A simple and cost-effective synthesis of sulfated β-cyclodextrin and its application as chiral mobile phase additive in the separation of cloperastine enantiomers

Journal of Inclusion Phenomena and Macrocyclic Chemistry - A simple and cost-effective method for the synthesis of sulfated β-cyclodextrin, one of the most widely used chiral mobile phase...     

Rotary disc bioreactor-based approach for bacterial nanocellulose production using Gluconacetobacter xylinus NCIM 2526 strain

Bacterial nanocellulose (BNC) is an indomitable biomaterial of utmost usage in different technological areas. Previously, the BNC production has been reported in the simplified bioreactors. Thus, pioneering bioreactor-assisted strategies are desirable for the commendable BNC production. Advanced bioreactors must be corroborated along with different bacterial strains to obtain creditable BNC yield. This study deals with BNC production in rotary disc bioreactor (RDBR) using Gluconacetobacter xylinus NCIM 2526 strain. RDBR-based production of BNC provided 189?±?14 gL^?1 of wet BNC, i.e., equivalent to 6.6?±?0.3 gL^?1 dry BNC yield in 10 days. However, in static cultivation mode, 56?±?12 gL^?1 wet weight of BNC, corresponding to 2.4?±?0.4 gL^?1 dry weight, was produced. Thus, BNC production was approximately 2.75 folds higher in RDBR than statically produced BNC from the same volume of the media. The sugar to BNC conversion yield (12.2?±?0.8%) was doubled in RDBR-based production as compared to static BNC production (6.2?±?1.4%) with efficient sugar consumption (90.0?±?3.3%). The maximum amount of BNC was produced at 7 RPM and pH 6. RDBR-based BNC showed a more hydrophilic nature than statically produced BNC. The RDBR might be appropriate for large-scale BNC production, especially for wet-end applications, as an ample amount of BNC can be produced from a single fermentation process. These BNC pellicles might have the potential for biomedical applications like wound dressings, biofacial masks, hydrogels, and tissue engineering scaffolds.

     

Magnetic Modulation in Heteroallene and Heterocumulene Based tert-butyl Nitroxide Diradicals: Spin Delocalization and Conformation Play Crucial Roles

We have theoretically investigated the magnetic properties of heteroallene (>C=C=X−) and heterocumulene (>C=C=C=X−) based tert-butyl nitroxide diradicals (X is P/As). Calculation of magnetic exchange coupling constant (J) shows ferromagnetic interaction in heteroallene based diradicals. Whereas, in heterocumulene based diradicals, tuning of J value from antiferro- to ferro-magnetic state is observed from Z- to E- isomer. Delocalization of spin density from radical site to the coupler (in planar arrangement) is observed in spin distribution analysis which is also advocated by molecular orbital analysis. The typical feature of tert-butyl nitroxide radical creates spin delocalization along with spin polarization within the coupler. The J values of all the diradicals strongly depend on the dihedral angle between radical center and coupler. Magneto-structural correlation shows that the change in dihedral angle tunes the magnetic property for both the Z- and E- isomers of heterocumulenes depending on the spin accumulation on two nearby magnetic centers. The extent of spin delocalization and conformation of spin centers on the molecular axis are important for the different J values observed in our designed systems.     

On the Control of Magnetic Anisotropy through an External Electric Field

The effect of an external electric field on the magnetic anisotropy of a single‐molecule magnet has been investigated, for the first time, with the help of DFT. The application of an electric field can alter the magnetic anisotropy from “easy‐plane” to “easy‐axis” type. Excitation analysis performed through time‐dependent DFT predicts that the external electric field facilitates metal to π‐acceptor ligand charge transfer, leading to uniaxial magnetic anisotropy and concomitant spin Hall effect in a single molecule.     

Nickel(II)-Mediated Reversible Thiolate/Disulfide Conversion as a Mimic for a Key Step of the Catalytic Cycle of Methyl-Coenzyme M Reductase

According to the well-accepted mechanism, methyl-coenzyme M reductase (MCR) involves Ni-mediated thiolate-to-disulfide conversion that sustains its catalytic cycle of methane formation in the energy saving pathways of methanotrophic microbes. Model complexes that illustrate Ni-ion mediated reversible thiolate/disulfide transformation are unknown. In this paper we report the synthesis, crystal structure, spectroscopic properties and redox interconversions of a set of Ni^II complexes comprising a tridentate N₂S donor thiol and its analogous N₄S₂ donor disulfide ligands. These complexes demonstrate reversible Ni^II-thiolate/Ni^II-disulfide (both bound and unbound disulfide-S to Ni^II) transformations via thiyl and disulfide monoradical anions that resemble a primary step of MCR's catalytic cycle.     

