Impact of Light Intensity on Control in Photoinduced Organocatalyzed Atom Transfer Radical Polymerization

被引:78
作者
Ryan, Matthew D. [1 ]
Pearson, Ryan M. [1 ]
French, Tracy A. [1 ]
Miyake, Garret M. [1 ,2 ]
机构
[1] Univ Colorado Boulder, Dept Chem & Biochem, Boulder, CO 80309 USA
[2] Univ Colorado Boulder, Mat Sci & Engn Program, Boulder, CO 80309 USA
基金
美国国家卫生研究院;
关键词
ELECTRON-TRANSFER; EXCHANGE-REACTION; EXCITED-STATES; PIVOTAL ROLE; NITROXIDE; REDUCTION; ALKOXYAMINE; CHEMISTRY; CROSSOVER; PERYLENE;
D O I
10.1021/acs.macromol.7b00502
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Organic photoredox catalysts have been shown to operate organocatalyzed atom transfer radical polymerizations (O-ATRP) using visible light as the driving force. In this work, the effect of light intensity from white LEDs was evaluated as an influential factor in control over the polymerization and the production of well-defined polymers. We posit the irradiation conditions control the concentrations of various catalyst states necessary to mediate a controlled radical polymerization. Systematic dimming of white LEDs allowed for consideration of the role of light intensity on the polymerization performance. The general effects of decreased irradiation intensity in photoinduced O-ATRP were investigated through comparing two different organic photoredox catalysts: perylene and an 3,7-di(4-biphenyl) 1-naphthalene-10-phenoxazine. Previous computational efforts have investigated catalyst photophysical and electrochemical characteristics, but the broad and complex effects of varied irradiation intensity as an experimental variable on the mechanism of O-ATRP have not been explored. This work revealed that perylene requires more stringent irradiation conditions to achieve controlled polymer molecular weight growth and produce polymers with dispersities <1.50. In contrast, the 3,7-di(4-biphenyl) 1-naphthalene-10-phenoxazine is more robust, achieving linear polymer molecular weight growth under relative irradiation intensity as low as 25%, to produce polymers with dispersities <1.50. This finding is significant, as the discovery of highly robust catalysts is necessary to allow for the adoption of successful O-ATRP in a wide scope of conditions, including those which necessitate low light intensity irradiation.
引用
收藏
页码:4616 / 4622
页数:7
相关论文
共 49 条
[1]   Photoinitiated Metal-Free Controlled/Living Radical Polymerization Using Polynuclear Aromatic Hydrocarbons [J].
Allushi, Andrit ;
Jockusch, Steffen ;
Yilmaz, Gorkem ;
Yagci, Yusuf .
MACROMOLECULES, 2016, 49 (20) :7785-7792
[2]  
[Anonymous], MACROMOL RAPID COMMU
[3]  
[Anonymous], J POLYM SCI A
[4]   The photophysics of photoredox catalysis: a roadmap for catalyst design [J].
Arias-Rotondo, Daniela M. ;
McCusker, James K. .
CHEMICAL SOCIETY REVIEWS, 2016, 45 (21) :5803-5820
[5]   Controlled/living radical polymerization: Features, developments, and perspectives [J].
Braunecker, Wade A. ;
Matyjaszewski, Krzysztof .
PROGRESS IN POLYMER SCIENCE, 2007, 32 (01) :93-146
[6]   Nitroxide-mediated polymerization:: The pivotal role of the kd value of the initiating alkoxyamine and the importance of the experimental conditions [J].
Chauvin, Florence ;
Dufils, Pierre-Emmanuel ;
Gigmes, Didier ;
Guillaneuf, Yohann ;
Marque, Sylvain R. A. ;
Tordo, Paul ;
Bertin, Denis .
MACROMOLECULES, 2006, 39 (16) :5238-5250
[7]   Light-Controlled Radical Polymerization: Mechanisms, Methods, and Applications [J].
Chen, Mao ;
Zhong, Mingjiang ;
Johnson, Jeremiah A. .
CHEMICAL REVIEWS, 2016, 116 (17) :10167-10211
[8]   Phenyl Benzo[b]phenothiazine as a Visible Light Photoredox Catalyst for Metal-Free Atom Transfer Radical Polymerization [J].
Dadashi-Silab, Sajjad ;
Pan, Xiangcheng ;
Matyjaszewski, Krzysztof .
CHEMISTRY-A EUROPEAN JOURNAL, 2017, 23 (25) :5972-5977
[9]   FLUORESCENCE OF BROMOPERYLENES AND REQUIREMENTS OF HEAVY-ATOM QUENCHING [J].
DREESKAMP, H ;
KOCH, E ;
ZANDER, M .
CHEMICAL PHYSICS LETTERS, 1975, 31 (02) :251-253
[10]   ELECTRON-TRANSFER REACTIONS IN ORGANIC-CHEMISTRY .2. AN ANALYSIS OF ALKYL HALIDE REDUCTION BY ELECTRON-TRANSFER REAGENTS ON THE BASIS OF THE MARCUS THEORY [J].
EBERSON, L .
ACTA CHEMICA SCANDINAVICA SERIES B-ORGANIC CHEMISTRY AND BIOCHEMISTRY, 1982, 36 (08) :533-543