Design of Low Offset and High Speed CMOS Comparator for Analog to Digital Converter

In today’s world everything is digitized but nature is analog, so it is necessary to have such a device which converts analog signal into digital and for this analog to digital converter is required. Now a day’s ADC’s require lesser power, better slew rate, high speed and less offset. Performance limiting component for ADC’s are amplifiers and comparators in which comparator is the most important.This paper presents the design of low offset low power dissipation and high speed  comparator. The proposed comparator consists of a preamplifier stage, decision stage and self biased output buffer stage. The proposed design uses a low power current mirror circuitry for providing a highly biased current. The circuit is designed using 90nm CMOS process for a supply voltage of 1V and reference voltage of 0.5V and power consumption is approximately 300?W. Keywords: CMOS Comparator, Current Mirror, Pre Amplifier, Output Buffe

Design of Low Voltage Improved performance Current Mirror

This paper proposes a low voltage current mirror circuit with low input impedance and high output impedance. These improvements are obtained by adding an amplifier which provides biasing voltage to the transistors. Its operation and results are compared with conventional and cascode current mirror circuits. The circuits are designed using Tanner EDA Tool in 90nm CMOS technology with 0.8V supply voltage. Simulation results shows that the minimum output voltage is reduced to 0.1 V, also input resistance is reduced to 0.179k? and consumes only 46µW power. Keywords: Current mirror, Input resistance Output resistance, Input compliance voltage, Output compliance voltage

Nickel(II) complexes having Imidazol-2-ylidene-N′-phenylurea ligand in the coordination sphere - Syntheses and solid state structures

We report the syntheses and structural studies of two nickel(II) complexes of imidazol-2-ylidene- N′-phenylureate ligand of composition [{Im tBuNCON(H)Ph}2Ni(acac)2](1) and [(C6H5NH2)2Ni(acac)2][ImMes NCON(H)Ph] (2). The nickel complex 1 was readily prepared by the reaction of nickel(II) acetylacetonate [Ni(acac)2] with imidazol-2-ylidene-N′-phenylureate ligand [Im tBuNCON(H)Ph] (L1) in THF under reflux condition for 72 h. The nickel complex 2 was obtained by the reaction of [Ni(acac)2], mesityl derivative of imidazol-2-ylidene-N′-phenylureate ligand [Im MesNCON(H)Ph] (L2) in the presence of aniline as base under reflux condition in THF. Both the paramagnetic complexes have been characterized by FT-IR spectroscopy and elemental analyses. Solid-state structures of both the new complexes were established by single crystal X-ray diffraction analysis. In the molecular structures of complexes 1 and 2, each nickel(II) ion is six fold coordinated and form a distorted octahedral geometry. The optical properties of both complexes have been explored. The Hirshfeld surfaces are used to view and analyze the intermolecular contacts in crystalline state for complex 2

Imidazol-2-ylidene-N′-phenylureate ligands in alkali and alkaline earth metal coordination spheres - heterocubane core to polymeric structural motif formation

The synthesis and isolation of two potassium, one lithium and two calcium complexes of imidazol-2-ylidene-N′-phenylureate ligands [ImRNCON(H)Ph] [(R = tBu (1a); Mes (1b) and Dipp (1c); Mes = mesityl, Dipp = 2,6-diisopropylphenyl] are described. Potassium complexes, [{κ2-(ImMesNCONPh)K}4] (2b) and [{κ3-(ImDippNCONPh)K}2{KN(SiMe3)2}2]n (2c), were prepared in good yields by the reactions of 1b and 1c, respectively, with potassium bis(trimethyl)silyl amide at ambient temperature in toluene. Lithium complex [{(2,6-tBu2-4-Me-C6H2O)Li(ImtBuNCON(H)Ph)}2{ImtBuNCON(H)Ph}] (3a) was isolated by a one-pot reaction between 1a and LiCH2SiMe3, followed by the addition of 2,6-tBu2-4-Me-C6H2OH in toluene. Calcium complex [{κ2-(ImtBuNCONPh)Ca{N(SiMe3)2}-{KN(SiMe3)2}]n (4a) was isolated by the one-pot reaction of 1a with [KN(SiMe3)2] and calcium diiodide in THF at ambient temperature. The solid-state structures of ligand 1a and complexes 2b, 2c, 3a and 4a were confirmed by single-crystal X-ray diffraction analysis. It was observed that potassium was coordinated to the oxygen atom of urea group and to the nitrogen atom of the imidazolin-2-imine group, in the solid-state structure of 2b. In complex 4a, the calcium ion was ligated to the monoanionic imidazol-2-ylidene-N′-phenylureate ligand in a bi-dentate (κ2) fashion through the oxygen and nitrogen atoms of the isocyanate building block leaving the imidazolin-2-imine fragment uncoordinated. In the solid state of the potassium complex 2c, tri-dentate (κ3) coordination from the imidazol-2-ylidene-N′-phenylureate ligand was observed through the oxygen and nitrogen atoms of the isocyanate building block and of the imidazolin-2-imine fragment. In contrast, in the dimeric lithium complex 3a, the neutral imidazol-2-ylidene-N′-phenylureate ligand was bound to the lithium centre in a mono-dentate fashion (κ1) through an oxygen atom of the isocyanate moiety. It is to be noted that in each complex thus observed, the elongated carbon-nitrogen bond distances indicate substantial electron delocalisation from the imidazole ring to the ureate group present in ligand 1

