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用于半导体螺旋状金属硫框架结晶的硫醇构建块的合成。

Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework.

作者信息

He Yonghe, Huang Jiahong, He Jun, Xu Zhengtao

机构信息

School of Chemical Engineering and Light Industry, Guangdong University of Technology.

School of Chemical Engineering and Light Industry, Guangdong University of Technology;

出版信息

J Vis Exp. 2018 Apr 9(134):57455. doi: 10.3791/57455.

Abstract

We present a method for preparing thioester molecules as the masked form of the thiol linkers and their utilization for accessing a semiconducting and porous metal-dithiolene network in the highly ordered single crystalline state. Unlike the highly reactive free-standing thiols, which tend to decompose and complicate the crystallization of metal-thiolate open frameworks, the thioester reacts in situ to provide the thiol species, serving to mitigate the reaction between the mercaptan units and the metal centers, and to improve crystallization consequently. Specifically, the thioester was synthesized in a one-pot procedure: an aromatic bromide (hexabromotriphenylene) reacted with excess sodium thiomethoxide under vigorous conditions to first form the thioether intermediate product. The thioether was then demethylated by the excess thiomethoxide to provide the thiolate anion that was acylated to form the thioester product. The thioester was conveniently purified by standard column chromatography, and then used directly in the framework synthesis, wherein NaOH and ethylenediamine serve to revert in situ the thioester to the thiol linker for assembling the single-crystalline Pb(II)-dithiolene network. Compared with other methods for thiol synthesis (e.g., by cleaving alkyl thioether using sodium metal and liquid ammonia), the thioester synthesis here uses simple conditions and economical reagents. Moreover, the thioester product is stable and can be conveniently handled and stored. More importantly, in contrast to the generic difficulty in accessing crystalline metal-thiolate open frameworks, we demonstrate that using the thioester for in situ formation of the thiol linker greatly improves the crystallinity of the solid-state product. We intend to encourage broader research efforts on the technologically important metal-sulfur frameworks by disclosing the synthetic protocol for the thioester as well as the crystalline framework solid.

摘要

我们提出了一种制备硫酯分子的方法,该硫酯分子作为硫醇连接体的掩蔽形式,并将其用于构建高度有序单晶态的半导体多孔金属二硫烯网络。与高反应活性的游离硫醇不同,游离硫醇易于分解并使金属硫醇盐开放框架的结晶过程复杂化,而硫酯会原位反应生成硫醇物种,有助于减轻硫醇单元与金属中心之间的反应,从而改善结晶效果。具体而言,硫酯是通过一锅法合成的:芳香族溴化物(六溴代三亚苯)在剧烈条件下与过量的硫代甲醇钠反应,首先形成硫醚中间产物。然后,硫醚被过量的硫代甲醇钠去甲基化,生成硫醇盐阴离子,该阴离子被酰化形成硫酯产物。硫酯可通过标准柱色谱法方便地纯化,然后直接用于框架合成,其中氢氧化钠和乙二胺用于将硫酯原位转化为硫醇连接体,以组装单晶态的Pb(II)-二硫烯网络。与其他硫醇合成方法(例如,使用金属钠和液氨裂解烷基硫醚)相比,此处的硫酯合成使用的条件简单且试剂经济。此外,硫酯产物稳定,易于处理和储存。更重要的是,与获得结晶态金属硫醇盐开放框架普遍存在的困难相反,我们证明使用硫酯原位形成硫醇连接体可大大提高固态产物的结晶度。我们希望通过公开硫酯以及晶体框架固体的合成方案,鼓励对技术上重要的金属硫框架进行更广泛的研究。

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