Methylthio BODIPY as a standard triplet photosensitizer for singlet oxygen production: a photophysical study.

A complete photophysical study on the iodinated-BODIPY, 3,5-dimethyl-2,6-diiodo-8-thiomethyl-pyrromethene (MeSBDP), demonstrated that it is an excellent triplet photosensitizer for singlet oxygen production in a broad range of apolar and polar solvents. Besides its absorption and fluorescence emission spectra, the dynamics of its excited states including its intersystem crossing rate was characterized by femtosecond transient experiments. The photophysical study of its triplet state by nanosecond transient absorption spectroscopy and phosphorescence emission concluded to a diffusion-controlled quenching of 3MeSBDP by O2 and to a fraction of triplet state quenching by O2 close to unity. The high (>0.87) and solvent-insensitive singlet oxygen quantum yield φΔ measured by singlet oxygen phosphorescence emission, together with the noticeable photostability of MeSBSP, as well as the absence of quenching of singlet oxygen by MeSBDP itself, allows claiming it as an alternative standard photosensitizer for singlet oxygen production, under excitation either in the UV or in the visible range.

Direct analysis of aldehydes and carboxylic acids in the gas phase by negative ionization selected ion flow tube mass spectrometry: Quantification and modelling of ion-molecule reactions.

RATIONALE: The concentrations of aldehydes and volatile fatty acids have to be controlled because of their potential harmfulness in indoor air or relationship with the organoleptic properties of agri-food products. Although several specific analytical methods are currently used, the simultaneous analysis of these compounds in a complex matrix remains a challenge. The combination of positive and negative ionization selected ion flow tube mass spectrometry (SIFT-MS) allows the accurate, sensitive and high-frequency analysis of complex gas mixtures of these compounds. METHODS: The ion-molecule reactions of negative precursor ions (OH- , O•- , O2 •- , NO2 - and NO3 - ) with five aldehydes and four carboxylic acids were investigated in order to provide product ions and rate constants for the quantification of these compounds by negative ion SIFT-MS. The results were compared with those obtained by conventional analysis methods and/or with already implemented SIFT-MS positive ionization methods. The modelling of hydroxide ion (OH- )/molecule reaction paths by ab-initio calculation allowed a better understanding of these gas-phase reactions. RESULTS: Deprotonation systematically occurs by reaction between negative ions and aldehydes or acids, leading to the formation of [M - H]- primary ions. Ab-initio calculations demonstrated the α-CH deprotonation of aldehydes and the acidic proton abstraction for fatty acids. For aldehydes, the presence of water in the flow tube leads to the formation of hydrated ions, [M - H]- .H2 O. With the NO2 - precursor ion, a second reaction channel results in ion-molecule association with the formation of M.NO2 - ions. CONCLUSIONS: Except for formaldehyde, all the studied compounds can be quantified by negative ion SIFT-MS with significant rate constants. In addition to positive ion SIFT-MS with H3 O+ , O2 + and NO+ precursor ions, negative ionization with O•- , O2 •- , OH- , NO2 - and NO3 - extends the range of analysis of aldehydes and carboxylic acids in air without a preparation or separation step. This methodology was illustrated by the simultaneous quantification in single-scan experiments of seven aldehydes and six carboxylic acids released by building materials.

Synthesis of Film-Forming Photoactive Latex Particles by Emulsion Polymerization-Induced Self-Assembly to Produce Singlet Oxygen.

