Revival of Degraded CsPbI3 Nanocrystals by Diselenide Ligand and Nanocrystal Self-Assembly on Nanofibrilar Ligand Template.

Among the lead halide perovskite (LHP) family, CsPbI3 is known to be significantly vulnerable to moisture, which hinders its use in real device applications. It is reported that chalcogen-based ligands can better stabilize CsPbI3 and revive nanocrystals (NCs). Here, diphenyl diselenide (DPhDSe) ligand is used to revive the degraded CsPbI3 NCs through a post-synthetic treatment of adding a small amount of DPhDSe in the degraded NC dispersion. DPhDSe in the dispersion formed nanofibrillar crystals at a low temperature through the π-π stacking of the phenyl ring. The nanofibrils played as a template on which the NCs self-assembled and they are attached side-by-side to form microfibers. The microfiber powder containing the NCs is optically stable at ambient conditions and morphologically self-healable by mild thermal annealing due to the dynamic Se─Se bond. The mechanism of the structural changes, optical transitions, and chemical changes has been systematically characterized through electron microscopy, diffraction, spectroscopy, and elemental analysis.

A Prompt Study on Recent Advances in the Development Of Colorimetric and Fluorescent Chemosensors for "Nanomolar Detection" of Biologically Important Analytes.

Fluorescent and colorimetric chemosensors for selective detection of various biologically important analytes have been widely applied in different areas such as biology, physiology, pharmacology, and environmental sciences. The research area based on fluorescent chemosensors has been in existence for about 150 years with the development of large number of fluorescent chemosensors for selective detection of cations as metal ions, anions, reactive species, neutral molecules and different gases etc. Despite the progress made in this field, several problems and challenges still exist. The most important part of sensing is limit of detection (LOD) which is the lowest concentration that can be measured (detected) with statistical significance by means of a given analytical procedure. Although there are so many reports available for detection of millimolar to micromolar range but the development of chemosensors for the detection of analytes in nanomolar range is still a challenging task. Therefore, in our current review we have focused the history and a general overview of the development in the research of fluorescent sensors for selective detection of various analytes at nanomolar level only. The basic principles involved in the design of chemosensors for specific analytes, binding mode, photophysical properties and various directions are also covered here. Summary of physiochemical properties, mechanistic view and type of different chemosensors has been demonstrated concisely in the tabular forms.

Molecular evaluation of the metabolism of estrogenic di(2-ethylhexyl) phthalate in Mycolicibacterium sp.

BACKGROUND: Di(2-ethylhexyl) phthalate (DEHP) is a widely detected plasticizer and a priority pollutant of utmost concern for its adverse impact on humans, wildlife and the environment. To eliminate such toxic burden, biological processes are the most promising ways to combat rampant environmental insults under eco-friendly conditions. The present study investigated the biochemical and molecular assessment of the catabolic potential of Mycolicibacterium sp. strain MBM in the assimilation of estrogenic DEHP. RESULTS: A detailed biochemical study revealed an initial hydrolytic pathway of degradation for DEHP followed by the assimilation of hydrolyzed phthalic acid and 2-ethylhexanol to TCA cycle intermediates. Besides the inducible nature of DEHP-catabolic enzymes, strain MBM can efficiently utilize various low- and high-molecular-weight phthalate diesters and can grow under moderately halotolerant conditions. Whole genome sequence analysis exhibited a genome size of 6.2 Mb with a GC content of 66.51% containing 6,878 coding sequences, including multiple genes, annotated as relevant to the catabolism of phthalic acid esters (PAEs). Substantiating the annotated genes through transcriptome assessment followed by RT-qPCR analysis, the possible roles of upregulated genes/gene clusters in the metabolism of DEHP were revealed, reinforcing the biochemical pathway of degradation at the molecular level. CONCLUSIONS: A detailed co-relation of biochemical, genomic, transcriptomic and RT-qPCR analyses highlights the PAE-degrading catabolic machineries in strain MBM. Further, due to functional attributes in the salinity range of both freshwater and seawater, strain MBM may find use as a suitable candidate in the bioremediation of PAEs.

Understanding the Effect of Internal Electrostatic Fields Created by Alkaline Earth Metal Ions Poised over Secondary Coordination Sphere of Molecular Iron Complexes.

