Synthesis and aggregation of cationic porphyrins

Autor: Chi K. Nguyen, Keiki-Pua S. Dancil, Amy M. Shachter, Kim U. Mai, Katherine S. Weddle, Richard G. Khoury, Lynn F. Hilario
Rok vydání: 1997
Předmět:
Zdroj: Journal of Heterocyclic Chemistry. 34:749-755
ISSN: 1943-5193
0022-152X
DOI: 10.1002/jhet.5570340308
Popis: Tetra(N-R-pyridinium-4-yl)porphyrin and tetra(N-R-pyridinium-3-yl)porphyrin derivatives were synthesized with R = 3, 6, and 8 carbon alkene, alcohol and carboxylic acid chains. Self-aggregation of these systems was studied at I = 0.1 using visible spectroscopy. N-Alkyl chain length and functionality were determined to play the dominant role in aggregation of the cationic porphyrins. Position of peripheral charge (meta vs. para) also influenced spectral changes and the nature of the aggregate.
Databáze: OpenAIRE