Instrumentation for multi-detector arrays

The new generation of detector arrays require complex instrumentation and data acquisition system to ensure increased reliability of operation, high degree of integration, software control and faster data handling capability. The main features of some of the existing multi-detector arrays like MSU 4π array, Gammasphere and Eurogam are summarized. The instrumentation for the proposed INGA array in India is discussed.     

Rotational structures in 123Cs

High-spin states in ¹²³Cs, populated via the ¹⁰⁰Mo ( ²⁸Si, p4n) fusion-evaporation reaction at E _lab = 130 MeV, have been investigated employing in-beam γ-ray spectroscopic techniques. Rotational bands, built on πg _7/2, πg _9/2 and the unique-parity πh _11/2 orbitals, have been extended and evolve into bands involving rotationally aligned ν(h _11/2)² and π(h _11/2)² quasiparticles. A three-quasiparticle band based on the high-K πh _11/2 ⊗ νg _7/2 ⊗ νh _11/2 configuration has also been observed. Total Routhian Surface (TRS) calculations have been used to predict the nuclear shape parameters ( β₂, β₄, γ) for the various assigned configurations. The assigned configurations have been discussed in the framework of a microscopic theory based on the deformed Hartree-Fock (HF) and angular-momentum projection techniques.     

Calorimetry and thermal analysis studies on the binding of 13-phenylalkyl and 13-diphenylalkyl berberine analogs to tRNAphe

The interaction of 13- monophenylalkyl and diphenylalkyl berberine analogs with tRNA^phe has been investigated using various thermochemical techniques like thermal melting, isothermal titration calorimetry, and differential scanning calorimetry experiments. Thermal melting studies revealed that all the analogs stabilized the tRNA^phe better than berberine. The binding affinity for the analogs was of the order of 10⁵ M^?1. Calorimetry results suggested that the binding of these analogs was predominantly entropy driven with small negative enthalpy contribution to the standard molar Gibbs energy. The temperature dependence of the standard molar enthalpy changes yielded negative values of standard molar heat capacity changes for the complexation revealing substantial hydrophobic contribution in the RNA binding of these analogs. An enthalpy–entropy compensation behavior was also seen in all the systems. The diphenylalkyl analogs were found to be more effective tRNA^phe binders compared to the monophenylalkyl analogs. The utility of the present work lies in understanding the structural and energetic aspects of the interaction of these berberine analogs with tRNA, which may be useful in the development of RNA-targeted drugs.     

Ambient temperature thermotropic liquid crystalline viologen bis(triflimide) salts

Two dicationic salts with bis(triflimide) as counterions exhibited crystal-to-smectic liquid crystalline phase transitions (T _m=41 and 37°C) and smectic-to-isotropic liquid phase transitions (T _i=112, 136°C). They had a broad liquid crystalline phase range (71–99°C) and an excellent range of thermal stability (360–364°C). Their mixtures of various compositions also displayed liquid crystalline properties from r.t. to an extended range of temperatures. They exhibited fluorescence in 1, 2-dimethoxyethane and methanol.     

Synthesis and characterisation of thermotropic liquid-crystalline properties of azomethine dimers

A series of azomethine dimers were prepared by condensation reactions of benzaldehyde, biphenylcarboxaldehyde and 9-anthraldehyde with various aromatic diamines of varying flexibility in ethanol in the presence of tosic acid. Their chemical structures were determined by Fourier transform infrared and ¹H and ¹³C nuclear magnetic resonance (NMR) spectroscopies, as well as elemental analysis. Their thermal properties were also examined by using a number of experimental techniques, including differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), polarising optical microscopy (POM) and variable temperature X-ray diffraction (VTXRD). Azomethine dimer, prepared from benzaldehyde and 1,9-bis(4-aminophenoxy)nonane, exhibited a monotropic, nematic liquid-crystalline (LC) phase. The majority of the azomethine dimers containing biphenyl moieties exhibited enantiotropic, nematic LC phase on melting at relatively low temperatures, since they developed typical Schlieren, threaded or marbled textures in their LC phase. They also had accessible isotropisation temperatures well below their decomposition temperatures. Azomethine dimers containing anthracene moieties did not exhibit LC properties, but exhibited polymorphism as determined by POM and VTXRD in two cases. All of these azomethine dimers in the series had excellent thermal stability that was in the broad range of temperatures of 307–400°C depending on their degrees of aromaticity index.     

Spin-parity measurements in the neutron-rich N ∼ 20 34P and 36S nuclei

Yrast and near-yrast energy levels in the neutron-rich N ∼ 20 nuclei ³⁴P, ³⁶S were populated using transfer/deep-inelastic processes following the ³⁴S + ¹¹⁵In reaction at an incident energy of 140MeV. The use of a multi-clover array has facilitated polarization measurements of the observed γ-rays and necessitated some changes in the previously known level scheme. The observation of the negative-parity levels in these nuclei on the periphery of the “island of inversion” is indicative of the influence of the intruder orbitals on the level structure at low spins. Shell-model calculations indicate that the inclusion of the orbitals from the upper pf shell is important even for the low-lying positive-parity states.     

Ambient temperature thermotropic liquid crystalline viologen bis(triflimide) salts

Two dicationic salts with bis(triflimide) as counterions exhibited crystal-to-smectic liquid crystalline phase transitions (T_m=41 and 37°C) and smectic-to-isotropic liquid phase transitions (T_i=112, 136°C). They had a broad liquid crystalline phase range (71-99°C) and an excellent range of thermal stability (360-364°C). Their mixtures of various compositions also displayed liquid crystalline properties from r.t. to an extended range of temperatures. They exhibited fluorescence in 1, 2-dimethoxyethane and methanol.     

High spin states in116Te

The high spin states in¹¹⁶Te were populated in the Ru(¹⁹F,p4n) reaction at E_lab=90MeV and the subsequent deexcitation was studied using the γ-ray spectroscopic techniques. Ninteen new transitions have been added to extend the level scheme. A ΔI=2 rotational band is identified for the first time in an even-A Tellurium nucleus.