Molecular imprinting surfaces

Fig. 14 Molecularly imprinted surface-bound nanofilaments. SEM images of the porous alumina template (a) and MIP nanofilaments after nanomolding (b). SEM images of 200 nm x 2 pm MIP (c) and of 50 nm x 5 pm nanofilaments (d). ESEM images of water microdroplets condensed on a surface with 200 nm x 1 pm nanofilaments (e) and on a flat surface consisting of the same polymer (f) [134, 135], Scale bars 1 pm (a, b), 100 pm (c, d)...

Recently, an in-depth review on molecular imprinted membranes has been published by Piletsky et al. [4]. Four preparation strategies for MIP membranes can be distinguished (i) in-situ polymerization by bulk crosslinking (ii) preparation by dry phase inversion with a casting/solvent evaporation process [45-51] (iii) preparation by wet phase inversion with a casting/immersion precipitation [52-54] and (iv) surface imprinting. 

Capture array Non-protein molecules that interact with proteins are immobilized on the surface. These may be broad capture agents based on surface chemistries such as the Ciphergen Protein Chip, or may be highly specific such as molecular imprinted polymers or oligonucleotide aptamers... 

Figure 8.9 Design of a molecular imprinting Rh2imp catalyst with Rh dimer structure on an Si02 surface.

Silica particles surface-imprinted with a TSA of a-chymotrypsin were applied for the enantio-selective hydrolyzation of amides. Surprisingly, the particles showed reverse enantio-selectivity, i. e., the sol-gel imprinted with the L-isomer of the enzyme s TSA showed a higher selectivity for the D-isomer of the substrate [125]. Also Ti02 gels have been imprinted, e.g., with 4-(4-propyloxypheny-lazo)benzoic acid. QCM coated with ultrathin films of this gel were prepared by an immersion process and showed selective binding of the template [ 126]. These examples demonstrate once more the broad applicability of the concept of molecular imprinting. 

Various novel imprinting techniques have also been presented recently. For instance, latex particles surfaces were imprinted with a cholesterol derivative in a core-shell emulsion polymerization. This was performed in a two-step procedure starting with polymerizing DVB over a polystyrene core followed by a second polymerization with a vinyl surfactant and a surfactant/cholesterol-hybrid molecule as monomer and template, respectively. The submicrometer particles did bind cholesterol in a mixture of 2-propanol (60%) and water [134]. Also new is a technique for the orientated immobilization of templates on silica surfaces [ 135]. Molecular imprinting was performed in this case by generating a polymer covering the silica as well as templates. This step was followed by the dissolution of the silica support with hydrofluoric acid. Theophylline selective MIP were obtained. 

This chapter focuses on several recent topics of novel catalyst design with metal complexes on oxide surfaces for selective catalysis, such as stQbene epoxidation, asymmetric BINOL synthesis, shape-selective aUcene hydrogenation and selective benzene-to-phenol synthesis, which have been achieved by novel strategies for the creation of active structures at oxide surfaces such as surface isolation and creation of unsaturated Ru complexes, chiral self-dimerization of supported V complexes, molecular imprinting of supported Rh complexes, and in situ synthesis of Re clusters in zeolite pores (Figure 10.1). 

Principle of Molecular Imprinting for Metal Complexes on Surfaces... 

Molecular Imprinting of Rh Dimers and Rh Monomers atSi02 Surfaces... 

Figure 10.5 Preparation of a molecular-imprinted [Rh-P(OCH3)3] dimer catalyst on a Si02 surface.

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