Experimental and theoretical insights into the influence of electronic density on proton-transfer reactions.

We report on the excited-state behavior of proton-transfer phenanthroimidazole derivatives, such as HPPI and NMHPPI, in solutions using steady-state and femto- to nanosecond time-resolved fluorescence spectroscopies. Experimental observations are supported by theoretical calculations (TDDFT). In dichloromethane (DCM) and acetonitrile (ACN), two different paths are found for the excited-state intramolecular proton-transfer (ESIPT) reactions following two different channels. A fast and direct channel (ESIPT1) in 1-2.5 ps and a slower one (ESIPT2) in 12-15 ps, the latter being more influenced by the solvent viscosity (30 ps for HPPI and 20 ps for NMHPPI in triacetin (TAC) solutions). The slowing down of the ESIPT2 reaction is explained in terms of an intramolecular charge transfer (ICT) reaction coupled to a twisting motion to reach a more suitable conformation of the involved parts in the proton-transfer motion. The absence of OH/OD exchange effects in the ultrafast and slow proton-transfer dynamics suggests that the ESIPT reactions, which involve intramolecular and solvent coordinates, do not occur via tunneling. These results reveal new insights into the photobehavior of proton-transfer dyes, which might help in designing photosensors or lighting devices.

Photochemistry and Photophysics in Silica-Based Materials: Ultrafast and Single Molecule Spectroscopy Observation.

Silica-based materials (SBMs) are widely used in catalysis, photonics, and drug delivery. Their pores and cavities act as hosts of diverse guests ranging from classical dyes to drugs and quantum dots, allowing changes in the photochemical behavior of the confined guests. The heterogeneity of the guest populations as well as the confinement provided by these hosts affect the behavior of the formed hybrid materials. As a consequence, the observed reaction dynamics becomes significantly different and complex. Studying their photobehavior requires advanced laser-based spectroscopy and microscopy techniques as well as computational methods. Thanks to the development of ultrafast (spectroscopy and imaging) tools, we are witnessing an increasing interest of the scientific community to explore the intimate photobehavior of these composites. Here, we review the recent theoretical and ultrafast experimental studies of their photodynamics and discuss the results in comparison to those in homogeneous media. The discussion of the confined dynamics includes solvation and intra- and intermolecular proton-, electron-, and energy transfer events of the guest within the SBMs. Several examples of applications in photocatalysis, (photo)sensors, photonics, photovoltaics, and drug delivery demonstrate the vast potential of the SBMs in modern science and technology.

A slowing down of proton motion from HPTS to water adsorbed on the MCM-41 surface.

We report on the steady-state and femtosecond-nanosecond (fs-ns) behaviour of 8-hydroxypyrene-1,3,6-trisulfonate (pyranine, HPTS) and its interaction with mesoporous silica based materials (MCM-41) in both solid-state and dichloromethane (DCM) suspensions in the absence and presence of water. In the absence of water, HPTS forms aggregates which are characterized by a broad emission spectrum and multiexponential behavior (τsolid-state/DCM = 120 ps, 600 ps, 2.2 ns). Upon interaction with MCM41, the aggregate population is found to be lower, leading to the formation of adsorbed monomers. In the presence of water (1%), HPTS with and without MCM41 materials in DCM suspensions undergoes an excited-state intermolecular proton-transfer (ESPT) reaction in the protonated form (ROH*) producing a deprotonated species (RO(-)*). The long-time emission decays of the ROH* in different systems in the presence of water are multiexponential, and are analysed using the diffusion-assisted geminate recombination model. The obtained proton-transfer and recombination rate constants for HPTS and HPTS/MCM41 complexes in DCM suspensions in the presence of water are kPT = 13 ns(-1), krec = 7.5 Å ns(-1), and kPT = 5.4 ns(-1), krec = 2.2 Å ns(-1), respectively, The slowing down of both processes in the latter case is explained in terms of specific interactions of the dye and of the water molecules with the silica surface. The ultrafast dynamics (fs-regime) of the HPTS/MCM41 complexes in DCM suspensions, without and with water, shows two components which are assigned to intramolecular vibrational-energy relaxation (IVR) (∼120 fs vs. ∼0.8 ps), and vibrational relaxation/cooling (VC), and charge transfer (CT) processes (∼2 ps without water and ∼5 ps with water) of the adsorbed ROH*. Our results provide new knowledge on the interactions and the proton-transfer reaction dynamics of HPTS adsorbed on mesoporous materials.

