76282-33-2Relevant articles and documents
C-H activation by a diselenido dinickel(II) complex
Wallick, Jessica,Riordan, Charles G.,Yap, Glenn P. A.
, p. 14972 - 14974 (2013)
Addition of selenium to the nickel(I) complex, [Ni(Me4[12] aneN4)(CO)]PF6, effects a redox reaction leading to the diselenido dinickel(II) complex, {[(Ni(Me4[12]aneN4)] 2(Se2)}(PF6)2, in 70% crystalline yield. The product's structure features a μ-η2: η2-Se2 ligand with Se-Se bond length of 2.379(13) A?. Upon mild heating, {[(Ni(Me4[12]aneN4)] 2(μ-η2:η2-Se2)}(PF 6)2 oxidizes 9,10-dihydroanthracene or 1,4-cyclohexadiene forming the terminal hydroselenide, [Ni(Me4[12]aneN 4)(SeH)]PF6, and anthracene or benzene, respectively. [Ni(Me4[12]aneN4)(SeH)]PF6 cleanly converts back to the diselenido dinickel(II) adduct upon addition of a phenoxy radical.
The Preparation, Characterization and Solution Chemistry of Some Nickel(II) and Copper(II) Complexes of 1,4,7,10-Tetramethyl-1,4,7,10-tetraazacyclododecane
Coates, John H.,Hadi, Dewan A.,Lincoln, Stephen F.
, p. 903 - 909 (2007/10/02)
The preparation of the new ligand 1,4,7,10-tetramethyl-1,4,7,10-tetraazacyclododecane, (-N(Me)(CH2)2-)4 (= L), and the complexes (ClO4)2, (ClO4)2, ClO4, (ClO4)2, and (ClO4)2, where Y = (-N(Me)(CH2)2N(Me)(CH2)3-)2, 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane, are described.The magnetic moments of the nickel(II) species are reported, and the labile low-spin/high-spin equilibria characterizing the 2+ and 2+ systems over a range of temperatures and ionic strengths in aqueous solution are discussed.The spectrophotometric titration of the aqua ligands in 2+, 2+, and 2+ against sodium hydroxide yields pKa values of 10.2+/-0.2, 12.0+/-0.3 and 10.7+/-0.2, respectively, and a study, using Job's method of continuous variations, of the formation of azide species shows + and + to be formed predominantly in aqueous solution.