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141.
Herein a polyurethane graft poly‐l ‐glutamate amphiphilic copolymer was synthesized from a polyurethane (PU)‐based macro‐initiator (containing pendant primary amine groups) through the ring opening polymerization of N‐carboxy anhydride of γ‐benzyl‐l ‐glutamate ( BLG‐NCA ). On average, twenty two l ‐glutamic acids were grafted from each amino group which was pendant on the polyurethane chain with 10 repeating units. The grafted polymer ( PU‐PP‐1 ) exhibits self‐assembly to produce a hydrogel in a wide pH window ranging from pH 5.0 to 8.0 with a critical gelation concentration (CGC) of 5.0 wt % (w/v) at pH 7.4. Furthermore, circular dichroism study revealed the transition of the α‐helix to a random coil upon increasing the pH. Due to the protonation of side chains at pH 4.0, PU‐PP‐1 adopted an α‐helical conformation whereas at pH >8.0 the side‐chain carboxylic acid groups of the PLGAs were ionized, leading to the formation of an extended random coil conformation as a result of charge repulsion. Conformational switching was also supported by FTIR spectroscopy. 相似文献
142.
Bhajendra N. Barman 《Journal of separation science》1993,16(7):404-406
Amperometric detection is shown to be highly selective and sensitive for the determination of tert-butylcatechol (TBC) added as an antioxidant in the circulating N-methyl-2-pyrrolidone (NMP) used for the purification of 1,3-butadiene by extractive distillation. The separation of TBC from numerous polar and nonpolar species present in the analyte is achieved on a 5-cm reversed-phase C-18 column using acetonitrile-water gradient conditions, both solvent components containing tetrabutyl ammonium dihydrogen phosphate as the amphiphilic modifier. The separation process is optimized for the resolution of TBC from nonpolar hydrocarbons as well as polar compounds, and a complete elution of all species from the column. An applied potential of 0.6 V relative to the Ag/AgCI electrode is found to provide an optimum sensitivity by the amperometric detector. It is also shown that the hydrocarbon content in NMP can be monitored simultaneously by coupling a spectrophotometric detector in series. 相似文献
143.
During the last two decades, massive efforts have been directed at uncovering different science concepts held by school age students. This particular study focused on identifying high school students' views regarding the nature of science. Thirty-two students were chosen from each of the following three countries: Canada, the United States, and Australia. Interviews were conducted with each student. The interview protocol contained the same core questions with an opportunity built in to allow both the student and the interviewer to seek clarification and extension as necessary. All of the interviews were audiotape recorded and transcribed. Some major differences and many commonalities were observed among the three groups of students. These results should be potentially useful to a wide range of science educators and curriculum developers in that one's ability to become scientifically literate is greatly impair ed when the nature of science is not completely understood. 相似文献
144.
Rama K. Barman Sanjay K. Singh Birinchi K. Das 《Journal of chemical crystallography》2002,32(10):369-375
A coordination polymer catena-chloro(4-pyridinecarboxylic acid)copper(I): [Cu(C6H5 O2N)Cl]n (1) has been prepared directly by reacting CuIICl2 2H2O and 4-cyanopyridine in the presence of disodium maleate under hydrothermal conditions at 140°C. Crystal data for 1 are as follows: monoclinic, P21/n, a = 16.4623(9) Å, b = 3.7795(2) Å, c = 24.7612(11) Å, = 101.534(1)°, V = 1509.5(1) Å3, Z = 4, D
calc. = 1.955 g cm–3, R1 = 0.0511, wR2 = 0.1060 for all 2666 reflections. In this 1-D stair-polymer, two [Cu–Cl–Cu]n zigzag chains are held together by weak interchain Cu–Cl bonds. The 4-pyridinecarboxylic acid ligands derived from the 4-CNpy molecules coordinate to the approximately tetrahedral Cu(I) centers through pyridyl-N atoms. The carboxyl ends of 4-pyridinecarboxylic acid participate in interchain hydrogen-bonding interactions to form a 2-D supramolecular network. 相似文献
145.
Srivastava P Barman J Pathmasiri W Plashkevych O Wenska M Chattopadhyaya J 《Journal of the American Chemical Society》2007,129(26):8362-8379
Two unusual reactions involving the 5-hexenyl or the 6-heptenyl radical cyclization of a distant double bond at C4' and the radical center at C2' of the ribofuranose ring of thymidine have been used as key steps to synthesize North-type conformationally constrained cis-fused bicyclic five-membered and six-membered carbocyclic analogues of LNA (carbocyclic-LNA-T) and ENA (carbocyclic-ENA-T) in high yields. Their structures have been confirmed unambiguously by long range 1H-13C NMR correlation (HMBC), TOCSY, COSY, and NOE experiments. The carbocyclic-LNA-T and carbocyclic-ENA-T were subsequently incorporated into the antisense oligonucleotides (AONs) to show that they enhance the Tm of the modified AON/RNA heteroduplexes by 3.5-5 degrees C and 1.5 degrees C/modification for carbocyclic-LNA-T and carbocyclic-ENA-T, respectively. Whereas the relative RNase H cleavage rates with carbocyclic-LNA-T, carbocyclic-ENA-T, aza-ENA-T, and LNA-T modified AON/RNA duplexes were found to be very similar to that of the native counterpart, irrespective of the type and the site modification in the AON strand, a single incorporation of carbocyclic-LNA and carbocyclic-ENA into AONs leads to very much more enhanced nuclease stability in the blood serum (stable >48 h) as compared to that of the native (fully degraded <3 h) and the LNA-modified AONs (fully degraded <9 h) and aza-ENA ( approximately 85% stable in 48 h). Clearly, remarkably enhanced lifetimes of these carbocyclic-modified AONs in the blood serum may produce the highly desired pharmacokinetic properties because of their unique stability and consequently a net reduction of the required dosage. This unique quality as well as their efficient use as the AON in the RNase H-promoted cleavage of the target RNA makes our carbocyclic-LNA and carbocyclic-ENA modifications excellent candidates as potential antisense therapeutic agents. 相似文献
146.
