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91.
92.
The absorption bands arising from overtones of the CH stretching vibration of liquid benzene were measured up to the v = 0–9 transition. The transition energies at the band maxima are expressed by a cubic equation. Their bandwidths and oscillator strengths are discussed.  相似文献   
93.
The heat capacity of thallium dihydrogen phosphate was measured from 12 to 300 K. A lambda anomaly with a small first order discontinuity was found at 229.76 K with the integrated enthalpy and entropy changes equal to 370 J mol-1 and 1.8 J K-1 mol-1, respectively. The entropy discontinuity at the first order transition is 0.25 J K-1 mol-1. The Landau theory of phase transitions of the second kind reproduces closely the temperature dependence of the anomalous heat capacity. This, together with the small discontinuity in the entropy, implies that the phase transition is close to a classical critical point of higher order. The relative dielectric permittivity ?r(b) along the b-axis at 1 kHz is anomalously large and strongly temperature dependent, while the ?r(a1) and ?r(c) are not. A broad absorption centered at 1700 cm-1 was observed in the infrared absorption spectrum, indicating presence of hydrogen bonding of the length ~ 0.25 nm. Occurrence of a phase transition at 127 ± 2 K was suggested by differential thermal analysis of thallium dideuterium phosphate.  相似文献   
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Surface corrugation has been photo-induced in a single-step process in hybrid sol-gel thin films. A model based on elastic deformation under photo-induced stress is developed to explain relief formation in this material. Computation is carried out with finite-element software. Theoretical and experimental values of relief amplitude variation with film thickness and grating period agree for small deformations. Mass transfer from illuminated to non-illuminated areas has to be associated with the elastic model to account for surface corrugation in the case of large photo-induced deformation. A comparison with a fluid mechanics model is presented. PACS 81.65.C; 81.20.F; 81.40.L  相似文献   
97.
Selective penta-addition of a methylcopper reagent followed by addition of a phenylcopper reagent to a suitably modified synthetic intermediate results in creation of 40pi-electron systems-hoop- and bowl-shaped cyclic benzenoid compounds, [10]cyclophenacene, and dibenzo-fused corannulene derivatives. The 40pi-electron cyclophenacene derivatives have been found to be chemically stable, yellow-colored, luminescent (560 nm), and EPR-silent. X-ray crystallographic analysis provided precision structural data sets. The dibenzo-fused corannulene derivatives exhibit blue-green (460 nm) to red (649 nm) fluorescence.  相似文献   
98.
Several studies have shown that UV irradiation may be effective for preventing vascular restenosis or vasopasm. However, the long-term effects of UV light on the physiological properties of vessels such as arterial tension have not been elucidated. We therefore studied the long-term effects of UV using rat carotid arteries treated with UV-B light (wavelength = 313 nm, total energy = 14 mJ/mm2). The animals were sacrificed at 1, 7 and 14 days after UV light exposure, and the carotid arteries were studied by light microscopy and the contractile responses of isolated arterial rings were recorded under isometric tension. UV treatment had induced a substantial loss of smooth muscle cells (SMC) along the entire circumference of the media on days 7 and 14, whereas loss of SMC on day 1 was negligible. Contractile responses of arteries that had been exposed to UV light were significantly reduced on days, 1, 7 and 14. The susceptibility of UV-treated arteries to phenylephrine and prostaglandin F2 alpha was significantly decreased on days 1 and 7, but decreased susceptibility was not seen on day 14. Acetylcholine-induced relaxations were not altered by UV treatment. These results suggest that the long-term effect of UV light is an attenuation of smooth muscle contractility without impairment of endothelial function.  相似文献   
99.
N-tert-Butylbenzenesulfenamide (1)-catalyzed oxidation of various primary and secondary alcohols to the corresponding aldehydes and ketones was efficiently carried out by using N-chlorosuccinimide (NCS) in the coexistence of potassium carbonate and molecular sieves 4 Å at easy-to-control temperatures ranging from 0°C to room temperature. The present catalytic oxidation was performed without giving any damage to the functional groups in alcohols, and was particularly effective in the oxidation of alcohols that formed labile aldehydes because of its mild reaction conditions. Further, selective oxidation of primary hydroxy groups took place in 1-catalyzed oxidation of several diols. Mechanistic investigation suggested that the chlorination of the sulfenamide 1 by NCS led to the formation of a key species, N-tert-butylbenzenesulfinimidoyl chloride (2), which in turn oxidized alcohols in the presence of potassium carbonate to afford carbonyl products by accompanying regeneration of the catalyst 1.  相似文献   
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