Engeldinger Eric, Armspach Dominique, Matt Dominique, Jones Peter G
Laboratoire de Chimie Inorganique Moléculaire Université Louis Pasteur, UMR 7513 CNRS 1 rue Blaise Pascal, 67008 Strasbourg Cedex, France.
Chemistry. 2003 Jul 7;9(13):3091-105. doi: 10.1002/chem.200304806.
The binding properties of two alpha-cyclodextrins, each containing two C(5)-linked "CH(2)PPh(2)" units, L 1 (A,D-substituted) and L 2 (A,C-substituted), have been investigated. Both ligands readily form transition-metal chelate complexes in which the metal centres are immobilised at the cavity entrance. Although diphosphane L 1 displays a marked tendency to behave only as a trans-spanning ligand, the ligand possesses a certain degree of flexibility, for example, allowing the stabilisation of a trigonal silver(I) complex in which the bite angle drops to 143 degrees. Another feature of L 1 concerns its ability to function as an hemilabile ligand. Together with four methoxy groups anchored onto the primary face, the two P(III) centres of L 1 form a circularly arranged P(2)O(4) 12-electron donor set able to complex an Ag(+) ion in a dynamic way, each of the four oxygen atoms coordinating successively to the silver ion. Furthermore, the particular structures of L 1 and L 2, characterised by the presence of P(III) units lying close to the cavity entrance, lead upon complexation to complexes whereby the first coordination sphere is partly entrapped in the cyclodextrin. Thus, when treated with metal chlorides, both ligands systematically produce complexes in which the Mbond;Cl unit is maintained inside the cyclodextrin through weak Cl.H-5 interactions. The chelate complex [Ag(L 1)]BF(4) reacts with acetonitrile in excess to afford a mixture of two equilibrating complexes, [Ag(acetonitrile)(L 1)]BF(4) and [Ag(acetonitrile)(2)(L 1)]BF(4), whose coordinated nitriles lie inside the cyclodextrin cavity. The inner-cavity ligands can be substituted by a benzonitrile molecule. The present study provides the first identification of an Ag(acetonitrile)(2)(phosphane)(2) ion. The unexpected stabilisation of this species probably rests on a cavity effect, the cyclodextrin walls favouring recombination of the complex after facile dissociation of the nitrile ligands.
研究了两种α-环糊精(分别含有两个通过C(5)连接的“CH(2)PPh(2)”单元)L 1(A、D取代)和L 2(A、C取代)的结合特性。两种配体都能很容易地形成过渡金属螯合物,其中金属中心固定在腔口处。尽管二膦配体L 1表现出明显的仅作为跨桥配体的倾向,但该配体具有一定程度的灵活性,例如,能稳定一种三角银(I)配合物,其咬合角降至143度。L 1的另一个特点是其作为半不稳定配体的功能。L 1的两个P(III)中心与锚定在主面上的四个甲氧基一起形成一个呈圆形排列的P(2)O(4) 12电子供体组,能够以动态方式络合一个Ag(+)离子,四个氧原子中的每一个依次与银离子配位。此外,L 1和L 2的特殊结构,其特征是P(III)单元靠近腔口,在络合后形成配合物,其中第一配位层部分被困在环糊精中。因此,当用金属氯化物处理时,两种配体都能系统地生成配合物,其中M—Cl单元通过弱的Cl…H-5相互作用保持在环糊精内部。螯合物[Ag(L 1)]BF(4)与过量乙腈反应,得到两种处于平衡状态的配合物[Ag(乙腈)(L 1)]BF(4)和[Ag(乙腈)₂(L 1)]BF(4)的混合物,其配位腈位于环糊精腔内。腔内配体可被苯甲腈分子取代。本研究首次鉴定出Ag(乙腈)₂(膦)₂离子。该物种意外的稳定性可能取决于腔效应,环糊精壁有利于腈配体容易解离后配合物的重组。