Surface modification and immobilization in poly(acrylic acid) of Ag/ZnO for photocatalytic degradation of endocrine‐disrupting compounds

Silver‐modified ZnO particles (Ag/ZnO) are effective catalysts for the photodegradation of water pollutants such as bisphenol‐A. However, until now, their use in continuous processes was back‐drawn because of difficulties associated with their recovery. To overcome this problem, the present work aimed at immobilizing Ag/ZnO in cross‐linked poly(acrylic acid) ‐PAA‐. Ag/ZnO was first silanized using (3‐glycidyloxypropyl)trimethoxysilane and thoroughly dispersed in a water‐acrylic acid solution. The suspension was then submitted to radical polymerization in presence of a cross‐linker (N,N′‐Methylenebisacrylamide). The resulting composites were characterized in terms of chemical structure, morphology, crystallinity, thermal properties, and photostability. Their analyses showed that the silanized particles were chemically anchored to PAA and homogeneously distributed in the matrix. UV‐assisted photocatalysis of bisphenol‐A aqueous solutions showed that immobilized Ag/ZnO can achieve photodegradation performances comparable to pure Ag/ZnO and allows its use in successive cycles and, consequently, in continuous processes. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43528.     

Light‐Activated Reversible Imine Isomerization: Towards a Photochromic Protein Switch

Mutants of cellular retinoic acid‐binding protein II (CRABPII), engineered to bind all‐trans‐retinal as an iminium species, demonstrate photochromism upon irradiation with light at different wavelengths. UV light irradiation populates the cis‐imine geometry, which has a high pK_a, leading to protonation of the imine and subsequent “turn‐on” of color. Yellow light irradiation yields the trans‐imine isomer, which has a depressed pK_a, leading to loss of color because the imine is not protonated. The protein‐bound retinylidene chromophore undergoes photoinduced reversible interconversion between the colored and uncolored species, with excellent fatigue resistance.     

Light‐Activated Triazabutadienes for the Modification of a Viral Surface

Chemical crosslinking is a versatile tool for the examination of biochemical interactions, in particular host–pathogen interactions. We report the critical first step toward the goal of probing these interactions by the synthesis and use of a new heterobifunctional crosslinker containing a triazabutadiene scaffold. The triazabutadiene is stable to protein conjugation and liberates a reactive aryl diazonium species upon irradiation with 350 nm light. We highlight the use of this technology by modifying the surface of several proteins, including the dengue virus envelope protein.     

Efficient visible photoinitiator with high‐spectrum stability in an acid medium for free‐radical and free‐radical‐promoted cationic photopolymerization based on erythrosine B derivatives

Three dye‐linked photoinitiators with excellent spectral stability in an acid medium were synthesized by the covalent bonding of a coinitiator (tertiary amine) and a benzoyl group or two coinitiators to the phenolic and carboxyl group position of erythrosine B. The combination of the iodonium salt and free tertiary amino used to initiate the free‐radical/cationic visible photopolymerization was investigated to acquire the relationship between the structure and performance. The photoinitiating ability of the derivative with the phenolic position bearing a coinitiator was poorer than of the derivative with the carboxyl group bearing one because of the strong back electron transfer of the former. For the derivative with a linked coinitiator on the carboxyl position, the proximity effect between the sensitizer and the coinitiator moiety resulted in an excellent photoinitiating ability for radical/cationic polymerization; this suggested its potential for application. Although radical/cationic photopolymerization could be initiated by the derivative/coinitiator/iodonium salt, the different component ratios between them had different effects on these two polymerizations; this provided useful information for the design of effective photoinitiators for different polymerizations. On the basis of the fluorescence quenching and photopolymerization results, a corresponding synergistic mechanism was proposed. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43035.     

Photochemical modulation of Ras-mediated signal transduction using caged farnesyltransferase inhibitors: activation by one- and two-photon excitation

The creation of caged molecules involves the attachment of protecting groups to biologically active compounds such as ligands, substrates and drugs that can be removed under specific conditions. Photoremovable caging groups are the most common due to their ability to be removed with high spatial and temporal resolution. Here, the synthesis and photochemistry of a caged inhibitor of protein farnesyltransferase is described. The inhibitor, FTI, was caged by alkylation of a critical thiol group with a bromohydroxycoumarin (Bhc) moiety. While Bhc is well established as a protecting group for carboxylates and phosphates, it has not been extensively used to cage sulfhydryl groups. The resulting caged molecule, Bhc-FTI, can be photolyzed with UV light to release the inhibitor that prevents Ras farnesylation, Ras membrane localization and downstream signaling. Finally, it is shown that Bhc-FTI can be uncaged by two-photon excitation to produce FTI at levels sufficient to inhibit Ras localization and alter cell morphology. Given the widespread involvement of Ras proteins in signal transduction pathways, this caged inhibitor should be useful in a plethora of studies.     

