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901.
“Aromatic nucleophilic substitution-rearrangement (SNAr-rearrangement)” mechanism provided a powerful tool to design fluorescent probes for the discrimination between biothiols. 相似文献
902.
Subluminal to superluminal light propagation in a V-type three-level atomic system interacting with squeezed vacuum 下载免费PDF全文
We study the light propagation properties in a V-type three-level atomic system interacting with two independent broadband squeezed baths. Using the graphic method, the dependences of the absorption and the dispersion of the system on the coupling field strength, the incoherent pumping field strength and the intensity of the squeezed vacuum are analysed. The result shows that the probe pulse propagation can be changed from subluminal to superluminal speed. 相似文献
903.
SPATIAL AND SEASONAL DISTRIBUTIONS OF ATMOSPHERIC CARBONACEOUS AEROSOLS IN PEARL RIVER DELTA REGION, CHINA 总被引:11,自引:0,他引:11
Concentrations and spatial distributions of organic carbon (OC) and elemental carbon (EC) in atmospheric particles were measured at 8 sites in four cities (Hong Kong, Guangzhou, Shenzhen and Zhuhai) of Pearl River Delta Region (PRDR), China during 2001 winter period and 2002 summer period. PM2.5 (particie diameter smaller than 2.5 um) and PM10 (particie diameter smaller than 10 um) samples were collected on pre-fired quartz filters with mini-volume samplers and analyzed using thermal optical reflectance (TOR) method. The average PM2.5and PM10 Ievel were 60.1 and 93.1 μg·m-3, respectively, with PM2.5 constituting 65.3% of the PM10 mass. The average OC and EC concentrations in PM2.5 were 12.0 and 5.1 μg·m-3, respectively, while those in PM10 were 16.0 and 6.5 μg·m-3, respectively. The carbo-naceous aerosol accounted for 37.2% of the PM2.5 and 32.8% of the PM10. The highest concentrations of OC and EC were observed at Guangzhou city in both vvinter and summer seasons. The average OC/EC ratios were 2. 相似文献
904.
SynthesisandCrystalStructureof(Et_4N)_2[Pd_2(mp)_2(mpH)_2]ShiJi-Cheng;HuangXiao-Ying;WenTing-Bin;DengYu-Heng;ChengChang-Neng;Li?.. 相似文献
905.
Two solid phase transitions of [Cd(H2O)6](BF4)2 occurring on heating at TC2=183.3 K and TC1=325.3 K, with 2 K and 5 K hysteresis, respectively, were detected by differential scanning calorimetry (DSC). High value of entropy changes indicated large orientational disorder of the high temperature and intermediate phase. Nuclear magnetic resonance (1H NMR and 19F NMR) relaxation measurements revealed that the phase transitions at TC1 and TC2 were associated with a drastic and small change, respectively, of the both spin-lattice relaxation times: T1(1H) and T1(19F). These relaxation processes were connected with the “tumbling” motions of the [Cd(H2O)6]2+, reorientational motions of the H2O ligands, and with the iso- and anisotropic reorientation of the BF4− anions. The cross-relaxation effect was observed in phase III. The line width and the second moment of the 1H and 19F NMR line measurements revealed that the H2O reorientate in all three phases of the title compound. On heating the onset of the reorientation of 3 H2O in the [Cd(H2O)6]+2, around the three-fold symmetry axis of these octahedron, causes the isotropic reorientation of the whole cation. The BF4− reorientate isotropically in the phases I and II, but in the phase III they perform slow reorientation only about three- or two-fold axes. A small distortion in the structure of BF4− as well as of [Cd(H2O)6]2+ is postulated. The temperature dependence of the bandwidth of the O-H stretching mode measured by Fourier transform middle infrared spectroscopy (FT-MIR) indicated that the activation energy for the reorientation of the H2O did not change much at the TC2 phase transition. 相似文献
906.
