کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1327582 | 977490 | 2006 | 8 صفحه PDF | دانلود رایگان |

A new class of Salpen analogues based on phosphorus derivatives where the classical alkylene backbone has been replaced by a N–P–N linkage is described. Such linkage both affords a very good stability in water and an additional (fifth) potentially complexing site. The classical ortho-OH groups have been also replaced by various ortho-substituents, including diphenylphosphino groups. The synthesis of these compounds is easy and their structure can be varied at will at several levels. Several ways of synthesis can be used to combine the various fragments constituting these Salpen analogues. The structure of one of these fragments, an azide, was determined by X-ray crystallography. A preliminary study of the complexation ability of some of these new ligands was carried out with groups 10 (Ni) and 11 (Au) elements. Depending on the type of substituents and the type of metals used, these compounds can act as mono-, or tetra-dentate ligands.
The synthesis of a new class of Salpen analogues based on phosphorus derivatives is described. Their structure can be easily varied at will, to afford a variety of ligands, possessing up to five complexing sites. Depending on the type of substituents Z and the type of metals used (groups 10 and 11 elements), these compounds can act as mono-, or tetra-dentate ligands.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 691, Issue 7, 15 March 2006, Pages 1333–1340