Search

Green synthesis of two coordination complexes of zinc acetate with N^N moiety on quercetin, which is a flavonoid is carried out. The complexes were obtained in high yields (> 97%) by grinding methods without the involvement of any solvent. Neither catalyst nor any additives were needed to perform the reactions. It was characterized by FT-IR, UV-Vis, NMR, HRMS, and elemental analysis. Antioxidant activity was done through the DPPH method which was compared with ascorbic acid and ligand (Quercetin). The study reveals that Complex 1 (IC50 163.093µg/ml) has significant free radical scavenging activity as compared to complex 2 (IC50 258.683µg/ml). Biological activity was performed against microbes (E. coli and S. aureus). MIC value of complex 1 (15.50µg/ml E. coli, 7.18µg/ml S. aureus) was found more significant as compared to complex 2 (22.51µg/ml E. coli, 18.62µg/ml S. aureus) and quercetin.

Chemical exchange saturation transfer (CEST) experiments are routinely used to study protein conformational exchange between a ‘visible’ major state and ‘invisible’ minor states because they can detect minor states with lifetimes varying from ~ 3 to ~ 100 ms populated to just ~ 0.5%. Consequently several 1H, 15N and 13C CEST experiments have been developed to study exchange and obtain minor state chemical shifts at almost all backbone and sidechain sites in proteins. Conspicuously missing from this extensive set of CEST experiments is a 1H CEST experiment to study exchange at glycine (Gly) 1Hα sites as the existing 1H CEST experiments that have been designed to study dynamics in amide 1H-15N spin systems and methyl 13CH3 groups with three equivalent protons while suppressing 1H-1H NOE induced dips are not suitable for studying exchange in methylene 13CH2 groups with inequivalent protons. Here a Gly 1Hα CEST experiment to obtain the minor state Gly 1Hα chemical shifts is presented. The utility of this experiment is demonstrated on the L99A cavity mutant of T4 Lysozyme (T4L L99A) that undergoes conformational exchange between two compact conformers. The CEST derived minor state Gly 1Hα chemical shifts of T4L L99A are in agreement with those obtained previously using CPMG techniques. The experimental strategy presented here can also be used to obtain methylene proton minor state chemical shifts from protein sidechain and nucleic acid backbone sites.

Resistive switching behavior of poly (4-vinylphenol):graphene oxide (PVP:GO) composite and ultrathin HfO x hybrid bilayer was explored for developing high-performance flexible resistive random access memory (RRAM) devices. These devices, fabricated with a PVP:GO equivolume solution spin-coated and atomic layer deposited ultrathin HfO x as an active bilayer, exhibited excellent bipolar switching behavior with set and reset voltages as low as 0.6 and −1.46 V, ${I}_{ \mathrm{\scriptscriptstyle ON}}/{I}_{ \mathrm{\scriptscriptstyle OFF}}$ of >105, and ac and dc switching endurance of over 1400 and 800 cycles, respectively. The same device configuration realized over a flexible polyethylene terephthalate (PET) substrate exhibited a memory window of >103 even after undergoing large mechanical strain (correspoding to a 5-mm bending radius). In addition, after 150 cumulative cycles of consecutive tensile and compressive strain at a 5-mm bending radius, flexible RRAMs demonstrated a clear memory window of $4\times 10^{{3}}$ for 104 s. Overall, the incorporation of GO into the PVP solution resulted in achieving better control over conductive filament (CF) growth and, therefore, improved repeatability and reliability. This article indicates that the strategy of incorporating composite and organic–inorganic active bilayer can lead toward the development of high-performance flexible RRAMs.

Actinyl ions can self-assemble in aqueous solution to form closed cage clusters ranging from 1.5 to 4.0 nm in diameter. The self-assembly, stability, and behavior of the nanoclusters depend on the nature of the aqueous environment, such as the pH and cations present. In this work, a classical force field for [(UO2)20(O2)30]20- (U20) peroxide nanoclusters in aqueous solution was developed from quantum-mechanical calculations. Using molecular dynamics simulations, the preferred binding sites of six cations (Li+, Na+, K+, Rb+, Cs+, and Ca2+) to the nanocluster were determined. Replica exchange molecular dynamics was used to equilibrate the structure and determine the equilibrium distribution of cations and water with respect to the nanocluster cage. In addition, the free energy barriers associated with cations entering the cluster were computed. Finally, the association of two cages was investigated by computing the free energy as a function of intercage distance. The free energy profiles reveal that the nanoclusters prefer to be associated when neutralized with divalent cations, but do not associate when neutralized with monovalent cations. This could explain the formation of tertiary structures observed experimentally.

Organic FETs (OFETs) with bilayer dielectric poly(4-vinylphenol) (PVP)/HfO2 and polyvinyl alcohol (PVA)/HfO2 were fabricated on a flexible low-cost Kapton tape substrate with TIPS -pentacene:polystyrene as an active layer. The devices exhibited average and maximum field-induced mobility of 0.25(±0.10) and 0.37 cm $^{{{2}}}\text{V}^{{-{1}}}\,\,\text{s}^{{-{1}}}$ for PVP/HfO2 devices, and 0.35(±0.18) and 0.69 cm $^{{{2}}}\text{V}^{{-{1}}}\,\,\text{s}^{{-{1}}}$ for PVA/HfO2 devices, respectively, with low threshold voltage and ${I}_{ \mathrm{\scriptscriptstyle ON}}$ to ${I}_{ \mathrm{\scriptscriptstyle OFF}}$ ratio approaching $10^{{{4}}}$ for both types of devices. Overlapping transfer multiple scans with very less performance variation under ambient conditions were observed. The devices were found to be fairly stable even when electrical stress was applied after a period of 5 months. Devices exhibited small degradation in ${I} _{{\text {DS}}}$ and small $\Delta {V} _{{\text {TH}}}$ with high degree of reliability and small performance spreads under combined effects of ambient exposure over a period of 5 months and successive electrical stress. In addition, inverter based on these OFETs with external load was also demonstrated.

