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Advanced tools for cell imaging are of great interest for the detection, localization, and quantification of molecular biomarkers of cancer or infection. We describe a novel photopolymerization method to coat quantum dots (QDs) with polymer shells, in particular, molecularly imprinted polymers (MIPs), by using the visible light emitted from QDs excited by UV light. Fluorescent core-shell particles specifically recognizing glucuronic acid (GlcA) or N-acetylneuraminic acid (NANA) were prepared. Simultaneous multiplexed labeling of human keratinocytes with green QDs conjugated with MIPGlcA and red QDs conjugated with MIP-NANA was demonstrated by fluorescence imaging. The specificity of binding was verified with a non-imprinted control polymer and by enzymatic cleavage of the terminal GlcA and NANA moieties. The coating strategy is potentially a generic method for the functionalization of QDs to address a much wider range of biocompatibility and biorecognition issues. [ABSTRACT FROM AUTHOR]

Advanced tools for cell imaging are of great interest for the detection, localization, and quantification of molecular biomarkers of cancer or infection. We describe a novel photopolymerization method to coat quantum dots (QDs) with polymer shells, in particular, molecularly imprinted polymers (MIPs), by using the visible light emitted from QDs excited by UV light. Fluorescent core-shell particles specifically recognizing glucuronic acid (GlcA) or N-acetylneuraminic acid (NANA) were prepared. Simultaneous multiplexed labeling of human keratinocytes with green QDs conjugated with MIPGlcA and red QDs conjugated with MIP-NANAwas demonstrated by fluorescence imaging. The specificity of binding was verified with a non-imprinted control polymer and by enzymatic cleavage of the terminal GlcA and NANA moieties. The coating strategy is potentially a generic method for the functionalization of QDs to address a much wider range of biocompatibility and biorecognition issues. [ABSTRACT FROM AUTHOR]

The field of imaging has developed considerably over the past decade and recent advances in the area of nanotechnology, in particular nanomaterials, have opened new opportunities. Polymeric nanoparticles are particularly interesting and a number of novel materials, characterized by stimuli-responsive characteristics and fluorescent tagging, have allowed visualization, intracellular labeling and real-time tracking. In some of the latest applications the nanoparticles have been used for imagining of tumor cells, both in vivo and ex vivo. [ABSTRACT FROM AUTHOR]

Three new hybrid gated mesoporous materials ( SN3-1, SNH2-2, and SN3-3) loaded with the dye [Ru(bipy)3]2+ (bipy=bipyridine) and capped with different tetrathiafulvalene (TTF) derivatives (having different sizes and shapes and incorporating different numbers of sulfur atoms) have been prepared. The materials SN3-1 and SN3-3 are functionalized on their external surfaces with the TTF derivatives 1 and 3, respectively, which were attached by employing the 'click' chemistry reaction, whereas SNH2-2 incorporates the TTF derivative 2, which was anchored to the solid through an amidation reaction. The final gated materials have been characterized by standard techniques. Suspensions of these solids in acetonitrile showed 'zero release', most likely because of the formation of dense TTF networks around the pore outlets. The release of the entrapped [Ru(bipy)3]2+ dye from SN3-1, SNH2-2, and SN3-3 was studied in the presence of selected explosives (Tetryl, TNT, TNB, DNT, RDX, PETN, PA, and TATP). SNH2-2 showed a fairly selective response to Tetryl, whereas for SN3-1 and SN3-3 dye release was found to occur with Tetryl, TNT, and TNB. The uncapping process in the three materials can be ascribed to the formation of charge-transfer complexes between the electron-donating TTF units and the electron-accepting nitroaromatic explosives. Finally, solids SNH2-2 and SN3-1 have been tested for Tetryl detection in soil with good results, pointing toward a possible use of these or similar hybrid capped materials as probes for the selective chromo-fluorogenic detection of nitroaromatic explosives. [ABSTRACT FROM AUTHOR]

