Department of Chemistry and Biochemistry, University of California, Los Angeles, 607 Charles E. Young Drive East, Los Angeles, California 90095, United States.
Department of Chemistry, United States Air Force Academy, 2355 Fairchild Drive, Suite 2N-255, Air Force Academy, Colorado 80840, United States.
J Am Chem Soc. 2020 Dec 9;142(49):20513-20518. doi: 10.1021/jacs.0c09361. Epub 2020 Nov 30.
High-affinity guests have been reported for the macrocyclic host cucurbit[7]uril (CB[7]), enabling widespread applications, but hindering CB[7] materials from being returned to their guest-free state for reuse. Here, we present polyhedral boron clusters (carboranes) as strongly binding, yet easily removable, guests for CB[7]. Aided by a Pd-catalyzed coupling of an azide anion, we prepared boron-functionalized 9-amino--carborane that binds to CB[7] with a ≈ 10 M. Upon basic treatment, -carborane readily undergoes deboronation to yield anionic -carborane, a poor guest for CB[7], facilitating recovery of guest-free CB[7]. We showcase the utility of the modified -carborane guest by recycling a CB[7]-functionalized resin. With this report, we introduce stimuli-responsive decomplexation as an additional consideration in the design of high-affinity host-guest complexes.
已报道大环主体葫芦[7]脲(CB[7])对高亲和力客体的结合,这使其得到广泛应用,但也阻碍了 CB[7]材料回复到其无客体状态以重复使用。在这里,我们将多面体硼簇(硼烷)作为强结合但易于去除的客体用于 CB[7]。在钯催化的叠氮阴离子偶联的辅助下,我们制备了硼功能化的 9-氨基--硼烷,其与 CB[7]的结合常数约为 10 M。经碱性处理,-硼烷容易发生去硼化反应生成阴离子 -硼烷,其对 CB[7]的亲和力较差,有利于回收无客体的 CB[7]。我们通过回收 CB[7]功能化树脂展示了改性 -硼烷客体的实用性。通过本报告,我们将响应性解络合作为设计高亲和力主客体配合物的另一个考虑因素引入。