全文获取类型
收费全文 | 1701篇 |
免费 | 45篇 |
国内免费 | 6篇 |
专业分类
化学 | 1074篇 |
晶体学 | 4篇 |
力学 | 35篇 |
数学 | 158篇 |
物理学 | 481篇 |
出版年
2021年 | 21篇 |
2020年 | 15篇 |
2019年 | 19篇 |
2017年 | 19篇 |
2016年 | 38篇 |
2015年 | 28篇 |
2014年 | 26篇 |
2013年 | 68篇 |
2012年 | 63篇 |
2011年 | 85篇 |
2010年 | 43篇 |
2009年 | 32篇 |
2008年 | 60篇 |
2007年 | 68篇 |
2006年 | 66篇 |
2005年 | 50篇 |
2004年 | 47篇 |
2003年 | 34篇 |
2002年 | 47篇 |
2001年 | 32篇 |
2000年 | 37篇 |
1999年 | 17篇 |
1998年 | 16篇 |
1997年 | 24篇 |
1996年 | 32篇 |
1995年 | 22篇 |
1994年 | 33篇 |
1993年 | 26篇 |
1992年 | 28篇 |
1991年 | 26篇 |
1990年 | 27篇 |
1989年 | 38篇 |
1988年 | 20篇 |
1987年 | 21篇 |
1986年 | 14篇 |
1985年 | 25篇 |
1984年 | 31篇 |
1983年 | 23篇 |
1982年 | 18篇 |
1981年 | 17篇 |
1980年 | 31篇 |
1979年 | 19篇 |
1978年 | 45篇 |
1977年 | 26篇 |
1976年 | 36篇 |
1975年 | 35篇 |
1974年 | 22篇 |
1973年 | 25篇 |
1972年 | 13篇 |
1969年 | 11篇 |
排序方式: 共有1752条查询结果,搜索用时 15 毫秒
71.
The azavinylidene osmium complex [(mes)Os(=N=CPh2(PiPr3)]PF6 (3; MES = 1.3.5-C6H3Me3), which was prepared in two steps from [(mes)OsCl2(PiPr3], CH3CO2Na/KPF6 and HN=CPh2, has been shown to react with trifluoracetic acid to give the isomeric heterocycle [(mes)
6H4)(Pi Pr3)]PF6 (4) in almost quantitative yield. With CF3CO2D, the monodeuterated compound 4-d4,containing a N---D unit in the five-membered ring, is obtained. An analogue of 4 with the composition [(mes)
6H4)(PMe3)]X(X = PF6 14a, SbF6 14b) has been made both from [(mes)Os(=N=CPh2)(PMe3)]PF6 12 and CF3CO2H and from [(mes)OsCl(NH= CPh2(PMe3)]SbF6 (13) and CF3CO2Ag. The reaction of 4 with NaH or KOtBu gives the uncharged heterocycle [(mes)
6 H4)(PiPr3)] (15), while treatment of [(mes)OsCl 2(NH=CPh2)] (19) with NaStBu gives the related complex [(mes)
6H4)(St Bu)] (20). The crystal structure of 4 has been determined. kw]Osmium; Azavinylidene; Cyclometallation; Crystal structure; Arene complexes 相似文献
72.
The photoluminescence (PL) of CdSe quantum dots (QD) in aqueous media has been studied in the presence of gold nanoparticles (NP) with different shapes. The steady state PL intensity of CdSe QD (1.5-2 nm in size) is quenched in the presence of gold NP. Picosecond bleach recovery and nanosecond time-resolved luminescence measurements show a faster bleach recovery and decrease in the lifetime of the emitting states of CdSe QD in the presence of quenchers. Surfactant-capped gold nanorods (NR) with aspect ratio of 3 and surfactant-capped and citrate-capped nanospheres (NS) of 12 nm diameter were used as quenchers in order to study the effect of shape and surface charge on the quenching rates. The Stern-Volmer kinetics model is used to examine the observed quenching behavior as a function of the quencher concentration. It was found that the quenching rate of NR is more than 1000 times stronger than that of NS with the same capping material. We also found that the quenching rate decreases as the length of the NR decreases, although the overlap between the CdSe emission and the NR absorption increases. This suggests that the quenching is a result of electron transfer rather than long-range (Forster-type) energy transfer processes. The quenching was attributed to the transfer of electron with energies below the Fermi level of gold to the trap holes of CdSe QD. The observed large difference between NR and NS quenching efficiencies was attributed to the presence of the [110] facets only in the NR, which have higher surface energy. 相似文献
73.
