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1.
Two novel migrated pimarane-type diterpenes named neoorthosiphols A (1) and B (2) were isolated from the water decoction of the leaves of Orthosiphon aristatus (Lamiaceae), which has been prescribed in Javanese traditional medicine (jamu) for the treatment of hypertension, etc. The absolute chemical structures have been elucidated on the basis of physicochemical properties. It has been found that two migrated pimarane-type diterpenes (1, 2), four isopimarane-type diterpenes (3, 4, 5, 6), three benzochromenes (7, 8, 9) and two flavones (12, 13) exhibit a suppressive effect on contractile responses in rat thoracic aorta, among thirteen chemical constituents (1-13) isolated from the leaves.  相似文献   

2.
短链氯化石蜡(SCCPs)组成复杂,具有远距离环境迁移的能力、环境持久性、生物蓄积性和一定的生物毒性,已被提议列入《关于持久性有机污染物的斯德哥尔摩公约》的附件A、B或C.我国是氯化石蜡生产和使用最多的国家,且尚未限制SCCPs的生产.几个研究已揭示了SCCPs在我国的环境中存量较高,因此应对其所引起的生态环境风险和人体健康风险给予关注.本文重点评述了SCCPs的分析方法,包括样品前处理、色谱分离、质谱检测、定量分析及国际实验室分析比对情况,同时也对SCCPs的环境行为、生物累积和毒性效应进行了综述.  相似文献   

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5.
Muscle strains are among the most prevalent causes for athletes' absence from sport activities. Low-level laser therapy (LLLT) has recently emerged as a potential contender to nonsteroidal anti-inflammatory drugs in muscle strain treatment. In this work we investigated effects of LLLT and diclofenac on functional outcomes in the acute stage after muscle strain injury in rats. Muscle strain was induced by overloading the tibialis anterior muscle of rats during anesthesia. The injured groups received either no treatment, or a single treatment with diclofenac 30 min prior to injury, or LLLT (810 nm, 100 mW) with doses of 1, 3, 6 or 9 J, at 1 h after injury. Functional outcome measures included a walking index and assessment of electrically induced muscle performance. All treatments (except 9 J LLLT) significantly improved the walking index 12 h postinjury compared with the untreated group. The 3 J group also showed a significantly better walking index than the drug group. All treatments significantly improved muscle performance at 6 and 12 h. LLLT dose of 3 J was as effective as the pharmacological agent in improving functional outcomes in the early phase after a muscle strain injury in rats.  相似文献   

6.
Hexavalent chromium, a major contaminant in most wastewater sites, is a potential health threat inducing cancer to humans while trivalent chromium is an essential element for the metabolism of sugar. The radiation-induced reduction of Cr(VI) metal ion to Cr(III) by the perhydroxyl radical (HO2 ?) and carboxyl radical anion (CO2 ??) produced by continuous radiolysis of water was investigated by steady state radiolysis of O2, Ar and N2O-saturated pH 3 solutions in the presence of formate. In all cases the removed Cr(VI) was a linear function of the absorbed dose. The added formate was favorable for removing Cr(VI). Its presence protects the solution from reverse radiolytic oxidation of Cr(III) to Cr(VI). The measured and calculated yield of removal of Cr(VI) do agree quite well at low formate concentration but at high formate concentration the measured yield was higher than the expected. When all formate is exhausted no recovery of Cr(VI) from Cr(III) was observed in case of O2- and Ar-saturated solutions whilst in the case of N2O-saturated solutions Cr(VI) recovers. The results obtained in this study highlight the potential of this technology for industrial wastewater treatment.  相似文献   

7.
The gas-phase radical-radical reaction dynamics of ground-state atomic oxygen [O((3)P)] with iso-propyl radicals, (CH(3))(2)CH, were investigated by applying a combination of high-resolution laser-induced fluorescence spectroscopy in a crossed-beam configuration and ab initio calculations. The nascent distributions of OH (X(2)Π: υ' = 0) from the major reaction channel O((3)P) + (CH(3))(2)CH → C(3)H(6) (propene) + OH showed substantial internal excitations with a bimodal feature of low- and high-N' components with neither spin-orbit nor Λ-doublet propensities. Unlike previous kinetic results, proposed to proceed only through the direct H-atom abstraction process, on the basis of the population analysis and comparison with the statistical theory, the title reaction can be described in terms of two competing mechanisms at the molecular level: direct abstraction process and indirect short-lived addition-complex-forming process with a ratio of 1.25?:?1.  相似文献   

8.

