Danilo Pedron

Novel heterocycle-based two-photon absorbing dyes.

[structure: see text]. The synthesis and nonlinear optical characterization of two novel heteroaromatic-based chromophores is described. The new dyes present an A-pi-D-pi-A general framework, where A is a pi-deficient heteroaromatic ring (pyridine, quinoline, benzothiazole) and D a pi-excessive pyrrolyl moiety. Both systems exhibit large two-photon absorption (TPA) values in the femtoseconds regime (TPA cross section as high as 150 x 10(-50) cm(4) s photon(-1) molecule(-1) with 150 fs laser pulses). Their TPA-based optical limiting activity is also shown.

Novel heteroaromatic-based multi-branched dyes with enhanced two-photon absorption activityElectronic supplementary information (ESI) available: Experimental section. See http://www.rsc.org/suppdata/cc/b3/b305995b/

The first examples of heterocycle-based multi-branched dyes with efficient two-photon absorption (TPA) activity are reported; the novel chromophores exhibit large TPA cross sections (as high as 1600 x 10(-50) cm4 s photon(-1) molecule(-1), measured with 150 fs laser pulses at 800 nm); a strong cooperative enhancement in the branched systems with respect to the one-dimensional sub-units is found.

“Nanogranite” and glassy inclusions: The anatectic melt in migmatites and granulites

Using as a case study a granulite from the Kerala Khondalite Belt, India, we show that a former anatectic melt can be preserved as tiny (<25 μm) droplets within refractory minerals, in this case garnet. The melt is either fully crystallized as a Qtz-Ab-Kfs-Bt cryptocrystalline aggregate (“nanogranite”), or completely glassy in inclusions <15 μm. Both nanogranite and glassy inclusions have a peraluminous, ultrapotassic granitic composition that, in this case, does not correspond to a “minimum melt” and points to high melting temperatures, in agreement with the ultrahigh-temperature origin of the rock. This discovery indicates that peritectic minerals, growing during incongruent melting reactions, act as hosts for inclusions of anatectic melt, and that in the general case of slow cooling of the crust these inclusions will occur as nanogranite. Exceptionally, in the smallest inclusions, glass may be present due to inhibition of crystallization. Our results extend the frontiers of petrological and geochemical research in crustal melting, as the composition of natural anatectic melts can be directly analyzed rather than assumed.

Photomodulation of the chiroptical properties of new chiral methacrylic polymers with side chain azobenzene moieties.

We have investigated the photoinduced optical properties of a new class of chiral methacrylic polymers characterised by the presence in the side chain of an optically active pyrrolidinyl ring linked to a trans-azoaromatic system. The homopolymers are enantiomerically pure and their strong optical activity indicates that the macromolecules assume, both in solution and in solid thin films, highly homogeneous conformations with a prevailing chirality. As expected, the studied polymers exhibit reversible linear dichroism and birefringence when irradiated with linearly polarised light. By irradiating with circularly polarised light, we have discovered that it is possible to photomodulate the chiroptical properties of the polymer films. After irradiation with L-polarised light, the CD spectra of the films show a net inversion of their relative sign. The effect is reversible and the original shape of the CD spectra can be restored by pumping with R-polarised radiation. This unexpected new phenomenon can be explained in terms of the ability of the L-polarised radiation to invert the prevailing helicity of the polymeric chains. The observed effect seems to open new possibilities for the use of azobenzene-containing materials as chiroptical switches.

Effective two-photon absorption cross section of heteroaromatic quadrupolar dyes: dependence on measurement technique and laser pulse characteristics.

The linear and nonlinear optical properties of the heteroaromatic push-pull-push two-photon absorbing dye N-methyl-2,5-bis[1-(N-methylpyrid-4-yl)ethen-2-yl]-pyrrole ditriflate (PEPEP) are reported. The determination of the two-photon absorption (TPA) cross-section spectrum has been performed with different techniques: femtosecond TPA-white light continuum probe experiments, two-photon-induced fluorescence, and open aperture Z-scan measurements using both nanosecond and femtosecond laser pulses. The measured TPA cross sections and their wavelength dispersion show a marked dependence on the parameters of the laser pulses and on the measurement technique employed. These properties are discussed in terms of the different microscopic mechanisms that can contribute to the multiphoton absorption processes, with different weight depending on the measurement conditions and on the photophysical parameters of the dye.

Photoinduced chiroptical bistability in new chiral methacrylic azobenzene-containing polymers

The photoinduced chiroptical properties of an optically active methacrylic polymer bearing in the side-chain a conjugated trans-azoaromatic chromophore linked to the main chain through a chiral cyclic pyrrolidine moiety of one prevailing absolute configuration have been investigated. The polymeric film is characterized by a strong optical activity that can be amplified and reversibly modulated by irradiation with circularly polarized (CP) light at 488 nm. A remarkable modification of the shape of the circular dichroism (CD) spectrum after the initial irradiation steps is observed, with an amplification of the CD signal upon increasing the total irradiation fluence. The most important results are connected with the handedness of the CP radiation: left circularly polarized (CP-L) light is able to reverse the relative sign of the CD spectra, whereas by pumping with right circularly polarized (CP-R) radiation, it is possible to recover the original shape of the signal. This well reproducible and reversible effect suggests the possibility to use the investigated material for chiroptical switching.

