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Metal coordination based recognition

Template-metal coordinative bonds have also been used in the imprinting and recognition of carbohydrates in aqueous media. A MIP, templated with glucose and using 4-(iV-vinylbenzyl)diethylenetriamine)Cu(H)]diformate as [Pg.20]


The previous section described the supramolecular side chain functionalization of polymers based on a single recognition motif. However, biological systems use a wide variety of noncovalent interactions such as hydrogen bonding, metal coordination, and hydrophobic interactions in an orthogonal fashion to introduce function,... [Pg.111]

Figure 5.8 Three recognition motifs based on (a) hydrogen bonding interactions between 2,6-diaminopyridine and thymine, (b) metal coordination of suUur-carbon-sulfur (SCS) Pd pincer with pyridine, (c) pseudorotaxane formation between dibenzo[24]crovvn-8 (DB24C8) and dibenzylammonium ions, and (d) fuUy functionaUzed terpolymer 5. Figure 5.8 Three recognition motifs based on (a) hydrogen bonding interactions between 2,6-diaminopyridine and thymine, (b) metal coordination of suUur-carbon-sulfur (SCS) Pd pincer with pyridine, (c) pseudorotaxane formation between dibenzo[24]crovvn-8 (DB24C8) and dibenzylammonium ions, and (d) fuUy functionaUzed terpolymer 5.
Arnold and co-workers have developed an approach that allows both the imprinting and the subsequent chiral separation of free amino acids to be carried out in aqueous solutions [39]. The recognition was based on metal coordination-chelation interactions using A-(4-vinylbenzyl)iminodiacetic acid as the functional monomer. (For a further discussion of this system see Chapters 6 and 9.) The method worked best for aromatic amino acids (Fig. 17.11). [Pg.409]

Fugii et al. [26] reported one of the earliest examples of selective recognition using metal coordinated molecular imprinting. They utilized a polymerizable cobalt (III) Schiff base complex as the recognition element in an MIP designed for the selective... [Pg.154]


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Metal coordination based recognition motifs

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