Synthesis, structure and spectral investigation of hydrogen bonded helical chain in mixed ligand Cu(II) pyrimidone complex.

A simple mono-aqua-dichloro copper(II) pyrimidone complex has been synthesized and characterized using various spectral techniques such as Infrared and Raman in addition to the single crystal X-ray diffraction. The single crystal X-ray analysis carried out for the complex under study brings out the fact that there are two molecules in the unit cell with parameters a = 9.657(2); b = 3.857(2); c = 10.781(2); alpha = 90 degrees; beta = 107.781 degrees; gamma = 90 degrees; V = 382.891 and are crystallized in monoclinic crystal system with Pn space group. In solid state the molecules are interconnected through strong hydrogen bonding [O4...H21-O2W = 2.644 angstroms; O4...H21 = 1.853 angstroms; angleO4...H21-O2W = 172.87 degrees;] formed between the coordinated water molecule (O2W) and the exocyclic ketonic oxygen of the pyrimidone ring (O4). This H-bonding interaction causing a twist in the C1=O1...H21 segment [angleC1=O1...H21 = 122.29 degrees] in combination with weak pi-pi stacking interaction (3.857 angstroms) of the adjacent pyrimidone rings brings the single stranded helical chain which possesses both P and M sense of supramolecular helical assembly. The internal and external modes of vibrations of the crystal under study have been estimated and discussed by applying group theoretical methods.

Vibrational spectroscopic analysis of cytosine monohydrate and its copper(II) complex.

Single crystals of cytosine monohydrate and its copper(II) complex were grown by slow evaporation in an aqueous solution at room temperature. The solubility studies were carried out at different temperatures in deionized water. Cytosine monohydrate and the copper(II) complex of cytosine were characterized by recording IR, Raman and UV spectra. The various vibrational modes of the crystals have been classified using factor group and site group analysis. Vibrational assignments were proposed for both the systems based on the spectral investigations.

Crystal growth, structural and spectroscopic analysis of hypoxanthinium chloride monohydrate.

Protonated form of hypoxanthinium chloride monohydrate single crystal has been grown from dilute hydrochloric acid. Single crystal X-ray analysis was carried out and the titled crystal belong to the monoclinic P2(1)/c space group. Hypoxanthine is protonated at N(1) with the hypoxanthine cations, linked to chlorine anion via weak bifurcated N-H...Cl hydrogen bonds and interconnected by hydrogen bonding contacts of the type N-H...O. Infrared, Raman and UV spectroscopic tools were applied to characterize hypoxanthinium chloride monohydrate. By applying group theoretical methods the internal and external modes of vibrations of the title crystal have been identified and discussed.

Membrane bound Indian clade C HIV-1 envelope antigen induces antibodies to diverse and conserved epitopes upon DNA prime/protein boost in rabbits.

The partial success of RV144 human clinical trial demonstrated that ALVAC prime/envelope protein boost vaccine regimen may represent a promising strategy for the development of an effective HIV-1 vaccine. Our earlier study demonstrated that a trimeric HIV-1 envelope gp145 from an Indian clade C isolate elicited cross clade neutralizing antibodies primarily towards Tier 1 isolates. In the present study, we examined the immunogenicity of DNA prime/envelope protein boost vaccine in rabbits using gp160 DNA of the Indian clade C isolate with various cytoplasmic tail truncations and trimeric gp145 protein. Cytoplasmic tail mutants of gp160 exposed epitopes that reacted strongly with a number of broadly neutralizing human monoclonal antibodies against HIV-1. Overall, envelope specific titers were found to be similar in all rabbit groups with higher pseudovirus neutralization in protein only immunized rabbits. The complete linear epitope mapping of rabbit immune sera revealed strong binding to C1, C2, V3, C3 and C4 domains of gp145. Importantly, reactivity of gp41 ecto-domain peptides was observed in DNA prime/protein boost sera but not in the sera of rabbits immunized with protein alone. Moreover, membrane anchored but not soluble envelope encoding DNA immunization elicited antibodies against linear epitopes on the conserved gp41 ecto-domain. Together, these results suggest that priming with DNA encoding cytoplasmic domains of Env alters the quality of antibodies elicited following protein boost and hence may be utilized to generate protective immunity by HIV-1 vaccine.

