Summary The new alkyl 2-(2-oxo-benzazoline-3-yl)-3-hydroxy dithiocrotonates and dithiocinnamates4 and the corresponding ketene dithioacetals2 and5 are obtained by dithiocarboxylation of the 3-acceptormethyl substituted benzazoline-2-ones1 or3. Alkylation at room temperature gives compounds4 whereas at higher alkylation temperature2 or5 are formed. The results of X-ray analyses performed for methyl 3-hydroxy-p-chloro-dithiocinnamate4d and of N-[1-(4-chloro-benzoyl)-2,2-bis(methylthio)-vinyl]-benzothiazoline-2-one5e are discussed. 相似文献
MNDO-PM3 and AM1 quantum chemical calculations of the molecular structure of N,N′-diphenyl-guanidine (DPG) prove that the
molecule preferably exists as an asymmetric tautomer with a basic center C = N−. IR and UV spectral data, dipole moments,
and average molecular weights of DPG solutions in nonpolar and low-polar solvents confirm the results of calculations, indicating
formation of hydrogen-bonded cyclic self-associates of DPG in solution.
Translated fromZhumal Strukturnoi Khimii, Vol. 39, No. 4, pp. 618–625, July–August, 1998. 相似文献
The linear sweep polarographic wave of the uranium-Xylidyl Blue I complex in ethylenediamine-1,10-phenanthroline-hydrochloric acid medium has been studied. The complex, corresponding to UO(2)(XBI)(2-)(2) with log beta' = 9.09 (by polarography), 8.81 (by spectrophotometry), is strongly adsorbed on the surface of the mercury electrode. The polarographic wave is attributed to the reduction of Xylidyl Blue I in the complex. The method is very sensitive with a detection limit of 3 x 10(-8)M. The wave height is proportional to the concentration of uranium over the range 8 x 10(-8)-7 x 10(-6)M. Solvent extraction is used to separate possible interferences. The recommended procedure has been applied to the determination of trace amounts of uranium in ores. 相似文献
Conclusions Reaction of SO2 or SO3/[B2O3] with terminal fluoroolefins or fluoroalkylbenzenes gives the corresponding fluoroalken-2-yl fluorosulfates and fluorobenzyl fluorosulfates.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2791–2795, December, 1982. 相似文献
The preparation of 2-amino-5-nitrothiophene, 2-formamido-5-nitrothiophene, 2-acetamido-5-nitrothiophene and 2-t-butyloxycarbonylamino-5-nitrothiophene are described. Abnormal values of the coupling constants J3.4 had been observed in the 1H-nmr spectra of compounds obtained. 相似文献
Photoresists are essential for the fabrication of flexible electronics through all-photolithographic processes. Single component semiconducting photoresist exhibits both semiconducting and photo-patterning properties, and as a result, the device fabrication process can be simplified. However, the design of semiconducting polymeric photoresist with ambipolar semiconducting property remains challenging. In this paper, we report a single component semiconducting photoresist (PFDPPF4T-N3) by incorporating azide groups and noncovalent conformation locks into the side alkyl chains and conjugated backbones of a diketopyrrolopyrrole-based conjugated polymer, respectively. The results reveal that PFDPP4FT-N3 exhibits ambipolar semiconducting property with hole and electron mobilities up to 1.12 and 1.17 cm2 V?1 s?1, respectively. Moreover, field effect transistors with the individual photo-patterned thin films of PFDPPF4T-N3 also show ambipolar semiconducting behavior with hole and electron mobilities up to 0.66 and 0.80 cm2 V?1 s?1, respectively. These results offer a simple yet effective design strategy for high-performance single component semiconducting photoresists, which hold great potential for flexible electronics processed by all photolithography.
The use of direct observation of nuclear reactions (p,p′γ) is discussed. The main characteristics of this method are presented
and applied to the case of the miroanalysis of Si, S and Zn in GaSb. 相似文献