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Excited state hydrogen atom transfer in ammonia-wire and water-wire clusters

机译:氨线和水线团簇中激发态氢原子的转移

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We review experimental and theoretical investigations of excited-state hydrogen atom transfer (ESHAT) reactions along unidirectionally hydrogen bonded solvent 'wire' clusters. The solvent wire is attached to the aromatic 'scaffold' molecule 7-hydroxyquinoline (7HQ), which offers an O - H and an N hydrogen bonding site, spaced far enough apart to form two- to four-membered wires. S-1 <-- S-0 photoexcitation renders the O - H group more acidic and the quinolinic N more basic. This provides a driving force for the enol --> keto tautomerization, probed by the characteristic fluorescence of the 7-ketoquinoline in the molecular beam experiments. For 7-hydroxyquinoline center dot (NH3)(3), excitation of ammonia-wire vibrations induces the tautomerization at similar to 200 cm(-1). Different reaction pathways have been explored by excited-state ab initio calculations. These show that the reaction proceeds by H-atom transfer along the wire as a series of Grotthus-type translocation steps. There is no competition with a mechanism involving successive proton translocations. The rate-controlling S-1 state barriers arise from crossings of a pi pi* with a Rydberg- type pi sigma* state and the proton and electron movements along the wire are closely coupled. The excited state reactant, H-transferred intermediates and product structures are characterized. The reaction proceeds by tunnelling, as shown by deuteration of the solvent molecules (ND3) in the wire. The first step of the reaction exhibits intra/intermolecular vibrational mode selectivity. Substitution of NH3 by one, two or three H2O molecules in the wire leads to increasing threshold with each additional H2O molecule, up to > 2000 cm(-1) for the 7-hydroxyquinoline center dot (H2O)(3) water-wire cluster. No 7-ketoquinoline fluorescence is observed upon insertion of even a single H2O molecule. The calculations show that insertion of each H2O molecule into the solvent wire introduces a high barrier, which blocks any further H-atom transfer.
机译:我们回顾了沿单向氢键键合溶剂“线”簇的激发态氢原子转移(ESHAT)反应的实验和理论研究。溶剂线连接到芳族“支架”分子7-羟基喹啉(7HQ),后者提供一个O-H和一个N氢键合位点,彼此间隔足够远,以形成两元至四元线。 S-1 <-S-0光激发使O-H基团更酸性,而喹啉N则更碱性。这为烯醇->酮互变异构提供了驱动力,在分子束实验中被7-酮喹啉的特征荧光探测到。对于7-羟基喹啉中心点(NH3)(3),氨线振动的激发在200 cm(-1)处引起互变异构。通过激发态从头算计算已经探索了不同的反应途径。这些表明反应是作为一系列Grotthus型移位步骤通过H原子沿着金属丝转移而进行的。涉及连续质子易位的机制是没有竞争的。速率控制的S-1状态势垒是由pi pi *与Rydberg型pi sigma *状态的交叉产生的,并且质子和电子沿导线的运动紧密耦合。表征了激发态反应物,H转移的中间体和产物结构。如线中的溶剂分子(ND3)氘化所示,反应通过隧穿进行。反应的第一步显示出内部/分子间的振动模式选择性。线中的一个,两个或三个H2O分子取代NH3会导致阈值随每个额外的H2O分子的增加而增加,对于7-羟基喹啉中心点(H2O)(3)水线簇,可达> 2000 cm(-1) 。即使插入单个H2O分子,也未观察到7-酮喹啉荧光。计算表明,将每个H2O分子插入溶剂线都会引入高势垒,从而阻碍任何进一步的H原子转移。

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