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Pseudohalogen Chemistry in Ionic Liquids with Non‐innocent Cations and Anions

机译:在离子液体中的伪化学化学与非无辜阳离子和阴离子

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摘要

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 [CO3Me]−, served as starting material and enabled facile access to pseudohalide salts by reaction with Me3Si−X (X=CN, N3, OCN, SCN). Starting with the synthesized Room temperature Ionic Liquid (RT‐IL) [nBu3MeN][B(OMe)3(CN)], we were able to crystallize the double salt [nBu3MeN]2[B(OMe)3(CN)](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)2]− and the temperature labile solvate anions [CN(HCN)n]− (n=2, 3). In addition, the highly labile anionic HCN solvates were obtained from [PPN]X ([PPN]=μ‐nitridobis(triphenylphosphonium), X=N3, OCN, SCN and OCP) and HCN. Crystals of [PPN][X(HCN)3] (X=N3, OCN) and [PPN][SCN(HCN)2] 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)2]−, crystallizing as HCN disolvate [PPN][P(CN⋅HCN)2]. Furthermore, we were able to isolate the novel cyanido(halido) silicate dianions of the type [SiCl0.78(CN)5.22]2− and [SiF(CN)5]2− and the hexa‐substituted [Si(CN)6]2− by temperature controlled halide/cyanide exchange reactions. By facile neutralization reactions with the non‐innocent cation of [Et3HN]2[Si(CN)6] with MOH (M=Li, K), Li2[Si(CN)6] ⋅ 2 H2O and K2[Si(CN)6] were obtained, which form three dimensional coordination polymers. From salt metathesis processes of M2[Si(CN)6] with different imidazolium bromides, we were able to isolate new imidazolium salts and the ionic liquid [BMIm]2[Si(CN)6]. When reacting [Mes(nBu)Im]2[Si(CN)6] with an excess of the strong Lewis acid B(C6F5)3, the voluminous adduct anion {Si[CN⋅B(C6F5)3]6}2− was obtained.
机译:在2017年开始的SPP 1708“材料合成附近的材料合成”中,我们能够利用离子液体(ILS)作为反应介质和反应物合成新的阴离子物种。 ILS,携带可分解和非无罪的碳酸甲酯阴离子[CO3ME] - ,用作原料,并通过与ME3SI-X(X = CN,N3,OCN,SCN,SCN)反应使得对伪卤化物盐的容纳进入。从合成室温离子液体(RT-IL)[NBU3men] [B(OME)3(CN)],我们能够使双盐[NBU3MEN] 2 [B(OME)3(CN)]结晶。 CN)。此外,我们研究了[WCC] SCN和[WCC] CN(WCC] CN(WCC =弱协调)与其相应的质子酸HX(X = SCN,CN)的反应,从而形成[H(NCS)2] - 和温度不稳定溶剂化阴离子[Cn(HCN)N] - (n = 2,3)。此外,高度不稳定的阴离子HCN溶剂化物是从[PPN] X([PPN] =μ-Nitridobis(三苯基膦酸铵),X = N3,OCN,SCN和OCP)和HCN获得。当在低温下进行结晶时,获得[PPN] [PPN] [PPN] [x(HCN)3](X = N 3,OCN)和[PPN] [SCN(HCN(HCN)2]的晶体。有趣的是,[PPN] OCP与HCN的反应被注意到,其导致形成[P(CN)2] - ,作为HCN Disolvate [PPN] [P(CN⋅HCN)2]结晶。此外,我们能够将新的Cyanido(Halido)硅酸盐褥疮分离出[SiCl0.78(CN)5.22] 2-和[SiF(CN)5] 2-和六甲酸(CN)6 ]通过温度控制的卤化物/氰化物交换反应。通过与[Et 3 Hl] 2 [Si(CN)6]的非无辜阳离子的体内和中和反应用MOH(M = Li,K),Li2 [Si(CN)6]≥2H2O和K2 [Si(CN)得到6],形成三维配位聚合物。通过用不同的咪唑溴铵的M2 [Si(CN)6]的盐复分解方法,我们能够分离新的咪唑鎓盐和离子液体[Bmim] 2 [Si(CN)6]。当用过量的强Lewis acid酸B(C6F5)3反应[MES(NBU)IM] 2 [Si(CN)6]时,体积加合物阴离子{Si [CN⋅B(C6F5)3] 6} 2-获得了。

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