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镧系苯六甲酸盐配位聚合物中压力诱导的配位数转变:结构与光谱学

Pressure-Induced Coordination Number Transition in Lanthanide Mellitate Coordination Polymers: Structure and Spectroscopy.

作者信息

Beck Nicholas, Gomez Martinez Daniela, Albrecht-Schönzart Thomas E

机构信息

Department of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida 32306, United States.

Department of Chemistry and Nuclear Science and Engineering Center, Colorado School of Mines, Golden, Colorado 80401, United States.

出版信息

Inorg Chem. 2023 Sep 25;62(38):15375-15381. doi: 10.1021/acs.inorgchem.3c00933. Epub 2023 Sep 12.

Abstract

High external pressure is found to induce a non-coordinated water molecule to bond to cerium in a previously studied mellitate coordination polymer, as determined by high-pressure single-crystal X-ray diffraction, resulting in a coordination number transition at 3.85 GPa from 9 to 9.5 where half the cerium ions are 10-coordinate. Also, bond length changes due to increased pressure are experimentally measured, whereas the cerium-carboxylate bond lengths overall change by -0.004(9) Å/GPa, the cerium-water bonds by -0.016(3) Å/GPa, and cerium-oxygen bonds overall by -0.010(6) Å/GPa, which corresponds well with theoretical bond length decreases determined for similar compounds. The high-pressure absorbance spectra of the analogous neodymium mellitate are examined and compared with the structural changes observed.

摘要

通过高压单晶X射线衍射测定发现,在先前研究的苯六酸配位聚合物中,高外部压力会促使一个未配位的水分子与铈结合,导致在3.85吉帕斯卡时配位数从9转变为9.5,此时一半的铈离子为10配位。此外,通过实验测量了由于压力增加导致的键长变化,苯甲酸盐-铈键长总体变化为-0.004(9) Å/吉帕斯卡,铈-水键长变化为-0.016(3) Å/吉帕斯卡,铈-氧键长总体变化为-0.010(6) Å/吉帕斯卡,这与类似化合物理论上确定的键长减小情况非常吻合。对类似的钕苯六酸盐的高压吸收光谱进行了检查,并与观察到的结构变化进行了比较。

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