ACS Nano
NanoPhotonics Centre, Cavendish Laboratory, Dept. of Physics, University of Cambridge, Cambridge CB3 0HE, U.K.
Published: March 2025
Stable radicals are spin-active species with a plethora of proposed applications in fields from energy storage and molecular electronics to quantum communications. However, their optical properties and vibrational modes are so far not well understood. Furthermore, it is not yet clear how these are affected by the radical oxidation state, which is key to understanding their electronic transport. Here, we identify the properties of 1,2,4-benzotriazin-4-yl, a stable doubly thiolated variant of the Blatter radical, using surface-enhanced Raman scattering (SERS). Embedding molecular monolayers in plasmonic nanocavities gives access to their vibrational modes, photoluminescence, and optical response during redox processes. We reveal the influence of the adjacent metallic surfaces and identify fluctuating SERS signals that suggest a coupling between the unpaired radical electron and a spatially overlapping vibrational mode. This can potentially be exploited for information-storage devices and chemically designed molecular qubits.
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http://dx.doi.org/10.1021/acsnano.4c09661 | DOI Listing |
ACS Nano
March 2025
NanoPhotonics Centre, Cavendish Laboratory, Dept. of Physics, University of Cambridge, Cambridge CB3 0HE, U.K.
Stable radicals are spin-active species with a plethora of proposed applications in fields from energy storage and molecular electronics to quantum communications. However, their optical properties and vibrational modes are so far not well understood. Furthermore, it is not yet clear how these are affected by the radical oxidation state, which is key to understanding their electronic transport.
View Article and Find Full Text PDFJ Org Chem
February 2025
Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, 90-363 Łódź, Poland.
Photocyclization of 8-aryloxy-3-phenylbenzo[][1,2,4]triazines leads to helicene radicals. Structural analysis of radicals forms by two-dimensional correlation nuclear magnetic resonance methods demonstrated that the photocyclization involves a Smiles rearrangement and exclusive formation of a single rearranged product for all substrates. Density functional theory investigations indicate that the mechanism requires the T state with (n, π*) character localized on the benzo[][1,2,4]triazine (BT) fragment and at least one occupied π molecular orbital (MO) localized on the aryloxy fragment with an energy that is higher than that of the n MO.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Faculty of Chemistry, University of Łódź, Tamka 12, 91403 Łódź, Poland.
Cofacial arrangement of two Blatter radicals enforced by the -naphthalene scaffold represents a new approach to stable diradicals with strong through-space interactions. Two stereoisomers of the naphthalene-diradicals, and , are investigated by XRD, VT-EPR, UV-vis, electrochemical, kinetic, and DFT methods. In solutions, both stereoisomers exist as open-shell singlets with Δ = -3.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, 90-363 Łódź, Poland.
Photocyclization of 8-aryloxy-3-phenylbenzo[][1,2,4]triazines leads to π-delocalized helicene radicals 1[n] ( = 5, 6, 7) containing the ring-fused 1,4-dihydro[1,2,4]triazin-4-yl as a spin source. Single crystal XRD revealed that the photocyclization to 1[n] involves a Smiles rearrangement. Radicals 1[n] were investigated by spectroscopic, electrochemical and DFT methods, while racemic helicene 1[7] was resolved and ECD spectra were recorded.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Department of Synthetic Chemistry and Biological Chemistry Graduate School of Engineering, Kyoto University Nishikyo-ku, Kyoto, 615-8510, Japan.
Herein, we report the synthesis and properties of triptycene-based C- and C-symmetric stable triradicals. SQUID magnetometry showed the propeller-shaped triradicals were both an antiferromagnetic equilateral triangle spin system with small spin-spin interactions J/k~-120 K and -106 K, leading to ca. 4/6 coexistence of the doublet/quartet states in thermal equilibrium at room temperature.
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