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![The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F54498.jpg&w=3840&q=50)
The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique
Published on: November 28, 2016
Solution-synthesized stable triaza[4]triangulene triradical with a quartet ground state
Xudong Bai1, Di Zhang1, Yushuang Zhang2
1Beijing National Laboratory for Molecular Sciences, Centre for the Soft Matter Science and Engineering, The Key Laboratory of Polymer Chemistry and Physics of the Ministry of Education, College of Chemistry, Peking University, Beijing, China.
None:
As a renowned class of open-shell molecules characterized by triangular nanographenic structures and novel magnetic properties with high-spin ground states, triangulenes are attractive targets to both synthetic chemists and molecular magnet researchers. Here, a highly stable aza-derivative of [4]triangulene triradical (1) is achieved, with a quartet ground state (S = 3/2). By virtue of the stability under ambient conditions (τ1/2 ~ 9 days in the solid state and 28 h in an air-saturated solution), thorough structural and magnetic characterizations are performed. Crystallographic analysis confirms that 1 has a planar triangular polycyclic aromatic skeleton embedded with delocalized spins. Concurrently, continuous-wave and pulsed EPR spectroscopies provide unambiguous evidence supporting its high-spin ground state. SQUID measurements reveal impressively large doublet-quartet energy gap (ΔED-Q = 3.18 kcal/mol), indicating very strong intramolecular ferromagnetic spin-spin exchanges (J/kB = +534 K) rendered by the triangulene structure.
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