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131.
基于支持向量机的羰基化合物红外光谱研究 总被引:1,自引:0,他引:1
设计了一个4层分等级分类系统,通过支持向量机技术对羰基化合物的红外光谱成功地进行了信息分类和提取,并与人工神经网络进行比较,结果表明:支持向量机对羰基类化合物红外光谱分类效果优于人工神经网络;另外详细探讨了表征酰胺类化合物的特征光谱峰片段对识圳伯仲叔酰胺的影响,证明了酰胺的N-H伸缩振动峰对识别伯仲叔酰胺贡献最大,为构建红外光谱智能解析系统提供了定量依据。 相似文献
132.
133.
用原子捕获技术提高火焰原子吸收光谱法的灵敏度 总被引:1,自引:0,他引:1
采用简易的石英原子捕获器,使Cu,Ag,Au,Zn,Cd,Pb,Sb,Bi等易挥发元素在空气-乙炔火焰原子吸收光谱法中的灵敏度提高了3~5倍,并有较好的精密度,相对标准偏差在1%左右,方法中用此技术测定了标准物质中Pb、Cd的含量,获得了满意的结果,它较之石墨炉原子吸收光地具有快速,简便的特点,具有较大的实用价值。 相似文献
134.
本文对几种人工光合作用反应中心系统,做一个简单的综述,其中包括叶绿素和细菌叶绿素二聚体,卟啉二聚体,卟啉-苯醌共价键络合物以及其他合成中心。 相似文献
135.
We show that two simple semiclassical strategies, one based on the Wilson–Sommerfeld rule and the other on the uncertainty principle, yield the exact modified form of the virial theorem for confined systems. An alternative, easier quantum mechanical route to arrive at this result is also sketched. Pilot calculations on confined oscillators reveal decisive trends. © 2004 Wiley Periodicals, Inc. Int J Quantum Chem, 2005 相似文献
136.
在242-260nm波氏范围通过CS2分子的共振增强多光子电离(REMPI)获得了母体离子CS和碎片离子的分质量激发谱.在λ<246.4nm区间,CS激发谱上呈现出来源于CS2双光子电离的弥散谱带,碎片离子激发谱的归属强烈提示多光子过程中有中性基电子态的CS和S(经由CS2的光解离)产生:(1)CS 的谱带主要来源于中性CS碎片经由单光子跃迁产生的(1+1)共振增强电离,(2)除了部分S 的谱峰来自CS 的光解外,多数S 的锐谱峰来自中性S原子经由3p3(2D0)4p,3p3(4S0)np(n=6,7,8)←3p43pJ(J=2,1,0)双光子跃迁产生的(2+1)共振增强电离. 相似文献
137.
D. Zorrilla Cuenca J. Sánchez Márquez M. Fernández Núñez R. Rodríguez Huertas 《International journal of quantum chemistry》2007,107(4):879-893
This project consists of two parts. In the first part, a series of test calculations is performed to verify that the integrals involved in the determination of atomic and molecular properties by standard self‐consistent field (SCF) methods can be obtained through Halton, Korobov, or Hammersley quasi‐random integration procedures. Through these calculations, we confirm that all three methods lead to results that meet the levels of precision required for their use in the calculation of properties of small atoms or molecules at least at a Hartree–Fock level. Moreover, we have ensured that the efficiency of quasi‐random integration methods that we have tested is Halton=Korobov>Hammersley?pseudo‐random. We also find that these results are comparable to those yielded by ordinary Monte Carlo (pseudo‐random) integration, with a calculation effort of two orders of smaller magnitude. The second part, which would not have been possible without the integration method previously analyzed, contains a first study of atoms constrained in spherical boxes through SCF calculations with basis functions adapted to the features of the problem: Slater‐type orbitals (STOs) trimmed by multiplying them by a function that yields 1 for 0 < r < (R‐δ), polynomial values for (R‐δ) < r < R and null for r > R, R being the radius of the box and δ a variationally determined interval. As a result, we obtain a equation of state for electrons of small systems, valid just in the limit of low temperatures, but fairly simple. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2007 相似文献
138.
Millar AJ Doonan CJ Smith PD Nemykin VN Basu P Young CG 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(11):3255-3267
Intermediates in the oxygen atom transfer from Mo(VI) to P(III), [Tp(iPr)MoOX(OPR3)] (Tp(iPr) = hydrotris(3-isopropylpyrazol-1-yl)borate; X = Cl-, phenolates, thiolates), have been isolated from the reactions of [Tp(iPr)MoO2X] with phosphines (PEt3, PMePh2, PPh3). The green, diamagnetic oxomolybdenum(IV) complexes possess local C(1) symmetry (by NMR spectroscopy) and exhibit IR bands assigned to nu(Mo==O) (approximately 950 cm(-1)) and nu(P==O) (1140-1083 cm(-1)) vibrations. The X-ray crystal structures of [Tp(iPr)MoOX(OPEt3)] (X = OC6H4-2-sBu, SnBu), [Tp(iPr)MoO(OPh)(OPMePh2)], and [Tp(iPr)MoOCl(OPPh3)] have been determined. The monomeric complexes exhibit distorted octahedral geometries, with coordination spheres composed of tridentate fac-Tp(iPr) and mutually cis monodentate terminal oxo, phosphoryl (phosphine oxide), and monoanionic X ligands. The electronic structures and stabilities of the complexes have been probed by computational methods, with the three-dimensional energy surfaces confirming the existence of a low-energy steric pocket that restricts the conformational freedom of the phosphoryl ligand and inhibits complete oxygen atom transfer. The reactivity of the complexes is also briefly described. 相似文献
139.
Electron impact and methane chemical ionization mass spectra were obtained following gas chromatography/mass spectrometry for several gem-difluoropropargyl compounds, which had been synthesized as potential intermediates for synthesis of gem-difluoromethylene-containing C-3 acetylenes. EI spectra were variable with respect to the presentation of molecular ions, depending on substituent functional groups present. Methane-CI spectra were characterized by loss of 19 mass units from molecular weight with all compounds examined. These [M − 19]+ ions often presented as base peaks of the CI spectra, and were more reliably present and abundant than [M + 1]+ ions for these compounds. These ions could have been formed by elimination of HF from the protonated molecules under conditions of methane chemical ionization. 相似文献
140.
E. T. Denisov 《Russian Chemical Bulletin》2005,54(4):914-923
Interatomic distances in the reaction centers of the addition reactions of (i) H· to the C=C, C=O, N≡C, and C≡C bonds, (ii) ·CH3 radical to the C=C, C=O, and C≡C bonds, and (iii) alkyl, aminyl, and alkoxyl radicals to olefin C=C bonds were determined
using a new semiempirical method for calculating transition-state geometries of radical reactions. For all reactions of the
type X· + Y=Z → X— Y—Z· the r
#
X...Y distance in the transition state is a linear function of the enthalpy of reaction. Parameters of this dependence were determined
for seventeen classes of radical addition reactions. The bond elongation, Δr
#
X...Y, in the transition state decreases as the triplet repulsion, electronegativity difference between the atoms X and Y in the
reaction center, and the force constant of the attacked multiple bond increase.
__________
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 894–902, April, 2005. 相似文献