作者: Kjetil Andreas Netland , Alexander Krivokapic , Mats Tilset
DOI: 10.1080/00958972.2010.505648
关键词: Medicinal chemistry 、 Ligand 、 Substituent 、 Chemistry 、 Carbene 、 Diimine 、 Imine 、 Moiety 、 Trans effect 、 Photochemistry 、 Protonolysis
摘要: A series of new L2PtMe2 and L2PtPh2 complexes have been prepared, where L2 = chelating diimine or NHC iminocarbene ligands with similar substituent patterns. These investigated by 1H- 13C-NMR spectroscopy single-crystal X-ray structure determinations to assess differences between the two ligand systems. All three approaches underscore strong trans influence N-heterocyclic carbene moiety relative imine group. This is supported trends in J(195Pt–H) J(195Pt–C) coupling constants hydrocarbyl NMR resonances as well Pt–ligand bond distances moieties. paralleled a clear effect protonolysis; treatment Pt(II) dimethyl diphenyl acid causes elimination methane benzene, respectively, selective loss methyl phenyl groups from position part ligand.