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New copolymers with thieno[3,2‐b]thiophene or dithieno[3,2‐b:2′,3′‐d]thiophene units possessing electron‐withdrawing 4‐cyanophenyl groups: Synthesis and photophysical,electrochemical, and electroluminescent properties 下载免费PDF全文
Drahomír Výprachtický Ilknur Demirtas Vagif Dzhabarov Veronika Pokorná Erdal Ertas Turan Ozturk Věra Cimrová 《Journal of polymer science. Part A, Polymer chemistry》2017,55(16):2629-2638
New monomers containing 4‐cyanophenyl (–PhCN) groups attached to a thieno[3,2‐b]thiophene (TT) or dithieno[3,2‐b:2′,3′‐d]thiophene (DTT) structure were synthesized and characterized as 4‐(2,5‐dibromothieno[3,2‐b]thiophen‐3‐yl)benzonitrile (Br–TT–PhCN) or 4,4′‐(2,6‐dibromodithieno[3,2‐b:2′,3′‐d]thiophene‐3,5‐diyl)dibenzonitrile (Br–DTT–PhCN). The Suzuki coupling of 9,9‐dioctylfluorene‐2,7‐diboronic acid bis(1,3‐propanediol)ester and the Br–TT–PhCN or Br–DTT–PhCN monomer was utilized for the syntheses of novel copolymers poly{9,9‐dioctylfluorene‐2,7‐diyl‐alt‐3‐(4′‐cyanophenyl)thieno[3,2‐b]thiophene‐2,5‐diyl} (PFTT–PhCN) and poly{9,9‐dioctylfluorene‐2,7‐diyl‐alt‐3,5‐bis(4′‐cyanophenyl)dithieno[3,2‐b:2′,3′‐d]thiophene‐2,6‐diyl} (PFDTT–PhCN), respectively. The photophysical, electrochemical, and electroluminescent (EL) properties of these novel copolymers were studied. Their photoluminescence (PL) exhibited the same emission maximum for both copolymers in solution. Red‐shifted PL emissions were observed in the thin films. The PL emission maximum of PFTT–PhCN was more significantly redshifted than that of PFDTT–PhCN, indicating more pronounced excimer or aggregate formation in PFTT–PhCN. The ionization potential (HOMO level) and electron affinity (LUMO level) values were 5.54 and 2.81 eV, respectively, for PFTT–PhCN and were 5.57 and 2.92 eV, respectively, for PFDTT–PhCN. Polymer light‐emitting diodes (LEDs) with copolymer active layers were fabricated and studied. Anomalous behavior and memory effects were observed from the current–voltage characteristics of the LEDs for both copolymers. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 2629–2638 相似文献
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Sevcan Ayaksz Ozturk Seda Kelestemur Mustafa Culha 《Journal of Raman spectroscopy : JRS》2013,44(2):183-189
Raman spectroscopy is a powerful tool to study molecular systems. The influence of the non‐covalent interactions of two different lengths of oligonucleotides, 10‐base and 25‐base, composed of polyA, polyT, polyG and polyC, on the electronic structure of single‐walled carbon nanotubes (SWCNTs) is first studied by means of Raman spectroscopy. Then, the possible changes in their electronic structure with chemical attachment of the oligonucleotides are investigated. The Raman data indicates that polyA with 10‐base wraps the SWCNTs at increased incubation time, while polyA with 25‐base wraps quickly, but increasing the incubation time reduces the efficient wrapping, possibly due to the self‐stacking. The polyT‐10 does not wrap around the SWCNTs very effectively even at increased incubation times, but the polyT‐25 wraps them effectively in 30 mins, but increasing the time again decreases the wrapping significantly. While polyG shows similar pattern to the case for the polyA, the polyC shows much higher affinity for the SWCNTs under all studied conditions. The chemical attachment of the same oligonucleotides does not alter the electronic properties of the SWCNTs significantly. These results suggest that oligonucleotides can be used to bring the SWCNTs into higher structures through DNA hybridization without significantly altering their unique properties. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
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The intersubband transitions in Si δ-doped GaAs structures is theoretically investigated for different applied electric fields. For an uniform distribution the electronic structure has been calculated by solving the Schrödinger and Poisson equations self-consistently. From our calculations, it is found that the subband energies and intersubband optical absorption is quite sensitive to the applied electric field. This gives a new degree of freedom in various device applications based on the intersubband transitions of electrons. 相似文献
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Serkan Unal Gozde Ozturk Kristin Sisson Timothy E. Long 《Journal of polymer science. Part A, Polymer chemistry》2008,46(18):6285-6295
Highly branched, poly(caprolactone) (PCL) containing segmented poly(ester urethane)s were synthesized via polymerization of A2 and oligomeric B3 type monomers. An isocyanate functional butanediol‐based A2 hard segment was synthesized and immediately reacted with a poly(caprolactone)‐based trifunctional (B3) soft segment. Characterization of thermal properties using DMA and DSC analysis demonstrated that the PCL segment remained amorphous in branched poly(ester urethane)s. Conversely, the crystallinity of PCL segment was retained to some extent in a linear analogue with equivalent soft segment molecular weight. Tensile testing revealed a slight decrease in Young's modulus and tensile strength for the highly branched polymers compared with a linear analogue. However, highly branched poly(ester urethane)s demonstrated lower hysteresis. In addition to synthesis of highly branched polymers, poly(ester urethane) networks were synthesized from a highly branched hydroxyl‐terminated precursor and a low molar mass diisocyanate as the crosslinking agent. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 6285–6295, 2008 相似文献
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Stojan Radenović Tatjana Došenović Vildan Ozturk Ćemal Dolićanin 《Journal of Fixed Point Theory and Applications》2017,19(4):2287-2295
In this paper we consider, discuss and slightly complement recent fixed point results for mappings in b-metric spaces established by Sintunavarat (J Fixed Point Theory Appl 18:397–416, 2016). Thus, all our results are with shorter proofs. In addition, an application to integral equations is given to illustrate the usability of our approach. 相似文献
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Murat Misir Temel Ozturk Mustafa Emirik Sevil S. Yilmaz 《Journal of polymer science. Part A, Polymer chemistry》2010,48(13):2896-2909
Cationic polymerization of tetrahydrofuran (THF) and epichlorohydrin (ECH) was performed with peroxy initiators synthesized from bis (4,4′‐bromomethyl benzoyl peroxide (BBP) or bromomethyl benzoyl t‐butyl peroxy ester (t‐BuBP) and AgSbF6 or ZnCl2 system at 0 °C to obtain the poly(THF‐b‐ECH) macromonomeric peroxy initiators. Kinetic studies were accomplished for poly(THF‐b‐ECH) initiators. Poly(THF‐b‐ECH‐b‐MMA) and poly(THF‐b‐ECH‐b‐S) block copolymers were synthesized by bulk polymerization of methyl methacrylate (MMA) and styrene (S) with poly(THF‐b‐ECH) initiators. The quantum chemical calculations for the block copolymers, the initiating systems of the cationic polymerization of THF and ECH were achieved using HYPERCHEM 7.5 program. The optimized geometries of the polymers were investigated with the quantum chemical calculations. Poly(THF‐b‐ECH) initiators having peroxygen groups were used for graft copolymerization of polybutadien (PBd) to obtain poly(THF‐b‐ECH‐g‐PBd) crosslinked graft copolymers. The graft copolymers were investigated by sol‐gel analysis. Swelling ratio values of the graft copolymers in CHCl3 were calculated. The characterizations of the polymers were achieved by FTIR, 1H NMR, GPC, SEM, TEM, and DSC techniques. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 2896–2909, 2010 相似文献