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Possible reaction pathways for self-condensation of melamine resins; reversibility of methylene bridge formation.

About 24 pages (7,125 words)

The Journal of Coatings Technology, January 1st, 1992

Acid catalyzed self-condensation reactions and NMR

spectra of three model compounds for methylolated

melamine-formaldehyde resins were studied. The

model compounds had a single --N(H) [CH.sub.2] [OCH.sub.3]

dyad, a single --N([[CH.sub.2] [OCH.sub.3]).sub.2] dyad, and three

--N([[CH.sub.2] [OCH.sub.3]).sub.2] dyads. Evidence from model

compound studies indicates that: (1) All self-condensation

reactions are reversible. (2) Acyclic methylene

bridges from readily from --N(H) [CH.sub.2] [OCH.sub.3] dyads

and from all dyads in the presence of water, but are

unstable. (3) Methylene bridg...

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Jones, Frank N.; Samaraweera, Upasiri. The Journal of Coatings Technology, January 1st, 1992. Possible reaction pathways for self-condensation of melamine resins; reversibility of methylene bridge formation.. Content provided by HighBeam Research.



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