Zhou Zheng, Johnson Matthew A, Wei Zheng, Bühringer Martina U, Garner Marc H, Tykwinski Rik, Petrukhina Marina A
Department of Chemistry, University at Albany, State University of New York, Albany, NY-12222, USA.
Department of Chemistry, University of Alberta, Edmonton, AB-T6G 2G2, Canada.
Chemistry. 2024 May 8;30(26):e202304145. doi: 10.1002/chem.202304145. Epub 2024 Mar 20.
Chemical reduction of a [4]cumulene with cesium metal was explored, and the structural changes stemming from electron acquisition are detailed using X-ray crystallography. It is found that the [4]cumulene undergoes dramatic geometric changes upon stepwise reduction, including bending of the cumulenic core and twisting of the endgroups from orthogonal to planar. The structural deformation is consistent with early theoretical reports that suggest that the twisting should occur upon reduction of both even and odd [n]cumulenes. The current results, on the other hand, are inconsistent with a previous experimental study of a [3]cumulene in which the predicted twisting is not observed upon reduction. DFT calculations reveal that the barrier to deformation is an order of magnitude lower in a [3]cumulene than a [4]cumulene, allowing the barrier to be overcome in the solid-state.
对用铯金属对[4]累积烯进行化学还原进行了探索,并使用X射线晶体学详细研究了电子获取引起的结构变化。研究发现,[4]累积烯在逐步还原时会发生剧烈的几何变化,包括累积烯核心的弯曲以及端基从正交扭曲到平面。这种结构变形与早期理论报告一致,该报告表明偶数和奇数[n]累积烯在还原时都会发生扭曲。另一方面,当前结果与先前对[3]累积烯的实验研究不一致,在该研究中,还原时未观察到预测的扭曲。密度泛函理论计算表明,[3]累积烯中变形的势垒比[4]累积烯低一个数量级,使得在固态下该势垒能够被克服。