A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Category: naphthyridines, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 106-49-0, Name is p-Toluidine, molecular formula is C7H9N. In an article, author is Powers, Ian G.,once mentioned of 106-49-0.
A 1,2-Addition Pathway for C(sp(2))-H Activation at a Dinickel Imide
A dinickel imido complex was synthesized using a redox-active naphthyridine-diimine supporting ligand. Upon coordination of an external ligand, the Ni-2 core was disrupted, triggering an aromatic C-H activation reaction to generate a Ni-2 (mu-NHAr)(Ar) species. This intermediate is capable of liberating free carbazole and phenanthridine products upon heating or treatment with excess tBuNC. Collectively, these studies establish a kinetically facile 1,2-addition mechanism for C(sp(2))-H activation, taking advantage of cooperative reactivity between two Ni centers.
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Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem