Ultrafast Photoelimination of Nitrogen from Upper Excited States of Diazoalkanes and the Fate of Carbenes Formed in the Reaction.

The photochemical reactivity of diphenyldiazomethane 1 and phenyl 1- and 2-adamantyl diazomethanes 2 and 3, respectively, was investigated by transient absorption spectroscopy (TA). Photoelimination of N2 upon UV excitation takes place in the anti-Kasha ultrafast photochemical reaction from the upper excited singlet states to deliver singlet carbenes, which were, in the case of 1 and 2, detected by fs-TA. The reactivity of the carbenes differs with respect to the substituent at the carbene center. The singlet car-1 in a nonpolar solvent delivers the triplet carbene by intersystem crossing (ISC). Singlet car-2 does not undergo ISC but reacts in the intermolecular insertion reactions into C-H bonds. Car-3 has an α-C-H bond next to the carbene center and reacts rapidly in the intramolecular C-H insertion reaction to deliver alkene, precluding its detection by fs-TA. However, the isolation of ketone photoproducts from 3 is highly indicative of triplet car-3's intermediate formation. The TA spectra from the S1-S3 states of 1-3 were computed using time-dependent density functional theory, while the multiconfigurational perturbation theory to the second order was used for the absorption spectra of the corresponding singlet and triplet carbenes. The modeled and measured spectra are in good agreement, and the computations corroborate the assignments of the key short-lived intermediates.

Photogeneration of quinone methide from adamantylphenol in an ultrafast non-adiabatic dehydration reaction.

The ultrafast photochemical reaction of quinone methide (QM) formation from adamantylphenol was monitored in real time using femtosecond transient absorption spectroscopy and fluorescence upconversion in solution at room temperature. Experiments were complemented by theoretical studies simulating the reaction pathway and elucidating its mechanism. Excitation with sub-20 fs UV pulses and broadband probing revealed ultrafast formation of the long-lived QM intermediate directly in the ground state, occurring with a time constant of around 100 fs. UV-vis transient absorption data covering temporal dynamics from femtoseconds to hundreds of milliseconds revealed persistence of the absorption band assigned to QM and partially overlapped with other contributions tentatively assigned to triplet excited states of the adamantyl derivative and the phenoxyl radical that are clearly distinguished by their evolution on different time scales. Our data, together with the computations, provide evidence of a non-adiabatic photodehydration reaction, which leads to the formation of QM in the ground state via a conical intersection, circumventing the generation of a transient QM excited state.

Femtosecond coherent anti-Stokes Raman scattering spectroscopy of hydrogen bonded structure in water and aqueous solutions.

Femtosecond coherent anti-Stokes Raman scattering (fsCARS) spectroscopy, together with perturbation theory based numerical calculation, is employed to study OH stretching (υOH) of pure water and aqueous lithium chloride solutions. Vibrational OH stretching (υOH) modes of aqueous solutions are Raman-excited by a pair of ultrashort, femtosecond laser pulses, and then probed through inelastic scattering of a third, time-delayed laser field. In order to overcome limited spectral resolution of fsCARS, numerical evaluation of the CARS signal through vibrational wave packet propagation was employed in order to confirm the position of distinctive OH stretching mode that is complicated by intramolecular and intermolecular vibrational coupling. Moreover, in order to come to a microscopic description of the observed CARS spectra for aqueous solutions, we have performed molecular dynamics simulations of aqueous lithium chloride solutions with varying concentrations at ambient conditions. To this end we have analyzed the equilibrium distributions of hydrogen bonds in the first solvation shells of the ions as well as in bulk water and also computed the average number of hydrogen bonds per water molecule. According to our experimental and theoretical results on time evolution of Raman OH stretching band of water, it can be inferred that the dissolved ions mainly influence hydrogen bond strength and structure of water molecules in the first hydration shell, the addition of lithium chloride primarily breaks the tetrahedral hydrogen bonding, promotes formation of the donor hydrogen bonding in water, and slightly increases the amount of free OH bonds.

