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排序方式: 共有146条查询结果,搜索用时 15 毫秒
1.
2.
许多实验对用CsI(Tl)闪烁晶体作为探测器来寻找和探测暗物质的可行性进行了研究.本工作利用8MeV单能中子轰击CsI(Tl)晶体探测器来研究Cs核和I核的QuenchingFactor.在数据处理中,运用脉冲形状甄别(PSD)方法来分辨反冲核信号和本底信号.实验结果表明,在7keV到132keV的能区中,Quench ingFactor随着反冲核能量的减少而增加.在探测暗物质的实验中,这一性质对于CsI(Tl)晶体探测器获得较低的能量阈值是很有利的. 相似文献
3.
An asymptotic expansion is constructed for the double integral
as +, where f(x, y) hasa curve of stationary points in D. The first two coefficientsof the expansion are explicitly calculated. 相似文献
4.
WONG Henry N. C. 《中国化学》2005,23(8):1106-1108
Trimethylsilyl groups have been used in our research as a director as well as a bulky and lipophilic group in our quest for natural and non-natural molecules. 相似文献
5.
A Minor New Flavone from Scutellaria baicalensis Georgi 总被引:1,自引:0,他引:1
A new flavone,6,2′-dihydroxy-5,7,8,6′-tetramethoxyflavone,was isolated from the roots of Scutellaria baicalensis. Its structure was established on the basis of spectral evidences. 相似文献
6.
LigandscontainingelectrochemicallyresponsivecentrearegoodsubjectsforthestUdyofintfamolecularandhost-guestillteraction.Forthisreason,tYemendousamoulltsofsuchligandsandtheircomplexeshavebeensynthesized.'-'AnobservationfromthestudiesofthesecomPlexesisthattheguestionhasapermrbationonthehostcelltre.2'7-9Forexample,itwasdocumelltedthatintroductionofCo(II)ionontoN-ferrocenylmethyl-l,4,7-triazacyclononane(fcmtacn)causesapositiveshiftintheredoxpotentialofferrocenylgroupfromthatofferrocenegroupinfree… 相似文献
7.
H. K. WONG 《Photochemistry and photobiology》1968,7(4):377-389
Abstract— Flash-photolysis of safranine in deoxygenated 5 per cent aqueous pyridine produces a transient bleaching, which disappears by a second order process. Very probably this transient species consists of a pair of radicals or radical ions and not of the safranine in the triplet state. These radicals are also produced in chlorophyll sensitized reactions. Present results combined with previous work by us[I] indicate that the chlorophyll sensitization of safranine bleaching involves the formation of these radicals.
The direct photochemical reduction of safranine to its leuco form occurs through the intermediate formation of the radicals. The appearance and disappearance of these radicals is fast compared to the role of photochemical formation and thermal disappearance of leuco safranine. Ascorbic acid influences but is not essential to the photo-bleaching of safranine in 5 per cent aqueous pyridine. An increase in ascorbic acid concentration increases the steady-state yield of the radicals but decreases the steady-state yield of the leuco safranine. In the absence of ascorbic acid or other added substance, safranine photobleaches irreversibly in deoxygenated 5 per cent aqueous pyridine. A plausible mechanism is proposed in explanation of the direct photochemical reduction of safranine. 相似文献
The direct photochemical reduction of safranine to its leuco form occurs through the intermediate formation of the radicals. The appearance and disappearance of these radicals is fast compared to the role of photochemical formation and thermal disappearance of leuco safranine. Ascorbic acid influences but is not essential to the photo-bleaching of safranine in 5 per cent aqueous pyridine. An increase in ascorbic acid concentration increases the steady-state yield of the radicals but decreases the steady-state yield of the leuco safranine. In the absence of ascorbic acid or other added substance, safranine photobleaches irreversibly in deoxygenated 5 per cent aqueous pyridine. A plausible mechanism is proposed in explanation of the direct photochemical reduction of safranine. 相似文献
8.