The design of photoactive polymer substrates producing singlet oxygen under visible light irradiation has great technological potential. Aqueous dispersion of novel photoactive core-shell particles was synthesized by surfactant-free reversible addition-fragmentation chain transfer (RAFT) emulsion polymerization of n-butyl acrylate. The surface of the nanoparticles is directly decorated thanks to the polymerization-induced self-assembly process using a hydrophilic macromolecular chain transfer agent (macro-CTA) functionalized with the organic photosensitizer. The macro-CTA was synthesized by statistical copolymerization of acrylic acid and 2-Rose Bengal ethyl acrylate (RBEA) at 80 °C mediated with 4-cyano-4-[(dodecylsulfanylthiocarbonyl)sulfanyl]pentanoic acid. Monitoring polymerization kinetics of RAFT polymerization highlights that increasing amount of RBEA induces retardation, still more pronounced when using the vinylbenzyl Rose Bengal comonomer. The present work provides insight into the quantum yield of singlet oxygen production in water (ΦΔ  = 0.2-0.6) for the three types of synthesized polymers (hydrophilic polymer, latex particles, and polymer film). The photoactive core-shell latex particles enabled the easy preparation of photoactive polymer film by simple casting.

Oxidative damage and impairment of protein quality control systems in keratinocytes exposed to a volatile organic compounds cocktail.

Compelling evidence suggests that volatile organic compounds (VOCs) have potentially harmful effects to the skin. However, knowledge about cellular signaling events and toxicity subsequent to VOC exposure to human skin cells is still poorly documented. The aim of this study was to focus on the interaction between 5 different VOCs (hexane, toluene, acetaldehyde, formaldehyde and acetone) at doses mimicking chronic low level environmental exposure and the effect on human keratinocytes to get better insight into VOC-cell interactions. We provide evidence that the proteasome, a major intracellular proteolytic system which is involved in a broad array of processes such as cell cycle, apoptosis, transcription, DNA repair, protein quality control and antigen presentation, is a VOC target. Proteasome inactivation after VOC exposure is accompanied by apoptosis, DNA damage and protein oxidation. Lon protease, which degrades oxidized, dysfunctional, and misfolded proteins in the mitochondria is also a VOC target. Using human skin explants we found that VOCs prevent cell proliferation and also inhibit proteasome activity in vivo. Taken together, our findings provide insight into potential mechanisms of VOC-induced proteasome inactivation and the cellular consequences of these events.

Adapting BODIPYs to singlet oxygen production on silica nanoparticles.

A modified Stöber method is used to synthesize spherical core-shell silica nanoparticles (NPs) with an external surface functionalized by amino groups and with an average size around 50 nm. Fluorescent dyes and photosensitizers of singlet oxygen were fixed, either separately or conjointly, respectively in the core or in the shell. Rhodamines were encapsulated in the core with relatively high fluorescence quantum yields (Φfl ≥ 0.3), allowing fluorescence tracking of the particles. Various photosensitizers of singlet oxygen (PS) were covalenty coupled to the shell, allowing singlet oxygen production. The stability of NP suspensions strongly deteriorated upon grafting the PS, affecting their apparent singlet oxygen quantum yields. Agglomeration of NPs depends both on the type and on the amount of grafted photosensitizer. New, lab-made, halogenated 4,4-difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPY) grafted to the NPs achieved higher singlet oxygen quantum yields (ΦΔ âˆ¼ 0.35-0.40) than Rose Bengal (RB) grafted NPs (ΦΔ âˆ¼ 0.10-0.27). Finally, we combined both fluorescence and PS functions in the same NP, namely a rhodamine in the silica core and a BODIPY or RB grafted in the shell, achieving the performance Φfl ∼ 0.10-0.20, ΦΔ âˆ¼ 0.16-0.25 with a single excitation wavelength. Thus, proper choice of the dyes, of their concentrations inside and on the NPs and the grafting method enables fine-tuning of singlet oxygen production and fluorescence emission.

Varying TiO2 macroscopic fiber morphologies toward tuning their photocatalytic properties.

