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61.
Chengcheng Yang Valter Castelvetro Dominique Scalarone Sabrina Bianchi Yongming Zhang 《Journal of polymer science. Part A, Polymer chemistry》2011,49(21):4518-4530
Stable colloidal dispersions of nanostructured semifluorinated acrylic particles with an unfluorinated core and an outer layer consisting of copolymers of the highly hydrophobic and lipophobic heptadecafluorodecyl methacrylate (FMA) were successfully synthesized with the assistance of three different cyclodextrins as phase‐transfer catalysts: β‐cyclodextrin (β‐CD), hydroxypropyl β‐cyclodextrin (HpCD), and methyl β‐cyclodextrin (MeCD). While all the cyclodextrins form a stable inclusion complex (IC) with FMA, only the ICs with the more hydrophilic HpCD and MeCD are soluble in water. Nevertheless, incorporation of FMA in the particle shell copolymer could be achieved also when using β‐CD. On the other hand, the morphology of the nanostructured particles was characterized by a “patchy” fluorinated shell dependent on the cyclodextrin used, the best results being obtained with MeCD. A monomer‐starved semicontinuous emulsion polymerization procedure was essential to favor the CD‐mediated incorporation of FMA into the copolymer structure and to achieve a stable colloidal dispersion even in the presence of small amounts of mixed anionic–nonionic surfactants. The thermal and surface properties of the latex films showed a good correlation with the shell composition and patchy nanostructured morphology of the particles. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
62.
Jun Araki 《Journal of polymer science. Part A, Polymer chemistry》2011,49(10):2199-2209
Four types of ionic polyrotaxane (PR) derivatives, that is, carboxymethylated, sulfoethylated, diethylaminoethylated, and trimethylammoniohydroxypropylated PRs, were successfully prepared starting from the same PR consisting of poly(ethylene glycol) as an axis and α‐cyclodextrins as ring molecules. The structures of the ionic PR derivatives were analyzed by 1H and 13C nuclear magnetic resonance (NMR), attenuated‐total reflection Fourier transform‐infrared, and colloidal titration. Degrees of substitution of the ionic PRs were calculated from results of 1H NMR and colloidal titrations; both sets of results satisfactorily agreed. Cross‐linking of sulfoethylated and quaternized PRs yielded ionic slide‐ring gels carrying sulfoethyl and quaternary ammonium groups on the mobile cross‐links, respectively. The former gel showed intriguing phenomena, including a large degree of swelling of up to 1147, drastic change in its swelling ratio by the presence of electrolyte and bending under a moderate applied electric field (7 V/cm). © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
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65.
Koji Kano Ryuhei Nishiyabu 《Journal of inclusion phenomena and macrocyclic chemistry》2002,44(1-4):355-359
A general mechanism for chiral recognition by native and modified cyclodextrins hasbeen proposed by reconsidering the data reported so far. Cyclodextrins in aqueoussolution adopt asymmetrically twisted structures, which seems to be the origin of chiralrecognition. 相似文献
66.
A. L. Nielsen M. B. O. Andersen T. V. Bugge C. F. Nielsen T. B. Nielsen R. Wimmer D. Yu K. L. Larsen 《Journal of polymer science. Part A, Polymer chemistry》2009,47(23):6619-6629
In this article, we present the synthesis and characterization of water‐soluble polymers with hydrophobic moieties. The polymers were synthesized in aqueous solutions utilizing β‐cyclodextrins as solubility enhancers to bring the hydrophobic monomers into solution. Polymers were made with different spacing between polymer backbone and phenyl moiety by using styrene, allylbenzene, and 4‐phenyl‐1‐butene as hydrophobic moieties, respectively. The effect of the presence of CDs during synthesis as well as this difference in spacing was investigated by rebinding free β‐CDs to the polymers. The interactions between polymers and CDs were studied by ITC and this revealed some differences between the polymers. Polymers made in the presence of CDs showed a markedly stronger binding to free CDs. The same was observed with polymers with a longer spacing between backbone and phenyl moiety. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 6619–6629, 2009 相似文献
67.
Miao Yu Sheng‐Zhen Zu Dr. Yong Chen Dr. Yu‐Ping Liu Dr. Bao‐Hang Han Prof. Dr. Yu Liu Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(4):1168-1174
A supramolecular hybrid is prepared by the supramolecular surface modification of single‐walled carbon nanotube (SWCNT) with cationic β‐cyclodextrin‐tethered ruthenium complexes through a spacer molecule that contains both an adamantane and a pyrene moiety. By employing the supramolecular hybrid, spatially controllable DNA condensation along the SWCNT skeleton is achieved by anchoring cationic ruthenium complexes on the surface. Furthermore, because of the unique physiological properties of SWCNTs, the cationic supramolecular hybrid can be used as a nonviral gene delivery system with the ruthenium complexes as a fluorescent probe to monitor uptake of DNA by cells. 相似文献
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Antonino Mazzaglia Luigi Monsu' Scolaro Raphael Darcy Ruth Donohue Bart Jan Ravoo 《Journal of inclusion phenomena and macrocyclic chemistry》2002,44(1-4):127-132
The entanglement process between porphyrins and some amphiphiliccyclodextrins and the occurrence of different species have been proved by the combination of UV-Visabsorption, fluorescence anisotropy, resonance light scattering and 1H NMR spectroscopy. 相似文献
70.