4.7 Article

Solution Dynamics of Redox Noninnocent Nitrosoarene Ligands: Mapping the Electronic Criteria for the Formation of Persistent Metal-Coordinated Nitroxide Radicals

期刊

INORGANIC CHEMISTRY
卷 54, 期 14, 页码 7110-7121

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.5b01252

关键词

-

资金

  1. U.S. National Science Foundation [CHE-0954710]
  2. Division Of Chemistry
  3. Direct For Mathematical & Physical Scien [1126889] Funding Source: National Science Foundation

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据