357980-96-2Relevant academic research and scientific papers
Cationic indium alkyl complexes incorporating aminotroponiminate ligands
Delpech, Fabien,Guzei, Ilia A.,Jordan, Richard F.
, p. 1167 - 1176 (2008/10/08)
The synthesis and structures of indium complexes incorporating the bidentate monoanionic ligand N,N′-diisopropylaminotroponiminate (iPr2-ATI) are described. The reaction of InCl3 with Li[iPr2-ATI] yields (iPr2-ATI)InCl2 (3), which is converted to (iPr2-ATI)InMe2 (4) by reaction with MeLi; 4 is also formed by the reaction of InMe3 with (iPr2-ATI)H. The reaction of 4 with [Ph3C] [B(C6F5)4] at 23 °C yields the diimine complex [{1,2-(NiPr)2-5-CPh3-cyclohepta-3,6-diene}InMe 2] [B(C6F5)4] (5) via addition of Ph3C- to the C5 carbon of 4. Thermolysis of 5 (75 °C) yields [(iPr2-ATI)InMe] [B(C6F5)4] (6) and Ph3CMe. 6 was isolated as the chlorobenzene solvate 6·PhCl. An X-ray diffraction study shows that there are two independent cations in the asymmetric unit of 6·PhCl. One cation (In(1)) is ion-paired with two B(C6F5)4- anions, while the second cation is complexed with two PhCl molecules and is disordered between two equally occupied positions (In(2) and In(3)). Dative In-ClPh bonding and PhCl/ATI π-stacking interactions contribute to the PhCl coordination in 6·PhCl. The reaction of 4 with B(C6F5)3 yields [(iPr2-ATI)InMe] [MeB(C6F5)3] (7), which decomposes slowly at 23 °C by C6F5- transfer reactions. The reaction of 4 with [HNMe2Ph] [B(C6F5)4] yields the labile amine adduct [(iPr2-ATI)In(Me)(NMe2Ph)] [B(C6F5)4] (10).