Background Malaria is a major public health problem in India and accounts for about 88% of malaria burden in South-East Asia. India alone accounted for 2% of total malaria cases globally. Anti-malarial drug resistance is one of the major problems for malaria control and elimination programme. Artemether-lumefantrine (AL) is the first-line treatment of uncomplicated Plasmodium falciparum in north eastern states of India since 2013 after confirming the resistance against sulfadoxine-pyrimethamine. In the present study, therapeutic efficacy of artemether-lumefantrine and k13 polymorphism was assessed in uncomplicated P. falciparum malaria. Methods This study was conducted at four community health centres located in Koraput district of Odisha, Bastar district of Chhattisgarh, Balaghat district of Madhya Pradesh and Gondia district of Maharashtra state. Patients with uncomplicated P. falciparum malaria were administered with fixed dose combination (6 doses) of artemether-lumefantrine for 3 days and clinical and parasitological response was recorded up to 28 days as per World Health Organization protocol. Nucleotide sequencing of msp1 and msp2 gene was performed to differentiate between recrudescence and reinfection. Amplification and sequencing of k13 propeller gene region covering codon 450–680 was also carried out to identify the polymorphism. Results A total 376 malaria patients who fulfilled the enrolment criteria as well as consented for the study were enrolled. Total 356 patients were followed up successfully up to 28 days. Overall, the adequate clinical and parasitological response was 98.9% and 99.4% with and without PCR correction respectively. No case of early treatment failure was observed. However, four cases (1.1%) of late parasitological failure were found from the Bastar district of Chhattisgarh. Genotyping of msp1 and msp2 confirmed 2 cases each of recrudescence and reinfection, respectively. Mutation analysis of k13 propeller gene showed one non-synonymous mutation Q613H in one isolate from Bastar. Conclusions The study results showed that artemether-lumefantrine is highly effective in the treatment of uncomplicated P. falciparum malaria among all age groups. No functional mutation in k13 was found in the study area. The data from this study will be helpful in implementation of artemether-lumefantrine in case of treatment failure by artesunate plus sulfadoxine-pyrimethamine.

In this work, a combination of a thin layer of Copper (II) phthalocyanine (CuPc) and TIPS-pentacene crystal was used to enhance the photo-sensing spectrum of photo- sensitive organic field-effect transistors (photo-OFETs). In TIPS-pentacene/CuPc bi-layer devices, the different conduction path not only reduced the total number of traps but also enhanced the sensing spectrum. It was found that, though the TIPS-pentacene was able to sense only blue and green colour well, and CuPc was able to sense only red and green colour well; the TIPS-pentacene/CuPc bi-layer were able to sense all three colors, enhancing the range of sensing. On illumination, bi-layer TIPS-pentacene/CuPc OFETs exhibited higher values of shift in threshold voltage (|ΔVTH|) compared to neat TIPS-pentacene and bare CuPc OFETs, due to change in the spatial distribution in the trap state density and associated pattern of trapping of photo-generated charge carriers. It was also found that the values of photo-responsivity (Rmax) and photo-detection time for the bi-layer OFETs were in between that for OFETs with TIPS-pentacene or CuPc.

Protein molecules sample different conformations in solution and characterizing these conformations is crucial to understanding protein function. 15N CEST experiments are now routinely used to study slow conformational exchange of protein molecules between a ‘visible’ major state and ‘invisible’ minor states. These experiments have also been adapted to measure the solvent exchange rates of amide protons by exploiting the one bond deuterium isotope effect on the amide 15N chemical shifts. However at moderately high temperatures (~ 50 °C) that are sometimes required to populate protein minor conformers to levels (~ 1%) that can be detected by CEST experiments solvent H/D exchange can lead to ‘dips’ in low B1 15N CEST profiles that can be wrongly assigned to the conformational exchange process being characterized. This is demonstrated in the case of ~ 18 kDa T4 Lysozyme (T4L) at 50 °C and the ~ 11 kDa E. coli hibernation promoting factor (HPF) at 52 °C. This problem is trivially solved by eliminating the exchangeable deuterons in the solvent by using either an external D2O lock or by using a small amount (~ 1–3%) of a molecule like d6-DMSO that does not contain exchangeable deuterons to lock the spectrometer.

Physics behind the improvement in breakdown voltage of AlGaN/GaN HEMTs with carbon-doping of GaN buffer is discussed. Modeling of carbon as acceptor traps and self-compensating acceptor/donor traps is discussed with respect to their impact on avalanche breakdown. Impact of carbon behaving as a donor as well as acceptor traps on electric field relaxation and avalanche generation is discussed in detail to establish the true nature of carbon in GaN that delays the avalanche action. This understanding of the behavior of carbon-doping in GaN buffer is then utilized to discuss design parameters related to carbon doped buffer. Design parameters such as undoped channel thickness and relative trap concentration induced by carbon-doping are discussed with respect to the performance metrics of breakdown voltage, leakage current, sheet charge density, and dynamic ON-resistance.

In part I of this paper, we developed physical insights into the role and impact of acceptor and donor traps—resulting from C-doping in GaN buffer—on avalanche breakdown in AlGaN/GaN HEMT devices. It was found that the donor traps are mandatory to explain the breakdown voltage improvement. In this paper, silicon doping is proposed and explored as an alternative to independently engineer donor trap concentration and profile. Keeping in mind the acceptor and donor trap relative concentration requirement for achieving higher breakdown buffer, as depicted in part I of this paper, silicon & carbon codoping of GaN buffer is proposed and explored in this paper. The proposed improvement in breakdown voltage is supported by physical insight into the avalanche phenomena and role of acceptor/donor traps. GaN buffer design parameters and their impact on breakdown voltage as well as leakage current are presented. Finally, a modified Si-doping profile in the GaN buffer is proposed to lower the C-doping concentration near GaN channel to mitigate the adverse effects of acceptor traps in GaN buffer.

