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Synthesis and Properties of N,C,S-Pincer Iron Carbonyl Complexes Bearing a Quinolyl Group

机译:含喹啉基的N,C,S-铅碳基复合物的合成与性质

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Dissociation of carbonyl ligands in transition metal complexes by electronic excitation is a useful property because the formed vacant coordination site can be utilized in catalytic reactions as well as synthetic chemistry. Furthermore, development of the controllable CO release from carbonyl complexes has become an important research area since CO was recognized as a signaling molecule in biological pathways. The wavelength dependence of the photoinduced dissociation of CO is highly related to the electronic structures of the carbonyl complexes. Previously we reported that near-infrared light-triggered release of CO is achievable by using N,C,S-pincer iron(III) carbonyl complexes with two axial phosphorus ligands. In this study, we newly designed an N,C,S-tridentate ligand with a quinolyl group to modulate the electronic structure.
机译:通过电子激发的过渡金属配合物中羰基配体的解离是一种有用的性质,因为所形成的空性配位位点可用于催化反应以及合成化学。此外,从羰基复合物的可控Co释放的发展已成为重要的研究区域,因为CO在生物途径中被认为是信号分子。 CO的光诱导离解的波长依赖性与羰基配合物的电子结构高度相关。此前,我们报道了通过使用具有两个轴向磷配体的N,C,S in型铁(III)羰基配合物可以实现近红外光触发释放。在这项研究中,我们设计了具有喹啉基的N,C,S三齿配体,以调节电子结构。

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