Department of Chemistry, University of Liverpool, Crown Street, Liverpool L69 7ZD, UK.
Langmuir. 2012 Jun 26;28(25):9797-806. doi: 10.1021/la301371q. Epub 2012 Jun 13.
Naphthalene dipeptides have been shown to be useful low-molecular-weight gelators. Here we have used a library to explore the relationship between the dipeptide sequence and the hydrogelation efficiency. A number of the naphthalene dipeptides are crystallizable from water, enabling us to investigate the comparison between the gel/fiber phase and the crystal phase. We succeeded in crystallizing one example directly from the gel phase. Using X-ray crystallography, molecular modeling, and X-ray fiber diffraction, we show that the molecular packing of this crystal structure differs from the structure of the gel/fiber phase. Although the crystal structures may provide important insights into stabilizing interactions, our analysis indicates a rearrangement of structural packing within the fibers. These observations are consistent with the fibrillar interactions and interatomic separations promoting 1D assembly whereas in the crystals the peptides are aligned along multiple axes, allowing 3D growth. This observation has an impact on the use of crystal structures to determine supramolecular synthons for gelators.
萘二肽已被证明是有用的低分子量凝胶剂。在这里,我们使用文库来探索二肽序列与水凝胶效率之间的关系。许多萘二肽可从水中结晶,使我们能够研究凝胶/纤维相与晶体相之间的比较。我们成功地直接从凝胶相中结晶出一个例子。使用 X 射线晶体学、分子建模和 X 射线纤维衍射,我们表明该晶体结构的分子堆积与凝胶/纤维相的结构不同。尽管晶体结构可能为稳定相互作用提供重要的见解,但我们的分析表明纤维内结构堆积的重新排列。这些观察结果与促进一维组装的纤维状相互作用和原子间分离一致,而在晶体中,肽沿多个轴排列,允许 3D 生长。这一观察结果对使用晶体结构来确定凝胶剂的超分子单体产生影响。