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Oxidation of carotenoids in dichloromethane and mesoporous molecular sieves: HPLC and spectroscopic studies.

机译:二氯甲烷和中孔分子筛中类胡萝卜素的氧化:HPLC和光谱研究。

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In the oxidation of the carotenoids, ethyl all-trans-8-apo-β-caroten-8-oate (I) and all-trans-β-carotene (II), with ferric chloride, several equilibria occur between Fe3+, Fe 2+, Cl, the neutral carotenoid, and its radical an electron from Fe2+. Isomerization of carotenoids occurs during the oxidation. In the presence of air a stable product is formed in high yield during the oxidation. 1H NMR, LC-MS and optical studies show that this product is the 5,8-peroxide of the starting material. A mechanism for the formation of this compound is proposed.; Carotenoid radical cations (Car·+) produced by oxidation with FeCl3 in CH2Cl2 solution were found to coexist as two species which were spectroscopically identified: the free radical cation (FCR) and an ion pair. The ion pair is formed by interaction between Car·+ and Cl. Optical and EPR studies show that the ion pair is solvent-separated (SSIP). The interaction causes a shift in the maximum absorption wavelength of Car·+ . The blue shift is for symmetrical Car·+ and the red shift is for asymmetrical Car·+. Semiempirical calculations predict these results and a theoretical explanation is given for these phenomena.; Electron transfer (ET) and isomerization of the carotenoids (Car) imbedded in MCM-41, Ti-MCM-41, Cu-MCM-41 and Fe-MCM-41 were studied. The ET efficiency in MCM-41 was highest for the carotenoid with the lowest oxidation potential. The presence of transition metal ions in the framework of MCM-41 increased the ET efficiency of all carotenoids, but the enhancement did not depend on oxidation potential, but rather on whether complexes are formed between carotenoids and metal ions. The presence of transition metal ions results in a large blue shift of the maximum absorption wavelength due to changes in the carotenoid conformation. A very high trans to cis isomerization efficiency of Car was found in these solid hosts. Isomer types of Car can be controlled by selecting different hosts.
机译:在类胡萝卜素的氧化过程中,乙基全- trans -8 '-apo-β-胡萝卜素-8 ' -oate( I )和全-β-胡萝卜素( II ),与氯化铁一起,Fe 3 + 之间会发生一些平衡,Fe 2 + ,Cl -,中性类胡萝卜素及其自由基是来自Fe 2 + 的电子。类胡萝卜素的异构化发生在氧化过程中。在空气存在下,在氧化过程中会以高收率形成稳定的产物。 1 H NMR,LC-MS和光学研究表明,该产物为起始原料的5,8-过氧化物。提出了形成该化合物的机理。发现在CH 2 Cl 2 溶液中用FeCl 3 氧化生成的类胡萝卜素自由基阳离子(Car ·+ )在光谱上被鉴定为两种共存:自由基阳离子(FCR)和离子对。离子对是由Car ·+ 和Cl -之间的相互作用形成的。光学和EPR研究表明离子对是溶剂分离的(SSIP)。相互作用导致Car ·+ 的最大吸收波长发生偏移。蓝色偏移表示对称的Car ·+ ,红色偏移表示不对称的Car ·+ 。半经验计算可以预测这些结果,并为这些现象提供理论解释。研究了嵌入在MCM-41,Ti-MCM-41,Cu-MCM-41和Fe-MCM-41中的类胡萝卜素(Car)的电子转移(ET)和异构化。在MCM-41中,对于具有最低氧化电位的类胡萝卜素,ET效率最高。 MCM-41框架中过渡金属离子的存在提高了所有类胡萝卜素的ET效率,但这种增强不取决于氧化电位,而是取决于类胡萝卜素和金属离子之间是否形成络合物。由于类胡萝卜素构象的变化,过渡金属离子的存在导致最大吸收波长发生大的蓝移。在这些固体宿主中,发现Car的[italic> trans cis 异构化效率非常高。可以通过选择不同的宿主来控制Car的异构体类型。

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