The risk of cancer development in offspring due to carcinogen exposure during pregnancy is a serious issue. In this study, we explored the involvement of the phosphatidylinositol 3-kinase (PI3K)/Akt pathway and microRNA-21 (miR-21) in transplacental lung tumorigenesis and its prevention by dietary compound inositol hexaphosphate (IP6) in F1 mice. Balb/c mice were exposed to the N-ethyl-N-nitrosourea (ENU) intraperitoneally on the 17th day of gestation. After weaning, half of the litters were fed with oral 2% IP6. At the end of 30, 120, or 240 days, we did not observe any effect on fetal viability or weight between ENU-exposed and non-exposed litters and the same was true of IP6. Altered expressions of the PI3K/Akt pathway were observed in F1 mice. Further, miR-21 expressions were found to be modulated at the respective time as well, along with the activation of matrix metalloproteinase (MMP-9) and vascular endothelial growth factor expression. Akt activation also enhanced the expression of cyclin D1, cyclooxygenase-2 (COX-2), nuclear factor-κB (NF-κBp50), and mammalian target of rapamycin (mTOR). IP6-fed F1 mice showed reduced tumorigenesis along with reduced expression of the PI3K/Akt pathway miR-21 and downstream targets. The PI3K/Akt pathway and miR-21 are involved in transplacental lung tumorigenesis, whereas IP6 seemed to affect lung tumorigenesis by suppressing the expression of the PI3K/Akt pathway in F1 mice.

With the increasing number of cases of inactive and drug-resistance tuberculosis, there is an urgent need to develop new potent molecules set for fighting this brutal disease. Medicinal chemistry concerns the discovery, the development, the identification, and the interpretation of the mode of action of biologically active compounds at the molecular level. Molecules bearing oxadiazoles are one such class that could be considered to satisfy this need. Oxadiazole regioisomers have been investigated in drug discovery programs for their capacity to go about as powerful linkers and as pharmacophoric highlights. Oxadiazoles can go about as bioisosteric substitutions for the hydrazide moiety which can be found in first-line anti-TB drugs, and some have been likewise answered to cooperate with more current anti-TB targets. This present review summarizes the current innovations of oxadiazole-based derivatives with potential antituberculosis activity and bacteria discussing various aspects of structure-activity relationship (SAR).

There has been a growing research interest in the development of light-emitting materials (phosphors) especially in the visible region for use in applications such as photonics, sensing, photoactivity, and solar cells. Phosphors made from rare earth–doped oxide hosts have been extensively investigated due to their intense luminescence features and thermal and chemical stability. In the past few decades, research interest in oxide materials has grown exponentially as observed from a growing number of publications based on these materials. Luminescence intensity of rare earth–doped oxide materials has been found to depend on the doping concentration and synthesis route. Therefore, in this chapter, the authors demonstrate the dependence of luminescence properties on different rare-earth dopant ions. The studied materials were evaluated for application in different types of light-emitting devices.

This study reports the synthesis and antibacterial evaluation of two novel complexes, [Cd (Q) (Bpy) (CH3COO)2, complex 1] and [Cd (Q) (Phen) (CH3COO)2, complex 2], based on quercetin ligand. The method of synthesis was by reacting natural flavonoid quercetin (Q) with a good chelator (Bpy = 2,2’-bipyridine, Phen= 1,10-phenanthroline and Q = quercetin) and metal ions. The produced metal complexes were studied in the solid state by Fourier-transform infrared (FTIR) spectroscopy and in solution by UV-Vis absorption. Further analysis included high resolution mass spectrometry (HRMS) for confirmation. To understand the nature and coordination of quercetin and its metal complexes, density functional theory (DFT) calculation was performed. The scavenging (DPPH radical), antibacterial, MTT, enzymatic and non-enzymatic antioxidant activity assay, cytotoxicity assay (fluorescence study) were done and quercetin was used for comparison. Both complex 1 and complex 2 induced loss of cell viability via impairment of metabolic activity, leakage of intracellular proteins, and increased oxidative stress. The free-radical scavenging activity of complex 2 (IC50 340.175 µg/mL) was statistically significantly more potent than that of complex 1. The MIC values of complex 2 (7.80 µg/mL Escherichia coli, 15.62 µg/mL Staphylococcus aureus) were higher as compared to complex 1 and quercetin in both test microorganisms. There was inhibition of cell proliferation in Escherichia coli treated with 2 µg/mL of complex 2, whereas Staphylococcus aureus did not show inhibition at this concentration. The cytotoxicity screening on MG 63 cell line showed that the compounds were safe up to 500 mg/L.

Previous success in improving the CO2 capacity of physical solvents for pre-combustion carbon capture by imparting poly(ethylene glycol) (PEG) functionality led us to compare tributyl phosphate (TBP), tri-isobutyl phosphate (TiBP) and three analogous organophosphate solvents in which the length of PEG-substitution was varied. The PEG-substituted solvents proved to have acceptable densities and viscosities for the application of interest, but all three solvents showed poorer CO2 absorption than TBP or TiBP. Inclusion of hydrophilic PEG groups in solvents (1) – (3) also led to the undesired absorption of larger amounts of water from humidified N2 compared to TBP and TiBP. Computational studies of the analogous organophosphate solvents revealed that all solvents had the lowest partial negative charges, closest CO2 interaction, and largest CO2 interaction energy at the double bonded phosphoryl O atom. The fractional free volumes were computed and was found to be largest for TiBP and grew progressively smaller as the length of the PEG group grew longer in solvents (1) – (3). Although introducing PEG groups to these molecules increased the number of interaction sites with CO2, solvents (1) – (3) showed poorer CO2 absorption than TBP and TiBP due to their decreased solvent fractional free volume.

