On-Surface Synthesis of Triaza[5]triangulene through Cyclodehydrogenation and its Magnetism

Donglin Li, Orlando J. Silveira, Takuma Matsuda, Hironobu Hayashi, Hiromitsu Maeda*, Adam S. Foster*, Shigeki Kawai*

*Corresponding author for this work

Research output: Contribution to journalArticleScientificpeer-review

1 Citation (Scopus)
9 Downloads (Pure)

Abstract

Triangulenes as neutral radicals are becoming promising candidates for future applications such as spintronics and quantum technologies. To extend the potential of the advanced materials, it is of importance to control their electronic and magnetic properties by multiple graphitic nitrogen doping. Here, we synthesize triaza[5]triangulene on Au(111) by cyclodehydrogenation, and its derivatives by cleaving C−N bonds. Bond-resolved scanning tunneling microscopy and scanning tunneling spectroscopy provided detailed structural information and evidence for open-shell singlet ground state. The antiferromagnetic arrangement of the spins in positively doped triaza[5]triangulene was further confirmed by density function theory calculations. The key aspect of triangulenes with multiple graphitic nitrogen is the extra pz electrons composing the π orbitals, favoring charge transfer to the substrate and changing their low-energy excitations. Our findings pave the way for the exploration of exotic low-dimensional quantum phases of matter in heteroatom doped organic systems.

Original languageEnglish
Article numbere202411893
Pages (from-to)1-6
Number of pages6
JournalAngewandte Chemie - International Edition
Volume63
Issue number45
DOIs
Publication statusPublished - 4 Nov 2024
MoE publication typeA1 Journal article-refereed

Keywords

  • density functional theory
  • graphitic nitrogen
  • on-surface synthesis
  • scanning tunneling microscopy/spectroscopy
  • triangulene

Fingerprint

Dive into the research topics of 'On-Surface Synthesis of Triaza[5]triangulene through Cyclodehydrogenation and its Magnetism'. Together they form a unique fingerprint.

Cite this