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排序方式: 共有1177条查询结果,搜索用时 15 毫秒
81.
Yusuf Akbaba Halis Türker Balaydın Süleyman Göksu Ertan Şahin Abdullah Menzek 《Helvetica chimica acta》2010,93(6):1127-1135
3,4‐Dibromo‐5‐[2‐bromo‐3,4‐dihydroxy‐6‐(methoxymethyl)benzyl]benzene‐1,2‐diol ( 2 ), a natural product, has been synthesized for the first time starting from (3‐bromo‐4,5‐dimethoxyphenyl)methanol ( 5 ) in five steps and with an overall yield of 34%. The reaction of some methoxymethyl‐substituted aryl methyl ethers with BBr3, followed by the addition of MeOH, afforded the corresponding methoxymethyl‐substituted arylphenols in high yields. 相似文献
82.
In this paper we apply computer algebra (Maple) techniques to calculate Jones polynomial of graphs of K(2,q)-Torus knots. For this purpose, a computer program was developed. When a positive integer q is given, the program calculate Jones polynomial of graph of K(2,q)-Torus knots. 相似文献
83.
A semi-analytical solution is presented for the virtual mass coefficient of an oblate-ellipsoidal bubble rising in liquid. The solution was found to be a function of Weber number. The present solution compared well with the numerical solution of the lattice Boltzmann method and the analytical solutions of other investigators. 相似文献
84.
S.F. Abdullah S. Radiman M.A. Abd. Hamid N.B. Ibrahim 《Colloids and surfaces. A, Physicochemical and engineering aspects》2006,280(1-3):88-94
The effect of calcination temperature on the surface morphology and crystallinity of tungsten (VI) oxide, WO3 nanorods prepared using colloidal gas aphrons (CGAs) as template was studied. The synthesized WO3 nanorods were calcined in a furnace for 4 h at four different temperatures, i.e., 400, 500, 600 and 700 °C. The morphology of the calcined WO3 nanorods have been characterized by both transmission electron microscope (TEM) and variable pressure scanning electron microscope (SEM) equipped with energy dispersive X-ray analysis (EDAX). The results showed that the calcination temperature influenced the shape and size of the WO3 nanorods produced. It is also found that the calcination at various temperature do not effect the composition and the purity of the WO3 nanorods. In order to characterize the crystalinity of WO3, X-ray diffraction (XRD) has been used. It shows that all the calcined WO3 produced are in crystalline form compared to the as-prepared WO3 nanorods, which is in amorphous form. 相似文献
85.
Roheena Abdullah Kinza Nisar Aafia Aslam Mehwish Iqtedar Shagufta Naz 《Natural product research》2015,29(11):1006-1011
This study is related to the isolation of fungal strain for xylanase production using agro-industrial residues. Forty fungal strains with xylanolytic potential were isolated by using xylan agar plates and quantitatively screened in solid-state fermentation. Of all the tested isolates, the strain showing highest ability to produce xylanase was assigned the code Aspergillus niger LCBT-14. For the enhanced production of the enzyme, five different fermentation media were evaluated. Out of all media, M4 containing wheat bran gave maximum enzyme production. Effect of different variables including incubation time, temperature, pH, carbon and nitrogen sources has been investigated. The optimum enzyme production was obtained after 72 h at 30°C and pH 4. Glucose as a carbon source while ammonium sulphate and yeast extract as nitrogen sources gave maximum xylanase production (946 U/mL/min). This study was successful in producing xylanase by A. niger LCBT-14 economically by utilising cheap indigenous substrate. 相似文献
86.
Mehwish Iqtedar Mohammad Nadeem Hira Naeem Roheena Abdullah Shagufta Naz Qurat ul Ain Syed 《Natural product research》2015,29(11):1012-1019
The industrialisation of lignocellulose conversion is impeded by expensive cellulase enzymes required for saccharification in bioethanol production. Current research undertakes cellulase production from pretreated Saccharum spontaneum through Trichoderma viride HN1 under submerged fermentation conditions. Pretreatment of substrate with 2% NaOH resulted in 88% delignification. Maximum cellulase production (2603 ± 16.39 U/mL/min carboxymethyl cellulase and 1393 ± 25.55 U/mL/min FPase) was achieved at 6% substrate at pH 5.0, with 5% inoculum, incubated at 35°C for 120 h of fermentation period. Addition of surfactant, Tween 80 and metal ion Mn+2, significantly enhanced cellulase yield. This study accounts proficient cellulase yield through process optimisation by exploiting cheaper substrate to escalate their commercial endeavour. 相似文献
87.
In this study, it was aimed to investigate the chemical composition and antioxidant activities of two Euphorbia species. The major component of the fatty acid compositions obtained from the petroleum ether extracts was identified as palmitic acid for Euphorbia gaillardotii and Euphorbia macroclada. The main constituents of the essential oils were identified as arachidic acid for E. gaillardotii and tetratetracontane for E. macroclada. Among the 27 studied compounds, hesperidin, rutin, hyperoside and quinic, malic, gallic and tannic acids were found to be the most abundant compounds in the two Euphorbia species. The methanol extracts of E. gaillardotii and E. macroclada showed strong antioxidant activity in all tested methods. Particularly, IC50 values of E. macroclada methanol extract that was the richest in terms of total phenolic-flavonoid contents were found to be lower than α-tocopherol and butylated hydroxytoluene in β-carotene bleaching, 2,2-diphenyl-1-picrylhydrazyl free and ABTS cation radical scavenging methods. 相似文献
88.
