Dudukovic Nikola A, Zukoski Charles F
Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.
Department of Chemical and Biological Engineering, University at Buffalo, Buffalo, New York 14222, USA.
J Chem Phys. 2014 Oct 28;141(16):164905. doi: 10.1063/1.4899905.
Solutions of the aromatic dipeptide derivative molecule fluorenylmethoxycarbonyl-diphenylalanine (Fmoc-FF) in dimethyl sulfoxide produce fibrous gels when mixed with water. We study the evolution of density fluctuations of this three-component system using X-ray photon correlation spectroscopy (XPCS) and compare these results to the macroscopic rheology of the gels and optical observations of the microstructure evolution. At the investigated scattering angles, the intensity autocorrelation functions do not follow behavior expected for simple diffusion of individual Fmoc-FF molecules localized within cages of nearest neighbors. Instead, the dynamics are associated with density fluctuations on length scales of ~10-100 nm arising from disaggregation and reformation of fibers, leading to an increasingly uniform network. This process is correlated with the growth of the elastic modulus, which saturates at long times. Autocorrelation functions and relaxation times acquired from XPCS measurements are consistent with relaxation rates of structures at dynamic equilibrium. This study provides further support to the concept of exploring peptide-based gelators as valence-limited patchy particles capable of forming equilibrium gels.
芴甲氧羰基 - 二苯基丙氨酸(Fmoc - FF)这种芳香族二肽衍生物分子在二甲基亚砜中的溶液与水混合时会形成纤维状凝胶。我们使用X射线光子相关光谱法(XPCS)研究了这个三元体系密度涨落的演变,并将这些结果与凝胶的宏观流变学以及微观结构演变的光学观察结果进行比较。在所研究的散射角度下,强度自相关函数并不遵循单个Fmoc - FF分子在最近邻笼中简单扩散所预期的行为。相反,动力学与纤维的解聚和重新形成所产生的~10 - 100 nm长度尺度上的密度涨落相关,从而导致网络越来越均匀。这个过程与弹性模量的增长相关,弹性模量在长时间后会饱和。从XPCS测量中获得的自相关函数和弛豫时间与动态平衡时结构的弛豫速率一致。这项研究进一步支持了将基于肽的凝胶剂作为能够形成平衡凝胶的价限补丁粒子进行探索的概念。