Černá Michaela, Seed John A, Garrido Fernandez Sara, Janicke Michael T, Scott Brian L, Whitehead George F S, Gaunt Andrew J, Goodwin Conrad A P
Centre for Radiochemistry Research, Department of Chemistry, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
Chemistry Division, Los Alamos National Laboratory, Los Alamos, New Mexico, 87545, USA.
Chem Commun (Camb). 2022 Nov 29;58(95):13278-13281. doi: 10.1039/d2cc04803e.
σ-Hydrocarbyl complexes of the form [M(η-PCMe)(μ-η:η-CHPh)K(η-arene)] (M = La, Ce, Pr, U, Np, Pu; arene = benzene or toluene) were synthesised in one-pot reactions from [MI(THF)], or [U(BH)(toluene)] (M = U). All complexes were examined by multinuclear (H, C{H}, P{H}) NMR and UV-vis-NIR spectroscopy, as well as single-crystal X-ray diffraction from which molecular metal-phosphorus bonds for Np and Pu, and a σ-hydrocarbyl metal-carbon bond for Pu, have been structurally authenticated.
通过一锅法反应,由[MI(THF)]或[U(BH)(甲苯)](M = U)合成了[M(η-PCMe)(μ-η:η-CHPh)K(η-芳烃)]形式的σ-烃基配合物(M = La、Ce、Pr、U、Np、Pu;芳烃 = 苯或甲苯)。通过多核(H、C{H}、P{H})核磁共振和紫外可见近红外光谱对所有配合物进行了研究,还通过单晶X射线衍射进行了研究,从中已对Np和Pu的分子金属-磷键以及Pu的σ-烃基金属-碳键进行了结构鉴定。