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Mesoporous Silica Materials (mesoporou + silica_material)
Selected AbstractsSelective Zinc(II)-Ion Fluorescence Sensing by a Functionalized Mesoporous Material Covalently Grafted with a Fluorescent Chromophore and Consequent Biological ApplicationsADVANCED FUNCTIONAL MATERIALS, Issue 2 2009Krishanu Sarkar Abstract A highly ordered 2D-hexagonal mesoporous silica material is functionalized with 3-aminopropyltriethoxysilane. This organically modified mesoporous material is grafted with a dialdehyde fluorescent chromophore, 4-methyl-2,6-diformyl phenol. Powder X-ray diffraction, transmission electron microscopy, N2 sorption, Fourier transform infrared spectroscopy, and UV-visible absorption and emission have been employed to characterize the material. This material shows excellent selective Zn2+ sensing, which is due to the fluorophore moiety present at its surface. Fluorescence measurements reveal that the emission intensity of the Zn2+ -bound mesoporous material increases significantly upon addition of various concentrations of Zn2+, while the introduction of other biologically relevant (Ca2+, Mg2+, Na+, and K+) and environmentally hazardous transition-metal ions results in either unchanged or weakened intensity. The enhancement of fluorescence is attributed to the strong covalent binding of Zn2+, evident from the large binding constant value (0.87,×,104M,1). Thus, this functionalized mesoporous material grafted with the fluorescent chromophore could monitor or recognize Zn2+ from a mixture of ions that contains Zn2+ even in trace amounts and can be considered as a selective fluorescent probe. We have examined the application of this mesoporous zinc(II) sensor to cultured living cells (A375 human melanoma and human cervical cancer cell, HeLa) by fluorescence microscopy. [source] Organically Functionalized Mesoporous Silica by Co-structure-Directing RouteADVANCED FUNCTIONAL MATERIALS, Issue 17 2010Chuanbo Gao Abstract This article provides a brief overview of functional mesoporous silica materials synthesized by the co-structure-directing route, which is distinct from conventional synthesis strategies. In these systems, organosilane serves as the co-structure-directing agent (CSDA), which provides critical interactions between the template and organic part of the organosilane to form mesostructures, thus retaining the organic groups on the pore surface after removal of the template by extraction. i) The formation of anionic-surfactant-templated mesoporous silicas (AMSs) has been achieved by the co-structure-directing route, which leads to a variety of mesostructures, porous properties and morphologies. ii) Other co-structure-directing systems for synthesizing mesoporous silicas have also been achieved, including systems using cationic surfactants and non-surfactants, and systems using DNA for constructing nanofibers and DNA,silica liquid crystalline complexes. iii) Evidence for the regular arrangement of functional groups on the pore surface resulted from the co-structure-directing effect has been discussed. Also included is a brief description of the application, future requirements, and trends in the development of mesoporous materials by the co-structure-directing route. [source] Tuning the Thermal Relaxation of a Photochromic Dye in Functionalized Mesoporous SilicaADVANCED FUNCTIONAL MATERIALS, Issue 13 2009Lea A. Mühlstein Abstract In this study, it is shown that the kinetics of the back-switching reaction of a photochromic spirooxazine dye encapsulated in mesoporous silica materials can be significantly influenced both by the space available to the dye molecules and by the functionalization of the silica wall. Steric hindrance of the ring-closing process due to high dye content or small pore size leads to a slow fading speed of the irradiated dye species. Further, the density of surface silanol-groups present at the silica walls has an effect on the switching behavior of the dye because of their ability to stabilize the zwitterionic merocyanine isomers, thereby slowing the fading process from the open to the closed form. This stabilization effect is further enhanced in the presence of acidic functional groups, while, in contrast, basic functional groups reduce the stabilization of the open-from dye isomers, and thus a faster decay