双环的同态定理

对双环的双子环、双环同态、双环同构、双理想子环、双商环等性质进行研究,给出了双环的2个同态定理.

Spatial and environmental effects on plant communities in the Yellow River Delta, Eastern China

Types and structure of plant communities in the Yellow River Delta were investigated by using detrended canonical correspondence analyses （DCCAs） and a two-way indicator species analysis （TWINSPAN）. The distribution pattern and influential factors of the plant communities were also analyzed by testing elevation, slope, soil characteristics, longitude and latitude of 134 vegetation samples collected by representative plot sampling methods. Results showed that all the 134 vegetation samples could be divided into seven vegetation groups, separately dominated by Robinia pseucdoacacia, Imperata cylindrical, Miscanthus saccharifleus, Suaeda salsa, Aeluropus sinensis, Phragmites australis and Tamarix chinensis. The vegetation distribution pattern was mainly related to elevation, ground water depth and soil characteristics such as salinity and soluble potassium. Among the factors affecting distribution pattern of the plant communities, the species matrix explained by non-spatial environmental variation accounts for 45.2% of total variation. Spatial variation and spatial-structured environmental variation explain 11.8%, and 2.2%, respectively. Remained 40.8% of undetermined variation is attributed to biological and stochastic factors.

Persistent Currents in the Double Aharonov-Bohm Ring Connected to Electron Reservoirs

We study persistent currents in the double Aharonov-Bohm ring connected to two electron reservoirs by quantum waveguide theory. It is found that the persistent currents in the double Aharonov-Bohm ring depend .on the direction of the current flow from one reservoir to another. When the direction of the current flow reverses, tl2e persistent current in each ring of the double Aharonov-Bohm ring changes. If the two rings are of the same size, the persistent currents in the left and the right rings exchange at the reversal of the current flow direction.

Biphenyl Bis [π-cyclopentadienyl ） iron] Dication as an Efficient Cationic Photoinitiator for Epoxy Polymerization

Ferrocenium monocations as photoinitiators for cationic photopolymerization suffer from a limitation of low absorption and low reactivity under high-pressure Hg lamp. Here, a ferrocenium dication salt, biphenyl bis [π-cyclopentadienyl）iron] hexafluorophosphate （[bis（Cp-Fe）-biphenyl] （PF6）2 was synthesized by the ligand exchange reaction between ferrocene and biphenyl. The chemical structure was characterized with FTIR and ^1HNMR. The separation of ferrocenium monocation cyclopentadien-iron-biphenyl hexafluorophosphate （[Cp-Fe-biphenyl] PF6） and dication [bis（Cp-Fe）-biphenyl] （PF6）2 was carried out by column chromatography. The photoactivity of initiating photopolyinerization of epoxide ER14221 was studied as a cationic photoinitiator. [Bis（Cp-Fe）-biphenyl] （PF6）2 can efficiently absorb radiation above 300nm and its photoactivity is higher than that of its monocation.

Conversion of methanol to propylene over SAPO-14:Reaction mechanism and deactivation

Methanol to olefins(MTO)reaction as an important non-oil route to produce light olefins has been industrialized,and received over 80% ethylene plus propylene selectivity.However,to achieve high single ethylene or propylene selectivity towards the fluctuated market demand is still full of challenge.Small-pore SAPO-14 molecular sieve is a rare MTO catalyst exhibiting extra-high propylene selectivity.It provides us a valuable clue for further understanding of the relationship between molecular sieve structure and MTO catalytic performance.In this work,a seconds-level sampling fixed-bed reactor was used to capture real-time product distributions,which help to achieve more selectivity data in response to very short catalytic life of SAPO-14.Changes in product distribution,especially during the low activity stage,reflect valuable information on the reaction pathway.Combined with in situ diffuse reflectance infrared Fourier-transform spectroscopy,in situ ultraviolet Raman measurements and ^(12)C/^(13)C isotopic switch experiments,a reaction pathway evolution from dual cycle to olefins-based cycle dominant was revealed.In addition,the deactivation behaviors of SAPO-14 were also investigated,which revealed that polymethylbenzenes have been the deactivated species in such a situation.This work provides helpful hints on the development of characteristic methanol to propylene(MTP)catalysts.

