聚乙二醇在乙腈中作为硝酸铈铵氧化黄嘌呤生物碱的高效催化剂:动力学和机理研究

S. Shylaja, K. Rajanna, K. Ramesh, K. Reddy, P. G. Reddy
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引用次数: 11

摘要

以硝酸铈铵(CAN)为催化剂,研究了黄嘌呤(XAN)、次黄嘌呤(HXAN)、咖啡因(CAF)、茶碱(TPL)和可可碱(TBR)等黄嘌呤类生物碱的氧化动力学。[CAN]和[黄嘌呤生物碱]的反应均服从一级动力学。高度缓慢的can -黄嘌呤生物碱反应(在乙腈介质中即使在高温下)在peg (PEG-200, -300, -400, -600)的存在下增强。[PEG]的增加线性地增加了氧化速率。这一观察结果加上在PEG存在下CAN的吸收变化,[H - (OCH2-CH2) n-O-NH4Ce (NO3)4(CH3CN)] (PEG结合的CAN物种)被认为比CAN更具反应性。PEG介质中的氧化机理已由Menger-Portnoy的酶模型解释。
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Polyethylene Glycols as Efficient Catalysts for the Oxidation of Xanthine Alkaloids by Ceric Ammonium Nitrate in Acetonitrile: A Kinetic and Mechanistic Approach
Kinetics of oxidation of xanthine alkaloids, such as Xanthine (XAN), hypoxanthine (HXAN), caffeine (CAF), theophylline (TPL), and theobromine (TBR), have been studied with ceric ammonium nitrate (CAN) using poly ethylene glycols (PEG) as catalysts. Reaction obeyed first order kinetics in both [CAN] and [Xanthine alkaloid]. Highly sluggish CAN-xanthine alkaloid reactions (in acetonitrile media even at elevated temperatures) are enhanced in presence PEGs (PEG-200, -300, -400, -600). An increase in [PEG] increased the rate of oxidation linearly. This observation coupled with a change in absorption of CAN in presence of PEG, [H–(OCH2–CH2)n–O–NH4Ce(NO3)4(CH3CN)] (PEG bound CAN species), is considered to be more reactive than CAN. The mechanism of oxidation in PEG media has been explained by Menger-Portnoy’s enzymatic model.
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