Energy transfer and spectroscopic characterization of a perylenetetracarboxylic diimide (PDI) hexamer.

We report a comprehensive study on a newly synthesized perylenetetracarboxylic diimide (PDI) hexamer together with its corresponding monomer and dimer by means of steady-state absorption and fluorescence as well as femtosecond broadband transient absorption measurements. The structure of the PDI hexamer is nearly arranged in a 3-fold symmetry by three identical and separated dimers. This unique structure makes the excited state energy relaxation processes more complex due to the existence of two different intramolecular interactions: a strong interaction between face-to-face PDIs in dimers and a relatively weak interaction between the three separated PDI dimers. The steady-state spectra and the ground state structural optimization show that the steric effect plays a dominant role in keeping the formation of the face-to-face stacked PDI-dimer within the PDI-hexamer, indicating that some level of a pre-associated excimer had formed already in the ground state for the dimer in the hexamer. Femtosecond transient absorption experiments on the PDI hexamer reveal a fast (∼200 fs) localization process and a sequential relaxation to a pre-associated excimer trap state from the delocalized exciton state with about 1.2 ps after the initially delocalized excitation. Meanwhile, excitation energy transfer among the three separated dimers within the PDI-hexamer is also revealed by the anisotropic femtosecond pump-probe transient experiments, where the hopping time is about 2.8 ps. A relaxed excimer state is further formed in 7.9 ps after energy hopping and conformational relaxation.

Atomic wave-packet dynamics and third-harmonic generation in sodium.

In femtosecond degenerate four-wave mixing experiments in sodium vapor, quantum beats are observed at the wavelength of the third harmonic when the fundamental beams are three-photon resonant. The period of beating, which corresponds to fine structure energy-level splitting, does not change with the atomic number density, buffer gas pressure, or laser intensity. Surprisingly, the third-harmonic signal is observed only at negative time delays for the transient grating pulse sequence. We relate this to the well-known interference effect between excitation pathways involving the fundamental and the third-harmonic fields, which leaves atoms virtually unexcited and prevents formation of population grating.

Excited state dynamics of ß-carotene studied by means of transient absorption spectroscopy and multivariate curve resolution alternating least-squares analysis.

Determination of the excited-state dynamics of carotenoids has attracted considerable interest, engendering a number of controversial hypotheses because of the strongly overlapping spectral peaks and complicated dynamics of transient species. In the present work, aiming for better understanding the complexity of excited-state processes in carotenoids, excited-state dynamics of all-trans-ß-carotene in ethanol was investigated by femtosecond pump-probe spectroscopy. Following the excitation of the strongly allowed S2 state of the ß-carotene, transient absorption spectra were recorded in the visible spectral range. For comparison, the time-resolved transient absorption spectra are analyzed in a conventional way, fitting kinetic traces with a multi-exponential function at chosen wavelengths from obtained spectra, and then again by means of the soft-modeling multivariate curve resolution alternating least-squares analysis (MCR-ALS) method for modeling pure profiles and the generalized two-dimensional (2D) correlation spectroscopy data analysis for providing additional information on the dynamics of spectral features. MCR-ALS analysis shows that both the dynamics of the S* state, identified using the 2D correlation spectra, and the S1 state develop on a different timescale than the relaxation of the vibrationally hot S1v' state. Hot S1v' and S* states are shown to have different species associated difference spectra. Results of our analysis indicate that the S* state observed in this work is not the hot S1v' state but instead a separate singlet state.

Intramolecular charge transfer and solvation dynamics of thiolate-protected Au20(SR)16 clusters studied by ultrafast measurement.

