On‐Surface Synthesis and Characterization of a High‐Spin Aza‐[5]‐Triangulene

Author:

Vilas‐Varela Manuel1ORCID,Romero‐Lara Francisco2ORCID,Vegliante Alessio2,Calupitan Jan Patrick34,Martínez Adrián1,Meyer Lorenz2,Uriarte‐Amiano Unai2,Friedrich Niklas2ORCID,Wang Dongfei2,Schulz Fabian2ORCID,Koval Natalia E.2ORCID,Sandoval‐Salinas María E.5,Casanova David46,Corso Martina3ORCID,Artacho Emilio267ORCID,Peña Diego1ORCID,Pascual José Ignacio26ORCID

Affiliation:

1. Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CiQUS) and Departamento de Química Orgánica Universidade de Santiago de Compostela 15782- Santiago de Compostela Spain

2. CIC nanoGUNE-BRTA 20018 Donostia-San Sebastián Spain

3. Centro de Física de Materiales CSIC/UPV-EHU-Materials Physics Center 20018 Donostia-San Sebastián Spain

4. Donostia International Physics Center (DIPC) 20018 Donostia-San Sebastián Spain

5. School of Physical and Chemical Sciences Queen Mary University of London UK

6. Ikerbasque, Basque Foundation for Science 48009 Bilbao Spain

7. Theory of Condensed Matter Cavendish Laboratory University of Cambridge J. J. Thomson Ave. Cambridge CB3 0HE UK

Abstract

AbstractTriangulenes are a class of open‐shell triangular graphene flakes with total spin increasing with their size. In the last years, on‐surface‐synthesis strategies have permitted fabricating and engineering triangulenes of various sizes and structures with atomic precision. However, direct proof of the increasing total spin with their size remains elusive. In this work, we report the combined in‐solution and on‐surface synthesis of a large nitrogen‐doped triangulene (aza‐[5]‐triangulene) on a Au(111) surface, and the detection of its high‐spin ground state. Bond‐resolved scanning tunneling microscopy images uncovered radical states distributed along the zigzag edges, which were detected as weak zero‐bias resonances in scanning tunneling spectra. These spectral features reveal the partial Kondo screening of a high‐spin state. Through a combination of several simulation tools, we find that the observed distribution of radical states is explained by a quintet ground state (S=2), instead of the quartet state (S=3/2) expected for the neutral species. This confirms that electron transfer to the metal substrate raises the spin of the ground state. We further provide a qualitative description of the change of (anti)aromaticity introduced by N‐substitution, and its role in the charge stabilization on a surface, resulting in an S=2 aza‐triangulene on Au(111).

Funder

H2020 Future and Emerging Technologies

Publisher

Wiley

Subject

General Chemistry,Catalysis

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