Synthesis of Antimalarial Bicyclic Hemiketal Peroxides Belonging to the G-factor Family

Structural analogues of bicyclic peroxides belonging to the G factors family have been synthesised under Mannieh type conditions, followed by an autoxidation step furnishing exclusively the peroxide. As electron transfer from heine or free iron to peroxide is the first step in the mode of action ofartemisinin -like compound, Fe（fl） induced reduction was studied and the reactivity of the intermediate C-centered radical formed was correlated to the antimalarial activity. Dissociative electron transfer was studied by electrochemistry and allowed the evaluation of the standard reduction potentials and other pertinent thermochemical information. These bicyclic peroxides were evaluated in vitro against Plasmodium falciparum and revealed moderate to good activity.

Crystal and Molecular Structure of Methylene-bis[benzobicyclo(diaza-diphenyl) stannoxide],[o-O■n(C_6H_5)_2]_2CH_2·1/2C_6H_6

Methylene-bis[benzobicyclo(diaza-diphenyl) stannoxide,C_(41)H_(34)N_4O_4Sn_2·1/2C_6H_6],Mr=923.19,m.p.126-127℃,triclinic,P1,a=9.780(4),b=14.485(2),c=15.122(6),α=74. 95(3),β=72.21(3),γ=82.68(2)°,V=1967(1) Z=2,Dx=1.56 g/cm￣3, MoKα(λ=0.71073),μ=13.20 cm-1,F(000)=922;final R=0.045, Rw=0.046 for 3637 observed reflections(I≥3σ(I)).The title compound is a bimetallo-heterocyclic complex prepared by condensation.Each tin atom has a trigonal bipyramidal coordination with two oxygen atoms occupying the axial positions.

A new approach to the bicyclo[3.3.1]nonane framework of huperzine A-like molecules via palladium-catalyzed intramolecular γ-arylation

In our synthetic studies toward huperzine A, a diastereoselective α＇-alkylation of the α-amido-γ-methyl hexenone 4 was real- ized through a dianion intermediate which significantly enhanced the reactivity. Under the attempted Heck reaction conditions, an unexpected and unprecedented palladium-catalyzed intramolecular T-arylation of 3 was observed, which generated 18 with bicyclo[3.3, l]nonane framework in satisfactory yield.

POCl_3-mediated H-bonding-directed one-pot synthesis of macrocyclic pentamers,strained hexamers and highly strained heptamers

Previously we have shown that POCl3-mediated H-bonding-directed one-pot macrocyclization allows for the highly selective preparation of five-residue macrocycles as the predominant product with low yields of hexamers and an undetectable occurrence of both tetramers and heptamers.Replacing the interiorly arrayed methyl groups with ethyl groups in these 4-7 residue macrocycles alters the relative stability order among them.Specifically,ethoxy-substituted six-residue macrocycle,rather than pentamer,turns out to be computationally the most stable,suggesting that ethoxy-containing hexamer possibly can be formed as the major product under suitable conditions.We have investigated this possibility by varying reaction temperatures and concentrations,invariably affording pentamer as the major macrocycle with strained circular hexamers and highly strained circular heptamers produced in substantial amounts.This discrepancy can be reasonably explained on the basis of bimolecular reactions between two oligomers higher than monomers via kinetic simulations.In this scenario,the acyclic pentamer is kinetically "trapped" to undergo an intramolecular cyclization to yield circular pentamer,rather than to produce acyclic hexamer.As a result,acyclic hexamer precursor is generated largely from sterically demanding bimolecular reactions between a dimer and a tetramer,or between two trimers that are kinetically slower than the pentamer-producing chain-growth reactions.We additionally found that one-pot macrocyclization proceeds to the largest extent at 40 ℃,an intriguing finding that highlights the low reactivities of acid chloride and amine groups in these H-bond-enforced acyclic oligomeric intermediates.