Highlights in Interface of Wastewater Treatment by Utilizing Metal Organic Frameworks: Purification and Adsorption Kinetics.

Polluted water has become a concern for the scientific community as it causes many severe threats to living beings. Detection or removal of contaminants present in wastewater and attaining purity of water that can be used for various purposes are a primary responsibility. Different treatment methods have already been used for the purification of sewage. There is a need for low-cost, highly selective, and reusable materials that can efficiently remove pollutants or purify contaminated water. In this regard, MOFs have shown significant potential for applications such as supercapacitors, drug delivery, gas storage, pollutant adsorption, etc. The outstanding structural diversity, substantial surface areas, and adjustable pore sizes of MOFs make them superior candidates for wastewater treatment. This Review provides an overview of the interaction science and engineering (kinetic and thermodynamic aspects with interactions) underpinning MOFs for water purification. First, fundamental strategies for the synthesis methods of MOFs, different categories, and their applicability in wastewater treatment are summarized, followed by a detailed explanation of various interaction mechanisms. Finally, current challenges and future outlooks for research on MOF materials toward the adsorption of hazardous components are discussed. A new avenue for modifying their structural characteristics for the adsorption and separation of hazardous materials, which will undoubtedly direct future work, is also summarized.

In situ growth of a redox-active metal-organic framework on electrospun carbon nanofibers as a free-standing electrode for flexible energy storage devices.

The rational construction of free-standing and flexible electrodes for application in electrochemical energy storage devices and next-generation supercapacitors is an emerging research focus. Herein, we prepared a redox-active ferrocene dicarboxylic acid (Fc)-based nickel metal-organic framework (MOF) on electrospun carbon nanofibers (NiFc-MOF@CNFs) via an in situ approach. This in situ approach avoided the aggregation of the MOF. The NiFc-MOF@CNF flexible electrode showed a high redox-active behavior owing to the presence of ferrocene and flexible carbon nanofibers, which led to unique properties, including high flexibility and lightweight. Furthermore, the prepared electrode was utilized in a supercapacitors (SC) without the use of any binder, which achieved a specific capacity of 460 C g-1 at 1 A g-1 with an excellent cyclic retention of 82.2% after 25 000 cycles and a good rate capability. A flexible asymmetric supercapacitor device was assembled, which delivered a high energy density of 56.25 W h kg-1 and a long-lasting cycling performance. Also, the prepared electrode could be used as a freestanding electrode in flexible devices at different bending angles. The obtained cyclic voltammetry curves showed negligible changes, indicating the high stability and good flexibility of the electrode. Thus, the use of the in situ strategy can lead to the uniform growth of redox-active MOFs or other porous materials on CNFs.

Exploring the antimicrobial potential of isoniazid loaded Cu-based metal-organic frameworks as a novel strategy for effective killing of Mycobacterium tuberculosis.

Tuberculosis (TB) remains one of the most infectious pathogens with the highest human mortality and morbidity. Biofilm formation during Mycobacterium tuberculosis (Mtb) infection is responsible for bacterial growth, communication, and, most essentially, increased resistance/tolerance to antibiotics leading to higher bacterial persistence. Thus, biofilm growth is presently considered a key virulence factor in the case of chronic disease. Metal-Organic Frameworks (MOFs) have recently emerged as a highly efficient system to improve existing antibiotics' therapeutic efficacy and reduce adverse effects. In this regard, we have synthesized Cu-MOF (IITI-3) using a solvothermal approach. IITI-3 was well characterized by various spectroscopic techniques. Herein, IITI-3 was first encapsulated with isoniazid (INH) to form INH@IITI-3 with 10 wt% loading within 1 hour. INH@IITI-3 was well characterized by PXRD, TGA, FTIR, and BET surface area analysis. Furthermore, the drug release kinetics studies of INH@IITI-3 have been performed at pH 5.8 and 7.4 to mimic the small intestine and blood pH, respectively. The results show that drug release follows first-order kinetics. Furthermore, the antimycobacterial activity of INH@IITI-3 demonstrated significant bacterial killing and altered the structural morphology of the bacteria. Moreover, INH@IITI-3 was able to inhibit the mycobacterial biofilm formation upon treatment and showed less cytotoxicity toward the murine RAW264.7 macrophages. Thus, this work significantly opens up new possibilities for the applications of INH@IITI-3 in biofilm infections in Mtb and further contributes to TB therapeutics.

