کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1325280 | 1499945 | 2009 | 5 صفحه PDF | دانلود رایگان |

New phosphenium cations stabilized by bidentate monoanionic N-isopropyl-2-(isopropylamino)troponiminate or 2-(isopropylamino)troponate units have been synthesized. These complexes were characterized by 31P, 1H and 13C NMR spectroscopies, and the molecular structures were determined by X-ray crystallography. These data indicate the formation of N,N′- and N,O-chelate derivatives having three-coordinate phosphorous atoms included in planar heterobicycles. Moreover, computational studies support the presence of high delocalization of the positive charge into the π-conjugated carbon backbone and of the high-lying phosphorus lone-pair orbital.
The syntheses and characterization of phosphenium cations stabilized by bidentate monoanionic N-isopropyl-2-(isopropylamino)troponate and 2-(isopropylamino)troponate ligands are presented. X-ray diffraction and computational studies support the existence of high delocalization of the positive charge into the π-conjugated carbon backbone.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 694, Issues 9–10, 15 April 2009, Pages 1562–1566