Chanda Arani, Ryabov Alexander D, Mondal Sujit, Alexandrova Larissa, Ghosh Anindya, Hangun-Balkir Yelda, Horwitz Colin P, Collins Terrence J
Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, PA 15213, USA.
Chemistry. 2006 Dec 13;12(36):9336-45. doi: 10.1002/chem.200600630.
Small-molecule synthetic homogeneous-oxidation catalysts are normally poorly protected from self-destruction under operating conditions. Achieving design control over both activity and half-life is important not only in advancing the utility of oxidation catalysts, but also in minimizing hazards associated with their use and disposal. Iron(III)-TAML (tetraamido-macrocyclic ligand) oxidant catalysts rapidly activate H(2)O(2) for numerous significant processes, exhibiting high and differing activity and varying half-lives depending upon the TAML design. A general approach is presented that allows for the simultaneous determination of the second-order rate constant for the oxidation of a targeted substrate by the active catalyst (k(II)) and the rate constant for the intramolecular self-inactivation of the active catalyst (k(i)). The approach is valid if the formation of the active catalyst from its resting state and the primary oxidizing agent, measured by the second-order rate constant k(I), is fast and the catalyst concentration is very low, such that bimolecular inactivation pathways can be neglected. If the oxidation process is monitored spectrophotometrically and is set up to be incomplete, the kinetic trace can be analyzed by using the equation ln(lnA(t))/A(infnity)=ln(k(II)/k(i)Fe(III)-k(i)t, from which k(II) and k(i) can be determined. Here, A(t) and A(infinity) are absorbances at time t and at the end of reaction (t=infinity), respectively, and Fe(III) is the total catalyst concentration. Several tools were applied to examine the validity of the approach by using a variety of different Fe(III)-TAML catalysts, H(2)O(2) and tBuOOH as oxidizing agents, and the dyes safranine O and orange II as target substrates. Learning how catalyst activities (k(II)) and catalyst half-lives (k(i)) can be controlled by ligand design is an important step in creating green catalysts that will not persist in the environment after they have achieved their purpose.
小分子合成均相氧化催化剂通常在操作条件下难以防止自身分解。实现对活性和半衰期的设计控制不仅对于提高氧化催化剂的效用很重要,而且对于将与其使用和处置相关的危害降至最低也很重要。铁(III)-TAML(四酰胺大环配体)氧化催化剂能迅速激活过氧化氢用于众多重要过程,根据TAML设计表现出高且不同的活性以及不同的半衰期。本文提出了一种通用方法,可同时测定活性催化剂氧化目标底物的二级速率常数(k(II))和活性催化剂分子内自失活的速率常数(k(i))。如果由静止状态的催化剂和主要氧化剂形成活性催化剂的过程(由二级速率常数k(I)衡量)很快,且催化剂浓度非常低,以至于双分子失活途径可忽略不计,那么该方法就是有效的。如果通过分光光度法监测氧化过程并使其不完全进行,则可以使用方程ln(lnA(t))/A(∞)=ln(k(II)/k(i)[Fe(III)]tot - k(i)t来分析动力学曲线,由此可确定k(II)和k(i)。这里,A(t)和A(∞)分别是时间t和反应结束时(t = ∞)的吸光度,[Fe(III)]tot是催化剂总浓度。应用了几种工具,通过使用各种不同的铁(III)-TAML催化剂、过氧化氢和叔丁基过氧化氢作为氧化剂,以及番红花红O和橙黄II染料作为目标底物,来检验该方法的有效性。了解如何通过配体设计控制催化剂活性(k(II))和催化剂半衰期(k(i))是创建绿色催化剂的重要一步,这种催化剂在达到其目的后不会在环境中持续存在。