Polymerizable composition, molded resin, and laminate
A technology of polymerizable compositions and complexes, applied in synthetic resin layered products, layered products, chemical instruments and methods, etc., can solve the problems of unstable properties, molecular weight and viscosity of cross-linking thermoplastic resins, etc. Achieve excellent dielectric properties, long pot life and stable polymerization activity
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Embodiment 1
[0147] The ruthenium carbene complex represented by the following formula (5) (dichloro three (isopropoxy) phosphine (3-phenyl-1H-inden-1-ylidene) [1,3-bis(2 ,4,6-trimethylphenyl)-4,5-dihydroimidazol-2ylidene)]ruthenium(II)(Tri(i-propoxy)phosphine(3-phenyl-1H-inden-1-ylidene 1 part of )[1,3-bis(2,4,6-trimethylph enyl)-4,5-dihydroimidazol-2-ylidene]ruthenium(II)dichloride, manufactured by STREM Corporation) was dissolved in 40 parts of tetrahydrofuran to prepare a catalyst liquid. In addition, 10 parts of tetracyclododecene (TCD) as a cycloolefin monomer and 90 parts of dicyclopentadiene were mixed with fumed silica (trade name "R715", manufactured by Japan Aerosil Corporation) as a filler. 2.5 parts, 3 parts of undecenyl methacrylate as a chain transfer agent, di-tert-butyl peroxide as a crosslinking agent (manufactured by Akzo Corporation, product name Kayabutyl D, 1 minute half-life temperature 192° C.) 3 parts and 10 parts of trimethylolpropane trimethacrylate as a crossli...
Embodiment 2
[0156] Using the polymerizable composition obtained in Example 1, the conditions during the polymerization reaction were changed to 110° C. for 3 minutes, except that, in the same manner as in Example 1, a crosslinkable resin (initial polymer and 24 hours After polymer), the evaluation was carried out in the same way. The results are shown in Table 1.
Embodiment 3
[0158] Using the polymerizable composition obtained in Example 1, except that the conditions during the polymerization reaction were changed to 95°C and 3 minutes, in the same manner as in Example 1, a crosslinkable resin (initial polymer and 24 hours After polymer), the evaluation was carried out in the same way. The results are shown in Table 1.
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