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41.
Supramolecular polymer gels from polystyrene bearing cyclic amidine Group and acrylic acid/n‐butyl acrylate copolymers
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Mina Sakuragi Naoto Aoyagi Yoshio Furusho Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2016,54(6):765-770
We have prepared supramolecular polymer gels by mixing solutions of a polystyrene bearing cyclic amidine pendant groups (Poly‐A) and copolymers of acrylic acid and n‐butyl acrylate (Poly‐C), followed by evaporation. FT‐IR analysis indicated that the gels were formed through three‐dimensional network of the amidinium‐carboxylate salt bridge. DSC study showed that the Poly‐A and the Poly‐C were miscible when the salt bridge content was high. On the other hand, the mixtures with small salt bridge content showed phase separation. Dynamic shear measurements showed that the gel prepared from Poly‐A and Poly‐C with acrylic acid unit content of 15% had G' higher than G″ over a temperature range of ?22 °C to 32 °C, in which the G' value reached almost 1 MPa. The gel had a crossover point of G' and G″ at 32 °C, very close to room temperature, which suggested facile processability. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 765–770 相似文献
42.
The purpose of this study was to investigate the effect of three vitrification procedures [conventional straw (CS), open pulled straw (OPS) and closed pulled straw (CPS)] on the development of two-cell mouse embryos. Two-cell mouse embryos were randomly divided into vitrified and non-vitrified control groups. Embryos in the vitrified group were cryopreserved within a combination of 5.5 M ethylene glycol and 1M sucrose as cryoprotectants, loaded within three different straws (CS, OPS and CPS) and warmed in stepwise sucrose solutions. The survived embryos from each procedure were cultured in human tubal fluid (HTF). The non-vitrified control embryos were also cultured in the same manner. The rates of the development in all the groups were daily determined and statistically compared. On day 4 of the cultivation period, several expanded blastocysts from each group were randomly selected and stained either with propidium iodide (PI) and bisbenzimide or with terminal transferase- mediate DNA end labeling (TUNEL) Technique. The mean number of the inner cell mass (ICM), trophoectoderm (TE), necrotic and apoptotic cells were counted and statistically compared. The survival rate of embryos in CPS was significantly higher than that in OPS and CS. The rate of hatched blastocysts did not differ in the three vitrification procedures, but in comparison with that of the control, CS and OPS showed a significant reduction. The mean number of ICM and TE decreased in CS and OPS, whereas in CPS it was almost identical to that of the control. The incidence of apoptosis and necrosis appeared to be almost similar in all the groups. In conclusion, CPS seems to be an effective, easy and rapid method for the cryopreservation of two-cell mouse embryos. 相似文献
43.
In vivo mapping of functional domains and axonal connectivity in cat visual cortex using magnetic resonance imaging 总被引:5,自引:0,他引:5
Kim DS Kim M Ronen I Formisano E Kim KH Ugurbil K Mori S Goebel R 《Magnetic resonance imaging》2003,21(10):1131-1140
Noninvasive cognitive neuroimaging studies based on functional magnetic resonance imaging (fMRI) are of ever-increasing importance for basic and clinical neurosciences. The explanatory power of fMRI could be greatly expanded, however, if the pattern of the neuronal circuitry underlying functional activation could be made visible in an equally noninvasive manner. In this study, blood oxygenation level-dependent (BOLD)-based fMRI and diffusion tensor imaging (DTI) were performed in the same cat visual cortex, and the foci of fMRI activation utilized as seeding points for 3D DTI fiber reconstruction algorithms, thus providing the map of the axonal circuitry underlying visual information processing. The methods developed in this study will lay the foundation for in vivo neuroanatomy and the ability for noninvasive longitudinal studies of brain development. 相似文献
44.
45.
