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101.
Steinberg Y Schroeder A Talmon Y Schmidt J Khalfin RL Cohen Y Devoisselle JM Begu S Avnir D 《Langmuir : the ACS journal of surfaces and colloids》2007,23(24):12024-12031
Liposomes prepared from a mixture of L-alpha-dipalmitoylphosphatidylcholine and the PEGilated phospholipid N-(carbonylmethoxypoly(ethylene glycol 2000))-1,2-distearoyl-sn-glycero-3-phosphoethanolamine were used as templates for the production of silica and alkylated silica approximately 100 nm capsules, "liposils", entrapping aqueous solutions of anionic dyes. Triggered release of this content was successfully affected by either low-frequency ultrasound or by microwave treatments. Cryo-TEM was used to follow the formation process of these particles, which are aggregated in a chain-like manner. A mechanism explaining this phenomenon is suggested. 相似文献
102.
Denekamp C Suwinska K Salman H Abraham Y Eichen Y Ben Ari J 《Chemistry (Weinheim an der Bergstrasse, Germany)》2007,13(2):657-665
Tripyrrolemethane- and bistripyrrolemethane-containing systems were recently reported to be efficient and selective hosts for anions. Nevertheless, the basic intrinsic properties of tripyrrolemethane as a ligand for anions have not yet been explored. Here we report the study of the anion-binding properties of the tripyrrolemethane group. We applied a combined experimental and theoretical approach to determine the affinity of the tripyrrolemethane system for different anions in the gas phase, in solution and in the crystalline state. In the crystal, the tripyrrolemethane group forms a number of different complexes with the bromide ion, some involving the participation of more than one ligand species. Despite the very similar basicity of fluoride and dihydrogen phosphate, the tripyrrolemethane ligand exhibits a clear preference for the fluoride anion in solution, which indicates an anion-binding system and not merely deprotonation. Although the affinity of the tripyrrolemethane ligand for other ions was negligible in solution, gas-phase studies show that complexation with larger halide ions is favoured over complexation with fluoride. 相似文献
103.
104.
Hui Dou Yuxuan Zheng Manyi Qu Peng Chen Chunlin He Michael Gozin Siping Pang 《Molecules (Basel, Switzerland)》2021,26(24)
The nitration of chitin monomer in a mixture of nitric acid and acetic anhydride was conducted and a highly nitrated (3R,4R,6R)-3-acetamido-6-((nitrooxy)methyl)tetrahydro-2H-pyran-2,4,5-triyl trinitrate (1) was obtained. Its structure was fully characterized using infrared spectroscopy, NMR spectroscopy, elemental analysis, and X-ray diffraction. Compound 1 possesses good density (ρ: 1.721 g·cm−3) and has comparable detonation performance (Vd: 7717 m·s−1; P: 25.6 GPa) to that of nitrocellulose (NC: Vd: 7456 m·s−1; P: 23 GPa; Isp = 239 s) and microcrystalline nitrocellulose (MCNC; Vd: 7683 m·s−1; P: 25 GPa; Isp = 250 s). However, Compound 1 has much lower impact sensitivity (IS: 15 J) than the regular nitrocellulose (NC; IS: 3.2 J) and MCNC (IS: 2.8 J). Compound 1 was calculated to exhibit a good specific impulse (Isp: 240 s), which is comparable with NC (Isp: 239 s) and MCNC (Isp: 250 s). By replacing the nitrocellulose with Compound 1 in typical propellants JA2, M30, and M9, the specific impulse was improved by up to 4 s. These promising properties indicate that Compound 1 has a significant potential as an energetic component in solid propellants. 相似文献
105.
Dr. Robert Langer Dr. Mark A. Iron Dr. Leonid Konstantinovski Dr. Yael Diskin‐Posner Dr. Gregory Leitus Yehoshoa Ben‐David Prof. Dr. David Milstein 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(23):7196-7209
The new, structurally characterized hydrido carbonyl tetrahydridoborate iron pincer complex [(iPr‐PNP)Fe(H)(CO)(η1‐BH4)] ( 1 ) catalyzes the base‐free hydrogenation of ketones to their corresponding alcohols employing only 4.1 atm hydrogen pressure. Turnover numbers up to 1980 at complete conversion of ketone were reached with this system. Treatment of 1 with aniline (as a BH3 scavenger) resulted in a mixture of trans‐[(iPr‐PNP)Fe(H)2(CO)] ( 4 a ) and cis‐[(iPr‐PNP)Fe(H)2(CO)] ( 4 b ). The dihydrido complexes 4 a and 4 b do not react with acetophenone or benzaldehyde, indicating that these complexes are not intermediates in the catalytic reduction of ketones. NMR studies indicate that the tetrahydridoborate ligand in 1 dissociates prior to ketone reduction. DFT calculations show that the mechanism of the iron‐catalyzed hydrogenation of ketones involves alcohol‐assisted aromatization of the dearomatized complex [(iPr‐PNP*)Fe(H)(CO)] ( 7 ) to initially give the Fe0 complex [(iPr‐PNP)Fe(CO)] ( 21 ) and subsequently [(iPr‐PNP)Fe(CO)(EtOH)] ( 38 ). Concerted coordination of acetophenone and dual hydrogen‐atom transfer from the PNP arm and the coordinated ethanol to, respectively, the carbonyl carbon and oxygen atoms, leads to the dearomatized complex [(iPr‐PNP*)Fe(CO)(EtO)(MeCH(OH)Ph)] ( 32 ). The catalyst is regenerated by release of 1‐phenylethanol, followed by dihydrogen coordination and proton transfer to the coordinated ethoxide ligand. 相似文献
106.
