Liquid templating

Synthesis of polymeric capsules involves polymer self-assembly on many levels and length scales. Approaches to their synthesis include cases where monomers are polymerized around a liquid template, premade polymers are assembled around liquid and solid templates, premade particles are assembled around templates, and small molecules or polymers assemble spontaneously. Each method offers unique challenges and advantages, and each allows the production of capsules with different properties. 

We can think of the previous methods for generating capsules as liquid templating, where self-assembly occurs around a hquid. An alternative is to use a solid template, usually called colloidal templating. The shell is generated around a solid particle that is later digested, leaving a hollow sphere (Caruso 2000). Deposition of... 

The cooperative self-assembly route is the most commonly used synthesis procedure for surfactant templated materials. It uses aqueous solutions at a much lower initial surfactant concentration than for the true liquid templating route, reducing the required amounts of expensive surfactant template. In these solutions, the surfactants are at a high enough concentration to form micelles, which may be spherical, elliptical, rod-like or vesicular, but do not form the ordered aggregates found in the final templated silica-surfactant composites. The solutions are in thermodynamic equilibrium so are stable at a given temperature until the silica precursors are added. Once added, a series of interactions between the inorganic species and the surfactant micelles occur, which involve simultaneous association of all components, hence the name, cooperative self-assembly. The result of the interactions is formation of the silica-surfactant composite, usually a precipitate, with an ordered nanoscale structure similar to those found in concentrated surfactant solutions. 

C. Choi, H. Yi, S. Hwang, D. Weitz, and C. Lee, Microfluidic fabrication of complex-shaped microfibers by liquid template-aided multiphase microflow, Lab on a Chip, 11, 1477-1483, 2011. 

Other approaches for the electrodeposition of structured Pt based films involved polystyrene spheres that were pre-self-assembled on the substrate prior to deposition. The film thickness and pore volume can be varied by using different diameters of polystyrene spheres. 3D nano-network structures were made in this manner. Both the lyotropic liquid template and the self-assembled polystyrene template method have been employed to form Pt and PtRu alloy films [75, 76]. An example of a macroporous Pt-based film made using polystyrene spheres is shown in Figure 9.7. 

Synthesis of ionic liquid templated zeolite like structures... 

C. J. Adams, A. E. Bradley, K. R. Seddon, The synthesis of mesoporous materials using novel ionic liquid templates in water, 2001, Aust. J. Chem., 54,679-681. 

Kresge C T, Leonowicz M E, Roth W J, Vartuli J C and Beck J S 1992 Ordered mesoporous molecular sieves synthesized by a liquid-crystal template mechanism Nature 359 710-12... 

The principle was demonstrated using triazine herbicides as templates and by varying the type of functional monomer and the monomer composition. With a final batch size of ca. 40 mg of monomer, the consumption of monomers and template is significantly reduced and the synthesis and evaluation can take place in standard high-performance liquid chromatography (UPLC) autosample vials. After synthesis. 

The approach consists of a liquid-phase oxidation using OH Fenton radicals from H2O2 for detemplation [148-150]. The radicals oxidize the organic template into CO2 and H2O while the porosity of the material is developed. The proof-of-principle of this concept is discussed for two case studies. 

The most important nanomaterial synthesis methods include nanolithography techniques, template-directed syntheses, vapor-phase methods, vapor-liquid-solid (VLS) methods, solution-liquid-solid (SLS) approaches, sol-gel processes, micelle, vapor deposition, solvothermal methods, and pyrolysis methods [1, 2]. For many of these procedures, the control of size and shape, the flexibility in the materials that can be synthesized, and the potential for scaling up, are the main limitations. In general, the understanding of the growth mechanism of any as-... 

Kokufuta, E Jinbo, E, A Hydrogel Capable of Facilitating Polymer Diffusion through the Gel Porosity and Its Application in Enzyme Immobilization, Macromolecules 25, 3549, 1992. Kresge, CT Leonowicz, ME Roth, WJ Vartuli, JC Beck, JS, Ordered Mesoporous Molecular Sieves Synthesized by a Liquid-Crystal Template Mechanism, Nature 359, 710, 1992. 

The use of ordered supramolecular assemblies, such as micelles, monolayers, vesicles, inverted micelles, and lyotropic liquid crystalline systems, allows for the controlled nucleation of inorganic materials on molecular templates with well-defined structure and surface chemistry. Poly(propyleneimine) dendrimers modified with long aliphatic chains are a new class of amphiphiles which display a variety of aggregation states due to their conformational flexibility [38]. In the presence of octadecylamine, poly(propyleneimine) dendrimers modified with long alkyl chains self-assemble to form remarkably rigid and well-defined aggregates. When the aggregate dispersion was injected into a supersaturated... 

The similarities of above experimental results inspired us to investigate the role of SE in heterogeneous catalytic enantioselective hydrogenation reactions. In heterogeneous catalytic reaction the SE means that a given template molecule interacts with the prochiral substrate in the liquid phase in such a way that one of the prochiral sites is preferentially shielded. If the substrate is shielded then its adsorption onto the metal can take place with its unshielded site resulting in ED. 

C -CP-MAS NMR provides subtle information about the degree of solvation of the polymer chains of a CFP in a given solvent and consequently it may be qualitatively correlated with the nanometer scale morphology of the polymer matrix. In fact, the prerequisite that enables a polymer framework to develop a nanoporosity is the ability of the polymer chains and its pendants to be suitably solvated by the liquid medium [26-28]. Therefore, C -CP-MAS NMR spectra provide the basis for a first level screening of the possibility of a CFP in a given solvent to be employed as an hexo-template, able to accommodate metal nanoclusters chemically produced in its interior (see below and Ref. [29]). 

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