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 |
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Rok vydání: | 1997 |
Předmět: |
chemistry.chemical_classification
biology Alkene Carboxylic acid Organic Chemistry Cationic polymerization chemistry.chemical_element Alcohol biology.organism_classification Photochemistry Porphyrin chemistry.chemical_compound Ultraviolet visible spectroscopy chemistry Polymer chemistry polycyclic compounds Tetra heterocyclic compounds Carbon |
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 |
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