Viscosity Behavior of Some Synthetic Polypeptides at Low Concentration

The viscosity of poly(γ-benzyl L-glutamate)(PBLG), poly -carbobenzoxy-L-lysine (PCBL), polyglycine (PG), and fivetricopolypeptides (glu^x-lys^y -gly^z) was studied as a function of concentration at 25°C. The solvents used include two random coil solvents, a theta solvent and a helicogenic solvent. The Huggins plots of all the systems except polyglycine showed anomalously high reduced viscosity values at low concentration of solutions. A variation of 20°C in the temperature of some of the systems did not show any marked effect on the abnormality in the Huggins plots. Various factors likely to cause abnormality were considered; disentanglement of the polypeptide chains appeared to be the prime factor responsible for the anomalous rise in the reduced viscosity.     

Vinyl Polymerization Initiated by Peroxydiphosphate. XI. Polymerization of Methyl Methacrylate Initiated by Peroxydiphosphate-Tartaric Acid Redox System

The polymerization of methyl methacrylate was studied using the peroxydiphosphate and tartaric acid redox system as the initiator. The rate of polymerization increases with increasing peroxydiphosphate concentration and the initiator exponent was computed to be 0.5. The rate of polymerization increases with increasing monomer concentration and the monomer exponent was computed to be unity. The reaction was carried out at three different temperatures, and the overall activation energy was computed to be 3.80 kcal/mol. The effect of certain surfactants on the rate of polymerization has been investigated and a suitable kinetic scheme has been proposed.     

Thermogravimetric analysis of the copper silicate mineral dioptase Cu6[Si6O18]·6H2O

There have been a few studies on the thermal decomposition of dioptase Cu₆[Si₆O₁₈]·6H₂O. The results of these analyses are somewhat conflicting and the conclusions vary among these thermo-analytical studies. The objective of this research is to report the thermal analysis of dioptase from different origins and to show the mechanism of decomposition. Thermal decomposition occurs over a very wide temperature range from around 400 to 730 °C with the loss of water. Two additional mass loss steps are observed at around 793 and 835 °C with loss of oxygen. The infrared spectra of dioptase in the hydroxyl stretching region enables the hydrogen bond distances of water molecules in the dioptase structure to be calculated. The large variation in the hydrogen bond distances offers an explanation as to why the decomposition of dioptase with loss of water occurs over such a wide temperature range.     

Popcorn‐Shaped Magnetic Core–Plasmonic Shell Multifunctional Nanoparticles for the Targeted Magnetic Separation and Enrichment,Label‐Free SERS Imaging,and Photothermal Destruction of Multidrug‐Resistant Bacteria

Over the last few years, one of the most important and complex problems facing our society is treating infectious diseases caused by multidrug‐resistant bacteria (MDRB), by using current market‐existing antibiotics. Driven by this need, we report for the first time the development of the multifunctional popcorn‐shaped iron magnetic core–gold plasmonic shell nanotechnology‐driven approach for targeted magnetic separation and enrichment, label‐free surface‐enhanced Raman spectroscopy (SERS) detection, and the selective photothermal destruction of MDR Salmonella DT104. Due to the presence of the “lightning‐rod effect”, the core–shell popcorn‐shaped gold‐nanoparticle tips provided a huge field of SERS enhancement. The experimental data show that the M3038 antibody‐conjugated nanoparticles can be used for targeted separation and SERS imaging of MDR Salmonella DT104. A targeted photothermal‐lysis experiment, by using 670 nm light at 1.5 W cm^?2 for 10 min, results in selective and irreparable cellular‐damage to MDR Salmonella. We discuss the possible mechanism and operating principle for the targeted separation, label‐free SERS imaging, and photothermal destruction of MDRB by using the popcorn‐shaped magnetic/plasmonic nanotechnology.     

A CSD analysis on H-bond patterns from phosphoric triamides to their coordination compounds, new complexes with (tBuNH)3PO ligand (PO): Cl2Ph2Sn(PO)2 and Fe(PO)2(NO3)3

The phosphoryl donor ligand (^tBuNH)₃PO (PO) was used for preparation of new tin(IV), Cl₂Ph₂Sn(PO)₂ (1), and iron(III), Fe(PO)₂(NO₃)₃ (2), complexes. These complexes are the first examples of using a phosphoric triamide containing a secondary nitrogen atom, [RNH]₃P(O), for preparation of an organotin(IV) complex of the type ([RNH]₃P(O))₂X₂Ph₂Sn, X = halide, and an iron(III) complex. In 1, the Sn coordination geometry is octahedral with the pair of similar ligands in a trans orientation. The Fe center in 2 is seven-coordinated with the two phosphoramide ligands in a trans fashion, too. This article also reviews the structures of analogous complexes with phosphoric triamide ligands, deposited in the CSD, aiming to classify hydrogen bond patterns in this category of compounds. Moreover, it is tried to find a relationship between the H-bond patterns in complexes and the related free ligands.     

