Viau Lydie, Knorr Michael, Knauer Lena, Brieger Lukas, Strohmann Carsten
Institut UTINAM UMR CNRS 6213, Université Bourgogne Franche-Comté, F-25030 Besançon, France.
Anorganische Chemie, Technische Universität Dortmund, Otto-Hahn-Straße 6, D-44227 Dortmund, Germany.
Dalton Trans. 2022 May 17;51(19):7581-7606. doi: 10.1039/d2dt00800a.
With the aim to elaborate novel and inexpensive sulphur-rich materials featuring unusual network architectures, the coordination chemistry of the tetradentate thiaheterocycle 1,2-di(1,3-dithian-2-yl)ethane L1 ligand toward CuX and HgX salts was investigated. When L1 is reacted with CuI in a 1 : 1 ratio, a two-dimensional CP [{Cu(μ-I)Cu}(μ-L1)] (CP1) is formed, in which two out of four S atoms of L1 remain non-coordinated. Upon treatment of L1 with CuI in a 1 : 2 ratio, [{Cu(μ-I)Cu}(μ-L1)] (CP2) is obtained, in which each S atom of L1 coordinates to one copper centre forming a 2D layer. Raising the ligand-to-CuI ratio to 1 : 4 affords the 2D material [{Cu(μ-I)(μ-I)Cu}(μ-L1)] (CP3), in which [Cu(μ-I)(μ-I)Cu] ribbons are interconnected through μ-bridging L1 ligands. Upon the reaction of L1 with CuBr in a 1 : 2 ratio, a 2D CP [{Cu(μ-Br)}(μ-L1)(μ-L1)] (CP4) is formed at room temperature and a 2D CP [{Cu(μ-Br)}(μ-L1)] (CP5) is obtained in refluxing propionitrile. In CP4 and CP5 Cu atoms are bridged by a single μ-Br ligand giving rise to [Cu(μ-Br)Cu] ribbons but CP4 differs from CP5 from the metal to ligand ratio and the presence of non-coordinated S atoms. Employing a 1 : 3 ratio, a 1D ribbon [{Cu(μ-Br)}(MeCN)(μ-L1)] (CP6) is generated, that contains both tetrahedral and trigonal copper atoms. CP6 also presents two different L1 ligands that differ by the coordination mode of the sulphur atoms (S acting as 2 or as 4 electron-donor). With CuCl, a 2D network [{Cu(μ-Cl)Cu}(μ-L1)] (CP7) is generated. L1 coordinates also on HgX salts to yield CPs whose architecture depends on the ligand-to-metal ratio. The meander-shaped 1D CP [(HgI)(μ-L1)] (CP8) and the linear 1D ribbons of CP9 and CP12 [(HgX)(μ-L1)] (X = Br, Cl) result from treatment with L1 in a 1 : 1 ratio. In the case of HgBr, using a 2 : 1 metal-to-ligand ratio, 1D polymeric [{BrHg(μ-Br)HgBr}(μ-L1)] (CP10) is produced. HgI and HgBr have also been reacted with 2-methyl-1,3-dithiane L2 yielding the molecular complexes [{IHg(μ-I)HgI}(κ-L2)] (D1) and [HgBr(κ-L2)] (M1). Two heterometallic 1D materials [{IHg(μ-I)HgI(μ-I){Cu(RCN)}(μ-L1)] (CP13) and (CP14) result from the treatment of CP1 with HgI in MeCN or EtCN. Performing the reaction of CP1 with HgBr in acetonitrile produces the zwitterionic 2D material [Cu(MeCN)}(HgIBr)(μ-L1)] (CP15).
为了制备具有新颖且廉价的、具有不寻常网络结构的富硫材料,研究了四齿硫杂环1,2 - 二(1,3 - 二硫杂环戊烷 - 2 - 基)乙烷L1配体与CuX和HgX盐的配位化学。当L1与CuI以1∶1的比例反应时,形成二维配位聚合物[{Cu(μ - I)Cu}(μ - L1)] (CP1),其中L1的四个S原子中有两个保持未配位状态。当L1与CuI以1∶2的比例处理时,得到[{Cu(μ - I)Cu}(μ - L1)] (CP2),其中L1的每个S原子与一个铜中心配位形成二维层。将配体与CuI的比例提高到1∶4,得到二维材料[{Cu(μ - I)(μ - I)Cu}(μ - L1)] (CP3),其中[Cu(μ - I)(μ - I)Cu]带通过μ - 桥连L1配体相互连接。当L1与CuBr以1∶2的比例反应时,在室温下形成二维配位聚合物[{Cu(μ - Br)}(μ - L1)(μ - L1)] (CP4),在回流的丙腈中得到二维配位聚合物[{Cu(μ - Br)}(μ - L1)] (CP5)。在CP4和CP5中,Cu原子由单个μ - Br配体桥连形成[Cu(μ - Br)Cu]带,但CP4与CP5在金属与配体比例以及未配位S原子的存在方面有所不同。采用1∶3的比例,生成一维带[{Cu(μ - Br)}(MeCN)(μ - L1)] (CP6),其中包含四面体和三角铜原子。CP6还呈现出两种不同的L1配体,它们在硫原子的配位模式上有所不同(S作为2或4电子供体)。与CuCl反应,生成二维网络[{Cu(μ - Cl)Cu}(μ - L1)] (CP7)。L1也与HgX盐配位生成配位聚合物,其结构取决于配体与金属的比例。以1∶1的比例用L1处理得到蜿蜒状的一维配位聚合物[(HgI)(μ - L1)] (CP8)以及CP9和CP12的线性一维带[(HgX)(μ - L1)] (X = Br, Cl)。对于HgBr,使用2∶1的金属与配体比例,生成一维聚合物[{BrHg(μ - Br)HgBr}(μ - L1)] (CP10)。HgI和HgBr也与2 - 甲基 - 1,3 - 二硫杂环戊烷L2反应生成分子配合物[{IHg(μ - I)HgI}(κ - L2)] (D1)和[HgBr(κ - L2)] (M1)。在MeCN或EtCN中用HgI处理CP1得到两种异金属一维材料[{IHg(μ - I)HgI(μ - I){Cu(RCN)}(μ - L1)] (CP13)和(CP14)。在乙腈中使CP1与HgBr反应生成两性离子二维材料[Cu(MeCN)}(HgIBr)(μ - L1)] (CP15)。