Kar Ketaki, Kar Sourav, Ghosh Sundargopal
Department of Chemistry, Indian Institute of Technology Madras Chennai 600036 India
Chem Sci. 2024 Feb 7;15(11):4179-4186. doi: 10.1039/d3sc06464f. eCollection 2024 Mar 13.
Since the pioneering electron counting rule for borane clusters was proposed by Wade, the structures and bonding of boron clusters and their derivatives have been elegantly rationalised. However, this rule and its modified versions faced problems explaining the electronic structures of less spherical deltahedra, unlike the core geometries of borate dianions [BH] ( = 6-12). Herein, we report the isolation of a series of osmaborane clusters [(CpOs)BH], 1-5, ( = 6-10) by the thermolysis of an generated intermediate, obtained from the rapid condensation of [CpOsBr] and [LiBH·THF], with [BH·THF] or [BH·SMe]. Interestingly, all these clusters show unusual less spherical deltahedral shapes that can be generated from canonical [BH] ( = 8-12) shapes by doing diamond-square-diamond (DSD) rearrangements. The DSD rearrangements led to the generation of higher degree vertices, which are occupied by Os atoms and also generated Os-Os bonds in these clusters. Theoretical calculations revealed that these CpOs⋯OsCp interactions in clusters 1-5 played a crucial role in their structural shape and electron count. These less spherical deltahedral clusters are rare, and most significantly, clusters 1-5 with (-1) skeleton electron pairs (SEPs) do not follow Wade-Mingos electron counting rules and can be classified as hypoelectronic clusters.
自从韦德提出硼烷簇合物的开创性电子计数规则以来,硼簇合物及其衍生物的结构和键合已得到精妙的阐释。然而,与硼酸盐二价阴离子[BH](= 6 - 12)的核心几何结构不同,该规则及其修改版本在解释不太规则的多面体的电子结构时面临问题。在此,我们报告了通过热解一种生成的中间体来分离一系列锇硼烷簇合物[(CpOs)BH],1 - 5(= 6 - 10),该中间体是由[CpOsBr]和[LiBH·THF]与[BH·THF]或[BH·SMe]快速缩合得到的。有趣的是,所有这些簇合物都呈现出不寻常的不太规则的多面体形状,这些形状可通过菱形 - 方形 - 菱形(DSD)重排从标准的[BH](= 8 - 12)形状生成。DSD重排导致产生更高价的顶点,这些顶点由Os原子占据,并且在这些簇合物中还生成了Os - Os键。理论计算表明,簇合物1 - 5中的这些CpOs⋯OsCp相互作用在其结构形状和电子计数中起着关键作用。这些不太规则的多面体簇合物很罕见,最重要的是,具有(-1)骨架电子对(SEP)的簇合物1 - 5不遵循韦德 - 明戈斯电子计数规则,可归类为贫电子簇合物。