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Conformational Landscape of meso-(1,3-Dithian-2-yl)porphyrins

  • An investigation of the conformational landscape of 1,3-dithian-2-yl bearing porphyrins and the rotational behavior of the dithianyl substituents in meso position was carried out by variable-temperature (VT) NMR spectroscopy. Additionally, theoretical results for alternative conformations and energy barriers were obtained by molecular modeling. The study revealed different NH trans tautomers with regard to the orientation of the dithianyl ligands for the free base porphyrins 1-3. Relatively ruffled porphyrin core conformations were established for the transition states of the dithianyl rotation, resulting in a lower rotational energy barrier for the nickel(II) complex 4 compared to that of the free base systems. The data obtained and the first depiction of a rotational transition state for the rotation of bulky meso-alkyl substituents illustrate the close structural interplay between meso-alkyl substituents and the macrocycle conformation in porphyrins.

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Metadaten
Author:Philipp Wacker, Katja Dahms, Mathias O. Senge, Erich Kleinpeter
URL:http://pubs.acs.org/doi/full/10.1021/jo0708700
DOI:https://doi.org/10.1021/Jo0708700
Document Type:Article
Language:English
Year of first Publication:2007
Year of Completion:2007
Release Date:2017/03/25
Source:Journal of Organic Chemistry. - 72 (2007), 16, S. 6224 - 6231
Organizational units:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Chemie
Peer Review:Nicht referiert