Boar Paul, Streitberger Markus, Lönnecke Peter, Hey-Hawkins Evamarie
Faculty of Chemistry and Mineralogy, Institute of Inorganic Chemistry, Universität Leipzig , Johannisallee 29, D-04103 Leipzig, Germany.
Inorg Chem. 2017 Jun 19;56(12):7285-7291. doi: 10.1021/acs.inorgchem.7b01046. Epub 2017 Jun 1.
Two bis-phospholane copper(I) metallamacrocycles were selectively synthesized starting from the same two building blocks, namely, ligand 1 and [Cu(NCCH)]BF. Reaction conditions (ligand:metal (L:M) ratio and dilution) can be tuned to obtain either a paddle-wheel- (2, L:M = 3:2) or box-type complex (3, L:M = 8:4). Their structures were unequivocally determined by X-ray crystallography. The solution P{H} NMR spectrum of complex 2 consists of a broad signal, as is common for such complexes, whereas complex 3 shows splitting of the P{H} NMR signal into a pseudoquartet due to Cu-P coupling, a rare occurrence exhibited only by highly symmetrical copper(I) phosphine complexes.
从相同的两个结构单元,即配体1和[Cu(NCCH)]BF开始,选择性地合成了两种双膦烷铜(I)金属大环化合物。反应条件(配体:金属(L:M)比例和稀释度)可以调节,以获得桨轮型(2,L:M = 3:2)或盒型配合物(3,L:M = 8:4)。它们的结构通过X射线晶体学明确确定。配合物2的溶液³¹P{¹H} NMR谱由一个宽信号组成,这对于此类配合物来说是常见的,而配合物3由于Cu-P耦合,³¹P{¹H} NMR信号分裂为一个伪四重峰,这种情况仅在高度对称的铜(I)膦配合物中罕见出现。