TY - JOUR
T1 - Actinide Coordination Chemistry on Surfaces
T2 - Synthesis, Manipulation, and Properties of Thorium Bis(porphyrinato) Complexes
AU - Rheinfrank, Erik
AU - Pörtner, Mathias
AU - Nuñez Beyerle, Maria del Carmen
AU - Haag, Felix
AU - Deimel, Peter S.
AU - Allegretti, Francesco
AU - Seufert, Knud
AU - Barth, Johannes V.
AU - Bocquet, Marie Laure
AU - Feulner, Peter
AU - Auwärter, Willi
N1 - Publisher Copyright:
© 2021 American Chemical Society
PY - 2021/9/15
Y1 - 2021/9/15
N2 - Actinide-based metal-organic complexes and coordination architectures encompass intriguing properties and functionalities but are still largely unexplored on surfaces. We introduce the in situ synthesis of actinide tetrapyrrole complexes under ultrahigh-vacuum conditions, on both a metallic support and a 2D material. Specifically, exposure of a tetraphenylporphyrin (TPP) multilayer to an elemental beam of thorium followed by a temperature-programmed reaction and desorption of surplus molecules yields bis(porphyrinato)thorium (Th(TPP)2) assemblies on Ag(111) and hexagonal boron nitride/Cu(111). A multimethod characterization including X-ray photoelectron spectroscopy, scanning tunneling microscopy, temperature-programmed desorption, and complementary density functional theory modeling provides insights into conformational and electronic properties. Supramolecular assemblies of Th(TPP)2as well as individual double-deckers are addressed with submolecular precision, e.g., demonstrating the reversible rotation of the top porphyrin in Th(TPP)2by molecular manipulation. Our findings thus demonstrate prospects for actinide-based functional nanoarchitectures.
AB - Actinide-based metal-organic complexes and coordination architectures encompass intriguing properties and functionalities but are still largely unexplored on surfaces. We introduce the in situ synthesis of actinide tetrapyrrole complexes under ultrahigh-vacuum conditions, on both a metallic support and a 2D material. Specifically, exposure of a tetraphenylporphyrin (TPP) multilayer to an elemental beam of thorium followed by a temperature-programmed reaction and desorption of surplus molecules yields bis(porphyrinato)thorium (Th(TPP)2) assemblies on Ag(111) and hexagonal boron nitride/Cu(111). A multimethod characterization including X-ray photoelectron spectroscopy, scanning tunneling microscopy, temperature-programmed desorption, and complementary density functional theory modeling provides insights into conformational and electronic properties. Supramolecular assemblies of Th(TPP)2as well as individual double-deckers are addressed with submolecular precision, e.g., demonstrating the reversible rotation of the top porphyrin in Th(TPP)2by molecular manipulation. Our findings thus demonstrate prospects for actinide-based functional nanoarchitectures.
UR - http://www.scopus.com/inward/record.url?scp=85114875022&partnerID=8YFLogxK
U2 - 10.1021/jacs.1c04982
DO - 10.1021/jacs.1c04982
M3 - Article
C2 - 34477375
AN - SCOPUS:85114875022
SN - 0002-7863
VL - 143
SP - 14581
EP - 14591
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 36
ER -