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121.
膜生物污染一直是膜生物反应器(membrane bioreactor,MBR)在废水处理工艺中需要解决的一大难题。最近研究表明:基于群体感应的淬灭技术可以作为MBR活性污泥体系中一种有效的膜生物污染防治策略。因而,识别和分析群体感应产生的信号分子是应用群体淬灭技术防治MBR中膜生物污染的关键。本文首先介绍了活性污泥体系中的群体感应机理和N-酰基高丝氨酸内脂(N-acyl homoserine lactone,AHL);其次,归纳近期研究中针对MBR中AHL定性和定量分析方法;最后,对MBR中AHL识别及分析技术应用进行了展望。 相似文献
122.
A convenient and efficient approach for difluoroalkyl-containing γ-butyrolactones via the radical addition reaction of iododifluoromethyl ketones with 4-pentenoic acids initiated by AIBN in CH3CN at 60 ℃ was reported. Various difluoroalkyl-containing δ-valerolactones were also synthesized under this reaction conditions. 相似文献
123.
Redeuil K Smarrito-Menozzi C Guy P Rezzi S Dionisi F Williamson G Nagy K Renouf M 《Journal of chromatography. A》2011,1218(29):4678-4688
This study reports a liquid chromatography-mass spectrometry method for the detection of polyphenol-derived metabolites in human plasma without enzymatic treatment after coffee consumption. Separation of available standards was achieved by reversed-phase ultra performance liquid chromatography and detection was performed by high resolution mass spectrometry in negative electrospray ionization mode. This analytical method was then applied for the identification and relative quantification of circulating coffee metabolites. A total of 34 coffee metabolites (mainly reduced, sulfated and methylated forms of caffeic acid, coumaric acid, caffeoylquinic acid and caffeoylquinic acid lactone) were identified based on mass accuracy (<4 ppm for most metabolites), specific fragmentation pattern and co-chromatography (when standard available). Among them, 19 circulating coffee metabolites were identified for the first time in human plasma such as feruloylquinic acid lactone, sulfated and glucuronidated forms of feruloylquinic acid lactone and sulfated forms of coumaric acid. Phenolic acid derivatives such as dihydroferulic acid, dihydroferulic acid 4'-O-sulfate, caffeic acid 3'-O-sulfate, dimethoxycinnamic acid, dihydrocaffeic acid and coumaric acid O-sulfate appeared to be the main metabolites circulating in human plasma after coffee consumption. The described method is a sensitive and reliable approach for the identification of coffee metabolites in biological fluids. In future, this analytical method will give more confidence in compound identification to provide a more comprehensive assessment of coffee polyphenol bioavailability studies in humans. 相似文献
124.
125.
Cdric G. Jaffredo Jean‐Franois Carpentier Sophie M. Guillaume 《Macromolecular rapid communications》2012,33(22):1938-1944
Basic organocatalysts of the guanidine (1,5,7‐triazabicyclo[4.4.0]dec‐5‐ene, TBD), amidine (1,8‐diazabicyclo[5.4.0]‐undec‐7‐ene, DBU), and phosphazene (2‐tert‐butylimino‐2‐diethylamino‐1,3‐dimethylperhydro‐1,3,2diazaphosphorine, BEMP) type do effectively polymerize β‐butyrolactone (BL). Poly(3‐hydroxybutyrate)s (PHBs) with controlled molecular features, that is, controlled molar masses, narrow molar mass distributions, and well‐defined functional end groups are thus formed at 60 °C from bulk monomer, with up to 21 500 g mol−1. The formation of α,ω‐guanidine/amidine/phosphazene,crotonate functionalized PHBs, as demonstrated by NMR, SEC, and MALDI–ToF mass spectrometry analyses, mechanistically suggests the formation of N‐acyl‐α,β‐unsaturated propagating species that originate from 1:1 guanidine/amidine/phosphazene:BL adducts. 相似文献
126.
Qiang Zhang Sizhe Li Maha Hachicha Mohamed Boukraa Laurent Soulre Mohamed L. Efrit Yves Queneau 《Molecules (Basel, Switzerland)》2021,26(17)
N-acyl homoserine lactones (AHLs) are small signaling molecules used by many Gram-negative bacteria for coordinating their behavior as a function of their population density. This process, based on the biosynthesis and the sensing of such molecular signals, and referred to as Quorum Sensing (QS), regulates various gene expressions, including growth, virulence, biofilms formation, and toxin production. Considering the role of QS in bacterial pathogenicity, its modulation appears as a possible complementary approach in antibacterial strategies. Analogues and mimics of AHLs are therefore biologically relevant targets, including several families in which heterocyclic chemistry provides a strategic contribution in the molecular design and the synthetic approach. AHLs consist of three main sections, the homoserine lactone ring, the central amide group, and the side chain, which can vary in length and level of oxygenation. The purpose of this review is to summarize the contribution of heterocyclic chemistry in the design of AHLs analogues, insisting on the way heterocyclic building blocks can serve as replacements of the lactone moiety, as a bioisostere for the amide group, or as an additional pattern appended to the side chain. A few non-AHL-related heterocyclic compounds with AHL-like QS activity are also mentioned. 相似文献
127.
