Recent progress in the development of highly active dyeing photoinitiators based on 1,3-bis(p-substituted phenylamino)squaraines for radical polymerization of acrylates
Literature Information
Alicja Balcerak, Janina Kabatc
Photopolymerization is a very popular technique used in the production of various polymeric materials. The key role in light-induced polymerization processes is played by a photoinitiator. One of the most common and desirable activators of photopolymerization is a dye-based photoinitiating system. Most often, these systems are composed of photosensitizer and other additives, such as co-initiators. The dye (photosensitizer) absorbs the irradiation selectively and interacts with other molecules to form reactive species that initiate a chain reaction. For this reason, design and development of novel photosensitizers, and hence photoinitiators, is crucial to improving the efficiency of photochemically initiated polymerization reactions. In recent years, an interesting group of light absorbers, i.e. squaraines, has been proposed as highly efficient photosensitizers. These dyes show excellent spectral properties, such as high molar extinction coefficients and a wide absorption range, which is one of the most important requirements of an effective photosensitizer. Therefore, it is worth paying attention to the high potential of squaraines for photoinitiation of polymerization reactions. In this review we summarized our recent reports on photoinitiating systems containing squarylium dyes for radical polymerization of acrylate monomers. We focused on the radical photoinitiators consisting of 1,3-bis(p-substituted phenylamino)squaraines in the role of sensitizers. The article highlights the development and progress of squaraine-based photoinitiators.
Recommended Journals
Related Literature
Molecular dynamics investigations of cello-oligosaccharide recognition by Cel9G–CBM3c from Clostridium cellulovorans
Penghui Li, Chunchun Zhang
DOI: 10.1039/C7CP07175B
Effect of chemical structure on the subglass relaxation dynamics of biobased polyesters as revealed by dielectric spectroscopy: 2,5-furandicarboxylic acid vs. trans-1,4-cyclohexanedicarboxylic acid
L. Genovese, M. Soccio, N. Lotti, A. Munari, A. Szymczyk, S. Paszkiewicz, A. Linares, A. Nogales, T. A. Ezquerra
DOI: 10.1039/C8CP01810C
Hexagonal SiC with spatially separated active sites on polar and nonpolar facets achieving enhanced hydrogen production from photocatalytic water reduction
Ning Liu, Zhongnan Guo, Wenjun Wang, Liwei Guo, Wenxia Yuan
DOI: 10.1039/C7CP08363G
Hydrogen detachment driven by a repulsive 1πσ* state – an electron localization function study of 3-amino-1,2,4-triazole
Andrzej Bil, Zdzisław Latajka, Malgorzata Biczysko
DOI: 10.1039/C7CP06744E
Structural stability and electronic properties of alkaline-earth metal induced Si(111)-(3 × 2) surfaces
Li-Fang Xu
DOI: 10.1039/C8CP04323J
Impact of screw and edge dislocations on the thermal conductivity of individual nanowires and bulk GaN: a molecular dynamics study
Anastasiia Salnikova, Imad Belabbas, David Lacroix, Joseph Kioseoglou
DOI: 10.1039/C7CP07821H
New insights into the plasmonic enhancement for photocatalytic H2 production by Cu–TiO2 upon visible light illumination
S. Hamid, F. Sieland, J. Sann, S. Xia, J. Schneider
DOI: 10.1039/C7CP07762A
Understanding interface (odd–even) effects in charge tunneling using a polished EGaIn electrode
Jiahao Chen, Thomas J. Giroux, Yen Nguyen, Atte A. Kadoma, Boyce S. Chang, Brett VanVeller, Martin M. Thuo
DOI: 10.1039/C7CP07531F
The interfacial electrostatic potential modulates the insertion of cell-penetrating peptides into lipid bilayers
Natalia Wilke, Luis S. Mayorga
DOI: 10.1039/C7CP07243K
A systematic study of various 2D materials in the light of defect formation and oxidation
A. K. A. Lu, D. Chiappe
DOI: 10.1039/C8CP05665J
You might also like
What are the main uses of 1-(3-Aminophenyl)-3-[(3R)-1-(3,3-dimethyl-2-oxobutyl)-2-oxo-5-(2-pyridinyl)-2,3-dihydro-1H-1,4-benzodiazepin-3-yl]urea (CAS: 155412-88-7)?
This compound is mainly used as an intermediate in the synthesis of antipsychoti...
How should waste containing 1-(D-Ribofuranosyl)-1,4-dihydro-3-pyridinecarboxamide (CAS: 19132-12-8) be handled?
Waste containing 1-(D-Ribofuranosyl)-1,4-dihydro-3-pyridinecarboxamide (CAS: 191...
What regulatory guidelines apply to 2-Methyl-2-propanyl 3-bromo-3-(hydroxymethyl)-1-azetidinecarboxylate (CAS: 2007919-81-3)?
2-Methyl-2-propanyl 3-bromo-3-(hydroxymethyl)-1-azetidinecarboxylate (CAS: 20079...
What is N-(4-Chloro-2-pyridinyl)acetamide (CAS: 245056-66-0)?
N-(4-Chloro-2-pyridinyl)acetamide (CAS: 245056-66-0) is a chemical compound with...
What is 5-Chloro-2-hydroxybenzoic acid (CAS: 321-14-2)?
5-Chloro-2-hydroxybenzoic acid, also known as 5-chlorosalicylic acid, is an arom...
What precautions should be taken when handling 1,1-Dichloro-1-fluoroethane (CAS: 1717-00-6)?
When handling 1,1-Dichloro-1-fluoroethane (CAS: 1717-00-6), it is important to u...
What are the physical and chemical properties of Fmoc-(2S,3R)-3-phenylpyrrolidine-2-carboxylic acid (CAS: 281655-32-1)?
Fmoc-(2S,3R)-3-phenylpyrrolidine-2-carboxylic acid is a white crystalline solid ...
What are the main uses of 4-Amino-5-bromo-2-pyridinecarboxylic acid (CAS: 1363381-01-4)?
4-Amino-5-bromo-2-pyridinecarboxylic acid is primarily used as a precursor in th...
What precautions should be taken when handling (S)-tert-butyl 2-((2-(4-bromophenyl)-2-oxoethyl)carbamoyl)pyrrolidine-1-carboxylate (CAS: 1007881-98-2)?
Handling this compound should be done with personal protective equipment (PPE) i...
What precautions should be taken when handling 8-bromo-2,2-dimethyl-3,4-dihydro-2H-1,4-benzoxazin-3-one (CAS: 688363-73-7)?
When handling 8-bromo-2,2-dimethyl-3,4-dihydro-2H-1,4-benzoxazin-3-one, use prop...
Source Journal
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.














