Department of Chemistry, University of Rochester, Rochester, New York 14627, United States.
Inorg Chem. 2011 Oct 3;50(19):9443-53. doi: 10.1021/ic201102v. Epub 2011 Sep 7.
Synthesis and characterization of new (PONOP) [2,6-bis(di-tert-butylphosphinito)pyridine] metal (Ni, Pd, Pt) complexes are reported. Surprisingly, these compounds [(PONOP)MCl]Cl in the presence of 1 equiv of superhydride (LiEt(3)BH) formed a new class of complexes (H-PONOP)MCl, in which the pyridine ring in the PONOP ligand lost its aromaticity as a result of hydride attack at the para position of the ring. The new Ni-H compound [(H-PONOP)NiH] was synthesized by reacting (H-PONOP)NiCl with 1 equiv of superhydride. Analogous Pd and Pt compounds were prepared. Reactivity of these new pincer complexes toward MeLi and PhLi also has been studied. These Ni complexes catalyzed the hydrosilylation of aldehyde. In some cases characterization of new (PONOP)M complexes was difficult because of high instability due to degradation of the P-O bond.
报告了新型(PONOP)[2,6-双(二-叔丁基膦亚基)吡啶]金属(Ni、Pd、Pt)配合物的合成与表征。令人惊讶的是,这些化合物[(PONOP)MCl]Cl 在 1 当量超氢化物(LiEt(3)BH)的存在下形成了一类新的配合物(H-PONOP)MCl,其中 PONOP 配体的吡啶环由于芳构性而失去了其芳构性由于环上对位的氢化物攻击。新的 Ni-H 化合物[(H-PONOP)NiH]通过与 1 当量的超氢化物反应合成。制备了类似的 Pd 和 Pt 化合物。还研究了这些新型钳形配合物对 MeLi 和 PhLi 的反应性。这些 Ni 配合物催化了醛的硅氢化反应。在某些情况下,由于 P-O 键的降解,新型(PONOP)M 配合物的稳定性很高,因此其表征很困难。