Dielectric loss of poly(vinylacetate) at electric fields of 400 kV/cm

Using quasi-steady-state and time-resolved high-field impedance techniques, the frequency-dependent dielectric permittivity of poly(vinylacetate) has been studied at electric field amplitudes as high as 400 kV/cm. The relative changes of the dielectric loss depend quadratically on the field amplitude and reach about 1 %. The magnitude and frequency-dependence of this non-linear dielectric effect and its time evolution after applying the high field are consistent with energy absorption from the field being at the source of the non-linear behavior. Based upon a phenomenological model of heterogeneous dynamics at isothermal conditions, the observed changes can be explained by locally increased configurational temperatures and the resulting accelerated dynamics.     

Quasi-diamagnetism and exchange anisotropy in Ni-Mn-In-Co Heusler alloys

The quasi-diamagnetism effect that manifests itself in the negative magnetic susceptibility observed in weak magnetic fields during cooling of samples below some critical temperature has been revealed in Ni₄₈Co₂Mn₃₅In₁₅ Heusler alloys. The effect has been attributed to a strong nonequilibrium of the system due to the presence of magnetic and structural disorders and exchange anisotropy.     

Investigation of the solid phase synthesis of tyrosine‐derived diphenol monomers with resin‐bound carbodiimide coupling reagents

Tyrosine‐derived pseudo‐polypeptides have recently been established as potential biomaterials. The bulk production of these polymers is dependant upon the convenient synthesis of tyrosine‐derived diphenolic monomers. Suitable solution phase methods for the synthesis of such monomers, with transient activated esters, have been reported previously by Kohn, J.; Langer, R. In Biomaterials Science: An Introduction to Materials in Medicine; Ratner, B. D.; Hoffman, A. S.; Schoen, F. J.; Lemons, J. E., Eds.; Academic Press: New York, 1996; pp 64–72. However, for all the methods reported by them, purification and isolation of the diphenol monomer involves rigorous extraction, column purification, or an extensive aqueous workup. These may lead to the incorporation of solvent‐based as well as inorganic impurities and also may lead to difficulties in the process scale‐up. In this article, an alternate and relatively more convenient method for the synthesis of tyrosine‐based diphenol monomers is reported. This involved the investigation of polymer resin‐bound carbodiimide in the solid‐phase synthesis of L‐tyrosine‐based diphenolic monomers. This method was found to eliminate the need for rigorous purification processes and was found to maintain reasonable yield as well as maintain purity of the final monomer product. The monomer was able to produce polymers of a reasonably high‐molecular‐weight and a narrow polydispersity. The amide bond formation by such a polymer‐tethered reagent can be described to follow a reverse‐Merrifield sense and the method is relatively convenient to scale up. The L‐tyrosine‐based diphenolic monomeric compound formed by this method was analyzed by NMR, Fourier transform infrared, and elemental microanalysis techniques for chemical structure and composition. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 4906–4915, 2004     

Decay of90m,g Rb

The decay of mass separated⁹⁰Rb has been studied usingβ,γ and conversion electron spectrometers in single and coincidence modes. The half-lives of the ground state and the isomeric level have been confirmed to be 162± 3 and 258±4 s, respectively. Theγ-rays from the decays of ground state and metastable state have been identified by measuring the decay of individual photopeaks using Ge(Li) detectors. The multipolarity of the 106.6 keV isomeric transition has been determined to beM3. Separate decay schemes of the ground and metastable states are presented. The levels of⁹⁰Sr are discussed in terms of the available experimental and theoretical information. Radioactivity.^90m,gRb [from²³⁸U(p, f)]; measuredT _1/2,E _γ,I _γ,γ—γ coin,I _ce,cc,E _β deduced logft,⁹⁰Sr levels, mass separated⁹⁰Rb.