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Synthesis and self-association of dibenzothiophene derivatives for simulation of hydrogen bonding interaction in asphaltenes
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作者 Ying-Hui Bian Shao-Tang Xu +4 位作者 Le-Chun Song Yu-Lu Zhou Li-Jun Zhu Yu-Zhi Xiang Dao-Hong Xia 《Petroleum Science》 SCIE CAS CSCD 2015年第3期501-508,共8页
The dibenzothiophene derivatives, namely 2-(dibenzothiophene-2-carbonyl)benzoic acid and 2-(diben- zothiophene-2-carbonyl)alkyl benzoate, were synthesized and characterized by nuclear magnetic resonance (1H NMR)... The dibenzothiophene derivatives, namely 2-(dibenzothiophene-2-carbonyl)benzoic acid and 2-(diben- zothiophene-2-carbonyl)alkyl benzoate, were synthesized and characterized by nuclear magnetic resonance (1H NMR), matrix-assisted laser desorption/ionization time of flight mass spectrometry, and elemental analysis. The self- association behavior of these dibenzothiophene derivatives in CH2C12 and CH3CN was investigated using UV-visible absorption spectroscopy, fourier transform infrared spec- troscopy, and atomic force microscopy. It was found that the carboxylic acid exhibited a strong self-association trend in CH2C12 solution at a concentration of about 5 × 10^-7 M. Hydrogen bonding of carboxyl in the dibenzoth- iophene derivatives was confirmed to be the main driving force for the formation of the carboxylic acid aggregates. 展开更多
关键词 dibenzothiophene derivatives Association Hydrogen bonding Simulation Asphaltenes
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