Fluorescent cyclodextrin carriers for a water soluble ZnII pyrazinoporphyrazine octacation with photosensitizer potential (Articolo in rivista)

Type
Label
  • Fluorescent cyclodextrin carriers for a water soluble ZnII pyrazinoporphyrazine octacation with photosensitizer potential (Articolo in rivista) (literal)
Anno
  • 2014-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1039/c3ra47034b (literal)
Alternative label
  • Anand R.; Manoli F.; Manet I.; Donzello M.P.; Viola E.; Malanga M.; Jicsinszky L.; Fenyvesi E.; Monti S. (2014)
    Fluorescent cyclodextrin carriers for a water soluble ZnII pyrazinoporphyrazine octacation with photosensitizer potential
    in RSC advances
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Anand R.; Manoli F.; Manet I.; Donzello M.P.; Viola E.; Malanga M.; Jicsinszky L.; Fenyvesi E.; Monti S. (literal)
Pagina inizio
  • 26359 (literal)
Pagina fine
  • 26367 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://www.scopus.com/inward/record.url?eid=2-s2.0-84903287248&partnerID=q2rCbXpz (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 4 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 50 (literal)
Note
  • Scopu (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Istituto per la Sintesi Organica e la Fotoreattività, Consiglio Nazionale Delle Ricerche, via P. Gobetti 101, I-40129 Bologna, Italy; Dipartimento di Chimica, Università degli Studi di Roma la Sapienza, P.le A. Moro 5, I-00185 Roma, Italy; CycloLab, Cyclodextrin RandD Ltd., Illatos út 7, H-1097 Budapest, Hungary (literal)
Titolo
  • Fluorescent cyclodextrin carriers for a water soluble ZnII pyrazinoporphyrazine octacation with photosensitizer potential (literal)
Abstract
  • A nitro-benzofurazan-triazolyl carboxymethylated b-cyclodextrin (NBFT-CMbCyD) and an oligomer of carboxymethyl b-cyclodextrin (sodium salt), crosslinked with epichlorohydrin and labeled with rhodaminyl groups (pbCyD-Rh), exhibit very high affinity in aqueous solution for octacationic photosensitizer [(CH3)8LZn]8+ neutralized by I? ions (L ¼ tetrakis-2,3-[5,6-di(2-(pyridiniumyl)pyrazino] porphyrazinato dianion). The photosensitizer (PS) forms complexes with 1 : 2 and 2 : 2 CyD:PS stoichiometry, which were characterized as binding constants and UV-Vis absorption and fluorescence properties. The self-association tendency of [(CH3)8LZn]8+, leading to a monomer-dimer equilibrium shift towards the dimer even at very low concentrations (z10?6 M), is not contrasted by either NBFTCMbCyD or the pbCyD-Rh oligomer, both of which completely convert the [(CH3)8LZn]8+ monomer fraction to the dimer form in the bound state. Quenching of fluorescence observed in [(CH3)8LZn]8+ upon binding with either hosts is consistent with the conversion of the monomer to the negligibly fluorescent dimer. The complexes formed with the CMbCyD units of the pbCyD-Rh oligomer have average association constants, which are larger by 6-7 orders of magnitude than those with the CMbCyD monomer in the NBFT-labeled derivative. (literal)
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