Studies on the thermal behaviour of mono- and di-imines of some diaminonaphthalenes

The mono- and di-imines of some diaminonaphthalenes were prepared using a solid solid reaction technique. Their structures were studied using elemental analysis, infrared and electronic spectra. The thermal behaviour of the obtained compounds and their solid solid preparation reactions have also been studied. The energies of activation as well as the reaction orders of those reactions were determined.     

A convenient synthesis of a novel fused tetracyclic heterocoumarin

New tetracyclic 6H‐[1]benzopyrano[3,4‐e]pyrazolo[1,5‐a]pyrimidin‐6‐ones ( 4a‐e ) have been synthesized through the condensation under acidic conditions of [1]benzopyrano[4,3‐c][1,5]‐benzodiazepin‐7(8H)‐one ( 1 ) and a series of 3,4‐disubsituted 5‐amino‐1H‐pyrazoles 3a‐e .     

Spectroscopic and Electrochemical Studies of Some Molybdenum and Ruthenium Complexes of N-[(2-pyridyl)methyl]-2,2′-dipyridylamine

Interaction of the tripodal ligand N-[(2-pyridyl)methyl]-2,2′-dipyridylamine (pmdpa) with [Mo(CO)₆] under reduced pressure gave two complexes [Mo(CO)₄(pmdpa)] and [Mo(CO)₂(pmdpa)₂], depending on the mole ratio and reaction time. The i.r. spectra of the two complexes gave patterns in the metal carbonyl region confirming the proposed structures. Reaction of [Ru₃(CO)₁₂] with pmdpa in benzene gave the mononuclear complex [Ru(CO)₃(pmdpa)]. The electronic absorption spectra of the complexes exhibited visible transitions due to metal-to-ligand charge transfers. Electrochemical investigation of the complexes showed some irreversible and quasi-reversible redox reactions due tautomeric interconversions through electron transfer.     

Electronically and sterically tuned trans labilization controls the substitution behaviour of cobaloximes

The kinetics of axial water substitution by cysteine in six different cobaloximes, viz.trans-RCo(Hdmg)(2)H(2)O, where Hdmg = dimethylglyoximate, R = cyclo-C(5)H(9) (c-P), CH(3)CH(2) (Et), CH(3) (Me), C(6)H(5)CH(2) (Bz), C(6)H(5) (Ph) and CF(3)CH(2), were studied as a function of cysteine concentration, temperature and pressure. It was found that cysteine substitutes the coordinated H(2)O molecule trans to the alkyl group with second order rate constants that follow the order of reactivity: c-P > Et > Bz > Me > Ph > CF(3)CH(2). Rate and activation parameters (Deltan H(++), Delta S(++) and Delta V(++)) enable the formulation of a reaction mechanism that can account for the substitution behaviour of the investigated alkylcobaloximes. In particular, a gradual mechanistic changeover from I(d) to I is observed along the series of R groups from c-P to CF(3)CH(2).     

Enzyme inhibitory constituents from Duranta repens

Isoprenylated flavonoids 5,7-dihydroxy-3'-(2-hydroxy-3-methyl-3-butenyl)-3,6,4'-trimethoxyflavone (1), 3,7-dihydroxy-3'-(2-hydroxy-3-methyl-3-butenyl)-5,6,4'-trimethoxyflavone (2) and an isoprenylated acetophenone derivative (3) have been isolated from Duranta repens along with known compounds, 5-hydroxy-3,6,7,4'-tetramethoxyflavone (4), rosenonolactone (5), 6,7-dimethoxycoumarin (6), 5alpha,8alpha-epidioxyergosta-6,22-dien-3beta-ol (7) and 5alpha,8alpha-epidioxyergosta-6,9(11),22-trien-3beta-ol (8), isolated for the first time from this species. Their structures and the relative configuration were determined by spectroscopic methods (1H- and 13C-NMR, IR, UV and MS) and two-dimensional (2D)-NMR experiments. The compounds 1-5 showed inhibitory activity against prolyl endopeptidase while 4 and 5 were also active against thrombin.     

