奇A 核的多声子γ振动带实验研究进展

对于近年来清华大学与美国合作研究组在原子核结构实验研究中有关奇A 核的多声子 振动带方面的进展进行了评述。研究人员通过有效的国际合作,识别了质量数A = 100 丰中子核区的奇A核103Nb,105Mo,107Tc 和109Tc中的两声子 振动带,这是迄今为止国际上在奇A 核的结构研究中发现的仅有的4 例这样的结构。对于实验方法、研究结果以及这些多声子 振动带的特性进行了评述,并对目前在多声子带其他方面的研究及今后进一步的工作进行了概述。The experimental research on multi-phonon γ-vibrational bands in odd-A nuclei by our international collaboration has been reviewed. The two phonon -vibrational bands in 103Nb, 105Mo, 107Tc and 109Tc in the A = 100 neutron-rich nuclear region were identified, which are the only four such bands discovered in nuclear structure studies until now. The experimental methods and results are summarized, and the characteristics for these band structures are discussed. The other aspects for our research on the multi-phonon vibrational bands as well as our future research work are also briefly reviewed.     

Method for improved secondary ion yields in cluster secondary ion mass spectrometry

A method to increase useful yields of organic molecules is investigated by cluster secondary ion mass spectrometry (SIMS). Glycerol drops were deposited onto various inkjet‐printed arrays and the organic molecules in the film were rapidly incorporated into the drop. The resulting glycerol/analyte drops were then probed with fullerene primary ions under dynamic SIMS conditions. High primary ion beam currents were shown to aid in the mixing of the glycerol drop, thus replenishing the probed area and sustaining high secondary ion yields. Integrated secondary ion signals for tetrabutylammonium iodide and cocaine in the glycerol drops were enhanced by more than a factor of 100 compared with an analogous area on the surface, and a factor of 1000 over the lifetime of the glycerol drop. Once the analyte of interest is incorporated into the glycerol microdrop, the solution chemistry can be tailored for enhanced secondary ion yields, with examples shown for cyclotrimethylenetrinitramine (RDX) chloride adduct formation. In addition, depositing localized glycerol drops may enhance analyte secondary ion count rates to high enough levels to allow for site‐specific chemical maps of molecules in complex matrices such as biological tissues. Published in 2010 by John Wiley & Sons, Ltd.     

Hydrodynamic chromatography of latex blends

The ability to characterize the size and shape distributions of broadly polydisperse analytes is a driving force in particle size analysis. Multi-detector hydrodynamic chromatography (HDC), which has previously shown promise in its ability to characterize the size and shape of monodisperse, spherical polystyrene latex standards, is applied here to include the characterization of bi-, tri-, and tetramodal latex blends and their constituents varying in size, chemistry, and compactness. The ability of multi-detector HDC to distinguish between similar-sized particles of different chemistry is realized by the coupling of a concentration-sensitive detector and two different types of light scattering detectors. The use of both multi-angle static and quasi-elastic light scattering permits for determination of two different size parameters across the elution profiles of the blends. Combining the size information obtained from both light scattering methods provides a measure of how particle compactness changes as a function of size in a latex blend. Multi-detector HDC was shown to be a rapid and precise method for characterizing particle size, shape, and their distributions of broadly polydisperse analytes.     

Nonlinear optical properties of CNHP4 nanofibers: Molecular dipole orientations and two photon absorption cross-sections

Polarized second harmonic measurements are used to determine the in- and out-of plane orientations of molecular dipoles in optical active, elongated, surface bound nanoaggregates. As a specific example, nonlinear optical active nanofibers grown from CNHP4 molecular dipoles on muscovite mica are investigated. The orientation of the dipoles relative to the substrate is found to be 7 ± 5°, whereas that of the dipoles relative to the long nanofiber axes is ± 13 ± 5°. Following 780 nm femtosecond laser excitation, the two photon action potential ησ₂ for CNHP4 is determined to be 4.7 × 10⁻⁵⁴ cm⁴ s/photon. For comparison, ησ₂ for para-hexaphenylene nanofibers is measured to be 12 × 10⁻⁵⁴ cm⁴ s/photon.     

Evidence of two dimensionality in quasi-one-dimensional cobalt oxides

The quasi-one-dimensional (Q1D) cobalt oxides A(N + 2)Co(n + 1)O(3n + 3) (A = Ca, Sr, and Ba, n = 1 - infinity) were investigated by muon-spin spectroscopy under applied pressures of up to 1.1 GPa. The relationship between the onset Néel temperature T(on)(N) and the interchain distance (d(ic)), which increases monotonically with n, is well fitted by the formula T(N)/T(N,0) = (1 - d(ic)/d(ic,o)(beta), here for T(on)(N) approximately 100 K for Ca(3)Co(2)O(6) (n = 1) and approximately 15 for BaCoCoO(3) (n = infinity at ambient P. The T(on)(N) - d(ic) curve also predicts a large dependence of Y(N) for the compounds with n > or = 5, i.e., in the vicinity of , while the compounds show only a very small effect. Indeed, our high-pressure mu(+) results show that of BaCoO(3) is enhanced by with a slope of 2.2 K(Gpa), whereas no detectable changes by P for both Ca(3)Co(2)O(6) and Sr(4)Co(3)O(9) (n = 2). This clearly confirms the role of the 2D-antiferromagnetic interaction on T(on)(N) in the Q1D cobalt oxides.     

Synthetic approaches to bicyclic diazenium salts

Bicyclic diazenium salts have been prepared from α-chloroazo species via a Lewis acid-mediated intramolecular cycloaddition. An alternative, more direct, route to these salts by the reaction of hydrazones with dimethylsulfonium ditriflate is also described. Terminal olefins provided mixtures of fused and bridged bicyclic diazenium salts. The ratio of the fused and bridged species was observed to depend on the electronics of the N-aryl substituent, which is explained by considering a concerted asynchronous cycloaddition mechanism.