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For example, it is soluble in various alcohols, such as methanol and ethanol, [30] as well as in more exotic solvents like the deep eutectic solvent formed by choline chloride and urea (Relin). [31] When dry it is a light flaky hygroscopic powder, readily absorbing up to 40% of its weight in atmospheric water. In solution, it has excellent ...
It is produced industrially by vinylation of 2-pyrrolidone, i.e. the base-catalyzed reaction with acetylene. [2] It is the precursor to polyvinylpyrrolidone (PVP), an important synthetic material. The NVP monomer is commonly used as a reactive diluent in ultraviolet and electron - beam curable polymers applied as inks , coatings or adhesives .
2-Pyrrolidone, also known as 2-pyrrolidinone or butyrolactam, is an organic compound consisting of a 5-membered lactam, making it the simplest γ-lactam. It is a colorless liquid that is miscible with water and most common organic solvents.
N-Methyl-2-pyrrolidone (NMP) is an organic compound consisting of a 5-membered lactam. It is a colorless liquid, although impure samples can appear yellow. It is miscible with water and with most common organic solvents. It also belongs to the class of dipolar aprotic solvents such as dimethylformamide and dimethyl sulfoxide.
Polyacrylic acid is a weak anionic polyelectrolyte, whose degree of ionisation is dependent on solution pH. In its non-ionised form at low pHs, PAA may associate with various non-ionic polymers (such as polyethylene oxide, poly-N-vinyl pyrrolidone, polyacrylamide, and some cellulose ethers) and form hydrogen-bonded interpolymer complexes. [17]
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Different methods can be used to synthesize PPy, but the most common are electrochemical synthesis and chemical oxidation. [6] [3] [7]Chemical oxidation of pyrrole:
An example is The preferred CRU is an acyclic subunit of 4 carbon atoms with 4 free valences, one at each atom, as shown. It is oriented so that the lower left atom has the lowest number. The free-valence locants are written before the suffix, and they are cited clockwise from the lower left position as: lower-left, upper-left:upper-right ...