Diastereoselective synthesis of 2,3,4,5-tetrasubstituted isoxazolidines via 1,3-dipolar cycloaddition

The 1,3-dipolar cycloaddition reactions of α-2-methoxyaryl nitrones with nitrostyrenes and chalcones have been investigated. The regiochemistry and stereochemistry of the resultant cycloadducts have been determined with the help of NMR spectroscopy and X-ray analysis. β-Nitrostyrenes add to nitrones to give two geometrical isomers, while the β-methyl-β-nitrostyrene gives a single isomer in relatively low yield. The chalcones give a single cycloadduct upon 1,3-dipolar addition.     

Inclusion of α-phenyl-N-p-methylphenyl Nitrone in β- Cyclodextrin: Formation of 1G : 1H and 1G : 2H Complexes and the Remarkably Fast 1,3-Dipolar Cycloaddition of the 1G : 2H Complex with Olefins in the Solid State

The nitrone is found to be included in the -cyclodextrin cavity in two different stoichiometries viz., 1G : 1H and 1G : 2H – the existence of which is proved by physical methods. The 1G : 2H complex of the nitrone serves as a good potent dipolarophile in the 1,3-dipolar cycloaddition reactions with olefins resulting in rate acceleration and regioselection.     

Multiobjective Optimization of Fabrication Parameters of Jute Fiber/Polyester Composites with Egg Shell Powder and Nanoclay Filler

In the present study, a model is presented to optimize the fabrication parameters of natural fiber reinforced polyester matrix composites with dual fillers. In particular, jute fiber mat was chosen as reinforcement and eggshell powder (ESP) and montmorillonite nanoclay (NC) were selected as fillers. The weight per square meter (GSM) of the fiber, the weight percentage of ESP and NC have been chosen as independent variables and the influence of these variables on tensile, flexural and impact strength of the composite has been inspected. The permutations of the different combinations of factors are intended to accomplish higher interfacial strength with the lowest possible number of tested specimens. The experiments were designed by the Taguchi strategy and a novel multi-objective optimization technique named COPRAS (COmplex PRoportional ASsessment of alternatives) was used to determine the optimal parameter combinations. Affirmation tests were performed with the optimal parameter settings and the mechanical properties were evaluated and compared. Experimental results show that fiber GSM and eggshell powder content are significant variables that improve mechanical strength, while the nanoclay appears less important.     

Single crystal EPR studies of an organic NLO material: methyl-p-hydroxy benzoate

Single crystals of an organic nonlinear optical (NLO) material methyl-p-hydroxy benzoate (MHB) were grown by solvent evaporation technique. EPR spectra were recorded for Er3+: MHB and gamma-irradiated MHB at room temperature at X-band frequencies. The angular variation studies of the spectra were observed and the principal values of g were determined. The grown crystals were characterized by single crystal X-ray diffraction studies.     

Identities for minors of the Laplacian, resistance and distance matrices

It is shown that if L and D are the Laplacian and the distance matrix of a tree respectively, then any minor of the Laplacian equals the sum of the cofactors of the complementary submatrix of D, up to sign and a power of 2. An analogous, more general result is proved for the Laplacian and the resistance matrix of any graph. A similar identity is proved for graphs in which each block is a complete graph on r vertices, and for q-analogues of such matrices of a tree. Our main tool is an identity for the minors of a matrix and its inverse.     

18‐Crown‐6 Catalyzed Microwave‐mediated Synthesis of Symmetric Bis‐Heterocyclic Compounds under Solvent‐free Condition

An efficient, solvent‐free and 18‐crown‐6 catalyzed method for the synthesis of N‐alkyl‐4‐(4‐(5‐(2‐(alkyl‐amino)thiazol‐4‐yl)pyridin‐3‐yl)phenyl)thiazol‐2‐amine, N‐alkyl‐4‐(5‐(2‐alkyamino)thiazol‐4‐yl)pyridine‐3‐yl)thiazol‐2‐amine, and 4,4′‐bis‐{2‐[amino]‐4‐thiazolyl}biphenyl bis‐heterocyclic derivatives via microwave accelerated cyclization is presented.     

