1997
DOI: 10.1002/(sici)1097-4628(19970613)64:11<2237::aid-app19>3.0.co;2-0
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Novel polymeric photoinitiators bearing side-chain ?-aminoacetophenone moieties for ultraviolet-curable pigmented coatings

Abstract: New polymeric photoinitiators with pendant a-aminoacetophenone moieties, such as the homopolymers of 1-(4-morpholinophenyl)-2-benzyl-2- [N-methyl-N-(3-methacryloyloxypropyl)]aminopropan-1-one and of 1-(4-morpholinophenyl)-2-benzyl-2-[N-methyl-N-(3-methacryloyloxypropyl)]aminobutan-1-one have been prepared and fully characterized. Their photoinitiation activity has been also checked in the ultraviolet cure of a standard acrylic mixture, under irradiation over 380 nm, thus simulating the absorption conditions of… Show more

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Cited by 9 publications
(6 citation statements)
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“…Second, the imide group may cause chain transfer reaction in the copolymerization,26 leading to low molecular weight of the final product. Finally, the electrophilic group in the para‐position of the aromatic N‐substituted maleimide will favor the copolymerization 39. However, the phenoxyl group belongs to electron‐donating group, which will certainly go against to attain high molecular weight product.…”
Section: Resultsmentioning
confidence: 99%
“…Second, the imide group may cause chain transfer reaction in the copolymerization,26 leading to low molecular weight of the final product. Finally, the electrophilic group in the para‐position of the aromatic N‐substituted maleimide will favor the copolymerization 39. However, the phenoxyl group belongs to electron‐donating group, which will certainly go against to attain high molecular weight product.…”
Section: Resultsmentioning
confidence: 99%
“…Examples of the Norrish type I photoinitiators are polymers bearing side-chain benzoin methyl ether moieties, 20 polymeric trichloro-and α-amino-acetophenones. 21 In addition, new polymeric systems with tethered thioxanthone, anthraquinone, camphorquinone, or benzyl moieties are developed intensively as well. 19 Most popular polymeric photoinitiators of the Norrish type II are based on benzophenone, mainly because of its relatively low cost.…”
Section: Introductionmentioning
confidence: 99%
“…17,18 MPIs are defined as polymer systems containing pendant or in-chain chromophores, which after the light absorption process can generate active species capable of initiating the polymerization and crosslinking of mono-and multi-functional monomers and oligomers. 17,[19][20][21][22][23] All of the free-radical photoinitiators can be divided into two main types: (i) those capable of photofragmention (Norrish type I), and (ii) those capable of free radicals generation through hydrogen-abstraction mechanism (Norrish type II). Examples of the Norrish type I photoinitiators are polymers bearing side-chain benzoin methyl ether moieties, 20 polymeric trichloro-and α-amino-acetophenones.…”
Section: Introductionmentioning
confidence: 99%
“…Macrophotoinitiators are defined as polymer systems containing pendant or in-chain chromophores, which through the light absorption process can generate active species capable of initiating the polymerization and crosslinking of mono-and multi-functional monomers and oligomers [3,[7][8][9][10][11]. All of the free-radical photoinitiators can be divided into two main types: i) those capable of photofragmention (Norrish type I), and ii) those capable of generating free radicals through hydrogen-abstraction mechanism (Norrish type II).…”
Section: Introductionmentioning
confidence: 99%
“…All of the free-radical photoinitiators can be divided into two main types: i) those capable of photofragmention (Norrish type I), and ii) those capable of generating free radicals through hydrogen-abstraction mechanism (Norrish type II). Examples of the Norrish type I photoinitiators are polymers bearing side-chain benzoin methyl ether moieties [8], polymeric trichloroand α-amino-acetophenones [9]. In the last years, new polymeric systems with tethered thioxanthone, anthraquinone, camphorquinone or benzyl moieties are intensively developed [7].…”
Section: Introductionmentioning
confidence: 99%