Recognition, kinetic

Table 8 Kinetic recognition of the size of end groups of bola-amphiphiles by a-CD kt[ ss, first order dissociation rate constant AGjiss, Eyring s free activation energy of dissociation...

Kinetic Recognition of Bulky Groups within Poly(bola-amphiphile)s... 

Porschke, D., Eigen, M. Cooperative nonenzymic base recognition. HI. Kinetics of the helix-coil transition of the oligoribouridylic oligoriboadenylic acid system and of oligoriboadenylic acid alone at acidic pH. J. Mol. Biol. 62 (1971) 361-381... 

Knowledge of the rate is important to design chemical reactors for industrial production. It is also important for optimizing the production and to define the safety limits of operation. As was mentioned in the introduction, various transfer processes can influence chemical rates. The recognition of such interference is of primary importance during any study of kinetics, especially in those studies that will serve as the basis of design for production reactors. 

The evidence supporting the duality of mechanisms is of several kinds. The kinetic behavior is an obvious feature. This is somewhat more complex than is implied by the preceding treatment. A quantitative description of the SnI mechanism requires recognition of the reversibility of the ionization step, thus... 

The purpose of the present review is to indicate the methods that have been used to obtain quantitative equilibrium and kinetic data for this water-addition reaction and to discuss the results that have so far been reported. It is hoped that by describing some of the characteristics of this reaction recognition of further examples may be facilitated. 

Chiral Recognition. The use of chiral hosts to form diastereomeric inclusion compounds was mentioned above. But in some cases it is possible for a host to form an inclusion compound with one enantiomer of a racemic guest, but not the other. This is caUed chiral recognition. One enantiomer fits into the chiral host cavity, the other does not. More often, both diastereomers are formed, but one forms more rapidly than the other, so that if the guest is removed it is already partially resolved (this is a form of kinetic resolution, see category 6). An example is use of the chiral crown ether (53) partially to resolve the racemic amine salt (54). " When an aqueous solution of 54 was... 

Bertrand T, Jolivalt C, Briozzo P, Caminade E, Joly N, Madzak C, Mougin C. 2002. Crystal structure of a four-copper laccase complexed with an arylamine Insights into substrate recognition and correlation with kinetics. Biochemistry 41 7325-7333. 

Goshe, A.J., Steele, I.M., Ceccarelli, C., Rheingold, A.L. and Bosnich, B. (2002) Supramolecular chemistry and self-assembly special feature supramolecular recognition on the kinetic lability of thermodynamically stable host-guest association complexes. Proceedings of the... 

Recognition that the kinetics of this reaction could be explained on the basis of the chain reaction mechanism presented above was one... 

Before we describe the chemistry of the compartments involved, note that like prokaryotes, a number of oxidative enzymes are found in the cytoplasm but they do not release damaging chemicals (see Section 6.10). We also observed that such kinds of kinetic compartments are not enclosed by physical limitations such as membranes. We have also mentioned that increased size itself makes for kinetic compartments if diffusion is restricted. In this section, we see many additional advantages of eukaryotes from those given in Section 7.4. How deceptive it can be to use just the DNA, the all-embracing proteome, metabolome or metallome in discussing evolution without the recognition of the thermodynamic importance of compartments and their concentrations These data could be useful both here and in simpler studies of single-compartment bacteria even in the analysis of species but not much information is available. 

To understand fully processes such as molecular recognition, reactivity and bioactivity, it is therefore imperative to obtain a detailed insight into the thermodynamic and kinetic properties of the metal-based anticancer agent at hand. 

The selective binding of molecules to form productive complexes is of central importance to pharmacology and medicinal chemistry. Although kinetic factors can influence the yields of different molecular complexes in cellular and other non-equilibrium environments,1 the primary factors that one must consider in the analysis of molecular recognition are thermodynamic. In particular, the equilibrium constant for the binding of molecules A and B to form the complex AB depends exponentially on the standard free energy change associated with complexation. 

Zinc interacts with numerous chemicals, sometimes producing greatly different patterns of accumulation, metabolism, and toxicity when compared to zinc alone. Recognition of these interactions is essential to the understanding of zinc kinetics in the environment. 

---