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收缩性和可伸展性的分子8字形结构。

Contractile and extensible molecular figures-of-eight.

作者信息

Niess Frédéric, Duplan Vincent, Diercks Christian S, Sauvage Jean-Pierre

机构信息

Institut de Science et d'Ingénierie Supramoléculaires (ISIS), Université de Strasbourg et CNRS, 8 allée Gaspard Monge, 67000 Strasbourg (France).

出版信息

Chemistry. 2015 Oct 5;21(41):14393-400. doi: 10.1002/chem.201502216. Epub 2015 Sep 1.

Abstract

Two large rings, 66- (m-66) and 78-membered (m-78) rings, each one incorporating two pairs of transition-metal-complexing units, have been prepared. The coordinating fragments are alternating bi- and tridentate chelating groups, namely, 2,9-diphenyl-1,10-phenanthroline (dpp) and 2,2',2',6''-terpyridine (terpy) respectively. Both macrocycles form molecular figures-of-eight in the presence of Fe(II) , affording a classical bis-terpy complex as the central core. The larger m-78 ring can accommodate a four-coordinate Cu(I) center with the formation of a {Cu(dpp)2 }(+) central complex and a highly twisted figure-of-eight backbone, whereas m-66 is too small to coordinate Cu(I) . Macrocycle m-78 thus affords stable complexes with both Fe(II) and Cu(I) ; the ligand around the metal changes from (terpy)2 to (dpp)2 . This bimodal coordination situation allows for a large amplitude rearrangement of the organic backbone. When coordinated to preferentially octahedrally coordinated Fe(II) or Cu(II) , the height of the molecule along the coordinating axis of the tridentate terpy ligands is only about 11 Å, whereas the height of the molecule along the same vertical axis is several times as large for the tetrahedral Cu(I) complex. Chemically or electrochemically driven contraction and extension motions along a defined axis make this figure-of-eight particularly promising as a new class of molecular machine prototype for use as a constitutive element in muscle-like dynamic systems.

摘要

已制备出两个大环,分别为含66个原子的环(m - 66)和含78个原子的环(m - 78),每个大环都包含两对过渡金属络合单元。配位片段是交替的双齿和三齿螯合基团,分别为2,9 - 二苯基 - 1,10 - 菲咯啉(dpp)和2,2',2'',6'' - 三联吡啶(terpy)。在Fe(II)存在下,这两种大环均形成分子8字形结构,以经典的双 - terpy络合物作为中心核。较大的m - 78环能够容纳一个四配位的Cu(I)中心,形成{Cu(dpp)₂ }(+)中心络合物和高度扭曲的8字形主链,而m - 66环太小,无法配位Cu(I)。因此,大环m - 78能与Fe(II)和Cu(I)都形成稳定的络合物;金属周围的配体从(terpy)₂变为(dpp)₂。这种双峰配位情况使得有机主链能够进行大幅度重排。当与优先八面体配位的Fe(II)或Cu(II)配位时,分子沿三齿terpy配体配位轴的高度仅约为11 Å,而对于四面体Cu(I)络合物,分子沿同一垂直轴的高度则是其几倍。沿定义轴进行化学或电化学驱动的收缩和伸展运动,使得这种8字形结构作为一类新型分子机器原型,有望成为肌肉样动态系统中的组成元件。

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