Synthesis and encapsulation of fluorescein in zeolite Y

被引:10
作者
Lukarska, Malgorzata [1 ]
Jankowska, Aldona [1 ]
Gapinski, Jacek [2 ,3 ]
Valable, Samuel [4 ]
Anfray, Clement [4 ]
Menard, Benjamin [4 ]
Mintova, Svetlana [5 ]
Kowalak, Stanislaw [1 ]
机构
[1] Adam Mickiewicz Univ, Fac Chem, Poznan, Poland
[2] Adam Mickiewicz Univ, Fac Phys, Poznan, Poland
[3] Adam Mickiewicz Univ, NanoBioMed Ctr, Poznan, Poland
[4] Univ Caen, CEA, CNRS, CERVOxy Grp, F-14050 Caen, France
[5] Univ Caen, ENSICAEN, LCS, CNRS, F-14050 Caen, France
关键词
Fluorescein; Synthesis; Zeolite Y; Encapsulation; Fluorescence; MOLECULES; BOTTLE; OXYGEN; STATE; SHIP;
D O I
10.1016/j.micromeso.2016.02.043
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Fluorescein was entrapped inside FAU type zeolite (Y) by generating it from resorcinol and phthalic anhydride. Prior to the formation of fluorescein, zeolite Y was modified with various cations (H, Zn, Ce, Na, K). The modified zeolite acted as catalysts for the fluorescein Friedel-Crafts reaction synthesis, while at the same time it played a role of matrix for the stabilization and homogeneous dispersion of the guest molecules. The nature of the different cations influenced the content of fluorescein generated in the zeolite, and favoured the formation of some dye isomers (i.e. anion, dianion, cation or transition metal complex). The contribution of different fluorescein derivatives in the products was reflected in their absorption and fluorescence properties. The H-, Ce-, and Zn- containing Y zeolites revealed the highest content of fluorescein due to their distinct acid active sites. The composites with H- and ZnY zeolites indicated much higher fluorescence than that of the pristine fluorescein. Moreover, fluorescein in zeolite Y matrices did not show any photobleaching under continuous illumination (lambda = 730 nm, in a two photon experiment for 180 s), which suggests that these materials could be used for biomedical applications. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:79 / 84
页数:6
相关论文
共 19 条
[1]   STRUCTURE OF RED AND ORANGE FLUORESCEIN [J].
ANTHONI, U ;
CHRISTOPHERSEN, C ;
NIELSEN, PH ;
PUSCHL, A ;
SCHAUMBURG, K .
STRUCTURAL CHEMISTRY, 1995, 6 (03) :161-165
[2]   Imaging the effect of a hydrothermal treatment on the pore accessibility and acidity of large ZSM-5 zeolite crystals by selective staining [J].
Aramburo, Luis R. ;
Ruiz-Martinez, Javier ;
Hofmann, Jan P. ;
Weckhuysen, Bert M. .
CATALYSIS SCIENCE & TECHNOLOGY, 2013, 3 (05) :1208-1214
[3]  
Azals T., 2006, CHEM MATER, V18, P6382
[4]   Solid state NMR characterisation of encapsulated molecules in mesoporous silica [J].
Babonneau, F ;
Yeung, L ;
Steunou, N ;
Gervais, C ;
Ramila, A ;
Vallet-Regi, M .
JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY, 2004, 31 (1-3) :219-223
[5]  
Chrétien MN, 2004, PHOTOCHEM PHOTOBIOL, V80, P434, DOI 10.1562/0031-8655(2004)080<0434:SSOFNA>2.0.CO
[6]  
2
[7]   Controlling J aggregation in fluorescein by bile salt hydrogels [J].
Das, Susmita ;
Chattopadhyay, Asoke P. ;
De, Swati .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2008, 197 (2-3) :402-414
[8]   Comparison of micro- and mesoporous inorganic materials in the uptake and release of the drug model fluorescein and its analogues [J].
Fisher, KA ;
Huddersman, KD ;
Taylor, MJ .
CHEMISTRY-A EUROPEAN JOURNAL, 2003, 9 (23) :5873-5878
[9]  
HERRON N, 1995, J INCLUS PHENOM MOL, V21, P283
[10]   A COBALT OXYGEN CARRIER IN ZEOLITE Y - A MOLECULAR SHIP IN A BOTTLE [J].
HERRON, N .
INORGANIC CHEMISTRY, 1986, 25 (26) :4714-4717