Anion relative complexation ability

Other experimental methods 319 5.6. Relative complexation ability of anions 342... 

The results discussed above unequivocally demonstrate that in moderately dissociating solvents, such as acetonitrile or propylene carbonate, most anions are involved in inner-sphere coordination to rare earth ions, in particular perchlorate and triflate. In this section, we examine the data pertaining to the relative complexing abilities of various anions. 

The relative initiator activities are not always simple functions of the reactivity of the free anion but probably involve contributions by complexing ability, ionization, or dissociation reactions [20-25],... 

Complex cyanides are compounds in which the cyanide anion is incorporated into a complex or complexes. These compounds are different in chemical and toxicologic properties from simple cyanides. In solution, the stability of the cyanide complex varies with the type of cation and the complex that it forms. Some of these are dissociable in weak acids to give free cyanide and a cation, while other complexes require much stronger acidic conditions for dissociation. The least-stable complex metallocyanides include Zn(CN)42 , Cd(CN)3 , and Cd(CN)42 moderately stable complexes include Cu(CN)2, Cu(CN)32, Ni(CN)42, and Ag(CN)2 and the most stable complexes include Fe(CN)64, and Co(CN)6. The toxicity of complex cyanides is usually related to their ability to release cyanide ions in solution, which then enter into an equilibrium with HCN relatively small fluctuations in pH significantly affect their biocidal properties. 

C5-derived peptide in serum. This molecule lacks anaphylatoxin activity (i.e. it cannot cause smooth muscle contraction), and its ability to cause che-motaxis in neutrophils is about 10-20 times lower than that of C5a. However, human serum also contains a heat-stable, anionic protein termed co-chemotaxin (relative molecular mass = 60 kDa), which acts in a concentration-dependent manner to permit C5a des Arg to act as a chemoattractant for neutrophils. Thus, C5a des Arg plus cochemotaxin working together probably account for most of the neutrophil chemoattractant activity in vivo following complement activation. The mechanism of action of cochemotaxin is unknown, but it may form a physical complex by attaching to a sialic acid residue on the oligosaccharide chain of C5a des Arg. Deglycosylation of C5a des Arg increases its chemoattractant activity more than 10-fold, and its dependency upon cochemotaxin is decreased. 

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