Rosai-Dorfman disease of the central nervous system.

Rosai-Dorfman disease (RDD) is an idiopathic, non-neoplastic, lymphoproliferative disorder characterized by sinus histiocytosis and massive lymphadenopathy. When RDD involves the central nervous system the lesion simulates a meningioma. Histological and immunohistochemical confirmation is essential for a definitive diagnosis. In this paper, ten cases of RDD confined to the central nervous system are reported. Another case with orbital RDD was excluded. Nine cases involved the cranial cavity alone; in one, the cervical extradural region was also involved. Treatment consisted of surgical excision or biopsy. Histology and immunohistochemistry revealed a mixed cell population of predominantly mature histiocytes with evidence of emperipolesis and strong positivity for S100 protein in all cases. No recurrence was observed during follow up ranging from three months to eight years.

Solvent extraction separation of hafnium with 4-methyl-3-pentene-2-one.

A new method for the extractive separation of hafnium from zirconium is presented. Zirconium is extracted with pure mesityl oxide from 4M nitric acid/4M sodium nitrate medium, followed by extraction of hafnium with mesityl oxide from 0.4M hydrochloric acid/2M ammonium thiocyanate medium. It is possible to accomplish clean separations of Hf from Zr in ratios from 1:20 to 1:200. The separation of hafnium from commonly associated elements such as scandium, yttrium, uranium, thorium, alkali and alkaline earth metals in 500:1 weight ratio to hafnium is also possible.

Liquid-liquid extraction of arsenic(III) with diluted tributyl phosphate.

A 40% tributyl phosphate solution in xylene was used for the quantitative extraction of arsenic(III) from 4M hydrochloric acid/2M lithium chloride. It was stripped from the organic phase with water and determined volumetrically with potassium bromate. The period of equilibration was 3 min. Arsenic was extracted in presence of copper, cobalt, nickel, tin, bismuth, iron, cadmium and other elements which are usually associated with it in sulphide minerals and alloys.

Non linear optical analyses of hexamine: phenol cocrystals based on hydrogen bonding: a comparative study.

Fourier-Transform Infrared (FT-IR) spectroscopy supported by Raman spectroscopy has been employed to explain the conventional and unconventional hydrogen bonding present in the 4,4'thiodiphenol: hexamine and 4,4'sulfonyldiphenol: hexamine cocrystals. The possible internal and external vibrational modes are predicted through factor group analysis. Influence of intra molecular charge transfer (ICT) interaction caused by the strong ionic ground state hydrogen bonding between charged species, giving rise to a non centro symmetric structure which is a criterion for second harmonic generation (SHG) efficiency has been discussed. Intense low wave number hydrogen bond vibrations in Raman which arise due to electron-phonon coupling are analyzed. Optical quality of adducts is identified through UV-Vis analysis. The second harmonic generation efficiency of both adducts is determined by Kurtz-Perry method.

Nonlinear optical analyses of organic N-(9-Anthrylmethylidene) methylamine Schiff base.

The organic NLO Schiff base of N-(9-Anthrylmethylidene) methylamine was synthesized by condensation process. The material was characterized through Powder XRD, FT-IR, and Raman techniques. The various planes of reflection are identified from the Powder XRD pattern. The formation of Schiff base is confirmed through FT-IR and Raman analysis. The intra molecular charge transfer interaction and the existence of the first-order molecular hyperpolarizability (ß) are identified from the red shift of the UV-Vis analysis. The structure of the molecule was optimized by density functional theory (DFT) using B3LYP method with 6-31G basis set. The NBO analysis is used to interpret the delocalization. The dipole moment and first hyperpolarizability values were also computed by HF/6-31G. These values indicate that the compound is a good candidate with nonlinear optical properties. This is the first time report on the existence of a second harmonic generation (SHG), χ(2), efficiency that has been identified by Powder Kurtz-Perry method.