A note on the almost-one-half holomorphic pinching

Motivated by a previous work by Zheng and the second-named author, we study pinching constants of compact Kähler manifolds with positive holomorphic sectional curvature. In particular, we prove a gap theorem on Kähler manifolds with almost-one-half pinched holomophic sectional curvature. The proof is motivated by the work of Petersen and Tao on Riemannian manifolds with almost-quarter-pinched sectional curvature.     

Synthesis of sulfonamides from azoles and sodium sulfinates at ambient temperature

NBS or NIS mediated direct SN bond formation between azoles and sodium sulfinates is described. The reaction shows good substrate scope and tolerates a wide range of functionalities in both azoles and sodium sulfinate substrates. Pyrazoles are also suitable for this method, various 4-halopyrazoles derivatives were obtained by using N-halosuccinimide (NXS) as the halogen source.     

A selective and cost-effective method for the reductive deuteration of activated alkenes

A new single electron transfer reaction for the reductive deuteration of activated alkenes has been developed for the selective synthesis of α,β-dideuterio compounds. A cheap, stable and commercially-available sodium dispersion with high specific surface area is employed as the electron donor to replace the traditionally used sodium/liquid ammonium system. Deuterium source is provided by EtOD-d₁. Excellent yields and deuterium incorporations were obtained across a broad range of activated alkenes with good functional group tolerance. This method provided a cheap, efficient and operationally-simple method for the synthesis of deuterium labeled compounds.     

气相色谱–质谱法测定棉花中苯氧羧酸类除草剂

采用气相色谱–质谱联用法检测棉花中3种苯氧羧酸类除草剂[2,4-D,2,4,5-T,2-甲-4-氯丁酸(MCPB)]的残留量。样品用甲酸酸化的丙酮提取,硫酸催化甲酯化反应,用气相色谱–质谱联用仪测定。采用HPLC法与GC–MS法对提取与衍生化步骤进行优化。2,4-D,2,4,5-T,MCPB 3种化合物在0.075~7.5 mg/kg范围内线性均良好,检出限分别为0.5,0.5,0.8μg/kg,测定结果的相对标准偏差分别为4.1%,4.3%,4.0%(n=5),方法回收率分别为93.6%,95.5%,93.9%。该方法各项指标均可满足检测要求。     

Resonant terahertz generation from InN thin films

Highly efficient conversion from ultrafast optical pulses to their terahertz (THz) counterparts has been achieved with InN thin films. An average THz output power as high as 0.931 microW has been obtained for an average pump power of 1 W, corresponding to a normalized conversion efficiency of 190% mm(-2). Based on our measured dependences of the THz output power on pump polarization, incident angle, pump power, and InN film thickness, resonance-enhanced optical rectification is one of the most plausible mechanisms for the THz generation in the InN films.     

Model of fluorescence intermittency in single enzymes

The intermittent emission of fluorescent light from single enzymes, quantum dots, and other nanoscale systems is often characterized by statistical correlations in the emitted signal. A one-dimensional model of such correlations in enzymes, based on a model of protein conformational fluctuations developed by Kou and Xie (Phys. Rev. Lett. 2004, 93, 180603), is formulated in the present paper in terms of the dynamics of a particle moving stochastically between "on" and "off" states under the action of fractional Gaussian noise. The model yields predictions for the short and long time behavior of the following quantities: the time correlation function, C(t), of the fluctuations of the signal intensity, the distribution, f(t), of time intervals between intensity fluctuations, and the Mandel parameter, Q(t), describing the extent of bunching or anti-bunching in the signal. At short times, C(t) and f(t) are found to decay exponentially, while, at long times, they are found to decay as power laws, the exponents being functions solely of the nature of the temporal correlations in the noise. The results are in good qualitative agreement with results from single-molecule experiments on fluorescence intermittency in the enzyme cholesterol oxidase carried out by Xie and co-workers (Science 1998, 282, 1877). The Mandel parameter, Q(t), for this model is positive at short and long times, indicating super-Poisson statistics in these limits, consistent with bunching of the fluorescent signal.     