Understanding the effect of the local electrical field around the reaction center in enzymes and molecular catalysis is an important topic of research. Herein, we explored the electrostatic field exerted by the alkaline earth metal ions (M2+ = Mg2+, Ca2+, Sr2+, and Ba2+) around Fe in FeIII(Cl) complexes by experimental and computational investigations. M2+ coordinated dinuclear FeIII(Cl) complexes (12M) were synthesized and characterized by X-ray crystallography and different spectroscopic techniques. EPR and magnetic moment measurements exhibited the presence of high-spin FeIII centers in the 12M complexes. Electrochemical investigations revealed FeIII/FeII reduction potential values shifted anodically in 12M complexes compared to 1. Likewise, 2p3/2 and 2p1/2 peaks in the XPS data were found to shift positively in the 12M complexes, demonstrating that redox-inactive metal ions make FeIII more electropositive. However, nearly similar λmax values in the UV-vis spectra were observed in 1 and 12M complexes. The first-principles-based computational simulations further revealed the impact of M2+ on stabilizing 3d-orbitals of Fe. The distortion in Laplacian distribution (∇2ρ(r)) of electron density around M2+ also indicates the possibility of having Fe-M interactions in these complexes. The absence of a bond critical point between FeIII and M2+ ions in the 12M complexes indicates dominant through-space interaction between these metal centers. Experimental and computational studies collectively imply that the installation of internal electrostatic fields exerted by M2+ ions in 12M complexes alters the electronic structure of FeIII.

Role of chemistry in bio-inspired liquid wettability.

Chemistry and topography are the two distinct available tools for customizing different bio-inspired liquid wettability including superhydrophobicity, superamphiphobicity, underwater superoleophobicity, underwater superoleophilicity, and liquid infused slippery property. In nature, various living species possessing super and special liquid wettability inherently comprises of distinctly patterned surface topography decorated with low/high surface energy. Inspired from the topographically diverse natural species, the variation in surface topography has been the dominant approach for constructing bio-inspired antiwetting interfaces. However, recently, the modulation of chemistry has emerged as a facile route for the controlled tailoring of a wide range of bio-inspired liquid wettability. This review article aims to summarize the various reports published over the years that has elaborated the distinctive importance of both chemistry and topography in imparting and modulating various bio-inspired wettability. Moreover, this article outlines some obvious advantages of chemical modulation approach over topographical variation. For example, the strategic use of the chemical approach has allowed the facile, simultaneous, and independent tailoring of both liquid wettability and other relevant physical properties. We have also discussed the design of different antiwetting patterned and stimuli-responsive interfaces following the strategic and precise alteration of chemistry for various prospective applications.

Designing a Network of Crystalline Polymers for a Scalable, Nonfluorinated, Healable and Amphiphobic Solid Slippery Interface.

The fluorinated-liquid infused amphiphobic slippery interfaces exhibiting superior sliding of the beaded oil/water droplets, often suffer from durability and contamination issues. Here, the ability of 1) hexagonal packing of hydrocarbon sides in a selected "comb-like" polymer and 2) its reversible phase transition at 51 °C was rationally exploited to achieve temperature-assisted rapid (<1 minute) and repetitive (50 times) self-healable amphiphobic solid-slippery coating on both planar and geometrically-complex substrates. The selected "comb-like" polymer was strategically infused in a porous, hydrophilic and thick (≈4.8 µm) polymeric coating. The resultant solid and smooth interface exhibited sliding of beaded droplets of various liquids, including droplets of water, polar (ethanol, 1-propanol, 1-hexanol, DMSO, DMF), and non-polar (decane, dodecane, diiodomethane) organic solvents, edible (vegetable oil), motor, engine (petrol, diesel, kerosene) and crude oils.

Non-Fluorinated and Robust Superhydrophobic Modification on Covalent Organic Framework for Crude-Oil-in-Water Emulsion Separation.

Covalent organic frameworks (COFs) having high specific surface area, tunable pore size and high crystallinity are mostly post modified following fluorine-based and complex synthetic approaches to achieve a bio-inspired liquid wettability, i.e. superhydrophobicity. Herein, a facile, non-fluorinated and robust chemical approach is introduced for tailoring the water wettability of a new COF-which was prepared through Schiff-base condensation reaction. A silane precursor was readily reacted with selected alkyl acrylates through 1,4-conjugate addition reaction, prior to grafting on the prepared C4-COF for tailoring different water wettability-including robust superhydrophobicity. The superhydrophobic C4-COF (SH-C4-COF) that displayed significantly enhanced (>5 times; from 220 wt. % to 1156 wt. %) oil-absorption capacity, was extended to address the relevant challenges of "oil-in-water" emulsion separation, rapidly (<1 minute) and repetitively (50 times) at diverse and harsh conditions.

High-Q diamond microresonators in the long-wave infrared.

