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1.
Wei-Yan Shao Ying-Nan Cao Wen-Jie Pan Xian-Zhang Bu Lin-Kun An Lian-Quan Gu Albert S.C. Chan 《Tetrahedron letters》2006,47(24):4085-4089
Seventeen unsymmetrical curcumin derivatives were synthesized in good yield and purity by a facile solid phase synthesis strategy. 相似文献
2.
构造了第孙中禹种强度不等的非对称三态叠加多模叠加态光场|ψ1(ABC)〉q.利用多模压缩态理论研究了态|ψ1(ABC)〉q第一正交分量高次和压缩.结果发现:①当构成态|ψ1(ABC)〉q的三个多模相干态光场的强度不相等时,在一定条件下,态|ψ1(ABC)〉q的第一正交分量可出现任意幂次的高次和压缩.②当上述的三个多模相干态光场强度相等时,态|ψ1(ABC)〉q的第一正交分量的高次和压缩现象消失.在这种情况下,态|ψ1(ABC)〉q的第一正交分量恒处于NH最小测不准态. 相似文献
3.
第Ⅰ种强度不对称三态叠加多模叠加态光场N次方Y压缩—第一正交相位分量的压缩情况 总被引:2,自引:0,他引:2
根据量子力学中的线性叠加原理,构造了由三个强度不等的多模相干态光场|{Zj(A)}>q、|{Zj(B)}>q和|{Zj(C)}>q的线性叠加所组成的第Ⅰ种强度不对称三态叠加多模叠加态光场|ψl(ABC)>q.利用多模压缩态理论,研究了态|ψl(ABC)>q的第一正交方分量(即磁场分量)的广义非线性等幂次N次方Y压缩特性.结果发现:①在上述各多模相干态光场中各模的强度和各模的初始相位各不相等的情况下,态|ψl(ABC)>q的第一正交分量-磁场分量在一定的条件下,总可呈现出周期性变化的、任意等幂次的N次方Y压缩效应;②当上述各多模相干态光场的强度和各模的初始相位相等时,态|ψl(ABC)>q的磁场分量的N次方Y压缩现象消失,态|ψl(ABC)>q可恒处于等幂次N-Y最小测不准态. 相似文献
4.
An unsymmetrical organic compound with carbazole (Cz) as donor and benzothiadiazole (BTD) as acceptor (D-π-A-π∗-D∗) was designed and synthesized via simple Heck reaction. The unique crystal structure of Cz-BTD-Cz∗ shows a ladder-like packing mode. A two molecule pair stacks parallelly with each other in each packing unit. In each cell, one Cz moiety is connected with BTD by vinylene bond in same plane. However, the other Cz group is connected to BTD by a one-end vinyl bond in almost perpendicular position to the coplanar part of the molecule. The shortest intermolecular plane distance is 3.48 ± 0.1 Å. The photophysical properties of Cz-BTD-Cz∗ in solution and in bulky crystalline powder state were studied. In bulk crystalline powder state, it has a red-shifted emission band peaked at 609 nm relative to that in solution, and the FWHM was reduced to only 58 nm. Electrochemical properties were also investigated. 相似文献
5.
Konrad Kowalski Janusz Zakrzewski S?awomir Domaga?a 《Journal of organometallic chemistry》2006,691(18):3902-3908
The synthesis of 1′-ethynyl-2,5-dimethylazaferrocene is reported along with its cyclic voltammetry measurements and the X-ray structure determination of its W(CO)5-complex. Basic coordination and organic chemistry of 1′-ethynyl-2,5-dimethylazaferrocene is also presented via derivatives incorporating cis-Pt(dppe) and Si(Et)3 units. 相似文献
6.
研究了Ni/Fe催化剂对废水中偏二甲肼臭氧化分解的催化作用,考察了组分含量、体系的pH值和偏二甲肼初始浓度对催化反应的影响.结果表明,Ni/Fe催化剂对水中偏二甲肼的臭氧化具有良好的催化活性.催化剂组分含量、体系的pH值和初始浓度对反应的影响程度不大.对催化剂的XRD表征结果表明,催化剂主要由尖晶石结构的铁酸盐和FeNi3合金相组成,催化剂的良好催化性能与催化剂中尖晶石结构的铁酸盐和FeNi3合金相的形成有关. 相似文献
7.
This report describes a new type of intra-intermolecular criss-cross cycloadditions. Thermal reactions of unsymmetrical allenylazines in the presence of alkynes led to three fused five-membered heterocycles in some cases. In the case of unsymmetrical substituted alkynes, a regioselectivity was observed. The molecular structures of all products are discussed. One X-ray crystal structure is also reported. 相似文献
8.
The reaction of the cluster Os3(CO)10(μ-H)(μ-γ-C5H3O2) (1) with a number of alkynes under thermal or visible light irradiation conditions, afforded in most cases the dinuclear complexes Os2(CO)6(μ-γ-C5H3O2)(μ-LH) (L=PhCCPh, tBuCCH, tBuCCMe or EtCCEt) (2) or the trinuclear chain complexes Os3(CO)9(μ-H)(μ-γ-C5H3O2)(μ-RCCHC6H4) (R=H, Ph) (3). In the case of PhCCPh, a new isomer of Os3(CO)8(PhCCPh)2, viz., Os3(CO)8(μ-PhCCPh)(μ-PhCCHC6H4) (7) has been isolated and characterised. 相似文献
9.
Three silylated γ-alkynylfurans were prepared and subjected to both gold and platinum catalysts. The TMS- and the TBDMS-substituted furans reacted. With AuCl3 and the binuclear [(Ph3PAu)2Cl][BF4] catalyst a hydroarylation of the alkyne was observed. Na[AuCl4] gave phenols as the product, but these were formed only after in situ desilylation of the starting material by the gold catalyst and thus the wrong isomer dominated. Only with PtCl2(MeCN)2 phenols with a silyl group were formed. The TBDPS-substituted furan failed to react. Two alkynylsilanes were synthesized, but they also failed to react. 相似文献
10.
A series of 4-halophosphaisocoumarins were prepared with high regioselectivity in good to excellent yields under mild conditions by the reaction of 2-(1-alkynyl)phenylphosphonic acid diesters with I2 in CHCl3 or ICl in CH2Cl2, or by the reaction of 2-(1-alkynyl)phenylphosphonic acid monoesters with NBS or NCS in DMF. Whether the alkynylphosphonates could cyclize or not was affected by the substituents, reaction solvents and electrophiles. A rationale for this reaction is discussed. 相似文献