Mojibola Adeolu, Dongmo-Momo Gilles, Mohammed Muzaffer, Aslan Kadir
Department of Chemistry, Morgan State University , 1700 East Cold Spring Lane, Baltimore, Maryland 21251 United States.
Cryst Growth Des. 2014 May 7;14(5):2494-2501. doi: 10.1021/cg500204t. Epub 2014 Mar 21.
In this work, we demonstrated that the change in the morphology of l-alanine crystals can be controlled with the addition of l-leucine using the metal-assisted and microwave accelerated evaporative crystallization (MA-MAEC) technique. Crystallization experiments, where an increasing stoichiometric amount of l-leucine is added to initial l-alanine solutions, were carried out on circular poly(methyl methacrylate) (PMMA) disks modified with a 21-well capacity silicon isolator and silver nanoparticle films using microwave heating (MA-MAEC) and at room temperature (control experiments). The use of the MA-MAEC technique afforded for the growth of l-alanine crystals with different morphologies up to ∼10-fold faster than those grown at room temperature. In addition, the length of l-alanine crystals was systematically increased from ∼380 to ∼2000 μm using the MA-MAEC technique. Optical microscope images revealed that the shape of l-alanine crystals was changed from tetragonal shape (without l-leucine additive) to more elongated and wire-like structures with the addition of the l-leucine additive. Further characterization of l-alanine crystals was undertaken by Fourier transform infrared (FT-IR) spectroscopy, Raman spectroscopy and powder X-ray diffraction (PXRD) measurements. In order to elucidate the growth mechanism of l-alanine crystals, theoretical simulations of l-alanine's morphology with and without l-leucine additive were carried out using Materials Studio software in conjunction with our experimental data. Theoretical simulations revealed that the growth of l-alanine's {011} and {120} crystal faces were inhibited due to the incorporation of l-leucine into these crystal faces in selected positions.
在这项工作中,我们证明了使用金属辅助和微波加速蒸发结晶(MA - MAEC)技术,通过添加L - 亮氨酸可以控制L - 丙氨酸晶体的形态变化。在使用微波加热(MA - MAEC)以及在室温下(对照实验),在由具有21孔容量的硅隔离器和银纳米颗粒膜修饰的圆形聚甲基丙烯酸甲酯(PMMA)圆盘上,进行了向初始L - 丙氨酸溶液中添加化学计量比不断增加的L - 亮氨酸的结晶实验。与在室温下生长的晶体相比,MA - MAEC技术使不同形态的L - 丙氨酸晶体的生长速度加快了约10倍。此外,使用MA - MAEC技术,L - 丙氨酸晶体长度从约380μm系统地增加到约2000μm。光学显微镜图像显示,添加L - 亮氨酸添加剂后,L - 丙氨酸晶体的形状从四方形状(无L - 亮氨酸添加剂)变为更细长的线状结构。通过傅里叶变换红外(FT - IR)光谱、拉曼光谱和粉末X射线衍射(PXRD)测量对L - 丙氨酸晶体进行了进一步表征。为了阐明L - 丙氨酸晶体的生长机制,结合我们的实验数据,使用Materials Studio软件对有和没有L - 亮氨酸添加剂的L - 丙氨酸形态进行了理论模拟。理论模拟表明,由于L - 亮氨酸在选定位置掺入到这些晶面中,L - 丙氨酸的{011}和{120}晶面的生长受到抑制。