ClaudiaG. Martínez Annette Neuner Cristina Martí Santi Nonell AndrM. Braun Esther Oliveros 《Helvetica chimica acta》2003,86(2):384-397
We have investigated the effect of a series of 18 solvents and mixtures of solvents on the production of singlet molecular oxygen (O2(1Δg), denoted as 1O2) by 9H‐fluoren‐9‐one (FLU). The normalized empirical parameter E derived from ET(30) has been chosen as a measure of solvent polarity using Reichardt's betaine dyes. Quantum yields of 1O2 production (ΦΔ) decrease with increasing solvent polarity and protic character as a consequence of the decrease of the quantum yield of intersystem crossing (ΦISC). Values of ΦΔ of unity have been found in alkanes. In nonprotic solvents of increasing polarity, ΦISC and, therefore, ΦΔ decrease due to solvent‐induced changes in the energy levels of singlet and triplet excited states of FLU. This compound is a poor 1O2 sensitizer in protic solvents, because hydrogen bonding considerably increases the rate of internal conversion from the singlet excited state, thus diminishing ΦΔ to values much lower than those in nonprotic solvents of similar polarity. In mixtures of cyclohexane and alcohols, preferential solvation of FLU by the protic solvent leads to a fast decrease of ΦΔ upon addition of increasing amounts of the latter. 相似文献
74.
Minkov I Gel'mukhanov F Friedlein R Osikowicz W Suess C Ohrwall G Sorensen SL Braun S Murdey R Salaneck WR Agren H 《The Journal of chemical physics》2004,121(12):5733-5739
High-resolution x-ray photoelectron emission (XPS) and near-edge x-ray absorption fine structure (NEXAFS) spectra of naphthalene are analyzed in terms of the initial state chemical shifts and the vibrational fine structure of the excitations. Carbon atoms located at peripheral sites experience only a small chemical shift and exhibit rather similar charge-vibrational coupling, while the atoms in the bridging positions differ substantially. In the XPS spectra, C-H stretching modes provide important contributions to the overall shape of the spectrum. In contrast, the NEXAFS spectrum contains only vibrational progressions from particular C-C stretching modes. The accuracy of ab initio calculations of absolute electronic transition energies is discussed in the context of minute chemical shifts, the vibrational fine structure, and the state multiplicity. 相似文献
75.
76.
77.
Sreekar Wunnava Christina F. Dirscherl Jakub Výravský Dr. Aleš Kovařík Dr. Roman Matyášek Prof. Jiří Šponer Prof. Dieter Braun Dr. Judit E. Šponer 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(70):17581-17585
The assembly of ancient informational polymers from nucleotide precursors is the central challenge of life's origin on our planet. Among the possible solutions, dry polymerization of 3’,5’-cyclic guanosine monophosphate (3’,5’-cGMP) has been proposed as a candidate to create oligonucleotides of 15–20 units in length. However, the reported sensitivity of the reaction to the presence of cations raised questions of whether this chemistry could be relevant in a geological context. The experiments in this study show that the presence of cations is not restrictive as long as the reaction is conducted in an acidic environment, in contrast to previous reports that suggested optimal conditions at pH 9. 相似文献
78.
79.
Hui Li Peng Tang Yan Zhao Shi‐Xia Liu Yves Aeschi Lijun Deng Jörg Braun Bin Zhao Yunqi Liu Songting Tan Wolfgang Meier Silvio Decurtins 《Journal of polymer science. Part A, Polymer chemistry》2012,50(14):2935-2943
Two well‐defined alternating π‐conjugated polymers containing a soluble electroactive benzo[1,2‐b:4,5‐b′]difuran (BDF) chromophore, poly(BDF‐(9‐phenylcarbazole)) (PBDFC), and poly(BDF‐benzothiadiazole) (PBDFBTD) were synthesized via Sonogashira copolymerizations. Their optical, electrochemical, and field‐effect charge transport properties were characterized and compared with those of the corresponding homopolymer PBDF and random copolymers of the same overall composition. All these polymers cover broad optical absorption ranges from 250 to 750 nm with narrow optical band gaps of 1.78–2.35 eV. Both PBDF and PBDFBTD show ambipolar redox properties with HOMO levels of ?5.38 and ?5.09 eV, respectively. The field‐effect mobility of holes varies from 2.9 × 10?8 cm2 V?1 s?1 in PBDF to 1.0 × 10?5 cm2 V?1 s?1 in PBDFBTD. Bulk heterojunction solar cell devices were fabricated using the polymers as the electron donor and [6,6]‐phenyl‐C61‐butyric acid methyl ester as the electron acceptor, leading to power conversion efficiencies of 0.24–0.57% under air mass 1.5 illumination (100 mW cm?2). These results indicate that their band gaps, molecular electronic energy levels, charge mobilities, and molecular weights are readily tuned by copolymerizing the BDF core with different π‐conjugated units. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
80.
Dr. Kaveh Matinkhoo Antonio A. W. L. Wong Dr. Chido M. Hambira Brandon Kato Charlie Wei Dr. Christoph Müller Dr. Torsten Hechler Dr. Alexandra Braun Dr. Francesca Gallo Dr. Andreas Pahl Prof. David M. Perrin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(40):10282-10292
Alpha-amanitin, an extremely toxic bicyclic octapeptide extracted from the death-cap mushroom, Amanita phalloides, is a highly selective allosteric inhibitor of RNA polymerase II. Following on growing interest in using this toxin as a payload in antibody-drug conjugates, herein we report the synthesis and biochemical evaluation of several new derivatives of this toxin to probe the role of the trans-hydroxyproline (Hyp), which is known to be critical for toxicity. This structure activity relationship (SAR) study represents the first of its kind to use various Hyp-analogs to alter the conformational and H-bonding properties of Hyp in amanitin. 相似文献