In a context of volatile organic compound photodecomposition, we have addressed TiO2-based macroscoscpic fiber generation. We have extruded hybrid sols of amorphous titania nanoparticles, latex nanoparticles, and nonionic surfactant (Tergitol) as structure-directing agents into a poly(vinyl alcohol) (PVA) solution bearing salts acting as a flocculating medium. The resulting nanocomposite TiO2/latex/PVA macroscopic fibers were thermally treated in air to open porosity by organic removal while generating the photocatalytically active anatase phase of TiO2 along with residual brookite. Considering the synthetic paths, we have varied both the diameter of the latex particles as well as their concentration within the starting sol. These parameters allow tuning both the voids created through the applied thermal treatment and the fiber final diameters. For gas-phase photocatalysis, we have shown that the fiber diameters, mesoscopic roughness, and macroscopic topological defects represent indeed important morphological parameters acting cooperatively toward both acetone degradation and its mineralization processes. Particularly, triggering the fiber morphological characteristics, we have increased their efficiency toward acetone degradation of around 550% when compared with previous work.

Immobilized organic photosensitizers with versatile reactivity for various visible-light applications.

Various photosensitizers were grafted by conventional peptide coupling methods to functionalized silica with several macroscopic shapes (powders, films) or embedded in highly transparent and microporous silica xerogel monoliths. Owing to the transparency and free-standing shape of the monoliths, the transient species arising from irradiation of the PSs could be analyzed and were not strikingly different from those observed in solutions. The observed reactivity for either liquid-solid (α-terpinene oxygenation vs dehydrogenation) or gas-solid (dimethylsulfide, DMS, solvent-free oxidation) reactions was consistent with the properties of the excited states of the PSs under consideration. Immobilized anthraquinone-derived materials preferentially react in both cases by electron transfer from the substrate to the triplet state of the sensitizer, in spite of an efficient singlet oxygen production. The recently developed 9,14-dicyanobenzo[b]triphenylene-3-carboxylic acid, DBTP-COOH, efficiently reacts via energy transfer to yield singlet oxygen from its triplet state. It was shown to perform better than 9,10-dicyanoanthracene and rose bengal for DMS oxidation and α-terpinene photooxygenation to ascaridole, respectively. Thus, by a proper choice of the organic immobilized photocatalyst, it is possible to develop efficient and reusable materials, activated under visible light, for various applications and to tune the reaction pathway, opening the way to green oxidation processes.

Transparent organosilica photocatalysts activated by visible light: photophysical and oxidative properties at the gas-solid interface.

The photophysical properties of several photosensitizers (PSs) included or grafted in silica monoliths were compared to their properties in solution. The effects of the solid support on their steady-state and transient absorption spectra, on their quantum yields of singlet oxygen ((1)O2) production, and on their ability to photoinduce the oxidation of dimethylsulfide (DMS) were investigated. Two cyanoanthracene derivatives (9,14-dicyanobenzo[b]triphenylene, DBTP, and 9,10-dicyanoanthracene, DCA), as well as three phenothiazine dyes (methylene blue, MB(+), new methylene blue, NMB(+), methylene violet, MV), were encapsulated in silica, analyzed and compared to two reference PSs (perinaphthenone, PN and rose bengal, RB). A DBTP derivative (3-[N-(N″-triethoxysilylpropyl-N'-hexylurea)]carboxamido-9,14-dicyanobenzo[b]triphenylene, 3) was also prepared and grafted onto silica. Thanks to the transparency and the free-standing shape of the monoliths, the complete spectroscopic characterization of the supported PSs was carried out directly at the gas-solid interface. The influence of the silica network, the PS, and the adsorption/grafting link between the PS and silica was investigated. The effects of PS concentration, gaseous atmosphere, humidity, and hydrophobicity on the production of (1)O2 were analyzed. With all PSs, (1)O2 production was very efficient (quantum yields of (1)O2 production, relative to PN, between 0.6 and 1), and this species was the only one involved in the pollutant photooxidation. The influence of the matrix on the PSs' photophysics could be considered as negligible. In contrast, the matrix effect on DMS photooxidation was extremely important: the gas diffusion inside the porous structure, and thus, the photoactivity of the materials, strictly depended on silica's surface area and porosity. Our results highlight the suitability of these silica structures as inert supports for the study of the photosensitizing properties at the gas-solid interface. Moreover, thanks to the adsorption properties of the matrix, the synthesized materials can be used as microphotoreactor for the (1)O2-mediated oxidation of volatile pollutants.

