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61.
Huey Wen Ooi Kevin S. Jack Andrew K. Whittaker Hui Peng 《Journal of polymer science. Part A, Polymer chemistry》2013,51(21):4626-4636
Despite the efficiency and robustness of the widely used copper‐catalyzed 1,3‐dipolar cycloaddition reaction, the use of copper as a catalyst is often not attractive, particularly for materials intended for biological systems. The use of photo‐initiated thiol‐ene as an alternative “click” reaction to synthesize “model networks” is investigated here. Poly(N‐isopropylacrylamide) precursors were synthesized by reversible addition fragmentation chain transfer (RAFT) polymerization and were designed to have trithiocarbonate moieties as end groups. This structure design provides opportunity for subsequent end‐group modifications in preparation for thiol‐ene “click.” Two reaction routes have been proposed and studied to yield thiol and ene moieties. The advantages and disadvantages of each reaction path were investigated to propose a simple but efficient route to prepare copper‐free “click” hydrogels. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 4626–4636 相似文献
62.
Prodip Sarker Saif U. R. Rehman Stephen Rimmer 《Journal of polymer science. Part A, Polymer chemistry》2013,51(8):1822-1830
Poly(1,1‐bis(ethoxycarbonyl)‐2‐vinyl cyclopropane (ECVP)‐graft‐dimethyl siloxane) copolymers were prepared using a macromonomer approach. Poly(dimethyl siloxane) (PDMS) macromonomers were prepared by living anionic polymerization of cyclosiloxanes followed by sequential chain‐end capping with allyl chloroformate. These macromonomers were then copolymerized with ECVP. MALDI‐ToF mass spectrometry and 1H NMR spectroscopy were used to show that the macromonomers had approximately 80% of the end groups functionalized with allyl carbonate groups. Gradient polymer elution chromatography showed that high yields of the graft copolymers were obtained, along with only small fractions of the PECVP and PDMS homopolymers. Differential scanning calorimetry showed that the low glass transition temperature (Tg) of the PDMS component could be maintained in the graft copolymers. However, the Tg was a function of polymer composition and the polymers produced had Tgs that ranged from ?50 to ?120 °C. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
63.
Wen Li Xiuqiang Zhang Jue Wang Xiao Qiao Kun Liu Afang Zhang 《Journal of polymer science. Part A, Polymer chemistry》2012,50(19):4063-4072
Tethering oligopeptides through one end densely packed onto a linear polymer main chain will greatly reduce freedom of the peptide chains, which affords an easy access to investigate the secondary structure of peptides under constrained condition. Herein, molecular brushes with densely grafted monodispersed Cbz‐protected oligolysine were efficiently synthesized via free radical polymerization of the macromonomer‐bearing lysine octamer, and the secondary structures of the oligopeptide side chains in solutions were investigated. To examine the architecture effects on helical conformation, circular dichroism spectra from the polymer were compared with that from the corresponding macromonomer. To check the chemical structural effects on conformation of the oligopeptide, Cbz groups from the molecular brushes were deprotected, and the secondary structures of the polymers were compared before and after the deprotection. Conformation of the deprotected polymer was further explored by varying solution pH values. Complexation of the positively charged, deprotected polymer with anionic surfactant provides an alternative route to mediate the secondary structures of the short peptides in the constrained environment. It has been found that oligolysine side chains within the molecular brushes can adopt enhanced α‐helical conformation through the crowding structures or can form β‐sheet by hydrophobic interactions between the complexed surfactants. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
64.
