CSIR-Central Salt & Marine Chemicals Research Institute , Bhavnagar 364002, Gujarat, India.
J Am Chem Soc. 2016 Sep 7;138(35):11113-6. doi: 10.1021/jacs.6b06312. Epub 2016 Aug 18.
The helical handedness in achiral self-assemblies is mostly complex due to spontaneous symmetry breaking or kinetically controlled random assembly formation. Here an attempt has been made to address this issue through chiral anion exchange. A new class of cationic achiral C3-symmetric gelator devoid of any conventional gelation assisting functional units is found to form both right- and left-handed helical structures. A chiral counteranion exchange-assisted approach is successfully introduced to control the chirality sign and thereby to obtain preferred homochiral assemblies. Formation of anion-assisted chiral assembly was confirmed by circular dichroism (CD) spectroscopy, microscopic images, and crystal structure. The X-ray crystal structure reveals the construction of helical assemblies with opposite handedness for (+)- and (-)-chiral anion reformed gelators. The appropriate counteranion driven ion-pair-assisted hydrogen-bonding interactions are found responsible for the helical bias control in this C3-symmetric gelator.
在非手性自组装中,螺旋手性大多是复杂的,因为自发对称破缺或动力学控制的随机组装形成。在这里,我们试图通过手性阴离子交换来解决这个问题。我们发现一种新型的手性阴离子交换辅助方法可以控制手性符号,从而获得优先的同手性组装。圆二色性(CD)光谱、微观图像和晶体结构证实了阴离子辅助手性组装的形成。X 射线晶体结构揭示了(+)-和(-)-手性阴离子重构凝胶剂形成的具有相反手性的螺旋组装体的构建。合适的抗衡阴离子驱动的离子对辅助氢键相互作用被认为是这种 C3 对称凝胶剂中螺旋偏差控制的原因。