This paper aims to describe the variability of particulate absorption properties using a unique hyperspectral dataset collected in the Red Sea as part of the TARA Oceans expedition. The absorption contributions by phytoplankton (aph) and non-algal particles (aNAP) to the total particulate absorption coefficients are determined using a numerical decomposition method (NDM). The NDM is validated by comparing the NDM derived values of aph and aNAP with simulated values of aph and aNAP are found to be in excellent agreement for the selected wavelengths (i.e., 443, 490, 555, and 676 nm) with high correlation coefficient (R2), low root mean square error (RMSE), mean relative error (MRE), and with a slope close to unity. Further analyses showed that the total particulate absorption coefficients (i.e., ap(443)average = 0.01995 m−1) were dominated by phytoplankton absorption (i.e., aph(443)average = 0.01743 m−1) with a smaller contribution by non-algal particles absorption (i.e., aNAP(443)average = 0.002524 m−1). The chlorophyll a is computed using the absorption based Line Height Method (LHM). The derived chlorophyll-specific absorption ((a*ph = aph(λ)/ChlLH)) showed more variability in the blue part of spectrum as compared to the red part of spectrum representative of the package effect and changes in pigment composition. A new parametrization proposed also enabled the reconstruction of a*ph(λ) for the Red Sea. Comparison of derived spectral constants with the spectral constants of existing models showed that our study A(λ) values are consistent with the existing values, despite there is a divergence with the B(λ) values. This study provides valuable information derived from the particulate absorption properties and its spectral variability and this would help us to determine the relationship between the phytoplankton absorption coefficients and chlorophyll a and its host of variables for the Red Sea.

Strong seasonal upwelling, downwelling, changes in current patterns and the volume of freshwater discharge from Cochin Estuary defines the coastal waters off Cochin. These coastal waters were investigated through monthly sampling efforts during March 2015 to February 2016 to study the seasonal and spatial variability in bio-optical properties for the four different seasons mainly Spring Inter Monsoon (SIM), South West Monsoon (SWM), Fall Inter Monsoon (FIM) and Winter Monsoon (WM). The Barmouth region is the meeting place where freshwater from Cochin Estuary directly enters to the sea through a single narrow outlet, was dominated by highly turbid waters during the entire period of study. Among the four seasons, chlorophyll a (Chl_a) concentration showed a high value during SWM, ranged from 2.90 to 11.66 mg m−3 with an average value of 6.56 ± 3.51 mg m−3. During SIM the distribution of coloured dissolved organic matter (CDOM) is controlled by decomposition of phytoplankton biomass and the river discharge, whereas during SWM the temporal distribution of CDOM is controlled only by river discharge. The highest value for CDOM spectral slope (SCDOM) was observed during SWM, ranged from 0.013 to 0.020 nm−1 with an average value of 0.015 ± 0.002 nm−1. During WM, the high SCDOM with lower aCDOM (443) indicates the photo-degradation affects the absorption characteristics of CDOM. The observed nonlinearity between Chl_a and the ratio of phytoplankton absorption aph (443)/aph (670) indicating the packaging effect and changes in the intercellular composition of pigments. During the study period, aph (670) was strongly correlated with Chl_a than aph (443), which explains the accessory pigment absorption dominating more than Chl_a in the blue part of the spectrum. Similarly, the results obtained from seasonal bio-optical data indicating that Chl_a significantly contributes light attenuation of the water column during SIM, whereas detritus (ad) significantly contributes light attenuation during SIM and WM. During the study period, the relative absorption of detritus materials dominates the relative absorption of phytoplankton and CDOM at 443, 555 and 670 nm wavelengths.

We report the dielectric and electrical behavior of thermally evaporated lithium fluoride (LiF)–tungsten trioxide (WO3) (x wt% WO3-doped LiF; x = 0, 1, 3, 5, 7, 10) nano-composite thin films at room temperature over a wide range of frequencies from 0.1 Hz to 1 MHz. Among the various doping concentrations of WO3, the 5 wt% WO3-doped LiF nano-composite thin film reaches to the maximum dielectric constant ~ 25, compared with those of pure LiF ~ 9 thin film. The electrical studies of the films have been done by complex impedance spectroscopy and show the presence of grain and grain boundaries contribution in the films for all doping concentrations. The relaxation behavior in the nano-composite films has been observed in the dielectric curve at low frequencies which is superimposed by electrode polarization. The non-Debye type of relaxation in the films has been observed in the impedance and modulus curve. The peaks appearing at low frequencies for each doping concentration in loss tangent spectrum show the presence of relaxing dipoles in the films. An increment in the ac conductivity has been observed with doping concentration up to 5%. The ac conductivity curves obey the jump relaxation power law where an electrode polarization effect can be seen at low-frequency region.

In this report, we have demonstrated the optical non-volatile memory characteristics using CuPc OFET. The memory operation was comprehensively demonstrated with different programming conditions. It was found that the programming of CuPc OFET with an electric pulse at the gate terminal under UV-light photo-illumination compared to other programming conditions, could substantially increase the memory window due to massive charge trapping in the polymer electret layer, which causes shift in the device transfer characteristics from low-conduction state (“OFF state”, or logic 0) to high conduction state (“ON state”, or logic 1) at VGS = 0V. From device operation at −50V, a memory window of greater than 45V could be achieved by applying a programming voltage of +70 V at the gate terminal under UV-light photo-illumination. Moreover, it was completely erased by applying −100 V at the gate terminal in dark.

The crucial role of molecular weight of the polymer dielectric in regulating the electrical performance and photo-response of TIPS-pentacene OFETs has been explored using poly(vinyl alcohol) (PVA) as the polymer dielectric layer. With increasing molecular weight of PVA, a degradation in the electrical and photo-response was observed. Atomic-force microscopy (AFM), Fourier-transform infrared spectroscopy (FTIR) and X-ray Diffraction (XRD) studies revealed that with increase in PVA molecular weight, polarizability of PVA dielectric layer and thus strength of the OFET channel reduced due to decreased hydroxyl group concentration oriented perpendicular to the PVA-semiconductor interface. Further, due to rising surface roughness of underlying PVA film with its molecular weight, macroscopic irregularities and therefore trap density in the active layer grown over it also increases. Therefore, both of these molecular weight dependent factors influence overall device performance and photo-response of OFETs in a critical way.