Wong CY Che CM Chan MC Han J Leung KH Phillips DL Wong KY Zhu N 《Journal of the American Chemical Society》2005,127(40):13997-14007
The synthesis and spectroscopic properties of trans-[RuL4(C[triple bond]CAr)2] (L4 = two 1,2-bis(dimethylphosphino)ethane, (dmpe)2; 1,5,9,13-tetramethyl-1,5,9,13-tetraazacyclohexadecane, 16-TMC; 1,12-dimethyl-3,4:9,10-dibenzo-1,12-diaza-5,8-dioxacyclopentadecane, N2O2) are described. Investigations into the effects of varying the [RuL4] core, acetylide ligands, and acetylide chain length for the [(-)C[triple bond]C(C6H4C[triple bond]C)(n-1)Ph] and [(-)C[triple bond]C(C6H4)(n-1)Ph] (n = 1-3) series upon the electronic and electrochemical characteristics of trans-[RuL4(C[triple bond]CAr)2](0/+) are presented. DFT and TD-DFT calculations have been performed on trans-[Ru(L')4(C[triple bond]CAr)2](0/+) (L' = PH3 and NH3) to examine the metal-acetylide pi-interaction and the nature of the associated electronic transition(s). It was observed that (1) the relationship between the transition energy and 1/n for trans-[Ru(dmpe)2{C[triple bond]C(C6H4C[triple bond]C)(n-1)Ph}2] (n = 1-3) is linear, and (2) the sum of the d(pi)(Ru(II)) --> pi*(C[triple bond]CAr) MLCT energy for trans-[Ru(16-TMC or N2O2)(C[triple bond]CAr)2] and the pi(C[triple bond]CAr) --> d(pi)(Ru(III)) LMCT energy for trans-[Ru(16-TMC or N2O2)(C[triple bond]CAr)2]+ corresponds to the intraligand pi pi* absorption energy for trans-[Ru(16-TMC or N2O2)(C[triple bond]CAr)2]. The crystal structure of trans-[Ru(dmpe)2{C[triple bond]C(C6H4C[triple bond]C)2Ph}2] shows that the two edges of the molecule are separated by 41.7 A. The electrochemical and spectroscopic properties of these complexes can be systematically tuned by modifying L4 and Ar to give E(1/2) values for oxidation of trans-[RuL4(C[triple bond]CAr)2] that span over 870 mV and lambda(max) values of trans-[RuL4(C[triple bond]CAr)2] that range from 19,230 to 31,750 cm(-1). The overall experimental findings suggest that the pi-back-bonding interaction in trans-[RuL4(C[triple bond]CAr)2] is weak and the [RuL4] moiety in these molecules may be considered to be playing a "dopant" role in a linear rigid pi-conjugated rod. 相似文献
9.
[reaction: see text] Effective epoxidation of lipophilic alkenes using hydrogen peroxide was accomplished with the manganese sulfate/bicarbonate catalytic system in an ionic liquid at room temperature. 相似文献
10.
Yuan-Jing Dai Ling Lin Pei-Wei Li Xiao-Ru Wang Kwok-Yin Wong 《International journal of environmental analytical chemistry》2013,93(8):607-617
Fiber-optical microbial sensors for determination of biochemical oxygen demand (BOD) are described. Sensing films consisting of layers of an oxygen-sensitive fluorescent material and two different kinds of seawater microorganisms immobilized in poly(vinyl alcohol) sol–gel matrix were investigated. Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) perchlorate was used as the oxygen fluorescent quenching indicator. After preconditioning, the BOD biosensors could consistently perform well for up to one month. For films of domestic bacilli and films of sieved bacteria from seawater, the linear fluctuant coefficients (R 2) in the range of 4–200?mg/L were 0.9975 and 0.9783 when a glucose/glutamate BOD standard was applied. The relative error of standard deviations for the two microorganism-immobilized BOD sensing films were within 4%?and 2%?of the mean value, respectively. The effects of temperature, pH and sodium chloride concentration on the two microbial films were also studied. For low biochemical oxygen demand, a film of sieved bacteria from seawater had superior sensitivity and is expected to be developed further. 相似文献