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1.
Two Isomeric pyridines were designed and prepared : 2-isopropyl-4,5,6-trimethyl-(3) and 2-isopropyl-3,4,6-trimethyl-pyridine (7); the latter, with a buttressed isopropyl, leads to much lower induced shifts by Eu(dpm)3 and Pr(dpm)3 than the former, owing to the conformation in which the Janus-type iPr group how to the LSR a t-butyl-like face.  相似文献   
2.
The photophysical properties of two polyrotaxanes ( PFBTh?PSβCD and PFBTh?PMeβCD ) composed of fluorene and bithiophene encapsulated into permodified β‐cyclodextrin cavities have been investigated and compared with those of the reference PFBTh . Rotaxane formation results in improvements of the thermal stability, solubility in common organic solvents, as well as better film forming ability combined with a high transparency. As expected PFBTh and its encapsulated forms absorb at wavelengths beyond 510 nm, and time‐resolved photoluminescence (PL) in solution shows a well‐define vibronic structures with a predominance of the 0‐0 transitions and an energy difference of 0.16 eV. The fluorescence lifetimes follow a monoexponential decay with a value τ = 630 ± 30 ps. Atomic force microscopy, AFM, indicated a tendency of polyrotaxanes to organize into fibers. The advancing contact angles indicated higher surface hydrophobicity and lower surface free‐energy values for polyrotaxanes compared with their unthreaded analogues. The device based on PFBTh?PSβCD: PCBM in a 1/1 w/w ratio under simulated AM 1.5G illumination at 100 mW cm?2 exhibited improved photovoltaic parameters of cells, resulted in high Voc (0.68 V), Jsc (1.65 mA cm?2), FF (31.6%), and PCE (0.35) values, compared with PFBTh or PFBTh?PMeβCD , respectively. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 460–471  相似文献   
3.
The study reports the synthesis of a copolymer based on 2‐hydroxyethyl methacrylate and 3,9‐divinyl‐2,4,8,10‐tetraoxaspiro[5.5]undecane (U) acquired through radical polymerization in the presence of 2,2′‐azobis(2‐methylpropionitrile). The attempt was to have a solid content as high as 10 wt %. The polymerization process was conducted in the presence of a classic ionic surfactant—sodium lauryl sulfate—and comparatively using two variants of protective colloid β‐cyclodextrin and poly(aspartic acid), respectively. The prepared dispersions were characterized from the viewpoint of their hydrodynamic radius, zeta potential, and conductivity evolution during syntheses. The mean particle size and size distribution and zeta potential and conductivity were also evaluated for the synthesized polymeric particles. The compositions of the polymers were confirmed by FTIR and 1H NMR spectra, and also, the thermal stability of the polymeric compounds was evaluated. SEM and AFM investigations of the polymer morphology are also presented. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011  相似文献   
4.
Polyfluorene PF?γCD rotaxane copolymer, composed of randomly distributed 9,9‐dioctylfluorene, methyltriphenylamine (electron‐donating) and 9‐dicyanomethylenefluorene complexed with γ‐cyclodextrin (γCD) (electron‐accepting) structural units, has been synthesized by Suzuki cross‐coupling reaction. The chemical structures were proved by FTIR and 1H NMR spectroscopy. The surface morphology, thermal, optical, electrochemical behavior, and adhesion characteristics of the obtained rotaxane copolymer have been investigated and compared with those of the nonrotaxane counterpart ( PF ). Relatively high fluorescence efficiency, almost identical normalized absorbance maximum in solution and solid‐state of PF?γCD rotaxane copolymer, and a more uniform and smoother surface with lower adhesion forces provides the role of γCD encapsulation on the lower aggregation propensity. PF?γCD and PF copolymers exhibit n‐ and p‐doping processes and blue‐light emission in the film state. The optical and electrochemical band gaps (ΔEg), as well as the highest occupied molecular orbital/lowest unoccupied molecular orbital positions in an energetic diagram indicate that both copolymers are promising blue‐emitting electroluminescent materials. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013  相似文献   
5.
