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Mireille Blanchard-Desce

Publications and source records attributed to Mireille Blanchard-Desce.

25 records · Page 2Linked to original sources

Improved transparency--nonlinearity trade-off with boroxine-based octupolar molecules.

A series of octupolar molecules derived from the boroxine framework were designed and their optical nonlinearities were investigated by performing harmonic light scattering experiments in solution; the molecules were found to combine excellent transparency in the near UV-visible region (lambdamax < or = 280 nm) and significant first-order hyperpolarisabilities (up to beta(0) = 56 x 10(-30) esu).

Journal Article↗

Resonance hyper-Raman scattering from conjugated organic donor-acceptor "push-pull" chromophores with large first hyperpolarizabilities.

Resonance hyper-Raman spectra have been obtained using 1064 nm excitation for several electron donor-acceptor-substituted, pi-conjugated "push-pull" molecules that have large second harmonic hyperpolarizabilities. The hyper-Raman spectra are nearly identical to the resonance Raman spectra measured with 532 nm excitation. This indicates that both the second harmonic hyperpolarizability and the linear absorption are dominated by the same, single electronic transition that is both one- and two-photon allowed. Comparison of resonance Raman and resonance hyper-Raman spectra is proposed as an experimental test of the common two-electronic-state model for the first hyperpolarizability.

Journal Article↗

Mechanisms of membrane potential sensing with second-harmonic generation microscopy.

We characterize the transmembrane voltage response of a novel second-harmonic generation (SHG) marker using a screening protocol with giant unilamellar vesicles. Two mechanisms are found to contribute to the voltage response: (1) an electro-optic-induced alteration of the molecular hyperpolarizability and (2) an electric-field-induced alteration of the degree of molecular alignment. We quantify the relative weights and of these contributions and provide an upper limit to their response time, which is found to be submillisecond. The identification of two voltage response mechanisms leads to new strategies for the molecular design of membrane potential markers.

Cell Membrane↗

Synthesis and photophysical properties of new conjugated fluorophores designed for two-photon-excited fluorescence.

[structure: see text] Novel elongated push-push fluorophores (e.g., 9) were synthesized by 2-fold Sonogashira or Wittigminus signHorner reactions. Modulation of the length and topology of the conjugated connectors allows tuning of their photophysical properties. In addition, their photoluminescence can be adjusted by playing on polarity. Derivatives combining enhanced two-photon absorption cross section (sigma2) in the visible red and high fluorescence quantum yield (Phi) have been obtained. Such fluorophores hold promise for nonlinear imaging of biological systems.

Journal Article↗

Multiple relaxation pathways in push-pull polyenes.

Subpicosecond absorption and gain spectroscopy are used to investigate the excited-state behavior of push-pull polyenes made of a diethylthiobarbituric acid electron-acceptor group and a dibutylaniline electron-donor group linked by a pi-conjugated chain. Four polyenes of increasing length, ranging from n = 2 to 5 double bonds, are compared. The relaxation path and relaxation kinetics are studied in dioxane and in cyclohexane, a polar and a nonpolar solvent, respectively. In dioxane, the results provide evidence for the formation of an emissive transient state on an ultrashort time scale (2-3 ps) attributed to a charge transfer (CT) state. The regular shift of the gain peak of this transient state with increase in the chain length (ca. 100 nm per added double bond) indicates that its structure is similar to that of a cyanine, i.e. with a fully conjugated polyenic chain. Its lifetime ranges from a few tens to a few hundreds of picoseconds depending on the chain length. When the number of double bonds increases from n = 2 to 3, the lifetime increases, then decreases continuously for longer chains. In cyclohexane, where the transient CT state is not formed, the decay of the initial excited state follows the same trend when the chain length increases but the lifetimes are shorter than that of the CT state in dioxane. In both solvents, the characterization of long-lived photoproducts by synchronizing two low repetition-rate subpicosecond laser systems demonstrates a change in the relaxation route as the chain length increases. Isomerization occurs for n = 2, whereas intersystem crossing to the triplet state occurs for n = 4. The change in the relaxation channel is observed for n = 3 in both solvents with however a solvent-dependent behavior. In dioxane, relaxation to the triplet state is already observed for n = 3, while an intermediate regime with a relaxation directly to the ground state is observed in cyclohexane. The photophysics of the studied push-pull polyenes is tentatively compared to that of polymethine cyanines and substituted carotenoids.

Journal Article↗