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Redox-active Phosphorus Ligands Bearing an Fe4C4-core Substituent. Complexation with Palladium and Platinum

机译:备用Fe4C4核取代基的氧化还原活性磷配体。钯和铂金络合

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Design of ancillary ligands is crucial for developing efficient catalysis of transition metal complexes. Introduction of a redox-active functionality into ligand frameworks enables alternation of reactivity and selectivity of metal centers through chemical or electrochemical modification of redox states. Wrighton et al. reported a representative example using a 1,1'-bis(diphenylphosphino)cobaltocene-coordinated rhodium(I) complex, which switches catalytic activities toward hydrosilylation and hydrogenation upon redox change of cobaltocene moiety. Considering multiple redox ability of polymetallic species, it is expected that introduction of such frameworks provides a new type of ligand capable of multistep tuning of catalytic property. Herein, we report the synthesis and property of a redox active-phosphorus ligand bearing an Fe4C4-core substituent. Its complexation with Pd(II) and Pt(II) will also be described.
机译:辅助配体的设计对于显影过渡金属配合物的有效催化是至关重要的。将氧化还原活性功能引入配体框架中,通过氧化还原态的化学或电化学改性,可以交替反应性和金属中心的选择性。 Wrighton等人。报道了使用1,1'-双(二苯基膦基)钴茂丙烯 - 配位铑(I)复合物的代表性实例,其将催化活性转换为钴茂的氧化还原变化时氢化硅烷化和氢化。考虑到多种多种物种的氧化还原能力,预计此类框架的引入提供了一种能够多步调整催化性质的新型配体。在此,我们报告了携带Fe4C4-核心取代基的氧化还原活性磷配体的合成和性质。还将描述其与Pd(II)和Pt(II)的络合。

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