Department of Chemistry, Indian Institute of Technology Bombay, Mumbai 400076, India.
Dalton Trans. 2018 Jul 10;47(27):9114-9127. doi: 10.1039/c8dt01148f.
The transmetalation reactions of a mercury precursor, [Pentyl(N^C^N)HgCl] (19), with selenium halides (SeCl4, SeBr4, and SeCl2) were attempted to obtain the corresponding organoselenium trichloride [Pentyl(N^C^N)SeCl3], tribromide [Pentyl(N^C^N)SeBr3], and monochloride [Pentyl(N^C^N)SeCl], respectively [(N^C^N) = 5-tert-butyl-1,3-bis-(N-pentyl-benzimidazol-2'-yl)phenyl]. However, in all the cases, a very facile ionization of the Se-halogen bond was observed leading to the isolation of a new class of air stable arylselenium(ii) complexes: [Pentyl(N^C^N)Se+]2[HgCl4]2- (20) and [Pentyl(N^C^N)Se+]2[HgBr4]2- (21). This is the first report on the formation of NCN pincer-based arylselenium(ii) cations via the transmetalation route. Similar reactions were further investigated with several tellurium precursors: {TeCl4, TeBr4 and TeI2} which resulted in the formation of analogous aryltellurium(ii) complexes: [Pentyl(N^C^N)Te+]2[HgCl4]2- (22), [Pentyl(N^C^N)Te+][Cl]- (23), [Pentyl(N^C^N)Te+]2[HgBr4]2- (24), [Pentyl(N^C^N)Te+][Br]- (25) and [Pentyl(N^C^N)Te+]4[Hg2Cl4.72I3.28]4- (26). These are only the second set of examples of aryltellurium cations (hypervalent 10-Te-3 species) with the NCN pincer-based ligand, characterised by X-ray crystallographic studies. The crystallographic studies show a strong SeN/TeN intramolecular interaction, which is confirmed by NBO calculations suggesting the donation of a lone pair of electrons on nitrogen to a lone p-vacancy on selenium/tellurium atoms. The analysis based on NPA derived charges indicates that the contribution of SeN interactions to the electrostatic stabilization energy is in the range of 40-60%, whereas TeN interactions have a contribution of about 84% and more, attributed to the differences in the electronegativity of selenium and tellurium. Furthermore, the formation of arylselenium(ii) and aryltellurium(ii) complexes was favoured due to the presence of the σ-hole on the Se/Te centres.
该汞前体[戊基(N^C^N)HgCl](19)与硒卤化物(SeCl4、SeBr4和 SeCl2)的transmetalation 反应试图获得相应的有机硒三氯化物[戊基(N^C^N)SeCl3]、三溴化物[戊基(N^C^N)SeBr3]和一氯化物[戊基(N^C^N)SeCl],分别为[(N^C^N)=5-叔丁基-1,3-双-(N-戊基-苯并咪唑-2'-基)苯基]。然而,在所有情况下,硒卤键都非常容易发生离解,导致一种新型的空气稳定的芳基硒(ii)配合物的分离:[戊基(N^C^N)Se+]2[HgCl4]2-(20)和[戊基(N^C^N)Se+]2[HgBr4]2-(21)。这是首次通过transmetalation 途径形成基于 NCN 钳形的芳基硒(ii)阳离子的报道。用几种碲前体进一步研究了类似的反应:{TeCl4、TeBr4 和 TeI2},结果形成了类似的芳基碲(ii)配合物:[戊基(N^C^N)Te+]2[HgCl4]2-(22)、[戊基(N^C^N)Te+][Cl]-(23)、[戊基(N^C^N)Te+]2[HgBr4]2-(24)、[戊基(N^C^N)Te+][Br]-(25)和[戊基(N^C^N)Te+]4[Hg2Cl4.72I3.28]4-(26)。这些只是第二组基于 NCN 钳形配体的芳基碲阳离子(高氧化态 10-Te-3 物种)的例子,通过 X 射线晶体学研究得到了证实。晶体学研究表明存在强烈的 SeN/TeN 分子内相互作用,这通过 NBO 计算得到了证实,表明氮上的孤对电子向硒/碲原子上的孤对空穴转移。基于 NPA 衍生电荷的分析表明,SeN 相互作用对静电稳定能的贡献在 40-60%范围内,而 TeN 相互作用的贡献约为 84%,甚至更高,这归因于硒和碲的电负性差异。此外,由于 Se/Te 中心存在σ-hole,芳基硒(ii)和芳基碲(ii)配合物的形成更有利。