An abstract Dirichlet problem in the Hilbert space

In the present paper, we consider an abstract partial differential equation of the form $\frac{{\partial ^2 u}}{{\partial t^2 }} - \frac{{\partial ^2 u}}{{\partial x^2 }} + A\left( {x,t} \right)u = f\left( {x,t} \right)$ , where $\left\{ {A\left( {x,t} \right):\left( {x,t} \right) \in \bar G} \right\}$ is a family of linear closed operators and $\bar G = G \cup \partial G,G$ is a suitable bounded region in the (x, t)-plane with boundary?G. It is assumed thatu is given on the boundary?G. The objective of this paper is to study the considered Dirichlet problem for a wide class of operatorsA(x, t). A Dirichlet problem for non-elliptic partial differential equations of higher orders is also considered.     

Detection of necking deformation along polypropylene fibres axis at low draw ratios using multiple-beam microinterferometry

A modified drawing device attached with an automated system for producing multiple-beam Fizeau fringes in transmission is used to study the mechanical deformation along polypropylene (PP) fibres at low draw ratios. Two drawing processes are used for drawing PP fibres. In the first process (fast drawing), the necking deformations are formed at draw ratios from 1.2 to 1.9 along the fibre axis. While in the other process (slow/step drawing), these deformations disappeared. The refractive indices calculated at different positions along the fibre axis during the fast- and slow-drawing processes. To overcome the formation of necking deformation along the PP fibres during fast-drawing process, the slow-drawing technique is recommended. Microinterferograms are given for illustration.     

Kinetics and mechanism of the catalysed decomposition of sodium perborate by the ethylenediaminetetraacetatoiron(III) complex

The rate of reaction of [Fe^IIIY] (Y = EDTA anion) with NaBO₃ was studied in aqueous 0.1 M NaNO₃ at various temperatures. The observed rate constant,k _obs = kKKK ₁[FeEDTA(H₂O)^-]/{[H⁺] + KK ₁[FeEDTA(H₂O)^-]}applies over the pH range studied. The monohydroxy complex, [FeEDTA (OH)]^2– is the catalyst which reacts with the peroxy ion to produce a violet intermediate complex. The composition of perborate confirms to Michaelis–Menten kinetics, the rate-determining step involving breakdown of the intermediate complex. The activation enthalpy and activation entropy were calculated.     

Detecting and avoiding the necking deformation along polypropylene fibre axis using the fringe pattern analysis of multiple-beam microinterferometry

A fibre-drawing device attached with the system for producing multiple-beam Fizeau fringes in transmission is used to optimize the optical properties during the cold drawing of polypropylene (PP) fibres. This system is automated for interference pattern analysis. Two drawing processes for the PP fibres are applied and investigated. The first one is fast drawing in which the necking deformation is predicted and the other is the slow (step) drawing in which the necking can be avoided. The refractive index profiles (n and n) of PP fibres are determined at different positions along the fibre axis during the fast and slow drawing processes. The fibre interference patterns are automatically digitized and stored in a computer storage media. The slow drawing technique for PP fibres is recommended to overcome the deformation difficulties along the fibre axis due to necking during the drawing processes. Microinterferograms in case of light vibrating parallel and perpendicular to the fibre axis are given for illustration.     

Crystallographic report: Bis{µ‐[O‐cyclopentyl(4‐methoxyphenyl) dithiophosphonato]1κ:S,2κ:S‐[O‐cyclopentyl(4‐methoxyphenyl)dithiophosphonato]1κ2S,S′} dizinc(II)

The centrosymmetric [Zn₂{CH₃OC₆H₄P(OC₅H₉)S₂}₄], features an eight‐membered Zn₂S₄P₂ ring as a result of two bidentate bridging thiolate ligands; the remaining ligands are chelating. Copyright © 2005 John Wiley & Sons, Ltd.