The Effect of varying Ground-state Aromaticity on the First Molecular Electronic Hyperpolarizabilites of Organic Donor-Acceptor Molecules

A series of compounds of the form 4-dimethylaminophenyl–polyene–acceptor, where the polyene ranges from nothing to all-trans-1,3,5-hexatriene and the acceptor is 2-nitrovinyl, formyl, or 2,2-dicyanovinyl has been prepared and their β values measured by solution electric-field-induced second-harmonic generation; these molecules, which lose only one aromatic resonance upon charge-transfer excitation, show enhanced β compared to bi-aromatic molecules with the same substitution and total conjugation length, such as 4-dimethylamino-4′-nitrostilbene (DANS), a well-known benchmark for high β organic molecules

The First Molecular Electronic Hyperpolarizabilities of Highly Polarizable Organic Molecules: 2,6-Di-tert-butylindoanilines

The first molecular hyperpolarizabilities (β) of a series of 2,6-di-tert-butylindoanilines, measured by electric-field-induced second harmonic generation are somewhat more sensitive to donor strength than was found for analogously substituted nitrostilbenes, and dimethylindoaniline has a β roughly twice that of its 2,6 di-tert-butylated analogue, measured in chloroform; solvatochromic measurements on the former compound suggest that this decrease in hyperpolarizability is consistent with a bound-solvent effect

Synthesis and First Hyperpolarizabilities of Acceptor-substituted β-apo-8’-Carotenal Derived Compounds

The synthesis and second-order nonlinear optical properties of acceptor-substituted biologically derived β-apo-8′-carotenal compounds are reported; electric field-induced second harmonic generation (EFISH) measurements give values of β(0) which are 2–6 times greater than for 4-N,N-dimethylamino-4′-nitrostilbene (DANS)

Universality of weakly bound dimers and Efimov trimers close to Li-Cs Feshbach resonances

We study the interspecies scattering properties of ultracold Li-Cs mixtures in their two energetically lowest spin channels in the magnetic field range between 800 G and 1000 G. Close to two broad Feshbach resonances we create weakly bound LiCs dimers by radio-frequency association and measure the dependence of the binding energy on the external magnetic field strength. Based on the binding energies and complementary atom loss spectroscopy of three other Li-Cs s-wave Feshbach resonances we construct precise molecular singlet and triplet electronic ground state potentials using a coupled-channels calculation. We extract the Li-Cs interspecies scattering length as a function of the external field and obtain almost a ten-fold improvement in the precision of the values for the pole positions and widths of the s-wave Li-Cs Feshbach resonances as compared to our previous work [Pires \textit{et al.}, Phys. Rev. Lett. \textbf{112}, 250404 (2014)]. We discuss implications on the Efimov scenario and the universal geometric scaling for LiCsCs trimers

The dependence of the molecular first hyperpolarizabilities of merocyanines on ground-state polarization and length

We report here the dipole moment (µ) and first hyperpolarizability (β) determined by electric field-induced second harmonic generation, for several merocyanine dyes containing an 1,3,3-trimethylindoline heterocycle as a ‘donor’ in which the ‘acceptor’ end of the molecule and the polyene bridge length was systematically varied; dyes with hexamethine bridges gave positive β, while that with a dimethine bridge gave a negative β value

Creation of a dipolar superfluid in optical lattices

We show that by loading a Bose-Einstein condensate (BEC) of two different atomic species into an optical lattice, it is possible to achieve a Mott-insulator phase with exactly one atom of each species per lattice site. A subsequent photo-association leads to the formation of one heteronuclear molecule with a large electric dipole moment, at each lattice site. The melting of such dipolar Mott-insulator creates a dipolar superfluid, and eventually a dipolar molecular BEC.Comment: 4 pages, 2 eps figure

Feshbach spectroscopy and scattering properties of ultracold Li+Na mixtures

We have observed 26 interspecies Feshbach resonances at fields up to 2050 G in ultracold $^6$Li+$^{23}$Na mixtures for different spin-state combinations. Applying the asymptotic bound-state model to assign the resonances, we have found that most resonances have d-wave character. This analysis serves as guidance for a coupled-channel calculation, which uses modified interaction potentials to describe the positions of the Feshbach resonances well within the experimental uncertainty and to calculate their widths. The scattering length derived from the improved interaction potentials is experimentally confirmed and deviates from previously reported values in sign and magnitude. We give prospects for $^7$Li+$^{23}$Na and predict broad Feshbach resonances suitable for tuning.Comment: 8 pages, 4 figures, version as published in PR

Feshbach spectroscopy and analysis of the interaction potentials of ultracold sodium

We have studied magnetic Feshbach resonances in an ultracold sample of Na prepared in the absolute hyperfine ground state. We report on the observation of three s-, eight d-, and three g-wave Feshbach resonances, including a more precise determination of two known s-wave resonances, and one s-wave resonance at a magnetic field exceeding 200mT. Using a coupled-channels calculation we have improved the sodium ground-state potentials by taking into account these new experimental data, and derived values for the scattering lengths. In addition, a description of the molecular states leading to the Feshbach resonances in terms of the asymptotic-bound-state model is presented.Comment: 11 pages, 4 figure