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Crystal engineering: From design of crystal structures to fabrication of composite crystals.

机译:晶体工程:从晶体结构设计到复合晶体的制造。

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This thesis reports how to design and control co-crystal structures from a kinetic point of view, and demonstrates the control of crystal morphology through understanding the kinetics and crystal structures. In chapter one, the in-situ atomic force microscope (AFM) was utilized to investigate how side chain on a glycine 2,5-diketopiperazine (GLYDKP) backbone can affect the assembly of GLYDKP, and showed that methyl groups cause larger energy barrier for crystallization. Because the introduction of functional group on the side chain could inevitably slow down the assembly process, a different approach should be considered. Chapter two shows that formic acid at low concentration can accelerate the assembly process without incorporating into the crystal structure. Because formic acid only crystallizes with GLYDKP in concentrated solution, these results prove that co-crystallization is a better method for incorporating functionalized molecules into a solid than direct modification of molecule itself.; Chapter three focuses on the rational design of GLYDKP cocrystals by utilizing the observation found in chapter two. Structure of GLYDKP and formic acid crystal was analyzed to search possible guest molecules for cocrystal studies. This method successfully identified eleven molecules that crystallize with GLYDKP, and proved that crystal structure can be controlled through weak interactions such as C-H•••O=C and C-H•••Cl interactions.; Chapter four and chapter five explore the possibility of using self-assembled process to control morphology of crystals and surface epitaxy. Metal(II) bis(imidazolium 2,b-pyridinedicarboxylate) complexes were chosen and two morphologies associated with different metal ions were found: rhombohedral (Type I) and rectangular (Type II) crystals. In this study, an additive was found to change the morphology of crystal from type I to type II, and then methods of producing various shapes of composite crystals were also established. These self-assembled procedures of making composite crystals at micron scale are very promising, because the fabrication will only relies on solvent, additives, or combination of them without using sophisticated crystallizers.
机译:本文从动力学的角度报道了如何设计和控制共晶结构,并通过了解动力学和晶体结构来证明对晶体形态的控制。在第一章中,使用了“斜体”原子力显微镜(AFM)来研究甘氨酸2,5-二酮哌嗪(GLYDKP)骨架上的侧链如何影响GLYDKP的组装。甲基会导致更大的能垒,从而阻碍结晶。由于在侧链上引入官能团会不可避免地减慢组装过程,因此应考虑使用其他方法。第二章表明,低浓度的甲酸可以加速组装过程,而不会引入晶体结构。因为甲酸仅在浓缩溶液中与GLYDKP一起结晶,所以这些结果证明,与直接修饰分子本身相比,共结晶是一种将功能化分子掺入固体的更好方法。第三章利用第二章中的观察,重点研究了GLYDKP共晶体的合理设计。分析了GLYDKP和甲酸晶体的结构,以寻找可能的客体分子用于共晶体研究。该方法成功鉴定了11个用GLYDKP结晶的分子,并证明可以通过弱相互作用(例如C-H••O = C和C-H••Cl相互作用)控制晶体结构。第四章和第五章探讨了使用自组装过程控制晶体形态和表面外延的可能性。选择了金属(II)双(咪唑鎓2,b-吡啶二羧酸盐)配合物,发现与不同金属离子相关的两种形态:菱形(I型)和矩形(II型)晶体。在这项研究中,发现了一种添加剂,可将晶体的形态从I型改变为II型,然后还建立了生产各种形状的复合晶体的方法。这些制造微米级复合晶体的自组装方法非常有前途,因为制造仅依赖于溶剂,添加剂或它们的组合,而无需使用复杂的结晶器。

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