Phosphorization Engineering on a MOF-Derived Metal Phosphide Heterostructure (Cu/Cu3P@NC) as an Electrode for Enhanced Supercapacitor Performance.

A highly conductive and rationally constructed metal-organic framework (MOF)-derived metal phosphide with a carbonaceous nanostructure is a meticulous architecture toward the development of electrode materials for energy storage devices. Herein, we report a facile strategy to design and construct a new three-dimensional (3D) Cu-MOF via a solvent diffusion method at ambient temperature, which was authenticated by a single-crystal X-ray diffraction study, revealing a novel topology of (2,4,7)-connected three-nodal net named smm4. Nevertheless, the poor conductivity of pristine MOFs is a major bottleneck hindering their capacitance. To overcome this, we demonstrated an MOF-derived Cu3P/Cu@NC heterostructure via low-temperature phosphorization of Cu-MOF. The electronic and ionic diffusion kinetics in Cu3P/Cu@NC were improved due to the synergistic effects of the heterostructure. The as-prepared Cu3P/Cu@NC heterostructure electrode delivers a specific capacity of 540 C g-1 at 1 A g-1 with outstanding rate performance (190 C g-1 at 20 A g-1) and cycle stability (91% capacity retention after 10,000 cycles). Moreover, the assembled asymmetric solid-state supercapacitor (ASC) achieved a high energy density/power density of 45.5 Wh kg-1/7.98 kW kg-1 with a wide operating voltage (1.6 V). Long-term stable capacity retention (87.2%) was accomplished after 5000 cycles. These robust electrochemical performances suggest that the Cu3P/Cu@NC heterostructure is a suitable electrode material for supercapacitor applications.

Heterostructures of MXenes and transition metal oxides for supercapacitors: an overview.

MXenes are a large family of two dimensional (2D) materials with high conductivity, redox activity and compositional diversity that have become front-runners in the materials world for a diverse range of energy storage applications. High-performing supercapacitors require electrode materials with high charge storage capabilities, excellent electrical conductivity for fast electron transfer, and the ability of fast charging/discharging with good cyclability. While MXenes show many of these properties, their energy storage capability is limited by a narrow electrochemically stable potential window due to irreversible oxidation under anodic potentials. Although transition metal oxides (TMOs) are often high-capacity materials with high redox activity, their cyclability and poor rate performance are persistent challenges because of their dissolution in aqueous electrolytes and mediocre conductivity. Forming heterostructures of MXenes with TMOs and using hybrid electrodes is a feasible approach to simultaneously increase the charge storage capacity of MXenes and improve the cyclability and rate performance of oxides. MXenes could also act as conductive substrates for the growth of oxides, which could perform as spacers to stop the aggregation of MXene sheets during charging/discharging and help in improving the supercapacitor performance. Moreover, TMOs could increase the interfacial contact between MXene sheets and help in providing short-diffusion ion channels. Hence, MXene/TMO heterostructures are promising for energy storage. This review summarizes the most recent developments in MXene/oxide heterostructures for supercapacitors and highlights the roles of individual components.

Multifaceted Carbon Dots: toward pH-Responsive Delivery of 5-Fluorouracil for In Vitro Antiproliferative Activity.

The synthesis of smart hybrid material to assimilate diagnosis and treatment is crucial in nanomedicine. Herein, we present a simple and facile method to synthesize multitalented blue-emissive nitrogen-doped carbon dots N@PEGCDs. The as-prepared carbon dots N@PEGCDs show enhanced biocompatibility, small size, high fluorescence, and high quantum yield. The N@PEGCDs are used as a drug carrier for 5-fluorouracil (5-FU) with more release at acidic pH. Furthermore, the mode of action of drug-loaded CD (5FU-N@PEGCDs) has also been explored by performing wound healing assay, DCFDA assay for ROS generation, and Hoechst staining. The drug loaded with carbon dots showed less toxicity to normal cells compared to cancer cells, making it a perfect candidate to be studied for designing next-generation drug delivery systems.