In this paper, the effects of pure water, SiO2/water nanofluid, and a phase-change material (PCM) as coolants on the performance of a photovoltaic thermal (PVT) system are numerically investigated. The simulations are performed on two modules of PVT with PCM (PVT/PCM module) and without (PVT module). Parameters including PV surface temperature, thermal, and electrical efficiencies of the systems are studied and compared with each other. Moreover, the results of nanofluid as a working fluid is compared with those obtained using pure water. The results show that in the water-based PVT/PCM, the average PV cell temperature is decreased by 16 °C compared to that of the PVT system. This results in an increase of 8% in the electrical efficiency and 25% in the thermal efficiency. In addition, using nanofluid (SiO2 with 1 and 3 mass% mass fraction) as a coolant in the PVT/PCM system increases the thermal efficiency by 3.51% and 10.40%, for 1 and 3 mass%, respectively, compared to that of the PVT/PCM with pure water as a coolant. This study shows that increasing the melting temperature of the phase-change material leads to an increase in the thermal efficiency of the PVT/PCM system.

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9.
It has been suggested that low-level laser therapy (LLLT) can modulate inflammatory processes. The aim of this experiment was to investigate what effects red laser irradiation with two different wavelengths (660 nm and 684 nm) on carrageenan-induced rat paw edema and histology. Thirty two male Wistar rats were randomly divided into four groups. One group received a sterile saline injection, while inflammation was induced by a sub-plantar injection of carrageenan (1 mg/paw) in the three other groups. After 1 h, LLLT was administered to the paw in two of the carrageenan-injected groups. Continuous wave 660 nm and 684 nm red lasers respectively with mean optical outputs of 30 mW and doses of 7.5 J/cm(2) were used. The 660 nm and 684 nm laser groups developed significantly (p<0.01) less edema (0.58 ml [SE+/-0.17] ml and 0.76 ml [SE+/-0.10] respectively) than the control group (1.67 ml [SE+/-0.19]) at 4h after injections. Similarly, both laser groups showed a significantly lower number of inflammatory cells in the muscular and conjunctive sub-plantar tissues than the control group. We conclude that both 660 nm and 684 nm red wavelengths of LLLT are effective in reducing edema formation and inflammatory cell migration when a dose of 7.5 J/cm(2) is used.  相似文献   

10.
Molybdenum-95 NMR chemical shifts are reported for a series of Mo(O) compounds of the type Mo(CO)4(pip)2−nLn(n = 1,2; L = substituted pyridine ligands). The σ(95Mo) values correlate well with the pKa values for the substituted pyridines; for the n = 1 series, σ (95Mo) ranges from − 1053 ppm (pKa = 1.86 for 4-CN) to − 1120 ppm (pKa = 9.61 for 4-NMe2). The effects of solvent polarity and some in situ reactivity studies are described and the nature of the MoL bond compared to that with piperidine and some other ligands is discussed.  相似文献   

11.
Conjugated molecules with a saturated alkyl linker between a thiol docking group and the pi-conjugated core have been shown to form self-assembled monolayers (SAMs) with a high degree of long-range order and uniformity. Additionally, pronounced odd-even effects have been observed in a number of properties characterizing these SAMs. We focus on omega-(biphenyl-4-yl)alkanethiols with n = 0-6 -(CH2)n- units deposited on Au(111) and investigate the microscopic origin of these odd-even effects in terms of the local sulfur-gold bonding geometry by employing first-principles calculations. An additional structural parameter, the torsion angle between the two phenyl rings in the biphenyl moiety, is identified and its relation to the experimentally observed odd-even effects is discussed. More importantly, we address relevant quantities for the application of these SAMs in molecular electronic devices, in particular, the modification of the work function of the underlying metal substrate and the energetic alignment of the molecular orbitals in the SAM with the Fermi level. While no clear trend emerges for the former, we find pronounced odd-even effects for the latter. Furthermore, the insertion of a single methylene unit between the biphenyl core and the thiol appears to largely decouple the valence electronic systems of the pi-conjugated segment and the gold substrate. Our results thus provide a solid theoretical basis for the interface energetics in this important class of systems.  相似文献   