Healable network polymers bearing flexible poly(lauryl methacrylate) chains via thermo‐reversible furan‐maleimide diels–alder reaction
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Sachin S. Patil Arun Torris Prakash P. Wadgaonkar 《Journal of polymer science. Part A, Polymer chemistry》2017,55(16):2700-2712
A new ATRP initiator containing two furyl rings, namely, bis(furan‐2‐ylmethyl) 2‐bromopentanedioate was synthesized starting from commercially available l ‐glutamic acid as a precursor. Well‐defined bisfuryl‐terminated poly(lauryl methacrylate) macromonomers with molecular weight and dispersity in the range 5000–12,000 g mol?1 and 1.30–1.37, respectively, were synthesized employing the initiator by atom transfer radical polymerization (ATRP). Independently, 1,1′,1″‐(nitrilotris(ethane‐2,1‐diyl))tris(1H‐pyrrole‐2,5‐dione) was synthesized as a tris‐maleimide counterpart for furan‐maleimide click reaction. Thermo‐reversible network polymer bearing flexible poly(lauryl methacrylate; (PLMA) chains was obtained by furan‐maleimide Diels–Alder click reaction of bisfuryl‐terminated PLMA with 1,1′,1″‐(nitrilotris(ethane‐2,1‐diyl))tris(1H‐pyrrole‐2,5‐dione). The prepared network polymer showed retro‐Diels–Alder reaction in the temperature range 110–170 °C as determined from DSC analysis. The presence of low Tg (–40 °C) PLMA chains induced chain mobility to the network structure which led to the complete scratch healing of the coating at 60 °C in five days due to furan‐maleimide adduct formation. The storage modulus of the network polymer was found to be 3.7 × 104 Pa at the constant angular frequency of 5 rad/sec and strain of 0.5%. The regular reversal of storage (G ′) and loss modulus (G ″) was observed with repeated heating (40 to 110 °C) and cooling cycles (110 to 40 °C) at constant angular frequency and strain. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55 , 2700–2712 相似文献
65.
Kazunori Se Tsuyoshi Iwata 《Journal of polymer science. Part A, Polymer chemistry》2011,49(18):3939-3950
Poly(n‐hexylisocyanate) (PHIC‐NH) as a rod‐like polymer having a ? NH group at one end of the polymer chain was found to instantly (less than a few seconds) be completely decomposed by CH3O?Na+ in tetrahydrofuran/CH3OH under a mild experimental condition ([CH3O?Na+] < 1 mol L?1 at room temperature).The mechanism of the decomposition for the PHIC‐NH consists of two steps: the first is abstraction of the proton for PHIC‐NH by Na+ with a slow reaction rate, and the second is the consequent depolymerization of PHIC‐N? based on the equilibrium polymerization with a rapid depolymerization rate. The decomposition rate constants (kd) depend on Mw of PHIC‐NH, namely kd ~ Mw?1.0. The decomposition of the PHIC‐NR having an end‐capped ? NR group was completely depressed. Using an “all or nothing” mechanism for the decomposition, the (PHIC)3.43 comb‐shaped polymer and polystyrene (PSt)‐graft‐(PHIC‐NH)4.28 graft copolymer were, respectively, decomposed to produce (PHIC‐NH)3.43–1.03 and PSt‐graft‐(PHIC‐NH)4.28–0 in a series with different numbers of PHIC‐NH combs and PHIC‐NH grafts by regulating the amount of CH3O?Na+ and the decomposition time. Molecular structure of (PHIC‐NH)3.43–1.03 and PSt‐graft‐(PHIC‐NH)4.28–0 was discussed from a viewpoint of PSt‐reduced chain dimension per molar mass. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
66.
The reactivity ratios for the styrene dimethylaminoethyl methacrylate (DMAEMA) copolymerization have been determined by accurate experimental procedures. The experimental results were analyzed using a completely numerical procedure developed from the equations of Skiest. The results obtained differ significantly from those previously published. 相似文献
67.
