Sequence, Stoichiometry, and Dimensionality Control in Porphyrin/bis-Calix[4]arene Self-Assemblies in Aqueous Solution (Articolo in rivista)

Type
Label
  • Sequence, Stoichiometry, and Dimensionality Control in Porphyrin/bis-Calix[4]arene Self-Assemblies in Aqueous Solution (Articolo in rivista) (literal)
Anno
  • 2010-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/chem.201000803 (literal)
Alternative label
  • Alessandro D'’Urso; Domenico Andrea Cristaldi; Maria Elena Fragalà; Giuseppe Gattuso; Andrea Pappalardo; Valentina Villari; Norberto Micali; Sebastiano Pappalardo; Melchiorre F. Parisi; Roberto Purrello (2010)
    Sequence, Stoichiometry, and Dimensionality Control in Porphyrin/bis-Calix[4]arene Self-Assemblies in Aqueous Solution
    in Chemistry (Weinh., Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Alessandro D'’Urso; Domenico Andrea Cristaldi; Maria Elena Fragalà; Giuseppe Gattuso; Andrea Pappalardo; Valentina Villari; Norberto Micali; Sebastiano Pappalardo; Melchiorre F. Parisi; Roberto Purrello (literal)
Pagina inizio
  • 10439 (literal)
Pagina fine
  • 10446 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 16 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 34 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Dipartimento di Scienze Chimiche, Universit?à di Catania Viale A. Doria 6, 95125 Catania (Italy) Dipartimento di Chimica Organica e Biologica, Universit?à di Messina Viale F. Stagno d?Alcontres 31, 98166 Messina (Italy) Istituto per i Processi Chimico-Fisici, CNR Viale F. Stagno d?Alcontres 37, 98158 Messina (Italy) (literal)
Titolo
  • Sequence, Stoichiometry, and Dimensionality Control in Porphyrin/bis-Calix[4]arene Self-Assemblies in Aqueous Solution (literal)
Abstract
  • The use of a water-soluble octacationic bis-calix[4]arene with divergent cavities (BC4) as a templating agent for the assembly of a tetraanionic porphyrin (CuTPPS) has allowed the noncovalent synthesis of 2D or 3D multiporphyrin assemblies. Self-assembly of CuTPPS and BC4 molecules proceeded under hierarchical control in a stepwise fashion to yield discrete and isolable supramolecular nanostructures containing up to 33 molecular elements (i.e., the CuTPPS/BC4 17:16 assembly, obtained in less than three hours). The formation of these species could be conveniently monitored by means of UV/Vis spectroscopy by following the absorbance of the Soret band at 412 nm. In particular, the attainment of the pivotal CuTPPS/BC4 5:4 species with a cruciform structure, as the key fork-point intermediate for the subsequent formation of the higher 2D and 3D assemblies, has been demonstrated by light-scattering studies and by an unequivocal synthesis of mixed-porphyrin/calixarene 5:4 species involving the use of two different types of metallated porphyrins, namely CuTPPS and MnTPPS. The remarkable stability of these assemblies permits a stepwise synthesis that makes it possible to choose the desired porphyrin sequence. (literal)
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