12.
Acetylene‐linked reactive intermediates of (nitrenoethynyl)‐X‐methylenes, (nitrenoethynyl)‐X‐silylenes, and (nitrenoethynyl)‐X‐germylenes are almost experimentally unreachable (X–M–C≡C–N; X=H ( 1 ), CN ( 2 ), OH ( 3 ), NH2 ( 4 ), NO2 ( 5 ), and CHO ( 6 ); M=C, Si, and Ge). The effects of the electron‐donating and electron withdrawing groups were compared and contrasted at seven levels of theory. All singlet species as ground states with one local open‐shell singlet carbene subunit (π1π1) and another local open‐shell singlet nitrene subunit (π1π1) were found to be more stable than their corresponding triplets including one local open‐shell singlet carbene (δ1π1) (or one local closed‐shell singlet carbene [δ2π0]) and another local triplet nitrene subunit (π1π1) with 45.94–77.996 kcal/mol singlet–triplet energy gap (ΔEs‐t). Their relative silylenes and germylenes made reduction of ΔEs‐t, so the triplet ground states were found for species 3 Si , 4 Si , 5 Si , 2 Ge , 3 Ge , 4 Ge , and 5 Ge . All the singlet silylenes/germylenes formed by one local closed‐shell singlet silylenes/germylenes (δ2π0) and one local closed‐shell singlet nitrene subunit (π2π0). Also, one local closed‐shell singlet silylene/germylene subunit (δ2π0) and one local triplet nitrene subunit (π1π1) were observed for triplet silylenes/germylenes. The singlet and triplet species 3 Si , 4 Si , 3 Ge , and 4 Ge , due to their electrophilic (Si4/Ge4) and nucleophilic (X5) centers, could be identified as intermediates in chemical reactions.  相似文献   

13.
The previously derived trajectory-based nonadiabatic molecular dynamics scheme [E. Tapavicza, I. Tavernelli, U. Rothlisberger, Phys. Rev. Lett. 98 (2007) 023001] is extended to include the coupling of the quantum system with a classically described environment. The dynamics is performed using LR-TDDFT energies and forces computed on-the-fly together with the nonadiabatic coupling vectors needed for the propagation of the nuclear coefficients according to Tully’s fewest-switches surface hopping algorithm. The resulting LR-TDDFT-QM/MM approach is applied to the study of the ultrafast relaxation of the photoexcited singlet metal-to-ligand-charge-transfer state (1MLCT) of [Ru(bpy)3]2+ (bpy = 2,2′-bipyridine) in water. The observed intersystem crossing dynamics with the triplet MLCT is in good agreement with available experimental results.  相似文献   

14.
A calometric study of the reactions of various phosphorous ligands (and t-BuNC) with di-1,5-cycloocatadienenickel shows that both the extent of reaction and mean Ni-P bond strengths tend to decrease with increasing ligand size. The steric strain energies in various NiL4 complexes and ΔG for their formation from nickel metal are estimated.  相似文献   

15.
About 30% of the proteins in mammalian systems are membrane bound or integrated (e.g., GPCRs). It is inherently difficult to investigate receptor-ligand interactions on a molecular level in their natural membrane environment. Here, we present a new method based on saturation transfer difference (STD) NMR to characterize at an atomic level binding interactions of cell surface proteins in living cells. Implemented as a double difference technique, STD NMR allows the direct observation of binding events and the definition of the binding epitopes of ligands. The binding of the pentapeptide cyclo(RGDfV) to the surface glycoprotein integrin alpha(IIb)beta3 of intact human blood platelets can be detected by saturation transfer double difference (STDD) NMR in less than an hour. A 5-fold higher STD response reflects a significantly higher affinity of integrin alpha(IIb)beta3 in native platelets than in liposomes, which demonstrates the importance of studying membrane proteins in their natural environment. Also, the binding mode of cyclo(RGDfV) in the arginine glycine region is slightly different when interacting with native integrin in platelets compared to integrin reintegrated into liposomes.  相似文献   

