Mixed-ligand based water-stable Mn(II)-MOF for quick, sensitive, and reusable IFE-PET-RET facilitated detection of formaldehyde and Cr(VI)-oxoanions in real-field samples like food and industrial water: experimental and theoretical insights.

We report the luminescence-based detection of Group-1 carcinogen formaldehyde (FA) and Cr(VI)-oxoanions with a mesoporous Mn(II)-MOF (1), featuring a uninodal 4-c net topology and linear 1D square channels forming a polymeric 2D network. The Mn-MOF , [Mn(phen)(hia)(HO)] was solvothermally constructed using π-conjugated, chelating phenanthroline (phen) and µ-η:η binding 5-hydroxyisophthalic acid (hia) ligands. The 2D rod-like crystallites of 1 demonstrated excellent phase purity, high thermal and photostability, and robustness under harsh conditions.

Assessment of the Inhibitory Efficacy of a Thiazole Derivative as an Efficient Corrosion Inhibitor for Augmenting the Resistance of MS in Acidic Environments.

Numerous thiazole compounds have been developed as cutting-edge inhibitors because of a rising fascination with using corrosion inhibitors (CIs) and preventative measures to prevent mild steel (MS) from deteriorating. In this study, the ability of a novel thiazole derivative, 2-hydrazono-3-methyl-2,3-dihydrobenzo[]thiazole hydrochloride (HMDBT), to prevent corrosion of MS (MS) in HCl has been reconnoitered using various approaches, Viz. gravimetric analysis, electrochemical (EC) analysis, and different surface characterizations.

Using eugenol scaffold to explore the explosive sensing properties of Cd(II)-based coordination polymers: experimental studies and real sample analysis.

Eugenol, the major constituent of clove oil, has been explored as an essential natural ingredient for ages owing to its versatile pharmacological properties. However, to date, the coordination chemistry of eugenol derivatives has not been much explored. In the present work, an eugenol-based Schiff base ligand (HL) was synthesized and structurally confirmed through ESI-MS, NMR, and FT-IR spectroscopy studies.

Mixed N,O-donor Directed Blue Emissive Nano-dispersed Mesoporous Mn(II)-MOF: Dual Sensing Probe for Recyclable and Ultrasensitive ppb-Level Recognition of TNP and Cr(VI)-Oxoanions.

A new mesoporous Mn(II)-MOF [Mn(phen)(nia)] with 4-c uninodal net topology and reiterating rectangular channels in its cargo-net like extension was synthesized using π-conjugated phenanthroline (phen) and syn-syn bridging 5-nitroisopthalic acid (nia) linkers. The MOF (1) exhibited phase purity, uniform morphology, photo and thermal stability, and robustness; duly triggered by the exceptional framework rigidity via intermolecular H-bonding and interlayer π-π stacking interactions. The bright-blue luminescence of the MOF nano-dispersion was explored for sensitive, specific and ultrafast detection of trinitrophenol (TNP) with extremely low LOD (90.

Integration of a Bismuth-Based Tris-Mononuclear Complex with 2D Functional Materials for Highly Efficient and Durable Aqueous Electrocatalytic Hydrogen Evolution.

The eminence of transitioning from traditional fossil fuel-based energy resources to renewable and sustainable energy sources is most evidently crucial. The potential of hydrogen as an alternative energy source has specifically focuses the electrocatalytic water splitting (EWS) as a promising technique for generating hydrogen. Development of efficient electrocatalysts to facilitate the EWS process while rationalizing the limitations of noble metal catalysts like platinum has become one of the daunting tasks.

CuAsO: Design, Hydrothermal Synthesis, Crystal Structure, Photocatalytic Dye Degradation, Hydrogen Evolution Reaction, Knoevenagel Condensation Reaction, and Thermal Studies.

