ABSTRACT
A strategy for the design of molecules with large two-photon absorption cross sections, delta, was developed, on the basis of the concept that symmetric charge transfer, from the ends of a conjugated system to the middle, or vice versa, upon excitation is correlated to enhanced values of delta. Synthesized bis(styryl)benzene derivatives with donor-pi-donor, donor-acceptor-donor, and acceptor-donor-acceptor structural motifs exhibit exceptionally large values of delta, up to about 400 times that of trans-stilbene. Quantum chemical calculations performed on these molecules indicate that substantial symmetric charge redistribution occurs upon excitation and provide delta values in good agreement with experimental values. The combination of large delta and high fluorescence quantum yield or triplet yield exhibited by molecules developed here offers potential for unprecedented brightness in two-photon fluorescent imaging or enhanced photosensitivity in two-photon sensitization, respectively.
Subject(s)
Aniline Compounds/chemistry , Fluorescence , Photons , Stilbenes/chemistry , Stilbenes/chemical synthesis , Chemical Phenomena , Chemistry, Physical , PhotochemistryABSTRACT
Photorefractive polymers with high diffraction efficiency in the visible and near-infrared regions of the electromagnetic spectrum have been developed. These polymers, which have a large dynamic range because of their high orientational birefringence, incorporate a dye designed to have a large dipole moment and a high linear polarizability anisotropy. Such polymers have enabled demonstrations of imaging through scattering media, using a holographic time-gating technique at a wavelength that is compatible with the transparency of biological tissues and with the emission of low-cost semiconductor laser diodes.
Subject(s)
Diagnostic Imaging/methods , Infrared Rays , Polymers , Birefringence , Coloring Agents , Image Processing, Computer-Assisted , Lasers , Refractometry , Scattering, Radiation , TemperatureABSTRACT
We demonstrate the use of a near-infrared-sensitive photorefractive polymer with high efficiency for imaging through scattering media, using an all-optical holographic time gate. Imaging through nine scattering mean free paths is performed at 800nm with a mode-locked continuous-wave Ti:sapphire laser.
ABSTRACT
Large two-photon absorptivities are reported for symmetrical bis-donor stilbene derivatives with dialkylamino or diphenylamino groups. These molecules exhibit strong optical limiting of nanosecond pulses over a broad spectral range in the visible. Relative to bis(di-n-butylamino)stilbene, bis(diphenylamino)stilbene exhibits a 90-nm red shift of its optical limiting band but only a minimal shift of ~13 nm of its lowest one-photon electronic absorption band. Mixtures of these compounds offer an unprecedented combination of broad optical limiting bandwidth and high linear transparency.
