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  • Title: Ni(II)/H(2)O(2) reactivity in bis[(pyridin-2-yl)methyl]amine tridentate ligand system. aromatic hydroxylation reaction by bis(mu-oxo)dinickel(III) complex.
    Author: Kunishita A, Doi Y, Kubo M, Ogura T, Sugimoto H, Itoh S.
    Journal: Inorg Chem; 2009 Jun 01; 48(11):4997-5004. PubMed ID: 19374371.
    Abstract:
    The nickel(II) complexes 1(X) supported by bis[(pyridin-2-yl)methyl]benzylamine tridentate ligands carrying m-substituted phenyl groups (X = OMe, Me, H, Cl, NO(2)) at the 6-position of pyridine donor groups (L(X), N,N-bis[(6-m-substituted-phenylpyridin-2-yl)methyl]benzylamine) have been synthesized and characterized. The X-ray crystallographic analyses have revealed that [Ni(II)(L(H))(CH(3)CN)(H(2)O)](ClO(4))(2) (1(H)), [Ni(II)(L(OMe))(CH(3)CN)(MeOH)](ClO(4))(2) (1(OMe)), [Ni(II)(L(Me))(CH(3)CN)(H(2)O)](ClO(4))(2) (1(Me)), and [Ni(II)(L(Cl))(CH(3)CN)(H(2)O)](ClO(4))(2) (1(Cl)) have a five-coordinate square pyramidal geometry, whereas [Ni(II)(L(NO(2)))(CH(3)CN)(2)(H(2)O)](ClO(4))(2) (1(NO(2))) exhibits a six-coordinate octahedral geometry having an additional CH(3)CN co-ligand. (1)H NMR spectra of the nickel(II) complexes 1(X) in CD(3)CN have indicated that all the complexes have a high spin ground state. The nickel(II) complexes 1(X) react with hydrogen peroxide (H(2)O(2)) in acetone to give bis(mu-oxo)dinickel(III) complexes 2(X) exhibiting a characteristic UV-vis absorption band at approximately 420 nm. In the case of 2(H), a resonance Raman band ascribable to a Ni(2)O(2) core vibration was observed at 611 cm(-1) that shifted to 586 cm(-1) upon H(2)(18)O(2). The bis(mu-oxo)dinickel(III) intermediates 2(X) undergo an efficient aromatic ligand hydroxylation reaction, producing a mononuclear nickel(II)-phenolate complexes 4(X) via a putative intermediate (mu-phenoxo)(mu-hydroxo)dinickel(II) (3(X)). The kinetic studies on the aromatic ligand hydroxylation process including m-substituent effects (Hammett analysis) and kinetic deuterium isotope effects (KIE) have indicated that the reaction of 2(X) to 3(X) involves an electrophilic aromatic substitution mechanism, where C-O bond formation and C-H bond cleavage occur in a concerted manner. Intermediate 3(H) was detected by ESI-MS during the course of the reaction, and the final product 4(H) was characterized by elemental analysis, ESI-MS, and X-ray crystallographic analysis.
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