Single-molecule studies of diffusion by oligomer-bound dyes in organically modified sol-gel-derived silicate films

被引:44
作者
Martin-Brown, SA [1 ]
Fu, Y [1 ]
Saroja, G [1 ]
Collinson, MM [1 ]
Higgins, DA [1 ]
机构
[1] Kansas State Univ, Dept Chem, Manhattan, KS 66506 USA
关键词
D O I
10.1021/ac0491511
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Single-molecule fluorescence spectroscopy is used to study dye diffusion within organically modified silicate (ORMOSIL) films. ORMOSIL films are prepared from sols containing tetraethoxysilane and isobutyltrimetboxysilane in 2:1 and 1:9 molar ratios. Nile red and a new silanized form of nile red that can be covalently attached to the silicate matrix are used as fluorescent probe molecules. The number and rate of single molecules diffusing through these films increases dramatically with increasing film organic content. Autocorrelation of the fluorescence images yields a quantitative measure of the relative populations of fixed and diffusing species. Surprisingly, both "free" and silicate-bound nile red exhibit relatively facile translational motions. Single-molecule/single-point fluorescence correlation spectroscopy (FCS) is used to measure the dye diffusion coefficients in submicrometer-scale film regions. The most common diffusion coefficients for "free" and silicate-bound nile red molecules in the 1:9 films are 3.9 x 10(-10) and 1.6 x 10(-10) cm(2)/s, respectively. The unexpectedly rapid diffusion of silicate-bound nile red is attributed to the presence of liquidlike silicate oligomers in the films. A lower bound for the molecular weight of the oligomers is estimated at 2900. Bulk solution-phase FCS experiments performed on "free" and silicate-bound nile red species extracted into chloroform solutions provide valuable support for these conclusions. Comparison of the results derived from experimental and simulated time transients indicates film heterogeneity occurs on sub-100-nm-length scales and likely results from the presence of inorganic- and organic-rich domains.
引用
收藏
页码:486 / 494
页数:9
相关论文
共 47 条
[1]   Catalytic hydrogenolysis of aromatic ketones by a sol-gel entrapped combined Pd-[Rh(cod)Cl]2 catalyst [J].
Abu-Reziq, R ;
Avnir, D ;
Blum, J .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2002, 187 (02) :277-281
[2]   ORGANIC-CHEMISTRY WITHIN CERAMIC MATRICES - DOPED SOL-GEL MATERIALS [J].
AVNIR, D .
ACCOUNTS OF CHEMICAL RESEARCH, 1995, 28 (08) :328-334
[3]   Nanoscale properties and matrix-dopant interactions in dye-doped organically modified silicate thin films [J].
Bardo, AM ;
Collinson, MM ;
Higgins, DA .
CHEMISTRY OF MATERIALS, 2001, 13 (08) :2713-2721
[4]  
Blum J, 1999, CHEMTECH, V29, P32
[5]   Fluorescence and NMR characterization and biomolecule entrapment studies of sol-gel-derived organic-inorganic composite materials formed by sonication of precursors [J].
Brennan, JD ;
Hartman, JS ;
Ilnicki, EI ;
Rakic, M .
CHEMISTRY OF MATERIALS, 1999, 11 (07) :1853-1864
[6]   Synthesis of functionalised fluorescent dyes and their coupling to amines and amino acids [J].
Briggs, MSJ ;
Bruce, I ;
Miller, JN ;
Moody, CJ ;
Simmonds, AC ;
Swann, E .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1997, (07) :1051-1058
[7]  
BRINKER J, 1989, SOL GEL SCI
[8]   EXCITED-STATE DYNAMICS IN THE STRUCTURAL CHARACTERIZATION OF SOLID ALKYLTRIMETHOXYSILANE-DERIVED SOL-GEL FILMS AND GLASSES CONTAINING BOUND OR UNBOUND CHROMOPHORES [J].
CHAMBERS, R ;
HARUVY, Y ;
FOX, MA .
CHEMISTRY OF MATERIALS, 1994, 6 (08) :1351-1357
[9]  
Collinson MM, 2002, TRAC-TREND ANAL CHEM, V21, P30
[10]  
Collinson MM, 2001, Handbook of advanced electronic and photonic materials and devices, P163