Lipika Ray Samir Barman Hemant Nanavati Prasenjit Ghosh 《Journal of organometallic chemistry》2007,692(20):4259-4269
Synthesis, structures, and catalysis studies of gold(I) complexes of N-heterocyclic carbenes namely, a di-O-functionalized [1-(2-hydroxy-cyclohexyl)-3-(acetophenone)imidazol-2-ylidene], a mono-O-functionalized [1-(2-hydroxy-cyclohexyl)-3-(benzyl)imidazol-2-ylidene] and a non-functionalized [1,3-di-i-propyl-benzimidazol-2-ylidene], are reported. Specifically, the gold complexes, [1-(2-hydroxy-cyclohexyl)-3-(acetophenone)imidazol-2-ylidene]AuCl (1c), [1-(2-hydroxy-cyclohexyl)-3-(benzyl)imidazol-2-ylidene]AuCl (2c), and [1,3-di-i-propyl-benzimidazol-2-ylidene]AuCl (3b), were prepared from the respective silver complexes 1b, 2b, and 3a by treatment with (SMe2)AuCl in good yields following the commonly used silver carbene transfer route. The silver complexes 1b, 2b, and 3a were synthesized from the respective imidazolium halide salts by the reactions with Ag2O. The N-heterocyclic carbene precursors, 1-(2-hydroxy-cyclohexyl)-3-(acetophenone)imidazolium chloride (1a) and 1-(2-hydroxy-cyclohexyl)-3-(benzyl)imidazolium chloride (2a), were synthesized by the direct reactions of cyclohexene oxide and imidazole with chloroacetophenone and benzyl chloride respectively. The gold (1c, 2c, and 3b) and the silver (3a) complexes along with a new O-functionalized imidazolium chloride salt (1a) have been structurally characterized by X-ray diffraction. The structural studies revealed that geometries around the metal centers were almost linear in these gold and silver complexes. The gold (1c, 2c, and 3b) complexes efficiently catalyze ring-opening polymerization (ROP) of l-lactide under solvent-free melt conditions producing polylactide polymer of moderate to low molecular weights with narrow molecular weight distributions. 相似文献
147.
A simple methodology has been developed for the synthesis of thieno[2,3‐b]pyrroles from N‐aryl‐diformylated‐pyrroles by base catalyzed condensation with thioglycolic ester. J. Heterocyclic Chem., 2011. 相似文献
148.
Amit Basak Subhendu Sekhar Bag Kakali Rani Rudra Jharna Barman Sumana Dutta 《ChemInform》2002,33(48):115-115
149.
Kaushik Kumar Bharadwaj Bijuli Rabha Siddhartha Pati Tanmay Sarkar Bhabesh Kumar Choudhury Arpita Barman Dorothy Bhattacharjya Ankit Srivastava Debabrat Baishya Hisham Atan Edinur Zulhisyam Abdul Kari Noor Haslina Mohd Noor 《Molecules (Basel, Switzerland)》2021,26(21)
Gold nanoparticles (AuNPs) have been widely explored and are well-known for their medical applications. Chemical and physical synthesis methods are a way to make AuNPs. In any case, the hunt for other more ecologically friendly and cost-effective large-scale technologies, such as environmentally friendly biological processes known as green synthesis, has been gaining interest by worldwide researchers. The international focus on green nanotechnology research has resulted in various nanomaterials being used in environmentally and physiologically acceptable applications. Several advantages over conventional physical and chemical synthesis (simple, one-step approach to synthesize, cost-effectiveness, energy efficiency, and biocompatibility) have drawn scientists’ attention to exploring the green synthesis of AuNPs by exploiting plants’ secondary metabolites. Biogenic approaches, mainly the plant-based synthesis of metal nanoparticles, have been chosen as the ideal strategy due to their environmental and in vivo safety, as well as their ease of synthesis. In this review, we reviewed the use of green synthesized AuNPs in the treatment of cancer by utilizing phytochemicals found in plant extracts. This article reviews plant-based methods for producing AuNPs, characterization methods of synthesized AuNPs, and discusses their physiochemical properties. This study also discusses recent breakthroughs and achievements in using green synthesized AuNPs in cancer treatment and different mechanisms of action, such as reactive oxygen species (ROS), mediated mitochondrial dysfunction and caspase activation, leading to apoptosis, etc., for their anticancer and cytotoxic effects. Understanding the mechanisms underlying AuNPs therapeutic efficacy will aid in developing personalized medicines and treatments for cancer as a potential cancer therapeutic strategy. 相似文献