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通过无溶剂热解黄原酸镓来获取 γ-GaS:一种低温下获得结晶产物的方法。

Accessing γ-GaS by solventless thermolysis of gallium xanthates: a low-temperature limit for crystalline products.

机构信息

School of Chemistry, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK and Chemistry Department, Faculty of Science and Arts, Al-Baha University, Al Makhwah, Saudi Arabia.

School of Chemistry, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK.

出版信息

Dalton Trans. 2019 Nov 7;48(41):15605-15612. doi: 10.1039/c9dt02061f. Epub 2019 Aug 7.

Abstract

Alkyl-xanthato gallium(iii) complexes of the form [Ga(SCOR)], where R = Me (1), Et (2), Pr (3), Pr (4), Bu (5), Bu (6) and Bu (7), have been synthesized and fully characterised. The crystal structures for 1 and 3-7 have been solved and examined to elucidate if these structures are related to their decomposition. Thermogravimetric analysis was used to gain insight into the decomposition temperatures for each complex. Unlike previously explored metal xanthate complexes which break down at low temperatures (<250 °C), to form crystalline metal chalcogenides, powder X-ray diffraction measurements suggest that when R ≥ Et these complexes did not produce crystalline gallium sulfides until heated to 500 °C, where γ-GaS was the sole product formed. In the case of R = Me, Chugaev elimination did not occur and amorphous GaS products were formed. We conclude therefore that the low-temperature synthesis route offered by the thermal decomposition of metal xanthate precursors, which has been reported for many metal sulfide systems prior to this, may not be appropriate in the case of gallium sulfides.

摘要

已合成并充分表征了式[Ga(SCOR)]的烷基-黄原酸镓(III)配合物,其中 R = Me(1)、Et(2)、Pr(3)、Pr(4)、Bu(5)、Bu(6)和 Bu(7)。已经解决了 1 和 3-7 的晶体结构,并对其进行了检查,以阐明这些结构是否与其分解有关。热重分析用于深入了解每个配合物的分解温度。与以前探索的金属黄原酸配合物不同,这些配合物在低温(<250°C)下分解,形成结晶金属硫族化物,粉末 X 射线衍射测量表明,当 R≥Et 时,这些配合物在加热至 500°C 之前不会产生结晶硫化镓,其中γ-GaS 是唯一形成的产物。对于 R = Me,Chugaev 消除没有发生,形成了无定形 GaS 产物。因此,我们得出结论,对于以前报道的许多金属硫化物系统,金属黄原酸前体的热分解提供的低温合成途径在硫化镓的情况下可能不合适。

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