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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Combining covalent bonding and electrostatic attraction to achieve highly viable species with ultrashort beryllium-beryllium distances: a computational design
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Combining covalent bonding and electrostatic attraction to achieve highly viable species with ultrashort beryllium-beryllium distances: a computational design

机译:结合共价粘合和静电吸引力,实现高度可行的物种,具有超短铍 - 铍距离:计算设计

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摘要

Though ultrashort metal-metal distances (USMMD, d(M-M) 1.900 angstrom) were primarily realized between transition metals, USMMDs between main group metal atoms such as beryllium atoms have also been designed previously using two strategies: (1) formation of multiple bonding orbitals or (2) having favourable electrostatic attraction. We recently turned our attention to the reported species IH Be2H2 IH (where IH denotes imidazol-2-ylidene) because the orbital energy level of its -type HOMO is noted to be very high, which may result in intrinsic instability. In the present study, we combined the abovementioned strategies to solve the high orbital energy level problem without losing the ultrashort Be-Be distances. It was found that breaking of such -type HOMO by addition of a -CH2- group onto the bridging position of two beryllium atoms led to the formation of IH Be2H2CH2 IH species, which not only possesses an ultrashort Be-Be distance in the -Be2H2CH2- moiety, but also has a relatively low HOMO energy level. Replacing the IH ligands with NH3 and PH3 resulted in the formation of NH3 Be2H2CH2 NH3 and PH3 Be2H2CH2 PH3 species with similar features. The electronic structure analyses suggest that the ultrashort Be-Be distances in these species are achieved by the combined effects of the formation of two Be-H-Be 3c-2e bonds and having favourable Coulombic attractions between the carbon atom of the -CH2- group and two beryllium atoms. Remarkably, when the IH, NH3, and PH3 ligands were replaced by large ligands with bulky groups, such as 1,3-bis(2,6-diisopropyl phenyl)imidazol-2-ylidene (IDip), triphenylamine (NPh3), and triphenylphoshpine (PPh3), respectively, the resultant species IDip Be2H2CH2 IDip, NPh3 Be2H2CH2 NPh3, and PPh3 Be2H2CH2 PPh3 exhibit good steric protection around the -Be2H2CH2- core. These species are thus examples for the experimental realization of species with ultrashort metal-metal distances between main group metals.
机译:虽然超短金属 - 金属的距离(USMMD,d(mm)及LT; 1.900埃)的过渡金属之间进行初步实现,主族金属原子之间USMMDs如铍原子也已经先前使用两种策略设计:多个(1)形成具有有利的静电引力键轨道或(2)。最近,我们把我们的关注报道物种IH Be2H2 IH(其中IH表示咪唑-2-叉),因为它的型HOMO的轨道能量水平注意到是非常高的,这可能导致内在的不稳定性。在本研究中,我们结合上述战略,以解决高轨道能级问题不失超短BE-要距离。结果发现,通过添加-CH 2 - 基团的上导致形成IH Be2H2CH2 IH种,其中不仅具有超短待要在-Be2H2CH2距离的两个铍原子的桥接位置打破这种型HOMO的 - 部分,而且还具有较低的HOMO能级。更换IH配体与NH 3和PH3导致NH 3 NH 3 Be2H2CH2和PH3 Be2H2CH2 PH3物种具有类似特征的形成。电子结构的分析表明,该超短BE-在这些物种距离由两个BE-H-3C成为-2E键的形成的综合影响,取得具有-CH 2 - 基团的碳原子之间的有利库仑景点和两个铍原子。值得注意的是,当IH,NH 3,和PH3的配体是由大的配体与大体积基团,替换为诸如1,3-双(2,6-二异丙基苯基)咪唑-2-亚基(IDIP),三苯胺(NPH3),和triphenylphoshpine(PPH 3),分别将所得物种IDIP Be2H2CH2 IDIP,NPH3 Be2H2CH2 NPH3,和PPh 3 Be2H2CH2 PPH3呈现围绕-Be2H2CH2-芯好位阻保护作用。这些物质,因此可用于实验实现物种的与主族金属之间超短金属 - 金属的距离的例子。

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    Shanxi Univ Inst Mol Sci Key Lab Mat Energy Convers &

    Storage Shanxi Prov Taiyuan 030006 Shanxi Peoples R China;

    Chinese Acad Sci Inst Coal Chem State Key Lab Coal Convers Taiyuan 030001 Shanxi Peoples R China;

    Shanxi Univ Inst Mol Sci Key Lab Mat Energy Convers &

    Storage Shanxi Prov Taiyuan 030006 Shanxi Peoples R China;

    Shanxi Univ Inst Mol Sci Key Lab Mat Energy Convers &

    Storage Shanxi Prov Taiyuan 030006 Shanxi Peoples R China;

    Shanxi Univ Inst Mol Sci Key Lab Mat Energy Convers &

    Storage Shanxi Prov Taiyuan 030006 Shanxi Peoples R China;

    Chinese Acad Sci Inst Coal Chem State Key Lab Coal Convers Taiyuan 030001 Shanxi Peoples R China;

    Chinese Acad Sci Inst Coal Chem State Key Lab Coal Convers Taiyuan 030001 Shanxi Peoples R China;

    Shanxi Univ Inst Mol Sci Key Lab Mat Energy Convers &

    Storage Shanxi Prov Taiyuan 030006 Shanxi Peoples R China;

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  • 正文语种 eng
  • 中图分类 化学 ; 无机化学 ;
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