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In supramolecular chemistry, [1] host–guest chemistry describes complexes that are composed of two or more molecules or ions that are held together in unique structural relationships by forces other than those of full covalent bonds. Host–guest chemistry encompasses the idea of molecular recognition and interactions through non-covalent ...
In organic chemistry, neighbouring group participation (NGP, also known as anchimeric assistance) has been defined by the International Union of Pure and Applied Chemistry (IUPAC) as the interaction of a reaction centre with a lone pair of electrons in an atom or the electrons present in a sigma or pi bond contained within the parent molecule but not conjugated with the reaction centre.
How do the spin–orbit coupling, other relativistic corrections, and inter-electron effects modify the chemistry of the trans-actinides? [1] [2] Is it possible to create a practically-useful lithium–air battery? [3]
In physical chemistry, supersaturation occurs with a solution when the concentration of a solute exceeds the concentration specified by the value of solubility at equilibrium. Most commonly the term is applied to a solution of a solid in a liquid , but it can also be applied to liquids and gases dissolved in a liquid.
Crystal structure of a nitrobenzene bound within a hemicarcerand reported by Cram and coworkers in Chem. Commun., 1997, 1303-1304.. In host–guest chemistry, a carcerand (from Latin carcer 'prison') is a host molecule that completely entraps its guest (which can be an ion, atom or other chemical species) so that it will not escape even at high temperatures. [1]
The enthalpy of solution is the solution enthalpy minus the enthalpy of the separate systems, whereas the entropy of solution is the corresponding difference in entropy. The solvation energy (change in Gibbs free energy) is the change in enthalpy minus the product of temperature (in Kelvin) times the change in entropy. Gases have a negative ...
The inert-pair effect is the tendency of the two electrons in the outermost atomic s-orbital to remain unshared in compounds of post-transition metals. The term inert-pair effect is often used in relation to the increasing stability of oxidation states that are two less than the group valency for the heavier elements of groups 13 , 14 , 15 and 16 .
In organic chemistry, steric effects are nearly universal and affect the rates and activation energies of most chemical reactions to varying degrees. In biochemistry, steric effects are often exploited in naturally occurring molecules such as enzymes , where the catalytic site may be buried within a large protein structure.