Microwave Assisted Synthesis of Chitosan Nanoparticles

Chitosan nanoparticles (CHN) were prepared based on ionotropic gelation between low moleculer weight chitosan and sodium tripolyphosphate (TPP) under microwave irradiation. Particle size, zeta potential, and FT-IR techniques were used for characterization of CHN. The influence of reaction time on the nanoparticle size distribution was investigated, and the results showed that the microwave irradiation method evidently decreases the reaction times and particle size over the conventional method. It was determined by the results of the zeta potential measurements that synthesized CHN under microwave irradiation clearly exhibits more homogeneous and stable dispersion.     

W-代数W(2,2)的单参数量子形变(英文)

众所周知,泛包络代数的量子形变所对应的量子群结构是依据所给代数的单根系给出的.我们构造了q-形变W代数Wq,并给出其非平凡的量子群结构.     

Photoelectron imaging study of the effect of monohydration on O2 - photodetachment

The photodetachment of the O(2)(-).H(2)O cluster anion at 780 and 390 nm is investigated in comparison with O(2)(-) using photoelectron imaging spectroscopy. Despite the pronounced shift in the photoelectron spectra, the monohydration has little effect on the photoelectron angular distributions: for a given wavelength and electron kinetic energy (eKE) range, the O(2)(-).H(2)O angular distributions are quantitatively similar to those for bare O(2)(-). This observation confirms that the excess electron in O(2)(-).H(2)O retains the overall character of the 2ppi(g) HOMO of O(2)(-). The presence of H(2)O does not affect significantly the partial wave composition of the photodetached electrons at a given eKE. An exception is observed for slow electrons, where O(2)(-).H(2)O exhibits a faster rise in the photodetachment signal with increasing eKE, as compared to O(2)(-). The possible causes of this anomaly are (i) the long-range charge-dipole interaction between the departing electron and the neutral O(2).H(2)O skeleton affecting the slow-electron dynamics; and (ii) the s wave contributions to the photodetachment, which are dipole-forbidden for pi(g)(-1) transitions in O(2)(-), but formally allowed in O(2)(-).H(2)O due to lower symmetry of the cluster anion and the corresponding HOMO.     

Collision-induced dissociation of HS-(HCN): unsymmetrical hydrogen bonding in a proton-bound dimer anion

The energy-resolved competitive collision-induced dissociation of the proton-bound complex [HS.H.CN](-) is studied in a guided ion beam tandem mass spectrometer. H(2)S and HCN have nearly identical gas-phase acidities, and therefore, the HS(-) + HCN and the CN(-) + H(2)S product channels exhibit nearly the same threshold energies, as expected. However, the HS(-) + HCN channel has a cross section up to a factor of 50 larger than CN(-) + H(2)S at higher energies. The cross sections are modeled using RRKM theory and phase space theory. The complex dissociates to HS(-)+ HCN via a loose transition state, and it dissociates to CN(-) + H(2)S via a tight transition state. Theoretical calculations show that the proton-transfer potential energy surface has a single minimum and that the hydrogen bonding in the complex is strongly unsymmetrical, with an ion-molecule complex of the form HS(-)..HCN rather than CN(-)..H(2)S or an intermediate structure. The requirement for proton transfer before dissociation and curvature along the reaction path impedes the CN(-) + H(2)S product channel.     

Indole diterpenoid synthetic studies. The total synthesis of (+)-nodulisporic acid F

[structure: see text] A stereocontrolled total synthesis of (+)-nodulisporic acid F, the simplest member of a family of novel ectoparasiticidal agents, has been achieved. Highlights of the effective modular synthetic strategy include anionic union of a tricyclic lactone with o-toluidine via our 2-substituted indole synthetic protocol, an optimized C-ring construction protocol, and a late-stage installation of the alpha,beta-unsaturated carboxylic acid side chain via the B-alkyl Suzuki-Miyaura cross-coupling tactic.     

A new modular indole synthesis. Construction of the highly strained CDEF parent tetracycle of nodulisporic acids A and B

[reaction: see text] Construction of the highly strained CDEF parent tetracycle, a structural motif found only in the potent ectoparasiticidal agents (+)-nodulisporic acids A and B and related congeners, has been achieved via a new modular indole synthesis, exploiting a sequential Stille cross-coupling/Buchwald-Hartwig union/cyclization tactic. The new indole synthesis holds the promise of rapid assembly of diverse, highly substituted indoles possessing uncommon substitution patterns.     

Indole diterpenoid synthetic studies. Construction of the heptacyclic core of (-)-nodulisporic acid D

[structure: see text] Construction of the heptacyclic core of (-)-nodulisporic acid D, a representative member of a recently discovered class of architecturally complex, ectoparasiticidal indole alkaloids, has been achieved. The modular synthetic strategy comprises an expedient, stereocontrolled synthesis of a tricyclic western hemisphere, in conjunction with union of an eastern hemisphere, exploiting the 2-substituted indole synthetic protocol introduced and developed in our laboratory.     

On exact solutions to epidemic dynamic models

In this study, we address an SIR (susceptible-infected-recovered) model that is given as a system of first order differential equations and propose the SIR model on time scales which unifies and extends continuous and discrete models. More precisely, we derive the exact solution to the SIR model and discuss the asymptotic behavior of the number of susceptibles and infectives. Next, we introduce an SIS (susceptible-infected-susceptible) model on time scales and find the exact solution. We solve the models by using the Bernoulli equation on time scales which provides an alternative method to the existing methods. Having the models on time scales also leads to new discrete models. We illustrate our results with examples where the number of infectives in the population is obtained on different time scales.     

Invariant Measures for Set-Valued Dynamical Systems

A continuous map on a compact metric space, regarded as a dynamical system by iteration, admits invariant measures. For a closed relation on such a space, or, equivalently, an upper semicontinuous set-valued map, there are several concepts which extend this idea of invariance for a measure. We prove that four such are equivalent. In particular, such relation invariant measures arise as projections from shift invariant measures on the space of sample paths. There is a similarly close relationship between the ideas of chain recurrence for the set-valued system and for the shift on the sample path space.

     

Fractionation of cigarette smoke condensate for chemical and biological testing

Large-scale fractionation of cigarette smoke condensate (CSC) was carried out by gel filtration and silicic acid column chromatography, and selected fractions and their subfractions were tested for tumorigenicity by mouse-skin bioassay. The weak-acid fraction was separated into four subfractions, the polynuclear aromatic hydrocarbon (PAH) fraction into two subfractions, and the polar neutral lipid fraction into three subfractions. Also, combinations of subfractions were examined for synergic effects and portions of all active material were subjected to chemical analyses by gel filtration, column, thinlayer and gas chromatography, and ultraviolet and mass spectrometry. A weak-acid subfraction (F-63) in which catechol was concentrated, and which comprized 3.27% CSC was shown to be tumorigenic, as were combinations of this sub fraction with the active PAH (F-67) sub fraction and a polar, neutral lipid (F-70) sub fraction, representing 0.01 and 0.05% CSC, respectively. The results indicated that catechol may be a potent cocarcinogen and that the PAH in CSC interact with other components to exert a tumorigenic effect.