From intra- to inter-molecular hydrogen bonds with the surroundings: steady-state and time-resolved behaviours.

We report on the photodynamics of 2-(2'-hydroxyphenyl)benzoxazole (HBO), compared to its amino derivatives, 6-amino-2-(2'-hydroxypheny)benzoxazole (6A-HBO) and 5-amino-2-(2'-hydroxypheny)benzoxazole (5A-HBO) in N,N-dimethylformamide (DMF) solutions. HBO at S0 shows a reversible deprotonation reaction leading to the production of anionic forms. However, for 6A-HBO and 5A-HBO, DMF containing KOH is necessary to produce the anions. Excited HBO in DMF exhibits intra- as well as inter-molecular proton transfer (ESIPT and ESPT) reactions. With excitation at 330 nm, we observed the open-enol, anti-enol and keto forms with different emission and lifetimes (620 ps, 1.5 ns, and 74 ps, respectively), while with the excitation at 433 nm, only the anionic species emission was detected (3.7 ns). Contrary to HBO, 6A-HBO and 5A-HBO do not exhibit any proton transfer process, and only the emissions of the open-enol charge-transferred forms (open-ECT) were observed, which are comparable to those of their methylated derivatives (6A-MBO and 5A-MBO). Femtosecond studies of 6A-MBO and 6A-HBO in DMF indicate that an intramolecular charge-transfer (ICT) reaction (∼80 fs) and solvent relaxation process (2 ps) take place at S1. Remarkably, the photoinduced breaking of the intramolecular hydrogen bond of 6A-HBO and the formation of an intermolecular hydrogen bond with DMF molecules occurs in 80 ps, while for 5A-HBO, this process occurs in less than 10 ps. In this study, we have demonstrated that the presence and position of the amino group in the HBO framework change both the S0 and S1 behaviours of the intramolecular H-bonds; a result which might be useful for the design and better understanding of supramolecular systems based on intra- and intermolecular H-bonds.

Direct observation of breaking of the intramolecular H-bond, and slowing down of the proton motion and tuning its mechanism in an HBO derivative.

We report on spectroscopic and photodynamical behaviours of 5-amino-2-(2'-hydroxyphenyl)benzoxazole (5A-HBO) in different solutions. The dye undergoes an ultrafast ICT reaction (<50 fs) (comparable to that observed for its methylated derivative, 5A-MBO), in agreement with the results of TD-DFT theoretical calculations (gas phase). Depending on the used solvent, the ICT reaction can be followed by a reversible/irreversible excited-state intramolecular proton transfer (ESIPT) reaction or by breaking of the intramolecular hydrogen bond (IHB). 5A-HBO in n-heptane solution exhibits an irreversible and slow (20 ps) ESIPT reaction, while that of the parent compound, HBO, takes place in less than 150 fs. Compared to excited HBO behaviour, theoretical calculations on 5A-HBO suggest a higher energy barrier (∼4 kcal mol(-1)) between the relaxed enol and keto tautomers, in addition to a less stabilization of the latter, which is in agreement with experiments in n-heptane. On the other hand, in dichloromethane, after the ICT reaction a subsequent and reversible proton motion occurs in an extraordinary slower regime (ns-time scale). No isotopic effect (OH/OD exchange) was observed in this solvent reflecting that the reversible ESIPT reaction evolves along the IHB and solvent coordinates. Using tetrahydrofurane and acetonitrile, we observed a breaking of the IHB due to specific intermolecular interactions with solvent molecules. This leads to the formation of open-enol forms, which undergo an ICT reaction as it occurs in 5A-MBO. These results bring new findings in the coupled ICT and ESIPT reactions. The photobehaviour of this new dye remarkably changes with the solvent nature, opening up the window for further research and possible applications in sensing polarity or H-bonding of media similar to that of the biological ones.

An abnormally slow proton transfer reaction in a simple HBO derivative due to ultrafast intramolecular-charge transfer events.

