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首页> 外文期刊>Inorganica Chimica Acta >Electron transfer reactions of copper(II)/(I) couples with bidentate and quadridentate polypyridine ligands: is gated behavior common among outer-sphere electron transfer reactions?
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Electron transfer reactions of copper(II)/(I) couples with bidentate and quadridentate polypyridine ligands: is gated behavior common among outer-sphere electron transfer reactions?

机译:铜(II)/(I)与双齿和四齿聚吡啶配体的电子转移反应:外球电子转移反应中门控行为是否常见?

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We examined redox behaviors of bis(2,9-diphenyl-1,10-phenanthroline)copper(II)/(I) couple and the oxidation reaction of structurally more constrained bis(1,2-bis(9-methyl-1,10-phenanthrolin-2-yl)ethane)dicopper(I) in acetnitrile: the electron transfer reactions of the former couple took place in an ordinary concerted manner with the self-exchange rate constant k(ex)(298) = 9.2 x 10(4) kg mol(-1) s(-1), while a dicopper(II) intermediate with a tetrahedral coordination geometry was spectrophotometrically detected during the course of the oxidation reaction of the latter compound. It was also found that the reduction of (1,2-bis(9-methyl-1,10-phenanthrolin-2-yl)ethane)copper(II), the oxidized form of the corresponding dicopper(I) species, proceeded through the dimerization process. The oxidation reaction of bis(1,2-bis(9-methyl-1,10-phenanthrolin-2-yl)ethane)dicopper(I) by [Ni(1,4,7-triazacyclononane)(2)](3+) in acetonitrile was a bi-phasic reaction involving fast electron transfer (ET) with k(ex)(298) = (4.8 +/- 1) x 10(4) kg mol(-1) s(-1) followed by the very slow monomerization of the intermediate [k(298) = (3.46 +/- 0.03) x 10(-4) s(-1)]. These observations indicate that the electron transfer reactions involving (1,2-bis(9-methyl-1,10-phenanthrolin-2-yl)ethane)copper(II)/bis(1,2-bis(9- methyl-1,10-phenanthrolin-2-yl)ethane)dicopper(I) couple are gated through the conformational change (Cu(II monomer-dimer). We re-examined the gated ET reactions of Cu(II)/(I) couples so far reported from the view point of the time scale of internal rearrangement and of the merit brought about by the geometric changes around either Cu(I) or Cu(II). We have reached a tentative conclusion that gated ET is observed only when the following conditions are fulfilled: (1) direct ET for either oxidation or reduction direction is non-adiabatic; and (2) a low energy CT perturbation is expected by the uneven structural change (change in the coordination geometry takes place only in the species which exhibits no low-lying CT band in its ground state). In addition to the above two conditions; (3) time scale of the structural change is slow compared with the lifetime of the encounter complex may be added. C) 2001 Elsevier Science B.V. All rights reserved. [References: 45]
机译:我们研究了bis(2,9-diphenyl-1,10-phenothroline)copper(II)/(I)对的氧化还原行为以及结构更受约束的bis(1,2-bis(9-methyl-1,乙腈中的10-菲咯啉-2-基)乙烷二铜(I):前两对的电子转移反应以通常的协同方式发生,自交换速率常数k(ex)(298)= 9.2 x 10 (4)kg mol(-1)s(-1),而在后者化合物的氧化反应过程中,通过分光光度法检测到具有四面体配位几何结构的双铜(II)中间体。还发现,还原(1,2-双(9-甲基-1,10-菲咯啉-2-基)乙烷)铜(II)(相应双铜(I)物种的氧化形式)通过二聚化过程。 [Ni(1,4,7-triazacyclononane)(2)](3)对双(1,2-双(9-甲基-1,10-菲咯啉-2-基)乙烷)二铜(I)的氧化反应+)在乙腈中是一个双相反应,涉及快速电子转移(ET),k(ex)(298)=(4.8 +/- 1)x 10(4)kg mol(-1)s(-1)通过中间体[k(298)=(3.46 +/- 0.03)x 10(-4)s(-1)的非常慢的单体化作用。这些观察结果表明涉及(1,2-双(9-甲基-1,10-菲咯啉-2-基)乙烷)铜(II)/双(1,2-双(9-甲基-1)的电子转移反应通过构象变化(Cu(II单体-二聚体),对10,菲咯啉-2-基)乙烷)双铜(I)进行门控。我们重新检查了Cu(II)/(I)对的门控ET反应,因此从内部重排的时间尺度以及由Cu(I)或Cu(II)周围的几何变化带来的优点来看,目前尚无报道,我们已经初步得出结论,只有在以下情况下才能观察到门控ET满足以下条件:(1)氧化或还原方向的直接ET是非绝热的;和(2)不均匀的结构变化会导致低能CT扰动(配位几何的变化仅在具有以下特征的物种中发生)除了以上两个条件外;(3)结构变化的时间尺度较wi慢。可能会增加相遇复合体的寿命。 C)2001 Elsevier Science B.V.保留所有权利。 [参考:45]

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