Comparison of the photophysical properties of three phenothiazine derivatives: transient detection and singlet oxygen production.

New methylene blue (NMB+) and methylene violet (MV) are known for their photosensitizing properties for singlet oxygen ((1)O2) generation upon visible-light irradiation, and various examples of their use in the photodynamic inactivation of microorganisms and for photomedicinal purposes have been reported. However, their photophysical properties have never been extensively and systematically analyzed and compared. In the current work, we studied their absorption and fluorescence behavior relative to their parent compound, methylene blue (MB+), detected the transient species generated upon excitation of the photosensitizers and determined their quantum yields of singlet oxygen production. We could measure very high quantum yields of singlet oxygen production for all the studied compounds. NMB+ appeared similar to MB+, even though it produces (1)O2 much more efficiently, and was slightly influenced by the solvent. MV, in contrast, was much more sensitive to the chemical environment, and the transient species formed upon irradiation were different in methanol and acetonitrile. It appeared to be a very good singlet oxygen sensitizer, but the influence of the chemical environment should be carefully considered for any application. The comparative characterization of these sensitizers will represent a support for the determination and the understanding of the photochemical mechanisms occurring by using these phenothiazine dyes for various photobiological applications.

Efficient cyanoaromatic photosensitizers for singlet oxygen production: synthesis and characterization of the transient reactive species.

In order to graft cyanoaromatic molecules onto various inert supports, we designed two new cyanoanthracene derivatives of benzo[b]triphenylene-9,14-dicarbonitrile (DBTP, 1), which already demonstrated good photosensitizing properties. We synthesized 3-(N-hydroxypropyl)carboxamido-9,14-dicyanobenzo[b]triphenylene, 3 and 3-(N-N0-Boc-aminohexyl)carboxamido-9,14-dicyanobenzo[b]triphenylene, 4 and compared their photophysical properties in acetonitrile relative to those of the parent compound 1 and its carboxylic derivative 9,14-dicyanobenzo[b]triphenylene-3-carboxylic acid, 2. The transient species were analysed and the quantum yields of singlet oxygen production (ΦΔ) determined in acetonitrile. The effect of chemical functionalization can be considered negligible, since absorption spectra, fluorescence emission spectra and fluorescence lifetimes do not significantly change with the substituent. The triplet-triplet absorption spectra and the triplet excited state lifetimes are similar for the whole series. For compounds 1-4 high values of ΦΔ, close to that of the standard sensitizer 1H-phenalen-1-one (PN, ΦΔ ≈ 1), and higher than that of the well-known photosensitizer 9,10-dicyanoanthracene (DCA), are due to very efficient intersystem crossing from the singlet to the triplet excited state and subsequent energy transfer to ground state oxygen ((3)O2). They belong to a class of very efficient photosensitizers, absorbing visible light and stable under irradiation, they may be functionalized without significant changes to their photophysical behaviour, and grafted onto various supports.

Photoactive, porous honeycomb films prepared from Rose Bengal-grafted polystyrene.

Honeycomb-structured porous polymer films based on photosensitizer-grafted polystyrene are prepared through the breath figure process. Rose Bengal (RB) photosensitizer is first attached to a well-defined poly(styrene-stat-4-vinylbenzyl chloride) statistical copolymer, synthesized by nitroxide-mediated radical polymerization. The RB grafted poly(styrene-stat-4-vinylbenzyl chloride) (ca. 20,000 g mol(-1) molar mass, 1.2 dispersity) leads to porous polymer films, with a hexagonal pore pattern, while a simple mixture of poly(styrene-stat-4-vinylbenzyl chloride) and the insoluble RB photosensitizer produced unstructured, nonporous films. The RB-grafted honeycomb films, compared with the corresponding nonporous flat films, are more efficient for oxidation of organic molecules via singlet oxygen production at a liquid/solid interface. The oxidations of 1,5-dihydroxynaphthalene to juglone and α-terpinene to ascaridole are followed in ethanol in the presence of both types of films. Oxidation of the organic molecules is a factor 5 greater with honeycomb compared to the nonporous films. This gain is ascribed to two factors: the specific location of the polar photosensitizer at the film interface and the greater exchange surface, as revealed by fluorescence and scanning electron microscopies.