Non‐Resonant z‐Scan Characterization of the Third‐Order Nonlinear Optical Properties of Conjugated Poly(thiophene azines)

The nonlinear optical properties of a functionalized poly(thiophene azine), namely, poly(3,4-didodecylthiophene azine), PAZ, at the optical telecommunication wavelength of 1550 nm are investigated by means of the closed-aperture z-scan technique in both thin films and solutions. Values of chi((3))=(2.4+/-0.4)x10(-13) esu, n(2)=(4.0+/-0.7)x10(-15) cm(2) W(-1), and gamma=(4.5+/-0.7)x10(-34) esu are estimated for the third-order (Kerr) susceptibility, the intensity-dependent refractive index, and the molecular second hyperpolarizability of solution samples, respectively. A very small dependence on the polymer chain length is found. Markedly higher values of (4.4+/-1.1)x10(-11) esu, (6.6+/-1.0)x10(-13) cm(2) W(-1), and (5.0+/-0.8)x10(-33) esu are measured for the corresponding quantities in thick (up to 20 mum) polymer films cast on quartz plates. The enhancement of the NLO responses on going from solution to solid samples is attributed to a partially ordered structure and to the presence of interchain interactions leading to greater pi-electron delocalization in the cast polymer films. The results are compared with those previously obtained by using third-harmonic generation (THG), taking into account that those data were measured under conditions of three-photon resonance, whereas our z-scan measurements are fully off-resonance.

Reversible chirality inversion of photochromic methacrylic polymers upon irradiation with one-handed circularly polarized light

Abstract Methacrylic polymers bearing in the side-chain the electron donor–acceptor conjugated trans -azoaromatic chromophore linked to the main chain through a chiral moiety of one prevailing absolute configuration, have been prepared and investigated as materials suitable to reversible optical storage. In addition to the induction of a significant birefringence, upon irradiation of the polymeric film with linearly polarized (LP) light, combined with a relevant stability and reproducibility after repeated writing–erasing cycles with linearly and circularly polarized (CP) light, respectively, the material exhibits inversion of chirality when the erasing step is performed with one-handed CP light of the opposite sense with respect to the original chirality handedness assumed by the material as a consequence of its intrinsically chiral structure. The process appears to be reversible, and the material may re-assume the original screw sense by irradiating with circularly polarized light of the appropriate sense, regardless previous ordering by irradiation with LP light has been performed. The sense of chirality assumed by the material upon irradiation with one-handed CP light is unaffected by heating; and annealing of the film at higher temperature, above the glass transition, produces an enhancement of the dichroic bands related to the electronic transitions of the azoaromatic chromophore.

Coupling of electrons to intermolecular phonons in molecular charge transfer dimers: A resonance Raman study

We report resonance Raman scattering (RRS) spectra and Raman excitation profiles (REP) of a system containing π dimers of identical molecular radical ions measured with laser excitation in resonance with the charge transfer (CT) transition. A Peierls–Hubbard (PH) Hamiltonian has been used to model the investigated system and to calculate its optical and RRS properties. Results are reported for two polyoxometallate salts of tetrathiafulvalene (TTF), namely (TTF)2(W6O19) and (TTF)2(Mo6O19) whose structures contain almost isolated (TTF+)2 dimers. The RRS spectra of (TTF)2(W6O19), measured in resonance with the CT absorption band centered at 832 nm, show three phonon modes located at 55, 90, and 116 cm−1 which are strongly resonance enhanced. These modes have been associated to the out‐of‐phase combinations of the translational motions of the two molecules composing the dimer. Such modes are effective in modulating the intradimer transfer integral, thus providing an efficient mechanism for coupling with the electronic system and for enhancement of the scattering intensity at resonance with the CT transition. The REP for the three strongly coupled modes of (TTF)2(W6O19) have been measured with laser excitation wavelengths ranging from 740 to 930 nm. Quantitative analysis of the REP data has been performed based on a perturbative solution of the PH model to second order in the electron‐molecular‐vibration (EMV) and electron‐intermolecular‐phonon (EIP) interactions. The CT absorption profile and the REP’s have been calculated using a time correlator technique and the model parameters have been optimized in order to fit the experimental REP data. Infrared vibronic absorptions of (TTF)2(W6O19), originated by the EMV coupling, have been measured and independent information on the electronic parameters of the PH model have been derived. This has made the choice of the fitting parameters used for the REP calculations rather unambiguous and has allowed us to obtain, for the first time, reliable experimental estimates of the EIP coupling constants.We report resonance Raman scattering (RRS) spectra and Raman excitation profiles (REP) of a system containing π dimers of identical molecular radical ions measured with laser excitation in resonance with the charge transfer (CT) transition. A Peierls–Hubbard (PH) Hamiltonian has been used to model the investigated system and to calculate its optical and RRS properties. Results are reported for two polyoxometallate salts of tetrathiafulvalene (TTF), namely (TTF)2(W6O19) and (TTF)2(Mo6O19) whose structures contain almost isolated (TTF+)2 dimers. The RRS spectra of (TTF)2(W6O19), measured in resonance with the CT absorption band centered at 832 nm, show three phonon modes located at 55, 90, and 116 cm−1 which are strongly resonance enhanced. These modes have been associated to the out‐of‐phase combinations of the translational motions of the two molecules composing the dimer. Such modes are effective in modulating the intradimer transfer integral, thus providing an efficient mechanism for coupling with the e...

Design and synthesis of heterocyclic multi-branched dyes for two-photon absorption

Abstract We report the first example of a heterocycle-based multi-branched two-photon absorption (TPA) dye. We show that the new chromophore presents a very large TPA cross-section in the femtoseconds (fs) regime. Comparison of the TPA cross-sections between the branched system and the corresponding “monomeric unit” shows a strong cooperative enhancement. A value of 22.6:1, corresponding to a 750% enhancement, was observed.