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Complexation Properties of Aza[n]phenacene Ligands.
Váňa, Lubomír ; Žádný, Jaroslav ; Storch, Jan ; Církva, Vladimír
This work is aimed at the synthesis of new aza[n]phenacenes 2 (n = 4 or 5, Ar = phenyl or 2-pyridyl), where [njphenacenes 1 with ö-lactam ring are used as starting material. The resulting compounds are subsequenttly investigated in terms of their complexation properties with transition metals (Cu, Ni, Co, Pt, Ir) due to their potential application as photoluminescent complexes.
Plný tet: 00206B6C274C191114122808 -  DOC
Plný text: content.csg - DOC
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Transition Metal Complexes with Aza[n]phenacene Ligands.
Váňa, Lubomír
This work is aimed at the synthesis of new aza[n]phenacenes 2(n = 4 or 5, Ar = phenyl or 2-pyridyl), where [n]phenacenes 1 with δ-lactam ring are used as starting material (Scheme 1). The resulting compounds are subsequently investigated in terms of their complexation properties with transition metals (Cu, Ni, Co, Pt, Ir) (e. g.Figure 1) due to their potential application as photoluminescent complexes.
Plný tet: SKMBT_C22019053108331 -  PDF
Plný text: content.csg - PDF
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Synthesis and Functionalization of Phenacenes Containing δ-Lactam Ring.
Váňa, Lubomír ; Církva, Vladimír ; Pfleger, Jiří ; Storch, Jan
This work is aimed at the development of a new efficient methodology towards the synthesis of various aza[5]phenacenes containing δ-lactam ring in their structure. Possibilities of their functionalization or derivatization are also discussed, along with complexation properties of suitable aza-derivatives as ligands in transition-metal complexes. The resulting compounds are investigated in terms of their material properties, especially for the formation of thin film structures capable of an efficient semi-conductivity or their potential application as photoluminescent complexes in OLEDs.
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Photochemical Synthesis of Aza-aromatic Compounds.
Kos, Martin ; Žádný, Jaroslav ; Storch, Jan ; Sýkora, Jan ; Církva, Vladimír
Herein we report synthesis of series of novel both aza- and diaza-helicenes, and phenacenes, which were prepared mainly by photocyclization of corresponding imine precursors. Reaction conditions of photocyclization (i.e. solvent, photocatalyst, type of irradiation, use of water scavenger) were optimized and enhanced. Usage of TEMPO as oxidizing agent leads to improvement of yields up to 72 %. Prepared 2-pyridyl substituted azaphenacenes will be utilized for preparation of potential semiconductive layers in cooperation with IMC of the CAS.
Plný tet: SKMBT_C22017111612580 - PDF
Plný text: content.csg - PDF
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Potential-driven On/Off Switch Strategy for the Electrosynthesis of [7]Helicene-derived Polymers.
Žádný, Jaroslav ; Storch, Jan ; Strašák, Tomáš ; Církva, Vladimír ; Hrbáč, J. ; Fekete, Ladislav ; Pokorný, Jan ; Bulíř, Jiří ; Vacek, J.
3-([7]H elicen-9-yl)-thiophene hybrid monomer was electrooxidized in acetonitrile by cyclic voltammetry with anodic potential limits of +1.5 V or +2.5 V, resulting in a conductive and non-conductive polymer, respectively. The electrochemical findings were supplemented by microscopy investigations; UV-Vis, fluorescence and vibrational spectroscopies, ellipsometry measurements and computational chemistry. The electrodeposited polymers could be used for the further development of materials applicable in organic electronics and sensing technologies.
Plný tet: SKMBT_C22017111612582 - PDF
Plný text: content.csg - PDF
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Preparation of Partially Fluorinated Polyaromatics by Photocyclization of Stilbenes.
Jakubík, Pavel ; Storch, Jan ; Žádný, Jaroslav ; Pfleger, Jiří ; Církva, Vladimír
Synthetic strategies to partially fluorinated polyaromatics by photocyclization were examined, leading to both 1,2,3,4-tetrafluoro[6]helicene (1) and 1,2,3,4,13,14,15,16-octafluoro[6]helicene (2), and to 1,2,3,4-tetrafluoro[5]phenacene (3) and 1,2,3,4-tetrafluoro[6]phenacene (4). Thin films of the prepared compounds were characterized for their electrical properties and incorporated into OFET structures.
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