Different researches have shown that long–term exposure to whole–body vibration can induce different injuries like back pain, injuries of the different part of the body, disturbing the physical and intellectual activities. The resulted diseases could be occasional or could be for ever. Bearing in mind that vibration is applied on the hand or feet, the health rick can be assessed if the forces transmitted in the shoulder during vibration are known. To estimate the forces a biomechanical model has been developed in which the shoulder, neck and head are represented by rigid bodies. The bodies are connected by visco–elastic joint elements. The applied forces are resulted from experimental measurements. To assess the health risk the forces must be divised in two components, an ascendant one and a descendent one. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   
6.
The effect of a continuous external magnetic field on the free radical polymerization of methyl methacrylate was studied with respect to some properties of the solvents used in the reaction. The studies were performed through dilatometric technique in and out a magnetic field of 0.25 T. Ten different solvents were used to underline the dependence between the magnetic field presence, the reaction medium, and the development of the polymerization process. The intervened magnetokinetic effects are attributed to the changes in the multiplicity of the radical pairs owing to the magnetic field influence. There is an interdependence among the viscosity and molar polarization of the solvents and the magnetic field effect. © 1996 John Wiley & Sons, Inc.  相似文献   
7.
8.
Poly[2,7-(9,9-dioctylfluorene-alt-2,7-fluorene/β-CD)] main chain polyrotaxane was synthesized through organometallic Suzuki coupling by reacting β-cyclodextrin/2,7-dibromofluorene inclusion complex with 9,9-dioctylfluorene-2,7-bis(trimethyleneborate). The IR, NMR and elemental analysis data support the presence of β-cyclodextrin in the copolymer structure. No glass transition or melting phenomena were detected in DSC curves of the polyrotaxane on the heating run in the 50-250 ° range. As compared with the reference copolymer obtained in the absence of β-cyclodextrin, the rotaxane copolymer is more hygroscopic and soluble in polar/non-polar solvent mixtures. The expected modification of the optical properties of the fluorene copolymer with rotaxane architecture in the main chain was proved by fluorescence and UV-vis spectroscopy and consists in a blue-shifted emission.  相似文献   
9.
Riboflavin under UVA radiation generates reactive oxygen species (ROS) that can induce various changes in biological systems. Under controlled conditions, these processes can be used in some treatments for ocular or dermal diseases. For instance, corneal cross-linking (CXL) treatment of keratoconus involves UVA irradiation combined with riboflavin aiming to induce the formation of new collagen fibrils in cornea. To reduce the damaging effect of ROS formed in the presence of riboflavin and UVA, the CXL treatment is performed with the addition of polysaccharides (dextran). Hyaluronic acid is a polysaccharide that can be found in the aqueous layer of the tear film. In many cases, keratoconus patients also present dry eye syndrome that can be reduced by the application of topical solutions containing hyaluronic acid. This study presents physico-chemical evidence on the effect of riboflavin on collagen fibril formation revealed by the following methods: differential scanning microcalorimetry, rheology, and STEM images. The collagen used was extracted from calf skin that contains type I collagen similar to that found in the eye. Spin trapping experiments on collagen/hyaluronic acid/riboflavin solutions evidenced the formation of ROS species by electron paramagnetic resonance measurements.  相似文献   
10.
Ru–BEA catalysts with 1.0–2.5 wt.% Ru were prepared by ion exchange. The acidic properties of these catalysts were investigated using deuterated acetonitrile, pyridine, and 2,6-di-tert-butyl-pyridine. The deposited Ru was studied by CO-FTIR spectroscopy. The materials were tested as catalysts in the hydrogenation of a conjugated cyclic keto–enol, namely, 5-hydroxymethylene-5H-6,7-dihydrodibenzo[a,c]cyclohepten-6-one. Beside hydrogenation, hydrogenolysis products were identified by GC–MS and 1H NMR techniques. Relations were sought between the selectivity and some physicochemical properties of the catalyst.  相似文献   
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