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排序方式: 共有453条查询结果,搜索用时 15 毫秒
1.
《Current Applied Physics》2015,15(11):1296-1302
One-dimensional ZnO materials have been promising for field-emission (FE) application, but how to facially control the alignment of ZnO emitters is still a great challenge especially for patterned display application. Here, we report the fabrication of novel ZnO nanowire (NW) line and bundle arrays for patterned field-electron emitters. The effects of PS template size and heating time on the resulted ZnO nanoarrays were systematically studied. The deformation degree of PS templates was controlled and hence utilized to adjust the alignment of electrochemically deposited ZnO arrays. It was found that the length of NW lines and the density of NW bundles can effectively tuned by the PS template heating time. The optimal FE performance with turn-on electric field as low as of 4.4 V μm−1 and the field-enhancement factor as high as of 1450 were achieved through decreasing the screening effect among the patterned field-electron emitters. 相似文献
2.
CeO2 nanotubes have been synthesized facilely using carbon nanotubes (CNTs) as templates by a liquid phase deposition method. The properties of the CeO2 nanotubes were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectrum (XPS) as well as thermogravimetry and differential thermal analysis (TG-DTA). The obtained CeO2 nanotubes with a polycrystalline face-centered cubic phase have a uniform diameter ranging from 40 to 50 nm. The CeO2 nanotubes are composed of many tiny interconnected nanocrystallites of about 10 nm in size. The pretreatment of CNTs and calcination temperature were confirmed to be the crucial factors determining the formation of CeO2 nanotubes. A possible formation mechanism has been suggested to explain the formation of CeO2 nanotubes. 相似文献
3.
Simon Doherty Julian G. Knight Tom H. Scanlan Mark R. J. Elsegood William Clegg 《Journal of organometallic chemistry》2002,650(1-2):231-248
The aprotic and protic bi- and multidentate iminophosphines 2-Ph2PC6H4N=CR1R2 (R1=H, R2=Ph=2a; R1=Me R2=Ph=2b; R1=H, R2=2-thienyl=2c; R1=H, R2=C6H4-2-PPh2=2d; R1=H, R2=C6H4-2-OH=2e, R1=H, R2=C6H4-2-OH-3-But=2f; R1=H, R2=CH2C(O)Me=2g) have been prepared by the acid catalyzed condensation of 2-(diphenylphosphino)aniline with the corresponding aldehyde–ketone. Iminophosphine 2d can be reduced with sodium cyanoborohydride to give the corresponding amino-diphosphine 2-Ph2PC6H4N(H)CH2C6H4-2-PPh2 (2h). In the presence of a stoichiometric quantity of acid, 2-(diphenylphosphino)aniline reacts in an unexpected manner with benzaldehyde, salicylaldehyde, or acetophenone to give the corresponding 2,3-dihydro-1H-benzo[1,3]azaphosphol-3-ium salts and with pyridine-2-carboxaldehyde to give N-(pyridin-2-ylmethyl)-2-diphenylphosphinoylaniline, the latter of which has been characterized by single-crystal X-ray crystallography, as its palladium dichloride derivative. The attempted condensation of 2-(diphenylphosphino)aniline with pyridine-2-carboxaldehyde to give the corresponding pyridine-functionalized iminophosphine resulted in an unusual transformation involving the diastereoselective addition of two equivalents of aldehyde to give 1,2-dipyridin-2-yl-2-(o-diphenylphosphinoyl)phenylamino-ethanol, which has been characterized by a single-crystal X-ray structure determination. The bidentate iminophosphine 2-Ph2PC6H4N=C(H)Ph reacts with [(cycloocta-1,5-diene)PdClX] X=Cl, Me) to give [Pd{2-Ph2PC6H4N=C(H)Ph}ClX] and the imino-diphosphine 2-Ph2PC6H4N=C(H)C6H4-PPh2 reacts with [(cycloocta-1,5-diene)PdClMe] to give [Pd{2-Ph2PC6H4N=C(H)C6H4---PPh2}ClMe] and each has been characterized by single-crystal X-ray crystallography. The monobasic iminophosphine 2-Ph2PC6H4N=C(Me)CH2C(O)Me reacts with [Ni(PPh3)2Cl2] in the presence of NaH to give the phosphino–ketoiminate complex [Ni{2-Ph2PC6H4N=C(Me)CHC(O)Me}Cl], which has been structurally characterized. Mixtures of iminophosphines 2a–h and a palladium source catalyze the Suzuki cross coupling of 4-bromoacetophenone with phenyl boronic acid. The efficiency of these catalysts show a marked dependence on the palladium source, catalysts formed from [Pd2(OAc)6] giving consistently higher conversions than those formed from [Pd2(dba)3] and [PdCl2(MeCN)2]. Catalysts formed from neutral bi- and terdentate iminophosphines 2a–d gave significantly higher conversions than those formed from their monobasic counterparts 2e–f. Notably, under our conditions the conversions obtained with 2a–c compare favorably with those of the standards; catalysts formed from tris(2-tolyl)phosphine and tris(2,4-di-tert-butylphenyl)phosphite and a source of palladium. In addition, mixtures of [Ir(COD)Cl]2 and 2a–h are active for the hydrosilylation of acetophenone; in this case catalysts formed from monobasic iminophosphines 2e–f giving the highest conversions. 相似文献
4.
