Synthesis of Nickel Oxide Nanoparticles from Thermal Decomposition of a New Precursor

Nickel oxide nanoparticles (25 nm) have been synthesized via decomposition of a new precursor nickel octanoate Ni(octa)₂ in the presence of oleylamine (C₁₈H₃₇N) and triphenylphosphine (C₁₈H₁₅P), in mild conditions. To control the particle size and morphology, combination of C₁₈H₁₅P and C₁₈H₃₇N were applied as surfactants. In this process, oleylamine was used as both the medium and the stabilizing reagent. C₁₈H₃₇N and C₁₈H₁₅P play an important role in preventing aggregation of NiO nanoparticles. The products were characterized by XRD, SEM, TEM, FT–IR, and TGA.     

Polycaprolactone composites with TiO(2) for potential nanobiomaterials: tunable properties using different phases

TiO(2) nanoparticles of different phases play a key role in property alteration of nanocomposite fibers. Polycaprolactone (PCL)/TiO(2) composite fibers were prepared using the electrospinning method. Pure anatase and rutile phases were synthesized using the sol-gel route for nanocomposite synthesis. The Effect of nanoparticle phases on crystallinity of fibers and interaction with polymer molecules have been studied using X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy, morphology through SEM, surface properties using BET method and wetting property of fibers commencing from contact angle measurement. Biocompatibility and biodegradation of hybrid materials have been studied in simulated body fluid (SBF) and phosphate buffer (PBS), respectively. The anatase phase with smaller particle dimensions exhibited significant improvement of most of the properties as compared to composites made of the rutile phase. Better interaction between polymer chain and anatase particle PCL-A nanocomposite fibers leads to better mechanical property and biocompatibility vis-à-vis PCL-R and pristine PCL fibers. Biocompatibility of PCL nanocomposite has been testified through proliferation of fibroblast cell and its adhesion; MTT (3-(4,5-dimethythiazol-2-yl)-2,5-diphenyl tetrazolium bromide) assay demonstrates good proliferation rate for cells on PCL-A nanocomposite fibres.     

Interactions of iodoperfluorobenzene compounds with gold nanoparticles

Understanding the interactions of small molecules with gold nanoparticles is important for controlling their surface chemistry and, hence, how they can be used in specific applications. The interaction of iodoperfluorobenzene compounds with gold nanoparticles was investigated by UV-Vis difference spectroscopy, surface enhanced Raman spectroscopy (SERS) and Synchrotron X-ray photoelectron spectroscopy (XPS). Results from UV-Vis difference spectroscopy demonstrated that iodoperfluorobenzene compounds undergo charge transfer complexation with gold nanoparticles. SERS of the small molecule-gold nanoparticle adducts provided further evidence for formation of charge transfer complexes, while Synchrotron X-ray photoelectron spectroscopy provided evidence of the binding mechanism. Demonstration of interactions of iodoperfluorobenzene compounds with gold nanoparticles further expands the molecular toolbox that is available for functionalising gold nanoparticles and has significant potential for expanding the scope for generation of hybrid halogen bonded materials.     

Inter- and intrastrand DNA crosslinks by 2-fluoro-substituted pyrrolobenzodiazepine dimers: stability, stereochemistry and drug orientation

A 2-fluoro-substituted pyrrolo[2,1-c][1,4]benzodiazepine (PBD) dimer with a 1,4-di-n-propyl piperazine linker was studied with respect to its binding and crosslinking capability towards double-helical DNA targets. Duplex thermal stabilizations upon drug binding as measured by UV melting experiments suggest that two guanine bases separated by four AT base pairs constitute the favorable binding site for the PBD dimer. Large stabilizations were observed for the self-complementary duplex d(AACAATTGTT)(2) as well as for the non-self-complementary duplex d(AAGAATTGTT)·d(AACAATTCTT) with both guanines located on the same strand. Formation of interstrand and intrastrand crosslinks by the covalent binding of both PBD moieties of the dimer to the exocyclic 2-amino group of the two guanine bases within the duplex minor groove was confirmed by NMR structural studies. In both the symmetric and non-symmetric DNA-PBD adducts the newly created stereogenic center at C11 of the tricyclic PBD subunits favors an S configuration. Different orientations of the PBD aromatic A-ring with respect to the covalently modified guanine as observed in the non-symmetric complex are shown to result in characteristic changes of PBD H11 and H11a proton chemical shifts. Based on a compilation of available NMR data on various PBD complexes, these differences may be used as valuable probes for the identification of PBD orientational preferences in DNA-PBD adducts.     