High quality factor (Q) photonic devices in the room temperature thermal infrared region, corresponding to deeper long-wave infrared with wavelengths beyond 9 microns, have been demonstrated for the first time. Whispering gallery mode diamond microresonators were fabricated using single crystal diamond substrates and oxygen-based inductively coupled plasma (ICP) reactive ion etching (RIE) at high angles. The spectral characteristics of the devices were probed at room temperature using a tunable quantum cascade laser that was free space-coupled into the resonators. Light was extracted via an arsenic selenide (As2Se3) chalcogenide infrared fiber and directed to a cryogenically cooled mercury cadmium telluride (HgCdTe) detector. The quality factors were tested in multiple microresonators across a wide spectral range from 9 to 9.7 microns with similar performance. One example resonance (of many comparables) was found to reach 3648 at 9.601 µm. Fourier analysis of the many resonances of each device showed free spectral ranges slightly greater than 40 GHz, matching theoretical expectations for the microresonator diameter and the overlap of the whispering gallery mode with the diamond.

Long-wave infrared absorption measurement of undoped germanium using photothermal common-path interferometry.

Germanium is one of the most commonly used materials in the longwave infrared ($\lambda \sim{8 {-} 12}\;\unicode{x00B5}{\rm m}$λ∼8-12µm), but ironically, its absorption coefficient is poorly known in this range. An infrared photothermal common-path interferometry system with a tunable quantum cascade pump laser is used to measure the absorption coefficient of ${ \gt }{99.999}\% $>99.999% pure undoped germanium as a function of wavelengths between 9 and 11 µm, varying between about 0.15 and ${0.45}\;{{\rm cm}^{ - 1}}$0.45cm-1 over this range.

Source apportionment of potentially toxic elements in street dust of a coal mining area in Chhattisgarh, India, using multivariate and lead isotopic ratio analysis.

Street dust of Korba, Chhattisgarh, an urban industrial hub in one of India's major coal mining areas, has been analysed for profiling and sourcing of Pb and other potentially toxic elements (PTEs). Lead isotopic ratio of dust, coal, diesel, fly ash and human blood of Korba is being reported for the first time in this study. The mean concentrations (in mg/kg) of Al, V, Cr, Fe, Mn, Ni, Cu, Zn, Cd and Pb were higher than World Background soil and Reference soil USA values and decreased in the order of Al (17000) > Fe (7550) > Mn (2740) > Cr (833) > Ni (571) > Zn (231) > Cu (152) > V (145) > Pb (98.6) > U (7.9) > Cd (1.34). About 25% of the sampled dust had Pb Igeo belonging to class IV category of heavy contamination. Dust from industrial areas was highly enriched with Cr, Cu, Pb and Mn, while those from coal mining areas had high mean V concentration. Principal component analysis extracted Al, Fe, Mn, Zn, Pb and U with the highest loading factors in Component 1 indicative of their lithogenic and anthropogenic sources. The lead isotopic ratios of the dust, coal, diesel, fly ash and eight human blood samples clustered linearly in the 207Pb/204Pb vs 208Pb/204Pb and 206Pb/204Pb vs 208Pb/204Pb plots. Airborne lead deposition from diesel-based traffic exhausts and fly ash contributed to the human blood lead level besides coal mining activities. Geospatially, while Pb was mainly concentrated in the residential, industrial and coal-mining areas, Zn and Mn were mainly distributed in the roadside areas of industrial centres.

Colorimetric and Fluorimetric DNA Detection with a Hydroxystyryl-Quinolizinium Photoacid and Its Application for Cell Imaging.

The combination of styryl dye properties with the acidity and strong photoacidity of the 2,2'-[(1''-hydroxy-4''-methyl-(E)-2'',6''-phenylene)]-bisquinolizinium enables the detection of DNA by distinct absorption and emission color changes and the fluorimetric detection of DNA in cells with epifluorescence and confocal fluorescence microscopy.

Cloning, overexpression and purification of a novel two-domain protein of Staphylococcus aureus phage Phi11.

The genome of aureophage Phi11 reveals the presence of the gene gp07 which codes for the putative antirepressor protein (GenBank accession no. NC_004615.1). Antirepressor proteins are mainly involved in lytic cycle determination mechanisms of various bacteriophages. The Phi11 protein Gp07 consists of two domains-an amino terminal Bro domain and a carboxy terminal KilA domain. Despite the important role of antirepressor proteins in the developmental pathway of phages, there are no reports on the purification and characterization of aureophage antirepressor proteins. Here we describe a method to clone, overexpress and purify the full length Gp07 as carboxy terminal hexa histidine tag variant. The recombinant protein was expressed in Escherichia coli BL21(λDE3) cells and gradient of imidazole and NaCl were used for successful purification of the soluble recombinant protein to homogeneity. The protein exists as a dimer in solution as is evident from our gel filtration chromatography and glutaraldehyde cross-linking data. Further, we found that temperature has huge impact on the structural conformation of the protein. We expect that the purification of Gp07 will further our work in characterizing the role played by this protein during phage induction.

Diphenylaminostyryl-substituted quinolizinium derivatives as fluorescent light-up probes for duplex and quadruplex DNA.

