Affiliation:
1. Beijing Key Laboratory for Science and Application of Functional Molecular and Crystalline Materials, Department of Chemistry, University of Science and Technology Beijing, Beijing 100083, China
Abstract
In this manuscript, unexpected supramolecular assembly of [Formula: see text]-conjugated molecules containing complex aromatic substituents was investigated. The air–water interfacial assembly of double-decker phthalocyanines containing sixteen phenol substituents (Ce(Pc2)[Formula: see text] and Y(Pc2)[Formula: see text] form aligned nanoparticles. Depending on the different surface pressure, the Ce(Pc2)[Formula: see text] self-assembled nanostructures can be regulated thoroughly. Although Ce(Pc2)[Formula: see text] and Y(Pc2)[Formula: see text] have only aromatic substituent groups, no H- or J-aggregation of [Formula: see text]-conjugated systems can be detected from the UV-vis spectra of the assemblies of these double-decker phthalocyanines. When the nanostructures of these assemblies were changed greatly, no corresponding changes of UV-vis spectra and FT-IR spectra could be detected. These unusual results can be understood from the balance between the hydrophilicity of aromatic substituents and the ether linkages of double-decker phthalocyanines and the surface pressure, and open new. approaches for supramolecular assembly of complex [Formula: see text]-conjugated systems.
Publisher
World Scientific Pub Co Pte Lt
Cited by
1 articles.
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1. Er(III) and Lu(III) complexes of 2(3),9(10),16(17),23(24)-tetrakis- and 2,3,9,10,16,17,23,24-octakis-[4-(1-methyl-1-phenylethyl)phenoxy]phthalocyaninato. Synthesis and spectroscopic properties;Journal of Porphyrins and Phthalocyanines;2019-04