Stüker Tony, Hohmann Thomas, Beckers Helmut, Riedel Sebastian
Anorganische Chemie, Institut für Chemie und Biochemie, Freie Universität Berlin, 14195, Berlin, Germany.
Angew Chem Int Ed Engl. 2020 Dec 14;59(51):23174-23179. doi: 10.1002/anie.202010950. Epub 2020 Oct 15.
The fluoronitrenoid metal complexes FNCoF and FNRhF as well as the first ternary Rh and Ir complexes NIrF and NRhF are described. They were obtained by the reaction of excited Group-9 metal atoms with NF and their IR spectra, isolated in solid rare gases (neon and argon), were recorded. Aided by the observed N isotope shifts and quantum-chemical predictions, all four stretching fundamentals of the novel complexes were safely assigned. The F-N stretching frequencies of the fluoronitrenoid complexes FNCoF (1056.8 cm ) and FNRhF (872.6 cm ) are very different and their N-M bonds vary greatly. In FNCoF , the FN ligand is singly bonded to Co and bears considerable iminyl/nitrene radical character, while the N-Rh bond in FNRhF is a strong double bond with comparatively strong σ- and π-bonds. The anticipated rearrangement of FNCoF to the nitrido Co complex is predicted to be endothermic and was not observed.
描述了氟氮烯类金属配合物FNCoF和FNRhF,以及首个三元铑和铱配合物NIrF和NRhF。它们是通过第9族激发态金属原子与NF反应得到的,并记录了在固体稀有气体(氖气和氩气)中分离得到的它们的红外光谱。借助观察到的氮同位素位移和量子化学预测,新型配合物的所有四个伸缩基频都得到了可靠归属。氟氮烯类配合物FNCoF(1056.8 cm⁻¹)和FNRhF(872.6 cm⁻¹)的F-N伸缩频率差异很大,它们的N-M键也有很大不同。在FNCoF中,FN配体与Co单键相连,具有相当大的亚氨基/氮烯自由基特征,而FNRhF中的N-Rh键是具有相对较强σ键和π键的强双键。预计FNCoF重排为氮基钴配合物是吸热反应,且未观察到该反应。