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pmid: 33051985
handle: 2158/1235500 , 2318/1765157
AbstractThe coherence time of the 17‐electron, mixed sandwich complex [CpTi(cot)], (η8‐cyclooctatetraene)(η5‐cyclopentadienyl)titanium, reaches 34 μs at 4.5 K in a frozen deuterated toluene solution. This is a remarkable coherence time for a highly protonated molecule. The intramolecular distances between the Ti and H atoms provide a good compromise between instantaneous and spin diffusion sources of decoherence. Ab initio calculations at the molecular and crystal packing levels reveal that the characteristic low‐energy ring rotations of the sandwich framework do not yield a too detrimental spin‐lattice relaxation because of their small spin–phonon coupling. The volatility of [CpTi(cot)] and the accessibility of the semi‐occupied, non‐bonding d orbital make this neutral compound an ideal candidate for single‐qubit addressing on surface and quantum sensing in combination with scanning probe microscopy.
quantum coherencetitanium, DFT; electron paramagnetic resonance; metallocene complexes; quantum coherence; titanium, electron paramagnetic resonance, Titanium, Metallocene complexes, Electron Paramagnetic Resonance, therahertz specroscopy, DFT, spin-phonon coupling, DFT, metallocene complexes
quantum coherencetitanium, DFT; electron paramagnetic resonance; metallocene complexes; quantum coherence; titanium, electron paramagnetic resonance, Titanium, Metallocene complexes, Electron Paramagnetic Resonance, therahertz specroscopy, DFT, spin-phonon coupling, DFT, metallocene complexes
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