Upcycling rust and plastic waste into an Fe MOF for effective energy storage applications: transformation of trash to treasure.

The upcycling of waste into valuable chemicals has gained significant attention in recent years as a way to reduce waste and promote the circular economy. The transition to a circular economy that includes waste upcycling is crucial for addressing the global challenge of resource depletion and waste management. To that end, an Fe-based metal-organic framework material (Fe-BDC(W)) has been synthesized completely via the utilization of waste materials. The upcycling of rust gives the Fe salt, whilst the benzene dicarboxylic acid (BDC) linker has been derived from waste polyethylene terephthalate plastic bottles. Sustainable energy storage from waste materials seeks to produce environmentally benign and economically viable energy storage technologies. The prepared MOF has been deployed as an active material for a supercapacitor, which achieves a specific capacitance of 752 F g-1 at 4 A g-1, comparable with the MOF produced from commercially available chemicals, Fe-BDC(C).

Cu-Metal Organic Framework Derived Multilevel Hierarchy (Cu/CuxO@NC) as a Bifunctional Electrode for High-Performance Supercapacitors and Oxygen Evolution Reaction.

The development of a MOFs-derived multilevel hierarchy in a single step still remains a challenging task. Herein, we have synthesized novel Cu-MOF via a slow diffusion method at ambient temperature and further utilized it as a precursor source for MOF-derived multilevel hierarchy (Cu/CuxO@NC, x = 1 and 2). This studies suggest that the organic ligands served as a source of an N-doped carbon matrix encapsulated with metal oxide nanoparticles which were confirmed by various characterization techniques; further BET analysis reveals a surface area of 178.46 m2/g. The synthesized multilevel hierarchy was utilized as an electro-active material in a supercapacitor that achieved a specific capacitance of 546.6 F g-1 at a current density of 1 A g-1 with a higher cyclic retention of 91.81% after 10 000 GCD cycles. Furthermore, the ASC device was fabricated using Cu/CuxO@NC as the positive electrode and carbon black as the negative electrode and utilized to enlighten the commercially available LED bulb. The fabricated ASC device was further employed for a two-electrode study which achieved a specific capacitance of 68 F g-1 along with a comparable energy density of 13.6 Wh kg-1. Furthermore, the electrode material was also explored for the oxygen evolution reaction (OER) in an alkaline medium with a low overpotential of 170 mV along with a Tafel slope of 95 mV dec-1 having long-term stability. The MOF-derived material has high durability, chemical stability, and efficient electrochemical performance. This work provides some new thoughts for the design and preparation of a multilevel hierarchy (Cu/CuxO@NC) via a single precursor source in a single step and explored multifunctional applications in energy storage and an energy conversion system.

Improved photovoltaic performance of Pb-free AgBi2I7 based photovoltaics.

Hybrid perovskites based on bismuth are good candidates for developing lead-free and air-stable photovoltaics, but they have historically been constrained by poor surface morphologies and large band-gap energies. Monovalent silver cations are incorporated into iodobismuthates as part of a novel materials processing method to fabricate improved bismuth-based thin-film photovoltaic absorbers. However, a number of fundamental characteristics prevented them from achieving better efficiency. We examine bismuth iodide perovskite made of silver with improvements in surface morphology and a narrow band gap, and we achieve high power conversion efficiency. AgBi2I7 perovskite was used in the fabrication of PSCs as a material for light absorption, and its optoelectronic proficiencies were also studied. We reduced the band gap to 1.89 eV and achieved a maximum power conversion efficiency of 0.96% using the solvent engineering approach. Additionally, simulation studies verified an efficiency of 13.26% by using AgBi2I7 as a light absorber perovskite material.

