ESR and 1H-,19F-ENDOR/TRIPLE Study of Fluorinated Diphenylnitroxides as Synthetic Bus Spin-Qubit Radicals with Client Qubits in Solution

Electron and nuclear spins as quantum bits (qubits) have been the focus of current issues in quantum information science/technology and related fields. From the viewpoint of chemistry, synthetic spin qubits are emerging. Diphenylnitroxide (DPNO) and its novel fluorine-substituted radicals are charac...

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Veröffentlicht in:The journal of physical chemistry letters 2011-03, Vol.2 (5), p.449-453
Hauptverfasser: Yoshino, Tomohiro, Nishida, Shinsuke, Sato, Kazunobu, Nakazawa, Shigeaki, Rahimi, Robabeh D, Toyota, Kazuo, Shiomi, Daisuke, Morita, Yasushi, Kitagawa, Masahiro, Takui, Takeji
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Sprache:eng
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Zusammenfassung:Electron and nuclear spins as quantum bits (qubits) have been the focus of current issues in quantum information science/technology and related fields. From the viewpoint of chemistry, synthetic spin qubits are emerging. Diphenylnitroxide (DPNO) and its novel fluorine-substituted radicals are characterized as synthetic electron bus spin-qubits by continuous-wave ESR and 1H-,19F-ENDOR/TRIPLE spectroscopy in solution and by DFT calculations. The partially fluorinated DPNOs have been synthesized to illustrate that they are candidates for the synthetic bus spin-qubits with well-defined client qubits. The fluorinated DPNOs undergo spin delocalization, dominating the robust spin polarization in the π-conjugation of phenyl rings, serving to increase the number of distinguishable client qubits from three to six.
ISSN:1948-7185
1948-7185
DOI:10.1021/jz101650z