Selective oxidation with nanoporous silica supported sensitizers: an environment friendly process using air and visible light.

Transparent and porous silica xerogels containing various grafted photosensitizers (PSs) such as anthraquinone derivatives, Neutral Red, Acridine Yellow and a laboratory-made dicyano aromatics (DBTP) were prepared. In most cases, the xerogels were shown to be mainly microporous by porosimetry. The PSs were characterized in the powdered monoliths (form, aggregation, concentration) by electronic spectroscopy which also proved to be a useful tool for monitoring the material evolution after irradiation. These nanoporous xerogels were used as microreactors for gas/solid solvent-free photo-oxygenation of dimethylsulfide (DMS) using visible light and air as the sole reactant. All these PSs containing monoliths were efficient for gas-solid DMS oxidation, leading to sulfoxide and sulfone in varying ratios. As these polar oxidation products remained strongly adsorbed on the silica matrix, the gaseous flow at the outlet of the reactor was totally free of sulfide and odorless. The best results in term of yield and initial rate of degradation of DMS were obtained with DBTP containing xerogels. Moreover, as these materials were reusable without loss of efficiency and sensitizer photobleaching after a washing regeneration step, the concept of recyclable sensitizing materials was approved, opening the way to green process.

A new cyanoaromatic photosensitizer vs. 9,10-dicyanoanthracene: systematic comparison of the photophysical properties.

The cyanoanthracene derivative, benzo[b]triphenylene-9,14-dicarbonitrile (1) can be prepared readily with a graftable function while maintaining (1)O(2) photosensitizing properties comparable to those of the standard compound 9,10-dicyanoanthracene (DCA). In view of the high potential of the derivatives of 1 for photooxidation reactions under heterogeneous conditions, we compared the photophysical properties of 1 in solution with those of DCA. In pursuing the comparison of 1 and DCA, we observed small but significant changes of the vibronic bands in the electronic absorption spectra of DCA in different solvents, which were well correlated with solvent polarity, similar to the pyrene polarity scale. The main difference between 1 and DCA is in the emission properties: we observed a much stronger sensitivity of the fluorescence emission spectrum to the electron-donating ability of the solvent than for DCA. The emission spectrum of 1 is in general structureless with a large Stokes shift. The ability of the singlet state of 1 to participate in charge transfer interactions with electron-donating solvents is proposed to account for these results. It makes 1 a highly sensitive probe to the surrounding medium. Reversible reduction was observed for both photosensitizers, with a small shift to more negative potentials for 1 compared to DCA. The reduction potential of the first singlet excited state is of the same order of magnitude in both cases. Several photo-oxidation reactions sensitized by 1 and DCA are compared in homogeneous solution and at the gas-solid interface by embedding 1 and DCA in silica monoliths. Our results confirmed the dual character of both cyanoanthracene derivatives as electron transfer and energy transfer sensitizers, highly efficient for singlet oxygen production.

Solvent-free production of singlet oxygen at the gas-solid interface: visible light activated organic-inorganic hybrid microreactors including new cyanoaromatic photosensitizers.