Direct Photomodification of Polymer Surfaces: Unleashing the Potential of Aryl‐Azide Copolymers

The possibility to impart surface properties to any polymeric substrate using a fast, reproducible, and industrially friendly procedure, without the need for surface pretreatment, is highly sought after. This is in particular true in the frame of antibacterial surfaces to hinder the threat of biofilm formation. In this study, the potential of aryl‐azide polymers for photofunctionalization and the importance of the polymer structure for an efficient grafting are demonstrated. The strategy is illustrated with a UV‐reactive hydrophilic poly(2‐oxazoline) based copolymer, which can be photografted onto any polymer substrate that contains carbon–hydrogen bonds to introduce antifouling properties. Through detailed characterization it is demonstrated that the controlled spatial distribution of the UV‐reactive aryl‐azide moieties within the poly(2‐oxazline) structure, in the form of pseudogradient copolymers, ensures higher grafting efficacy than other copolymer structures including block copolymers. Furthermore, it is found that the photografting results in a covalently bound layer, which is thermally stable and causes a significant antiadherence effect and biofilm reduction against Escherichia coli and Staphylococcus epidermidis strains while remaining noncytotoxic against mouse fibroblasts.     

Photochemical Reactions of Uranium(VI) in Aqueous Phosphoric Acid Solutions

Photochemical reactions of U(VI) ion with halogen and pseudohalogen anions. I^?, Br^?, Cl^? and NCS^?, were studied in aqueous phosphoric acid solutions under irradiation of nitrogen laser. The formation of U(IV) was observed in the reactions with I^?, Br^? and NCS^?, but not with CI^?. The yield of U(IV) increased in the order Br^?<NCS^?<I^?. This order was the same as the quenching rate constants of the excited U (VI) ion with these anions, but the reverse of their standard redox potentials. These facts are consistent with the electron transfer mechanism between excited U (VI) and these anions. The rates of the formation of U (IV) in the presence of Br^? were measured by the spectrophotometric method. It was found that the rate equation was first order in both U (VI) and Br^?. The results were reasonably interpreted by a series of reaction processes involving U(V) and Br radical. The photo-oxidation of tris(1, 10-phenanthroline)-Fe (II) ion by U (VI) was also studied in the same procedures. Based on the rate law, we proposed a one-electron transfer mechanism involving U(V) as an intermediate.     

Neptunium Valence Adjustment through Photochemically Induced Redox Reactions at Low Concentrations

Photochemically induced redox reactions of Np(VI) and Np (IV) to Np (V) are experimentally studied in nitric acid solution of low Np concentration less than 10^?4 mo].dm⁸ using a Kr-F excimer laser. The preparations of the initial solution of Np (VI) or Np (IV) are based on the addition of chemical redox reagents. The extraction chromatography is used to analyze the fraction of the neptunium valences. The result of redox experiments with laser radiation shows that the fractions of Np(V)/Np(VI) or Np(V)/Np(IV) photochemically increase up to the steady-state values against initially oxidizing or reducing conditions respectively. The steady- state values are different from those at thermal equilibrium states. It is concluded that, in low Np concentration as is observed in the normal Purex process, laser application to valence adjustment of Np gives another redox condition which is different from that determined thermochemically.     

Photoswitching Emission with Rhodamine Spiroamides for Super-resolution Fluorescence nanoscopies

Spatial resolution in far-field fluorescence microscopy is limited by diffraction to about 200 nm. With the aid of photoswitchable fluorophores, the diffraction barrier has been successfully overcome, allowing unprecedented resolution in the order of single biomolecules. The imaging process demands markers with strict and reliable control of the switching, to keep most of the markers in a non-emissive state most of the time and to bring a tiny number back to an emissive state, and detection at the single-molecule level. Herein, we describe the use of rhodamine spiroamides with unique photophysical properties as molecular probes for super-resolution techniques based on the localization of single emitters. This family of photochromic and fluorescent compounds fulfils the stringent requirements for such imaging methods; these compounds are robust and capable of enduring single-molecule detection in diverse environments. This has allowed meaningful images with resolution down to a few nanometres. Their design, synthesis and implementation is discussed along with imaging applications in material and life sciences.