RADICAL COPOLYMERIZATION OF PARA-(2-GLYCIDYLOXYMETHYL)CYCLOPROPYL STYRENE WITH 2,3-DIMETHYLBUTADIENE-1,3 AND PROPERTIES OF THEIR COPOLYMERS
Keywords:
copolymerization, radical polymerization, cross-linking, para-(2-glycidyloxymethyl)cyclopropyl styrene, photosensitivityAbstract
The radical copolymerization of para-(2-glycidyloxymethyl)cyclopropyl styrene (GOMCPSt) with 2,3dimethylbutadiene-1,3 (DMB) has been investigated. It has been shown that the copolymerization proceeds with opening of double bond of vinyl group of GOMCPSt and 1,4-addition with DMB. The dependence of copolymer composition on composition of the initial monomer mixture has been revealed, the copolymerization constants have been determined and the factors of activity and also polarity of the used monomers have been calculated. It has been shown that the synthesized copolymers due to availability of double bond, three-carbon cycle and epoxide group are capable for structuring under action of UV-irradiation and show good negative photosensitive properties.
References
Moro U. Mikrolitografiya : principy, metody, materialy. // Per.s angl. pod. red. D.H.Timerovoj. M.: Mir; 1990. [Moro U. Mikrolitografiya: printsipy, metody, materialy. // Per. s angl. pod. red. D.Kh.Timerovoy. Moscow: Mir; 1990. (In Russ)].
Hou H., Jiang J., Ding M. Ester-type precursor of polyimide and photosensitivity. Eur. Polym. J. 1999;(35):1993-2000. https://doi.org/10.1016/S0014-3057(98)00290-0
Bajner A. Ya., Dyumaev K.M. Negativnye fotorezisty na osnove nenasyshennyh proizvodnyh poliamidokislot // Him. Prom-st. 1989. №7. S.483-487. [Vayner A.Ya., Dyumayev K.M. Negativnye fotorezisty na osnove nenasyshhennyh proizvodnyh poliamidokislot. Khim.Prom-st. 1989;(7):483-487. (In Russ).]
Decker C. Photoinitiated crosslinking polymerization. Prog. Polym. Sci. 1996;(21):593-650. https://doi.org/10.1016/0079-6700(95)00027-5 5. Vajner A. Ya., Dyumaev K.M., Lihacheva I.A. i dr. Metakrilatnye proizvodnye karboksilsoderzhashih poliimidov: sintez i fotohimicheskie prevrasheniya // Dokl. RAN. 2004. T.396. №3. S.362-365. [Vayner AYa, Dyumayev KM, Likhacheva IA, et al. Methacrylate derivatives of carboxyl-containing polyimides: synthesis and photochemical transformations. DOKLADY PHYSICAL CHEMISTRY. 2004;396(3);115-118]. 10.1023/B:DOPC.0000029167.69210.4c 6. Guliev K.G., Ponomareva G.Z., Guliev A.M. Fotochuvstvitelnost polimerov na baze epoksizameshennyh vinilfenilciklopropanov //Zhurn. Prikladnoj Himii. 2006. T.79. №3. S.497500. [Guliyev KG, Ponomaryeva GZ, Guliyev AM. Photosensitivity of polymers based on epoxysubstituted vinylphenylcyclopropanes. Russian Journal of Applied Chemistry. 2006;79(3):488-491.] 10.1134/S1070427206030323
Guliev K.G., Ponomareva G.Z., Guliev A.M. Sintez i svojstva epoksisoderzhashih policiklopropilstirolov // Vysokomolek. soed. Ser. B. 2007. T.49. №8. S.1577-1581. Guliyev KG, Ponomaryeva GZ, Guliyev AM. Synthesis and properties of epoxy-containing poly(cyclopropylstyrenes). Polymer Science. Series B. 2007;49(7-8):196-199.] 10.1134/S1560090407070068
Guliev K.G. Sintez, polimerizaciya i sopolimerizaciya 2-formil-1-(nvinilfenil)ciklopropana so stirolom // Zhurn. Prikladnoj himii. 2008. T.81. №4. S.636-639. [Guliyev KG. Synthesis of 2-formyl-1-(pvinylphenyl)cyclopropane and its polymerization and copolymerization with styrene. Russian Journal of Applied Chemistry. 2008;81(4):672-675.] 10.1134/S1070427208040204
Guliev K.G., Nazaraliev H.G., Guliev A.M. Sintez i polimerizaciya p-(2zameshennyh)ciklopropilstirolov // Azerb. Himicheskij zhurnal. 1999. №1. S.87-90. [Guliyev KG, Nazaraliyev KhG, Guliyev AM Sintez i polimerizacija p-(2-zameshhennyh)ciklopropilstirolov. Azerb. Khimicheskiy zhurnal. 1999;(1):87-90. (In Russ).]
Toropceva A.M., Belogorodskaya K.V., Bondarenko V.M. Laboratornyj praktikum po himii i tehnologii vysokomolekulyarnyh soedinenij. L.: Himiya; 1972. [Toroptseva AM, Belogorodskaya KV, Bondarenko VM Laboratorniy praktikum po khimii i tekhnologii vysokomolekulyarnykh soyedineniy. Leningrad: Khimiya; 1972. (In Russ)].
Guliev K.G., Ponomareva G.Z., Mamedli S. B., Guliev A.M. Ultrafioletovye spektry poglosheniya 2-zameshennyh-1-(pvinilfenil)ciklopropanov Zhurnal strukturnoj himii. 2009. T.50. №4. S.720-722. [Guliyev KG, Ponomaryeva GZ, Mamedli SB, Guliyev AM Ultraviolet absorption spectra of 2-substituted-1-(p-vinylphenyl)cyclopropanes. Journal of structural chemistry. 2009;50(4):693-695.] 10.1007/s10947-0090105-0
Zilberman E.N. Parametry mikrostruktury mnogokomponentnyh sopolimerov // Vysokomolek. soed. Seriya B. 1979. T.21. №1. S.33-36. [Zilberman EN Parametry mikrostruktury mnogokomponentnykh sopolimerov. Vysokomolek. soyed. Seriya B. 1979;21(1):33-36. (In Russ).]
Farall M.I., Alxis M., Trecarten M. Chemically modified polystyrene containing pendant vinyl groups: a photosensitive polymer exhibiting chemical amplification. Polymer. 1983;(24):114-116. https://doi.org/10.1016/0032-3861(83)90091-5
A.s. SSSR № 622036, 1978. [A.s. SSSR № 622036, 1978.]
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