Abstract
Metal complexes at surfaces and interfaces play a prominant role in many
areas of modern technology, including catalysis, sensors, and organic
electronics. An important aspect of these interfaces is the possible
exchange of the metal center, because this reaction can drastically
alter the properties of the metal complex and thus of the interface.
Here, we demonstrate that such metal exchange reactions are indeed
possible and can proceed already at moderate temperatures even in the
absence of solvents. Specifically, we studied the redox transmetalation
of a monolayer of lead(II)-tetraphenylporphyrin (PbTPP) with copper from
a Cu(111) surface under ultrahigh-vacuum (UHV) conditions using
multiple surface-sensitive techniques. Temperature dependent X-ray
photoelectron spectroscopy (XPS) reveals that the Pb/Cu exchange starts
already below 380 K and is complete at 600 K. The identity of the
reaction product, CuTPP, is confirmed by mass spectrometric detection in
a temperature-programmed reaction (TPR) experiment. Scanning tunneling
microscopy (STM) sheds light on the adsorbate structure of PbTPP at 300 K
and uncovers the structural changes accompanying the transmetalation
and side-reactions of the phenyl substituents. Moreover, individual free
Pb atoms are observed as a product of the metal exchange. Our study
suggests that surfaces functionalized with metal complexes may consist
of other species than intended under operation conditions, which often
involve elevated temperatures.
Supplementary materials
Title
Herritsch Transmetalation supporting ChemRxiv 12.12.2020
Description
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