2008
DOI: 10.1002/pat.1114
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Synthesis and characterization of mono‐ and di‐methoxy substituted acrylate polymers containing photocrosslinkable pendant chalcone moiety

Abstract: Two acrylate monomers – 4‐(2′‐methoxycinnamoyl)phenyl acrylate, and 4‐(2′,5′‐dimethoxycinnamoyl)phenyl acrylate – comprising photocrosslinkable pendant chalcone moiety and a free radical polymerizable group were synthesized. The monomers were polymerized in the presence of ethyl methyl ketone at 70°C using benzoyl peroxide as the initiator. The polymers were characterized by UV, FT‐IR, 1H‐NMR, and 13C‐NMR spectra. The weight and number average molecular weights of the polymers were determined by gel permeation… Show more

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Cited by 9 publications
(3 citation statements)
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“…Absorbance value of this band decreased rapidly with irradiation time from 0 to 315 min, and a new band at 284 nm, which is attributed to a new structure, arised. It is well known that the chalcone double bonds transform to cyclobutane ring with UV irradiation [11,14,[31][32][33]. The formation of cyclobutane ring by 2π + 2π addition of pendant chalcone units of the copolymer causes a decrease in the intensity of the band at 356 nm and formation of a new absorption band at 284 nm.…”
Section: Uv-vis Absorption Spectroscopic Study After Uv-irradiationmentioning
confidence: 99%
See 1 more Smart Citation
“…Absorbance value of this band decreased rapidly with irradiation time from 0 to 315 min, and a new band at 284 nm, which is attributed to a new structure, arised. It is well known that the chalcone double bonds transform to cyclobutane ring with UV irradiation [11,14,[31][32][33]. The formation of cyclobutane ring by 2π + 2π addition of pendant chalcone units of the copolymer causes a decrease in the intensity of the band at 356 nm and formation of a new absorption band at 284 nm.…”
Section: Uv-vis Absorption Spectroscopic Study After Uv-irradiationmentioning
confidence: 99%
“…Synthetic chalcones are commonly synthesized with the reaction of aromatic ring bonded to acetyl group and benzaldehyde derivatives via the Claisen-Schmidt condensation in presence of bases or acids catalyst [2][3][4][5][6][7]. One of the important characteristics of the chalcones is that they have the ability to photocrosslinking under ultraviolet light [8][9][10][11][12][13]. Photochemical reactions may provoke many changes in physicochemical properties such as solubility, dielectric constant, electrical conductivity, optical transparency and refractive index [14,15].…”
mentioning
confidence: 99%
“…Ⅲ 4-Hydroxyl chalcone [7]. A solution of 0.05mol NaOH in 3 ml deionized water was added to 0.05mol acetophenone in 60 ml of ethanol.…”
Section: Synthesis Of ⅲ ⅲ ⅲmentioning
confidence: 99%