A UNIQUE SUPRAMOLECULAR STRUCTURE OF POLY [μ-OXO -BIS(1,1,2,3,4,5-HEXAHYDRO-1-NITRATOTELLUROPHENE)] [(C4H8TENO3)2O]N WITH—0-TE-0-TE-0—CROSS LINKED CHAINS

Abstract

Poly [μ-oxo bis(1,1,2,3,4.5-hexahydro- 1-nitratotellurophene)] 1, is prepared by the room temperature reaction of 1,1,2,3,4,5-hexahydro- 1.1 -diiodotellurophene with silver nitrate in deionised water. Crystals of 1 are monoclinic. space group CUc with a=13.930(2) Å, b =11.665(2) Å, c=10.0682(11) Å, β=116.264(8)^O and Z=A. The monomeric unit of the title compound is centrosymmetric, with an angular TeOTe skeleton containing bridging O atom at the centre of symmetry. These monomeric units are linked together through —O-Te-O-Te-O—cross linked chains and the nitrate groups are asymmetrically bidentate with a primary Te-ONO₂ and a secondary Te—O semibonding interaction. Each nitrate group further participates in another Te–O semibonding interaction forming another asymmetric Te(NO₃)₂Te bridge. The structural characteristics of 1 are compared with related complexes.     

A facile,catalyst-free synthesis of new polycyclic pyrrolo[1,2-b]pyrazolone derivatives

A convenient and efficient procedure has been developed for the synthesis of a new ring system, pyrrolo[1,2-b]pyrazolone, via two-component coupling reaction followed by base mediated intramolecular cyclization. Single-pot synthesis replacing the two step process has also been successfully carried out. A series of polycyclic pyrrolo[1,2-b]pyrazolone derivatives have been obtained by employing the procedure along with some fused pyrrol-1-ylamine system. The products were formed very rapidly in catalyst free condition in a good yield (up to 75%) and also it had tolerance to a wide scope of substrates.     

Radiofrequency pulse sequences which compensate their own imperfections. 1980

Radiofrequency pulse sequences are described which have the same overall effect as a single 90° or 180° pulse but which compensate the undesirable effects of resonance offset and spatial inhomogeneity of the radiofrequency field H₁. These “composite” pulses are built up from a small number of conventional pulses which rotate the nuclear magnetization vectors about different axes in the rotating frame, while in the intervals between pulses a limited amount of free precession may be allowed to occur. Insight into the way in which pulse imperfections are compensated is obtained by computer simulation of trajectories of families of nuclear spin “isochromats” representing a distribution of H₁ intensity or resonance offset. Composite 90° pulses are suggested as a method of reducing systematic errors in spin-lattice relaxation times derived from progressive saturation or saturation-recovery experiments, and as the preparation pulse of a spin-locking experiment. A test of the effectiveness of the composite 180° pulse sequence has been made by using it for population inversion in a spin-lattice relaxation measurement, where T₁ is derived from the null point in the recovery curve, a technique known to be very sensitive to pulse imperfections.     

State feedback stabilization of uncertain linear time‐delay systems: A nonlinear matrix inequality approach

A nonlinear matrix inequality is derived as a stabilizability condition of linear uncertain time‐delay systems. This inequality is seen as a less conservative one as well as efficient for numerical computation than the existing results as seen when solving by cone‐complementary algorithm. Copyright © 2010 John Wiley & Sons, Ltd.     

Stability criteria with less LMI variables for linear system with additive time-delays

In this technical note, equivalent stability criterion with minimal number of variables for three recently reported stability criteria is proposed for a class of linear systems with additive time-varying delays. The existing delay-dependent stability criteria for additive time-delay systems have more number of matrix variables in the LMI; and hence, they require more computational cost. The proposed equivalent criteria, unlike the original ones, encompass only the matrix variables that are associated in the Lyapunov-Krasovskii functional, making the criteria mathematically less complex and computationally more attractive. The complexity involved in the existing stability criteria is attributed to the fact the cross-terms that emanate from the time-derivative of the Lyapunov-Krasovskii functional are dealt with free-weighting matrices. Hence, apart from the matrix variables that are associated in the corresponding Lyapunov-Krasovskii functional, the existing criteria also have additional matrix variables in them. In this paper, we have devised techniques to eliminate the free-weighting matrices in the existing stability criteria without sacrificing the conservatism. The resulting equivalent stability criteria, therefore, have least possible number of variables in the LMI; and hence, have minimum computational burden. The effectiveness of the proposed equivalent criteria is validated on a numerical example.