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钌卡宾复分解催化剂的气相热化学

Gas-phase thermochemistry of ruthenium carbene metathesis catalysts.

作者信息

Torker Sebastian, Merki Daniel, Chen Peter

机构信息

Laboratorium für Organische Chemie, ETH Zürich, Wolfgang-Pauli-Strasse 10, CH-8093 Zürich, Switzerland.

出版信息

J Am Chem Soc. 2008 Apr 9;130(14):4808-14. doi: 10.1021/ja078149z. Epub 2008 Mar 15.

Abstract

Quantitative energy-resolved collision-induced dissociation cross-sections by tandem ESI-MS provide absolute thermochemical data for phosphine binding energies in first- and second-generation ruthenium metathesis catalysts of 33.4 and 36.9 kcal/mol, respectively. Furthermore a study of the ring-closing metathesis in the second-generation system to liberate norbornene by forming the 14-electron reactive intermediate from the intramolecular pi-complex gives an estimate of the olefin binding energy to the 14-electron complex of around 18 kcal/mol, assuming a loose transition state. The results reported here are in remarkably good agreement with the latest DFT calculations using the M06-L functional.

摘要

通过串联电喷雾电离质谱法获得的定量能量分辨碰撞诱导解离截面,分别为第一代和第二代钌复分解催化剂中膦结合能提供了绝对热化学数据,其结合能分别为33.4千卡/摩尔和36.9千卡/摩尔。此外,对第二代体系中的闭环复分解反应进行研究,通过分子内π络合物形成14电子反应中间体来释放降冰片烯,假设过渡态较松散,则可估算出烯烃与14电子络合物的结合能约为18千卡/摩尔。此处报道的结果与使用M06-L泛函的最新密度泛函理论计算结果非常吻合。

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