Heinl Sebastian, Balázs Gábor, Bodensteiner Michael, Scheer Manfred
University of Regensburg, Universitätsstr. 31, 93040 Regensburg, Germany.
Dalton Trans. 2016 Feb 7;45(5):1962-6. doi: 10.1039/c5dt01750e. Epub 2015 Jun 22.
The use of the highly sterically demanding Cp(BIG) ligand (Cp(BIG) = C5(4-nBuC6H4)5) and white phosphorus (P4) enables the synthesis of new P-rich derivatives of the rare Pn ligand complexes of manganese. The obtained complexes, [{Cp(BIG)Mn}2(μ,η(5:5)-P5)] (2) and [{Cp(BIG)Mn}2(μ,η(2:2)-P2)2] (3), exhibit the highest number of P atoms in this class of manganese compounds identified by X-ray structure analyses. The EPR spectrum of the 29 VE triple-decker complex 2 shows one unpaired electron coupling with two 5/2 spin Mn nuclei.
使用空间位阻要求很高的Cp(BIG)配体(Cp(BIG) = C5(4-nBuC6H4)5)和白磷(P4)能够合成锰的稀有Pn配体配合物的新型富磷衍生物。所得到的配合物[{Cp(BIG)Mn}2(μ,η(5:5)-P5)](2)和[{Cp(BIG)Mn}2(μ,η(2:2)-P2)2](3),通过X射线结构分析确定,在这类锰化合物中具有最多的磷原子。29价电子三层夹心配合物2的电子顺磁共振谱显示一个未成对电子与两个5/2自旋的锰核耦合。