Synthesis and characterization of thermally robust amidinato group 13 hydride complexes

被引:64
作者
Cole, ML
Jones, C
Junk, PC
Kloth, M
Stasch, A
机构
[1] Univ Cardiff Wales, Sch Chem, Ctr Fundamental & Appl Main Grp Met Chem, Cardiff CF10 3AT, Wales
[2] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
关键词
aluminum; amidinates; gallium; hydrides; structure elucidation;
D O I
10.1002/chem.200500278
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reactivity of two sterically bulky amidines, ArNC(R)N(H)Ar (Ar = 2,6-diisopropylphenyl; R = H (HFiso); tBu, (HPiso)) towards LiMH4, M = Al or Ga, [AlH3(NMe3)], and [GaH3(quin)] (quin = quinuclidine) has been examined. This has given rise to a variety of very thermally stable aluminum and gallium hydride complexes. The structural motif adopted by the prepared complexes has been found to be dependent upon both the amidinate ligand and the metal involved. The 1:1 reaction of HFiso with LiAlH4 yielded dimeric [{AlH3(mu-Fiso)Li(OEt2)}(2)]. Amidine HFiso reacts in a 1:1 ratio with [AlH3(NMe3)] to give the unusual hydride-bridging dimeric complex, [[AIH(2)(Fiso)](2)], in which the Fiso(-) ligand is nonchelating. The equivalent reaction with the bulkier amidine, HPiso, yielded a related hydride-bridging complex, [[AlH2(PiSO))(2)], in which the Piso(-) ligand is chelating. In contrast, the treatment of [GaH3(quin)] with one equivalent of HFiso afforded the four-coordinate complex [GaH2-(quin)(Fiso)], in which the Fiso(-) ligand acts as a localized monodentate amido-imine ligand. The 2:1 reactions of HFiso with [AlH3(NMe3)] or [GaH3-(quin)] gave the monomeric complexes [MH(Fiso)(2)], which are thermally robust and which exhibit chelating amidinate ligands. In contrast, HPiso did not give 2:1 complexes in its reactions with either of the Group 13 trihydride precursors. For sake of comparison, the reactions of [AlH3(NMe3)] and [GaH3(quin)(])Fiso ligand is nonchelating. The equivalent reaction with the bulkier amidine, HPiso, yielded a related hydride-bridging complex, [(AlH2(Piso)(2)], in which the Piso- ligand is chelating. In contrast, the treatment of [GaH3(quin)] with one equivalent of HFiso afforded the four-coordinate complex [GaH3(quin)(Fiso)], in which the Fiso- ligand acts as a localized monodentate(quin)] with the bulky carbodiimide ArN=C=NAr and the thiourea Ar(H)NC(=S)N(H)Ar were examined. These last reactions afforded the five-coordinate thioureido complexes, [MH{N(Ar)C[N(H)(Ar)]S}(2)], M=Al or Ga.
引用
收藏
页码:4482 / 4491
页数:10
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