Donor properties of the nitrone function in copper(II) complexes of some 2-hydroxy-1-naphthylnitrones

Summary Copper(II) complexes of the type CuL₂, 2H₂O and CuL₂. Py where L=-(2-hydroxy-1-naphthyl)-N-R-nitrone (R= methyl, phenyl and variously substituted phenyls) have been isolated and characterised. They have normal magnetic moments. Their ligand field spectra indicate an octahedral geometry for the dihydrates and a five-coordinate environment for the pyridine adducts. Increased (C=N) and considerably decreased (N-O) frequencies in these complexes reveal the presence of - and -interactions of the ligand with copper through nitrone oxygen. The effect of pyridine adduct formation is to increase the Cu-O -interaction.     

Asymmetric induction during electron transfer mediated photoreduction of carbonyl compounds: role of zeolites

Photochemistry of 17 aryl alkyl ketones included within cation exchanged zeolites has been examined. In solution five of the 17 ketones undergo intramolecular hydrogen abstraction reaction even in the presence of a chiral amine and the rest are photoreduced to the corresponding alcohol. Within zeolites all 17 ketones yielded in presence of a chiral amine, the corresponding alcohol as the major product. When a chiral amine was used as the coadsorbent within alkali ion exchanged zeolites, enantiomerically enriched alcohol was formed in all cases. The best chiral induction was obtained with phenyl cyclohexyl ketone (enantiomeric excess: 68%). 1H-13C Cross Polarization Magic Angle Spinning (CP-MAS) experiments, with a model ketone (perdeuterated acetophenone) and chiral amine (pseudoephedrine) included within MY zeolites, suggested that the cation brings the reactant and the chiral amine closer. The role of the cation in such a process is also revealed by the computation results. The results presented here highlight the importance of a supramolecular structure in forcing a closer interaction between a reactant and a chiral inductor that could be used to achieve asymmetric induction in photoproducts.     

Generic pole assignability,structurally constrained controllers and unimodular completion

In this paper we assume dynamical systems are represented by linear differential-algebraic equations (DAEs) of order possibly higher than one. We consider a structured system of DAEs for both the to-be-controlled plant and the controller. We model the structure of the plant and the controller as an undirected and bipartite graph and formulate necessary and sufficient conditions on this graph for the structured controller to generically achieve arbitrary pole placement. A special case of this problem also gives new equivalent conditions for structural controllability of a plant. Use of results in matching theory, and in particular, ‘admissibility’ of edges and ‘elementary bipartite graphs’, make the problem and the solution very intuitive. Further, our approach requires standard graph algorithms to check the required conditions for generic arbitrary pole placement, thus helping in easily obtaining running time estimates for checking this. When applied to the state space case, for which the literature has running time estimates, our algorithm is faster for sparse state space systems and comparable for general state space systems.     

Crystal growth of phase matchable new organic nonlinear optical material for UV laser generation

L-histidinium tetrafluorosuccinate (L-HFS), an organic nonlinear optical material has been synthesized and characterized by the elemental analysis, FT-IR, FT-NMR and X-ray diffraction studies. Solubility of L-HFS was found to be higher in water than ethanol. Single crystals with dimensions 10 mm x 6 mm x 3 mm were grown in an aqueous solution by the slow evaporation technique at 30 degrees C. The thermal stability of L-HFS has been analyzed by thermogravimetric and differential thermal analyses (TGA and DTA). The UV-vis spectral study reveals that the material has a wide optical transparency in the entire visible region with the lower cutoff wavelength at 235 nm. The phase matching condition was obtained by Kurtz powder second harmonic generation (SHG) efficiency test. The laser damage threshold of the grown crystal was measured using a Q-Switched Nd:YAG laser (1064 nm).