Supramolecular porphyrin polymers in solution and at the solid-liquid interface

被引:93
作者
van Hameren, Richard [1 ]
van Buul, Arend M. [1 ]
Castriciano, Maria A. [2 ]
Villari, Valentina [3 ]
Micali, Norberto [3 ]
Schon, Peter [1 ]
Speller, Sylvia [1 ]
Scolaro, Luigi Monsu [2 ]
Rowan, Alan E. [1 ]
Elemans, Johannes A. A. W. [1 ]
Nolte, Roeland J. M. [1 ]
机构
[1] Radboud Univ Nijmegen, Inst Mol & Mat, NL-6525 ED Nijmegen, Netherlands
[2] Univ Messina, Dipartimento Chim Inorgan Chim Analit & Chim Fis, I-98166 Messina, Italy
[3] CNR, IPCF, I-98158 Messina, Italy
关键词
D O I
10.1021/nl072563f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have investigated in detail the self-assembly of, a chiral porphyrin trimer in different solvents and correlated this behavior to the aggregation of the molecule at a solid-liquid interface. In n-hexane and cyclohexane, CID spectroscopy and dynamic and static light scattering studies showed that the porphyrin trimer self-assembles already at micromolar concentrations into long, chiral supramolecular polymers, which precipitate as fibers when the solution is drop-cast onto a mica surface. In contrast, in chloroform, the compound is molecularly dissolved up to concentrations of 0.2 mM and when micromolar solutions are drop-cast onto mica, no precipitation of large assemblies occurs. Instead, at the moment that the chloroform film becomes subject to spinodal dewetting and the porphyrin trimers; within this film start to self-assemble, extended patterns of equidistant lines of single molecule thick columnar stacks are formed.
引用
收藏
页码:253 / 259
页数:7
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