Supramolecular architecture built of Co(II) and a tripodal ligand containing 1-D water tapes with (H2O)16 cluster units

The reaction of Co(NO₃)₂?·?6H₂O with a tripodal ligand leads to a new complex {[Co(L)]?·?2NO₃?·?8H₂O} (1) confirmed by single-crystal X-ray diffraction, infrared spectroscopy, and elemental analysis. The particular interest of 1 is in the formation of a 1-D water tape consisting of (H₂O)₁₆ cluster units, the neighboring water tapes are connected by free nitrate anions via hydrogen bonds into a 2-D guest layer. These guest layers are alternately packed face-to-face with the 2-D host layers along the a-axis to form a 3-D supramolecular architecture. There exist C–H?···?N and C–H?···?O weak hydrogen bonds between the guest layer and host layer. These weak hydrogen bonds and water–nitrate, water–water hydrogen bonds are important for the stability of the overall structure.     

Naphthalene derivatives of a conformationally locked GFP chromophore with large stokes shifts

The active development of fluorescence microscopy requires an increase in the variety of the dyes and their characteristics. Compounds with a large Stokes shift, i.e., a large difference between the positions of the absorption and emission maxima, have attracted the interest of researchers as a tool that can be used for multicolor labeling. One of the known approaches to increase the Stokes shift is the introduction of additional polycyclic fragments. Herein, we report novel derivatives of a conformationally locked GFP chromophore containing the naphthalene ring. The proposed modification leads not only to the enhancement of the Stokes shift up to 100 nm but also leads to the noticeable red-shift of the emission and absorption spectra in contrast with the corresponding derivatives with one benzene ring.     

Selective extraction of U(VI), Th(IV), and La(III) from acidic matrix solutions and environmental samples using chemically modified Amberlite XAD-16 resin

A new grafted polymer has been developed by the chemical modification of Amberlite XAD-16 (AXAD-16) polymeric matrix with [(2-dihydroxyarsinoylphenylamino)methyl]phosphonic acid (AXAD-16-AsP). The modified polymer was characterized by a combination of ¹³C CPMAS and ³¹P solid-state NMR, Fourier transform-NIR-FIR-Raman spectroscopy, CHNPS elemental analysis, and thermogravimetric analysis (TGA). The distribution studies for the extraction of U(VI), Th(IV), and La(III) from acidic solutions were performed using an AXAD-16-AsP-packed chromatographic column. The influences of various physiochemical parameters on analyte recovery were optimized by both static and dynamic methods. Accordingly, even under high acidities (>4 M), good distribution ratio (D) values (10²–10⁴) were achieved for all the analytes. Metal ion desorption was effective using 1 mol L^–1 (NH₄)₂CO₃. From kinetic studies, a time duration of <15 min was sufficient for complete metal ion saturation of the resin phase. The maximum metal sorption capacities were found to be 0.25, 0.13, and 1.49 mmol g^–1 for U(VI); 0.47, 0.39, and 1.40 mmol g^–1 for Th(IV); and 1.44, 1.48, and 1.12 mmol g^–1 for La(III), in the presence of 2 mol L^–1 HNO₃, 2 mol L^–1 HCl, and under pH conditions, respectively. The analyte selectivity of the grafted polymer was tested in terms of interfering species tolerance studies. The system showed an enrichment factor of 365, 300, and 270 for U(VI), Th(IV), and La(III), and the limit of analyte detection was in the range of 18–23 ng mL^–1. The practical applicability of the polymer was tested with synthetic nuclear spent fuel and seawater mixtures, natural water, and geological samples. The RSD of the total analytical procedure was within 4.9%, thus confirming the reliability of the developed method.     

Hydrolysis kinetics of p-nitrophenylpicolinate catalyzed by schiff base Mn(III) complexes in Gemini 16-2-16 micellar solutiony

Two mono-Schiff base Mn(III) complexes (MnL₂Cl, L=L¹ and L²) were synthesized and employed as artificial hydrolases in catalyzing the hydrolysis of p-nitrophenylpicolinate (PNPP) in Gemini 16-2-16 micellar solution. The effect of different micelles and their complex structures on the catalytic hydrolysis of PNPP is discussed in detail. The observations showed that MnL₂²Cl exhibited higher catalytic activity over MnL₁²Cl under a comparable condition, which confirmed that an open active centre is essential for modulating the activities of the two enzyme mimics. Moreover, under the conditions employed, hydrolytic rates of PNPP induced by these Mn(III) complexes were faster in Gemini 16-2-16 micelles than that in the micellar solution of cetyltrimethylammonium bromide (CTAB), a conventional analogue of Gemini 16-2-16. Electronic Supplementary Material  Supplementary material is available for this article at and is accessible for authorized users.     

Macrolactones built from the bis-3,4(indol-1-yl)maleimide scaffold

15, 16, and 17-Membered lactones based on the bis-3,4(indol-1-yl)maleimide framework were obtained using intramolecular esterification reaction starting from 3-(1-ω-carboxyalkyl-2,3-dihydroindol-1-yl)-4-(1-ω-hydroxyalkyl-2,3-dihydroindol-1-yl)-maleimides. 3,4-Dibromo-maleimide, ω-(2,3-dihydroindol-3-yl)alkanoic acids, and ω-(2,3-dihydroindol-3-yl)alkanoles were used as starting compounds. Substitution of Br for the substituted indolines followed by the intramolecular cyclization of O-silylated hydroxyl acids derivatives led to macrolactones that incorporated 4-(dihydroindol-1-yl)-3-(indol-1-yl)maleimide moieties. Indoline nuclei in these compounds were dehydrogenated by DDQ in refluxing toluene to give 15, 16 or 17-membered lactones 3-[(ω-3-carboxyalkylindol-1-yl)-4-(ω-hydroxyalkylindol-1-yl)maleimides. Quantum chemical calculations showed that the formation of macrolactones of smaller size (13-membered) corresponds to the higher Gibbs energy ΔG^# and correlates with the absence of the target reaction product.     

Studies on the New Constituents of Sal via Miltiorrhiza Bunge

Two novel constituents were isolated from the roots of Chinese medicinal herbs, Salvia miltiorrhiza. Their structures were determined by spectroscopic technique. The compounds were named 13,14-dihydroxy-15-methyl-benzo[2,3-a]-7,7-dimethyl-12-oxa-tricyclo[4,4,21.4,0]dodecane(1) and 16-methyl-tropono[2,3-c]-7,7-dimethyl-12-oxa-tricyclo[4,4,21.4,0]dodecane(2).     

高质量数字声音广播系统

本文就现行模拟声音广播系统与数字声音广播系统的差异，提出发展高质量数字声音广播系统的意义，介绍了发达国家对该课题研究的概况，讲座了数字声音卫星广播和数字声音地面广插系统的特点，并详细阐述了其主要构成部分：信源编码、信道编码及数字调制技术。     

Incompressible Viscous Fluid Flows in a Thin Spherical Shell

Linearized stability of incompressible viscous fluid flows in a thin spherical shell is studied by using the two-dimensional Navier–Stokes equations on a sphere. The stationary flow on the sphere has two singularities (a sink and a source) at the North and South poles of the sphere. We prove analytically for the linearized Navier–Stokes equations that the stationary flow is asymptotically stable. When the spherical layer is truncated between two symmetrical rings, we study eigenvalues of the linearized equations numerically by using power series solutions and show that the stationary flow remains asymptotically stable for all Reynolds numbers.