Alireza Banaei Afshin Saadat Mina Mohammad Goli Patrick McArdle Eslam Pourbasheer Parinaz Pargolghasemi 《Heteroatom Chemistry》2016,27(6):353-360
Two novel dithiophosphonate ligands, HS2P(p‐C6H4OMe)(OCH2CH2CH(CH3)2) ( 1 ) and HS2P(p‐C6H4OMe)(OCH(CH3)2) ( 2 ), were synthesized and characterized by multinuclear (1H, 31P, and 13C) NMR, infrared spectroscopy as well as elemental analysis. The reactions of 1 and 2 with NiCl2·6H2O and Cd(NO3)2·4H2O in methanol led to novel complexes 3 and 4 . The single crystal X‐ray structures of 3 and 4 showed tetracoordinated structure with square planar geometry for the nickel complex, while it showed pentacoordinated structure with distorted square‐pyramid environment for the cadmium complex. 相似文献
46.
Bamoharram Fatemeh F Roshani Mina Heravi Majid M Mahdavi Masoumeh Javid Ali Emampour Jalal Sh 《中国化学》2010,28(6):974-976
Isoxazolo[5,4‐d]pyrimidine‐4,6(5H,7H)diones 2a – 2f have been synthesized from the reaction of ethyl 5‐amino‐3‐methyl‐4‐isoxazole carboxylate ( 1 ) with aryl isocyanates in the presence of Keggin heteropolyacid H3[PW12O40] as a green solid acid catalyst at room temperature in a one‐pot process in good yields. 相似文献
47.
Ramin Ghorbani-Vaghei Seyedeh Mina Malaekehpour 《Central European Journal of Chemistry》2010,8(5):1086-1089
N,N,N,’N’-Tetrabromobenzene-1,3-disulfonamide [TBBDA] is found to be a reusable catalyst for efficient synthesis of various amidoalkyl
naphthols from β-naphthol, aromatic aldehydes and urea in good to high yields under solvent-free conditions.
相似文献
48.
Majid M. Heravi Mina Saeedi Yahya S. Beheshtiha Hossein A. Oskooie 《Molecular diversity》2011,15(1):239-243
Abstract
One-pot synthesis of different benzochromeno-pyrazole derivatives has been reported via reaction of aldehydes, 3-methyl-1H-pyrazol-5(4H)-one and α-naphthol/β-naphthol in the presence of sulfamic acid. 相似文献49.
Heravi Majid M. Bakhtiari Khadijeh Alinejhad Hamideh Saeedi Mina Malakooti Reihane 《中国化学》2010,28(2):269-272
β‐Aminoalcohols were synthesized in high yields by reaction of epoxides with amines in the presence of MCM‐41 as a green and reusable catalyst under solvent‐free conditions. 相似文献
50.
Mina Mazzeo Marina Lamberti Ilaria D'Auria Stefano Milione Jonas C. Peters Claudio Pellecchia 《Journal of polymer science. Part A, Polymer chemistry》2010,48(6):1374-1382
New Group 3 metal complexes of the type [LM(CH2SiMe3)2(THF)n] supported by tridentate phosphido‐diphosphine ligands [(o‐C6H4PR2) 2 PH; L1‐H : R = iPr; L2‐H : R = Ph] have been synthesized by reaction of L1‐H and L2‐H with [M(CH2SiMe3)3(THF)2)] (M = Y and Sc). All the new complexes [(o‐C6H4PR2) 2 PM(CH2SiMe3)2(THF)n] [M = Y, R = iPr (1), R = Ph (2); M = Sc, R = iPr (3), R = Ph (4)] were studied as initiators for the ring opening polymerization of lactide. The yttrium complexes ( 1 and 2 ) exhibited high activity and good polymerization control, shown by the linear fits in the plot of number‐averaged molecular weight (Mn) versus the percentage conversion and versus the monomer/initiator ratio and by the low polydispersity index values. Interestingly, very good molar‐mass control was observed even when L ‐Lactide was polymerized in the absence of solvent at 130 °C. A good molar‐mass control but lower activities were observed in the polymerization reaction of lactide promoted by the analogous scandium complexes 3 and 4 . © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1374–1382, 2010 相似文献