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9月 7日讲座:Optimizing Old Reactions vs. Exploring New Reactions–What is the Most Promising Way for On-Surface Synthesis?

报告题目Optimizing Old Reactions vs. Exploring New Reactions–What is the Most Promising Way for On-Surface Synthesis?


报 告 人:  Markus Lackinger, Technische Universität München & Deutsches Museum


报告时间:  2017-09-07 14:00


报告地点:  实验三楼102


主办单位:  化学与分子工程学院


备注: CV of Markus Lackinger:

Educational and Professional Experiences:

-studies: physical engineering at the University of Applied Sciences Munich

-PhD in experimental physics from TU Chemnitz (Prof. Michael Hietschold)

-research stay at Columbia University (Prof. George W. Flynn)

-postdoc at the LMU München (Prof. Wolfgang M. Heckl)

-postdocs at the University of California Irvine (Prof. Wilson Ho)

-substitute professorship (LMU München)

-habilitation in material science (LMU München)

-habilitation in experimental physics (TU München)

-adjunct professor (LMU München)

-independent research group leader at the Deutsches Museum in cooperation with TU München


讲座摘要:

     The presentation will discuss recent advancements and challenges in the on-surface synthesis of extended covalent nanostructures. A particularly important and widespread coupling reaction is the so called surface-assisted Ullmann coupling, where halogenated precursors recombine by forming interlinking C-C bonds after the thermally activated dehalogenation on the surface. Here it is particularly instructive to focus on differences between seemingly very comparable metal surfaces, i.e. Au(111) vs. Ag(111). On the other hand, even though quite challenging, the tool box of on-surface synthesis is continuously enlarged by newly discovered or developed coupling reactions. In most cases these are inspired by solution chemistry, but transferring the coupling reactions onto surfaces can have implications that reach significantly beyond imposed geometrical constraints. Exemplarily, the thermally induced surface chemistry of a three-fold thiol functionalized monomer on Au(111) will be discussed.


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