We report on the steady-state, picosecond and femtosecond time-resolved studies of a charge and proton transfer dye 6-amino-2-(2'-hydroxyphenyl)benzoxazole (6A-HBO) and its methylated derivative 6-amino-2-(2'-methoxyphenyl)benzoxazole (6A-MBO), in different solvents. With femtosecond resolution and comparison with the photobehaviour of 6A-MBO, we demonstrate for 6A-HBO in solution, the photoproduction of an intramolecular charge-transfer (ICT) process at S1 taking place in ∼140 fs or shorter, followed by solvent relaxation in the charge transferred species. The generated structure (syn-enol charge transfer conformer) experiences an excited-state intramolecular proton-transfer (ESIPT) reaction to produce a keto-type tautomer. This subsequent proton motion occurs in 1.2 ps (n-heptane), 14 ps (DCM) and 35 ps (MeOH). In MeOH, it is assisted by the solvent molecules and occurs through tunneling for which we got a large kinetic isotope effect (KIE) of about 13. For the 6A-DBO (deuterated sample in CD3OD) the global proton-transfer reaction takes place in 200 ps, showing a remarkable slow KIE regime. The slow ESIPT reaction in DCM (14 ps), not through tunnelling as it is not sensitive to OH/OD exchange, has however to overcome an energy barrier using intramolecular as well as solvent coordinates. The rich ESIPT dynamics of 6A-HBO in the used solutions is governed by an ICT reaction, triggered by the amino group, and it is solvent dependent. Thus, the charge injection to a 6A-HBO molecular frame makes the ICT species more stable, and the phenol group less acidic, slowing down the subsequent ESIPT reaction. Our findings bring new insights into the coupling between ICT and ESIPT reactions on the potential-energy surfaces of several barriers.

Switching to a reversible proton motion in a charge-transferred dye.

We report on the steady-state, pico- and femtosecond time-resolved emission studies of 6-amino-2-(2-methoxyphenyl)benzoxazole (6A-MBO) and 6-amino-2-(2-hydroxyphenyl)benzoxazole (6A-HBO) in different solvents. We observed an intramolecular charge transfer (ICT) reaction following by slow (relatively) solvent relaxation, which happened in the same time domain for both molecules. The ultrafast ICT reaction happens in 80-140 fs whereas the solvent relaxation occurs in 0.5-1.1 ps. In 6A-MBO the excited CT species has a lifetime of ∼2.5 ns. However, in 6A-HBO and after the ICT reaction, a reversible excited-state intramolecular proton transfer (ESIPT) reaction takes place in the formed enol charge transfer (ECT*) species producing a keto (K*) type tautomer. Depending on the solvent, the forward ESIPT reaction (ECT* → K*) happens in 40-175 ps while that of the reverse one (ECT* ← K*) occurs in 240-990 ps. Kinetic isotopic effect (OH/OD exchange) study in acetone shows that the reversible ESIPT reaction occurs via tunneling, while we suggest that in acetonitrile solution it evolves along the IHB and solvent coordinates. Our results show a reversible proton motion coupled to charge-transfer reactions opening the way to new explorations of charge- and proton-transfer dynamics and spectroscopy.

Photodynamics of a Proton-Transfer Dye in Solutions and Confined Within NaX and NaY Zeolites.

We report on steady-state, picosecond and femtosecond time-resolved emission studies of 2-(2'-hydroxyphenyl)benzoxazole (HBO) in solutions and interacting with NaX and NaY zeolites. In solutions, an ultrafast (less than 150 fs) excited-state intramolecular proton-transfer (ESIPT) reaction takes place in syn-enol form, and leads to keto-type tautomer. We also observed a torsional motion in the keto form (~20 ps in dichloromethane, DCM). For NaX and NaY DCM suspensions, anionic forms interacting with the zeolites at S0 and S1 states are generated. They show two fluorescence lifetimes in both zeolites (720 ps and 2.4 ns for NaY and 960 ps and 2.7 ns for NaX), while those of the enol bonded to the zeolite framework and of the free keto forms are ~100 and 250 ps, respectively. The ultrafast dynamics of the anion in alkaline solutions reveals two deactivation pathways: an intramolecular charge transfer (ICT, 1.2 ps) and a twisting motion, affected by the viscosity of the solvent (12 and 20 ps for MeOH and ethylene glycol). When HBO is interacting with NaX and NaY the twisting motion is cancelled, while the ICT becomes slower as a result of a combination of several environment effects. HBO anions within the faujasite framework show also a ~ 30 ps decay associated to a non-fluorescent (n, π*) state. Our results demonstrate how intermolecular H-bonds, the confinement and the electrostatic interactions of HBO with the used materials, affect its ground as well as its excited state properties. Our findings add new knowledge on the interactions of silica-based nanomaterials containing the H-bonding guests.