COPOLYMERIZATION OF MONO-ACRYLOYLETHOXY, DI-ACRYLOYLETHOXY, AND TRI-ACRYLOYLETHOXY FLUOROISOPHTHALONITRILES WITH METHYL-METHACRYLATE, STYRENE, AND DIALLYL PHTHALATE
T. Kikuchi et al., COPOLYMERIZATION OF MONO-ACRYLOYLETHOXY, DI-ACRYLOYLETHOXY, AND TRI-ACRYLOYLETHOXY FLUOROISOPHTHALONITRILES WITH METHYL-METHACRYLATE, STYRENE, AND DIALLYL PHTHALATE, Kobunshi ronbunshu, 50(12), 1993, pp. 909-917
AF derivatives (AF, 4-acryloylethoxy-2, 5, 6-trifluoroisophthalonitril
e; DAF, 4, 6-diacryloylethoxy-2, 5 -difluoroisophthalonitrile, and TAF
, 2,4,6-triacryloylethoxy-5-fluoroisophthalonitrile) were synthesized
from tetrafluoroisophthalonitrile, and radical homopolymerizations or
copolymerizations of these monomers with vinyl monomers were investiga
ted. The order of copolymer yields of the AF derivatives with methyl m
ethacrylate (MMA) or styrene (St) was TAF>DAF>AF. The copolymer yield
of AF with diallyl isophthalate (DAIP) or diallyl terephthalate (DATP)
was larger than homopolymer yield of DAIP or DATP. The copolymers of
DAF or TAF with diallyl phthalate (DAP) were heat-resistant and insolu
ble in usual organic solvents.