Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Kimberly C. Mullane"'
Autor:
Thibault Cheisson, Ji Young Park, Mu-Hyun Baik, Lauren N. Grant, Daniel J. Mindiola, Brian C. Manor, Eric J. Schelter, Patrick J. Carroll, Ho Ryu, Kimberly C. Mullane
Publikováno v:
Journal of the American Chemical Society. 140:11335-11340
Uranium complexes in the +3 and +4 oxidation states were prepared using the anionic PN– (PN– = (N-(2-(diisopropylphosphino)-4-methylphenyl)-2,4,6-trimethylanilide) ligand framework. New complexes include the halide starting materials, (PN)2UIIII
Autor:
Matthias Zeller, Kimberly C. Mullane, Suzanne C. Bart, Eric J. Schelter, Sharon E. Bone, Phillip E. Fanwick, Scott A. Pattenaude, Stosh A. Kozimor, Juan S. Lezama Pacheco, Maryline G. Ferrier, Benjamin W. Stein
Publikováno v:
Inorganic Chemistry. 57:6530-6539
Uranium complexes (MesDAE)2U(THF) (1-DAE) and Cp2U(MesDAE) (2-DAE) (MesDAE = [ArN-CH2CH2-NAr]; Ar = 2,4,6-trimethylphenyl (Mes)), bearing redox-innocent diamide ligands, have been synthesized and characterized for a full comparison with previously pu
Autor:
Eric J. Schelter, Christopher Uyeda, Kimberly C. Mullane, Cholpisit Kiattisewee, Ian G. Powers
Publikováno v:
Chemistry – A European Journal. 23:7694-7697
A dinickel imido complex was synthesized using a redox-active naphthyridine-diimine supporting ligand. Upon coordination of an external ligand, the Ni2 core was disrupted, triggering an aromatic C-H activation reaction to generate a Ni2 (μ-NHAr)(Ar)
Publikováno v:
Chemistry – A European Journal. 23:5748-5757
Organic azides that contain naphthyl functional groups were used to prepare uranium(V) imido complexes UV [=NC(2-naph)Ph2 ][N(SiMe3 )2 ]3 (2), UV [=NC(2-naph)3 ][N(SiMe3 )2 ]3 (3), and UV [=N(2-naph)][N(SiMe3 )2 ]3 (4), and their properties were comp
Autor:
Patrick J. Carroll, Haolin Yin, Jerald E. Hertzog, Eric J. Schelter, Jessica M. Anna, Brian C. Manor, Kimberly C. Mullane, Yi Jin
Publikováno v:
Journal of the American Chemical Society. 138:16266-16273
The hexachlorocerate(III) anion, [CeIIICl6]3–, was found to be a potent photoreductant in acetonitrile solution with an estimated excited-state reduction potential of −3.45 V versus Cp2Fe0/+. Despite a short lifetime of 22.1(1) ns, the anion exhi