Role of Coster-Kronig transitions in multiply-ionized states formed in heavy-ion collisions

The usually allowed Coster-Kronig L₁L_2,3M transitions are found not to be energetically possible for all electronic configurations with a single K-shell and multiple L-shell vacancies of Al. Consideration of these effects as related to X-ray measurements in heavy-ion-atom collisions are presented.     

Nitro,Nitrito and Nitrato Derivatives of Dicyclopentadienyl Thallium(III) Chloride and Bis Indenyl Thallium(III) Chloride

Six new complexes of thallium(III) of the formula (π-D)₂Tl(L) (where D= cyclopentadienyl or indenyl group and L=nitro, nitrito or nitrato group) have been prepared and characterised on the basis of I. R. studies and some thermal properties of these complexes.     

Synthesis and biological evaluation of bile acid dimers linked with 1,2,3-triazole and bis-beta-lactam

We report herein the synthesis and biological evaluation of bile acid dimers linked through 1,2,3-triazole and bis-beta-lactam. The dimers were synthesized using 1,3-dipolar cycloaddition reaction of diazido bis-beta-lactams , and terminal alkynes derived from cholic acid/deoxycholic acid in the presence of Cu(i) catalyst (click chemistry). These novel molecules were evaluated in vitro for their antifungal and antibacterial activity. Most of the compounds exhibited significant antifungal as well as antibacterial activity against all the tested fungal and bacterial strains. Moreover, their in vitro cytotoxicities towards HEK-293 and MCF-7 cells were also established.     

Ratiometric sensing of Hg2+ based on the calix[4]arene of partial cone conformation possessing a dansyl moiety

A new fluorescent chemosensor based on the calix[4]arene of partial cone conformation possessing a dansyl moiety has been synthesized. The chemosensor demonstrates selective optical recognition of Hg(2+) and Cu(2+) in two contrasting modes. The receptor exhibited ratiometric sensing of Hg(2+) and "ON-OFF" type of fluorescence behavior in the presence of Cu(2+). The compound behaves as a fluorescent molecular switch upon chemical inputs of Hg(2+) and Cu(2+) ions.     

A novel synthesis of 2-substituted 2H-imidazo[1,5-<Emphasis Type="Italic">b</Emphasis>]isoquinoline-1,5-diones by <Emphasis Type="Italic">in situ</Emphasis> desulfurization

A novel synthesis of 2-substituted 2H-imidazo[1,5-b]isoquinoline-1,5-diones by reductive desulfurization of a variety of 2-substituted 3-thioxo-2H-imidazo[1,5-b]isoquinoline-1,5-diones is reported with nickel boride in dry methanol at ambient temperature. __________ Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 404–408, March, 2008.     

Polysaccharide-Silica Hybrids: Design and Applications

This article discusses and reviews the current status and future perspectives of silica hybrids of polysaccharides and biosilicas derived thereof. The hybrids have been produced in various morphological shapes and utilized in water remediation, separation, enzyme immobilization, sensor, and biomedical fields. The polysaccharides show templating and structure directing influence in manipulation of sol gel silica hybrid materials which can be calcined to derive functional biosilicas. The development of energy storage devices and white light emitting solid phosphors may be the fields of future research.     

Development and validation of stability indicating analytical method for Ilaprazole

The objective of the present study was to develop and validate a rapid and simple stability indicating analytical method for estimating Ilaprazole. Ilaprazole was subjected to different stress conditions prescribed by International Conference on Harmonization (ICH) such as hydrolysis, oxidation, photolytic and dry heat degradation conditions. The drug was very susceptible to degradation under hydrolysis and photolytic conditions, less susceptible to oxidation and stable under dry heat degradation condition. An acceptable separation of drug and its degradants was achieved by using a C-18 column and mobile phase composed of ammonium acetate buffer (pH 3.2)—acetonitrile (55: 45, v/v). Flow rate was 1 mL/min and detection wavelength was set at 303 nm. Retention time of drug was found to be 6.6 min and analysis can be completed within 10 min. The method was validated with respect to linearity, precision, accuracy, robustness, LOD and LOQ as per ICH. The method was linear (R² = 0.996) in the range of 2.5–250 μg/mL. The recovery was in the range from 99.2–100.2%.     

Diastereoselective synthesis of novel 3-aryloxy/alkoxy-4-benzothiazolylpyrazolyl-β-lactams: Potential synthons for novel aminoacids/nanocopolymers

A fast, efficient, and diastereoselective synthesis of novel 3-oxo-4-benzothiazolylpyrazolyl-β-lactams is described. The reaction between 2-aryloxy/alkoxyacetic acid and novel benzothiazolylpyrazole-substituted imines afforded exclusive formation of trans-β-lactams. The scope of the reaction was investigated by varying different groups on substrates (R¹, R², R³, Z). All the novel compounds were characterized using various spectroscopic techniques such as FT-IR, ¹H NMR, ¹³C NMR, elemental analysis, and mass spectrometry in representative cases. No report has been listed in the literature for the synthesis of these types of β-lactam heterocycles so far.     

Stereoselective synthesis of novel C-3 functionalized 3-sulfonyl-β-lactams: Promising biologically active heterocyclic scaffolds

An efficient and operationally simple strategy for the stereoselective synthesis of novel C-3 functionalized 3-sulfonyl-β-lactam heterocycles is described. The C-3 functionalized 3-phenyl/benzylsulfonyl-β-lactams 3/3′, 5/5′ has been synthesized via Michael addition using different Michael acceptors on trans-3-phenyl/benzylsulfonyl-β-lactams 2(a–f) using K₂CO₃ as a base and acetonitrile/DMF as solvents. The reaction furnished exclusively cis-β-lactam adducts 3(a–r) using sterically less hindered Michael acceptors. Further, the effect of steric bulk and chiralilty of Michael acceptors was explored to achieve target C-3 functionalized β-lactams 3(s-u)/3′(s-u) and 5(a–c)/5′(a–c). The structural and stereochemical analysis of novel β-lactams were carried out using FT-IR, NMR (¹H, ¹³C, ¹H-¹H COSY, ¹H-¹³C COSY and ¹³C DEPT-135), elemental analysis (CHNS), mass spectrometry (EIMS and LCMS) in representative cases and single crystal X-ray crystallographic studies (3e). The cis or trans configuration of the Michael acceptor (E) at C-3 was assigned with respect to C4-H.