首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Nanocluster formation and stabilization fundamental studies: Investigating 'solvent-only' stabilization en route to discovering stabilization by the traditionally weakly coordinating anion BF4- plus high dielectric constant solvents
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Nanocluster formation and stabilization fundamental studies: Investigating 'solvent-only' stabilization en route to discovering stabilization by the traditionally weakly coordinating anion BF4- plus high dielectric constant solvents

机译:纳米团簇的形成和稳定化基础研究:研究“纯溶剂”稳定化方法,以通过传统上弱配位的阴离子BF4-和高介电常数溶剂发现稳定剂

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摘要

The nanocluster literature contains a wide variety of nanocluster stabilizing agents. In addition to the plethora of putative stabilizing additives, 12 claims appear of "solvent- only" stabilization of transition-metal nanoclusterssa hypothesis that is tested for the first time as part of the present studies. When the two main modes of nanocluster stabilization, electrostatic and steric are considered, "solvent- only" stabilization can only be steric (i.e., is not electrostatic). Solvent-only stabilization would, therefore, require that a strongly coordinated, perhaps even kinetically nonlabile, solvent be present on the nanocluster surface. Hence, an investigation has been conducted into potential sources for the stabilization of prototype Ir(0)(n) transition-metal nanoclusters prepared from [(1,5-COD)Ir(CH3CN)(2)][BF4] in five different solvents, with a special focus on the formulation and testing of alternative hypotheses regarding the true source of the nanocluster stabilization in putative solvent-only stabilization conditions. Seven total hypotheses are tested with five being initially ruled out; they are, namely, stabilization by (i) trace chloride (ii), surface hydrides, (iii) scavenged charge, (iv) solvent oxidative addition reactions with the nanocluster surface, or (v) polymerized solvent. This led in turn to two additional main alternative hypotheses: (vi) nanocluster surface ligation by highdonor number solvents (i.e., in the absence of anions) and (vii) nanocluster stabilization by surface-coordination of the traditionally weakly coordinating anion BF4-. Our results reveal a significant contribution to nanocluster stability from the traditionally weakly coordinating BF4- in high dielectric constant solvents, such as propylene carbonate. Literature claims of solvent-only nanocluster stabilization are not supported by our findings. Overall, DLVO (Derjaugin- Landau-Verwey-Overbeek) theory of colloidal stability is supported and found to apply to even traditionally weakly coordinating anions.
机译:纳米簇文献包含各种各样的纳米簇稳定剂。除了过多的可能的稳定添加剂外,还有12项声称是过渡金属纳米团簇假说的“仅溶剂”稳定化研究,该假说作为本研究的一部分进行了首次测试。当考虑纳米团簇稳定化的两种主要模式时,静电和空间位阻,“仅溶剂”稳定化只能是空间位阻(即,不是静电的)。因此,仅溶剂稳定化将需要在纳米簇表面上存在强烈配位的,甚至在动力学上不稳定的溶剂。因此,已经对由[[1,5-COD] Ir(CH3CN)(2)] [BF4]制备的五种不同形式的原型Ir(0)(n)过渡金属纳米簇的稳定来源进行了研究。溶剂,特别是关于在假定的仅溶剂稳定条件下纳米簇稳定的真正来源的替代假设的制定和测试。共检验了七个假设,其中五个被初步排除。它们是通过(i)痕量氯化物(ii),表面氢化物,(iii)清除的电荷,(iv)与纳米簇表面的溶剂氧化加成反应或(v)聚合的溶剂来稳定化。这又导致了另外两个主要的替代假设:(vi)通过高供体数溶剂(即,在没有阴离子的情况下)进行纳米团簇表面连接,以及(vii)通过传统上弱配位的阴离子BF4-的表面配位来稳定纳米团簇。我们的结果表明,在高介电常数溶剂(例如碳酸亚丙酯)中,传统上弱配位的BF4-对纳米簇的稳定性有重要贡献。我们的发现不支持仅溶剂型纳米簇稳定化的文献主张。总体而言,DLVO(Derjaugin-Landau-Verwey-Overbeek)胶体稳定性理论得到了支持,并被发现甚至适用于传统上弱配位的阴离子。

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