takes place at each stage of an overall chemical reaction. The detailed steps of a reaction are not observable in most cases.
The propagation mechanisms appear to involve both ionic and radical species. Plasma polymerization offers a potentially unique method of forming thin polymer films for uses such as thin-film capacitors, antireflection coatings, and various types of thin membranes. [1] Sonication: The polymerization is initiated by high-intensity ultrasound ...
In polymer chemistry, chain termination is any chemical reaction that ceases the formation of reactive intermediates in a chain propagation step in the course of a polymerization, effectively bringing it to a halt.
In chemistry, initiation is a chemical reaction that triggers one or more secondary reactions. Initiation creates a reactive centre on a molecule which produces a chain reaction . [ 1 ] The reactive centre generated by initiation is usually a radical , but can also be cations or anions . [ 2 ]
Chain-growth includes both initiation and propagation steps (at least), and the propagation of chain-growth polymers proceeds by the addition of monomers to a growing polymer with an active centre. In contrast step-growth polymerization involves only one type of step, and macromolecules can grow by reaction steps between any two molecular ...
In organosulfur chemistry, the thiol-ene reaction (also alkene hydrothiolation) is an organic reaction between a thiol (R−SH) and an alkene (R 2 C=CR 2) to form a thioether (R−S−R'). This reaction was first reported in 1905, [ 1 ] but it gained prominence in the late 1990s and early 2000s for its feasibility and wide range of applications.