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131.
132.
Chunhua Fu Changshun Ruan Ya Fu Yuanliang Wang 《Polymer Degradation and Stability》2010,95(4):485-490
The multi-arm star polymer (ESOPLA) was obtained by ring-opening polymerization of dl-lactide using multifunctional epoxidized soybean oil (ESO) as an initiator in the presence of a stannous actuate (SnOct2) catalyst. Gel permeation chromatography with multi-angle laser light scattering (GPC-MALLS), FTIR, 1H NMR, thermal analysis and in vitro degradation were used to qualitatively characterize the synthesized polymers. The results revealed that ESO plays an important role in increasing the molecular weight, polymerization rate and monomer conversion rate. Degradation analysis demonstrated that the decrease in molecular weight and the weight loss ratio of the star-shaped ESOPLA were lower than that of linear poly(dl-lactide) (PDLLA). The surface topography of pre- and post-degradation materials was characterized by scanning electron microscopy (SEM). These SEM images showed that the linear PDLLA films underwent water erosion more readily than the star-shaped polymer films. 相似文献
133.
Xiao‐Shuang Feng Cai‐Yuan Pan 《Journal of polymer science. Part A, Polymer chemistry》2001,39(13):2233-2243
A novel hexafunctional discotic initiator, 2,3,6,7,11,12‐hexakis(2‐bromobutyryloxy)triphenylene (HBTP), was synthesized by the esterification of 2,3,6,7,11,12‐hexahydroxytriphenylene with 2‐bromobutyryl chloride. Atom transfer radical polymerizations of styrene, methyl acrylate, and n‐butyl acrylate were carried out in 50 vol % tetrahydrofuran with HBTP/copper(I) bromide/2,2′‐bipyridyl as an initiation system. The polymers produced had well‐controlled molecular weights and narrow molecular weight distributions (<1.2). On the basis of 1H NMR spectra of the star polymer and its hydrolyzed products, we can conclude that the initiator quantitatively initiated the polymerization of vinyl monomers and that a star polymer with a discotic core was obtained. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 2233–2243, 2001 相似文献
134.
Asghar Bodaghi 《先进技术聚合物》2019,30(11):2827-2832
Novel A2B2‐type energetic miktoarm star‐shaped copolymers composed of two PGN arms and two PCL arms was synthesized by the combination of ring‐opening polymerization (ROP) and “click” chemistry. Initially, diazido end‐functionalized two‐arm PGN, (PGN)2‐(N3)2, was synthesized by ROP of glycidyl nitrate monomers. Subsequently, (PGN)2‐(PCL)2 was obtained from the click reaction between diazido end‐functionalized (PGN)2‐(N3)2 polymers and propargyl‐terminated poly(ε‐caprolactone) (PTPCL). This star copolymer solves problems of PCL (lake of energy) and PGN (low Tg). The Fourier‐transform infrared (FT‐IR), 1H nuclear magnetic resonance (NMR), and gel permeation chromatography (GPC) studies revealed that (PGN)2‐(PCL)2 was successfully obtained. The thermal behavior of star polymer was investigated by thermogravimetric analysis (TGA) and derivative thermogravimetry. The results show that (PGN)2‐(PCL)2 decomposed at two stages. The first stage is seen at 212.6°C which related to degradation of –ONO2 group and second stage attributed to degradation of PCL group which is seen at 346.1°C. 相似文献
135.
Dongyi Liu Ahmed M. El‐Zohry Maria Taddei Clemens Matt Laura Bussotti Zhijia Wang Jianzhang Zhao Omar F. Mohammed Mariangela Di Donato Stefan Weber 《Angewandte Chemie (International ed. in English)》2020,59(28):11591-11599
We prepared conceptually novel, fully rigid, spiro compact electron donor (Rhodamine B, lactam form, RB)/acceptor (naphthalimide; NI) orthogonal dyad to attain the long‐lived triplet charge‐transfer (3CT) state, based on the electron spin control using spin‐orbit charge transfer intersystem crossing (SOCT‐ISC). Transient absorption (TA) spectra indicate the first charge separation (CS) takes place within 2.5 ps, subsequent SOCT‐ISC takes 8 ns to produce the 3NI* state. Then the slow secondary CS (125 ns) gives the long‐lived 3CT state (0.94 μs in deaerated n‐hexane) with high energy level (ca. 2.12 eV). The cascade photophysical processes of the dyad upon photoexcitation are summarized as 1NI*→1CT→3NI*→3CT. With time‐resolved electron paramagnetic resonance (TREPR) spectra, an EEEAAA electron‐spin polarization pattern was observed for the naphthalimide‐localized triplet state. Our spiro compact dyad structure and the electron spin‐control approach is different to previous methods for which invoking transition‐metal coordination or chromophores with intrinsic ISC ability is mandatory. 相似文献
136.
