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Absorption spectrum of an aqueous solution of potassium permanganate, showing a vibronic fine structure in the LMCT band. The tetraoxides of d 0 metal centers are often deeply colored for the first row metals. This coloration is assigned to LMCT, involving transfer of nonbonding electrons on the oxo ligands to empty d-levels on the metal.
In chemistry, charge-transfer (CT) complex, or electron donor-acceptor complex, describes a type of supramolecular assembly of two or more molecules or ions. The assembly consists of two molecules that self-attract through electrostatic forces, i.e., one has at least partial negative charge and the partner has partial positive charge, referred ...
Protein folding problem: Is it possible to predict the secondary, tertiary and quaternary structure of a polypeptide sequence based solely on the sequence and environmental information? Inverse protein-folding problem: Is it possible to design a polypeptide sequence which will adopt a given structure under certain environmental conditions?
For example, the colour of chromate, dichromate and permanganate ions is due to LMCT transitions. Another example is that mercuric iodide , HgI 2 , is red because of a LMCT transition. A metal-to-ligand charge transfer (MLCT) transition will be most likely when the metal is in a low oxidation state and the ligand is easily reduced.
Absorption spectrum of an aqueous solution of potassium permanganate. As an example from inorganic chemistry the permanganate ion, MnO − 4, in aqueous solution has an intense purple colour due to an O → Mn ligand-to-metal charge transfer band (LMCT) in much of the visible region. [22]
For example, the d-d transitions for [Cr(NH 3) 5 Cl] 2+ are weak (ε < 100) even though the complex is only of C 4v symmetry. [5] The Laporte rule helps explain the intense colors often observed for the tetrahedral complexes. The tetrahedral point group lacks the inversion operation, so the Laporte rule does not apply. [6]
Origin of title phenomenon in crystallographic defects. Shown is a two-dimensional slice through a primitive cubic crystal system showing the regular square array of atoms on one face (open circles, o), and with these, places where atoms are missing from a regular site to create vacancies, displaced to an adjacent acceptable space to create a Frenkel pair, or substituted by a smaller or larger ...
Diffusion control is more likely in solution where diffusion of reactants is slower due to the greater number of collisions with solvent molecules. Reactions where the activated complex forms easily and the products form rapidly are most likely to be limited by diffusion control. Examples are those involving catalysis and enzymatic reactions.