Platts James A, Kariuki Benson M, Newman Paul D
School of Chemistry, Cardiff University, Cardiff CF10 3AT, UK.
Molecules. 2024 Mar 5;29(5):1150. doi: 10.3390/molecules29051150.
The controlled formation of mixed-metal bimetallics was realised through use of a -[Re(CO)(,'-bpy-P)Cl] complex bearing an exogenous 2,4,6-trioxa-1,3,5,7-tetramethyl-8-phosphaadamantane donor at the 5-position of the bpy. The introduction of gold, silver, and rhodium with appropriate secondary ligands was readily achieved from established starting materials. Restricted rotation about the C-P bond was observed in several of the bimetallic complexes and correlated with the relative steric bulk of the second metal moiety. Related chemistry with the 6-substituted derivative proved more limited in scope with only the bimetallic Re/Au complex being isolated.
通过使用一种在联吡啶(bpy)的5位带有外源2,4,6-三氧杂-1,3,5,7-四甲基-8-磷金刚烷供体的-[Re(CO)(′-bpy-P)Cl]配合物,实现了混合金属双金属的可控形成。从已有的起始原料中很容易引入带有适当二级配体的金、银和铑。在几种双金属配合物中观察到围绕C-P键的旋转受限,并且这与第二种金属部分的相对空间体积相关。事实证明,与6-取代衍生物的相关化学在范围上更有限,仅分离出了双金属Re/Au配合物。