Chemical effect on FKα X-ray satellites produced by 6 MeV/amu p,α and C4+

The excitation conditions where both direct Coulomb and shake-off processes concur to multiply ionize fluorineK andL shells were adopted in this experiment; 6MeV/amu p,α and C⁴⁺ impacts. The ion induced FKα satellites, measured for a series of F bearing compounds, showed significant chemical effects on their intensity distributions. Such effects are explained well with an FL-vacancy rearrangement model. Without any theoretical prediction, rearrangement probabilities or widths of FL shells were estimated by use of a reference compound with high ionicity, i.e. NaF. A linear relationship between FL widths and covalencies of compounds was found for a wide variety of fluorides. For the same compounds, the absolute values of the FL-vacancy rearrangement probabilities or the FL-shell widths obtained here were the same as those estimated from pure direct Coulomb and pure shake-off excitations, respectively. Other models than theL-vacancy rearrangement's are also discussed and eliminated.     

Steady-state thermodynamics of Langevin systems

We study Langevin dynamics describing nonequilibirum steady states. Employing the phenomenological framework of steady-state thermodynamics constructed by Oono and Paniconi [Prog. Theor. Phys. Suppl. 130, 29 (1998)], we find that the extended form of the second law which they proposed holds for transitions between steady states and that the Shannon entropy difference is related to the excess heat produced in an infinitely slow operation. A generalized version of the Jarzynski work relation plays an important role in our theory.     

Jamming Transition in Kinetically Constrained Models with Reflection Symmetry

A class of kinetically constrained models with reflection symmetry is proposed as an extension of the Fredrickson–Andersen model. It is proved that the proposed model on the square lattice exhibits a freezing transition at a non-trivial density. It is conjectured by numerical experiments that the known mechanism of the singular behaviors near the freezing transition in a previously studied model (spiral model) is not responsible for that in the proposed model.     

Synthesis of Asymmetrically Substituted Terpyridines by Palladium‐Catalyzed Direct C?H Arylation of Pyridine N‐Oxides

The synthesis of asymmetrically substituted 2,2′:6′,2′′‐terpyridines is reported. First, palladium‐catalyzed C? H arylation of pyridine N‐oxides with substituted bromopyridines gave 2,2′‐bipyridine N‐oxides, which were further arylated in a second step to form 2,2′:6′,2′′‐terpyridine N‐oxides. Yields of up to 77 % were obtained with N‐oxides bearing an electron‐withdrawing ethoxycarbonyl substituent in the 4‐position. Pd(OAc)₂ with either P(tBu)₃ or P(o‐tolyl)₃ was used as the catalyst. Cyclometalated complexes derived from Pd(OAc)₂ and these phosphines were also effective. K₃PO₄ as the base gave better results than K₂CO₃. Subsequent deoxygenation with H₂ and Pd/C as the catalyst gave the asymmetrically substituted 2,2′:6′,2′′‐terpyridines in near quantitative yield. This reaction sequence significantly reduces the number of steps required in comparison with known cross‐coupling methods and therefore allows convenient and scalable access to substituted terpyridines.     

Selective synthesis combined with chemical separation of single-walled carbon nanotubes for chirality selection

Single-walled carbon nanotubes (SWNTs) are potential materials for future nanoelectronics. Since the electronic and optical properties of SWNTs strongly depend on tube diameter and chirality, obtaining SWNTs with narrow (n,m) chirality distribution by selective growth or chemical separation has been an active area of research. Here, we demonstrate that a new, bimetallic FeRu catalyst affords SWNT growth with narrow diameter and chirality distribution in methane CVD. At 600 degrees C, methane CVD on FeRu catalyst produced predominantly (6,5) SWNTs according to UV-vis-NIR absorption and photoluminescence excitation/emission (PLE) spectroscopic characterization. At 850 degrees C, the dominant semiconducting species produced are (8,4), (7,6), and (7,5) SWNTs, with much narrower distributions in diameter and chirality than materials grown by other catalysts. Further, we show that narrow diameter/chirality growth combined with chemical separation by ion exchange chromatography (IEC) greatly facilitates achieving single (m,n) SWNT samples, as demonstrated by obtaining highly enriched (8,4) SWNTs with near elimination of metallic SWNTs existing in the as-grown material.     