Effect of Electrolytic Cations on a 3D Cd-MOF for Supercapacitive Electrodes.

A cadmium-based metal-organic framework (Cd-MOF) is synthesized in a facile manner at ambient temperature by an easy slow diffusion process. The three-dimensional (3D) structure of Cd-MOF is authenticated by single-crystal X-ray diffraction studies and exhibits a cuboid-shaped morphology with an average edge length of ∼1.13 µm. The prepared Cd-MOF was found to be electroactive in nature, which resulted in a specific capacitance of 647 F g-1 at 4 A g-1 by maintaining a retention of ∼78% over 10,000 successive cycles in the absence of any binder. Further, to distinguish the efficiency of Cd-MOF electrodes, different electrolytes (NaOH, KOH, and LiOH) were explored, wherein NaOH revealed a higher capacitive response due to its combined effect of ionic and hydrated ionic radii. To investigate the practical applicability, an asymmetric supercapacitor (ASC) device is fabricated by employing Cd-MOF as the positive electrode and activated carbon (AC) as the negative electrode, enabling it to light a commercial light-emitting diode (LED) bulb (∼1.8 V). The as-fabricated ASC device delivers comparable energy density and power density.

Insight into the Modulation of Carbon-Dot Optical Sensing Attributes through a Reduction Pathway.

Oxidized/reduced carbon dots (CDs) with tunable optical features have emerged as a new class of CDs having a common "molecular origin" but different fluorescence (FL) behaviors. In the present work, using "banana peel" as a sole carbon source followed by doping with fluorine (F), boron (B), and nitrogen (N) over CDs, banana peel-derived carbon dots (BP-CDs) were synthesized using a well-known hydrothermal synthesis method. Moreover, as-synthesized BP-CDs were further reduced to "rBP-CDs" by NaBH4. At post reduction, the FL performance (i.e., quantum yield) of rBP-CDs were found to be enhanced compared with the BP-CDs, along with variations in excitation and emission wavelengths. Interestingly, the optical sensing attributes of BP-CDs and rBP-CDs were varied, that is, BP-CDs selectively sense "Co2+ with a limit of detection (LOD) value of 180 nM", whereas rBP-CDs detected Co2+ (with an LOD value of 242 nM) as well as Hg2+ (with an LOD value of 190 nM). To the best of our knowledge, this work presents the very first report on the modulation of CDs' sensing behavior after reduction. The modulation in the sensing behavior with the common carbon precursor and reduction paves a new possibility for exploring CDs for different commercial applications.

Fluorene-Chloroquine Hybrids: Synthesis, in†vitro Antiplasmodial Activity, and Inhibition of Heme Detoxification Machinery of Plasmodium falciparum.

Fluorene-chloroquine hybrids have been identified as a new promising class of antiplasmodial agents. The most active compound 9 d exhibited good in vitro antiplasmodial activity against a chloroquine-sensitive NF54 strain of the human malaria parasite Plasmodium falciparum with an IC50 value of 139 nM. UV-visible absorption, FTIR spectral and 1 H NMR titration data corroborated the binding of 9 d to monomeric and µ-oxodimeric heme as well as inhibition of ß-hematin formation, which collectively supported the inhibition of heme detoxification machinery in P. falciparum. In silico docking studies revealed the binding interactions of the hybrids in the active site of the wild type as well as quadruple mutant of Pf-DHFR-TS dihydrofolate enzyme. Further, the ADMET parameters were predicted and were in good agreement with the expected values, suggesting the drug likeness of the synthesized hybrid molecules.

Recent Development of Morphology-Controlled Hybrid Nanomaterials for Triboelectric Nanogenerator: A Review.