Dongyi Liu Dr. Ahmed M. El-Zohry Maria Taddei Clemens Matt Laura Bussotti Dr. Zhijia Wang Prof. Jianzhang Zhao Prof. Omar F. Mohammed Prof. Mariangela Di Donato Prof. Stefan Weber 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(28):11688-11696
We prepared conceptually novel, fully rigid, spiro compact electron donor (Rhodamine B, lactam form, RB)/acceptor (naphthalimide; NI) orthogonal dyad to attain the long-lived triplet charge-transfer (3CT) state, based on the electron spin control using spin-orbit charge transfer intersystem crossing (SOCT-ISC). Transient absorption (TA) spectra indicate the first charge separation (CS) takes place within 2.5 ps, subsequent SOCT-ISC takes 8 ns to produce the 3NI* state. Then the slow secondary CS (125 ns) gives the long-lived 3CT state (0.94 μs in deaerated n-hexane) with high energy level (ca. 2.12 eV). The cascade photophysical processes of the dyad upon photoexcitation are summarized as 1NI*→1CT→3NI*→3CT. With time-resolved electron paramagnetic resonance (TREPR) spectra, an EEEAAA electron-spin polarization pattern was observed for the naphthalimide-localized triplet state. Our spiro compact dyad structure and the electron spin-control approach is different to previous methods for which invoking transition-metal coordination or chromophores with intrinsic ISC ability is mandatory. 相似文献
137.
Photophysical and photochemical processes of riboflavin (vitamin B_2) by means of the transient absorption spectra in aqueous solution 总被引:1,自引:0,他引:1
Using time-resolved techniques of 337 and 248 nm laser flash photolysis, the photo-physical and photochemical processes of riboflavin (RF, vitamin B2) were studied in detail in aqueous solution. The excited triplet state of riboflavin (3RF*) was produced with 337 nm laser, while under 248 nm irradiation, both 3RF* and hydrated electron (eaq) formed from photoionizationcould be detected. Photobiological implications have been inferred on the basis of reactivity of 3RF* including energy transfer, electron transfer and hydrogen abstraction. The RF.+ was generated by oxidation of SO4.- radical with the aim of confirming the results of photolysis. 相似文献
138.
Using time-resolved techniques of 337 and 248 nm laser flash photolysis, the photo physical and photochemical processes of
riboflavin (RF, vitamin B2) were studied in detail in aqueous solution. The excited triplet state of riboflavin (3RF*) was produced with 337 nm laser, while under 248 nm irradiation, both3RF* and hydrated electron (eaq) formed from photoionization could be detected. Photobiological implications have been inferred on the basis of reactivity
of3RF* including energy transfer, electron transfer and hydrogen abstraction. The RF·+ was generated by oxidation of SO4
·-radical with the aim of confirming the results of photolysis. 相似文献
139.
V.?V.?BryukhanovEmail author A.?M.?Ivanov I.?G.?Samusev 《Journal of Applied Spectroscopy》2005,72(6):804-808
The processes of homo-and hetero-triplet—triplet annihilation (TTA) of Bengali rose on the spongy silicon surface have been
investigated. It has been found that upon pulse photoexcitation on the silica surface photophysical processes involving the
triplet states of monomers and their associates can develop. It has been shown that the processes of hetero-TTA are inhibited
due to the decomposition of associates under the influence of hexane molecules in the molecular clusters of the dye adsorbates.
__________
Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 72, No. 6, pp. 734–737, November–December, 2005. 相似文献
140.
Gurkan Hizal Umit Tunca Amitav Sanyal 《Journal of polymer science. Part A, Polymer chemistry》2011,49(19):4103-4120
Functional polymeric materials with desired properties can be designed by precise control of macromolecular architectures. Over the recent years, click reactions have enabled efficient synthesis of a variety of polymers with different topologies via efficient polymer–polymer conjugations. While the copper catalyzed Huisgen type (3+2) dipolar cycloaddition between azide and alkyne has been widely used toward this goal, the Diels–Alder (DA) reaction offers an alternative click reaction that allow efficient macromolecular conjugations, oftentimes without the need of any additional reagent or catalyst. This article highlights, with illustrative examples, the power of the DA “click” reaction to efficiently synthesize a variety of different well‐defined macromolecular constructs in a modular fashion. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献