Auwärter Willi, Weber-Bargioni Alexander, Brink Susan, Riemann Andreas, Schiffrin Agustin, Ruben Mario, Barth Johannes V
Departments of Chemistry and Physics & Astronomy, University of British Columbia, Vancouver, B.C. V6T 1Z4, Canada.
Chemphyschem. 2007 Feb 2;8(2):250-4. doi: 10.1002/cphc.200600675.
We report a bottom-up approach for the fabrication of metallo-porphyrin compounds and nanoarchitectures in two dimensions. Scanning tunneling microscopy and tunneling spectroscopy observations elucidate the interaction of highly regular porphyrin layers self-assembled on a Ag(111) surface with iron monomers supplied by an atomic beam. The Fe is shown to be incorporated selectively in the porphyrin macrocycle whereby the template structure is strictly preserved. The immobilization of the molecular reactants allows the identification of single metalation events in a novel reaction scheme. Because the template layers provide extended arrays of reaction sites, superlattices of coordinatively unsaturated and magnetically active metal centers are obtained. This approach offers novel pathways to realize metallo-porphyrin compounds, low-dimensional metal-organic architectures and patterned surfaces which cannot be achieved by conventional means.
我们报道了一种自下而上的方法,用于二维制备金属卟啉化合物和纳米结构。扫描隧道显微镜和隧道光谱观察阐明了自组装在Ag(111)表面的高度规则卟啉层与原子束提供的铁单体之间的相互作用。结果表明,Fe被选择性地掺入卟啉大环中,从而严格保留了模板结构。分子反应物的固定化使得在一种新颖的反应方案中能够识别单个金属化事件。由于模板层提供了扩展的反应位点阵列,因此获得了配位不饱和且具有磁活性的金属中心的超晶格。这种方法为实现金属卟啉化合物、低维金属有机结构和图案化表面提供了新途径,而这些是传统方法无法实现的。