Entangling remote nuclear spins linked by a chromophore.

Molecular nanostructures may constitute the fabric of future quantum technologies, if their degrees of freedom can be fully harnessed. Ideally one might use nuclear spins as low-decoherence qubits and optical excitations for fast controllable interactions. Here, we present a method for entangling two nuclear spins through their mutual coupling to a transient optically excited electron spin, and investigate its feasibility through density-functional theory and experiments on a test molecule. From our calculations we identify the specific molecular properties that permit high entangling power gates under simple optical and microwave pulses; synthesis of such molecules is possible with established techniques.

Ion-induced manipulation of photochemical pathways in crown ether compounds based on fluorinated oligophenylenevinylenes: the border between ultrafast photoswitches and photoproduced nanomaterials.

The photochemical and photophysical properties of the crown ethers trans,trans-1,4-bis[2-(3',4'-benzo 15-crown 5)ethenyl]-2,3,5,6-tetrafluorobenzene (1) and trans,trans-1,4-bis[2-(3',4'-benzo 18-crown 6) ethenyl]-2,3,5,6-tetrafluorobenzene (2) were investigated in the absence and presence of groups I and II metal ions. The photophysical methods used include steady state flurescence, uv spectroscopy, and ultrafast transient absorption spectroscopy. Both compounds showed solvatochromic behavior, due to intramolecular charge transfer state formation, and efficient fluorescence in polar solvents. Photophysical behavior was dependent on the metal ion. The addition of metal ions that completely fit into the crown ether cavity resulted in significant blue shifts in the fluorescence emission spectra (chemosensing properties). Partially fitting ions changed the fluorescence spectra slightly. Transient absorption measurements revealed fast and slow decay components with time constants of 10-20 and 500-600 ps for all fitting ions, respectively. The latter is assigned to a trans-cis photoisomerization process, which decreased in efficiency in the presence of partially fitting ions, i.e., increasing ion size. Steady state irradiation showed clear evidence of a change in the absorption spectra. Trans-cis photoisomerization and [2 + 2] photocycloaddition were found to compete with fluorescence. The ions Li+, Na+, and Ca2+, which fit into the cavity, direct the photoisomerization. Larger ions (K+, Rb+, Sr2+ and Ba2+) that partially fit the cavity cause photocycloaddition. Quantum yields of the photoreaction are between 0.1 and 0.3. Analysis of the photo-product obtained for the 1-Sr2+ system revealed a compound with a molecular weight of nanosize dimension, which was equivalent to seven mass units of 1. The higher molecular weight product was formed due to alternately stacked supramolecular assemblies.