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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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Ruthenium (II) Complexes with 6,7-Diaza[5]phenacene.
Beránek, Tomáš ; Žádný, Jaroslav ; Jakubík, Pavel ; Církva, Vladimír ; Storch, Jan
In this work we focused on preparation of novel bidentate and fully aromatic N,N-ligand and its ruthenium complexes. 6,7-Diaza[5]phenacene (1) was synthetized from 4-bromoisoquinoline by microwave-assisted tandem Hyama-Heck cross coupling reaction3 followed by photocyclization (Scheme 1). With 6,7-diaza[5]phenacene (1) in our hand, we prepared some new ruthenium(II) complexes (e.g. 2) , characterized them from structural point of view and determined some of their electronic and optical properties with regard to their application potential.
Plný tet: SKMBT_22316112114160 -  PDF
Plný text: content.csg - PDF
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Synthesis of [n]Phenacenes
Jakubík, Pavel ; Církva, Vladimír ; Storch, Jan
The goal of this work was to develop a multigram scale photochemical syntesis of [n]phenacenes and their derivatives from stilbene-type precursors. Vast effort was made to examine [n]phenacenes-based organic P-type semicondutors in the past. This work is also focused on an introduction of electron-acceptor substituents (fluorine, nitrogen) into or onto phenacene skeleton. The proper choice of substitutions can lead to change in semiconductivity of [n]phenacenes so their properties could be easily modulated.
Plný tet: SKMBT_C22015011213301 - PDF
Plný text: content.csg - PDF
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