氢的一个新系列契约驱动的 heterodimers 在从基于一种肺结核特效药的单体的氯仿自我装配。在充满电子的二度(p苯撑)之间的另外的分子间的施主领受人相互作用联合起来的 -34-crown-10 和联合起来的电子缺乏的萘 diimide 被利用了增加 dimmers 的稳定性,并且二分离非共有原子价的显著 cooperativity 强迫稳定更暗淡被量的 1H ( 2D )揭示了 NMR 和紫外力的实验。
A new series of hydrogen bonding-driven heterodimers have been self-assembled in chloroform from hydrazide-based monomers. Additional intermolecular donor-acceptor interaction between the electron-rich bis(p-phenylene)-34-crown-10 unit and the electron-deficient naphthalene diimide unit has been utilized to increase the stability of the dimmers, and pronounced cooperativity of the two discrete non-covalent forces to stabilize the dimer has been revealed by the quantitative ^1H (2D) NMR and UV-Vis experiments.