Axial Imidazole Binding Strengths in Porphyrinoid Cobalt(III) Complexes as Studied by Tandem Mass Spectrometry

The Co(II) complexes of twelve meso-tetraaryl-porphyrins, -chlorins, and chlorin analogues containing non-pyrrolic heterocycles were synthesized and converted in situ to the corresponding Co(III) complexes coordinated to one or two imidazoles. Electrospray ionization tandem mass spectrometry (ESI-MS/MS) in conjunction with the energy-variable collision-induced dissociation (CID) technique was used to compare the relative gas-phase binding strength of the axially coordinated imidazoles to the octahedral and square planar Co(III) porphyrinoid complex ions. The observed binding energies of these ligands were rationalized in terms of the effects of porphyrinoid core structure and meso-substitution on the electron density on the central Co(III) centers. Some of these trends were supported by DFT-based computational studies. The study highlights to which extend porphyrins vary from chlorins and chlorin analogues in their coordination abilities and to which extraordinary degree meso-thienyl-substituents influence the electronic structure of porphyrins. The study also defines further the scope and limits CID experiments can be used to interrogate the electronic structures of metalloporphyrin complexes.     

A novel,green 1-glycyl-3-methyl imidazolium chloride-copper(Ⅱ) complex catalyzed C-H oxidation of alkyl benzene and cyclohexane

A variety of alkyl-arenes and cyclohexane were converted to the corresponding ketones with NaCIO as the oxidant in the presence of l-glycyl-3-methyl imidazolium chloride-copper(Ⅱ) complex.This method contains simplified product isolation and catalyst recycling,affording benzylic C-H oxidation of alkyl-arenes imparting high yield of ketones.Furthermore,complex could be reused seven times without a significant loss of its catalytic activity.     

High-throughput cell cycle synchronization using inertial forces in spiral microchannels

Efficient synchronization and selection of cells at different stages of the cell replication cycle facilitates both fundamental research and development of cell cycle-targeted therapies. Current chemical-based synchronization methods are unfavorable as these can disrupt cell physiology and metabolism. Microfluidic systems developed for physical cell separation offer a potential alternative over conventional cell synchronization approaches. Here we introduce a spiral microfluidic device for cell cycle synchronization, using the combined effects of inertial forces and Dean drag force. By exploiting the relationship between cell diameter and cell cycle (DNA content/ploidy), we have successfully fractionated several asynchronous mammalian cell lines, as well as primary cells comprising bone marrow-derived human mesenchymal stem cells (hMSCs), into enriched subpopulations of G0/G1 (>85%), S, and G2/M phases. This level of cell cycle enrichment is comparable to existing microfluidic systems, but the throughput (～ 15 × 10(6) cells per h) and viability (～ 95%) of cells thus synchronized are significantly greater. Further, this platform provides rapid collection of synchronized cells or of diameter-sorted cells post-separation, to enable diverse applications in the study and manipulation of cell proliferation.     

Synthesis and characterization of novel quinoline selenium compounds: X-ray structure of 6-methoxy-3H-[1,2]diselenolo[3,4-b]quinoline

A series of novel and synthetically important quinoline selenium compounds have been successfully synthesized using an efficient and simple strategy. The method employed leads to the synthesis of both cyclic as well as open chain quinoline selenium compounds. The prepared selenium compounds have been characterized with the help of various spectroscopic techniques viz., NMR (¹H, ¹³C), FT-IR, mass spectrometry. The structure of 6-methoxy-3H-[1,2]diselenolo[3,4-b]quinoline has been determined by X-ray crystallography.     

Dynamic analysis of multilayered welded aluminum cantilever beams

Welded joints are often used to fabricate assembled structures in machine tools, automotive and many such industries requiring high damping. Vibration suppression in these applications can enhance the dynamic stability significantly. A little amount of work has been reported till date on the damping capacity of welded aluminum structures. The present work outlines the basic formulation for the slip damping mechanism in multilayered and tack welded aluminum beams, vibrating under dynamic conditions. It is observed that there are a number of vital parameters that govern the damping capacity of these structures. The developed damping model is found to be fairly in good agreement with experimental results.     

Synthesis and Antimicrobial Activity of 2‐(Pyridine‐3‐yl)‐4H‐chromen‐4‐one Derivatives

An efficiently synthesis of chromones via cyclodehydration of corresponding 1‐(2‐hydroxyphenyl)‐3‐(pyridine‐3‐yl)propane‐1,3‐dione is described under ultrasound irradiation. A series of novel 2‐(pyridine‐3‐yl)‐4H‐chromen‐4‐one derivatives was confirmed on the basis of ¹H‐NMR, mass, IR spectral data, and elemental analysis. The synthesized compounds were evaluated for their antibacterial and antifungal activities. Most of the compounds were found to be comparable potent than the reference standard drugs. Utilization of ultrasound irradiation, simple reaction conditions, isolation, and purification makes this manipulation very interesting from an economic and environmental perspective.     

Room temperature synthesis of water repellent silica coatings by the dip coat technique

The present paper describes the room temperature synthesis of dip coated water repellent silica coatings onto stainless steel substrates using 1,1,1,3,3,3-hexamethyldisilazane as a surface modifying agent. The hydrophobic property of the silica coating was enhanced by increasing its surface roughness, which was achieved by a proper control over the MeOH/TMOS molar ratio (S) during the synthesis. The contact angle of a water droplet (10 μl) increased from 72° to 145° with an increase in the S value from 9.1 to 36.4. The silica coating showed a minimum sliding angle of 15° for a water droplet of 10 μl. The water repellent silica coatings are thermally stable up to a temperature of 340 °C. The results have been discussed by taking into consideration the contact angle measurements, surface morphology and sol-gel parameters.     

Frequency dependence of acoustic parameters of freshly excised tissues of Sprague Dawley rats

A modified version of the pulse echo technique was used to measure the velocity of propagation and attenuation of ultrasound in excised tissue of young-adult Sprague-Dawley rats. The measurements were made at ultrasonic frequencies of 1.0, 2.25, 5.0, 7.5 and 10.0 MHz. The temperature of the tissues was monitored continuously to within ± 0.1°C of the ambient temperature. The acoustic parameters were measured in the liver, kidney, cardiac muscle and gastrocnemius muscle. All measurements were carried out in the near field region of the ultrasonic beam. It was observed that the velocity of propagation in tissues showed a slight dispersion with frequency. The attenuation in tissues increased with increasing frequency.     

A simple microwave kit to convert an X-band ESR spectrometer for K-band operation

A kit for the conversion of an X-bandesr spectrometer for K-band operation is described and its performance has been tested withp-benzosemiquinone, vanadyl acetyl acetonate and 2, 5-ditertiary butyl semiquinone. The easy conversion of the X-band spectrometer to K-band operation enables us to distinguish between magnetic field dependent and field independent parameters. A varactor harmonic generator is used as a frequency doubler driving the fundamental power from the existing X-band source to give a power output at K-band without having to modify the electronic circuit; the modification of the microwave circuitry is proposed.     

On the oscillation of a second-order delay equation

The oscillatory nature of two equations (r(t) y′(t))′ + p₁(t)y(t) = f(t), (r(t) y′(t))′ + p₂(t) y(t ? τ(t))= 0, is compared when positive functions p₁ and p₂ are not “too close” or “too far apart.” Then the main theorem states that if h(t) is eventually negative and a twice continuously differentiable function which satisfies (r(t) h′(t))′ + p₁(t) h(t) ? 0, then this inequality is necessary and sufficient for every bounded solution of (r(t) y′(t))′ + p₂(t) y(t ? τ(t)) = 0 to be nonoscillatory.