首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Cyclometalated ruthenium complexes with carboxylated ligands from a combined experimental/computational perspective
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Cyclometalated ruthenium complexes with carboxylated ligands from a combined experimental/computational perspective

机译:与组合的实验/计算视角的环素烯化的钌配合物用羧化配体

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摘要

The syntheses and characterization of nine new cyclometalated ruthenium complexes are reported. These structures consist of Ru(II) with bipyridine and phenylpyridine ligands which are substituted with ester or carboxylate groups. Two of the complexes were extensively studied and their properties were compared to those of two previously reported structures. The identities of the compounds were confirmed by NMR, HR-MS and single crystal XRD, and the electronic properties were investigated by UV-Vis spectroscopy. DFT and TD-DFT calculations showed that the intense absorbances in the visible region of the spectrum of these cyclometalated complexes are due to electronic excitations to virtual orbitals located on the carboxylated ligands. These results indicate that the compounds are promising candidates as sensitizers for more efficient photocatalysis with sunlight. Further, the carboxylate groups should facilitate their use as linkers in metal-organic frameworks.
机译:据报道了九种新的环素晶型钌配合物的合成和表征。 这些结构由ru(ii)组成,与酯或羧酸酯基团取代的丙啶和苯基吡啶配体。 广泛研究了两种复合物,并将其性质与两个先前报道的结构进行了比较。 通过NMR,HR-MS和单晶XRD证实化合物的标识,通过UV-Vis光谱研究了电子性质。 DFT和TD-DFT计算表明,这些环状叠络合物的光谱的可见区域中的强烈吸光度是由于位于羧化配体上的虚拟轨道的电子激发。 这些结果表明,该化合物是具有阳光更有效的光催化的敏感剂的候选者。 此外,羧酸盐基团应促进其用作金属有机框架中的接头。

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