Being cognizant of modern electronic devices, the scientists are continuing to investigate renewable green-energy resources for a decade. Amid different energy harvesting systems, the triboelectric nanogenerators (TENGs) have been found to be the most promising mechanical harvesting technology and have drawn attention to generate electrical energy. Thanks to its instant output power, choice to opt for wide-ranging materials, low maintenance cost, easy fabrication process and environmentally friendly nature. Due to numerous working modes of TENGs, it is dedicated to desired application at ambient conditions. In this review, an advance correlation of TENGs have been explained based on the variety of nanostructures, including 0D, 1D, 2D, 3D, metal organic frameworks (MOFs), coordination polymers (CPs), covalent organic frameworks (COFs), and perovskite materials. Moreover, an overview of previous and current perspectives of various nanomaterials, synthesis, fabrication and their applications in potential fields have been discussed in detail.

Doxycycline detection and degradation in aqueous media via simultaneous synthesis of Fe-N@carbon dots and Fe3O4-carbon dot hybrid nanoparticles: a one arrow two hawk approach.

The overuse of antibiotics in recent years presents a huge challenge to society for their removal from the environment. The prolonged presence of antibiotics as environmental pollutants results in the emergence of drug-resistant bacteria faster than new antibiotics to treat diseases they cause. Therefore, a rapid, sensitive, and cost-effective method is urgently required to detect and degrade antibiotics. Given this, a novel strategy has been devised for synthesizing Fe-doped carbon dots (Fe-N@CDs) and iron oxide-carbon dot hybrid nanoparticles (Fe3O4-CDs) in a single step for doxycycline detection and its degradation. For the very first time, the formation of two simultaneous products, i.e., Fe-N@CDs (0 D fluorescent carbon dots) and Fe3O4-CDs (magnetic nanoparticles) in a single step hydrothermal carbonization process by using a sole iron salt (FeCl2) and carbon precursor (citric acid) in the presence of ethylenediamine is reported. The as prepared Fe-N@CDs selectively detect doxycycline with a limit of detection value of 66 ng mL-1 and in the linear range from 0 mg mL-1 to 50 mg mL-1, whereas the other formed products, i.e., Fe3O4-CDs, degrade doxycycline by 70.26% in just 5 min by applying shear force using simply a kitchen blender. The results demonstrated the suitability and application scope in food and environment safety.

Diruthenium and triruthenium compounds of the potential redox active non-chelated η1-N,η1-N-benzothiadiazole bridge.

In the present study, a series of non-chelated BTD (2,1,3-benzothiadiazole)-bridged diruthenium(II) ([{(CH3CN)(acac)2RuII}2(µ-BTD)] 1, [{CH3CN(acac)2RuII}(µ-BTD){RuII(acac)2(η1-N-BTD)}] 2, [{(η1-N-BTD)(acac)2RuII}2(µ-BTD)] 3), and triruthenium ([{(acac)2RuII}3(µ-BTD)2(η1-N-BTD)2] 4) complexes with varying ratios of η1-N and µ-bis-η1-N,η1-N modes of BTD were studied. Complexes 1-4 (S = 0) were obtained via the one-pot reaction of electron-rich Ru(acac)2(CH3CN)2 and electron-deficient BTD in refluxing acetone. The relatively low Ru(II)/Ru(III) potential of 1-4 (0.08-0.44 V versus SCE) further facilitated the isolation of the corresponding mixed valent RuIIRuIII (S = 1/2) and RuIIRuIIRuIII (S = 1/2)/RuIIRuIIIRuIII (S = 1) forms [1]ClO4-[3]ClO4 and [4]ClO4/[4](ClO4)2, respectively. The single-crystal X-ray structures of the representative mixed valent [1]ClO4 and [3]ClO4 established (i) Ru⋯Ru distances of 6.227 Å and 6.256 Å (molecule A)/6.184 Å (molecule B), respectively, (ii) a significant variation of the N-S distance of BTD in [3]ClO4 as a function of its binding mode µ versus η1 and (iii) similar Ru-N (µ-BTD) distances in each case corresponding to a valence delocalised situation. The mixed valent diruthenium (1+-3+) and triruthenium (4+/42+) complexes exhibited metal-based anisotropic electron paramagnetic resonance (EPR) and moderately intense low-energy intervalence charge-transfer (IVCT) transitions in the near-infrared region of 1730-1890 nm. Analysis of the IVCT band using the Hush treatment revealed a valence delocalised class III mixed valent state with the electronic coupling Vab of ≈2640-2890 cm-1, as also corroborated by the Kc values of 105-108, solvent independency of the IVCT band and uniform spin distribution between the metal ions in the singly occupied state(s). Furthermore, the involvement of the BTD (η1 and µ)-based orbitals in the reduction processes was evident by its free radical EPR feature.