Photo-response of solution processed flexible TIPS-pentacene organic field-effect transistors is evaluated under illumination with visible light of red, green, and blue colors having minimum wavelengths of 620, 520, and 460 nm. For −10 V operation, pristine photo-OFETs exhibited average field-effect mobility of 0.11 cm $^{2}\text{V}^{-1}\text{s}^{-1}$ , near zero threshold voltage, and current ON–OFF ratio of ~105. These photo-OFETs exhibited prevalent photovoltaic characteristics with shift in the threshold voltage upon illumination, which was found to increase with rising intensity, illumination time, and gate bias during illumination. For low-voltage operation at −5 V, maximum current modulation of $4\times 10^{4}$ and 102, and photo-responsivity of 17 mA/W and 35 mA/W, respectively, were achieved for blue (intensity of 1.7 mW/cm2) and green (intensity of 0.4 mW/cm2) light illuminations. However, these photo-OFETs did not show significant response to red light. A fast dynamic response to periodic pulses of illumination was also observed. For a gate bias of +10 V and illumination time of 500 s, maximum current modulation of 105 was achieved for blue light illumination.

Phase separation induced high carrier mobility and electrical stability are achieved in organic field-effect transistors using TIPS-pentacene:polystyrene blends. Rigid Si/SiO 2 substrate was especially chosen to explore the phase separation. A vertical phase separation between TIPS-pentacene and polystyrene as confirmed from scanning electron microscopic image, evetually leads to excellent carrier mobility in polymer blend devices compared to that of neat TIPS-pentacene. Maximum hole mobility improved from 0.2 cm 2 V −1 s −1 for neat TIPS-pentacene on SiO 2 to 2.6 cm 2 V −1 s −1 for TIPS-pentacene blends with PS, with average value of 1.5 cm 2 V −1 s −1 . Apart from higher mobility, TIPS-pentacene:PS blend devices also showed much lower decay in drain current (∼30%) during a constant bias-stress of 2 h, compared to neat devices (∼80%). Interestingly, This decay was fully recovered for blend devices under rest conditions. The corresponding shift in the threshold voltage due to bias-stress was lower for TIPS-pentacene:PS device due to better quality of interface as confirmed by lower values of density of interface traps and higher trapping time. High electrical stability in TIPS-pentacene:polystyrene blend devices was also supported by repeatabiliiy studies, which exhibited nearly unchanged device characteristics.

This paper for the first time presents a comprehensive computational modeling approach for AlGaN/GaN high electron mobility transistors. Impact of the polarization charge at different material interfaces on the energy band profile as well as parasitic charge across the epitaxial stack is modeled and studied. Furthermore, impact of surface and bulk traps on two-dimensional electron gas, device characteristics, and gate leakage is accounted in this paper. For the first time, surface states modeled as donor type traps were correlated with gate leakage. Moreover, a new approach to accurately model the forward gate leakage in Schottky gate devices is proposed. Finally, impact of lattice and carrier heating is studied, while highlighting the relevance of carrier heating, lattice heating, and bulk traps over the device characteristics. In addition to this, modeling strategy for other critical aspects like parasitic charges, quantum effects, S/D Schottky contacts, and high field effects is presented.

In this work, we have explored the effect of TIPSpentacene: polystyrene (PS) blend on electrical performance and photo-response of solution processed organic field-effect transistors (OFETs). It was observed that though the blend OFETs show better electrical performance, the photo-responsivity (R) of neat TIPS-pentacene OFETs was significantly better. This study was performed for different color lights such as blue, red, and green, as well as for ultraviolet light (UV). R was highest for blue color (~2600 mA/W for neat, ~230 mA/W for blend), and smaller for other cases. Low R value in blend devices is attributed to less trapping of photo-generated charge carriers during photo-illumination compared to their neat counterparts.

We report on the fabrication of bottom gate top contact organic field effect transistors with hybrid gate dielectric and TIPS-Pentacene:PS blend as active layer on PowerCoat™ HD 230 paper substrate. The hybrid dielectric layer leads the devices operated at relatively low voltage of −10 V with avg. and maximum field effect mobility of $0.52(\pm 0.16)$ and 0.78 cm2 V−1 S−1 respectively, with near zero threshold voltage and on-off current ratio approaching ~104. The devices have shown excellent operational stability when tested with DC bias stress of $\mathrm{V}_{\mathrm{DS}}=\mathrm{V}_{\mathrm{GS}}=-10\ \mathrm{V}$ for 1 h and minuscule changes in electrical characteristics were observed with continuous multiple transfer cycle scans. In addition, we have demonstrated a resistive load inverter circuit with varying the load resistance with these paper OFETs.

Effect of UV irradiation $( \lambda _{Peak} \quad =365$ nm) on the electrical performance of the OFETs with CuPc as active layer is demonstrated. The devices have shown stable electrical performance under dark with avg. and max. field effect mobility of $( 1.0 \pm 0.3 ) \times 10 ^{-2}$ and $1.4 \times 10 ^{-2}$ cm $^{2}\, \mathrm {V}^{-1}\, \mathrm {s}^{-1}$ respectively. Under UV illumination there found a shift in threshold voltage and change in ON current along with fast response and recovery time of 0.4 s and 2 s respectively with periodic UV ON-OFF pulses.

We report the effect of varying the semiconductor:polymer blend ratio on the electrical performance and bias-stress stability of the organic field effect transistors (OFETs) with TIPS-Pentacene and polystyrene as semiconductor and polymer combination. Device performance was found to improve with increasing polymer content in the solution. Devices with 1:3 TIPS-Pentacene:polystyrene blend outperformed the other counterparts with high performance, and demonstrated least performance variation with regular 100 transfer measurement cycles. In addition, 1:3 blend devices have shown the least normalized drain current decay of $\sim$ 8.5 % with the bias stress condition of V DS = V GS = -30 V for 2 h, as compared to the 1:1, 3:1 and neat devices with the decay of 15 %, 37 % and 71 % respectively. Additionally, a better recovery of electrical characteristics was observed in blend devices with larger polymer fractions from the deteriorating effects of gate bias stress.

