首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Discrete Silver(I)‐Palladium(II)‐Oxo Nanoclusters, {Ag4Pd13} and {Ag5Pd15}, and the Role of Metal–Metal Bonding Induced by Cation Confinement
Authors:Dr Peng Yang  Dr Yixian Xiang  Dr Zhengguo Lin  Zhongling Lang  Dr Pablo Jiménez‐Lozano  Dr Jorge J Carbó  Prof Josep M Poblet  Dr Linyuan Fan  Prof Changwen Hu  Prof Ulrich Kortz
Institution:1. Department of Life Sciences and Chemistry, Jacobs University, Bremen, Germany;2. Department de Química Física i Inorgànica, Universitat Rovira I Virgili, Tarragona, Spain;3. Key Laboratory of Cluster Science, Ministry of Education of China;4. Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, School of Chemistry, Beijing Institute of Technology, Beijing, P.R. China
Abstract:We introduce the class of discrete silver(I)‐palladium(II)‐oxo nanoclusters with the preparation of {Ag4Pd13} and {Ag5Pd15}. Both polyanions represent the first examples of noble metal‐capped polyoxo‐noble‐metalates in a fully inorganic assembly, featuring an unprecedented host–guest mode containing hetero‐ and homometallic Ag–Pd and Ag–Ag bonding interactions. Comprehensive theoretical calculations suggest that the Ag–Pd metallic bonds originate partially from surface confinement of AgI guest ions onto the anionic polyoxopalladate host that is induced by strong electrostatic forces. This work opens the field of fully inorganic silver‐palladium‐oxo nanoclusters, which can be considered as discrete mixed noble metal precursors for the formation of monodisperse core–shell nanoparticles, with high relevance for catalysis.
Keywords:DFT  metal-metal bonding  palladium  polyoxometalates  silver
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号