CuAsO has been explored as a heterogeneous catalyst in the fields of photocatalysis, electrocatalysis, and solvent-free organic transformation reactions. The homogeneity has been successfully attained for the first time by designing a pH-assisted hydrothermal synthesis technique. Single-crystal X-ray diffraction studies reveal that no phase transition has been observed by lowering the temperature up to 103 K with no existence of satellite reflections.

Exploitation of a 1D coordination polymer as a portable kit for an eye-catching fluorometric response towards sensing of trivalent cations.

The development and utilization of coordination polymers (CPs) have drawn interest for potential applications in different fields. Detection of metal ions in efficient and selective manners is an important field of research. It paves the way to protect human health by balancing toxic metal ions and biologically active metal ions in the atmosphere.

Facile construction of an anthracene-decorated highly luminescent coordination polymer for the selective detection of explosive nitroaromatics and the mutagenic pollutant TNP.

Explosive nitroaromatic compounds (epNACs) are a group of chemicals that have caused significant human casualties through terrorist attacks and they also pose health risks. For the benefit of homeland security and environmental health, there is room for advancing research on the precise detection of epNACs. Coordination polymers (CPs) successfully serve this purpose because of their binding abilities and quenching capabilities.

Drug delivery using biocompatible covalent organic frameworks (COFs) towards a therapeutic approach.

Covalent organic frameworks (COFs) are constructed exclusively with lightweight organic scaffolds, which can have a 2D or 3D architecture. The ease of synthesis, robust skeleton and tunable properties of COFs make them superior candidates among their counterparts for a wide range of uses including biomedical applications. In the biomedical field, drug delivery or photodynamic-photothermal (PDT-PTT) therapy can be individually considered a potential parameter to be investigated.

AIEE activated Pyrene-Dansyl coupled FRET probe for discriminating detection of lethal Cu and CN: Bio-Imaging, DNA binding studies and prompt prognosis of Menke's disease.

In present work a pyrene-dansyl dyad functionalized chemoreceptor, DPNS is unveiled towards ultrasensitive chromo-fluorogenic detection of heavy and transition metal ions (HTMs) like Cu and pernicious CN. It demonstrated distinct chromogenic responses; colorless to faint yellow (Cu), intense yellow (CN) from contaminant aqueous sources. Cu instigated alteration in DPNS fluorescence from feeble emission to sparkling green with LOD: 37.

Anion-directed structural tuning of two azomethine-derived Zn complexes with optoelectronic recognition of Cu in aqueous medium with anti-cancer activities: from micromolar to femtomolar sensitivity with DFT revelation.

Herein, two novel mononuclear transition metal Zn complexes [Zn(HL)(N)(OAc)] (NS-1) & [Zn(HL)(ClO)] (NS-2) have been synthesised using a tridentate clickable Schiff base ligand, HL (2-methyl-2-((pyridin-2-ylmethyl)amino)propan-1-ol), and the polyatomic monoanions N and ClO for NS-1 and NS-2 respectively. Interestingly, NS-1 and NS-2 have been explored for the detection of Cu with an LOD of 48.6 fM (response time ∼6 s) and 2.

A strategically synthesized arseno-discriminatory tetra-phenoxido hetero-trinuclear complex envisioned for the recognition of iAs and oAs from sp. and aquatic crustaceans.

A heterotrimetallic [Mn(Cu)(CHNO)] complex VBCMERI has been unveiled herein to monitor its synergistic propensity towards aqueous phase As3+ (iAs and oAs) detection. VBCMERI was structurally probed by numerous analytical tools like ESI-MS, FT-IR, and SCXRD. The aqueous phase selective chromogenic alteration of the sensory probe from greenish-yellow to colorless was observed owing to interaction with As (cationic form, iAs).

A Ni-MOF as Fluorescent/Electrochemical Dual Probe for Ultrasensitive Detection of Picric Acid from Aqueous Media.

