作者: Eric J. Chan , Simon A. Cotton , Jack M. Harrowfield , Brian W. Skelton , Alexandre N. Sobolev
DOI: 10.1071/CH19130
关键词: Crystallography 、 Supramolecular chemistry 、 Picrate 、 Denticity 、 Solvation 、 Coordination sphere 、 Coordination number 、 Ligand 、 Chemistry 、 Ionic liquid
摘要: Addition of various oxygen-donor ligands (L, all dipolar, aprotic solvents), to a solution hydrated scandium picrate in weakly coordinating solvents (S), has yielded several crystalline adducts the form Sc(pic)3(L)m(·nS) which L are coordinated, subsequently characterised by series single crystal X-ray studies. For L = dmso, m = 3 and anions bound as phenoxide-O donor units, while for nmp, dma, tmp, hmpa, m = 2 one picrates becomes bidentate through phenoxide- nitro-O donation. L = ompa, two is displaced from primary coordination sphere. All complexes contain six-coordinate ScIII, confirming that this number consequence ligand bulk.