High-performance solution processed flexible organic field-effect transistors with 6,13(bis-triisopropylsily-lethynyl) pentacene and polystyrene blend are demonstrated with high electro-mechanical stability. For −5 V operation, field-effect mobility up to 1.1 cm $^{2}~\text{V}^{\mathrm {-1}}~\text{s}^{\mathrm {-1}}$ and threshold voltage as low as −0.1 V were obtained with high current on–off ratios of $\sim 10^{5}$ due to high quality dielectric–semiconductor interface developed during solvent evaporation. Stable electrical characteristics were achieved with increasing duration of mechanical strain, and after multiple cycles of tensile and compressive strain. Drain current decay of 10%, very large trapping time of $\sim 10^{8}$ s, and a very small threshold voltage shift of 0.3 V were observed during bias stress of 1 h, signifying low charge carrier trapping and a high quality of dielectric–semiconductor interface, which was retained largely after two days of continuous tensile strain. Moreover, after 100 cycles of tensile and compressive strain, the corresponding shift in threshold voltage due to bias stress was still $\sim 0.5$ V. Overall, a high performance and stability were demonstrated under collective effects of mechanical and electrical stress.

Flexible organic field-effect transistors (OFETs) with TIPS-pentacene: polystyrene (PS) blend are demonstrated to exhibit enhanced mobility and significantly improved electrical stability compared to neat TIPS-pentacene on poly(4-vinylphenol) (PVP) dielectric (bi-layer OFETs), along with high mechanical stability. Due to merit of high quality dielectric-semiconductor interface, pristine TIPS-pentacene: PS blend OFETs exhibited maximum mobility of 0.93 cm2 V−1 s−1 with average of 0.44(±0.25) cm2 V−1 s−1 compared to 0.14(±0.10) cm2 V−1 s−1 for bi-layer OFETs with high current on-off ratios on the order 105 for both. Both types of devices exhibited high electrical stability upon bending with increasing magnitude of strain or its duration up to 5 days. However, significant differences in electrical stability of devices were observed upon applying constant bias-stress for 40 min to 1 h. Pristine blend devices exhibited outstanding electrical stability with very low drain current decay of

The effect of structural dissimilarity of the additive solvent from the main solvent on the properties of the solution and resulting crystals for solution processed organic field-effect transistors (OFETs) is comprehensively studied. Organic semiconductor TIPS-Pentacene was explored with toluene as the main solvent and benzene, cyclohexane, and hexane as additives for making semiconductor solutions. The solution formation with various solvents is explained by Hansen’s solubility theory, according to which the binary solvent with higher structural dissimilarity between constituent solvents is a weaker solvent of the organic semiconductor; which eventually supports better molecular aggregation and crystallinity in the resulting crystallites. As investigated by XRD, the degree of crystalline order systematically increased with rising dissimilarity in component solvents; integrated intensity ratio rising from 0.52 for toluene to 0.54, 0.69 and 0.72 respectively for toluene/benzene, toluene/cyclohexane, and toluene/hexane. The variation in degree of crystallinity is also reflected in electrical properties of OFETs, where the field-effect mobility improved from 0.05 cm2/(V.s) for toluene solvent to higher than 0.1 cm2/(V.s) for toluene/hexane.

Flexible organic field-effect transistors with high electrical stability upon bending are demonstrated on indium tin oxide coated polyethylene terephthalate substrates with TIPS-Pentacene semiconductor crystals formed by drop casting on a hybrid gate dielectric consisting hafnium dioxide grown by atomic layer deposition and spin coated poly(4-vinylphenol). Fabricated devices exhibited excellent p-channel characteristics with field-effect mobility up to 0.12 cm2/Vs with high current on/off ratio >104 and low threshold voltage of −0.2 V. Device performance was slightly affected by mechanical strain applied by bending for 5 min with radius varying from 12.5 mm to as low as 5.0 mm; and a high stability in performance was demonstrated upon applying constant tensile strain for more than 48 h at bending radius of 5.0 mm. It was found that strain induced changes in the device performance primarily occur due to increase in dielectric surface roughness; and the semiconductor-dielectric interface uniformity is influenced more with magnitude of strain rather than its duration.

An efficient strategy for nucleophilic ring opening of donor-acceptor (DA)-cyclopropanes with electron rich arenes to provide 2-(2,2-diarylethyl)malonates in excellent yields is described. The reaction was found to be successful with heteroarenes as the nucleophile as well. Reaction of enantiopure DA-cyclopropane with arene/heteroarene as the nucleophiles afforded the corresponding 2-(2,2-diarylethyl)malonates with high yield and enantioselectivity (ee 95%). The synthetic utility of the products was demonstrated by converting them easily into other important synthetic scaffolds like functionalized cyclohexene and malonic acid derivatives.

Skin cancer is among the most common cancers worldwide and identifiable molecular changes for early and late stage of skin tumorigenesis can suggest the better targets for its control. In this study, we investigated the status of K-Ras-PI3K-AKTpathway followed by NF-κB, cyclin D1, MMP-9 and regulatory micro RNA during 7, 12-dimethylbenz[a]anthracene (DMBA) induced mouse skin tumorigenesis and its prevention by butyric acid (BA), nicotinamide (NA) and calcium glucarate (CAG), individually or in combination with respect to time. DMBA upregulated the K-Ras, PI3K, Akt, NF-κB, cyclin D1 and MMP-9, but downregulated the PTEN in a time dependent manner. DMBA also reduced the levels of micoRNA let-7a but induced the levels of miR-21 and miR-20a as a function of time. BA, NA and CAG were found to prevent DMBA induced changes, but they were most effective when used together in a combination. Reduced let-7a and miR-211 were correlated with the overexpression of K-Ras and MMP-9. Overexpression of miR-21 and miR-20a was correlated with the down regulation of PTEN and overexpression of Cyclin D1. Collectively, the enhanced chemopreventive potential of natural compound in combination via regulation of K-Ras-PI3K-AKTpathway along with regulatory micro RNAs provide a newer and effective mean for cancer management.