A water-stable, microporous, luminescent Ni(II)-based metal-organic framework (MOF) () with a 4- uninodal topology was solvothermally synthesized using mixed N-, O-donor-directed π-conjugated co-ligands. The extraordinary performance of this MOF toward rapid monitoring of mutagenic explosive trinitrophenol (TNP) in aqueous and vapor phases by the fluorescence "Turn-off" technique with an ultralow detection limit of 66.43 ppb (: 3.

Explicating the recognition phenomenon of hazardous nitro-aromatic compound from contaminated environmental and cellular matrices by rationally designed pyridine-functionalized molecular probes.

In the quest of recognizing hazardous nitro-aromatic compounds in water, two pyridine-functionalized Schiff-base chemosensors, DMP ((E)-N-(3,4-dimethoxybenzylidene)(pyridin-2-yl)methanamine)) and MP (4-((E)-((pyridin-2-yl)methylimino)methyl)-2-ethoxyphenol) have been synthesized to detect mutagenic 2,4,6-Trinitrophenol (TNP) in soil, water as well as cellular matrices by producing turn-off emission responses as a combined consequence of PET and RET processes. Several experimental analyses including ESI-MS, FT-IR, photoluminescence, H NMR titration, and the theoretical calculations ascertained the formation and sensing efficacies of the chemosensors. The analytical substantiations revealed that structural variation of the chemosensors played a significant role in improving the sensing efficiency, which would certainly be worthwhile in developing small molecular TNP sensors.

Metal-organic frameworks/cellulose hybrids with their modern technological implementation towards water treatment.

Metal-organic frameworks (MOFs) are amongst the most attractive porous polymeric networks with appealing properties. However, their inherent fragility, powder nature, low processibility, and handling present some exceptional challenges for high-tech commercial applications. Currently, economic and environmental concerns drive the development of some bioinspired polymeric matrices containing MOFs.

Electrochemical Nanosensors for Sensitization of Sweat Metabolites: From Concept Mapping to Personalized Health Monitoring.

Sweat contains a broad range of important biomarkers, which may be beneficial for acquiring non-invasive biochemical information on human health status. Therefore, highly selective and sensitive electrochemical nanosensors for the non-invasive detection of sweat metabolites have turned into a flourishing contender in the frontier of disease diagnosis. A large surface area, excellent electrocatalytic behavior and conductive properties make nanomaterials promising sensor materials for target-specific detection.

Selective Low-Level Detection of a Perilous Nitroaromatic Compound Using Tailor-Made Cd(II)-Based Coordination Polymers: Study of Photophysical Properties and Effect of Functional Groups.

Three coordination polymers (CPs -) are prepared based on diverse electron-donating properties and coordination arrangements of conjugated ligands. Interestingly, this is also reflected in their photophysical properties. The distinguishable high emissive nature of the luminescent coordination polymer shows its potentiality toward the detection of the perilous substance 2,4,6-trinitrophenol (TNP) or picric acid (PA).

Regioselective synthetic approach for key precursors of 6-arylbenzo[]phenanthridin-10-ol derivatives: a useful compound for selective chromogenic recognition of fluoride.

A regioselective synthetic strategy for 6-aryl-8,9-dihydrobenzo[]phenanthridine-10(7)-ones (4) is accomplished using a one-pot four-component reaction by fine-tuning the reaction temperature. DMSO is excellently used as a reactant-cum-solvent to introduce a carbonyl functionality regioselectively at the C-10 position of the benzophenanthridine backbone, an MCR, which is unknown yet. The elegant features of this strategy are the formation of two CC, one CN, and one CO bonds in a single step, without using a base and an activator for the oxygenation process.

"Caught in the Act" @ disruption of A-ET-E process in the recognition of F by a lamellar Eu-MOF in heterogeneous manner with logic gate construction: From protagonist idea to implementation world.

Development of cost-effective and reliable fluoride sensor for assessing water quality of natural water samples is of immense importance in developing countries as they can provide an easy platform for safeguarding human health. These sensors should be as simple as possible to be fabricated locally by layman. In this context, Eu-based MOFs provide trustable platform with bright luminescence in the visible region due to their absorbance-energy transfer-emission (A-ET-E) process.