X-ray analysis of ZnO nanorods grown by microwave irradiation heating on ZnO films

Utilizing microwave irradiation heating, 100-nm-diameter ZnO nanorods were grown from aqueous solution on sputtered ZnO films on glass substrates. Its out-of-plane X-ray diffraction (XRD) measurement indicated that the ZnO nanorods were grown with c-axis orientation, similar with the underlying ZnO films. In the in-plane XRD measurement, intensity of the () diffraction was comparable with that of the () one, suggesting their intensity ratio would contain useful information on nanorods density.     

Development of an <Emphasis Type="Italic">Agrobacterium</Emphasis>-Mediated Transformation Method and Evaluation of Two Exogenous Constitutive Promoters in Oleaginous Yeast <Emphasis Type="Italic">Lipomyces starkeyi</Emphasis>

The biogenic iron oxide/hydroxide materials possess useful combination of physicochemical properties and are considered for application in various areas. Their production does not require special investments because these compounds are formed during cultivation of neurophilic iron bacteria. Bacteria from genus Leptothrix develop intensively in the Sphaerotilus-Leptothrix group of bacteria isolation medium and feeding media of Fedorov and Lieske. These media are different in their composition which determined the present study as an attempt to clear up the reasons that define the differences in the composition of the laboratory-obtained biomasses and the natural biomass finds. FTIRS, Mössbauer spectroscopy, and XRD were used in the research. Comparative analysis showed that the biomass and control samples contain iron compounds (α-FeOOH, γ-FeOOH, β-FeOOH, γ-Fe₂O₃) in different ratios. The biomass samples were enriched in oxyhydroxides of higher dispersion. Organic residuals of bacterial origin, SO₄, CO₃, and PO₄ groups were registered in the biogenic materials.     

Indirect detection of nitrogen-14 in solid-state NMR spectroscopy.

NMR spectra of (14)N (spin I=1) are obtained by indirect detection in powders spinning at the magic angle. The method relies on the transfer of coherence from a neighboring "spy" nucleus with S=1/2, such as (13)C or (1)H, to single- or double-quantum transitions of (14)N nuclei. The transfer of coherence can occur through a combination of scalar and residual dipolar splittings (RDS); the latter are also known as second-order quadrupole-dipole cross terms. The two-dimensional NMR spectra reveal powder patterns determined by second- and third-order quadrupolar couplings. These spectra depend on the quadrupolar coupling constant C(Q) (typically a few megahertz), on the asymmetry parameter eta(Q) of the (14)N nucleus, and on the orientation of the internuclear vector r(IS) between the I ((14)N) and S (spy) nuclei with respect to the quadrupolar tensor. These parameters, which can be subject to motional averaging, can reveal valuable information about the structure and dynamics of nitrogen-containing solids. Application of this technique to various amino acids, either enriched in (13)C or with natural carbon isotope abundance, with spectra recorded at various magnetic fields, illustrates the scope of the method.     

A unique approach to development of near-infrared fluorescent sensors for in vivo imaging

Near-infrared (NIR) fluorescent sensors have emerged as promising molecular tools for imaging biomolecules in living systems. However, NIR fluorescent sensors are very challenging to be developed. Herein, we describe the discovery of a new class of NIR fluorescent dyes represented by 1a/1c/1e, which are superior to the traditional 7-hydroxycoumarin and fluorescein with both absorption and emission in the NIR region while retaining an optically tunable hydroxyl group. Quantum chemical calculations with the B3LYP exchange functional employing 6-31G(d) basis sets provide insights into the optical property distinctions between 1a/1c/1e and their alkoxy derivatives. The unique optical properties of the new type of fluorescent dyes can be exploited as a useful strategy for development of NIR fluorescent sensors. Employing this strategy, two different types of NIR fluorescent sensors, NIR-H(2)O(2) and NIR-thiol, for H(2)O(2) and thiols, respectively, were constructed. These novel sensors respond to H(2)O(2) or thiols with a large turn-on NIR fluorescence signal upon excitation in the NIR region. Furthermore, NIR-H(2)O(2) and NIR-thiol are capable of imaging endogenously produced H(2)O(2) and thiols, respectively, not only in living cells but also in living mice, demonstrating the value of the new NIR fluorescent sensor design strategy. The new type of NIR dyes presented herein may open up new opportunities for the development of NIR fluorescent sensors based on the hydroxyl functionalized reactive sites for biological imaging applications in living animals.