Eun Won Seo Ji Hee Han Cheol Ho Heo Prof. Dr. Jae Ho Shin Prof. Dr. Hwan Myung Kim Prof. Dr. Bong Rae Cho 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(39):12388-12394
Two‐photon microscopy (TPM) has become an indispensable tool in the study of biology and medicine due to the capability of this method for molecular imaging deep inside intact tissues. For the maximum utilization of TPM, a variety of two‐photon (TP) probes for specific applications are needed. In this article, we report a small‐molecule TP probe (ANO1) for nitric oxide (NO) that shows a rapid and specific NO response, a 68‐fold fluorescence enhancement in response to NO, and a maximum TP‐action cross‐section of 170 GM (GM: 10?50 cm4 photon?1) upon reaction with excess NO. This probe can be easily loaded into cells and tissues and can real‐time monitor NO in living tissues at 100–180 μm depth for longer than 1200 s through the use of TPM, with minimum interference from other biologically relevant species. 相似文献
907.
Joong-Ho Kwon Myung-Woo Byun Kang-Soo Kim Il-Jun Kang 《Radiation Physics and Chemistry》2000,57(3-6):309-313
The hygienic, physicochemical, and organoleptic qualities of white ginseng were monitored during 6 months under accelerated conditions (40°C, 90% r.h.) by observing its microbial populations, disinfestation, and some quality attributes following either gamma irradiation at 2.5–10 kGy or commercial phosphine (PH3) fumigation. In a comparative study, both treatments were found to be effective for disinfecting the stored samples. Phosphine showed no appreciable decontaminating effects on microorganisms contaminated including coliforms, while 5 kGy irradiation was sufficient to control all microorganisms related to the quality of the packed samples. Irradiation at 5 kGy caused negligible changes in physicochemical attributes of the samples, such as ginsenosides, amino acids, fatty acids, and organoleptic properties, whereas phosphine fumigation was found detrimental to sensory flavor (P<0.01). Quality deterioration occurred in the commercially-packed samples was in the following order: the control, 10 kGy-, phosphine-, and 2.5–5 kGy-treated samples. Accordingly, irradiation at <5 kGy was found to be an effective alternative to phosphine fumigation for white ginseng. 相似文献
908.
Dong Cao Huogao Huang Ming Hu Lin Cui Fanglan Geng Ziyu Rao Hongyun Niu Yaqi Cai Yuehui Kang 《Analytica chimica acta》2015
Natural organic matter (NOM) is a complex and non-uniform mixture of organic compounds which plays an important role in environmental processes. Due to the complexity, it is challenging to obtain fully detailed structural information about NOM. Although Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS) has been demonstrated to be a powerful tool for providing molecular information about NOM, multiple ionization methods are needed for comprehensive characterization of NOM at the molecular level considering the ionizing selectivity of different ionization methods. This paper reports the first use of matrix assisted laser desorption/ionization (MALDI) method coupled with FT-ICR-MS for molecular characterization of NOM within a mass range of 200–800 Da. The mass spectral data obtained by MALDI were systematically compared with data generated by electrospray ionization (ESI). It showed that complementary molecular information about NOM which could not be detected by ESI, were provided by MALDI. More unsaturated and aromatic constituents of NOM with lower O/C ratio (O/C ratio < 0.5) were preferentially ionized in MALDI negative mode, whereas more polar constituents of NOM with higher O/C ratio were preferentially ionized in ESI negative mode. Molecular anions of NOM appearing at even m/z in MALDI negative ion mode were detected. The results show that NOM molecules with aromatic structures, moderate O/C ratio (0.7 > O/C ratio > 0.25) and lower H/C ratio were liable to form molecular anions at even m/z, whereas those with higher H/C ratio are more likely to form deprotonated ions at odd m/z. It is speculated that almost half of the NOM molecules identified by MALDI may be aromatic or condensed aromatic compounds with special groups which are liable to absorb electron from other molecules to generate free radical anions during MALDI ionization. 相似文献
909.
Reaction of the semi-rigid ligand 2,4-bis(1-imidazolylmethyl)-mesitylene (m-bimms) with CdCl2 afforded a boat-like molecular rectangle [Cd(m-bimms)Cl2]2 · 1/2H2O (1), with the orientation of the two imidazolyl arms of the ligand in syn-conformation and bridging chloride ions bisecting the macrocycle. Weak Cl· · ·H—C interations further extended the dimers into 1D infinite chains with nanoscopic channels. An analogous reaction with Cd(NO3)2 gave a 1D coordination polymer [Cd(m-bimms)2(NO3)2]n · 2nH2O (2) composed of nanoscopic metallamacrocycles, where the two imidazolyl arms adopt an anti-conformation. Different anions result in different ligand conformations and thus determine the varied molecular architectures. 相似文献
910.