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迈向用于将 CO 固定为环状碳酸酯的中性单组分脒基碘化物铝催化剂。

Toward a Neutral Single-Component Amidinate Iodide Aluminum Catalyst for the CO Fixation into Cyclic Carbonates.

作者信息

Saltarini Sebastián, Villegas-Escobar Nery, Martínez Javier, Daniliuc Constantin G, Matute Ricardo A, Gade Lutz H, Rojas René S

机构信息

Laboratorio de Química Inorgánica, Facultad de Química y Farmacia, Pontificia Universidad Católica de Chile, Casilla 306, Santiago-22 6094411, Chile.

Centro Integrativo de Biología y Química Aplicada (CIBQA), Universidad Bernardo OHiggins, Santiago 8370854, Chile.

出版信息

Inorg Chem. 2021 Jan 18;60(2):1172-1182. doi: 10.1021/acs.inorgchem.0c03290. Epub 2020 Dec 29.

Abstract

A new iodide aluminum complex ({AlI(κ-naphbam)}, ) supported by a tetradentate amidinate ligand derived from a naphthalene-1,8-bisamidine precursor (naphbamH, ) was obtained in quantitative yield via reaction of the corresponding methyl aluminum complex ({AlMe(κ-naphbam)}, ) with 1 equiv of I in CHCl at room temperature. Complexes and were tested and found to be active as catalysts for the cyclic carbonate formation from epoxides at 80 °C and 1 bar of CO pressure. A first series of experiments were carried out with 1.5 mol % of the alkyl complex and 1.5 mol % of tetrabutylammonium iodide (TBAI) as a cocatalyst; subsequently, the reactions were carried out with 1.5 mol % of iodide complex as a single-component catalyst. Compound is one of the first examples of a nonzwitterionic halide single-component aluminum catalyst producing cyclic carbonates. The full catalytic cycle with characterization of all minima and transition states was characterized by quantum chemistry calculations (QCCs) using density functional theory. QCCs on the reaction mechanism support a reaction pathway based on the exchange of the iodine contained in the catalyst by 1 equiv of epoxide, with subsequent attack of I to the epoxide moiety producing the ring opening of the epoxide. QCCs triggered new insights for the design of more active halide catalysts in future explorations of the field.

摘要

通过相应的甲基铝配合物({AlMe(κ - naphbam)}, )与1当量的I在室温下于CHCl中反应,以定量产率获得了一种由萘 - 1,8 - 双脒前体(naphbamH, )衍生的四齿脒基配体支撑的新型碘化物铝配合物({AlI(κ - naphbam)}, )。对配合物 和 进行了测试,发现它们在80℃和1巴CO压力下作为由环氧化物形成环状碳酸酯的催化剂具有活性。首先进行了一系列实验,使用1.5摩尔%的烷基配合物 和1.5摩尔%的四丁基碘化铵(TBAI)作为助催化剂;随后,反应以1.5摩尔%的碘化物配合物 作为单组分催化剂进行。化合物 是产生环状碳酸酯的非两性离子卤化物单组分铝催化剂的首批实例之一。使用密度泛函理论通过量子化学计算(QCC)对具有所有极小值和过渡态表征的完整催化循环进行了表征。关于反应机理的QCC支持一种反应途径,该途径基于催化剂中所含的碘与1当量的环氧化物交换,随后I进攻环氧化物部分导致环氧化物开环。QCC为该领域未来探索中设计更具活性的卤化物催化剂引发了新的见解。

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