Astrophysical S-factors from asymptotic normalization coefficients

S-factors for direct capture reactions can be found at astrophysical energies from asymptotic normalization coefficients which provide the normalization of the tail of the overlap function. For example the overlap for ⁸B → ⁷Be+p defines the S-factor for ⁷Be (p, γ)⁸B. Peripheral transfer reactions offer a technique to determine these asymptotic normalization coefficients. As a test of the technique, the ¹⁶O(³He, d)¹⁷F reaction has been used to determine asymptotic normalization coefficients for transitions to the ground and first excited states of ¹⁷F. The S-factors for ¹⁶O(p, γ)¹⁷F calculated from these ¹⁷F → ¹⁶O+p asymptotic normalization coefficients are found to be in very good agreement with recent measurements. Following the same technique, the ¹⁰B(⁷Be, ⁸B)⁹Be and ¹⁴N(⁷Be, ⁸B)¹³C reactions have been used to measure the asymptotic normalization coefficient for ⁷Be(p, γ)⁸B. This result provides an indirect determination of S ₁₇(0).     

关于n+k相多体系(k≥4)封闭网的构造

本文证明了n+k多体系(k≥4)的全部可能的封闭网均可以通过若干相应的子n+3相多体系的拼合运算得出,从而为具体构造n+k相多体系(k≥4)的全部合理的封闭网,提供了基本方法。     

超导临界温度理论(Ⅱ)

在文献[1]中,我们导出了超导临界温度T-c的一个严格级数表式.本文讨论这个级数的收敛范围,以及通过解析延拓来扩展收敛范围的可能性.结论是:我们的T_c级数(指文献[1]原来的级数,或者经过延拓后的级数)在∞>λ>λ₀的整个范围内,都是收敛的.这里λ₀是Matsubara表象中使决定T_c的方程具有正实数解的最小的λ值.它实际上就是库伦赝势.因此,也许除了少数非常弱耦合的超导体以外,我们的T_c级数能适用于一切超导体.     

EPR of Mn2+ in Cd(COO)2· 3H2O single crystals

The electron paramagnetic resonance spectrum of Mn²⁺ has been investigated in cadmium oxalate trihydrate single crystals at room temperature. The spectrum, recorded in the X-band, consists of a set of lines all of which correspond to a single type of environment. None of the principal axes coincides with any crystallographic axis. The spectrum is satisfactorily described by a spin Hamiltonian with a rhombic crystalline electric field. The separations of the forbidden doublets (Δm = ± 1) in different electronic transitions have been calculated and compared with the observed doublet separations.     

New Aminoethylsulfanyl-Substituted Tribenzoporphyrazines

Unsymmetrical metal-free and metalo-porphyrazines (M=Mg, Zn, Co) made up of three phthalonitrile units and a single maleonitrile moiety on the periphery were prepared by cyclization of bis(2-dimethylaminoethylthio)maleonitrile and phthalonitrile. The magnesium derivative (Mgpz) was converted into the quaternized product by reaction with methyl iodide. The new compounds were characterized by elemental analysis, IR, NMR, mass, and electronic spectra.     

裂缝的张开位移和应变的关系

本文采用Kármán-钱处理亚音速流动方法的精神。处理了弹塑性断裂力学问题.通过建立的“双弹性”模型,从理论上得到了裂缝端部的张开位移和应变的方程组.实例计算结果表明,理论值全部落在实验结果的分散带内.文中并从理论上解释了实验结果与材料的性质及实验条件的关系.本文的结果不仅为宽板实验所证实,也被文献[2]的实验所证实.同时也表明。公式(37)用于工程,能够分析压力容器上应变裂缝的容许极限.     

Weighted tridiagonal matrix enhanced multivariance products representation (WTMEMPR) for decomposition of multiway arrays: applications on certain chemical system data sets

This work focuses on the utilization of a very recently developed decomposition method, weighted tridiagonal matrix enhanced multivariance products representation (WTMEMPR) which can be equivalently used on continuous functions, and, multiway arrays after appropriate unfoldings. This recursive method has been constructed on the Bivariate EMPR and the remainder term of each step therein has been expanded into EMPR from step to step until no remainder term appears in one of the consecutive steps. The resulting expansion can also be expressed in a three factor product representation whose core factor is a tridiagonal matrix. The basic difference and novelty here is the non-constant weight utilization and the applications on certain chemical system data sets to show the efficiency of the WTMEMPR truncation approximants.     

Photoinduced intramolecular charge separation in donor/acceptor-substituted bicyclohexylidene and bicyclohexyl

The photophysical properties of a bicyclohexylidene (1DA) and a bicyclohexyl (2DA) substituted with an anilino electron donor and a dicyanoethylene electron acceptor have been studied. Quenching of local donor emission is observed for these compounds as well as quenching of the "pseudo-local" acceptor emission. Transient absorption spectra show dialkylanilino-type radical-cation and dicyanoethylene-type radical-anion absorptions. These results show that intramolecular charge separation takes place in 1DA and 2DA. This was corroborated by time-resolved microwave conductivity measurements from which large excited-state dipole moments were found for both 1DA and 2DA. Time-resolved fluorescence spectroscopy revealed that in the charge-separated state in cyclohexane for 2DA, molecular folding takes place on a nanosecond timescale. For 1DA in cyclohexane, either charge separation takes place in a (fully) folded conformation or very rapid (subnanosecond timescale) folding takes place subsequent to charge separation. In addition to this difference in conformational behavior, the presence of the exocyclic double bond between the cyclohexyl-type rings results in efficient quenching of the anilino donor triplet state and acceleration of the charge recombination rate by a factor of 20.     

多光束共振光压作用下钠原子束的偏转

本文报道了多光束共振光压作用下钠原子束偏转的实验研究结果。文中提出了用多光束与原子束相互作用以增大原子束的偏转量,并可大大降低对激光功率的要求。用一台染料激光器照射钠原子束得到1×10^-2rad的偏转角,偏转距离约7.2mm,并用激光诱导原子束荧光的方法检测原子束的偏转。