Arlt Sören, Bläsing Kevin, Harloff Jörg, Laatz Karoline Charlotte, Michalik Dirk, Nier Simon, Schulz Axel, Stoer Philip, Stoffers Alrik, Villinger Alexander
Anorganische Chemie, Institut fur Chemie, Universität Rostock, A.-Einstein-Str. 3a, 18059, Rostock, Germany.
Anorganische Chemie, Institut für Chemie, Philipps-Universität Marburg, Hans-Meerwein-Straße 4, 35032, Marburg, Germany.
ChemistryOpen. 2021 Feb;10(2):62-71. doi: 10.1002/open.202000252. Epub 2020 Nov 10.
Within the second funding period of the SPP 1708 "Material Synthesis near Room Temperature",which started in 2017, we were able to synthesize novel anionic species utilizing Ionic Liquids (ILs) both, as reaction media and reactant. ILs, bearing the decomposable and non-innocent methyl carbonate anion [CO Me] , served as starting material and enabled facile access to pseudohalide salts by reaction with Me Si-X (X=CN, N , OCN, SCN). Starting with the synthesized Room temperature Ionic Liquid (RT-IL) [nBu MeN][B(OMe) (CN)], we were able to crystallize the double salt [nBu MeN] B(OMe) (CN). Furthermore, we studied the reaction of [WCC]SCN and [WCC]CN (WCC=weakly coordinating cation) with their corresponding protic acids HX (X=SCN, CN), which resulted in formation of [H(NCS) ] and the temperature labile solvate anions [CN(HCN) ] (n=2, 3). In addition, the highly labile anionic HCN solvates were obtained from [PPN]X ([PPN]=μ-nitridobis(triphenylphosphonium), X=N , OCN, SCN and OCP) and HCN. Crystals of [PPN][X(HCN) ] (X=N , OCN) and [PPN][SCN(HCN) ] were obtained when the crystallization was carried out at low temperatures. Interestingly, reaction of [PPN]OCP with HCN was noticed, which led to the formation of [P(CN) ] , crystallizing as HCN disolvate [PPN][P(CN⋅HCN) ]. Furthermore, we were able to isolate the novel cyanido(halido) silicate dianions of the type [SiCl (CN) ] and [SiF(CN) ] and the hexa-substituted [Si(CN) ] by temperature controlled halide/cyanide exchange reactions. By facile neutralization reactions with the non-innocent cation of [Et HN] [Si(CN) ] with MOH (M=Li, K), Li [Si(CN) ] ⋅ 2 H O and K [Si(CN) ] were obtained, which form three dimensional coordination polymers. From salt metathesis processes of M [Si(CN) ] with different imidazolium bromides, we were able to isolate new imidazolium salts and the ionic liquid [BMIm] [Si(CN) ]. When reacting [Mes(nBu)Im] [Si(CN) ] with an excess of the strong Lewis acid B(C F ) , the voluminous adduct anion {Si[CN⋅B(C F ) ] } was obtained.
在2017年开始的德国科学基金会优先项目1708“近室温材料合成”的第二个资助期内,我们能够利用离子液体(ILs)作为反应介质和反应物来合成新型阴离子物种。带有可分解且非惰性碳酸甲酯阴离子[CO₂Me]的离子液体用作起始原料,并通过与Me₃Si - X(X = CN、N₃、OCN、SCN)反应,方便地制备出拟卤化物盐。从合成的室温离子液体(RT - IL)[nBu₃MeN][B(OMe)₂(CN)]出发,我们成功结晶出复盐[nBu₃MeN]₂B(OMe)₂(CN)。此外,我们研究了[WCC]SCN和[WCC]CN(WCC = 弱配位阳离子)与它们相应质子酸HX(X = SCN、CN)的反应,反应生成了[H(NCS)₂]和温度不稳定的溶剂化阴离子[CN(HCN)ₙ](n = 2、3)。另外,通过[PPN]X([PPN]=μ - 氮杂双(三苯基鏻),X = N₃、OCN、SCN和OCP)与HCN反应得到了高活性的阴离子HCN溶剂化物。当在低温下进行结晶时,得到了[PPN][X(HCN)ₙ](X = N₃、OCN)和[PPN][SCN(HCN)₃]的晶体。有趣的是,观察到[PPN]OCP与HCN的反应,该反应生成了[P(CN)₆]³⁻,以HCN二溶剂化物[PPN][P(CN⋅HCN)₃]形式结晶。此外,通过温度控制的卤化物/氰化物交换反应,我们能够分离出[SiCl₂(CN)₂]²⁻和[SiF(CN)₅]²⁻类型的新型氰基(卤代)硅酸盐二阴离子以及六取代的[Si(CN)₆]⁴⁻。通过用[Et₃HN]₂[Si(CN)₆]的非惰性阳离子与MOH(M = Li、K)进行简便的中和反应,得到了Li₂[Si(CN)₆]⋅2H₂O和K₂[Si(CN)₆],它们形成三维配位聚合物。通过M₂[Si(CN)₆]与不同咪唑鎓溴化物的盐复分解过程,我们能够分离出新的咪唑鎓盐和离子液体[BMIm]₂[Si(CN)₆]。当[Mes(nBu)Im]₂[Si(CN)₆]与过量的强路易斯酸B(C₆F₅)₃反应时,得到了体积庞大的加合物阴离子{Si[CN⋅B(C₆F₅)₃]₃}⁻。