Abstract:
:Three amphiphilic antimony(V)-phthalocyanines have been synthesized by treating [Sb(R(4)Pc)(OH)(2)](+) salts in concentrated H(2)SO(4) and isolated as zwitter ions, [Sb(R(4)Pc)(SO(4)H)(SO(4))], where R(4)Pc denotes tetra-substituted phthalocyaninate; R(4)Pc=pc (R=H), tbpc (R=(t)Bu), and tObpc (R=O(n)Bu). Their solubility (R=tbpc>pc >tObpc in H(2)O (much improved by the presence of surfactant or alcohol) while tbpc>tObpc >pc in CH(2)Cl(2)) and aggregation behaviors are highly sensitive to the nature of the peripheral substituents. The pc and tbpc derivatives form well-behaved J-aggregates in aqueous media in the presence of surfactant or alcohol.
journal_name
J Inorg Biochemjournal_title
Journal of inorganic biochemistryauthors
Isago H,Kagaya Y,Oyama Y,Fujita H,Sugimori Tdoi
10.1016/j.jinorgbio.2012.02.021subject
Has Abstractpub_date
2012-06-01 00:00:00pages
91-8eissn
0162-0134issn
1873-3344pii
S0162-0134(12)00065-7journal_volume
111pub_type
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