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单卟啉分子在 Cu(110)表面上的热和振动诱导互变异构。

Thermally and vibrationally induced tautomerization of single porphycene molecules on a Cu(110) surface.

机构信息

Department of Physical Chemistry, Fritz-Haber Institute of the Max-Planck Society, Faradayweg 4-6, 14195 Berlin, Germany.

Surface Science Research Centre and Department of Chemistry, University of Liverpool, Liverpool L69 3BX, United Kingdom.

出版信息

Phys Rev Lett. 2013 Dec 13;111(24):246101. doi: 10.1103/PhysRevLett.111.246101. Epub 2013 Dec 11.

Abstract

We report the direct observation of intramolecular hydrogen atom transfer reactions (tautomerization) within a single porphycene molecule on a Cu(110) surface by scanning tunneling microscopy. It is found that the tautomerization can be induced via inelastic electron tunneling at 5 K. By measuring the bias-dependent tautomerization rate of isotope-substituted molecules, we can assign the scanning tunneling microscopy-induced tautomerization to the excitation of specific molecular vibrations. Furthermore, these vibrations appear as characteristic features in the dI/dV spectra measured over individual molecules. The vibrational modes that are associated with the tautomerization are identified by density functional theory calculations. At higher temperatures above ∼75  K, tautomerization is induced thermally and an activation barrier of about 168 meV is determined from an Arrhenius plot.

摘要

我们通过扫描隧道显微镜直接观察到了铜(110)表面卟吩分子内的氢原子转移反应(互变异构)。实验发现,在 5 K 时,通过非弹性电子隧穿可以诱导互变异构。通过测量同位素取代分子的偏压相关的互变异构速率,我们可以将扫描隧道显微镜诱导的互变异构归因于特定分子振动的激发。此外,这些振动在单个分子上测量的 dI/dV 谱中表现为特征。通过密度泛函理论计算确定了与互变异构相关的振动模式。在高于约 75 K 的较高温度下,互变异构是热诱导的,通过 Arrhenius 图确定了约 168 meV 的活化能垒。

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