首页> 外文期刊>Inorganica Chimica Acta >Intensity enhancement of intraligand singlet-triplet pi-pi* transition for the coordinated beta-diketonate in Ni(II) complexes with a nitroxide radical
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Intensity enhancement of intraligand singlet-triplet pi-pi* transition for the coordinated beta-diketonate in Ni(II) complexes with a nitroxide radical

机译:Ni(II)配合物中带有氮氧化物自由基的配体β-二酮酸酯的配体内单重态-三重态pi-pi *跃迁的强度增强

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摘要

Room temperature and low temperature magnetic circular dichroism (MCD) in the intraligand spin-forbidden ringlet-triplet n-n` transition for the coordinated beta-diketonate ligands were observed for the beta-diketonato Ni(II) complexes with a chelated imino or nitronyl nitroxide radical, but not for the beta-diketonato Ni(II) complexes without the radical ligands. This is elucidated by the borrowing mechanism from the singlet-singlet pi-pi* transition through the hypothetical interligand beta-diketonate-to-radical charge transfer (LLCT) in contrast to the case of Cr(III) complexes. (c) 2006 Elsevier B.V. All rights reserved.
机译:观察到配体β-二酮基Ni(II)配合物与螯合的亚氨基或亚硝基硝基氮自由基的配体自旋禁带自旋-三重态nn`跃迁中的室温和低温磁性圆二色性(MCD) ,但不适用于没有自由基配体的β-二酮镍(II)配合物。与Cr(III)络合物的情况相比,借由单峰-单峰pi-pi *过渡通过假设的配位体从β-二酮到自由基的电荷转移(LLCT)的借入机制阐明了这一点。 (c)2006 Elsevier B.V.保留所有权利。

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