507264-46-2Relevant academic research and scientific papers
Organo-rare-earth complexes supported by chelating diamide ligands
Estler, Frank,Eickerling, Georg,Herdtweck, Eberhardt,Anwander, Reiner
, p. 1212 - 1222 (2008/10/08)
The synthesis of a series of heteroleptic ate-complex-free rare-earth(III) diamide complexes by alkane and amine elimination reactions, starting from Ln(CH2SiMe3)3(THF)2 and Ln-(NiPr2)3(THF)x (x = 1, Ln = Sc, Lu; x = 2, Ln = Y), respectively, is described. 2,6-Bis(((2,6-diisopropylphenyl)amino)methyl)pyridine (H2BDPPpyr) formed monomeric complexes of the types (BDPPpyr)Ln(CH2SiMe3)(THF)x (x = 1, Ln = Sc, Lu; x = 2, Ln = Y) and (BDPPpyr)-Ln(NiPr2)(THF) (Ln = Sc, Lu), which display enhanced stability for the smaller metal center scandium, for diisopropylamide coordination, and in donor solvents such as THF. Conversion of the silylalkyl complexes into their amide derivatives via secondary alkane elimination, i.e., reaction with HNEt2 and HN(SiHMe2)2, increased the complex stability. The mono-THF adduct complexes (BDPPpyr)Sc(L)(THF) show a nonfluxional structure in solution, which contrasts the dynamic behavior of the corresponding bis-THF adduct complexes of the larger elements lutetium and yttrium. Sterically less encumbered 2,6-bis((mesitylamino)-methyl)pyridine (H2BMespyr) gave the less stable complexes (BMespyr)Ln(CH2SiMe3)(THF)x (x = 1, Ln = Sc; x = 2, Ln = Lu; the Y derivative could not be isolated). Again, subsequent silylalkyl/silylamide ligand exchange gave the complexes (BMespyr)Ln[N(SiHMe2)2](THF), exhibiting considerably increased stability. The complexes (BDPPoxyl)Ln(CH2SiMe3)(THF) (Ln = Sc, Lu, Y), derived from a nonfunctionalized diamide ligand (H2BDPPoxyl = 1,2-bis-(((2,6-diisopropylphenyl)amino)methyl)benzene), were isolated in high yields. The 4- and 5-coordinate complexes (BDPPoxyl)Sc(CH2SiMe3)(THF) and (BDPPpyr)Sc(CH2SiMe3)(THF), respectively, were also characterized by X-ray diffraction structure determinations. All of the 5-coordinate scandium complexes derived from the BDPPpyr ligand effectively polymerize methyl methacrylate in a living manner (Mw/Mn 1.5), affording mainly atactic polymer at ambient temperature.