Regulation of aggregation and morphology of cyanine dyes on monolayers via gemini amphiphiles

The aggregation of dyes is of considerable importance in relating to their functions and applications. In this paper, we have investigated the regulation on the aggregation and morphology of two cyanine dyes, 3,3'-disulfopropyl-4,5,4',5'-dibenzo-9-methylthiacarbocyanine triethylammonium salt (MTC) and 3,3'-disulfopropyl-4,5,4',5'-dibenzo-9-phenylthiacarbocyanine triethylammonium salt (PTC), using a series of gemini amphiphiles (bis(2'-heptadecyl-3'-ethylimidazolium)-1,n-alkane dibromide, abbreviated as Gn, n=2, 4, 6, 8, 10). It has been found that both of the dyes could be adsorbed onto the monolayers of the gemini amphiphiles through the electrostatic and pi-pi interaction and stacked into H- or J-aggregate. The spacer of the gemini amphiphile showed good control over the aggregation of MTC: H-aggregate was favored when gemini amphiphiles with short spacer were applied, while J-aggregation was preferred in the case of longer spacer. Only J-aggregate was observed for PTC on gemini monolayer, regardless of the structure of the gemini amphiphiles. Interesting morphologies were observed for all the gemini/dye complex monolayers. Network structure and nanofibers were formed for the gemini/MTC films transferred below the plateau surface pressure and close to the collapse pressure, respectively. The ability of the complex monolayers to form nanofibers strongly depended on the component amphiphiles, G2>G4>G6, and no nanofibers were observed for G8/MTC and G10/MTC after the collapse. Only squared domains were observed for gemini/PTC monolayers. When both G2 and G10 were mixed, an individual control of the gemini amphiphiles over the aggregation of MTC in the complex monolayers was observed. The relationship among the spacer, dye structure, and aggregation was revealed.     

Thermoresponsive triblock copolymer aggregates investigated by laser light scattering

Narrowly distributed polystyrene-b-poly(N-isopropylacrylamide)-b-polystyrene (PS-b-PNIPAM-b-PS) triblock copolymer with trithiocarbonate group in the middle of PNIPAM block was synthesized by using reversible addition fragmentation chain transfer (RAFT) polymerization. Such copolymer chains form a micelle-like aggregate with PNIPAM interlocking rings and associating PS blocks as the core and PNIPAM rings as the corona. The hydrolysis of the trithiocarbonate group leads the rings in the corona to be cut into open linear coils. Using laser light scattering, we have investigated the temperature-induced collapse of the aggregates with the rings and coils in the corona. Our results reveal that the former shrink much less than the latter due to the topological effect of PNIPAM blocks in the corona. On the other hand, the aggregates with long coils exhibit a sharper collapse transition than those with shorter coils.     

Anion bridged nanosheet from self-assembled G-quadruplexes

A novel, non-covalent polymeric nanosheet has been produced through small molecule self-assembly; the structure has been characterized by solution NMR, solid-state NMR, powder XRD and AFM.     

Fabrication of a poly(styrene-octadecene-divinylbenzene) monolithic column and its comparison with a poly(styrene-divinylbenzene) monolithic column for the separation of proteins

In this paper, a poly(styrene-octadecene-divinylbenzene) (PS-OD-DVB) monolithic column was prepared in one step by introducing a C18 carbon chain as monomer. N,N-Dimethylformamide and decanol served as porogens to make a homogeneous polymerization mixture in a fused silica capillary (320 microm inner diameter). Its physical and chromatographic properties were compared with those of poly(styrene-divinylbenzene) (PS-DVB) monolithic column, which was also fabricated by in-situ polymerization in a fused silica capillary with the same inner diameter. Six standard proteins were used to evaluate the columns and their potential application for the separation of human hemoglobin was also discussed. It was shown that the PS-OD-DVB and PS-DVB monoliths appeared to have similar efficiency for rapid separation of six proteins within 3.5 min. The PS-OD-DVB monolith was found to have higher loading capacity and higher resolution for the separation of alpha and beta chains of hemoglobin because of the introduction of C18 carbon chains, and shows great potential for the separation of bio-macromolecules.