Synthesis and polymerization studies of formaldehyde oxime and its derivatives

✍ Scribed by Dallas D. Parker; Anne Buyle; Padias H. K. Hall Jr.

• Publisher: John Wiley and Sons
• Year: 2000
• Tongue: English
• Weight: 112 KB
• Volume: 38
• Category: Article
• ISSN: 0887-624X
• DOI: 10.1002/(sici)1099-0518(20000515)38:10<1866::aid-pola740>3.0.co;2-a

✦ Synopsis

Formaldehyde oxime and three O-alkyl derivatives were examined as potential imine monomers. Formaldehyde oxime spontaneously polymerized below 60 °C and did not polymerize above 60 °C (ceiling temperature), even in the presence of free-radical or cationic initiators. The O-benzoyl derivative was isolated as the cyclic trimer but could not be converted into the monomeric form. Formaldehyde O-benzyloxime was synthesized and isolated. Attempted homopolymerizations in the presence of free-radical initiators only led to oligomers, whereas with cationic initiators only cyclic trimer was obtained. Copolymerizations with appropriate vinyl monomers and free-radical and anionic initiators yielded only low molecular weight polymers. Cationic copolymerizations gave higher molecular weights and polymer yields, but the polymers containing appreciable amounts of imine function had very low molecular weights. We conclude that the polymerizability of imines is extremely sensitive to the substitution pattern: imines with only a substituent on nitrogen are unstable and readily polymerize, whereas imines with more substituents generally do not polymerize. Electronwithdrawing substituents are more favorable to polymerizability.