Dynamic Motion of Organic Ligands in Polar Layered Cobalt Phosphonates

Zhong Sheng Cai, Norihisa Hoshino, Song Song Bao, Jiage Jia, Tomoyuki Akutagawa, Li Min Zheng

    研究成果: Article査読

    3 被引用数 (Scopus)


    By introducing the polar methoxy group into phenyl- or benzyl-phosphonate ligands, four cobalt phosphonates with layered structures are obtained, namely, [Co(4-mopp)(H2O)] (1), [Co(4-mobp)(H2O)] (2), [Co(3-mopp)(H2O)] (3), and [Co(3-mobp)(H2O)] (4), where 4- or 3-moppH2 is (4- or 3-methoxyphenyl)phosphonic acid and 4- or 3-mobpH2 is (4- or 3-methoxybenzyl)phosphonic acid. Compounds 1, 2, and 4 crystallize in the polar space groups Pmn21 or Pna21, whereas compound 3 crystallizes in the centrosymmetric space group P21/n. The layer topologies in the four structures are similar and can be viewed as perovskite type, where the edge-sharing [Co4O4] rhombi are capped by the PO3C groups. The phenyl and MeO groups in compounds 1–3 are heavily disordered, whereas that in 4 is ordered. Structural comparison based on the data at 296 and 123 K reveals distinct dynamic motion of the organic groups in compounds 1 and 2. The fluctuation of the polar MeO groups in these two compounds is confirmed by dielectric relaxation measurements. In contrast, the fluctuation of polar groups in compounds 3 and 4 is not evident. Interestingly, the dehydrated samples of 3 and 4 (i.e., 3-de and 4-de) exhibit one-step and two-step phase transitions associated with the motion of polar organic groups, as proven by DSC and dielectric measurements. The magnetic properties of compounds 1–4 are investigated, and strong antiferromagnetic interactions are found to mediate between the magnetic centers through μ-O(P) and O-P-O bridges.

    ジャーナルChemistry - A European Journal
    出版ステータスPublished - 2018 9 12

    ASJC Scopus subject areas

    • 触媒
    • 有機化学


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