Michal Segal-Rosenheimer Yael Dubowski 《Journal of photochemistry and photobiology. A, Chemistry》2010,209(2-3):193-202
The present study focuses on the photodegradation of methyl-parathion thin films, an organophosphate insecticide, under different atmospheric conditions. The latter include nitrogenated, oxygenated and ozonated atmospheres, under low and high relative humidity conditions. Addition of oxygen to the atmospheric mixture did not seem to affect the reaction rates and quantum yields. Relative humidity affect was minor, with a small enhancement in reaction rate under 254 nm radiation. The addition of ozone (to either dry or humid atmosphere), at all concentrations tested, largely enhanced degradation rates. In the absence of ozone, the obtained quantum yields for photolysis of methyl-parathion thin films under 254 and 313 nm were 0.024 ± 0.007 and 0.012 ± 0.005, respectively. These values are higher than the values previously reported for solutions of methanol and water. Although the presence of molecular oxygen and water vapors did not seem to affect much the reaction rates, it did have a certain effect on the resulted products. More polar products were obtained under oxygenated and ozonated atmospheres, as well as dimers under ozone conditions. The reaction on thin films has yielded more toxic products than usually found in solutions, adding alkylphosphate esters in addition to the oxons formed normally. 相似文献
107.
Kalid O Mense M Fischman S Shitrit A Bihler H Ben-Zeev E Schutz N Pedemonte N Thomas PJ Bridges RJ Wetmore DR Marantz Y Senderowitz H 《Journal of computer-aided molecular design》2010,24(12):971-991
Folding correctors of F508del-CFTR were discovered by in silico structure-based screening utilizing homology models of CFTR. The intracellular segment of CFTR was modeled and three cavities were identified at inter-domain interfaces: (1) Interface between the two Nucleotide Binding Domains (NBDs); (2) Interface between NBD1 and Intracellular Loop (ICL) 4, in the region of the F508 deletion; (3) multi-domain interface between NBD1:2:ICL1:2:4. We hypothesized that compounds binding at these interfaces may improve the stability of the protein, potentially affecting the folding yield or surface stability. In silico structure-based screening was performed at the putative binding-sites and a total of 496 candidate compounds from all three sites were tested in functional assays. A total of 15 compounds, representing diverse chemotypes, were identified as F508del folding correctors. This corresponds to a 3% hit rate, ~tenfold higher than hit rates obtained in corresponding high-throughput screening campaigns. The same binding sites also yielded potentiators and, most notably, compounds with a dual corrector-potentiator activity (dual-acting). Compounds harboring both activity types may prove to be better leads for the development of CF therapeutics than either pure correctors or pure potentiators. To the best of our knowledge this is the first report of structure-based discovery of CFTR modulators. 相似文献
108.
Uncovering the physics of electroweak symmetry breaking (EWSB) is the raison-d’etre of the LHC. Flavor questions, it would seem, are of minor relevance for this quest, apart from their role in constraining the possible structure of EWSB physics. In this short review article, we outline, using flavor-dependent slepton physics as an example, how flavor can affect both searches for supersymmetry, and future measurements aimed at understanding the nature of any new discoveries. If the production cross-sections for supersymmetry are relatively low, as indicated by the fact that it has not revealed itself yet in standard searches, the usual assumptions about the superpartner spectra need rethinking. Furthermore, one must consider more intricate searches, such as lepton-based searches, which could be susceptible to flavor effects. We start by reviewing the flavor structure of existing frameworks for mediating supersymmetry breaking, emphasizing flavor-dependent models proposed recently. We use the kinematic endpoints of invariant mass distributions to demonstrate how flavor dependence can impact both searches for supersymmetry and the Inverse Problem. We also discuss methods for measuring small-mass splittings and mixings at the LHC, both in models with a neutralino LSP and in models with a charged slepton (N)LSP. 相似文献
109.
110.
Multivalency as a Key Factor for High Activity of Selective Supported Organocatalysts for the Baylis–Hillman Reaction
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Dr. Kerem Goren Jeny Karabline‐Kuks Yael Shiloni Einav Barak‐Kulbak Prof. Scott J. Miller Prof. Moshe Portnoy 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(3):1191-1197
The polystyrene‐supported N‐alkylimidazole‐based dendritic catalysts for the Baylis–Hillman reaction exhibit one of the strongest beneficial effects of multivalent architecture ever reported for an organocatalyst. The yields in the model reaction of methyl vinyl ketone with p‐nitrobenzaldehyde are more than tripled when a non‐dendritic catalyst is replaced by a second‐ or third‐generation analogue. Moreover, the reaction of the less active substrates will not occur with the non‐dendritic catalyst and will proceed to a significant extent only with the analogous catalysts of higher generations. A substantial additional enhancement of the reaction yield could be achieved by increasing the content of water in the reaction solvent. The plausible cause of the dendritic effect is the assistance of the second, nearby imidazole moiety in the presumably rate‐determining proton transfer in the intermediate adduct, after the first imidazole unit induced the formation of the new carbon–carbon bond. 相似文献