超临界流体色谱在金属络合物和金属有机化合物中的分析应用

超临界流体色谱（SFC）在色谱分离过程中能在较低的温度下分析对热不稳定性的化合物,包括金属络合物和金属有机化合物。本文总结了近来文献报道的各种过渡金属、重金属、镧系和锕系以及铅、汞和锡的金属有机化合物的SFC分离,还讨论了SFC检测系统和金属有机化合物的溶解度的测定。     

Analysis ofK→3Π decays in chiral perturbation theory

Using the recently proposed higher-order chiral Lagrangians determined from the integration of nontopological chiral anomalies, we calculate corrections to the current-algebra analysis ofK→3Π decay amplitudes expanded in powers of the Dalitz variables. Effects of quartic-derivative weak chiral Lagrangians are determined through the use of short-distance effective weak Hamiltonian and the factorization method. We find that (1) the constant and linear terms in the amplitude for ΔI=1/2K→3Π are in excellent agreement with experiment; the previous discrepancy of (20–35)% between current algebra and data is thus accounted for by the higher-order effective Lagrangians, (2) the penguin interaction does not play an essential role in the ΔI=1/2 rule, for otherwise it will lead to a large disagreement for the constant and linear terms, (3) one of the two quadratic terms in the ΔI=1/2 process, which arise from the quartic chiral Lagrangians, is in accord with data within experimental errors, while the other is off by four standard deviations, (4) the linear term in the ΔI=3/2 transitions is in good agreement with experiment and contributions from quadratic terms are sizable.     

A companion matrix approach to the study of zeros and critical points of a polynomial

In this paper, we introduce a new type of companion matrices, namely, D-companion matrices. By using these D-companion matrices, we are able to apply matrix theory directly to study the geometrical relation between the zeros and critical points of a polynomial. In fact, this new approach will allow us to prove quite a number of new as well as known results on this topic. For example, we prove some results on the majorization of the critical points of a polynomial by its zeros. In particular, we give a different proof of a recent result of Gerhard Schmeisser on this topic. The same method allows us to prove a higher order Schoenberg-type conjecture proposed by M.G. de Bruin and A. Sharma.     

Synthesis and light‐emitting properties of platinum‐containing oligoynes and polyynes derived from oligo(fluorenyleneethynylenesilylene)s

A series of blue‐light‐emitting oligo(fluorenyleneethynylenesilylene)s (OFESs) of the general formula HC?CRC?C(EC?CRC?C)_mEC?CRC?CH (E = SiPh₂, SiMe₂, or SiMe₂? SiMe₂; m = 0–2; R = 9,9‐dihexylfluorene‐2,7‐diyl) and their phosphorescent platinum‐containing oligoynes and polyynes were synthesized and characterized. The solution properties and regiochemical structures of this new structural class of organosilicon‐based polyplatinayne polymers {trans‐[? Pt(PBu₃)₂C ?CRC?C(EC?CRC?C)_mEC?CRC?C? ]_n} were studied with IR and NMR (¹H, ¹³C, ²⁹Si, and ³¹P) spectroscopy. The optical absorption and photoluminescence spectra of these metallopolymers were examined and compared with their discrete oligomeric model complexes. Our studies led to a novel approach of using the sp³‐silyl moiety as a conjugation interrupter to limit the effective conjugation length in metal polyynes, which could boost the phosphorescence decay rates essential for light‐energy harvesting from the triplet excited state. The influence of the heavy platinum atom and the group 14 silyl unit possessing different side‐group substituents on the thermal and phosphorescence properties was investigated in detail. We also established the goal of studying the evolution of the lowest singlet and triplet excited states with chain length m of OFESs and the nature of E in these metallopolymers. This work indicated that the phosphorescence emission efficiency harnessed through the heavy‐atom effect of platinum in the main chain did not change very much with oligomer chain length m but generally decreased with the E group in the order SiMe₂ > SiMe₂? SiMe₂ > SiPh₂. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4804–4824, 2006     

一类Markov链的强逼近

本文给出了一类非时齐的Markov链的强逼近.作为应用,建立了临床试验中Markov链自适应设计的强相合性,重对数律和弱收敛.     

Some addition reactions of bisgermavinylidene

The reaction of bisgermavinylidene [(Me₃SiN?PPh₂)₂C?Ge→Ge?C(PPh₂?NSiMe₃)₂] ( 1 ) with AdNCO (Ad = Adamantyl) afforded the [2 + 2] cycloadditon product [(Me₃SiN?PPh₂)₂CGeC(O) NAd] ( 2 ). Similar reaction of 1 with Ph₃SiOH in tetrahydrofuran (THF) yielded the base‐stabilized germanium(II) triphenylsiloxide [H₂C(PPh₂?NSiMe₃)₂Ge(OSiPh₃)₂] ( 3 ). The results suggested that reactive germavinylidene may exist in solution and is capable of forming addition reaction products. The X‐ray structures of 2 and 3 were determined. Copyright © 2007 John Wiley & Sons, Ltd.     

Synthesis of novel 7-substituted 5,6-dihydroindol-2-ones via a Suzuki-Miyaura cross-coupling strategy

A versatile method for the synthesis of new 7-substituted 5,6-dihydroindol-2-ones is described. The synthetic strategy proceeds through the use of the established palladium-catalyzed Suzuki-Miyaura cross-coupling reaction of halogenated indol-2-ones and arylboronic acids/esters.     

Optical gain of interdiffused GaInNAs/GaAs quantum wells

A self-consistent model for the band structure and optical gain spectra in interdiffused Ga_xIn_1-xN_0.04As_0.96/GaAs single quantum wells are studied theoretically using Fick’s Law and the Fermi Golden Rule. Due to quantum-well interdiffusion, the peak gain and its peak vary with the annealing time. Our results show that the interdiffusion technique can be used to tune the operation wavelength for multi-wavelength applications without degradation of device performance. Received: 18 April 2001 / Accepted: 19 September 2001 / Published online: 20 December 2001