Shedding light on azopolymer brush dynamics by fluorescence correlation spectroscopy

被引:5
|
作者
Kollarigowda, R. H. [1 ,2 ,3 ]
De Santo, I. [1 ,2 ]
Rianna, C. [1 ,2 ,4 ]
Fedele, C. [1 ,2 ]
Manikas, A. C. [1 ,5 ]
Cavalli, S. [1 ]
Netti, P. A. [1 ,2 ]
机构
[1] Ist Italiano Tecnol, Ctr Adv Biomat Healthcare, Largo Barsanti & Matteucci 53, I-80125 Naples, Italy
[2] Univ Naples Federico II, Dipartimento Ingn Chim Mat & Prod Ind, DICMAPI, Piazzale Tecchio 80, I-80125 Naples, Italy
[3] Univ Alberta, Dept Chem & Mat Engn, Natl Inst Nanotechnol NINT, 11421 Saskatchewan Dr, Edmonton, AB, Canada
[4] Univ Bremen, Inst Biophys, Otto Hahn Allee 1, D-28359 Bremen, Germany
[5] Fdn Res & Technol Hellas FORTH ICE HT, Inst Chem Engn Sci, Stadiou Str, GR-26504 Patras, Hellas, Greece
关键词
DENSITY POLYMER BRUSHES; AZOBENZENE POLYMERS; FILMS; FIELD; SUPERRESOLUTION; DISPERSE-RED-1; FLUCTUATIONS; ORIENTATION; TEMPERATURE; MECHANISM;
D O I
10.1039/c6sm01482h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Understanding the response to illumination at a molecular level as well as characterising polymer brush dynamics are key features that guide the engineering of new light-stimuli responsive materials. Here, we report on the use of a confocal microscopy technique that was exploited to discern how a single molecular event such as the photoinduced isomerisation of azobenzene can affect an entire polymeric material at a macroscopic level leading to photodriven mass-migration. For this reason, a set of polymer brushes, containing azobenzene (Disperse Red 1, DR) on the side chains of poly(methacrylic acid), was synthesised and the influence of DR on the polymer brush dynamics was investigated for the first time by Fluorescence Correlation Spectroscopy (FCS). Briefly, two dynamics were observed, a short one coming from the isomerisation of DR and a long one related to the brush main chain. Interestingly, photoinduced polymer aggregation in the confocal volume was observed.
引用
收藏
页码:7102 / 7111
页数:10
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