Cooperative supramolecular polymerization of an amine-substituted naphthalene-diimide and its impact on excited state photophysical properties

被引:44
|
作者
Kar, Haridas [1 ]
Gehrig, Dominik W. [2 ]
Allampally, Naveen Kumar [3 ,4 ]
Fernandez, Gustavo [3 ,4 ]
Laquai, Frederic [2 ]
Ghosh, Suhrit [1 ]
机构
[1] Indian Assoc Cultivat Sci, Polymer Sci Unit, 2A & 2B Raja SC Mullick Rd, Kolkata 700032, India
[2] Max Planck Inst Polymer Res, Max Planck Res Grp Organ Optoelect, Ackermannweg 10, D-55128 Mainz, Germany
[3] Univ Wurzburg, Inst Organ Chem, D-97074 Wurzburg, Germany
[4] Univ Wurzburg, Ctr Nanosyst Chem, D-97074 Wurzburg, Germany
关键词
PI; CONSTRUCTION; PHOTOSYSTEMS; TRANSISTORS; NANOTUBES; CATALYSIS; POLYMERS; ACCEPTOR; TUBULES; DYES;
D O I
10.1039/c5sc03462k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A donor-acceptor-donor (D-A-D) type naphthalene-diimide (NDI-H) chromophore exhibits highly cooperative J-aggregation leading to nanotubular self-assembly and gelation in n-decane, as demonstrated by UV/Vis, FT-IR, photoluminescence and microscopy studies. Analysis of temperature-dependent UV/Vis spectra using the nucleation-elongation model and FT-IR data reveals the molecular origin of the cooperative nature of the self-assembly. The supramolecular polymerization is initiated by H-bonding up to a degree of polymerization similar to 20-25, which in a subsequent elongation step promotes J-aggregation in orthogonal direction leading to possibly a sheet-like structure that eventually produces nanotubes. Time-resolved fluorescence and absorption measurements demonstrate that such a tubular assembly enables very effective delocalization of excited states resulting in a remarkably prolonged excited state lifetime.
引用
收藏
页码:1115 / 1120
页数:6
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