Controlling the aggregation of 5,10,15,20-tetrakis-(4-sulfonatophenyl)- porphyrin by the use of polycations derived from polyketones bearing charged aromatic groups

Claudio Toncelli, Juan Pablo Pino-Pinto, Naoki Sano, Francesco Picchioni, Antonius A. Broekhuis, Hiroyuki Nishide, Ignacio Moreno-Villoslada

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

The interaction between 5,10,15,20-tetrakis-(4-sulfonatophenyl)-porphyrin and different polycations is studied by UVevis spectroscopy. Two polycations containing charged aromatic residues (imidazolium and pyridinium) have been easily synthesized by PaaleKnorr reaction of alternating aliphatic polyketones with histamine and 4-picolylamine. It was found that these polymers stabilize the tetra-anionic form of the porphyrin at acidic conditions, and avoid the formation of H- and J-type self-aggregates. Other polycations such as poly(allylamine) and poly(decylviologen) enhance porphyrin selfaggregation. As the latter polymer has also aromatic charged groups, the influence of the polymer structure as a whole in the behavior of the porphyrin/polycation system is highlighted. In this context, similar but not equal results have been found comparing the influence of the polyketone derivative containing pyridinium groups and the polycation poly(4-vinylpyridine) on the porphyrin selfaggregation and acidebase behavior.

Original languageEnglish
Pages (from-to)51-63
Number of pages13
JournalDyes and Pigments
Volume98
Issue number1
DOIs
Publication statusPublished - 2013 Jul

Keywords

  • Aromatic polycations
  • Aromatic-aromatic interactions
  • Polyelectrolyteedye interactions
  • Polyketone derivatives
  • Porphyrin aggregation
  • TPPS

ASJC Scopus subject areas

  • Chemical Engineering(all)
  • Process Chemistry and Technology

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