Langmuir-Blodgett Films of Diketopyrrolopyrroles with Tunable Amphiphilicity

被引:8
作者
Hupfer, Maximilian L. [1 ,2 ]
Koszarna, Beata [3 ]
Ghosh, Soumik [1 ,4 ]
Gryko, Daniel T. [3 ]
Presselt, Martin [1 ,2 ,4 ,5 ]
机构
[1] Leibniz Inst Photon Technol IPHT, D-07745 Jena, Germany
[2] Friedrich Schiller Univ Jena, Inst Phys Chem, D-07743 Jena, Germany
[3] Polish Acad Sci, Inst Organ Chem, PL-01224 Warsaw, Poland
[4] SciClus GmbH & Co KG, D-07745 Jena, Germany
[5] Friedrich Schiller Univ Jena, Ctr Energy & Environm Chem Jena CEEC Jena, D-07743 Jena, Germany
关键词
DENSITY-FUNCTIONAL THEORY; SIDE-CHAINS; FLUORESCENCE; ABSORPTION; MONOLAYERS; DISCOVERY; DYNAMICS; BEHAVIOR; PROBES; IMPACT;
D O I
10.1021/acs.langmuir.1c01113
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work, we present the formation of H- and J-aggregates of amphiphilic centrosymmetric diketopyrrolopyrroles containing aliphatic or aromatic amino groups. The inherent amphiphilicity of these dyes predestines their assembly at interfaces to form ordered supramolecular structures. In this work, we employed the Langmuir-Blodgett (LB) technique to generate, manipulate, and deposit such supramolecular structures. The aforementioned amines provide an additional means to control the formation of the supramolecular assemblies. In the resulting LB films, both H- and J-aggregates of the dyes can be realized, leading to very broad absorption spectra. In contrast to many reports on Hand J-aggregates, the interactions between the symmetric diketopyrrolopyrroles are controlled via interface assembly and p-stacking and not by dipolar interactions. We show that in the case of the aliphatic, but not for the aromatic amine functionalization, the usage of an acidic subphase enables the transition from H- to J-aggregate-dominated LB films via an increase in the surface pressure during deposition.
引用
收藏
页码:10272 / 10278
页数:7
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