Evaluation of antioxidant potential of Emblica officinalis and Murraya koenigii and their role in modulation of cognitive function in diabetic rats

Background: Hyperglycaemia and hyperlipidaemia seen in diabetes mellitus result in oxidative stress and pose significant risk of cognitive decline that may lead to Alzheimer’s disease. Approved anti-diabetic drugs have so far failed to demonstrate anti-oxidant and anti-hyperlipidemic activity, apart from saroglitazar. Therefore, this study was done to find a suitable anti-diabetic drug that possesses anti-hyperglycaemic, anti-oxidant and anti-hyperlipidemic activities and can reverse cognitive decline.Methods: Emblica officinalis (250 mg/kg, p.o. and 500 mg/kg, p.o.) and Murraya koenigii (250 mg/kg, p.o. and 500 mg/kg, p.o.) were chosen to study these activities in Wistar rats. Diabetes was induced by single intraperitoneal injection of streptozotocin [STZ] (50 mg/kg). Fasting blood glucose levels and lipid profile were measured on day 1 and day 30 of the experiment. Cognitive function was assessed by measuring transfer latency (TL) on elevated plus maze, step-down latency (SDL) on passive avoidance apparatus and retention latency (RL) and quadrant time (QT) in Morris water maze. Oxidative stress was assessed at end of study by measuring brain MDA and GSH levels. Cholinergic marker of cognition, AChE was measured in brain at end of study.Results: Both E. officinalis and M. koenigii showed dose dependent anti-hyperglycemic, anti-hyperlipidemic and anti-oxidant effects in diabetic rats with 500 mg/kg dose showing significantly higher effect. Both 250 mg/kg and 500 mg/kg dose of E. officinalis and M. koenigii partially reversed cognitive decline in diabetic rats by day 30.Conclusions: 500 mg/kg p.o. dose of E. officinalis or M. koenigii has potential to reverse cognitive decline in diabetic patients.

Synthesis and solid state structures of Chalcogenide compounds of Imidazolin-2-ylidene-1,1-Diphenyl-phosphinamine

We report the synthesis and solid state structures of 1,3-di-aryl-imidazolin-2-ylidine-1,1-diphenylphosphinamine [(aryl = mesityl (1a) and aryl = 2,6-diisopripyl (1b)] and their chalcogenide compounds 1, 3-di-aryl-imidazolin-2-ylidine- P,P-diphenylphosphinicamide (2a,b), 1,3-di-aryl-imidazolin-2-ylidine-P,P-diphenyl-phosphinothioicamide (3a,b) and 1,3-diaryl-imidazolin-2-ylidine- P,P-diphenyl-phosphinoselenoic-amide (4a,b). The compounds 1a,b were prepared in good yield by the reaction of 1,3-di-aryl-imidazolin-2-imine and chlorodiphenylphosphine in the presence of triethylamine in toluene. The reactions of 1a,b with elemental sulphur and selenium afforded the corresponding chalcogenide compounds 3a,b and 4a,b respectively. The corresponding oxo- derivative (2a,b) was obtained by reacting compound 1a,b with 30% aqueous hydrogen peroxide in THF. The molecular structures of 1a, 2a, 3a and 4a,b have been established by single crystal X-ray diffraction analyses. The molecular structures reveal that even C1–N1–P1 angle (124.62 ∘) in compound 1a is less obtuse compared to the corresponding C1–N1–Si1 angles (157.8 ∘) observed in related N-silylated 2-iminoimidazolines and trimethylsilyl iminophosphoranes. C1–N1–P1 angles are further widened in compounds 2a, 3a, and 4a,b due to the attachment of chalcogen atoms onto phosphorus atom

Formation of BH3 Adducts with Pyridine-2-Methylaminophosphine ligands: An experimental and computational study

The reaction of pyridine-2-methylaminophosphine [C5H4N-CH2NHPPh2] (1) and pyridine-2-methylphosphinoselenoic amide [C5H4N-CH2NHP(Se)Ph2] (2) with BH3⋅SMe2 yields the corresponding adducts [C5H4N(BH3)-CH2NHP(BH3)Ph2] (1a), and [C5H4N(BH3)-CH2NHP(Se)Ph2] (2a), respectively. The solid state structures of both the compounds were established by single crystal X-ray diffraction analysis. The phosphorus and the pyridine nitrogen atoms are coordinated to the boron atom in the case of 1a whereas only pyridine nitrogen atom is attached to the BH3 group in the case of 2a. To understand the nature of P-B/ N-B bonds and to compare the basicities of pyridine nitrogen, amino nitrogen and phosphorus atoms, density functional theoretical (DFT) calculations were performed on the BH3 adducts 1a and 2a. The results are consistent with the experimental results