Jijun Qiu Weidong Yu Xiangdong Gao Xiaomin Li 《Journal of Sol-Gel Science and Technology》2007,44(3):235-239
Ordered porous TiO2 films, including TiO2 nanotube arrays, are fabricated by a sol-gel dip-coating approach via ZnO nanorod templates obtained from aqueous solution
approach. The results indicate that the morphologies of ordered porous TiO2 films have been great affected by the sol-gel dip-coating cycle number. Open-ended TiO2 nanotube arrays can be obtained in optimum dip-coating cycle numbers. The TiO2 nanotubes with the inner diameter matching well with the diameters of ZnO nanorods, are well assembled and separate each
other. When the cycle number is less than this optimum value, no intact porous TiO2 film can be obtained. As the cycle number is larger than this optimum value, an ordered porous TiO2 film with many throughout holes is formed. The evolutive mechanism of ordered porous TiO2 films is proposed. 相似文献
5.
Andrew R. Leach Keith Prout Daniel P. Dolata 《Journal of computer-aided molecular design》1988,2(2):107-123
Summary The results of a wide-ranging investigation into some of the different methods available for performing the joining of templates to build molecular models show that the choice of algorithm can significantly affect the quality of the results obtained, and different algorithms are most suited to particular categories of join. 相似文献
7.
Summary The condensation of 2,6-diacetylpyridine andm-phenylenediamine in the presence of scandium(III) perchlorate as a template agent affords a new 20-membered macrocyclic complex of formula ScL(ClO4)3·4H2O, whereL is Me4
bzo
2
pyo
2[20]octaene-N6.
Scandium(III) als Matrix für die Synthese eines makrocyclischen Hexaazaliganden
Zusammenfassung Die Kondensation von 2,6-Diacetylpyridin undm-Phenylendiamin in Gegenwart von Scandium(III)perchlorat als Matrix liefert einen neuen makrocyclischen Komplex der Zusammensetzung ScL(ClO4)3·4H2O (L=Me4 bzo 2 pyo 2[20]octaen-N6).相似文献
8.
Template Reaction of Bis(acetylacetonato)-dioxo-molybdenum(VI) with Benzoylhydrazone By reaction of bis(acetylacetonato)-dioxo-molybdenum(VI) with benzoylhydrazine benzoylhydrazido(2?)-acetylacetonebenzoylhydrazonato(2?)-oxo-molybdenum(VI) was formed beside another species. The compound was characterized by mass spectrometry and X-ray structural analysis. Crystallographic data see ?Inhaltsübersicht”?. 相似文献
9.
分子筛的合成通常是采用含碱金属离子的强碱性体系,通过水热晶化法实现~[1,2]的.得到的分子筛原粉不但必须通过铵离子交换和焙烧才能转变为氢型催化剂,而且在该体系中晶体的粒度也较小.Guth等人~[3]首次报道了在非碱性介质F-离子存在下直接合成铵型ZSM-5的工作.除用四丙基溴化铵合成ZSM-5及其杂原子分子筛外~[4],尚未见到在非碱性介质中合 相似文献
10.
Macrocyclic Lewis acidic hosts with structures incorporating electron-withdrawing icosahedral carboranes and electrophilic mercury centers bind a variety of electron-rich guests. These compounds, the so-called mercuracarborands, are synthesized by a kinetic halide ion template effect that affords tetrameric cycles or in the absence of halide ion templates, cyclic trimers. Both types of mercuracarborands form stable host–guest complexes with anionic and neutral electron-rich molecules. The multidentate structure of mercuracarborand hosts has made these unique molecules ideal for catalytic and ion-sensing applications as well as for the assembly of supramolecular architectures. 相似文献