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Metal Coordination-Based Recognition Motifs

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.
See other pages where Metal Coordination-Based Recognition Motifs is mentioned: [Pg.84]    [Pg.84]    [Pg.222]    [Pg.105]    [Pg.130]    [Pg.575]    [Pg.1064]    [Pg.121]    [Pg.205]    [Pg.229]    [Pg.129]    [Pg.3579]    [Pg.415]   


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