Shigeki Ohno Krzysztof Matyjaszewski 《Journal of polymer science. Part A, Polymer chemistry》2006,44(19):5454-5467
Atom transfer radical polymerization (ATRP) was used for the preparation and subsequent copolymerization of two acryloyl‐terminated poly(n‐butyl acrylate) macromonomers with different degrees of polymerization (DPnBA = 25 and 42). Homopolymerization of the higher molecular weight macromonomer ( MM1 ; PnBA42‐A, Mn = 5600, DPMM = 42, Mw/Mn = 1.18) resulted in preparation of a densely grafted polymer with a narrow molecular weight distribution (Mw/Mn = 1.14), but with the limited degree of polymerization DP = 12. The ultimate degree of homopolymerization for the lower molecular weight macromonomer ( MM2 ; PnBA25‐A, Mn = 3400, DPMM = 25, Mw/Mn = 1.20) was higher, and DP increased from 12 to 22. The limited DP could be because of progressively increasing steric congestion for macromonomers in approaching the growing chain ends of densely grafted polymers. When MMs were copolymerized with nBA, the reactivity of MM was nearly the same as that of nBA monomer irrespective of the differences in the degree of polymerization of the MMs and the initial molar ratio of nBA to MM. Well‐defined graft polymers with different lengths of backbone and side chains, and different graft density were successfully prepared by “grafting through” ATRP. Tadpole‐shaped and dumbbell‐shaped graft polymers were also synthesized by ATRP. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5454–5467, 2006 相似文献
68.
Andreas Nystrm Anders Hult 《Journal of polymer science. Part A, Polymer chemistry》2005,43(17):3852-3867
A series of polymers tethered with bis‐MPA dendrons was synthesized by a combination of divergent growth and atom transfer radical polymerization (ATRP). Macromonomers of first and second generation were synthesized utilizing the acetonide protected anhydride of bis‐MPA as the generic esterfication agent. The macromonomers were polymerized in a controlled fashion by ATRP utilizing Cu(I)/Cu(II) and N‐propyl‐2‐pyridylmethanamine as the halogen/ligand system. The end‐groups of these polymers were further tailored to achieve hydroxyl, acetate, and aliphatic hexadecyl functionality. With this approach all polymers will emanate from the same backbone, enabling for an evaluation of both the generation and end‐group dependent properties. Furthermore, a dendronized tri‐block copolymer was synthesized. All materials were analyzed by 1H and 13C NMR, as well as size‐exclusion chromatography (SEC). The SEC analysis revealed that the molecular weights of the divergently grown dendronized polymers increased with increasing generation while the polydispersity (PDI) was kept low. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 3852–3867, 2005 相似文献
69.
Hideyuki Kaneko Shin‐ichi Kojoh Nobuo Kawahara Shingo Matsuo Tomoaki Matsugi Norio Kashiwa 《Journal of polymer science. Part A, Polymer chemistry》2005,43(21):5103-5118
Graft and star copolymers having poly(methacrylate) backbone and ethylene–propylene random copolymer (EPR) branches were successfully synthesized by radical copolymerization of an EPR macromonomer with methyl methacrylate (MMA). EPR macromonomers were prepared by sequential functionalization of vinylidene chain‐end group in EPR via hydroalumination, oxidation, and esterification reactions. Their copolymerizations with MMA were carried out with monofunctional and tetrafunctional initiators by atom transfer radical polymerization (ATRP). Gel‐permeation chromatography and NMR analyses confirmed that poly(methyl methacrylate) (PMMA)‐g‐EPR graft copolymers and four‐arm (PMMA‐g‐EPR) star copolymers could be synthesized by controlling EPR contents in a range of 8.6–38.1 wt % and EPR branch numbers in a range of 1–14 branches. Transmission electron microscopy of these copolymers demonstrated well‐dispersed morphologies between PMMA and EPR, which could be controlled by the dispersion of both segments in the range between 10 nm and less than 1 nm. Moreover, the differentiated thermal properties of these copolymers were demonstrated by differential scanning calorimetry analysis. On the other hand, the copolymerization of EPR macromonomer with MMA by conventional free radical polymerization with 2,2′‐azobis(isobutyronitrile) also gave PMMA‐g‐EPR graft copolymers. However, their morphology and thermal property remarkably differed from those of the graft copolymers obtained by ATRP. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5103–5118, 2005 相似文献
70.