Synthesis and Characterization of Palladium(II) and Nickel(II) Alcoholate-Functionalized NHC Complexes and of Mixed Nickel(II)–Lithium(I) Complexes
The synthesis of Pd(II) and Ni(II) alcohol-functionalized N-heterocyclic carbene (NHC) complexes was explored to examine the possible influence of the functional arm attached to the NHC backbone on their structure and reactivity and, in the case of a Ni(II) complex, on its catalytic properties in et...
Gespeichert in:
Veröffentlicht in: | Inorganic chemistry 2014-05, Vol.53 (10), p.5189-5200 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The synthesis of Pd(II) and Ni(II) alcohol-functionalized N-heterocyclic carbene (NHC) complexes was explored to examine the possible influence of the functional arm attached to the NHC backbone on their structure and reactivity and, in the case of a Ni(II) complex, on its catalytic properties in ethylene oligomerization. Starting from the alcohol-functionalized imidazolium salt [ImDiPP(C2OH)]Cl (2), the new functionalized NHC palladium(II) complex [PdCl(acac){ImDiPP(C2OH)-C NHC}] (3) was synthesized and fully characterized. Two byproducts, [PdCl{μ-ImDiPP(C2O)-C NHC ,O}]2 (4) and trans-[PdCl2{ImDiPP(C2OH)-C NHC}2] (5), formed during the synthesis of 3, were also fully characterized. Acids promoted the transformation of 3 into the new CNHC-bound complex [PdCl(μ-Cl){ImDiPP(C2OH)-C NHC}]2 (6), unveiling the lability of the acac ligand and the resistance of the Pd–NHC bond to acids. Complex 6 reacted with a base to afford complex 4, in which alkoxide coordination to Pd(II) has occurred to generate a CNHC,O chelate. The stability of 3 was also assessed under basic conditions, and the new complex [Pd(acac){ImDiPP(C2O)-C NHC ,O}] (7) was characterized. The new nickel(II) alcoholate-functionalized NHC complex [NiCl{μ-ImDiPP(C2O)-C NHC ,O}]2 (8) was synthesized by the reaction of the imidazolium salt 2 with n-BuLi and [NiCl2(dme)]. The reaction of 8 with HCl regenerates the imidazolium and alcohol functions to give [ImDiPP(C2OH)]2[NiCl4] (9). The mixed-metal Ni(II)–Li(I) complexes [Ni2{μ-ImDiPP(C2O)-C NHC,μ-O}4Li]BF4 (10), [Ni2{μ-ImDiPP(C2O)-C NHC,μ-O}4Li]Cl (11), and [Ni{ImDiPP(C2O)-C NHC,μ-O}2LiBr] (12) were isolated and characterized. However, it was not possible to synthesize a Ni(II) alcohol-functionalized NHC complex in high yield. Small amounts of the square-planar complex [NiCl2{ImDiPP(C2OH)-C NHC}2] (13) could be isolated, and this complex was characterized by single-crystal X-ray diffraction. In 13, only the CNHC atom of the alcohol-functionalized NHC ligand is bound to the metal. The structures of the imidazolium salt 2·2H2O and of the complexes 3, 4, 4-polymorph, 5, 6·CH2Cl2, and 8–13 were established by single-crystal X-ray diffraction. |
---|---|
ISSN: | 0020-1669 1520-510X |
DOI: | 10.1021/ic500349t |