Das Paramita, Kumar Atul, Howlader Prodip, Mukherjee Partha Sarathi
Inorganic and Physical Chemistry Department, Indian Institute of Science, Bangalore, 560012, India.
Chemistry. 2017 Sep 12;23(51):12565-12574. doi: 10.1002/chem.201702263. Epub 2017 Aug 10.
A water-soluble Pd trigonal prism (A) was synthesized by two-component coordination-driven self-assembly of a Pd 90° acceptor with a tetraimidazole donor. The walls of the prism are constructed by three conjugated aromatic building blocks, which means that the confined pocket of the prism is hydrophobic. In addition to the hydrophobic cavity, large product egress windows make A an ideal molecular vessel to catalyze otherwise challenging pseudo-multicomponent dehydration reactions in its confined nanospace in aqueous medium. This study is an attempt at selective generation of the intermediate tetraketones and xanthenes by fine-tuning the reaction conditions employing a supramolecular molecular vessel. Moreover, either poor or no yield of the dehydrated products in the absence of A under similar reaction conditions supports the ability of the confined space of the barrel to promote such reactions in water. Furthermore, we focused on the rigidification of the tetraphenylethylene-based tetraimidazole unit anchored within the Pd coordination architecture; enabling counter-anion dependent aggregation induced emission in the presence of water.
通过钯 90°受体与四咪唑供体的双组分配位驱动自组装合成了一种水溶性钯三角棱柱(A)。棱柱的壁由三个共轭芳香结构单元构成,这意味着棱柱的受限腔是疏水的。除了疏水腔外,大的产物出口窗口使 A 成为一种理想的分子容器,可在水介质中的受限纳米空间内催化原本具有挑战性的准多组分脱水反应。本研究尝试通过使用超分子分子容器微调反应条件来选择性生成中间体四酮和呫吨。此外,在类似反应条件下,没有 A 时脱水产物的产率很低或根本没有产率,这支持了桶状受限空间在水中促进此类反应的能力。此外,我们专注于固定在钯配位结构内的基于四苯基乙烯的四咪唑单元的刚性化;在有水存在的情况下实现了基于抗衡阴离子的聚集诱导发光。