http://www.cnr.it/ontology/cnr/individuo/prodotto/ID176866
Role of counteranions in acid-induced aggregation of isomeric tetrapyridylporphyrins in organic solvents (Articolo in rivista)
- Type
- Label
- Role of counteranions in acid-induced aggregation of isomeric tetrapyridylporphyrins in organic solvents (Articolo in rivista) (literal)
- Anno
- 2005-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/jp0448797 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Giovanna De Luca; Andrea Romeo; Luigi Monsù Scolaro (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://pubs.acs.org/doi/abs/10.1021/jp0448797 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Univ Messina, Dipartimento Chim Inorgan Chim Analit & Chim Fis, I-98166 Messina, Italy (literal)
- Titolo
- Role of counteranions in acid-induced aggregation of isomeric tetrapyridylporphyrins in organic solvents (literal)
- Abstract
- The effect of adding various kinds of acids HX (X = Cl, Br, I, CF3COO, CF3SO3, TFPB ((3,5-(CF3)2C6H3)4B) to isomeric tetra(2-pyridyl)porphyrin, tetra(3-pyridyl)porphyrin, and tetra(4-pyridyl)porphyrin (TpyP(2), TpyP(3), and TpyP(4)) in dichloromethane solution has been investigated through the combined use of UV/vis absorption, fluorescence emission, and resonance light scattering (RLS) techniques. The experimental evidence points to a marked dependence of the protonation and aggregation behavior on the nature of both acids and porphyrins. In general, three different trends can be recognized: (i) formation of a fully protonated species, followed by aggregation; (ii) formation of a tetraprotonated species, which aggregates and, on further addition of acid, disaggregates; and (iii) protonation of the four pyridyl moieties, leading to a tetraprotonated ion pair, in the unique case of the bulky TFPB- anion. In all cases, the protonated species and the resulting aggregates exhibit spectroscopic features that are markedly influenced by the nature of the counteranions. A model for J-aggregation has been proposed on the basis of an interplay of hydrogen bonding, electrostatic interactions, and dispersive interactions. Kinetic control of the aggregation process allows for a fine-tuning of the spectroscopic properties of the final aggregated species. (literal)
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