George Tanner, Grant Tamika, Munhoz Isadora Schumann, Do Thai, Masuda Jason D
Department of Chemistry, Saint Mary's University, Halifax, Nova Scotia, Canada B3H 3C3.
Dalton Trans. 2024 Aug 6;53(31):13107-13118. doi: 10.1039/d4dt01561d.
A new triazene ligand was prepared by the reaction of the bulky aryl azide, TerMesN, (2,6-bis(2,4,6-trimethylphenyl)phenyl azide), with the bulky N-heterocyclic carbene (NHC), SIPr (,'-2,6-bis(diisopropylphenyl)-3,4-dihydroimidazol-2-ylidene). The steric bulk of these two groups leads to perpendicular bonding of the NHC-N plane and the aryl group which provides immense steric crowding around the triazene core. The corresponding π-conjugated triazene ligand was utilized as a neutral, monodentate ligand which results in monomeric Cu(I)Cl, Ag(I)OTf, and Au(I)Cl complexes. Instability of the π-conjugated triazene Au(I)Cl complex was observed, even under inert conditions. When dissolved and photolyzed in THF with workup in isopropanol, the compound decomposes forming [(SIPrNH)Au(I)][Au(I)Cl] a relatively stable compound to light, moisture, and water - alongside the formation of gold nanoparticles which were characterized using scanning electron microscopy with energy dispersive spectroscopy.
通过大位阻芳基叠氮化物TerMesN(2,6-双(2,4,6-三甲基苯基)苯基叠氮化物)与大位阻N-杂环卡宾(NHC)SIPr(1,3-双(2,6-二异丙基苯基)-3,4-二氢咪唑-2-亚基)反应制备了一种新型三氮烯配体。这两个基团的空间位阻导致NHC-N平面与芳基垂直键合,在三氮烯核心周围产生巨大的空间拥挤。相应的π共轭三氮烯配体用作中性单齿配体,得到单体Cu(I)Cl、Ag(I)OTf和Au(I)Cl配合物。即使在惰性条件下,也观察到π共轭三氮烯Au(I)Cl配合物的不稳定性。当在四氢呋喃中溶解并光解,然后在异丙醇中后处理时,该化合物分解形成[(SIPrNH)Au(I)][Au(I)Cl],一种对光、湿气和水相对稳定的化合物,同时形成金纳米颗粒,使用扫描电子显微镜和能量色散光谱对其进行了表征。