16.
Two diastereomeric derivatives of norbornene, dimethyl (1R,2R,3S,4S)-bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate and dimethyl (1R,2S,3S,4S)-bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate, were synthesized and polymerized using ring-opening metathesis polymerization (ROMP). For comparative purposes, diastereomeric derivatives of Dewar benzene, dimethyl (1R,2S,3R,4S)-bicyclo[2.2.0]hex-5-ene-2,3-dicarboxylate and dimethyl (1R,2S,3S,4S)-bicyclo[2.2.0]hex-5-ene-2,3-dicarboxylate, were also synthesized and polymerized using ROMP. The polymerization reactions proceeded in a controlled manner as evidenced in part by linear relationships between the monomer-to-catalyst feed ratios and the molecular weights of the polymer products. Chain extension experiments were also conducted which facilitated the formation of block copolymers. Although the poly(norbornene) derivatives exhibited glass transition temperatures that were dependent on their monomer stereochemistry (cis: 115°C vs. trans: 125°C), more pronounced differences were observed upon analysis of the polymers derived from Dewar benzene (cis: 70°C vs. trans: 95°C). Likewise, microphase separation was observed in block copolymers that were prepared using the diastereomeric monomers derived from Dewar benzene but not in block copolymers of the norbornene-based diastereomers. The differential thermal properties were attributed to the relative monomer sizes as reducing the distances between the polymer backbones and the pendant stereocenters appeared to enhance the thermal effects.  相似文献   

17.
The interactions of dihydronicotinamide adenine dinucleotide (NADH) with Al(III) in near neutral aqueous solutions were studied by means of multinuclear (31P, 27Al, 1H and 13C)-NMR and fluorescence spectra techniques. The results suggested that Al(III) interacts with NADH by occupying the binding sites of pyrophosphate oxygen atoms and locks the adenine moiety of coenzyme in an anti folded conformation Meanwhile, the weak attractive interactions ('association') may occur between Al(III) and the hydroxyl groups of ribose rings through the intramolecular hydrogen bonding. Furthermore, at biologically relevant pH and concentrations of Al(III) and NADH (pH 6.5, C(Al)=10(-6)-10(-5) M), Al(III) could increase the amount of folded forms of NADH, which will result in reducing the coenzyme NADH activity in hollow-dehydrogenases reaction systems. However, in the presence of possible competing organic acids such as citrate, oxalate and tartate, could detoxify these Al(III) toxic effect.  相似文献   

18.
In order to investigate the physical and chemical effects of neutron capture reaction, a neutron in-beam Mössbauer spectroscopic study on two isomorphs of iron disulfide: pyrite and marcasite, were carried out with a parallel plate avalanche counter at room temperature. In both compounds only two major products accounted for the obtained spectrum: one with Mössbauer parameters close to the parent compound and the other one considered to be a new product. The yield of the parent-like species was different in the two isomorphs.  相似文献   

19.
the IR wavenumbers and half-band width's of the carbonyl stretching vibrations of several substituted 7r-(tricarbonylchromium)benzenes in isooctane solution are reported. only small perturbations of C3,.symmetry are observed. the shape of the out-of-phase band is influenced by electronic effects, conformer distribution and solute-solvent interaction. the asymmetry of the E-band in (1'-t-butyl-2',2'-dimetliylpropyl)-7r-(tricarbonylchromium)benzene is ascribe to a direct steric effect. ,me correlation between the CO force constants and electronic substituent parameters is satisfactory for the monosubstituted complexes. the substituent effects are approximately additive for the di- and tri-alkylsubstituted benzene complexes.  相似文献   

20.
Ethanol in an acidic solution-Pt(110) interface was studied by SFG spectroscopy (between 1820 and 2325 cm(-1)) to explore primarily the effects of the alcohol concentration. Stretching bands of H-Pt (ca. 1970 or 2050 cm(-1)) and CO (ca. 1980 and 2040 cm(-1)) species, produced by the ethanol oxidation, were detected during the adsorption and oxidation of 0-1 mol L(-1) ethanol in a 0.1 mol L(-1) HClO(4) solution on the electrode surface. Hydrogen and CO coadsorb stably on Pt(110) between 0.05 and 0.15 V in ethanol-containing solutions. In this potential range, the blue shift of the hydrogen resonance (ca. 80 cm(-1)) reveals a weakening of the hydrogen bonding between adsorbed hydrogen and water molecules in the double layer. After the hydrogen desorption (0.15 V), the formation of compact CO islands, depending on the ethanol concentration, lifts the Pt(110) surface reconstruction. In ethanol-free solution, the surface remains reconstructed. The lower-frequency CO band is assigned to the CO species adsorbed on (1 x 2) reconstructed Pt(110) domains, having smaller local coverages, while the higher-frequency CO band is attributed to the close-packed CO species adsorbed on (1 x 1) patches. The reaction pathway forming CO(2) is less favored with increasing ethanol concentration.  相似文献   

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