Conformational chirality in buckled molecular silicenes: a precursor for chiral magnets

The chirality effect in bulk silicene has been studied under uniaxial tension, and Dirac Fermion chirality has also been observed in silicene on Ag (111). Despite these significant findings in bulk and surface-supported silicene, the existence and nature of chirality in molecular silicene, remain unknown. Herein, we report the "conformational chirality" in molecular silicene rings. This work also reports a computational study on silicene-based chiral magnetic systems that combines the structural flexibility of silicon with the spin functionality of organic radicals. Structural distortion introduces conformational chirality, making silicene an ideal platform for developing chiral magnetic materials. By coupling with silicene frameworks, organic nitronyl nitroxide (NN) radicals, a new class of diradicals are designed that exhibit both magnetism and chirality. These findings establish silicene-based chiral diradicals as promising candidates for applications in spintronics, quantum information science, and light-induced spin manipulation, setting the pathway for silicon-centered materials that describe chirality and magnetism.

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Publication Details

Journal
RSC Advances
Published
2026-01-01
DOI
https://doi.org/10.1039/d6ra01088a
Primary Topic
Synthesis and Properties of Aromatic Compounds
Type
article
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article

Conformational chirality in buckled molecular silicenes: a precursor for chiral magnets

Suranjan Shil, Debojit Bhattacharya, Muskan
RSC Advances
Synthesis and Properties of Aromatic Compounds
article

Conformational chirality in buckled molecular silicenes: a precursor for chiral magnets

Suranjan Shil, Debojit Bhattacharya, Muskan
article en

Abstract

The chirality effect in bulk silicene has been studied under uniaxial tension, and Dirac Fermion chirality has also been observed in silicene on Ag (111). Despite these significant findings in bulk and surface-supported silicene, the existence and nature of chirality in molecular silicene, remain unknown. Herein, we report the "conformational chirality" in molecular silicene rings. This work also reports a computational study on silicene-based chiral magnetic systems that combines the structural flexibility of silicon with the spin functionality of organic radicals. Structural distortion introduces conformational chirality, making silicene an ideal platform for developing chiral magnetic materials. By coupling with silicene frameworks, organic nitronyl nitroxide (NN) radicals, a new class of diradicals are designed that exhibit both magnetism and chirality. These findings establish silicene-based chiral diradicals as promising candidates for applications in spintronics, quantum information science, and light-induced spin manipulation, setting the pathway for silicon-centered materials that describe chirality and magnetism.

RSC AdvancesVol. 16(18)
Manipal Academy of Higher Education (IN), North Bengal University (IN)
Openalex Percentile: Top 12%
Synthesis and Properties of Aromatic Compounds
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Conformational chirality in buckled molecular silicenes: a precursor for chiral magnets — Suranjan Shil, Debojit Bhattacharya, et al. · RSC Advances (2026) | TGRS Research Map | TGRS