It is accepted that the monolayer ligand shell in monolayer-protected gold nanoclusters (MPCs) plays an important role in stabilizing the metal core structure. Previous reports have shown that the core and shell do not interact chemically, and very few studies investigating the intramolecular charge transfer (ICT) between the core and ligand shell in clusters have been reported. The underlying excited state relaxation mechanisms about the influence of solvents, the optically excited vibration, and the roles of the core and shell in charge transfer remain unknown to a large extent. Here we report a femtosecond transient absorption study of a Au20(SR)16 (R = CH2CH2Ph) cluster in toluene and tetrahydrofuran. The ICT from the outside shell to the inside core upon excitation in Au20(SR)16 is identified. The observed solvation-dependent oscillations in different solvents further confirm the photoinduced ICT formation in Au20(SR)16. The results provide a fundamental understanding of the structure-property relationships about the solvation-dependent core-shell interaction in Au MPCs.

Spectroscopic evidence for unusual microviscosity in imidazolium ionic liquid and tetraethylene glycol dimethyl ether cosolvent mixtures.

The rotational dynamics of coumarin 153 (C153) in imidazolium-based ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim][PF(6)]) and tetraethylene glycol dimethyl ether (TEGDME) mixtures across all mole fractions have been investigated to determine the local viscosity of the microenvironment surrounding the probe molecules. The excimer-to-monomer fluorescence emission intensity ratio (I(E)/I(M)) of a well-known microviscosity probe, 1,3-bis(1-pyrenyl)propane (BPP), is also employed to study the microviscosity of the mixtures as a complementary measurement. The rotational dynamics of C153 show that there are incompact and compact domains within the heterogeneous structural [bmim][PF(6)], resulting in fast and slow components of C153 rotational dynamics. The microviscosity in different structural domains of [bmim][PF(6)] before and after adding cosolvent TEGDME with different mole fractions is further investigated by studying the fluorescence anisotropy decay of probe molecules. The obtained average rotation time constants show that the microviscosity of [bmim][PF(6)] is enhanced after mixing with a certain amount of TEGDME, although the bulk viscosity of TEGDME itself is much lower than that of the ionic liquid. This unusual behavior of microviscosity enhancement is further proven by the steady state fluorescence measurement with the microviscosity probe of BPP. The microviscosity enhancement is reasonably demonstrated by the fast time constant of C153 rotational dynamics and the departure between the experimentally observed and calculated ratio of I(E)/I(M) of BPP, which shows that this effect is most pronounced at intermediate mole fractions of the [bmim][PF(6)] and TEGDME mixtures. The strengthening effects caused by the molecular interactions between TEGDME and structural heterogeneous ionic liquid [bmim][PF(6)] are proposed to interpret the unusual microviscosity behaviors.

Localized emitting state and energy transfer properties of quadrupolar chromophores and (multi)branched derivatives.

In order to better understand the nature of intramolecular charge and energy transfer in multibranched molecules, we have synthesized and studied the photophysical properties of a monomer quadrupolar chromophore with donor-acceptor-donor (D-A-D) electronic push-pull structure, together with its V-shaped dimer and star-shaped trimers. The comparison of steady-state absorption spectra and fluorescence excitation anisotropy spectra of these chromophores show evidence of weak interaction (such as charge and energy transfer) among the branches. Moreover, similar fluorescence and solvation behavior of monomer and branched chromophores (dimer and trimer) implies that the interaction among the branches is not strong enough to make a significant distinction between these molecules, due to the weak interaction and intrinsic structural disorder in branched molecules. Furthermore, the interaction between the branches can be enhanced by inserting π bridge spacers (-C═C- or -C≡C-) between the core donor and the acceptor. This improvement leads to a remarkable enhancement of two-photon cross-sections, indicating that the interbranch interaction results in the amplification of transition dipole moments between ground states and excited states. The interpretations of the observed photophysical properties are further supported by theoretical investigation, which reveal that the changes of the transition dipole moments of the branched quadrupolar chromophores play a critical role in observed the two-photon absorption (2PA) cross-section for an intramolecular charge transfer (ICT) state interaction in the multibranched quadrupolar chromophores.