X-ray Structure of <Emphasis Type="Italic">mer</Emphasis>-[Mo(CO)<Subscript>3</Subscript>(PPh<Subscript>3</Subscript>)(<Emphasis Type="Italic">κ</Emphasis><Superscript>2</Superscript>-dppm)]

Abstract  

Treatment of [Mo(CO)₃(NCMe)₃] with bis(diphenylphosphino)methane (dppm) and triphenylphosphine (PPh₃) at 50 °C afforded mer-[Mo(CO)₃(PPh₃)(κ ²-dppm)] (1) in 55% yield which has been characterized by single crystal X-ray diffraction studies and spectroscopic measurements. Compound 1 crystallizes in the triclinic space group P−1 with a = 10.3449(6), b = 11.1570(6), c = 17.8961(10) ?, β = 80.8400(10)°, Z = 2 and V = 1959.8(2) ?³.     

Abnormal switching behavior of nanoparticle composite systems

We have investigated the properties of liquid crystals (LCs) doped with ZnO (8% Cu doped) nanoparticles. The electro-optic properties of LCs have changed with varying concentration of ZnO nanoparticles. The dielectric anisotropy obtained from the values of dielectric permittivity at 5 kHz in the nematic and smectic phases was found to increase with increasing concentration of nanoparticles in LCs. It has been established that the effect of nanoparticles on the dielectric anisotropy depends on the physical properties of LCs; the nanoparticle disturbs the orientation ordering of LC molecules. The nanoparticle also influences the switching behavior, splay elastic constant, rotational viscosity and threshold voltage of pure LCs. A small quantity of nanoparticles causes slight reduction of the splay elastic constant and rotational viscosity of LC cells.     

On supplementation and generalized projective modules

Discrete (quasi) modules form an important class in module theory, they are studied extensively by many authors. The decomposition theorem for quasidiscrete modules plays an important rule in the better understanding of such modules. In fact, every quasidiscrete module is a direct sum of hollow submodules. Here we introduce some new concepts (weak quasidiscrete, and S ₁- and S ₂-supplemented modules) which generalize the concept of quasidiscrete module. We show that some of the properties of quasidiscrete modules still hold in the class of weak quasidiscrete modules. We also obtain some properties of weak quasidiscrete modules, which are similar to the properties known for quasidiscrete modules. We introduce the concept of generalized relative projectivity (relative S-projectivemodules), and use it to characterize direct sums of hollowmodules. In fact, relative S-projectivity is an essential condition for direct sums of hollow modules to be weak quasidiscrete modules.     

Net-convergence and weak separation axioms in (L, M)-fuzzy topological molecular lattices

In this paper, we used the concept of (L, M)-fuzzy remote neighborhood system to study and establish the convergence theory of molecular nets. Next, we introduce the T_i-axioms (i = ?1, 0, 1, 2) in (L, M)-fuzzy topological molecular lattices, and discuss some of their characterizations. Finally, we show that the T_i-axioms (i = ?1, 0, 1, 2) are preserved under homeomorphisms.     

Some Character Degree Conditions Implying Solvability of Finite Groups

Let cd(G) be the set of all irreducible complex character degrees of a finite group G. In this paper, we show that if a, b, and c are pairwise relatively prime integers and ${\rm{cd}} \left(G\right) \subseteq \{1, a, b, c, ab, ac\}$ , then either G is solvable or {a, b, c}?=?{2 ^f ???1, 2 ^f , 2 ^f ?+?1} for some $f \geqslant 2$ and cd (G)?=?{1, a, b, c}.     

Coating of powder-blasted channels for high-performance microchip electrophoresis

Channels in microfluidic glass chips manufactured with the alternative powder blasting technology were permanently coated with poly(vinyl alcohol) (PVA) in order to improve the performance in microchip electrophoresis. The performance of coated and uncoated powder-blasted (pb) devices as well as coated and uncoated wet chemical etched (wc) chips was compared in electrophoretic separations of fluorescently labeled test compounds. The limited electrophoretic resolution obtained in pb-chips could significantly be improved by coating the channels with PVA. The resolution of test compounds in such coated pb-devices was even higher than in uncoated wc-chips. PVA-coated pb-chips could also successfully be applied in chiral separations. While in an uncoated pb-chip using a cyclodextrins buffer only one broad signal was obtained, two well-resolved signals were obtained in a coated device.