Bilepton production in $ e^-\gamma $ collisions

We study the production of bileptons, new gauge bosons of lepton number two, in the minimal 3-3-1 model in high energy collisions. If the bilepton masses are in the range of 300 GeV the reaction will give observable cross-sections in future colliders.Received: 5 August 2003, Published online: 23 March 2004Dang Van Soa: On leave of absence from Department of Physics, Hanoi University of Education, Hanoi, VietnamHoang Ngoc Long: On leave of absence from Institute of Physics, NCST, P.O. Box 429, Bo Ho, Hanoi 10000, Vietnam     

1.517 μm附近水汽分子谱线加宽系数的腔衰荡光谱测量

 以超低膨胀系数微晶玻璃为腔体,以分布反馈式激光器为光源,建立了一套等噪声测量灵敏度为3.2×10^-9 cm^-1的调腔式连续波腔衰荡光谱系统。应用该系统对1.517 μm附近(6 586.5~6 596.5 cm^-1范围内)的7条水汽吸收谱线进行了实验研究,测得了这些谱线在氮气、空气环境下的谱线加宽系数。根据测得的结果,得到了此波段水汽的空气加宽系数与氮气加宽系数之比为0.896 9±0.068 7(3倍标准误差范围内),并就测得水汽的谱线加宽系数与HITRAN2004数据库数据进行了比较。     

Interim Anatase Coating Layer Stabilizes Rutile@CrxOy Photoanode for Visible‐Light‐Driven Water Oxidation

Ternary core–shell heterostructured rutile@anatase@Cr_xO_y nanorod arrays were elaborately designed as photoanodes for efficient photoelectrochemical water splitting under visible‐light illumination. The four‐fold enhanced and stabilized visible‐light photocurrent highlights the unique role of the interim anatase layer in accelerating the interfacial charge transfer from the Cr_xO_y chromophore to rutile nanorods.     

Binding and photodissociation of CO in iron(II) complexes for application in positron emission tomography (PET) radiolabelling

(R-DAB)FeI(2) complexes containing bidentate diimide ligands (R-DAB = RN=CH-CH=NR; R = (i)Pr, c-C(6)H(11)) have been investigated for their ability to react with carbon monoxide to form iron(II) dicarbonyl complexes, (R-DAB)FeI(2)(CO)(2). Solution IR spectroscopy revealed two νCO stretches between 2000 and 2040 cm(-1) corresponding to a cis-arrangement of the carbonyl ligands around the iron. Photochemical decarbonylation was achieved by UV irradiation (365 nm), which occurred within 5 min as evidenced by solution IR spectroscopy. (c-C(6)H(11)-DAB)FeI(2) has been characterised by X-ray crystallography. Reactions using (11)C-labelled carbon monoxide were investigated and revealed that both (R-DAB)FeI(2) species were not effective as trapping complexes due to the low concentrations of [(11)C]CO used in these experiments. A Fe(TPP)(THF)(x) (TPP = tetraphenylporphyrin) complex was investigated with unlabelled CO and the monocarbonyl adduct Fe(TPP)(THF)CO was formed in situ as identified by IR spectroscopy (νCO = 1966 cm(-1)) yet was stable to CO loss upon UV irradiation. Carbonylation reactions of in situ-generated Fe(TPP)(THF)(x) using [(11)C]CO revealed that 97% of the [(11)C]CO stream could be trapped in one pass of the gas at room temperature and at atmospheric pressure.     

Lp空间中随机变量的g-期望与条件g-期望

利用倒向随机微分方程的Lp解定义了Lp空间中随机变量g-期望与条件g-期望,扩张了g-期望与条件g-期望的定义空间;证明了用Lp解定义的g-期望与文[5]用算子连续扩张方法定义的一般g-期望的一致性,得到了Lp空间中随机变量的g-期望与条件g-期望的一些性质.     

Search for f(J)(2220) in radiative J/ψ decays

We present a search for f(J)(2220) production in radiative J/ψ→γf(J)(2220) decays using 460 fb?1 of data collected with the BABAR detector at the SLAC PEP-II e(+)e? collider. The f(J)(2220) is searched for in the decays to K(+)K? and K(S)?K(S)?. No evidence of this resonance is observed, and 90% confidence level upper limits on the product of the branching fractions for J/ψ→γf(J)(2220) and f(J)(2220)→K(+)K?(K(S)?K(S)?) as a function of spin and helicity are set at the level of 10??, below the central values reported by the Mark III experiment.     

开链冠醚Schiff碱-稀土配合物的合成、表征及近红外发光光谱研究

合成了3个新型开链冠醚Schiff碱-稀土离子三元配合物RE(H2L)(Mq)(NO3)3,其中RE=Nd3 ,Er3 ,Yb3 ,配体H2L=N,N-双(邻羟苯亚甲基)-3,6-二氧杂-1,8-二氨基辛烷,Mq为8-羟基喹哪啶.采用元素分析、红外光谱(IR)、紫外-可见吸收光谱(UV-vis)、热重-差热分析(TG-DTG)等手段对配合物的组成结构进行了表征.测定了3种新型结构稀土三元配合物在不同温度(77 K和300 K)时的近红外发光光谱.     

Determination of 77Se-77Se and 77Se-13C J-coupling parameters for the clusters [Re5OsSe8(CN)6]3- and [Re4Os2Se8(CN)6]2-

We have investigated rarely observed 77Se J-couplings (spin-spin couplings) in the mixed-metal face-capped octahedral clusters [Re5OsSe8(CN)6]3- and [Re4Os2Se8(CN)6]2- at natural abundance. To the best of our knowledge, these are the first observations of Se-Se spin-spin interactions between mu3-Se sites, important for stereochemical assignments in hexarhenium analogues, Chevrel phase materials, and similar cluster materials. NMR techniques such as COSY, INADEQUATE, and 2D J-resolved spectroscopy have been used in conjunction to study these interactions. The two isomers (cis and trans) of [Re4Os2Se8(CN)6]2- were distinguishable, and selective isotopic labeling of [Re5OsSe8(CN)6]3- with 13CN ligands enabled resonances to be assigned by observing the 2J (Se-M-C) couplings. For [Re5OsSe8(CN)6]3-, two different 2J (Se-M-Se) couplings were measurable on a single cluster, and these are related to one another through spin-spin interactions across a face diagonal or along an edge of the cube of inner selenium ligands. A rigorous analysis based on combinatorial math has been invoked to assign the couplings on the basis of the probability of multiple-spin interactions. The face diagonal association is found to result in a J-coupling interaction larger in magnitude than that from coupling along an edge of the cube-information critical for making stereochemical assignments of selenium sites.     

A New Two‐Dimensional Coordination Polymer of Mercury(II) with very High Thermal Stability

A 2D Hg^II coordination polymer containing ligands 1,2,4‐triazole (Htrz) and thiocyanate, [Hg(μ₃‐trz)(SCN)]_n ( 1 ) has been synthesized and characterized by elemental analysis and IR spectroscopy. The single‐crystal X‐ray data show the coordination number of Hg atoms is four and the ligand trz^? acts as a three‐fold donor. The thermal stability of compound 1 was studied by thermal gravimetric and differential thermal analyses. The composition and formation of the complex in methanol solution were found to be in support of its solid state structure.