Xu Jia, Zhou Mingfei
Department of Chemistry and Laser Chemistry Institute, Shanghai Key Laboratory of Molecular Catalysts and Innovative Materials, Fudan University, Shanghai 200433, P. R. China.
J Phys Chem A. 2006 Sep 14;110(36):10575-82. doi: 10.1021/jp063776g.
The reactions of early lanthanide metal atoms Nd, Sm, and Eu with water molecules have been investigated using matrix isolation infrared spectroscopy and density functional calculations. The reaction intermediates and products were identified on the basis of isotopic labeled experiments and density functional frequency calculations. The ground state metal atoms react with water to form the M(H2O) and M(H2O)(2) complexes spontaneously on annealing (M = Nd, Sm, Eu). The M(H2O) complexes isomerize to the inserted HMOH molecules under red light irradiation, which further decompose to give the metal monoxides upon UV light irradiation. The Nd(H2O)(2) complex decomposes to form the trivalent HNd(OH)(2) molecule, while the Sm(H2O)(2) and Eu(H2O)(2) complexes rearrange to the divalent Sm(OH)(2) and Eu(OH)(2) molecules under red light irradiation.
利用基质隔离红外光谱法和密度泛函计算研究了早期镧系金属原子钕(Nd)、钐(Sm)和铕(Eu)与水分子的反应。基于同位素标记实验和密度泛函频率计算确定了反应中间体和产物。基态金属原子与水反应,在退火时自发形成M(H₂O)和M(H₂O)₂配合物(M = Nd、Sm、Eu)。M(H₂O)配合物在红光照射下异构化为插入的HMOH分子,在紫外光照射下进一步分解生成金属氧化物。Nd(H₂O)₂配合物分解形成三价HNd(OH)₂分子,而Sm(H₂O)₂和Eu(H₂O)₂配合物在红光照射下重排为二价Sm(OH)₂和Eu(OH)₂分子。