Academic Journal

Synthetic, structural, and spectroscopic studies of bis(porphyrinzinc) complexes linked by two-atom conjugating bridges

التفاصيل البيبلوغرافية
العنوان: Synthetic, structural, and spectroscopic studies of bis(porphyrinzinc) complexes linked by two-atom conjugating bridges
المؤلفون: Harper, Shannon R., Pfrunder, Michael C., Esdaile, Louisa J., Jensen, Paul, McMurtrie, John C., Arnold, Dennis P.
بيانات النشر: Wiley - VCH
سنة النشر: 2015
المجموعة: The University of Queensland: UQ eSpace
مصطلحات موضوعية: Peripherally-Metalated Porphyrins, Density-Functional Theory, Crystal-Structure, 2-Photon Absorption, Electrochemical Properties, Heck Reaction, Dimers, Diporphyrins, State, Coordination
الوصف: Four Zn-II 5,10,15-triphenylporphyrin (TriPP) complexes meso-meso linked by two-atom bridges, namely, C2H2 (2), C-2 (3), CH= N (4), and N-2 (5), were prepared, for comparison of ground-state inter-porphyrin conjugation. The X-ray crystal structure of azoporphyrin 5 center dot py(2) (py = pyridine) was determined: it exhibits a stepped-offset shape and a porphyrin- azo torsion angle of 34.8 degrees. Some new monoporphyrin starting materials were prepared, and ZnTriPPNH(2) (27), ZnTriPPCHO (23), NiTriPPCHO (7), and ZnTriPPCH(2)CH(2)Ph (18), as well as the byproduct butadiyne-linked dimer 26 were characterized by single-crystal X-ray crystallography. The conjugation in the dimers was assessed by electronic absorption and steady-state fluorescence spectroscopy. All show variously split B bands: azoporphyrin 5 clearly has the strongest ground-state inter-porphyrin interactions. Imine 4 and azo 5 show strongly quenched fluorescence emission, which indicates the presence of efficient relaxation pathways afforded by the N-containing linkers.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 1434-193X
1099-0690
Relation: orcid:0000-0002-2270-7141
الاتاحة: https://espace.library.uq.edu.au/view/UQ:80486db
رقم الانضمام: edsbas.A870287C
قاعدة البيانات: BASE