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A unified picture of acid-base behavior in aprotic organic solvents is presented, based on an extensive survey of the literature and experimental results of the author and associates. Evidence given to support this picture includes data pertaining to colligative properties of acids, bases, and salts and also conductance, dielectric constants, distribution between immiscible solvents, and spectral absorption in the infrared, visible, and ultraviolet. The acids upon which attention is centered are proton-donor compounds that are measurably ionized in water, such as aliphatic and aromatic carboxylic acids, substituted phenols and mineral acids. The bases of principal interest are likewise compounds capable of forming ions in water, for example, aliphatic and aromatic amines and derivatives of guanidine or pyridine. The solvents emphasized are hydrocarbons and halohydrocarbons, but data for dipolar aprotic solvents (for example, acetone, acetonitrile, and nitrobenzene) are included. Contrasts in acid-base behavior and in acidity and basicity scales in aprotic and water-like solvents are discussed. The role of hydrogen bonding in aprotic solvents is discussed at length. Important types of hydrogen-bonded structures include chelate rings; self-associated acids, bases, and salts; hydrogen-bonded ion pairs; and homo- and heteroconjugate cations and anions. Examples are given in which hydrogen bonding of these types affects such properties as the absorption spectrum of a salt, the catalytic effect of an acid, and the accurate location of a titration endpoint. (Author).
An attempt is made to summarize a year's progress on the technical projects of the Section in such a way as to stress the program and capabilities of the organizational unit as a whole. A description of facilities and equipment is presented, and the directions of the programs are indicated. Brief summaries of several lines of work now under way are given. The main areas include the measurement of acidity, with progress toward the establishment of standards for pH, pH*, and pD being reported. Studies of the behavior of glass electrodes in deuterium oxide are described and solvent effects on ionic processes are discussed. Equilibrium data for certain ionic systems have been obtained, modifications of a precision conductance bridge are described, and a method for titrating hydrogen fluoride in dimethylformamide is outlined. The survey concludes with lists of the members of the Section staff, publications and manuscripts produced during the year, talks given by the staff, and committee assignments. (Author).
The main challenge in modern solvent extraction separation is that most techniques are mainly empirical, specific and particular for narrow fields of practice and require a large degree of experimentation. This concise and modern book provides a complete overview of both solvent extraction separation techniques and the novel and unified competitive complexation/solvation theory. This novel and unified technique presented in the book provides a key for a preliminary quantitative prediction of suitable extraction systems without experimentation, thus saving researchers time and resources. - Analyzes and compares both classical and new competitive models and techniques - Offers a novel and unified competitive complexation / solvation theory that permits researchers to standardize some parameters, which decreases the need for experimentation at R&D - Presents examples of applications in multiple disciplines such as chemical, biochemical, radiochemical, pharmaceutical and analytical separation - Written by an outstanding scientist who is prolific in the field of separation science