Fluorescent organic-inorganic mesoporous hybrid materials have been prepared and characterised, and their behaviour against nitroaromatic explosives have been tested. MCM-41 silica was used as an inorganic scaffold and pyrene ( P derivative containing trialkoxysilane moieties), dansyl and fluorescein ( D and F derivatives also containing trialkoxysilane groups, respectively) fluorophores have been anchored on hybrid materials by a co-condensation method to obtain a homogenous distribution of dyes into the pores of the support. Six sensing materials have been prepared, of which SP, SD, SF were hydrophilic and SPh, SDh, SFh were hydrophobic. Template-free hydrophilic materials ( SP, SD, SF) were obtained after repeated NH4NO3/ethanol extractions under temperature from as-synthesised ( MP, MD and MF supports, respectively) solids. Hydrophobic materials (SPh, SDh, SFh) were prepared by using excess 1,1,1,3,3,3-hexamethyldisilazane with template-free hydrophilic ( SP, SD and SF) materials. The six final materials displayed the typical emission bands of the grafted fluorophores. In particular, SP and SPh show the typical pyrene monomer (370-420 nm) and excimer (430-600 nm) emissions. SD and SDh exhibit the broad dansyl fluorescence band in the 450-600 nm range, whereas solids SF and SFh present sharp fluorescein emission centred at 525 nm. The fluorescent behaviour of the six final materials was tested in the presence of explosives (pentaerythritol tetranitrate (PETN), hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), nitrobenzene (NB), 1,3,5-trinitrobenzene (TNB), 2,4,6-trinitrotoluene (TNT), 2,4-dinitrotoluene (DNT), 2,4,6-trinitrophenylmethylnitramine (Tetryl) and picric acid (PA)). Only nitroaromatic compounds were able to induce emission quenching. As a general trend, the quenching degree depended on the nature of the final material. The best response was obtained with explosives PA and Tetryl, which were able to significantly quench the emission of the sensing supports. The observed quenching was ascribed to the π-π stacking interactions between the electron-donor fluorophores and the electron-withdrawing nitroaromatic explosives. When using SPh for Tetryl and PA, the limits of detection were 8.5 and 1.4 ppm, respectively, whereas they were 14.4 and 1.2 ppm for SDh. Principal component analysis algorithms were applied to the fluorescence measurements taken with the six hybrid materials and the seven explosives. The obtained score plot showed well-defined clusters for the seven explosives tested. Finally, solid SDh was applied to detect trace amounts of Tetryl in soil samples with good results. [ABSTRACT FROM AUTHOR]

Review: [62 refs. [ABSTRACT FROM AUTHOR]

Despite the current advancements, yet improving the intrinsic structure and external environmental stability of hybrid metal halide perovskite nanomaterials is required for developing efficient perovskite‐based devices. Up‐to‐date, a very attractive method is growing and/or embedding perovskite nanocrystals within organic polymeric matrices, or into porous inorganic and hybrid nano/micromaterials (e. g. metal‐organic frameworks, mesoporous silica, zeolites, and others), favored through confinement effect within the pores. In this review, we highlighted the last two years of research progress on enhancing the stabilization of perovskite nanoparticles based on methylammonium cations. In the future generation of optoelectronic and photovoltaic devices along with other interesting applied fields, it is predicted that an effective way to trigger the widespread use of this type of perovskite nanocrystals may involve combining different functional host materials, acting as a smarter protection method for the guest nanocrystals. [ABSTRACT FROM AUTHOR]

This work reports a reversible braking system for micromotors that can be controlled by small temperature changes (≈5 °C). To achieve this, gated‐mesoporous organosilica microparticles are internally loaded with metal catalysts (to form the motor) and the exterior (partially) grafted with thermosensitive bottle‐brush polyphosphazenes to form Janus particles. When placed in an aqueous solution of H2O2 (the fuel), rapid forward propulsion of the motors ensues due to decomposition of the fuel. Conformational changes of the polymers at defined temperatures regulate the bubble formation rate and thus act as brakes with considerable deceleration/acceleration observed. As the components can be easily varied, this represents a versatile, modular platform for the exogenous velocity control of micromotors. [ABSTRACT FROM AUTHOR]