Genetic diversity and haplotype structure of 21 Y‐STRs,including nine noncore loci,in South Tunisian Population: Forensic relevance 下载免费PDF全文
Faten Makki‐Rmida Arwa Kammoun Nadia Mahfoudh Adnene Ayadi Abdullah Ahmed Gibriel Bakhta Mallek Leila Maalej Zouheir Hammami Samir Maatoug Hafedh Makni Saber Masmoudi 《Electrophoresis》2015,36(23):2908-2913
Y chromosome STRs (Y‐STRs) are being used frequently in forensic laboratories. Previous studies of Y‐STR polymorphisms in different groups of the Tunisian population identified low levels of diversity and discrimination capacity (DC) using various commercial marker sets. This definitely limits the use of such systems for Y‐STRs genotyping in Tunisia. In our investigation on South Tunisia, 200 unrelated males were typed for the 12 conventional Y‐STRs included in the PowerPlex® Y System. Additional set of nine noncore Y‐STRs including DYS446, DYS456, DYS458, DYS388, DYS444, DYS445, DYS449, DYS710, and DYS464 markers were genotyped and evaluated for their potential in improving DC. Allele frequency, gene diversity, haplotype diversity (HD), and DC calculation revealed that DYS464 was the most diverse marker followed by DYS710 and DYS449 markers. The standard panel of 12 Y‐STRs (DC = 80.5%) and the nine markers were combined to obtain DC of 99%. Among the 198 different haplotypes observed, 196 haplotypes were unique (HD = 99.999). Out of the nine noncore set, six Y‐STRs (DYS458, DYS456, DYS449, DYS710, DYS444, and DYS464) had the greatest impact on enhancing DC. Our data provided putative Y‐STRs combination to be used for genetic and forensic applications. 相似文献
89.
A New and Facile Synthesis of Novel Pyrazolothienopyrimidines and Imidazopyrazolothienopyrimidines 下载免费PDF全文
4‐Amino‐3‐methyl‐1‐phenyl‐1H‐thieno[2,3‐c]pyrazole‐5‐carboxamide ( 5 ), which was synthesized by an innovative method, was used as a versatile precursor for synthesizing pyrazolothienopyrimidines and imidazopyrazolothienopyrimidines compounds. Reaction of amino thienopyrazole carboxamide 5 with triethyl orthoformate afforded thienopyrazolopyrimidine 6 . Chlorination of the latter compound, using phosphorus oxychloride afforded the chloro pyrazolothienopyrimidine 7 , which underwent nucleophilic substitution reactions with various primary and secondary amines to give the alkyl (aryl) amino pyrimidine compounds 8a–d . On the other hand, the reaction of chloropyrimidine 7 with thiourea afforded the pyrimidine thione compound 9 , which was alkylated with α‐halogentaed compounds to afford the S‐alkylated derivatives 10a–c . Also, chloroacetylation of the amino carboxamide 5 using chloroacetyl chloride yielded the chloromethyl pyrazolothienopyrimidine 12 , which underwent nucleophilic substitu‐ tion reactions with various primary and secondary amines to afford the alkyl (aryl) aminomethyl compounds 13a–f . The latter Compounds underwent Mannich reaction to give imidazopyrimidothieno‐ pyrazoles 14a–c . The newly synthesized compounds and their derivatives were fully characterized by elemental and spectral analysis. 相似文献
90.
Nurul Hidayah Abdullah Kamyar Shameli Ezzat Chan Abdullah Luqman Chuah Abdullah 《中国化学快报》2017,28(7):1590-1596
A facile and green synthetic approach for fabrication of starch-stabilized magnetite nanoparticles was implemented at moderate temperature. This synthesis involved the use of iron salts, potato starch,sodium hydroxide and deionized water as iron precursors, stabilizer, reducing agent and solvent respectively. The nanoparticles(NPs) were characterized by UV-vis, PXRD, HR-TEM, FESEM, EDX, VSM and FT-IR spectroscopy. The ultrasonic assisted co-precipitation technique provides well formation of highly distributed starch/Fe_3O_4-NPs. Based on UV–vis analysis, the sample showed the characteristic of surface plasmon resonance in the presence of Fe_3O_4-NPs. The PXRD pattern depicted the characteristic of the cubic lattice structure of Fe_3O_4-NPs. HR-TEM analysis showed the good dispersion of NPs with a mean diameter and standard deviation of 10.68 4.207 nm. The d spacing measured from the lattice images were found to be around 0.30 nm and 0.52 nm attributed to the Fe3O4 and starch, respectively. FESEM analysis confirmed the formation of spherical starch/Fe_3O_4-NPs with the emission of elements of C, O and Fe by EDX analysis. The magnetic properties illustrated by VSM analysis indicated that the as synthesized sample has a saturation magnetization and coercivity of 5.30 emu/g and 22.898 G respectively.Additionally, the FTIR analysis confirmed the binding of starch with Fe_3O_4-NPs. This method was cost effective, facile and eco-friendly alternative for preparation of NPs. 相似文献