Objective Ayurvedic formulations are preferred over other formulations as well as commercialized on broad level to treat various ailments. The World Health Organization has established certain guidelines for quality control of heavy metals and pesticide residues. Bacopa monnieri, a popular herb with immunomodulator and memory-enhancing properties is the chief constituent of several Ayurvedic formulations, which include Brahmi Vati (BV), Brahmi Ghrita (BG) and Saraswat Churna (SC), etc. In view of the World Health Organization guidelines, two products of each formulation from six different manufacturers were purchased from Ayurvedic Pharmacy, Bulanala-Varanasi, India for testing heavy metal and pesticide residue. Methods In the present study, all the formulations—BV, BG and SC—were selected for estimation of four heavy metals namely lead (Pb), cadmium (Cd), chromium (Cr) and nickel (Ni) by a plasma emission spectrophotometer. Organochlorine pesticidal residues were estimated for dichlorodiphenyl trichloroethane, isomers of hexachlorocyclohexane (HCH) and α-endosulfan, etc. in total 12 samples of test formulations containing Bacopa monnieri L. using gas chromatography technique. Results Out of 12 samples, Pb, Cd, Cr and Ni were present in all samples but below the permissible limit. Although atrazine, aldrin, dialdrin were in below detection limit, but other pesticides were detected in some samples as oxamyl, hexachlorocyclohexanes (α-HCH, β-HCH and γ-HCH), dichlorodiphenyl trichloroethane and dichlorodiphenyl dichloroethylene. Conclusion The presence of heavy metals in the formulations was low to cause toxicity. However evaluation of heavy metals and pesticide residue in every batch is necessary.

Rare earth doped/codoped phosphors have been extensively studied for different types of applications based on their intense luminescence features. For this, researchers have tried to choose the inorganic host matrices having both a low phonon cut-off frequency and a high refractive index. Many articles have been published on oxide based phosphor materials, but due to their high cut-off phonon frequency, use of these materials is restricted for optical based applications. This is why additional research has been carried out on fluoride based host materials because of their low phonon frequencies, low composition degradation, and high quantum efficiency. In this paper, the authors review the rare earth fluoride based host nano- and micromaterials for different applications and discuss possible mechanisms.Rare earth doped/codoped phosphors have been extensively studied for different types of applications based on their intense luminescence features. For this, researchers have tried to choose the inorganic host matrices having both a low phonon cut-off frequency and a high refractive index. Many articles have been published on oxide based phosphor materials, but due to their high cut-off phonon frequency, use of these materials is restricted for optical based applications. This is why additional research has been carried out on fluoride based host materials because of their low phonon frequencies, low composition degradation, and high quantum efficiency. In this paper, the authors review the rare earth fluoride based host nano- and micromaterials for different applications and discuss possible mechanisms.

We explored the basis of the combinatorial chemopreventive effect of butyric acid (BA), nicotinamide (NA) and calcium glucarate (CAG) on mouse skin exposed to 7,12-dimethylbenz(a)anthracene (DMBA). We studied the effects of topical application of DMBA in the presence or absence of BA, NA and CAG on the regulators of apoptosis. DMBA treatment suppressed Bax, Bax/Bcl-2 ratio, release of cyt c, Apaf1, caspase-9, -3 mediated apoptosis. Downregulation of p21 and upregulation of Bcl-2, mut p53 were also observed in only DMBA treated mice. Simultaneous application of BA, NA and CAG induced a mitochondria-mediated apoptosis, characterized by a rise in the Bax, Bax/Bcl-2 ratio, release of cyt c, upregulation of Apaf1 with down-stream activation of caspase-9, -3. Furthermore treatment with BA, NA and CAG demonstrated an upregulation of p21 and downregulation of Bcl-2, mut p53. But this effect was enhanced in the presence of all the three compounds together in combination. Chemoprevention by a combination of BA, NA and CAG by inducing the apoptosis, the natural cell death, suggest the importance of the potential combinational strategies capable of preventing skin tumor development.

In this work, a TCAD based approach is presented to model electrical behavior of TIPS-Pentacene: polymer blend organic field-effect transistors (OFETs). Stress induced and temperature induced effects are also captured, thereby accurately modeling the device behavior under different operating conditions. The framework is validated against experimental results and is then used to estimate the effect of temperature on characteristics of inverter circuit using this device.

Effect of thermal annealing on the performance of flexible OFETs was investigated. Annealing at low temperatures up to 50 °C enhanced the molecular ordering and granular arrangement leading to improved device performance, however, a permanent degradation was induced at high temperature annealing due to loss in crystallinity and crack generation. An annealed device exhibited a larger decay in drain current than a pristine device under constant bias stress. Under combined effects of mechanical and thermal stress, effect of thermal stress was found to be dominant at higher annealing temperatures, resulting in monotonic performance degradation.

An atom transfer radical addition elimination (ATRE) reaction of terminal alkenes with perfluoroalkyl halides under visible light is described. The photoredox catalysis with Eosin Y provides perfluoroalkenes in good yields. The reaction has been utilized for the late stage perfluoroalkenylation of an estrone-derived alkene.

In the present study, we showed the correlation of EZH2, SUV39H1 or G9a expression and histone modifications with the urethane induced mouse lung tumorigenesis in the presence or absence of antitumor agent, inositol hexaphosphate (IP6). Tumorigenesis and the molecular events involved therein were studied at 1, 4, 12 or 36 weeks after the exposure. There were no tumors at 1 or 4 weeks but tumors started appearing at 12 weeks and grew further till 36 weeks after urethane exposure. Among the molecular events, upregulation of EZH2 and SUV39H1 expressions appeared to be time dependent, but G9a expression was altered significantly only at later stages of 12 or 36 weeks. Alteration in miR-138 expression supports the upregulation of its target, EZH2. H3K9me2, H3K27me3 or H4K20me3 was found to be altered at 12 or 36 weeks. However, ChIP analysis of p16 and MLH1 promoters showed their binding with H3K9me2 and H3K27me3 which was maximum at 36 weeks. Thus, histone modification and their interactions with gene promoter resulted in the reduced expression of p16 and MLH1. IP6 prevented the incidence and the size of urethane induced lung tumors. IP6 also prevented the urethane induced alterations in EZH2, SUV39H1, G9a expressions and histone modifications. Our results suggest that the alterations in the histone modification pathways involving EZH2 and SUV39H1 expressions are among the early events in urethane induced mouse lung tumorigenesis and could be exploited for cancer control.

