Synthesis and Characterization of Octaalkyl Metallo and Metal-Free Phthalocyanines and Decaalkyl Uranyl Superphthalocyanines.
Abstract
A straightforward, efficient, and generalizable synthesis of symmetrically substituted 2,3,9,10,16,17,23,24-octaalkyl phthalocyanines and 2,3,9,10,16,17,23,24,30,31-decaalkyl uranyl superphthalocyanines from o-dialkyl benzenes is described. For phthalocyanines, the approach is illustrated for methyl and n-butyl substituents. and both metal-free and nickel complexes are reported. Uranyl superphthalocyanines have been prepared with methyl and n-butyl substituents. The new complexes have been characterized by a variety of chemical and physicochemical methods. Quantitative determination of the solubilities of substituted and unsubstituted phthalocyanine and superphthalocyanine complexes in both 1,2,4-trichlorobenzene and toluene demonstrates decreasing solubility in the order (4,5-Bu2)5SPcUO2 > (4-Me)5SPcUO2 > (4,5-Me2)5SPcUO2 - SPcUO2 > (4-Me)4PcH2 > Ni(4,5-Bu2)Pc > Ni(4,5-Me2) 4Pc - NiPc. Attempts to displace the uranyl ion from (4,5-R2)5SPcUO2 with acids or Cu(OAc)2 lead to the formation of (4,5-R2)4PcH2 or Cu(4,5-R2)4Pc, respectively. (Author)
Document Details
- Document Type
- Technical Report
- Publication Date
- May 13, 1981
- Accession Number
- ADA099529
Entities
People
- Edward A. Cuellar
- Tobin J. Marks
Organizations
- Northwestern University