Chemicals binding properties

Montmorillonite is a laminar and expandable clay with wet binding properties and widely available throughout the world. The layers have permanent negative charges due to isomorphic substitutions. The scientific interest of montmorillonite lies in its physical and chemical properties as well as its low price. Consequently, the industrial application of montmorillonite is an attractive process [1]. On the other hand, among numerous reports published so far, crystallization of zeolite Beta draws much attention because of its unique characteristics, in particular, acidity and acid catalysis. It is reasonable to conceive that a catalyst system based on Beta/montmorillonite composite with suitable composition should provide a good catalytic capacity. 

The rates of hydrolysis and binding to DNA of anti-DE-I, syn-DE-I, anti-DE-II, syn-DE-II, and anti-1,2-dihydroxy-3,4-epoxy-1,2,3,4-tetrahydrochrysene (anti-chrysene-DE) were studied in order to relate the chemical reactivity of these dihydrodiol epoxides to their biological activities. The half-lives of the dihydrodiol epoxides in cacodylate buffer at pH 7.0 and 37°C are summarized in Table III and their relative extents of binding to DNA in Table IV. It is clear that the rates of hydrolysis of the dihydrodiol epoxides do not correlate with their DNA binding properties. 

Disregarding such chemical-specific properties as dissociation constants (in the case of ionic compounds), particle size, and polymorphism, as well as side effects of viscosity, binding to vehicle components, complex formulation, and the like, the following formulation principles arise ... 

Using a simple amphoteric model for the mineral surface, we have demonstrated the role specific chemical binding reactions of potential determining Ions In determining the electrical properties and thermodynamics of the oxide/solution interfaces. A by-product of our study Is that under appropriate conditions, an amphoteric surface can show marked deviations from ideal Nernstlan behaviour. The graphical method also serves to Illustrate the... 

What was the distinction between quantum chemistry and chemical physics After the Journal of Chemical Physics was established, it was easy to say that chemical physics was anything found in the new journal. This included molecular spectroscopy and molecular structures, the quantum mechanical treatment of electronic structure of molecules and crystals and the problem of chemical binding, the kinetics of chemical reactions from the standpoint of basic physical principles, the thermodynamic properties of substances and calculation by statistical mechanical methods, the structure of crystals, and surface phenomena. 

Abstract Recently, the interest on biomaterials and especially in tannins was growing and some attractive results were obtained in the adsorption of some metals by tannin adsorbents. Tannins are widely distributed in nature and have multiple adjacent polyhydroxyphenyl groups in their chemical structure which have extremely high afiSnity for heavy metal ions. This study will describe how tannin can be used as an effective zinc and lead sorbent by the use of tannin resins. Batch method was used in the experiments in which pH profde, adsorption time, adsorbent/liquid ratios, initial concentration of metal ions, adsorbent amount and temperature were investigated to determine binding properties of adsorbent for the Zn(II) and Pb(ll) ions. 

The cause of the cell cycle specificity of the bisindole alkaloids may be associated with the ability of these compounds to interact with the protein tubulin and thereby inhibit the polymerization (and depolymerization) of microtubules (16,17). In this respect the cellular pharmacology of vinca alkaloids is similar to that of other cytotoxic natural products such as colchicine or podophyllotoxin. On closer inspection, however, Wilson determined that the specific binding site on tubulin occupied by vinblastine or vincristine is chemically distinct from the site occupied by the other natural products (18). Subsequent experiments have determined that the maytansinoids, a class of ansa-macrocycles structurally distinct from the bisindoles, may bind to tubulin at an adjacent (or overlapping) site (19). A partial correlation of the antimitotic activity of these compounds with their tubulin binding properties has been made, but discrepancies in cellular uptake probably preclude any quantitative relationship of these effects (20). 

The values AE, and AH, are considered at some temperature, usually 25°C, specifically, under working conditions of practical interest. These quantities include contributions from internal rotations that are more or less free in some cases and hindered in others, but need not be considered at 0 K. Zero-point vibrational energies ate to be taken into proper account, as these energies, like the thermal ones, cannot be fairly apportioned among bonds or atoms in a molecule since they are not truly additive properties, nor can they be regarded as a part of chemical binding. These reasons prompt us to smdy a molecule in its hypothetical vibrationless state at OK, whose atomization energy is AEl. 

Amoxapine has been found to be effective in several double-blind studies (Table 7-4 and Table 7-6). It is a dibenzoxazepine derivative that has both NE and serotonin uptake inhibiting properties. Amoxapine is converted into 8-hydroxyamoxapine, which has considerable dopamine receptor binding properties (i.e., radioreceptor bioassays on patients given amoxapine have found activity levels similar to those of patients on typical antipsychotics), a chemical structure similar to loxapine, and effects similar to antipsychotics (1Q3). As a result of this metabolite, amoxapine theoretically may have unique beneficial effects in psychotically depressed patients. However, this possibility has never been adequately tested. Nevertheless, this metabolite is likely responsible for some of the antidopamine effects reported in patients taking amoxapine, including acute and chronic extrapyramidal side effects and elevated prolactin levels ( 104). Like TCAs, amoxapine can be lethal in... 

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