Thiazolothiazole based donor-π-acceptor fluorophore: Protonation/deprotonation triggered molecular switch, sensing and bio-imaging applications.

Stimuli modulated photophysical properties of a new asymmetric multifunctional molecular probe, 2-(pyren-1-yl)-5-(pyridin-4-yl)thiazolo [5,4-d]thiazole (PYTZ-P) bearing electron-rich pyrene and electron-deficient pyridine units linked through a π-conjugated thiazolo [5,4-d]thiazole (TTz) bridge are reported. Its sensitivity towards protons (TFA) in solution is manifested in the form of bathochromically shifted emission that spreads all over the visible region, and is related to the increased acceptor strength of pyridine upon protonation and subsequent enhanced magnitude of intramolecular charge-transfer in the probe. Similar modulation of the luminescence behaviour of the probe was also observed in the solid state. These observations are well rationalised by the theoretical calculations. The applicability of the sensitivity of the probe towards TFA has been demonstrated by developing the ready-to-use portable paper strips. Furthermore, PYTZ-P showed different acid/base induced absorption/emission switching property. Interestingly, when the response of the probe was noted in the presence of several cations, modulation of the electronic properties was observed only in the presence of Hg2+ ions, with the lowest detection limit of 8.43 × 10-8 M. Additionally, the sensitivity of the probe towards TFA and Hg2+ ions in solution and solid states is convincingly mimicked in the fluorescence imaging of HeLa and A375 cancer cells.

Photoactivatable carbon dots as a label-free fluorescent probe for picric acid detection and light-induced bacterial inactivation.

The zero-dimensional carbon nanostructure known as carbon dots showed attractive attributes such as multicolour emission, very high quantum yield, up-conversion, very good aqueous solubility, eco-friendliness, and excellent biocompatibility. These outstanding features of the carbon dots have raised significant interest among the research community worldwide. In the current work, water-soluble nitrogen, silver, and gold co-doped bimetallic carbon dots (BCDs) were prepared using the one-pot hydrothermal method with citric acid as a sole carbon source. As prepared BCDs showed size in the range of 4-8 nm and excitation-independent emission behaviour with maximum emission observed at 427 nm. Additionally, these BCDs showed a very high quantum yield value of 50% and fluorescence lifetime value of 10.1 ns respectively. Interestingly, as prepared BCDs selectively sense picric acid (PA) by exhibiting "selective fluorescence turn-off" behaviour in the presence of PA with a limit of detection value (LOD) of 46 nM. Further, as prepared BCDs were explored for photodynamic therapy to inactivate bacterial growth in the presence of light (400-700 nm) by generating singlet oxygen. Thus as prepared BCDs offer lots of potentials to use a nanoprobe to detect picric acid in an aqueous medium and to design next-generation antibacterial materials.

Cancer-Targeted Chitosan-Biotin-Conjugated Mesoporous Silica Nanoparticles as Carriers of Zinc Complexes to Achieve Enhanced Chemotherapy In Vitro and In Vivo.

