Durola Fabien, Lux Jacques, Sauvage Jean-Pierre
Institut Le Bel, Université Louis Pasteur, 4 Rue Blaise Pascal, 67070 Strasbourg, France.
Chemistry. 2009;15(16):4124-34. doi: 10.1002/chem.200802510.
Fast-track changes: The synthesis of a new copper-based molecular shuttle is described, with a coordinating macrocycle based on a nonhindering but endocyclic ligand (see scheme), which makes the ligand exchange easier, and thus the motions of the ring along the thread faster.The present report deals with the synthesis of a two-station [2]rotaxane consisting of a dpbiiq-incorporating macrocycle (dpbiiq: 8,8'-diphenyl-3,3'-biisoquinoline) threaded by a coordinating fragment whose complexing units are a dpp and a terpy ligand (dpp: 2,9-diphenyl-1,10-phenanthroline; terpy: 2,2',6',2"-terpyridine). The [2]rotaxane was prepared in 11 steps from commercially available or easy-to-make molecules, without taking into account the preparation of the dpbiiq-containing 39-membered ring, which was available in our group. The ring-incorporated bidentate chelate is at the same time endocyclic and sterically nonhindering, which is a specific property of the dpbiiq-coordinating unit. This unique feature has a profound influence on the rate of the ring-and-copper translation motion between the two stations of the axle. Based on an analogous multistep strategy, a related molecular shuttle has also been prepared that contains exactly the same axle and stoppers as the first compound but whose threaded ring incorporates the sterically hindering dpp chelate. The translation motions of this other system are several orders of magnitude slower than the corresponding movements of the dpbiiq-based compound. The motion corresponding to the rearrangement of the unstable five-coordinate copper(I) form of the compounds is relatively fast for both shuttles; the half lifetime of the five-coordinate Cu(I) species being below 20 ms for the dpbiiq-containing system and below 1 s for the dpp-based molecule. The reverse motion corresponding to the rearrangement of the four-coordinate copper(II) complexes is much slower, especially for the dpp-based system. It is of the order of several hours for the dpp-based shuttle and only one second or less for the dpbiiq system, under exactly the same conditions. The remarkable difference between the motion rates for the two two-station shuttles demonstrates that the use of a very open chelate such as dpbiiq is extremely beneficial in the context of fast-moving molecular machines.
本文描述了一种新型铜基分子梭的合成,其配位大环基于一种无阻碍的内环状配体(见方案),这使得配体交换更容易,从而环沿着链的运动更快。本报告涉及一种双站[2]轮烷的合成,该轮烷由一个包含dpbiiq的大环(dpbiiq:8,8'-二苯基-3,3'-联异喹啉)和一个配位片段构成,该配位片段的络合单元是一个dpp和一个三联吡啶配体(dpp:2,9-二苯基-1,10-菲咯啉;三联吡啶:2,2',6',2''-三联吡啶)。该[2]轮烷由市售或易于制备的分子通过11步反应制备而成,无需考虑含dpbiiq的39元环的制备,该环在我们小组中是可得的。环内的双齿螯合物同时是内环状且空间位阻小,这是dpbiiq配位单元的一个特殊性质。这一独特特征对轴的两个站点之间环与铜的平移运动速率有深远影响。基于类似的多步策略,还制备了一种相关的分子梭,它与第一种化合物具有完全相同的轴和封端,但其穿线环包含空间位阻较大的dpp螯合物。该另一体系的平移运动比基于dpbiiq的化合物的相应运动慢几个数量级。对于两种分子梭,与化合物不稳定的五配位铜(I)形式的重排相对应的运动都较快;对于含dpbiiq的体系,五配位Cu(I)物种的半衰期低于20毫秒,对于基于dpp的分子则低于1秒。与四配位铜(II)配合物重排相对应的反向运动要慢得多,特别是对于基于dpp的体系。在完全相同的条件下,基于dpp的分子梭的反向运动速率约为几小时,而对于dpbiiq体系则仅为一秒或更短。这两种双站分子梭运动速率的显著差异表明,在快速移动的分子机器中使用非常开放的螯合物如dpbiiq极其有益。