The syntheses of amphiphilic antimony(V) -phthalocyanines and spectral investigation on their aggregation behaviors in aqueous and non-aqueous solutions
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作者:
Isago, Hiroaki
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Natl Inst Mat Sci, Tsukuba, Ibaraki 3050047, JapanNatl Inst Mat Sci, Tsukuba, Ibaraki 3050047, Japan
Isago, Hiroaki
[1
]
Kagaya, Yutaka
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Natl Inst Mat Sci, Tsukuba, Ibaraki 3050047, JapanNatl Inst Mat Sci, Tsukuba, Ibaraki 3050047, Japan
Kagaya, Yutaka
[1
]
Oyama, Youichi
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Natl Inst Mat Sci, Tsukuba, Ibaraki 3050047, JapanNatl Inst Mat Sci, Tsukuba, Ibaraki 3050047, Japan
Oyama, Youichi
[1
]
Fujita, Harumi
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Natl Inst Mat Sci, Tsukuba, Ibaraki 3050047, JapanNatl Inst Mat Sci, Tsukuba, Ibaraki 3050047, Japan
Fujita, Harumi
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]
Sugimori, Tamotsu
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Toyama Univ, Grad Sch Med & Pharmaceut Sci, Toyama 9300194, JapanNatl Inst Mat Sci, Tsukuba, Ibaraki 3050047, Japan
Sugimori, Tamotsu
[2
]
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[1] Natl Inst Mat Sci, Tsukuba, Ibaraki 3050047, Japan
[2] Toyama Univ, Grad Sch Med & Pharmaceut Sci, Toyama 9300194, Japan
Three amphiphilic antimony(V)-phthalocyanines have been synthesized by treating [Sb(R4Pc)(OH)(2)](+) salts in concentrated H2SO4 and isolated as zwitter ions, [Sb(R4Pc)(SO4H)(SO4)], where R4Pc denotes tetra-substituted phthalocyaninate; R4Pc = pc (R = H), tbpc (R = Bu-t), and tObpc (R = (OBu)-Bu-n). Their solubility (R = tbpc > pc >> tObpc in H2O (much improved by the presence of surfactant or alcohol) while tbpc > tObpc >> pc in CH2Cl2) 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. (C) 2012 Elsevier Inc. All rights reserved.