化学
吸附
结晶学
分子
晶体结构
金属
无机化学
作者
Katharina Ueltzen,Sebastian Schmitz,Marco Moors,Maria Glöß,M. Börner,Irina Werner,Ziyan Warneke,Jonas Warneke,Bernd Abel,Kirill Yu. Monakhov
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2021-06-30
卷期号:60 (14): 10415-10425
被引量:4
标识
DOI:10.1021/acs.inorgchem.1c00994
摘要
The controlled adsorption of polynuclear coordination compounds with specific structural and electronic characteristics on surfaces is crucial for the prospective implementation of molecule–surface interfaces into practical electronic devices. From this perspective, a neutral 3d,4f-coordination cluster [Mn II 3 Mn IV Yb 3 O 3 (OH)(L·SMe) 3 (OOCMe) 9 ]·2MeCN·3EtOH ( 1 ·2MeCN·3EtOH), where L·SMe – is a Schiff base, has been synthesized and fully characterized and its adsorption on two different solid substrates, gold and graphite, has been studied. The mixed-valence compound with a bilayered metal core structure and the structurally exposed thioether groups exhibits a substantially different surface bonding to metallic gold and semimetallic graphite substrates. While on graphite the adsorption takes place only on distinguished attraction points with a locally increased number of potential bonding sites such as terrace edges and other surface defects, on gold the molecules were found to adsorb rather weakly on randomly distributed adsorption sites of the surface terraces. This entirely different behavior provides important information for the development of advanced surface materials that may enable well-distributed ordered molecular assemblies.
科研通智能强力驱动
Strongly Powered by AbleSci AI