National Repository of Grey Literature 4 records found  Search took 0.01 seconds. 
EPR-Electrochemical Study of Reduction Mechanism of Pyrene-Cyclobutene Conjugates
Koláčná, Lucie ; Polák, P. ; Klíma, Jiří ; Tobrman, T. ; Ludvík, Jiří
Reduction mechanism of pyrene-cyclobutene conjugates were studied electrochemically and\nspectro-electrochemically. Analysis and interpretation of spectro-electrochemical data of\nconjugates revealed intramolecular communication of electrons and enabled determination of\nredox mechanism of conjugates. This knowledge is fundamental for tuning the required redox\nproperties of molecules just by chemical modification. Studied molecules represent promising\nmaterial for organic semiconductor materials.
Electrochemistry of Phospholes
Koláčná, Lucie ; Liška, Alan ; Ludvík, Jiří
Seventeen pentasubstituted phospholes with expected application in organic electronics were\nsynthesized and characterized electrochemically and by UV-vis spectra. Quantum chemical\ncalculations ofredox potentials and HOMO-LUMO energies were performed and experimental\nand theoretical data were successfully correlated. Tuning of redox properties can be achieved\nby combination of induction and resonance effects of substituents, extension / diminution of\nthe pi- delocalized system and by steric changes which affect intramolecular electron\ncommunication.
Electrochemical Study of Selected Pyrene Derivatives as Precursors to Organic Semiconductors
Koláčná, Lucie ; Tobrman, T. ; Ludvík, Jiří
A series of 9 precursors for pyrene based biodegradable organic (semi)conductors having tetrasubstituted double bond as a central organic core and photo- or redox active centers attached at this core were electrochemically investigated in order to determine the influence of individual parts of the molecule on the redox properties, to describe the location of the reduction center and to understand the structure - redox activity relationship of the mentioned compounds.
Redox Properties of Fluorinated Derivativers of 1,3-Diphenylisobenzofuran-Chromophores for Singlet Fission
Šimková, Ludmila ; Ludvík, Jiří
Derivatives of 1,3-diphenylisobenzofuran attract interest because they should be efficient as the molecules for singlet fission. The understanding of singlet fission in isolated molecules might be advantageous for use as solar cell sensitizers. This study is focused on fluorinated derivatives of 1,3-diphenylisobenzofuran and the effect of the position of fluorine atoms on their redox properties. For characterization of the redox properties standard electrochemical methods, and in situ UV-vis and EPR spectroscopy techniques were used.

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