Dhimba George, Muller Alfred, Lammertsma Koop
Department of Chemical Sciences, University of Johannesburg, Auckland Park, Johannesburg 2006, South Africa.
Department of Chemistry and Pharmaceutical Sciences, Faculty of Sciences, Vrije Universiteit Amsterdam, De Boelelaan 1108, Amsterdam 1081 HZ, The Netherlands.
Inorg Chem. 2022 Sep 26;61(38):14918-14923. doi: 10.1021/acs.inorgchem.2c00824. Epub 2022 Aug 18.
Chiral -MoO(acac) racemizes via four pathways that agree with and extend upon Muetterties' topological analysis for dynamic MX(chel) complexes. Textbook Ray-Dutt and Bailar twists are the least favored with barriers of 27.5 and 28.7 kcal/mol, respectively. Rotating both acac ligands of the Bailar structure by 90° gives the lower Conte-Hippler twist (20.0 kcal/mol), which represents a valley-ridge inflection that invokes the trans isomer. The most favorable is a new twist that was found by 90° rotation of only one acac ligand of the Bailar structure. The gas-phase barrier of 17.4 kcal/mol for this Dhimba-Muller-Lammertsma twist further decreases upon inclusion of the effects of solvents to 16.3 kcal/mol (benzene), 16.2 kcal/mol (toluene), and 15.4 kcal/mol (chloroform), which are in excellent agreement with the reported experimental values.
手性-MoO(acac) 通过四条途径外消旋,这些途径与穆特蒂耶斯对动态MX(chel)配合物的拓扑分析一致并有所扩展。教科书式的雷-达特扭曲和贝拉尔扭曲最不常见,其能垒分别为27.5和28.7千卡/摩尔。将贝拉尔结构的两个acac配体都旋转90°会产生能量较低的孔泰-希普勒扭曲(20.0千卡/摩尔),这代表了一种谷-脊拐点,会产生反式异构体。最有利的是一种新的扭曲,它是通过仅将贝拉尔结构的一个acac配体旋转90°发现的。这种迪姆巴-米勒-拉默茨马扭曲的气相能垒为17.4千卡/摩尔,计入溶剂效应后进一步降低至16.3千卡/摩尔(苯)、16.2千卡/摩尔(甲苯)和15.4千卡/摩尔(氯仿),与报道的实验值非常吻合。