Ligand Effects on the Spin Relaxation Dynamics and Coherent Manipulation of Organometallic La(II) Potential Qu d its
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Nodaraki, Lydia E.
Ariciu, Ana-Maria
Huh, Daniel N.
Liu, Jingjing
Martins, Daniel O. T. A.
Ortu, Fabrizio
Winpenny, Richard E. P.
Chilton, Nicholas F.
McInnes, Eric J. L.
Mills, David P.
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We present pulsed electron paramagnetic resonance (EPR) studies on three La(II) complexes, [K(2.2.2-cryptand)][La(Cp′) 3] (1), [K(2.2.2-cryptand)][La(Cp″) 3] (2), and [K(2.2.2-cryptand)][La(Cp tt) 3] (3), which feature cyclopentadienyl derivatives as ligands [Cp′ = C 5H 4SiMe 3; Cp″ = C 5H 3(SiMe 3) 2; Cp tt = C 5H 3(CMe 3) 2] and display a C 3 symmetry. Long spin-lattice relaxation (T 1) and phase memory (T m) times are observed for all three compounds, but with significant variation in T 1 among 1-3, with 3 being the slowest relaxing due to higher s-character of the SOMO. The dephasing times can be extended by more than an order of magnitude via dynamical decoupling experiments using a Carr-Purcell-Meiboom-Gill (CPMG) sequence, reaching 161 μs (5 K) for 3. Coherent spin manipulation is performed by the observation of Rabi quantum oscillations up to 80 K in this nuclear spin-rich environment ( 1H, 13C, and 29Si). The high nuclear spin of 139La (I = 7/2), and the ability to coherently manipulate all eight hyperfine transitions, makes these molecules promising candidates for application as qudits (multilevel quantum systems featuring d quantum states; d >2) for performing quantum operations within a single molecule. Application of HYSCORE techniques allows us to quantify the electron spin density at ligand nuclei and interrogate the role of functional groups to the electron spin relaxation properties.
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Journal of the American Chemical Society
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