Invited for the cover of this issue is the group of Ian Teasdale and Yolanda Salinas at the Johannes Kepler University Linz. The image depicts the self‐propelled Janus micromotors reported in this work. Read the full text of the article at10.1002/chem.202004792. [ABSTRACT FROM AUTHOR]

Manganese ions are embedded in microporous silica nanoparticles to catalyse the degradation of the H SB 2 sb O SB 2 sb "fuel" to water and gaseous oxygen. Keywords: bottle-brush polymers; mesoporous silica; micromotors; microparticles; polyphosphazenes EN bottle-brush polymers mesoporous silica micromotors microparticles polyphosphazenes 3187 3187 1 02/17/21 20210215 NES 210215 B Self-propelled micromotors b with a reversible braking system are shown. Manganese ions are embedded in microporous silica nanoparticles to catalyse the degradation of the H SB 2 sb O SB 2 sb "fuel" to water and gaseous oxygen. [Extracted from the article]

The incorporation of an extraneous on–off braking system is necessary for the effective motion control of the next generation of micrometer‐sized motors. Here, the design and synthesis of micromotors is reported based on mesoporous silica particles containing bipyridine groups, introduced by cocondensation, for entrapping catalytic cobalt(II) ions within the mesochannels, and functionalized on the surface with silane‐derived temperature responsive bottle‐brush polyphosphazene. Switching the polymers in a narrow temperature window of 25–30 °C between the swollen and collapsed state, allows the access for the fuel H2O2 contained in the dispersion medium to cobalt(II) bipyridinato catalyst sites. The decomposition of hydrogen peroxide is monitored by optical microscopy, and effectively operated by reversibly closing or opening the pores by the grafted gate‐like polyphosphazene, to control on demand the oxygen bubble generation. This design represents one of the few examples using temperature as a trigger for the reversible on–off external switching of mesoporous silica micromotors. [ABSTRACT FROM AUTHOR]

Herein, the impact of thin layer of polyphosphazene derivatives, as a buffer layer between the electron‐transporting layer and the back metal‐contact in mixed‐cation mixed‐halide perovskite solar cells (PSCs), is explored. PSCs with a poly[bis(allylamino)phosphazene] (PPz) interlayer exhibit enhanced rectification in the photo‐induced current density–voltage (J–V) curves, which show improved photovoltaic performance and photostability with reduced hysteresis. The thickness of the interlayer is optimized and the optimized PSCs with PPz buffer layer shows an average open‐circuit voltage (VOC) of ≈1.05 V, a short‐circuit current density (JSC) of around 23.5 mA cm−2, a fill factor of ≈72%, and a power conversion efficiency of about 17.3% for the forward and reverse scans under simulated AM1.5G illumination. Moreover, the application of PPz as an electron‐transporting interlayer in organic solar cells reveals that PPz interfacial layer improves the electron extraction at the cathode. The merit of applying PPz interlayer extends to the possibility of using different metals (such as aluminum, gold, copper, and silver) as the top contact in the prepared PCSs. In general, these experiments reveal a very promising approach to tackle the issue of interfacing, and to improve the performance and stability of PSCs. [ABSTRACT FROM AUTHOR]

To celebrate International Women′s Day on March 8th 2016, Chemistry – A European Journal is publishing a special issue dedicated to women around the world currently working in chemical research. The cover picture shows the frontispieces of the Concept, Review, and Minireview articles published in this issue, highlighting the broad range of chemistry that is currently being carried out by female researchers. In the top row from left to right: S. Harutyunyan et al. (page 3558 ff.), J. Sponer et al. (page 3572 ff.), and M. Brimble et al. (page 3622 ff.). In the middle row from left to right: M. Resmini et al. (page 3612 ff.), the logo for International Women′s Day 2016 (http://www. internationalwomensday.com/), and Y. Xie and J. Xie (page 3588 ff.). In the bottom row from left to right: I. Beletskaya and P. Sazonov (page 3644 ff.), T. Gaich and M. Pfaffenbach (page 3600 ff.), and A. Lattanzi and S. Meninno (page 3632 ff.). [ABSTRACT FROM AUTHOR]