1,1,1,1-Tetrakis(o-fluorophenylamino)silane tris[titanium(IV) chloride]. Evidence for a new titanium cation [Ti2Cl7]+

Si(NHC₆H₄F-o)₄ · 3TiCl₄ (1) has been obtained from the disproportionation of (CF₃CH₂O)₃SiNHC₆H₄F-o and TiCl₄ in petroleum ether (40–60 °C) at –10 °C. The analytical (elemental analysis, molar conductance) and spectral (i.r., ¹H- and ¹⁹F-n.m.r.) data suggested that (1) behaves as [Si(NHC₆H₄F-o)₄ · Ti₂Cl₇]⁺ [TiCl₅]^–. The presence of these ions has been confirmed by characterising the products of metathetical reactions of (1) with R₄NX (R = Bu and Et; X = I and Br) and with AgNO₃. The data suggest the presence of a new titanium cation [Ti₂Cl₇]⁺.     

Macroscopic recognition of iodide by polymer appended calix[4]amidocrown resin

ABSTRACT

The current study reveals the synthesis of polymer appended Calix[4]amidocrown-5 with specific binding affinity for iodide at ppm-level. The low detection limits are observed via UV-vis and fluorescence spectroscopy. The time-dependent solution and solid-state ¹²⁷I NMR studies with 18.8 and 19 ppm shifts, indicate a strong sensing nature of resin towards iodide ion. A significant reduction in surface area and pore volume with higher thermostability of resin after iodide uptake indicated iodide inclusion in the amidocrown cavity. The mechanism of iodide sensing may be governed by noncovalent interactions of NH and OH protons present in amidocrown and phenyl ring as observed in terms of emission enhancement in fluorescence spectroscopy. The binding affinity and stoichiometric determinations are determined by Benesi-Hildebrand and Jobs plots, respectively.     

Vibration and deflection analysis of thin cracked and submerged orthotropic plate under thermal environment using strain gradient theory

Nonlinear Dynamics - Based on a non-classical plate theory, a nonlinear analytical model is proposed to analyze transverse vibration of thin partially cracked and submerged orthotropic plate in the...     

A facile deprotection of oximes using glyoxylic acid in an aqueous medium

Oximes of ketones and aldehydes are efficiently deprotected with glyoxylic acid in an aqueous medium at room temperature. Oximes can be cleaved selectively in the presence of a TBDMS group. This method is high yielding, fast, clean, safe, cost effective, and therefore very suitable for practical organic synthesis.     

Absorption and fluorescence spectral studies of the interaction of sulpha drugs with α-cyclodextrin

The spectral characteristics of different drugs i.e. sulfanilamide, sulfanilic acid, sulfosalicylic acid dihydrate (SSAD) and sulfamethoxazole in aqueous α-cyclodextrin (CD) have been investigated at neutral pH. The formation of inclusion complexes of sulfa drugs with α-CD leads to the changes in fluorescence and absorption spectra which further enable the calculation of association constant of the bind processes by implementing the non-linear regression on the experimental data. The standard Gibbs energy ΔG was also calculated for the systems in which complex formation was observed. The α-CD study indicates that the sulpha drugs form 1:1 inclusion complex with α-CD.     

Uniqueness of the standard model neutral current predictions

In view of an excellent agreement between the recently determinedv _μ-hadron couplings and predictions of the standard model, the basic question discussed is how far its neutral current predictions can be mimiced in going either from the isodoublet to an isotriplet (or an even higher isospin) left-handed representation or from SU _L (2) × U(1) toG × U(1), whereG is a simple group of rank two. This question is addressed with reference to a sufficiently broad class of schemes. Their most distinctive properties are: in the higher isospin scheme, neutrino couplings are precisely in the form obtainable with standard l.h. representation; the higher g.g. scheme isL+R type in which, to each light fermion of evenRU parity, a superheavy fermion of the same charge and oddRU parity is associated, parity conservation forbidding their mixing. Reasons for excluding theL-type andG ₂ higher g.g. schemes are given. Their neutral current predictions are compared with those of the standard model. A higher isospin representation can mimic the predictions of the standard model in inclusive and semi-inclusivev _μ-hadron reactions but is conclusively discriminated from the isodoublet representation by elasticv _μ ⁽⁻ p scattering. TheG × U(1) scheme can mimic standard model neutrino sector but is conclusively discriminated from minimal scheme by parity violating effects.