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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 ...
The resulting enone 3 is a charge transfer complex molecule. A knoevenagel condensation. The Knoevenagel condensation is a key step in the commercial production of the antimalarial drug lumefantrine (a component of Coartem): [8] Final step in Lumefantrine synthesis
Many materials may be characterized as organic superconductors. These include the Bechgaard salts and Fabre salts which are both quasi-one-dimensional, and quasi-two-dimensional materials such as k-BEDT-TTF 2 X charge-transfer complex, λ-BETS 2 X compounds, graphite intercalation compounds and three-dimensional materials such as the alkali ...
In the 1950s, researchers discovered that polycyclic aromatic compounds formed semi-conducting charge-transfer complex salts with halogens. In particular, high conductivity of 0.12 S/cm was reported in perylene–iodine complex in 1954. [3] This finding indicated that organic compounds could carry current.
An intermediate case between Frenkel and Wannier excitons is the charge-transfer (CT) exciton. In molecular physics, CT excitons form when the electron and the hole occupy adjacent molecules. [ 18 ] They occur primarily in organic and molecular crystals; [ 19 ] in this case, unlike Frenkel and Wannier excitons, CT excitons display a static ...
Fig. 1. The parabolas of outer-sphere reorganisation energy of the system two spheres in a solvent. Parabola i: the charge on the first, transfer to the second, parabola f: the charge on the second, transfer to the first. The abscissa is the transferred amount of charge Δe or the induced polarization P, the ordinate the Gibbs free energy.
This method was first developed by Benesi and Hildebrand in 1949, [2] as a means to explain a phenomenon where iodine changes color in various aromatic solvents. This was attributed to the formation of an iodine-solvent complex through acid-base interactions, leading to the observed shifts in the absorption spectrum.
Structure of the charge-transfer complex between pyrene with the electron-deficient 1,3,5-trinitrobenzene. [3] Alternatively, electron-deficiency describes molecules or ions that function as electron acceptors. Such electron-deficient species obey the octet rule, but they have (usually mild) oxidizing properties.
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