Ligands principles

Designing segmental ligands Principles and synthetic routes... 

The principle of specific chemical recognition is common to ligand—macromolecule interactions, but this alone does not suffice to define a receptor in the pharmacologic sense. Rather, it is the combination of chemical specificity or recognition and the capacity to initiate biological response or transduction that define the pharmacologic receptor (1,10,11). 

The world of zinc-containing DNA-binding proteins is by no means exhausted by these three subfamilies. Several other subfamilies are already known with different three-dimensional structures and different sequence patterns of cysteine and histidine residues that form the zinc ligands. Further subfamilies may well be discovered as the genomes of different species are sequenced whether or not any fundamentally new principles for DNA-protein recognition will be discovered amongst these new subfamilies remains to be seen. 

As a result of the systematic application of coordination-chemistry principles, dozens of previously unsuspected stnicture types have been synthesized in which polyhedral boranes or their anions can be considered to act as ligands which donate electron density to metal centres, thereby forming novel metallaboranc elusters, ". Some 40 metals have been found to act as acceptors in this way (see also p. 178). The ideas have been particularly helpful m emphasizing the close interconnection between several previously separated branches of chemistry, notably boron hydride clu.ster chemistry, metallaboranc and metallacarbaborane chemistry (pp. 189-95). organometallic chemistry and metal-metal cluster chemistry. All are now seen to be parts of a coherent whole. 

This is in principle possible in any compound containing an ambidentate ligand. However, that... 

The ratios of these slopes for L- and D-esters are shown in Table 12. The kL/kD values of the acylation step in the CTAB micelle are very close to those in Table 9, as they should be. It is interesting to note that the second deacylation step also occurs enantioselectively. Presumably it is due to the deacylation ocurring by the attack of a zinc ion-coordinated hydroxide ion which, in principle, should be enantioselective as in the hydroxyl group of the ligand. Alternatively, the enantioselectivity is also expected when the free hydroxide ion attack the coordinated carbonyl groups of the acyl-intermediate with the zinc ion. At any rate, the rates of both steps of acylation and deacylation for the L-esters are larger than those for the D-esters in the CTAB micelle. However, in the Triton X-100 micelle, the deacylation step for the D-esters become faster than for the L-esters. 

You know die charge of die complex and those of the ligands. To find the formulas of the coordination compounds, apply the principle of electrical neutrality. 

In principle, any molecule or anion with an unshared pair of electrons can act as a Lewis base. In other words, it can donate a lone pair to a metal cation to form a coordinate covalent bond. In practice, a ligand usually contains an atom of one of die more electronegative elements (C, N, O, S, F, Cl, Br, I). Several hundred different ligands are known. Those most commonly encountered in general chemistry are NH3 and HzO molecules and CN , Cl-, and OH- ions. 

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