Pregled bibliografske jedinice broj: 482862
Formation, photophysics, and photochemistry of cadmium(II) complexes with 5,10,15,20-tetrakis(4-sulphonatophenyl)porphyrin and its octabromo derivative: the effects of bromination and the axial hydroxo ligand
Formation, photophysics, and photochemistry of cadmium(II) complexes with 5,10,15,20-tetrakis(4-sulphonatophenyl)porphyrin and its octabromo derivative: the effects of bromination and the axial hydroxo ligand // Journal of photochemistry and photobiology. A, Chemistry, 218 (2011), 1; 143-155 doi:10.1016/j.jphotochem.2010.12.014 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 482862 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Formation, photophysics, and photochemistry of cadmium(II) complexes with 5,10,15,20-tetrakis(4-sulphonatophenyl)porphyrin and its octabromo derivative: the effects of bromination and the axial hydroxo ligand
Autori
Valicsek, Zsolt ; Horváth, Ottó ; Lendvay, György ; Kikaš, Ilijana ; Škorić, Irena
Izvornik
Journal of photochemistry and photobiology. A, Chemistry (1010-6030) 218
(2011), 1;
143-155
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
water-soluble porphyrin ; sitting-atop complex ; cadmium(II) ion ; photochemistry
Sažetak
In slightly alkaline solution (pH = 8) Cd(II) ion and 5, 10, 15, 20-tetrakis(4- sulphonatophenyl)porphyrin form a kinetically labile complex, in which the metal center is located out of the ligand plane, partly due to the effect of the axial hydroxo ligand. Both acidification and irradiation at the Soret-band can result in the dissociation of the axial ligand, forming a less distorted structure. Besides, irradiation of both types of metalloporphyrins promotes an irreversible ligand- to-metal charge transfer leading to the oxidative degradation of the coordinated porphyrin. Under same conditions, in the case of the octabromo derivative of this water-soluble porphyrin the distorted structure accelerates the formation of the corresponding complex with Cd(II), compared to its reaction with the parent, unbrominated ligand. The structure of this porphyrin strongly distorted by the bromo substituents significantly affects the characteristic features of the absorption (and emission) spectra, red-shifting the position of the main bands of this metalloporphyrin compared to those of the complex with the non-brominated ligand.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
MZOS-125-0982933-2926 - Heteropolicikli, strukturne osnove za bioaktivne spojeve. Sinteza i fotokemija (Škorić, Irena, MZOS ) ( CroRIS)
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Irena Škorić
(autor)
Poveznice na cjeloviti tekst rada:
Pristup cjelovitom tekstu rada doi www.sciencedirect.com dx.doi.orgCitiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
Uključenost u ostale bibliografske baze podataka::
- CA Search (Chemical Abstracts)