(E)-2-[1'-((Diphenylamino)styryl)quinolizinium (3a) and 2,2'-{(phenylimino)-bis[(E)-1'',1'''-styryl]}-bis[quinolizinium] (3b) were synthesized, and their interactions with duplex DNA and quadruplex DNA were investigated with a particular focus on their ability to operate as DNA-sensitive fluorescent probes. Due to the significantly different size and steric demand of these quinolizinium derivatives they exhibit different binding modes. Thus, 3a intercalates into duplex DNA and binds through π stacking to quadruplex DNA, whereas 3b favours groove binding to both DNA forms. The emission intensity of these compounds is very low in aqueous solution, but it increases drastically upon association with duplex DNA by a factor of 11 (3a) and >100 (3b) and with quadruplex DNA by a factor of >100 (3a) and 10 (3b), with emission bands between 600 and 750 nm.

Inclusion of Ln(III) in the Complexes of Co(II) with a Mannich Base Ligand: Development of Atmospheric CO2 Fixation and Enhancement of Catalytic Oxidase Activities.

The reaction of the Mannich base ligand (H2L = N, N'-dimethyl- N, N'-bis(2-hydroxy-3-methoxy-5-methylbenzyl)ethylenediamine) with Co(OAc)2·4H2O and Ln(III) nitrate salts (Ln = Gd, Tb, and Dy) under basic conditions afforded three carbonato-bridged isostructural tetranuclear heterometallic Co(II)-Ln(III) complexes (Co2Gd2L2(µ4-CO3)2(NO3)2] (1), [Co2Tb2L2(µ4-CO3)2(NO3)2] (2), and [Co2Dy2L2(µ4-CO3)2(NO3)2] (3)) by atmospheric CO2 fixation. In all structures, two dinuclear [(CoIIL)LnIII(NO3)] units are linked via two µ4-carbonato groups to form the tetranuclear CoII2LnIII2 core. The geometry around two penta-coordinated Co(II) ions is distorted square pyramid, and that around two nona-coordinated Ln(III) ions is intermediate between "spherical tricapped trigonal prism" and "spherical capped square antiprism" in all complexes. The complexes (1-3) showed catecholase-like and phenoxazinone-synthase-like catalytic activities. The kcat values calculated for the catecholase-like reaction were 254.5, 272.4, and 291.3 h-1, and for the phenoxazinone-synthase-like reaction they were 2930.6, 2965.2, and 2998.5 h-1 for complexes 1-3, respectively. The probable pathways for these two oxidase reactions have been proposed by the analyses of mass spectral data. For all of the compounds, the variable temperature magnetic susceptibility and isothermal magnetization data were investigated. The complexes exhibited overall ferromagnetic behavior, which was evident from the isothermal magnetization curves. AC magnetic susceptibility measurements revealed the slow relaxation of magnetization in complexes 2 and 3 but very negligible in 1. The activation energy barriers ( Ueff) for the slow relaxation process were evaluated and found to be 1.99, 2.79, and 8.98 K for 1, 2, and 3, respectively.

Light-Cone Spreading of Perturbations and the Butterfly Effect in a Classical Spin Chain.

We find that the effects of a localized perturbation in a chaotic classical many-body system-the classical Heisenberg chain at infinite temperature-spread ballistically with a finite speed even when the local spin dynamics is diffusive. We study two complementary aspects of this butterfly effect: the rapid growth of the perturbation, and its simultaneous ballistic (light-cone) spread, as characterized by the Lyapunov exponents and the butterfly speed, respectively. We connect this to recent studies of the out-of-time-ordered commutators (OTOC), which have been proposed as an indicator of chaos in a quantum system. We provide a straightforward identification of the OTOC with a natural correlator in our system and demonstrate that many of its interesting qualitative features are present in the classical system. Finally, by analyzing the scaling forms, we relate the growth, spread, and propagation of the perturbation with the growth of one-dimensional interfaces described by the Kardar-Parisi-Zhang equation.

A concentration dependent auto-relay-recognition by the same analyte: a dual fluorescence switch-on by hydrogen sulfide via Michael addition followed by reduction and staining for bio-activity.

H2S is shown, for the first time, to play an extraordinary dual role due to its nucleophilicity and reducing property with our single chemosensor, PND [4-(piperidin-1-yl) naphthalene-1,2-dione]. The initial nucleophilic attack via Michael addition (a lower concentration of H2S, blue fluorescence) is followed by the reduction of the 1,2-diketo functionality (a higher concentration of H2S, green fluorescence). This chemosensor, which also shows biological response, is remarkably effective in sensing the same analyte (H2S) at its different concentrations in a relay pathway via a fluorescence "off-on-on" mechanism, and this is also supported by DFT calculation and Cyclic voltammograms.