A Low-Complexity Multiuser Detector for Asynchronous CDMA QPSK Adaptive Antenna Array Systems

This paper proposes a low complexity joint space-time multiuser detection algorithm for asynchronous DS/CDMA antenna array systems. The proposed multiuser detector is composed of an adaptive antenna array, used as a linear beamformer, and a sliding window decorrelator. A QPSK modulation scheme is used in order to increase bandwidth efficiency. Numerical results are given in terms of Bit Error Rate (BER) under the assumption of a frequency-selective Rayleigh slow fading channel. In particular, the proposed receiver is shown to be near-far resistant, even in worst fading cases, and to exploit completely array introduction while maintaining acceptable computational complexity. The proposed architecture avoids linear filter realization of the decorrelator, which is impractical in the case of a large number of users, and operates with relatively short data frames instead of the complete information sequence. Finally, this receiver is very flexible to changes in timing configuration.     

Fifty years of the Siberian Division of the Russian Academy of Sciences

This is a write-up on the foundation of the Sobolev Institute of Mathematics in 1957.     

逻辑函数在布尔减-异或、布尔除-符合代数系统中的规范展开式

证明了布尔减、异或运算以及布尔除、符合运算的完备性,并从与-异或及或-符合代数系统中的RM、CRM展开式出发,分别推导了任意逻辑函数在布尔减-异或及布尔除-符合代数系统中的规范展开式.举例说明了与-或-非代数系统中规范展开式与布尔减-异或、布尔除-符合代数系统中的规范展开式之间的转换.     

Rearrangement during cyclisation of some 3-(2-pyrrolyl) propionic acids and related compounds

Cyclisation of the title compounds leads to mixtures of the expected 4H-cyclopental[b]pyrrol-4-ones (1), the corresponding 6-ones (3) by a single rearrangement, and the cyclopenta[c]pyrrol-4-ones (4) by a double rearrangement, the proportions depending upon the substituents.The ¹H NMR spectra of 2-methyl-4H-cyctopenta[b]thiophen-6-one (3f) shows 6J long range $\text{CH}{}_3\text{CH}{}_2$ coupling, but this is absent in the corresponding pyrroles (3c,d). The ¹³C spectra of 1 and 3 cannot be interpreted on the basis of substituent chemical shifts in pyrroles and thiophens, and are clearly -CH = CH-X (X = NMe, NPh, S) bridged derivatives of cyclopent-2-enone.     

An electron-diffraction study of the molecular structure of gaseous perbromyl fluoride and calculation of its force field and vibrational amplitudes

The molecular structure of FBrO₃ has been studied by gas-phase electron diffraction. Least-squares refinements of the molecular geometry using fixed spectroscopic amplitudes revealed two geometrical minima. Initially, the amplitudes employed were derived from diagonal force fields obtained by spectroscopic least-squares refinements to fit observed and calculated wave numbers; for each geometry there are two spectroscopic minima. In the lowest geometrical minimum the wave number agreement is poor, however, the introduction of the ∠OBrO/∠FBrO interaction force constant removed the discrepancies; the resulting force field is F(Br-O) = 6.92 ± 0.02 mdyn Å^?1F(Br-F) = 3.22 ± 0.03 mdyn Å^?1, F(∠OBrO) = 1.06 ± 0.02 mdyn Å, F(∠FBrO) = 0.81 ± 0.03 mdyn Å, F(∠OBrO/∠FBrO) = ?0.19 ± 0.02 mdyn Å. In the corresponding geometrical minimum r_g(Br-O) = 1.582 ± 0.001 Å, r_g(Br-F) = 1.708 ± 0.003 Å, r_α(∠OBrO) = 114.9 ± 0.3°, r_α(∠FBrO) = 103.3 ± 0.3°. Perpendicular amplitude correction coefficients, calculated for each force field employed, were used throughout to relate the interatomic distances through the r_α-structure. The geometries of the r_α^o- and r_e-structures are estimated.     

Relative raman line intensities for H2 and for D2. Correction factors for molecular non-rigidity

Ab initio calculations are presented for H₂ and D₂ relative Raman intensities originating from common rotational levels for both vibrational-rotational and pure rotational transitions. Factors f(J) required to correct measured intensities for molecular non-rigidity (e.g. in temperature measurements) are tabulated. The calculations are compared with literature perturbation-theory equations (significant differences at large J in vibration-rotation) and with experiment.     

Fluorescence decay of tertiary aliphatic amines

The fluorescence decay of the tertiary aliphatic animes trimethylamine (TMA), triethylamine (TEA) and tri-n-propylamine (TPA) in the vapour phase excited between 260 and 215 nm has been shown to consist of a single, wavelength-dependent, component when the first excited state is uniquely excited, but two components when the first and second excited states are simultaneously excited. This dual exponentiality persists at pressures as low as 10 mTorr, and it is argued that the two-component decay does not arise from collisional vibrational relaxation.     

Separation and gravimetric determination of cerium and lanthanum with N-m-tolyl-m-nitrobenzohydroxamic acid

Cerium and lanthanum were determined gravimetrically by selective precipitation with N-m-tolyl-m-nitrobenzohydroxamic acid and separated from several metal ions such as Ag(+), Be(2+) , Pb(2+) , Mn(2+) , Cu(2+), Zn(2+) , Cd(2+) , Hg(2+) , Pd(2+) , Ga(3+) A1(3+) , Bi(3+) , Sb(3+), Sn(4+), Ce(3+) , Pr(3+) , Nd(3+) , Ti(4+), Zr(4+), Th(4+), V(5+) , Mo(6+) and U(6+) . The precipitates were weighted directly after drying at 110 degrees . The analytical results indicated the composition of the complexes to be (C(14)H(11)N(2)O(4))(n)M.     

二维同步OCDMA系统的性能分析

构造了一种用于二维同步光码分多址(OCDMA)系统的修正素数跳频码(MPC/PC),分析了码字的自相关和互相关性能,研究了二维同步OCDMA系统的误码率和吞吐量性能.结果表明,与一维同步OCDMA系统相比,二维同步OCDMA系统的可接入用户数大大增加,误码率大大降低,吞吐量明显提高.     

GF(2p)LDPC编码的相位调制OFDM系统在瑞利衰落信道的性能

OFDM是一项能有效对抗高速无线通信中多径衰落的关键技术，为了进一步提高OFDM系统的误码性能，许多信道编码技术已被应用于OFDM系统中，二元域LDPC码以其近香农限的误码性能和较低的译码复杂度成为研究的热点。在AWGN信道下，多元域LDPC码比等效码长的二元域LDPC码有更好的纠错性能。本文提出了一种将多元域LDPC码经过MPSK调制后用于OFDM系统的新方法。仿真结果表明，在多径衰落信道下，通过合理选择多元LDPC码域的阶数和调制的方法，多元域LDPC编码的高阶调制OFDM系统比等效码长的二元域LDPC编码OFDM系统具有更好的性能，并且由于采用了多元域LDPC的快速BP译码，译码复杂度只是稍有增加。