Národní úložiště šedé literatury Nalezeno 2 záznamů.  Hledání trvalo 0.01 vteřin. 
Stereoelectrochemistry of Calixarenes
Liška, Alan ; Ludvík, Jiří ; Vojtíšek, P.
The relationship between the stereochemical properties (shape or molecular geometry in\ngeneral sense) and electrochemical ones (typically number of separate redox proceses, their\nnature and potentials) is very fundamental, however, not easily answerable. The nitro\nsubstituted calix[4]arenes appeared to be suitable series of compounds enabling correlation of\nelectrochemical data (redox potential, current, reversibility) with actual shape, conformation\nand dynamic behavior of the molecules dissolved in solution due to their well defined\ngeometry and clear polarographic and voltammetric response. Electrochemical methods can\nbe therefore used as a straightforward alternative to e.g. temperature dependent NMR\nspectroscopy. The present contribution is focused on thiacalix[4]arenes, their similarities and\ndistinctions from their methylene bridged analogues.\n
Redox Properties of Quasi Dimer of 1,3-diphenylisobenzofuran for Singlet Fission
Šimková, Ludmila ; Ludvík, Jiří
Molecules on the base of 1,3-diphenylisobenzofuran attract an interest because of their\npossible efficiency for singlet fission This study is focused on electrochemical behaviour of\nthe „quasi dimer“ of 1,3-diphenylisobenzofuran. For characterization of reduction mechanism\nin situ UV-vis and EPR spectroscopy were used. The monomer 1,3-diphenylisobenzofuran\nand its CH2 dimer were added to this study for comparison. The redox properties of both\ncompared molecules are similar. The location and the nature of the covalent bridging unit in\nCH2dimer have small effect onthe redox potentials. But the pi-conjugation in the molecule of\nquasi dimer causes approximately 0.2 V easier oxidization and reduction.

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