Iron Oxide Nanoparticles Labeled with an Excited-State Intramolecular Proton Transfer Dye

被引:6
作者
de Oliveira, Elisa M. N. [2 ]
Coelho, Felipe L. [1 ]
Zanini, Mara L. [2 ]
Papaleo, Ricardo M. [2 ]
Campo, Leandra F. [1 ]
机构
[1] Univ Fed Rio Grande do Sul, Appl Organ Photochem, Inst Chem, Ave Bento Goncalves 9500, BR-90650001 Porto Alegre, RS, Brazil
[2] Pontificia Univ Catolica Rio Grande do Sul, Multidisciplinary Ctr Nanosci & Micronanotechnol, Ave Ipiranga 6681, BR-90619900 Porto Alegre, RS, Brazil
关键词
excited-state intramolecular proton transfer; fluorescent probes; magnetic properties; nanoparticles; sol-gel processes; FLUORESCENT MAGNETIC NANOPARTICLES; SILICA-BASED NANOMATERIALS; ALZHEIMERS-DISEASE; TRANSFER ESIPT; PHOTOPHYSICS; PROBE; FUNCTIONALIZATION; CHROMOPHORES; PARTICLES; DYNAMICS;
D O I
10.1002/cphc.201600472
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
Excited-state intramolecular proton transfer (ESIPT) is a particularly well known reaction that has been very little studied in magnetic environments. In this work, we report on the photophysical behavior of a known ESIPT dye of the benzothiazole class, when in solution with uncoated superparamagnetic iron oxide nanoparticles, and when grafted to silica-coated iron oxide nanoparticles. Uncoated iron oxide nanoparticles promoted the fluorescence quenching of the ESIPT dye, resulting from collisions during the lifetime of the excited state. The assembly of iron oxide nanoparticles with a shell of silica provided recovery of the ESIPT emission, due to the isolation promoted by the silica shell. The silica network gives protection against the fluorescence quenching of the dye, allowing the nanoparticles to act as a bimodal (optical and magnetic) imaging contrast agent with a large Stokes shift.
引用
收藏
页码:3176 / 3180
页数:5
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