Gougeon Patrick, Salloum Diala, Cuny Jérôme, Le Pollès Laurent, Le Floch Marie, Gautier Régis, Potel Michel
Sciences Chimiques de Rennes, UMR CNRS 6226, Université de Rennes 1, Ecole Nationale Supérieure de Chimie de Rennes, 35042 Rennes Cedex, France.
Inorg Chem. 2009 Sep 7;48(17):8337-41. doi: 10.1021/ic900960g.
The ternary reduced molybdenum sulphide Cs(1)Mo12S14 has been synthesized by solid-state reaction at 1400 degrees C for 96 h in sealed molybdenum crucibles. The compound crystallizes in the trigonal space group P31c with the following lattice parameters: a = 9.9793 (2) A, c = 6.3730 (2) A, Z = 1. Its crystal structure was determined from single crystal X-ray diffraction data and consists of interconnected Mo6S8(i)S6(a) units forming an original three-dimensional framework in which large tunnels are occupied randomly by the Cs+ ions. 133Cs static NMR studies are in favor of a static cesium disorder. Unlike Ba4Mo12S18 where some Mo6S8(i)S6(a) units are also connected through S(i-i) ligands, this connection mode does not lead to significant interactions in the title compound. Single-crystal resistivity measurements show that Cs(1)Mo12S14 presents a metallic behavior with a superconducting transition at 7.7 K as confirmed by magnetic measurements.
三元还原硫化钼Cs(1)Mo12S14是在密封的钼坩埚中于1400℃通过固态反应合成96小时得到的。该化合物结晶于三方空间群P31c,具有以下晶格参数:a = 9.9793(2) Å,c = 6.3730(2) Å,Z = 1。其晶体结构由单晶X射线衍射数据确定,由相互连接的Mo6S8(i)S6(a)单元组成,形成一个原始的三维框架,其中大隧道被Cs+离子随机占据。133Cs静态核磁共振研究支持静态铯无序。与Ba4Mo12S18不同,在Ba4Mo12S18中一些Mo6S8(i)S6(a)单元也通过S(i-i)配体连接,这种连接方式在标题化合物中不会导致显著的相互作用。单晶电阻率测量表明,Cs(1)Mo12S14呈现金属行为,磁测量证实其在7.7 K发生超导转变。