67974-40-7Relevant academic research and scientific papers
Chemical Oxidation of a Coordinated PNP-Pincer Ligand Forms Unexpected Re-Nitroxide Complexes with Reversal of Nitride Reactivity
Connor, Gannon P.,Mercado, Brandon Q.,Lant, Hannah M.C.,Mayer, James M.,Holland, Patrick L.
, p. 10791 - 10801 (2019)
Because of the thermodynamic demands of N2 cleavage, N2-derived nitride complexes are often unreactive. The development of multistep N2 functionalization reactions hinges on methods for modulating nitride reactivity with s
Terminal NiII?OH/?OH2complexes in trigonal bipyramidal geometries derived from H2O
Lau, Nathanael,Sano, Yohei,Ziller, Joseph W.,Borovik
, p. 179 - 185 (2017)
The preparation and characterization of two NiIIcomplexes are described, a terminal NiII–OH complex with the tripodal ligand tris[(N)-tert-butylureaylato)-N-ethyl)]aminato ([H3buea]3?) and a terminal NiII/
Conformational Change with Steric Interactions Affects the Inner Sphere Component of Concerted Proton-Electron Transfer in a Pyridyl-Appended Radical Cation System
Welker, Evan A.,Tiley, Brittney L.,Sasaran, Crina M.,Zuchero, Matthew A.,Tong, Wing-Sze,Vettleson, Melissa J.,Richards, Robert A.,Geruntho, Jonathan J.,Stoll, Stefan,Wolbach, Jeffrey P.,Rhile, Ian J.
, p. 8705 - 8712 (2015/09/15)
Proton-coupled electron transfer (PCET) model systems combine one-electron oxidants and bases to generate net hydrogen atom acceptors. We have generated two persistent pyridyl-appended radical cations: 10-(pyrid-2-yl)-10H-phenothiazinium (PPT?+) and 3-(pyrid-2-yl)-10-methyl-10H-phenothiazinium (MPTP?+). EPR spectra and corresponding calculations indicate phenothiazinium radical cations with minimal spin on the pyridine nitrogen. Addition of hindered phenols causes the radical cations to decay, and protonated products and the corresponding phenoxyl radicals to form. The ΔG° values for the formation of intermediates (determined through cyclic voltammetry and pKa measurements) rule out a stepwise mechanism, and kinetic isotope effects support concerted proton-electron transfer (CPET) as the mechanism. Calculations indicate that the reaction of PPT?+ + tBu3PhOH undergoes a significant conformational change with steric interactions on the diabatic surface while maintaining the hydrogen bond; in contrast, MPTP?+ + tBu3PhOH maintains its conformation throughout the reaction. This difference is reflected in both experiment and calculations with (Formula presented.) (Formula presented.). Experimental results with 2,6-di-tert-butyl-4-methoxyphenol are similar. Hence, despite the structural similarity between the compounds, differences in the inner sphere component for CPET affect the kinetics.
Reduction-Oxidation Properties of Organotransition-metal Complexes. Part 12. Formation of Carbon-Carbon Bonds via the Oxidative Dimerisation of 4-C8H8)> and the Reduction of 5:η'5-C16H16)>2+
Connelly, Neil G.,Kelly, Raymond L.,Kitchen, Maureen D.,Mills, Rona M.,Stansfield, Robert F. D.,et al
, p. 1317 - 1326 (2007/10/02)
The complexes 4-cot)> undergo chemically irreversible one-electron oxidation in Ch2Cl2 at a platinum electrode.Chemical generation of the highly reacti