Despite being the most common component of numerous metalloenzymes in the human body, zinc complexes are still under-rated as chemotherapeutic agents. Herein, the present study opens up a key route toward enhanced chemotherapy with the help of two ZnII complexes (ZnMBC) synthesized alongside Mannich base ligands to upsurge biological potency. Further, well-established mesoporous silica nanoparticles (MSNs) have been chosen as carriers of the titled metallodrugs in order to achieve anticancer drug delivery. A pH-sensitive additive, namely, chitosan (CTS) conjugated with biotin is tagged to MSNs for the targeted release of core agents inside tumors selectively. In general, CTS blocks ZnMBC inside the mesopores of MSNs, and biotin acts as a targeting ligand to improve tumor-specific cellular uptake. CTS-biotin surface decoration significantly enhanced the cellular uptake of ZnMBC through endocytosis. A panel of four human cancer cell lines has revealed that ZnMBC (1/2)@MSNs-CTS-biotin nanoparticles (NPs) exhibits unprecedented enhanced cytotoxicity toward cancer cells with IC50 values ranging from 6.5 to 28.8 µM through induction of apoptosis. NPs also possess great selectivity between normal and cancer cells despite this potency. Two-photon-excited in vitro imaging of normal (HEK) and cancer (HeLa) cells has been performed to confirm the biased drug delivery. Also, NP-induced apoptosis was found to be dependent on targeting DNA and ROS generation. Moreover, a lower range of LD50 values (153.6-335.5 µM) were observed upon treatment zebrafish embryos with NPs in vivo. Because of the anatomical similarity to the human heart, the heart rate of NP-treated zebrafish has been analyzed in assessing the cardiac functions, which is in favor of the early clinical trials of ZnMBC (1/2)@MSNs-CTS-biotin candidates for their further evaluation as a chemotherapeutic and chemopreventive agent toward human cancers, especially adenocarcinoma.

A fluorene based probe: Synthesis and "turn-on" water sensitivity of the in-situ formed Cu2+ complex: Application in bio-imaging.

A new fluorene based probe (FTH) has been evaluated for its photo-physical properties in solution as well as in the aggregated state/viscous environment. Addition of a poor solvent (water) to the solution of the probe in a good (acetonitrile) solvent significantly enhanced the otherwise weak emission due to aggregation induced emission (AIE). The emission enhancement is also related to the increase in viscosity of the solution, leading to the restricted intramolecular rotation of the peripheral (phenyl) groups. Interestingly, the emission behaviour of the non-emissive in-situ formed Cu2+ complex is drastically modulated in the presence of water. The solution of the putative Cu2+ complex of the probe turns highly emissive (yellow colour) upon addition of a small fraction of water (up to 7.6 wt %), but the yellow emission diminishes upon increasing higher water fraction. We propose that the initially formed Cu2+ complex undergoes hydrolysis in the presence of higher water content releasing the free amine possessing the diaryl amino rotors thus rendering the solution non-emissive. Thus the current probe being reported herein discloses its potential to generate trace water sensitive turn-on Cu2+ complex. Additionally, the bio-imaging potential of FTH for live cancer cells and its sensitivity towards intracellular presence of Cu2+ ions has been demonstrated.

Construction of a Cu-Based Metal-Organic Framework by Employing a Mixed-Ligand Strategy and Its Facile Conversion into Nanofibrous CuO for Electrochemical Energy Storage Applications.

Recently, metal-organic frameworks (MOFs) have been widely employed as a sacrificial template for the construction of nanostructured materials for a range of applications including energy storage. Herein, we report a facile mixed-ligand strategy for the synthesis of a Cu-MOF, [Cu3(Azopy)3(BTTC)3(H2O)3·2H2O]n (where BTTC = 1,2,4,5-benzenetetracarboxylic acid and Azopy = 4,4'-azopyridine), via a slow-diffusion method at room temperature. X-ray analysis authenticates the two-dimensional (2D)-layered framework of Cu-MOF. Topologically, this 2D-layered structure is assigned as a 4-connected unimodal net with sql topology. Further, nanostructured CuO is obtained via a simple precipitation method by employing Cu-MOF as a precursor. After analysis of their physicochemical properties through various techniques, both materials are used as surface modifiers of glassy carbon electrodes for a comparative electrochemical study. The results reveal a superior charge storage performance of CuO (244.2 F g-1 at a current density of 0.8 A g-1) with a high rate capability compared to Cu-MOF. This observation paves the pathway for the strategic design of high-performing supercapacitor electrode materials.