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由氯化镓稳定的芳烃-汞配合物:H/D和芳烃交换的相对速率

Arene-mercury complexes stabilized by gallium chloride: relative rates of H/D and arene exchange.

作者信息

Branch Catherine S, Barron Andrew R

机构信息

Department of Chemistry and Center for Nanoscale Science and Technology, Rice University, Houston, Texas 77005, USA.

出版信息

J Am Chem Soc. 2002 Nov 27;124(47):14156-61. doi: 10.1021/ja0206590.

Abstract

We have previously proposed that the Hg(arene)(2)(GaCl(4))(2) catalyzed H/D exchange reaction of C(6)D(6) with arenes occurs via an electrophilic aromatic substitution reaction in which the coordinated arene protonates the C(6)D(6). To investigate this mechanism, the kinetics of the Hg(C(6)H(5)Me)(2)(GaCl(4))(2) catalyzed H/D exchange reaction of C(6)D(6) with naphthalene has been studied. Separate second-order rate constants were determined for the 1- and 2-positions on naphthalene; that is, the initial rate of H/D exchange = k(1i)[Hg][C-H(1)] + k(2i)[Hg][C-H(2)]. The ratio of k(1i)/k(2i) ranges from 11 to 2.5 over the temperature range studied, commensurate with the proposed electrophilic aromatic substitution reaction. Observation of the reactions over an extended time period shows that the rates change with time, until they again reach a new and constant second-order kinetics regime. The overall form of the rate equation is unchanged: final rate = k(1f)[Hg][C-H(1)] + k(2f)[Hg][C-H(2)]. This change in the H/D exchange is accompanied by ligand exchange between Hg(C(6)D(6))(2)(GaCl(4))(2) and naphthalene to give Hg(C(10)H(8))(2)(GaCl(4))(2,) that has been characterized by (13)C CPMAS NMR and UV-visible spectroscopy. The activation parameters for the ligand exchange may be determined and are indicative of a dissociative reaction and are consistent with our previously calculated bond dissociation for Hg(C(6)H(6))(2)(AlCl(4))(2). The initial Hg(arene)(2)(GaCl(4))(2) catalyzed reaction of naphthalene with C(6)D(6) involves the deuteration of naphthalene by coordinated C(6)D(6); however, as ligand exchange progresses, the pathway for H/D exchange changes to where the protonation of C(6)D(6) by coordinated naphthalene dominates. The site selectivity for the H/D exchange is initially due to the electrophilic aromatic substitution of naphthalene. As ligand exchange occurs, this selectivity is controlled by the activation of the naphthalene C-H bonds by mercury.

摘要

我们之前曾提出,Hg(芳烃)₂(GaCl₄)₂催化C₆D₆与芳烃的H/D交换反应是通过亲电芳香取代反应发生的,其中配位的芳烃使C₆D₆质子化。为了研究该机理,我们研究了Hg(C₆H₅Me)₂(GaCl₄)₂催化C₆D₆与萘的H/D交换反应的动力学。分别测定了萘1位和2位的二级速率常数;即,H/D交换的初始速率 = k₁ᵢ[Hg][C-H₁] + k₂ᵢ[Hg][C-H₂]。在所研究的温度范围内,k₁ᵢ/k₂ᵢ的比值在11到2.5之间,这与所提出的亲电芳香取代反应相符。对反应进行较长时间的观察表明,速率随时间变化,直到它们再次达到一个新的恒定二级动力学状态。速率方程的总体形式不变:最终速率 = k₁բ[Hg][C-H₁] + k₂բ[Hg][C-H₂]。H/D交换的这种变化伴随着Hg(C₆D₆)₂(GaCl₄)₂与萘之间的配体交换,生成了Hg(C₁₀H₈)₂(GaCl₄)₂,已通过¹³C CPMAS NMR和紫外可见光谱对其进行了表征。可以确定配体交换的活化参数,这些参数表明是解离反应,并且与我们之前计算的Hg(C₆H₆)₂(AlCl₄)₂的键解离一致。最初Hg(芳烃)₂(GaCl₄)₂催化萘与C₆D₆的反应涉及配位的C₆D₆使萘氘化;然而,随着配体交换的进行,H/D交换的途径发生变化,变为配位的萘使C₆D₆质子化占主导。H/D交换的位点选择性最初是由于萘的亲电芳香取代。随着配体交换的发生,这种选择性由汞对萘C-H键的活化控制。

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