Strategic optimization of phase-selective thermochemically amended terra-firma originating from excavation-squander for geogenic fluoride adsorption: a combined experimental and in silico approach.

An inimitable adsorbent "FI-TM-BWCC," emanated from meta-phase-selective thermochemical modulation of excavation-squander (mine waste)-derived terra-firma (blackish white china clay, i.e., BWCC), is explored in the present work for fluoride (F) adsorption purpose.

Unveiling of a smartphone-mediated ratiometric chemosensor towards the nanomolar level detection of lethal CN: combined experimental and theoretical validation with the proposition of a molecular logic circuitry.

A promising naphthalene-functionalized ratiometric chemosensor ()-1-((naphthalen-5-yl) methylene)-2-(2,4-dinitrophenyl) hydrazine (DNMH) is unveiled in the present work. DNMH demonstrates brisk discernible colorimetric response from yellow to red in the presence of CN, a lethal environmental contaminant, in a near-perfect aqueous medium with a LOD of 278 nM. The "key role marker" controlling the electrochemical and non-covalent H-bonding interaction between DNMH and CN is through the commendable role of acidic -NH functionalities.

A Ni(II) Metal-Organic Framework with Mixed Carboxylate and Bipyridine Ligands for Ultrafast and Selective Sensing of Explosives and Photoelectrochemical Hydrogen Evolution.

We report a (nickel metal-organic framework), , synthesized by using two linkers 5-sulfoisophthalic acid (SIP) and 4,4'-bipyridine (BPY) simultaneously. It displays an orthorhombic crystal system with the 2 space group: = 31.425 Å, = 19.

Selective recognition of ammonia and aliphatic amines by C-N fused phenazine derivative: A hydrogel based smartphone assisted 'opto-electronic nose' for food spoilage evaluation with potent anti-counterfeiting activity and a potential prostate cancer biomarker sensor.

In real day scenario, it is an urge to provide a single solution of multiple problems. In this regard, herein rapid, selective and highly efficient chromo-fluorogenic detection of ammonia/aliphatic amines over aromatic amines has been investigated by means of a novel "opto-electronic nose", CN-2, synthesized in a single-step via multiple inter/intramolecular C-N fusion reactions. The in-situ generated mono-protonated CN-2 can selectively detect primary to secondary to even tertiary aliphatic amines over aromatic amines within ∼40 S with extremely low detection threshold values of 27.

Knoevenagel condensation triggered synthesis of dual-channel oxene based chemosensor: Discriminative spectrophotometric recognition of F, CN and HSO with breast cancer cell imaging, real sample analysis and molecular keypad lock applications.

A novel oxene based unusual sensory receptor (HyMa) has been synthesized via.Knoevenagel condensation triggered carbon-heteroatom (oxygen) intramolecular bond formation reaction at room temperature for discriminative detection of multi-analytes like HSO, CN & F by spectro-photometric alterations with profound selectivity with the detection limit of 38 ppb, 18 ppb & 94 ppb respectively. Examination of the sensing mechanism was exhaustively investigated through several spectroscopic means like H NMR, FT-IR, absorption and fluorescence spectra etc.

Amine-substituent induced highly selective and rapid "turn-on" detection of carcinogenic 1,4-dioxane from purely aqueous and vapour phase with novel post-synthetically modified d-MOFs.

Herein, an amine decorated Cd(II) metal-organic framework (MOF) with a uninodal 6-c topology was synthesized as a suitable platform for facile post-synthetic modification (PSM). The as-synthesized parent d-MOF (1) with free -NH centers, when functionalized with two different carbonyl substituents (1-naphthaldehyde and benzophenone) of varying conjugation, produces two novel luminescent MOFs (LMOFs) PSM-1 and PSM-2. The judicious incorporation of carbonyl substituents into the skeleton of 1 was rationalized ESI-MS, H-NMR, FT-IR and PXRD analyses.