We synthesized new cyanoaromatics, benzo[b]triphenylene-9,14-dicarbonitrile (DBTP) 1a and a graftable derivative, 9,14-dicyanobenzo[b]triphenylene-3-carboxylic acid (DBTP-COOH) 1b, easily prepared from commercial reagents. Their photosensitizing properties were investigated. Hybrid porous silica monoliths loaded with encapsulated 1a or grafted 1b were prepared, and their adsorption, spectroscopic and photosensitizing properties, as well as stability, were compared. Solvent-free, efficient oxidation of dimethylsulfide (DMS) was observed at the gas-solid interface under visible light irradiation. Quantum yields of formation of 1O2 inside the porous monoliths are comparable to those of phenalenone. Singlet oxygen lifetimes (approximately 25 micros) were found to be longer in silica monoliths than in usual polar solvents such as methanol or ethanol. This new class of hybrid materials work as porous, transparent, and highly efficient microreactors for oxidation reactions under visible light.

Hybrid functional mesostructured thin films with photo-oxidative properties in the visible range.

Hybrid mesostructured thin films functionalised with organic photosensitiser molecules demonstrated high efficiency for the decontamination of polluted atmosphere via singlet oxygen production.

Singlet oxygen in microporous silica xerogel: quantum yield and oxidation at the gas-solid interface.

The quantum yields of singlet oxygen ((1)O(2)) production (Phi(Delta)) and (1)O(2) lifetimes (tau(Delta)) at the gas-solid interface in silica gel material are determined. Different photosensitizers (PS) are encapsulated in parallelepipedic xerogel monoliths (PS-SG). PS were chosen according to their known photooxidation properties: 9,10-dicyanoanthracene (DCA), 9,10-anthraquinone (ANT), and a benzophenone derivative, 4-benzoyl benzoic acid (4BB). These experiments are mainly based on time-resolved (1)O(2) phosphorescence detection, and the obtained Phi(Delta) and tau(Delta) values are compared with those of a reference sensitizer for (1)O(2) production, 1H-phenalen-1-one (PN), included in the same xerogel. The trend between their ability to oxidize organic pollutants in the gas phase and their efficiency for (1)O(2) production is investigated through photooxidation experiments of a test pollutant dimethylsulfide (DMS). The Phi(Delta) value is high for DCA-SG relative to the PN reference, whereas it is slightly lower for 4BB-SG and for ANT-SG. Phi(Delta) is related to the production of sulfoxide and sulfone as the main oxidation products for DMS photosensitized oxidation. Additional mechanisms, leading to C--S bond cleaveage, appear to mainly occur for the less efficient singlet oxygen sensitizers 4BB-SG and ANT-SG.

Photo-oxidation of di-n-butylsulfide by various electron transfer sensitizers in oxygenated acetonitrile.

The selective activation of different photosensitizers has been carried out under comparable conditions and their efficiency towards di-n-butylsulfide oxidation in oxygenated acetonitrile compared from the product distribution after 150 minutes of irradiation. As expected, the best selectivity towards sulfoxide is obtained with a conventional energy transfer sensitizer such as Rose Bengal (RB), but also with a quinone with a low-lying triplet state, 2,3,5,6-tetrachloro-1,4-benzoquinone (chloranil or CHLO) and with 9,10-dicyanoanthracene (DCA). More significant yields in sulfonic and sulfuric acids are obtained under sensitization with 9,10-anthraquinone (ANT) or a derivative of benzophenone, 4-benzoyl benzoic acid (4-BB), with which additional experiments were carried out in order to discuss the involvement of either singlet oxygen or superoxide radical anion. Triphenyl pyrylium tetrafluoroborate (TPT+) is inefficient under the selected conditions and sulfide photo-oxidation can only be achieved with higher TPT+ concentrations with simultaneous total TPT+ bleaching. With TPT+, 1,2,4,5-tetracyanobenzene (TCNB) and TiO2, the product distribution and the low selectivity as well as the formation of numerous common by-products are indicative of radical mechanisms. All these results are discussed according to the possible formation of activated oxygen species, such as singlet oxygen, superoxide radical anion or alkylperoxy radicals.