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排序方式: 共有750条查询结果,搜索用时 15 毫秒
11.
I. Schmelzer 《Foundations of Physics》2009,39(1):73-107
We present the bundle (Aff(3)⊗ℂ⊗Λ)(ℝ3), with a geometric Dirac equation on it, as a three-dimensional geometric interpretation of the SM fermions. Each (ℂ⊗Λ)(ℝ3) describes an electroweak doublet. The Dirac equation has a doubler-free staggered spatial discretization on the lattice
space (Aff(3)⊗ℂ)(ℤ3). This space allows a simple physical interpretation as a phase space of a lattice of cells.
We find the SM SU(3)
c
×SU(2)
L
×U(1)
Y
action on (Aff(3)⊗ℂ⊗Λ)(ℝ3) to be a maximal anomaly-free gauge action preserving E(3) symmetry and symplectic structure, which can be constructed using two simple types of gauge-like lattice fields: Wilson
gauge fields and correction terms for lattice deformations.
The lattice fermion fields we propose to quantize as low energy states of a canonical quantum theory with ℤ2-degenerated vacuum state. We construct anticommuting fermion operators for the resulting ℤ2-valued (spin) field theory.
A metric theory of gravity compatible with this model is presented too. 相似文献
12.
分子筛改性对一步法合成二甲醚的影响 总被引:3,自引:2,他引:3
采用浸渍法制备了MgO、CaO、ZnO改性的HZSM 5分子筛,并以改性HZSM 5为脱水剂与JC207甲醇合成催化剂组成双功能催化剂,在固定床反应器上考察了其对一步法合成二甲醚影响。结果表明,适量碱性氧化物的引入,引起分子筛表面的B酸中心(强酸中心)向L酸中心(弱酸中心)转变,而弱酸和中强酸中心是甲醇脱水生成二甲醚的活性中心,强酸中心会造成二甲醚进一步脱水生成烃类副产品,所以改性后产物中二氧化碳和烃类的选择性下降,二甲醚选择性升高。这种趋势在CaO/HZSM 5脱水剂上表现的更为明显。 相似文献
13.
14.
本文研究了2,2'-偶氮二异丁酸二甲酯的合成及其在甲苯、二甲苯中的热分解反应动力学,得到了其热分解反应速度常数与反应温度的关系式:K_d=1.63×100 ̄(-14)exp(-123.3KJ/RT)2,2'-偶氮二异丁酸二甲酯作为苯乙烯自由基聚合的引发剂,其单体转化率随引发剂用量的增加而增高,产物分子量则随之下降;引发剂用量在5%以上时,可得到分子量低于10 ̄3的含有酯基端基的聚合物。 相似文献
15.
R. HekmatShoar S. Souri F. Faridbod 《Phosphorus, sulfur, and silicon and the related elements》2013,188(7):1457-1461
An efficient process that converts 2-hydroxybenzaldehyde and their derivetives to chromene derivatives via intramolecular Wittig reaction is described. 相似文献
16.
以天然长叶薄荷酮[R-(+)-Pulegone]为起始原料,经过一系列立体选择性化学反应步骤,成功地建立了3个手性中心,从而完成了具有抗艾滋病活性Didemnaketals类似物的关键中间体3,7-二甲基-5,6-二羟基-辛-7-烯醛中间体的合成.发现PCC与三级环氧醇8和9的非对映选择性反应,使得9被完全氧化,而8以93%的产率回收,其de值高达98%. 相似文献
17.
Morphology and mechanical properties of poly(vinyl alcohol) and starch blends prepared by gelation/crystallization from solutions 总被引:1,自引:0,他引:1
In an attempt to produce biodegradation materials, poly(vinyl alcohol) (PVA)–starch (ST) blends were prepared by gelation/crystallization
from semidilute solutions in dimethyl sulfoxide (Me2SO) and water mixtures and elongated up to 8 times. The content of mixed solvent represented as Me2SO/H2O (volume percent) was set to be 60/40 assuring the greatest drawability of PVA homopolymer films. The PVA/ST compositions
chosen were 1/1, 1/3, and 1/5. The elongation up to 8 times could be done for the 1/1 blend but any elongation was impossible
for blends whose ST content was beyond 50%. When the blends were immersed in water at 20 or 83 °C, the solubility became considerable
for an undrawn blend with 1/5 composition and a drawn 1/1 blend with λ=8. To avoid this phenomenon, cross-linking of PVA chains
was carried out by formalization under formaldehyde vapor. Significant improvement could be established by the cross-linking
of PVA chains. For the 1/1 blend, the amount of ST dissolved in water at 23 °C was less than 3% for the undrawn state and
25% for the drawn film. The decrease in the ST content was enough for use as biodegradation materials. Namely, the water content
relating to the biodegradation in soil is obviously different from such a serious experimental condition that a piece of blend
film was immersed in a water bath. At temperatures above 0 °C, the storage modulus of the formalization blends became slightly
higher than those of the nonformalization blends. The Young's modulus of the drawn films with a draw ratio of 8 times was
2 GPa at 20 °C.
Received: 23 June 2000 Accepted: 30 October 2000 相似文献
18.
Mervat S. Sammor Ahmad Q. Hussein Firas F. Awwadi Mustafa M. El-Abadelah 《Tetrahedron》2018,74(1):42-48
3,10-Dihydro-2H-1,3-oxazepino[7,6-b]indoles are synthesized via a convenient one-pot three-component 1,4-dipolar cycloaddition reaction, involving 3-alkyl(aryl)imidazo[1,5-a]pyridines, dimethyl acetylenedicarboxylate (DMAD) and N-alkylisatins. Structures of the newly synthesized heterocycles are evidenced from spectral data and further confirmed by single crystal X-ray diffraction. A plausible reaction mechanism is advanced, whereby the intermediate 1,4-dipole, generated in situ from imidazo[1,5-a]pyridine and DMAD, initially adds to the keto group of N-alkylisatins to form the corresponding 1,3-oxazin-spiro-oxindole cycloadduct. The latter undergoes subsequent unprecedented skeletal rearrangement through a cascade of bond breaking and bond making processes, eventually leading to ring enlargement, furnishing the tricyclic oxazepino[7,6-b]indole ring system as the end product. 相似文献
19.
Benan K?lba?Author VitaeMetin BalciAuthor Vitae 《Tetrahedron》2011,67(13):2355-2389
20.
Xiaolu Jiang 《Tetrahedron》2010,66(52):9828-9834
Gold(I) and (III) salts have been found to be highly effective at the catalysis of ether formation from alcohols. Intramolecular ether formation of a 1,5-diol was also achieved, with a stereoselectivity that indicates that an SN1 mechanism predominates. In an attempt to form a seven-membered ring, a stable 14-membered dimer product was also formed. Attempts to control the diastereoselectivity of the reaction using a chiral anionic counterion did not give products with a high de. 相似文献