New Versatile Strategy towards Zinc(II)-, Copper(II)- and Cobalt(II)-Metallated Thiophene/Porphyrin-Hybrids

0348873 - ÚOCHB 2011 RIV DE eng J - Článek v odborném periodiku
Zöllner, M. J. - Becker, E. - Jahn, Ullrich - Kowalsky, W. - Johannes, H. H.
New Versatile Strategy towards Zinc(II)-, Copper(II)- and Cobalt(II)-Metallated Thiophene/Porphyrin-Hybrids.
European Journal of Organic Chemistry. -, č. 23 (2010), s. 4426-4435. ISSN 1434-193X. E-ISSN 1099-0690
Grant ostatní: DLR(DE) FKZ 01BI565
Výzkumný záměr: CEZ:AV0Z40550506
Klíčová slova: porphyrinoids * ligand design * hybrid monomers * UV/Vis spectroscopy * cyclic voltammetry
Kód oboru RIV: CC - Organická chemie
Impakt faktor: 3.206, rok: 2010

A series of linear and lateral functionalised porphyrin–thiophene hybrid molecules was synthesised. Directly linked metal-free conjugates were synthesised by a successive bromination/cross-coupling sequence and transformed subsequently into zinc, copper and cobalt porphyrins. In the lateral connection mode, diverse strategies were necessary to obtain zinc and cobalt porphyrins, whereas the synthesis of the copper derivative followed an established route. All compounds were investigated by cyclic voltammetry. Within the series, the cobalt derivatives were exceptional because the cobalt porphyrin oxidation proved to be in competition with the thiophene oxidation. These results lead to a better understanding of the redox behaviour because such hybrid molecules consist of two independent redox centres. Furthermore, in the linear case, the absorption spectra clearly indicated an electronic influence of the thiophene periphery on the porphyrin, although conjugation is hindered strongly.
Trvalý link: http://hdl.handle.net/11104/0189280