首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Reaction of tris(bipyridine)ruthenium(III) with hydroxide and its application in a solar energy storage system
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Reaction of tris(bipyridine)ruthenium(III) with hydroxide and its application in a solar energy storage system

机译:三联吡啶钌(III)与氢氧化物的反应及其在太阳能存储系统中的应用

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摘要

Irradiation of Ru(bipy)32+ (bipy = 2,2′-bipyridine) with light below 560 nm results in the formation of a charge-transfer excited state potentially capable of reducing water to dihydrogen with concomitant production of Ru(bipy)33+. The latter may be reduced by hydroxide [Formula: see text] to form dioxygen and regenerate the starting complex. The use of these reactions in a cell designed to bring about the photochemical decomposition of water is proposed.The stoichiometry, kinetics, and mechanism of the Ru(bipy)33+-hydroxide reaction have been investigated by conventional and stopped-flow spectrophotometry. The dioxygen yield is a sharp function of pH, attaining its maximum value (about 80%) at pH 9. At low pH (3 and 4.8) the production of ruthenium(II) is first order with kobsd = (1.41 ± 0.04) × 10-4 sec-1 (25°, ionic strength μ = 1.00 M with sodium sulfate). In the intermediate pH range (7.9-10.0) complex kinetics are observed. In the hydroxide range 0.01-0.50 M, ruthenium(II) production is predominantly first order with kobsd = ka[OH-] + kb[OH-]2 sec-1; ka = 148 M-1 sec-1 and kb = 138 M-2 sec-1 (25°, μ = 1.00 M, sodium sulfate). For the ka term, the activation parameters are ΔH = 15.3 ± 1.0 kcal mol-1 and ΔS = 7 ± 3 cal deg-1 mol-1 (1 cal = 4.184 J). An intermediate species (λmax 800 nm) forms at the same rate as ruthenium(II) in this hydroxide range. It disappears with kobsd = 1.2 + 1.1 × 102 [OH-] sec-1 at 25°. Similarly absorbing (λmax 750 to 800 nm) species are generated by the addition of hydroxyl radical to M(bipy)32+/3+ [M = Fe(II), Os(II), Ru(II), Cr(III), Ru(III)] in pulse radiolysis experiments. The kinetics above pH 7 are described in terms of rate-determining nucleophilic attack by hydroxide on the bound bipyridine ring. The hydroxide adduct so generated is tentatively identified with that observed in the pulse radiolysis experiments with Ru(bipy)32+.For reduction of Ru(bipy)33+ by hydrogen peroxide ruthenium(II) production is first order with kobsd = kc[HO2-] + kd[H2O2] where kc = 5.4 × 107 M-1 sec-1 and kd = 8.3 M-1 sec-1 (25°, μ = 1.00 M, pH 3.5 to 9.7). This reaction produces dioxygen in 83 ± 15% yield at pH 6.8 and in 1.0 N sulfuric acid.
机译:低于560 nm的光照射Ru(bipy)3 2 + (bipy = 2,2'-bipyridine)会形成电荷转移激发态,可能将水还原为二氢Ru(bipy)3 3 + 的伴随产生。后者可以被氢氧化物还原[分子式:见正文]以形成双氧并再生起始配合物。提出了将这些反应用于引起水的光化学分解的反应池中。研究了Ru(bipy)3 3 + -氢氧化物反应的化学计量,动力学和机理。常规分光光度法。双氧产量是pH的一个急剧函数,在pH 9时达到最大值(约80%)。在低pH(3和4.8)下,钌(II)的产生是一阶的,kobsd =(1.41±0.04)× 10 -4 -1 (25°,离子强度μ= 1.00 M,带硫酸钠)。在中等pH范围(7.9-10.0)中,观察到复杂的动力学。在0.01-0.50 M的氢氧化物范围内,钌(II)的生成主要为一阶,其中kobsd = ka [OH -] + kb [OH -] 2 sec -1 ; ka = 148 M -1 sec -1 和kb = 138 M -2 sec -1 (25° ,μ= 1.00M,硫酸钠)。对于ka项,激活参数为ΔH = 15.3±1.0 kcal mol -1 和ΔS = 7±3 cal deg < sup> -1 mol -1 (1 cal = 4.184 J)。在此氢氧化物范围内,以与钌(II)相同的速率形成中间物种(λmax800 nm)。它在25°时以kobsd = 1.2 + 1.1×10 2 [OH -] sec -1 消失。通过在M(bipy)3 2 + / 3 + [M = Fe(II),Os(II),Ru (II),Cr(III),Ru(III)]进行脉冲放射分解实验。 pH值高于7的动力学描述了速率,该速率决定了氢氧化物对结合的联吡啶环的亲核攻击。初步确定了所生成的氢氧化物加合物与在Ru(bipy)3 2 + 的脉冲辐射分解实验中观察到的氢氧化物加成物有关。为了减少Ru(bipy)3 3 + 的还原性,一氧化氢钌(II)的生产是一阶的,其中k obsd = k c [HO 2 -] + k d [H 2 O 2 ]其中,k c = 5.4×10 7 M -1 sec -1 和k d = 8.3 M -1 sec -1 < / sup>(25°,μ= 1.00 M,pH 3.5至9.7)。该反应在pH 6.8和1.0 N硫酸中以83±15%的产率产生双氧。

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