The Khok Kruat Formation is the upper part of the Khorat Group,which consists of upper Lower Cretaceous non-marine sedimentary rocks in northeastern *** dinosaur footprints have been known from the upper Lower Cretace...
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The Khok Kruat Formation is the upper part of the Khorat Group,which consists of upper Lower Cretaceous non-marine sedimentary rocks in northeastern *** dinosaur footprints have been known from the upper Lower Cretaceous(Aptian-Albian)Khok Kruat Formation at the Huai Dam Chum(Tha Uthen)site,northeastern *** 600 tracks occur in thin mudstone layer of the northern part of the outcrop at the Huai Dam Chum track *** types of footprints,small-sized theropod and crocodylomorph are imprinted with mud cracks and ripple marks on the thin mud *** of footprints are referred to ***,and are imprinted by small-sized theropoda,probably *** tracks are mainly separated into two groups,Group A and Group *** ichnological viewpoints,the small-sized theropod track assemblage indicates the herd behaviour and its idiosyncratic group *** particular,the histogram of size-frequency measurements of Group A shows the anomalous bimodal *** consider that there are two hypotheses;the first one is due to the male-female difference,and the second is a result of the different growing stage.
Because imines could be used as convenient starting materials in various fields, the development of an easy synthetic method of imine was strongly desired. In response to this demand, we thought that it would be an ef...
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Because imines could be used as convenient starting materials in various fields, the development of an easy synthetic method of imine was strongly desired. In response to this demand, we thought that it would be an effective synthesis method if an aldehyde and an amine could be reacted to give an imine in good yield under solvent- and catalyst-free conditions. In fact, we tried the reaction of benzaldehyde with various amines under solvent- and catalyst-free conditions followed by removal of water that was produced in the reaction system by a vacuum pump, and desired imines could be obtained in good yields. Observation of this reaction using a nuclear magnetic resonance spectrometer revealed that the reaction rate was extremely fast at the initial stage but slowed over time. However, the reaction of benzaldehyde with aniline differed greatly, and the reaction rate dramatically improved in 47 - 48 minutes after the start of the reaction. At this time, we found that the reaction system underwent a phase transition from the liquid phase to the solid phase.
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