A branch-and-cut method for 0-1 mixed convex programming

We generalize the disjunctive approach of Balas, Ceria, and Cornuéjols [2] and devevlop a branch-and-cut method for solving 0-1 convex programming problems. We show that cuts can be generated by solving a single convex program. We show how to construct regions similar to those of Sherali and Adams [20] and Lovász and Schrijver [12] for the convex case. Finally, we give some preliminary computational results for our method. Received January 16, 1996 / Revised version received April 23, 1999?Published online June 28, 1999     

Effect of a cocatalyst modifier in the synthesis of ultrahigh molecular weight polyethylene having reduced number of entanglements

The use of a hindered phenol to trap free trimethylaluminum (TMA) in methylaluminoxane (MAO) solutions has been reported to improve the performance of single‐site, homogeneous catalysts for olefin polymerization. In the present study, with the help of rheological analyses, we have investigated and compared the molecular weight, molecular weight distribution and entanglement density of ultrahigh molecular weight polyethylene synthesized with a single‐site catalyst activated by MAO and phenol‐modified MAO. While the number average molecular weight (M_n) of the obtained polymers remains the same for both activations, a higher yield and a higher entanglement density are found in the initial stages of polymerization on using phenol‐modified MAO as the cocatalyst. These results suggest that on using the phenol‐modified MAO as activator, a higher number of active sites are obtained. Surprisingly in the presence of untreated MAO, a tail in the higher molecular mass region is produced. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013     

Recent advances in the synthesis of C-5-substituted analogs of 3,4-dihydropyrimidin-2-ones: A review

3,4-Dihydropyrimidin-2-ones act as a versatile scaffold in organic synthesis, which serves as a significant template for the development of various therapeutic agents and shows a wide spectrum of activities. The attractive application of 3,4-dihydropyrimidin-2-ones in organic synthesis is undoubtedly owing to C-5 ester group, which is responsible for the change in its bioactivity. Introduction of various groups like electron-withdrawing and electron-donating groups at positions 1, 2, 3, 5, and 6 greatly increased biological activity. Significant efforts have been undertaken to exploit different synthetic routes to synthesize various derivatives of 3,4-dihydropyrimidin-2-ones. This review article gives a comprehensive account of the synthetic utility of C-5 substitution of 3,4-dihydropyrimidin-2-ones used in the design and synthesis of different types of compounds with greater emphasis on recent literature.     

New Chromogenic Spray Reagent for Detection and Identification of Carbosulfan

JPC – Journal of Planar Chromatography – Modern TLC - A new chromogenic spray reagent has been used for detection and identification of carbosulfan in HPTLC. Alkaline hydrolysis of...     

Ionic liquid: an efficient and recyclable medium for the synthesis of octahydroquinazolinone and biscoumarin derivatives

Abstract  

A facile and environmentally benign procedure for the synthesis of octahydroquinazolinone and biscoumarin derivatives in ionic liquids is reported. Octahydroquinazolinones were synthesized in the presence of trimethylsilyl chloride (TMSCl) while the synthesis of biscoumarins required no additive. The ability to reuse the ionic liquid, the high yields, and ease of purification are the important features of this process.     

A short and efficient synthesis of furo[2,3-b]indoles

Application of Wittig olefination-Claisen rearrangement protocol for the short synthesis of furo[2,3-b]indoles is described.     

Ultrasound Promoted and Ionic Liquid Catalyzed Cyclocondensation Reaction for the Synthesis of 4(3H)-Quinazolinones

4(3H)‐Quinazolinones were synthesized in high yields by one‐pot three‐component condensation of anthranilic acid, carboxylic acid and aniline in the presence of ionic liquid such as 1‐n‐butyl‐3‐methylimidazolium tetrafluoroborate (BMImBF₄) as catalyst under solvent free and neutral conditions.     

From beads-to-wires-to-fibers of tungsten oxide: electrochromic response

Suitable host lattice and morphology for easy intercalation and deintercalation process are crucial requirements for electrochromic device. In this investigation, the evolution of structural and morphological changes and their effect on electrochromic (EC) properties of spray-deposited WO₃ thin films are studied. Films of different morphologies were deposited from an ammonium tungstate precursor solution using a novel pulsed spray pyrolysis technique (PSPT) on tin-doped indium oxide (ITO) coated glass substrates by varying quantity of spraying solution. Interesting morphological transition from beads-to-wires-to-fibers as a function of quantity of sprayed solution has been demonstrated. The porosity, crystallinity and “open” structures in the films consisting of beads, wires, and fiber-like morphology enabled us to correlate these aspects to their EC performance. WO₃ films comprising wire-like morphology (20 cc spraying quantity) exhibited better EC properties both in terms of coloration efficiency (42.7 cm²/C) and electrochemical stability (10³ colored/bleached cycles) owing to their adequate open structure, porosity, and amorphicity, compared with the films having bead/fiber-like morphology.     

On paving matroids and a generalization of MDS codes

We define a class of codes that corresponds to a class of matroids called paving matroids. This class of codes includes maximum-distance-separable (MDS) codes, and some other interesting codes such as the (12,6) ternary Golay code. Some basic properties of these codes are established using techniques from matroid theory. Our results raise a natural existence question to which we obtain partial answers using known results about the non-existence of Steiner systems of the type S(t–1,t,2t).     

Wetting and phase separation at surfaces

We study the problem ofsurfacedirected spinodal decomposition, viz., the dynamical interplay of wetting and phase separation at surfaces. In particular, we focus on the kinetics of wetting-layer growth in a semi-infinite geometry for arbitrary surface potentials and mixture compositions. We also present representative results for phase separation in confined geometries, e.g., cylindrical pores, thin films, etc.