of the irradiated species is observed. Control over the fading speed of photochromic dyes is interesting for applications requiring a particularly fast or slow fading speed. [source] Templated Synthesis of Mesoporous Superparamagnetic Polymers,ADVANCED FUNCTIONAL MATERIALS, Issue 14 2007B. Fuertes Abstract We present a novel synthetic strategy for fabricating superparamagnetic nanoparticles randomly dispersed in a mesoporous polymeric matrix. This method is based on the use of mesoporous silica materials as templates. The procedure used to obtain these mesoporous magnetic polymers consisted in: a),generating iron oxide ferrite magnetic nanoparticles (FMNP) of size ,,7,8,nm within the pores of the silica, b),loading the porosity of the silica/FMNP composite with a polymer (Polydivinylbenzene), c),selectively removing the silica framework from the resulting silica/FMNP/polymer composite. Such magnetic porous polymeric materials exhibit large surface areas (up to 630,m2,g,1), high pore volumes (up to 0.73,cm3,g,1) and a porosity made up of mesopores. In this way, it is possible to obtain superparamagnetic mesoporous hybrid nanocomposites that are easily manipulated by an external magnetic field and display different magnetic behaviours depending on the textural properties of the template employed. [source] A Study on the Effect of Template Chain Length on the Synthesis of Mesoporous Silica in An Acidic ConditionJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 11 2007Yang Yu-Xiang Hexagonal mesoporous silica materials were synthesized in an acidic medium using different chain length of the quaternary ammonium surfactants as a template. The effects of chain length on the physical property, morphology of mesoporous materials, and the temperature on synthesis of materials in CnTMBr,TEOS,HNO3,H2O (n=12,14,16,18) system were systematically studied. The synthesized products were characterized by X-ray diffraction patterns, scanning electron microscopy, transmission electron microscopy, and nitrogen sorption analysis. It was found that degree of ordering, the d spacing values, and pore size all increase with an increase in the chain length of the template. The optimum synthesis temperature for mesoporous silica using C18TMBr,TEOS,HNO3,H2O system is slightly higher than the Krafft point. The temperature and pH can all affect the expandability of micelles, and so an increase in temperature and decrease in pH all lead to an increase in the pore size. It is also found that the shear flow and chain length are two key factors inducing the formation of millimeter-scaled silica ropes and micrometer-scaled rope fibers. [source] Organic,inorganic hybrid mesoporous silicas: functionalization, pore size, and morphology controlTHE CHEMICAL RECORD, Issue 1 2006Sung Soo Park Abstract Topological design of mesoporous silica materials, pore architecture, pore size, and morphology are currently major issues in areas such as catalytic conversion of bulky molecules, adsorption, host,guest chemistry, etc. In this sense, we discuss the pore size-controlled mesostructure, framework functionalization, and morphology control of organic,inorganic hybrid mesoporous silicas by which we can improve the applicability of mesoporous materials. First, we explain that the sizes of hexagonal- and cubic-type pores in organic,inorganic hybrid mesoporous silicas are well controlled from 24.3 to 98.0,Å by the direct micelle-control method using an organosilica precursor and surfactants with different alkyl chain lengths or triblock copolymers as templates and swelling agents incorporated in the formed micelles. Second, we describe that organic,inorganic hybrid mesoporous materials with various functional groups form various external morphologies such as rod, cauliflower, film, rope, spheroid, monolith, and fiber shapes. Third, we discuss that transition metals (Ti and Ru) and rare-earth ions (Eu3+ and Tb3+) are used to modify organic,inorganic hybrid mesoporous silica materials. Such hybrid mesoporous silica materials are expected to be applied as excellent catalysts for organic reactions, photocatalysis, optical devices, etc. © 2006 The Japan Chemical Journal Forum and Wiley Periodicals, Inc. Chem Rec 6: 32,42; 2006: Published online in Wiley InterScience (www.interscience.wiley.com) DOI 10.1002/tcr.20070 [source] | ||||||||||