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Long-range proton-coupled electron transfer in phenol-Ru(2,2'-bipyrazine)3~(2+) dyads

机译:苯酚-Ru(2,2'-联吡嗪)3〜(2+)二元化合物中的远程质子耦合电子转移

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摘要

Two dyads in which either 4-cyanophenol or un-substituted phenol is connected via a p-xylene spacer to a Ru(bpz)3~(2+) (bpz = 2,2'-bipyrazine) complex were synthesized and investigated. Selective photo-excitation of Ru{bpz)3~(2+) at 532 nm in a CH3CN-H2O mixture leads to the formation of 4-cyanophenolate or phenolate along with Ru(bpz)3~(2+) in its electronic ground state. This apparent photoacid behavior can be understood on the basis of a reaction sequence comprised of an initial photoinduced proton-coupled electron transfer (PCET) during which 4-cyanophenol or phenol is oxidized and deprotonated, followed by a thermal electron transfer event in the course of which 4-cyanophenoxyl or phenoxyl is reduced by Ru(bpz)3~+ to 4-cyanophenolate or phenolate. Conceptually, this reaction sequence is identical to a sequence of photoinduced charge-separation and thermal charge-recombination events as observed previously for many electron transfer dyads, with the important difference that the initial photoinduced electron transfer process is proton-coupled. The dyad containing 4-cyanophenol reacts via concerted-proton electron transfer (CPET) whereas the dyad containing un-substituted phenol appears to react predominantly via a stepwise PCET mechanism. Long-range PCET is a key reaction in photosystem II. Understanding the factors that govern the kinetics of long-range PCET is desirable in the broader context of light-to-energy conversion by means of proton-electron separation across natural or artificial membranes.
机译:合成并研究了其中通过对二甲苯间隔基将4-氰基苯酚或未取代的苯酚连接到Ru(bpz)3〜(2+)(bpz = 2,2'-联吡嗪)络合物的两个二元化合物。在CH3CN-H2O混合物中Ru(bpz)3〜(2+)在532 nm处选择性光激发会导致4-氰基酚盐或酚盐与Ru(bpz)3〜(2+)在其电子基底中形成州。可以根据以下反应顺序来理解这种明显的光酸行为,该反应顺序包括初始的光致质子偶联电子转移(PCET),在此期间4-氰基苯酚或苯酚被氧化和去质子化,随后在反应过程中发生热电子转移事件。 Ru(bpz)3〜+将4-氰基苯氧基或苯氧基还原为4-氰基苯酚盐或酚盐。从概念上讲,该反应序列与先前对许多电子转移二元化合物所观察到的光诱导电荷分离和热电荷重组事件的序列相同,但重要的区别在于初始光诱导电子转移过程是质子耦合的。包含4-氰基苯酚的二元化合物通过协调质子电子转移(CPET)反应,而包含未取代苯酚的二元化合物似乎主要通过逐步PCET机制进行反应。远程PCET是光系统II中的关键反应。在更广泛的光到能量转换背景下,通过跨天然或人造膜的质子电子分离,了解控制远程PCET动力学的因素是合乎需要的。

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