Complex ions properties

Actinide ions form complex ions with a large number of organic substances (12). Their extractabiUty by these substances varies from element to element and depends markedly on oxidation state. A number of important separation procedures are based on this property. Solvents that behave in this way are thbutyl phosphate, diethyl ether [60-29-7J, ketones such as diisopropyl ketone [565-80-5] or methyl isobutyl ketone [108-10-17, and several glycol ether type solvents such as diethyl CeUosolve [629-14-1] (ethylene glycol diethyl ether) or dibutyl Carbitol [112-73-2] (diethylene glycol dibutyl ether). 

The stability of tin over the middle pH range (approximately 3-5-9), its solubility in acids or alkalis (modified by the high hydrogen overpotential), and the formation of complex ions are the basis of its general corrosion behaviour. Other properties which have influenced the selection of tin for particular purposes are the non-toxicity of tin salts and the absence of catalytic promotion of oxidation processes that may cause changes in oils or other neutral media affecting their quality or producing corrosive acids. 

The physical and chemical properties of complex ions and of the coordination compounds they form depend on the spatial orientation of ligands around the central metal atom. Here we consider the geometries associated with the coordination numbers 2,4, and 6. With that background, we then examine the phenomenon of geometric isomerism, in which two or more complex ions have the same chemical formula but different properties because of their different geometries. 

Two or more species with different physical and chemical properties but the same formula are said to be isomers of one another. Complex ions can show many different kinds of isomerism, only one of which we will consider. Geometric isomers are ones that differ only in the spatial orientation of ligands around the central metal atom. Geometric isomerism is found in square planar and octahedral complexes. It cannot occur in tetrahedral complexes where all four positions are equivalent... 

Until about 20 years ago, the valence bond model discussed in Chapter 7 was widely used to explain electronic structure and bonding in complex ions. It assumed that lone pairs of electrons were contributed by ligands to form covalent bonds with metal atoms. This model had two major deficiencies. It could not easily explain the magnetic properties of complex ions. 

Organic Polymers, Natural and Synthetic 610 Appendix 1 Units, Constants, and Reference Data 635 Appendix 2 Properties of the Elements 641 Appendix 3 Exponents and Logarithms 643 Appendix 4 Nomenclature of Complex Ions 648 Appendix 5 Molecular Orbitals 650... 

An investigation of the physical-chemical properties and IR spectra of melts with relatively low metal concentrations indicated that heptafluorometalate ions, TaF72, are also present in the melt. These measurements initiated the second conceptual step and it was assumed that there are two types of complex ions, namely octafluorometalate, MeF83 , and heptafluorometalate, MeF72, that determine the melt s various properties. 

The third step consisted of the direct investigation of IR emission spectra for a wide range of concentrations. The investigation showed the tendency of the metals to reduce their coordination number when moving from solid to molten state. This property of the melt depends on the equilibrium between two types of complex ions, MeF72 and MeF6 ... 

Physicochemical properties of molten systems have an applied significance due to their wide use in both technological process planning and in production equipment design. Analysis of various melt properties versus different parameters of the melt enables to infer the interaction mechanism between the initial components, and in some cases, even to estimate the possible composition of the main complex ions formed in the melt [312]. From this point of view, the analysis of isotherms of physicochemical properties versus melt composition and of the magnitude of their deviation from ideal conditions is of most interest. 

Electro-conductivity of molten salts is a kinetic property that depends on the nature of the mobile ions and ionic interactions. The interaction that leads to the formation of complex ions has a varying influence on the electroconductivity of the melts, depending on the nature of the initial components. When the initial components are purely ionic, forming of complexes leads to a decrease in conductivity, whereas associated initial compounds result in an increase in conductivity compared to the behavior of an ideal system. Since electro-conductivity is never an additive property, the calculation of the conductivity for an ideal system is performed using the well-known equation proposed by Markov and Shumina (Markov s Equation) [315]. 

The results were presented in the form of isotherms, in which the properties are plotted versus the concentration. Nevertheless analysis of the isotherms was made based on available melting diagrams approach that the melts consist of TaFg3 and TaF7Cl3 complex ions. However, according to this general conception [312-314], the isotherm of the surface tension must, in such a case, have either a minimum or at least display prominence of the dependence in the direction of the concentration axis. 

Analysis of the physicochemical properties of fluoride and oxyfluoride melts reveals that the complex ions are characterized by coordination numbers that do not exceed seven. Fluoride melts consist of the complex ions MeF72 and MeFe. Molten chloride-fluoride systems initiate the formation of heteroligand complexes of the form MeFgCl2 . Oxyfluoride and oxyfluoride-chloride melts can contain oxyfluoride complexes MeOF63 at relatively low concentrations. The behavior of the more concentrated melts can be attributed to the formation of oxyfluorometalate polyanions. 

Examples of deductions regarding atomic arrangement, bond angles and other properties of molecules and complex ions from magnetic data, with the aid of calculations involving bond eigenfunctions, are given. 

Amphoteric metals (such as Al, Zn, Pb, and Hg) have properties that may be intermediate between those of metals and those of nonmetals. They will react with a base to form a complex ion with oxygen. This is a rare problem. 

Condensed-phase flame retardant mechanisms, 44 484—485 Condensed phosphates, 18 841-852 colloidal properties of, 48 851 complex ion formation in,... 

Properties of hydrogen Properties of metals Band theory Properties of nonmetals Properties of transition metals Coordination compounds Crystal-held theory Complex ions... 

Our goal in this chapter is to familiarize you with some properties of the elements, as well as the periodic trends that you can observe in these properties. You might want to review briefly the periodic trends we discussed in Chapter 8. We will also discuss coordination compounds and complex ions. Again— Practice, Practice, Practice. 

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