We investigated the chemopreventive effects of naturally occurring compounds like butyric acid (BA), nicotinamide (NA) and calcium glucarate (CAG) individually or in combination in 7, 12-dimethylbenz [a] anthracene (DMBA) treated mouse skin at 4 and 16 weeks, the time before and after the tumor development. DMBA application did not show any skin tumors at 4 weeks but well defined tumors appeared at 16 weeks. BA, NA or CAG prevented the tumor development significantly but the protection was highly enhanced when all these compounds were given together. In order to see the molecular changes progressing with tumors, we showed the downregulation of tumor suppressor miR-203 at 16 weeks and upregulation of histone deacetylases (HDAC), DNA methyltransferase, promoter methylation of miR-203 at 4 or 16 weeks. Regulators of micro RNA biogenesis such as DICER1 and Ago2 were also deregulated by DMBA. Proto-oncogene c-myc and BMI1 were upregulated and tumor suppressor gene p16 was downregulated by DMBA as a function of time. Effects of BA, NA or CAG were more pronounced after 16 weeks as compared to 4 weeks in preventing the tumor development and altered gene expression. Concomitant administration of BA, NA and CAG tried to prevent these alterations more effectively than that of individual compound possibly by regulating miR-203 status through epigenetic or biogenetic modulations before and after the tumor development. Study provides a rationale for chemoprevention by combination of different compounds targeting miR-203.

An unprecedented and domino synthetic strategy for the synthesis of highly functionalized carbocyclic β-enaminoesters bearing an all-carbon quaternary center via Yb(OTf)3-catalyzed ring-opening cyclization/decarboxylative tautomerization of donor-acceptor cyclopropanes with 2-alkyl malononitriles in excellent yields is described. The products are obtained as a single diastereomer in most cases where the nitrile and aryl groups are aligning in a cis orientation across the ring.

Inverter circuits based on neat TIPS-pentacene and TIPS-pentacene: polystyrene blend organic field-effect transistors (OFETs) with external resistive load has been studied. Resistive loads of 28 ΜΩ, 40 ΜΩ, 68 ΜΩ and 108 ΜΩ were used to study the inverter transfer characteristics. Transfer characteristics of both types of inverters are improved with increasing load resistance. Inverter with a representative OFET with neat TIPS-pentacene shows a DC voltage gain of −6.9, swing of 40 V, and static power dissipation of 9.5 μW with load of 108 ΜΩ and 50 V power supply. Similarly, inverter with a representative TIPS-pentacene: polymer blend OFET shows a DC voltage gain of −8.7, swing of 44 V, and static power dissipation of 10.2 μW with the same load. For both neat TIPS-pentacene and TIPS-pentacene: polymer blend inverters, maximum DC gain and voltage swing are achieved with highest value of resistive load. However, switching thresholds near V DD /2 are obtained with moderate resistive loads.

The aim of the present study was to standardize Brahmi vati (BV) by simultaneous quantitative estimation of Bacoside A3 and Piperine adopting HPLC-UV method. BV very important Ayurvedic polyherbo formulation used to treat epilepsy and mental disorders containing thirty eight ingredients including Bacopa monnieri L. and Piper longum L.An HPLC-UV method was developed for the standardization of BV in light of simultaneous quantitative estimation of Bacoside A3 and Piperine, the major constituents of B. monnieri L. and P. longum L. respectively. The developed method was validated on parameters including linearity, precision, accuracy and robustness.The HPLC analysis showed significant increase in amount of Bacoside A3 and Piperine in the in-house sample of BV when compared with all three different marketed samples of the same. Results showed variations in the amount of Bacoside A3 and Piperine in different samples which indicate non-uniformity in their quality which will lead to difference in their therapeutic effects.The outcome of the present investigation underlines the importance of standardization of Ayurvedic formulations. The developed method may be further used to standardize other samples of BV or other formulations containing Bacoside A3 and Piperine.

An efficient and practical strategy for the synthesis of highly functionalized racemic and non-racemic 4,5-dihydropyrroles via domino ring-opening cyclization (DROC) of activated aziridines with malononitrile in excellent yield and stereoselectivity is described. The reaction serves as a tool for the synthesis of a large variety of substituted 4,5-dihydropyrroles in enantiomerically pure forms.

Infrared to visible upconversion fluorescent nanoparticles of Gd2O3 codoped with Ho3+/Yb3+ ions are synthesized via thermal decomposition process. The X-ray diffraction analysis of as-synthesized nanoparticles and annealed sample at 1000 °C has shown body-centered cubic phase of Gd2O3. The synthesized phosphor has shown intense green emission upon 980-nm excitation. High-contrast latent fingermarks on some difficult semi-porous and non-porous surfaces under 980-nm diode laser excitation were developed through powder dusting and colloidal solution spraying techniques and the results are compared with the commercial green luminescent fingermark powder. The latent fingermarks were developed on transparent (biological glass slides), single-color (aluminum foil) and multicolor (plywood, plastic bottle and book cover page) background surfaces. The present study depicts that the upconversion-based latent fingermarks detection using Gd2O3:Ho3+/Yb3+ phosphor material is suitable over the other conventional powders and has potential for practical applications in forensic science.

Organic field effect transistors (OFETs) have been widely explored for their popular applications in flat panel displays and various kinds of affordable sensors. The overall performance of the device depends on the quality of semiconductor-dielectric interface, and degree of crystalline order in the active layer, close to the above said interface. In the special league of solution processed OFETs, semicondutor: polymer blends have been reported as one of the best possible ways to achieve an intimate, uniform and defect free semiconductor-dielectric interface in a single step. In addition, degree of crystalline order can be further ameliorated through solvent vapor annealing (SVA), which essentially controls the evaporation time of the solvent.

We report on high-mobility top-gate organic field-effect transistors (OFETs) and complementary-like inverters fabricated with a solution-processed molecular bis(naphthalene diimide)-dithienopyrrole derivative as the channel semiconductor and a CYTOP/Al2O3 bilayer as the gate dielectric. The OFETs showed ambipolar behavior with average electron and hole mobility values of 1.2 and 0.01 cm2 V−1 s−1, respectively. Complementary-like inverters fabricated with two ambipolar OFETs showed hysteresis-free voltage transfer characteristics with negligible variations of switching threshold voltages and yielded very high DC gain values of more than 90 V/V (up to 122 V/V) at a supply voltage of 25 V.