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极性溶剂化沸石中的电子俘获

Electron trapping in polar-solvated zeolites.

作者信息

Ellison Eric H

机构信息

Department of Chemistry and Biochemistry, 322 Coulter Hall, University of Mississippi, University, MS 38677, USA.

出版信息

J Phys Chem B. 2005 Nov 3;109(43):20424-32. doi: 10.1021/jp053617h.

Abstract

Of current interest in our laboratory is the nature of photoinduced processes in the cavities of zeolites completely submerged in polar solvents, or polar-solvated zeolites (PSZ). The present study addresses the nature of electron trapping in PSZ with emphasis on the zeolites NaX and NaY. Free electrons were generated by two-photon, pulsed-laser excitation of either pyrene or naphthalene included in zeolite cavities. Trapped electrons were monitored by diffuse transmittance, transient absorption spectroscopy at visible wavelengths. In anhydrous alcohols, electron trapping by Na(4)(4+) ion clusters was observed in both NaX and NaY. The resulting trapped electrons decayed over the course of tens of milliseconds. No evidence for alcohol-solvated electrons was found. More varied results were observed in solvents containing water. In NaX submerged in CH(3)OH containing 5% or higher water, species having microsecond lifetimes characteristic of solvated electrons were observed. By contrast, a 2 h exposure of NaY to 95/5 CH(3)OH/H(2)O had no effect on electron trapping relative to anhydrous CH(3)OH. The difference between NaX and NaY was explained by how fast water migrates into the sodalite cage. Prolonged exposure to water at room temperature or exposure to water at elevated temperatures was necessary to place water in the sodalite cages of NaY and deactivate Na(4)(4+) as an electron trap. Additional studies in NaY revealed that solvent clusters eventually become lower energy traps than Na(4)(4+) as the water content in methanol increases. In acetonitrile-water mixtures, electron trapping by Na(4)(4+) was eliminated and no equivalent species characteristic of solvated electrons in methanol-water mixtures was observed. This result was explained by the formation of low energy solvated electrons which cannot be observed in the visible region of the spectrum. Measurements of the rate of O(2) quenching in anhydrous solvents revealed rate constants for the quenching of ion cluster trapped electrons that were 2-4 times higher than that for pyrene triplets. In NaX, the rate constant in methanol was 10(4) times smaller than that in cyclohexane, showing greater inhibition of O(2) reactivity in the medium of PSZ. The results of this study point out the conditions under which Na(4)(4+) is active as an electron trap in PSZ and that water must be present in the sodalite cage to produce solvated electrons in the supercage.

摘要

目前我们实验室感兴趣的是完全浸没在极性溶剂中的沸石空腔,即极性溶剂化沸石(PSZ)中的光诱导过程的本质。本研究探讨了PSZ中电子俘获的本质,重点研究了沸石NaX和NaY。通过对包含在沸石空腔中的芘或萘进行双光子脉冲激光激发来产生自由电子。通过漫透射率、可见光波长下的瞬态吸收光谱来监测俘获电子。在无水醇中,在NaX和NaY中均观察到Na(4)(4+)离子簇对电子的俘获。所产生的俘获电子在几十毫秒内衰减。未发现醇溶剂化电子的证据。在含水溶剂中观察到了更多样化的结果。在浸没于含5%或更高水的CH(3)OH中的NaX中,观察到了具有溶剂化电子特征的微秒寿命的物种。相比之下,将NaY暴露于95/5 CH(3)OH/H(2)O中2小时,相对于无水CH(3)OH,对电子俘获没有影响。NaX和NaY之间的差异是由水迁移到方钠石笼中的速度来解释的。需要在室温下长时间暴露于水或在升高的温度下暴露于水,才能使水进入NaY的方钠石笼中并使Na(4)(4+)作为电子陷阱失活。对NaY的进一步研究表明,随着甲醇中水含量的增加,溶剂簇最终会成为比Na(4)(4+)能量更低的陷阱。在乙腈 - 水混合物中,Na(4)(4+)对电子的俘获被消除,并且在甲醇 - 水混合物中未观察到与溶剂化电子等效的物种。这一结果是由形成了在光谱可见光区域无法观察到的低能量溶剂化电子来解释的。在无水溶剂中对O(2)猝灭速率的测量表明,离子簇俘获电子的猝灭速率常数比芘三线态的猝灭速率常数高2 - 4倍。在NaX中,甲醇中的速率常数比环己烷中的小10(4)倍,表明在PSZ介质中对O(2)反应性的抑制作用更大。本研究结果指出了Na(4)(4+)在PSZ中作为电子陷阱起作用的条件,以及方钠石笼中必须存在水才能在超笼中产生溶剂化电子。

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