Magnetic circular dichroism of transition metal ions in solids—II K2NaGaF6: Cr3+

The absorption and MCD spectra of the ${}^4\text{A}{}_{\mathrm{2g}}\text{→}{}^4\text{T}{}_{\mathrm{2g}}$, ${}^4\text{A}{}_{\mathrm{2g}}$, ${}^4\text{A}{}_{\mathrm{2g}}\text{→}{}^4\text{T}{}_{\mathrm{1g}}{}^{\mathrm{a}}$ and ${}^4\text{A}{}_{\mathrm{2g}}\text{→}{}^4\text{T}{}_{\mathrm{1g}}{}^{\mathrm{b}}$ spin-allowed transitions of Cr³⁺ in K₂NaGaF₆ are reported. It is shown that transitions to the ${}^4\text{T}{}_{\mathrm{1g}}$. states are induced by T_1u vibratio the other spin-allowed transition, ${}^4\text{A}{}_{\mathrm{2g}}\text{→}{}^4\text{T}{}_{\mathrm{2g}}$, there are three competing intensity mechanisms: electric dipole induced by T_1u vibrations, electric dipole induced by T_2u vibrations and magnetic dipole, and an estimate is made of the relative importance of these. The magnetic dipole ${}^4\text{A}{}_{\mathrm{2g}}\text{→}{}^2\text{E}{}_{\mathrm{g}}$ zero-phonon line is observed to be accompanied by a vibrational sideband for which the coupling is predominantly with T_2u vibrations. Other weak transitions are observed in MCD spectra and their origin briefly discussed.     

Pd Uptake and H2S Sensing by an Amphoteric Metal–Organic Framework with a Soft Core and Rigid Side Arms

Molecular components of opposite character are often incorporated within a single system, with a rigid core and flexible side arms being a common design choice. Herein, molecule L has been designed and prepared featuring the reverse design, with rigid side arms (arylalkynyl) serving to calibrate the mobility of the flexible polyether links in the core. Crystallization of this molecule with Pb^II ions led to a dynamic metal–organic framework (MOF) system that not only exhibits dramatic, reversible single‐crystal‐to‐single‐crystal transformations, but combines distinct donor and acceptor characteristics, allowing for substantial uptake of PdCl₂ and colorimetric sensing of H₂S in water.     

Improved rejection of multiply scattered photons in confocal microscopy using dual-axes architecture

We perform Monte Carlo simulations to show that the dual-axes (DA) confocal architecture has superior rejection of multiply scattered photons in tissue to that of single axis. As a result, the DA configuration provides improved signal-to-noise ratio and dynamic range, and thus is sensitive to ballistic photons from deeper within tissue, features that are particularly useful for performing vertical cross-sectional reflectance images in tissue.     

Low-temperature Mössbauer studies of FeNb2O6

Fe⁵⁷ Mössbauer spectra of FeNb₂O₆ were obtained from 15.0K down to 1.9 K. The isomer shift, 1.42±0.01 mm sec^?1 relative to Cr, was found to be temperature independent, whereas the magnitude of the quadrupole splitting was observed to decrease slightly with temperature. The quadrupole splitting and the hyperfine field at 1.9 K are -2.41±0.01 mm sec^?1 and 34.6±0.3 kOe respectively. The directions of the hyperfine fields experienced by the Fe nuclei are in the a-c plane symmetrically displaced with respect to the crystallographic axes.     

两种可溶性聚乙炔衍生物的飞秒发光动力学研究

采用飞秒频率上转换技术测量了两种可溶聚乙炔衍射生物ｐｏｌｙ（ｐｈｅｎｙｌａｃｅｔｙｌｅｎｅ（ＰＰＡ）和ｐｏｌｙ（１－ｐｈｅｎｙｌ－１－ｂｕｔｙ１）ＰＰＢ）的发光动力学过程。采用非均匀展宽态密我规行走理论对上述结果进行了分析。     

Lp-spectra of strongly Carleman pseudo-differential operators

The spectrum and essential spectrum in L^p($\text{R}$ⁿ) of a strongly Carleman pseudo-differential operator with symbol of class S_?,0^m, 0 ? p ? 1, are shown to coincide with the range of the symbol for some (but need not be all) p different from 2. The absolutely continuous spectra of perturbations of operators with strongly Carleman symbols (but without the assumption of being in S_?,0^m) are also investigated.     

The absence of physical-aging effects on the surface relaxations of rubbed polystyrene

Extensive experimental results are presented to reveal the relaxations of polystyrene surface deformed by rubbing with a velvet cloth. We found that surface topographic features, such as ditches and ridges created by rubbing, relax at temperatures at about 20^° C below the bulk glass transition temperature of the polystyrene for a molecular weight of 442 kg/mol, even though we estimate the Laplace Pressure driving the relaxation to be 1/500 of the yield limit. The relaxation is independent of the thermal history before the rubbing process, and post rubbing thermal history below 55^° C . In other words, physical-aging processes at 23^° C for up to 7 days and at 50^° C for 2 days, which would have drastic effects on the relaxations of bulk polymers, have little effects on the relaxations of rubbed surfaces. This is consistent with the mobility enhancement in the surface layer previously reported in the literature.     

Solid-State NMR Spectroscopy: A Powerful Technique to Directly Study Small Gas Molecules Adsorbed in Metal–Organic Frameworks

Metal–organic frameworks (MOFs) have shown great potential in gas separation and storage, and the design of MOFs for these purposes is an on-going field of research. Solid-state nuclear magnetic resonance (SSNMR) spectroscopy is a valuable technique for characterizing these functional materials. It can provide a wide range of structural and motional insights that are complementary to and/or difficult to access with alternative methods. In this Concept article, the recent advances made in SSNMR investigations of small gas molecules (i.e., carbon dioxide, carbon monoxide, hydrogen gas and light hydrocarbons) adsorbed in MOFs are discussed. These studies demonstrate the breadth of information that can be obtained by SSNMR spectroscopy, such as the number and location of guest adsorption sites, host–guest binding strengths and guest mobility. The knowledge acquired from these experiments yields a powerful tool for progress in MOF development.