Titlebook: On-Surface Synthesis II; Proceedings of the I Dimas G. de Oteyza,Celia Rogero Conference proceedings 2018 Springer International Publishing

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Mechanistic Insights into Surface-Supported Chemical Reactions,btain fascinating and unprecedented insights into the mechanisms of chemical transformations. Particularly exciting are recent advances in atomic force microscopy that allow bond-resolved imaging and thus make the chemical identification of organic molecular reaction intermediates and products possi

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緊張過度

Reactivity , and , Graphene Layers: Scanning Probe Microscopy Reveals,ng (STM) and atomic force microscopies (AFM). We place particular emphasis on the diversity of reactions, systems and synthetic strategies that are now available to surface scientists working in various fundamental and applied research fields. Using imine formation as the model reaction we discuss c

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macrophage

On-Surface Ullmann Reaction for the Synthesis of Polymers and Macrocycles,n situ characterizations of products with large molecular weight are required. This article covers the on-surface synthesis of hydrocarbon polymers and macrocycles via an Ullmann type reaction of haloarenes on metal single-crystal surfaces. The related formation of stable organometallic reaction int

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Parabola

,Aryl–Aryl Covalent Coupling on Rutile TiO2 Surfaces,directly on a supporting surface. So far, selected noble metals have been mostly used as substrates for such on-surface chemical reactions. For the sake of practical applications the semiconductor surfaces clearly represent much more attractive platforms. Especially transition metal oxides exhibitin

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On-Surface Coupling Reactions with Extrinsic Catalysts,e catalytic effects of Cu and Pd deposits in the on-surface Ullmann coupling and Sonogashira cross-coupling reactions. The stepwise reaction paths, intermediates, and activation energies are deliberated at a single molecular level using scanning tunneling microscopy (STM). Such studies offer mechani

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