20 research outputs found

    Genetic Enhancement Perspectives and Prospects for Grain Nutrients Density

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    Diet-induced micronutrient malnutrition continues to be a major challenge globally, especially in the developing world. With the ever-increasing population, it becomes a daunting task to feed millions of mouths with nutritious food. It is time to reorient agricultural systems to produce quality food to supply the calorie and nutrient requirements needed by the human body. Biofortification is the process of improving micronutrients density by genetic means. It is cheaper and sustainable and complements well with the nutrient supplementation and fortification— the short-term strategies that are currently deployed to address the micronutrient malnutrition. Sorghum is one of the important food crops globally, adapted to semi-arid tropics, and there is increased awareness on its nutritional importance. Further, there is great opportunity to improve sorghum for nutritional quality. This chapter deals about the genetic enhancement perspectives and prospects for improving the nutritional quality with main emphasis on grain micronutrient density in sorghum

    1H NMR Study of Molecular Motions and Phase Transitions in Methyl Ammonium Hexabromo Selenate [(CH3NH3)2SeBr6]

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    The temperature dependence of 1H spin-lattice relaxation time, T1, and that of the second moment, M2, are analysed in the temperature range 390 K to 77 K. A plot of T1 vs inverse temperature shows three phase transitions at 250 K, 167 K and 111 K. At 167 K, T1 displays a large jump while it shows changes in slope at 250 K and 111 K. In the high temperature phase (> 167 K), the correlated motion of CH3 and NH3 groups is found to cause the relaxation while their uncorrelated motion takes over in the low temperature phases (< 167 K). The unusual T1 behaviour in phase II (250 K-167 K) is ascribed to the small angle torsion of the cation. A constant M2 value of ∼ 9.7 G2, throughout the range of temperature studied, indicates the presence of reorientation of CH3 and NH3 groups

    NMR study of molecular dynamics in trimethyl ammonium hexabromo selenate [NH(CH3)3]2SeBr6[NH(CH_3)_3]_2SeBr_6

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    Temperature dependence of 1H^1H relaxation time, T1T_1, in the temperature range 387 to 77 K shows the presence of inequivalent trimethyl ammonium ions and methyl groups. The relaxation in the temperature range below 100 K is ascribed to the small angle torsion of the methyl groups. The variation of the second moment with temperature also reflects these internal motions (20 refs.

    NMR study of molecular dynamics and phase transitions in dimethyl ammonium hexabromo selenate [NH2(CH3)2]2SeBr6[NH_2(CH_3)_2]_2SeBr_6

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    1H^1H spin lattice relaxation study in the temperature range 439–77 K has been carried out in dimethyl ammonium (DMA) hexabromo selenate. A high temperature phase transition is observed as a dip in T1T_1 around 360 K, followed by a slope change a 222 K, and a discontinuous jump in T1T_1 at 154 K, which are also attributed to phase transitions. DMA diad axis motion and spin– rotation interaction are found to be the dominant mechanisms responsible for the observed T1T_1 behaviour above 222 K, while between 222 and 154 K, DMA torsional oscillations contribute significantly. Below 154 K the relaxation is governed by the methyl group dynamics. The motional effects are also reflected in the second moment variation with temperature

    Proton NMR Study of Molecular Dynamics and Phase Transitions in Trimethyl Ammonium Hexachloro Plumbate [NH(CH3)3]2PbCl6{[NH{(CH_3)}_3]}_2PbCl_6 and Tetramethyl Ammonium Hexachloro Plumbate [N(CH3)4]2PbCl6{[N{(CH_3)}_4]}_2PbCl_6

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    The proton spin lattice relaxation time (T1)(T_1) measured as a function of temperature in the range 424 to 119 K in trimethyl ammonium hexachloro plumbate [(TrMA)2PbCl6][(TrMA)_2PbCl_6] shows phase transitions at 340 and 119 K. The observed badly resolved minima in this compound are explained on the basis of C3 reorientations of inequivalent trimethyl ammonium and methyl groups. The computed second moment values, suggest the freezing of both types of reorientation around 117 K. Proton T1T_1 studies in tetramethyl ammonium hexachloro plumbate [(TMA)2PbCl6][(TMA)_2PbCl_6] in the temperature range 295 to 106 K shows a deep T1T_1 minimum at 180 K and a shallow one around 111 K, which are interpreted in terms of inequivalent tetramethyl ammonium (TMA) ions as well as CH3CH_3 reorientation

    Molecular dynamics in tetramethylammonium hexabromoselenate [N(CH3)4]2SeBr(6)[N(CH_3)_4]2SeBr(6). A proton NMR study

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    1H^1H spin-lattice relaxation time T1T_1 and second moment M2 have been studied as a function of temperature over the temperature range 445 to 77 K. A discontinuous change in T1T_1 at 365 K, indicates the presence of a phase transition, while the slope change at 152 K, is attributed to a change in the TMA ion dynamics from tumbling to torsion. The T1T_1 results could be explained in terms of inequivalent TMA ions and their small angle torsional oscillations. A second moment (M2) transition occurs around 160 K and is ascribed to the freezing of TMA tumbling and CH3CH_3 reorientation
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