Mona-Katharina Bill Stephan Brinkmann Markus Oberpaul Maria A. Patras Benedikt Leis Michael Marner Marc-Philippe Maitre Peter E. Hammann Andreas Vilcinskas Sren M. M. Schuler Till F. Schberle 《Molecules (Basel, Switzerland)》2021,26(17)
The ‘core’ metabolome of the Bacteroidetes genus Chitinophaga was recently discovered to consist of only seven metabolites. A structural relationship in terms of shared lipid moieties among four of them was postulated. Here, structure elucidation and characterization via ultra-high resolution mass spectrometry (UHR-MS) and nuclear magnetic resonance (NMR) spectroscopy of those four lipids (two lipoamino acids (LAAs), two lysophosphatidylethanolamines (LPEs)), as well as several other undescribed LAAs and N-acyl amino acids (NAAAs), identified during isolation were carried out. The LAAs represent closely related analogs of the literature-known LAAs, such as the glycine-serine dipeptide lipids 430 (2) and 654. Most of the here characterized LAAs (1, 5–11) are members of a so far undescribed glycine-serine-ornithine tripeptide lipid family. Moreover, this study reports three novel NAAAs (N-(5-methyl)hexanoyl tyrosine (14) and N-(7-methyl)octanoyl tyrosine (15) or phenylalanine (16)) from Olivibacter sp. FHG000416, another Bacteroidetes strain initially selected as best in-house producer for isolation of lipid 430. Antimicrobial profiling revealed most isolated LAAs (1–3) and the two LPE ‘core’ metabolites (12, 13) active against the Gram-negative pathogen M. catarrhalis ATCC 25238 and the Gram-positive bacterium M. luteus DSM 20030. For LAA 1, additional growth inhibition activity against B. subtilis DSM 10 was observed. 相似文献
128.
Atsushi Sudo Akane Suzuki Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2013,51(19):4213-4220
Cationic copolymerization of n‐butyl glycidyl ether (BGE) and 3‐isochromanone (ICM) was investigated using trifluoromethanesulfonic acid (TfOH) as an initiator at 100 °C. In the copolymerization, the reactive site of ICM with the propagating cation was completely different from that in its homopolymerization: in the former, the propagating cation reacted with the carbonyl oxygen of ICM, while in the latter, the propagating cation reacted with the aromatic ring of ICM. In spite of the potential of ICM to undergo the homopolymerization, in the present copolymerization, ICM was consumed smoothly only in the presence of epoxide. As a result, the copolymerization proceeded in a statistic manner to afford the corresponding copolymer bearing ICM‐derived ester linkages distributed in the main chain. Cationic copolymerization of bisphenol A‐diglycidyl ether and ICM was also performed to synthesize the corresponding networked polymer. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 4213–4220 相似文献
129.
Clémence Guillaume Noureddine Ajellal Jean‐François Carpentier Sophie M. Guillaume 《Journal of polymer science. Part A, Polymer chemistry》2011,49(4):907-917
The controlled ring‐opening polymerization of racemic allyl‐β‐butyrolactone (rac‐BLallyl) in toluene or in bulk, catalyzed by the discrete β‐diiminate zinc amido [(BDIiPr)Zn(N(SiMe3)2)] ( 1 ) or {amino‐methoxy‐bis(phenolate)}yttrium amido [(ONOOtBu)Y(N(SiHMe2)2)(THF)] ( 2 ) complexes, in association with an alcohol, gave poly(β‐hydroxyalkanoate)s (PHAs) with allylic side chains. These PHAsallyl exhibit either a slightly isotactic‐enriched (Pm = 0.61) or highly syndiotactic‐enriched (Pr = 0.82) backbone structure, respectively, with high molar mass (M n up to 21,100 g mol?1) and narrow molar mass distribution values (1.05 < M w/M n < 1.28), as evidenced by detailed 13C NMR and size exclusion chromatography analyses. Postpolymerization rhodium‐catalyzed hydroboration of the resulting PHAsallyl with pinacolborane quantitatively afforded the corresponding PHAsboron. Introduction of boron into the pendant chains did not alter neither the structure of the polymer backbone nor the macromolecular features (M n, M w/M n, and stereoregularity). However, differential scanning calorimetry analyses revealed a significant increase of the glass transition temperature on modifying the allyl for the boron function in these PHAs. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
130.