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          Institute: MPI für bioanorganische Chemie     Collection: MPI für bioanorganische Chemie     Display Documents



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ID: 712716.0, MPI für bioanorganische Chemie / MPI für bioanorganische Chemie
Solution Dynamics of Redox Noninnocent Nitrosoarene Ligands: Mapping the Electronic Criteria for the Formation of Persistent Metal-Coordinated Nitroxide Radicals
Authors:Barnett, Brandon R.; Labios, Liezel A.; Moore, Curtis E.; England, Jason; Rheingold, Arnold L.; Wieghardt, Karl; Figueroa, Joshua S.
Language:English
Date of Publication (YYYY-MM-DD):2015
Title of Journal:Inorganic Chemistry
Journal Abbrev.:Inorg. Chem.
Volume:54
Issue / Number:14
Start Page:7110
End Page:7121
Review Status:Internal review
Audience:Experts Only
Abstract / Description:The redox-noninnocence of metal-coordinated C-organo nitrosoarenes has been established on the basis of solid-state characterization techniques, but the solution-phase properties of this class of metal-coordinated radicals have been relatively underexplored. In this report, the solution-phase properties and dynamics of the bis-nitrosobenzene diradical complex trans-Pd(kappa(1)-N-PhNO)(2)(CNArDipp2)(2) are presented. This complex, which is best described as containing singly reduced phenylnitroxide radical ligands, is shown to undergo facile nitrosobenzene dissociation in. solution to form the metalloxaziridine Pd(eta(2)-N,O-,PhNO)(CNArDipp2)(2) and thus is not a persistent species in solution. An equilibrium between trans-Pd(kappa(1)-N-PhNO)(2)(CNArDipp2)(2), Pd(eta(2)-N,O-PhNO)(CNArDipp2)(2), and free nitrosobenzene is established in solution, with the metalloxaziridine being predominantly favored. Efforts to perturb this equilibrium by the addition of excess nitrosobenzene reveal that the formation of trans-Pd(kappa(1)-N-PhNO)(2)(CNArDipp2)(2) is in competition with insertion-type chemistry of Pd(eta(2)-N,O-PhNO)(CNArDipp2)(2) and is therefore not a viable strategy for the production of a kinetically persistent bis-nitroxide radical complex. Electronic modification of the nitrosoarene framework was explored as a means to generate a persistent trans-Pd(kappa(1)-N-ArNO)(2)(CNArDipp2)(2) complex. While most substitution schemes failed to significantly perturb the kinetic lability of the nitrosoarene ligands in the corresponding trans-Pd(kappa(1)-N-ArNO)(2)(CNArDipp2)(2) complexes, utilization of para-formyl or para-cyano nitrosobenzene produced bis-nitroxide diradical complexes that display kinetic persistence in solution. The origin of this persistence is rationalized by the ability of para-formyl-and para-cyano-aryl groups to both attenuate the trans effect of the corresponding nitrosoarene and, more importantly, delocalize spin density away from the aryl-nitroxide NO unit. The results presented here highlight the inherent instability of metal-coordinated nitroxide radicals and suggest a general synthetic strategy for kinetically stabilizing these species in solution.
Comment of the Author/Creator:Date: 2015, JUL 20 2015
External Publication Status:published
Document Type:Article
Version Comment:Automatic journal name synchronization
Communicated by:N. N.
Affiliations:MPI für bioanorganische Chemie
External Affiliations:[Barnett,B.R.; Labios,L.A.; Moore,C.E.; Rheingold,A.L.; Figueroa,J.S.]Univ.Calif.San Diego, Dept.Chem.& Biochem., La Jolla, CA 92093 USA.
Identifiers:ISI:000358549300052 [ID No:1]
ISSN:0020-1669 [ID No:2]
DOI:10.1021/acs.inorgchem.5b01252 [ID No:3]
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