Wen Mei, Medel Robert, Zasimov Pavel V, Riedel Sebastian
Institut für Chemie und Biochemie-Anorganische Chemie, Freie Universität Berlin, Fabeckstrasse 34/36, Berlin 14195, Germany.
Inorg Chem. 2025 Mar 17;64(10):5105-5112. doi: 10.1021/acs.inorgchem.4c05418. Epub 2025 Mar 5.
We report on the generation of FB-As═BF, an arsinoborene (boranylidenearsane) with a genuine As═B double bond, where both the As and B atoms are two-coordinate. It was obtained from the reaction of AsF with laser-ablated boron atoms under cryogenic conditions in neon and argon matrices. In addition, the single-bonded arsenic-boron radicals FB-AsF and FB-AsF were characterized. These species were identified by infrared spectroscopy and B isotope substitution in conjunction with quantum-chemical calculations at the B3LYP and CCSD(T) levels of theory. The isomerization from FB-AsF to FB-AsF can be triggered by irradiation with ultraviolet light (λ = 275 nm) in argon. This discovery of the arsinoborene FB-As═BF further extends the series of multiple-bonded systems between heavy main group elements and boron.
我们报道了FB-As═BF(一种具有真正As═B双键的胂硼烯(硼亚烷基胂))的生成,其中As和B原子均为二配位。它是在低温条件下,于氖气和氩气基质中通过AsF与激光烧蚀的硼原子反应得到的。此外,还对单键连接的砷硼自由基FB-AsF和FB-AsF进行了表征。这些物种通过红外光谱以及结合B3LYP和CCSD(T)理论水平的量子化学计算的B同位素取代得以鉴定。在氩气中用紫外线(λ = 275 nm)照射可引发FB-AsF到FB-AsF的异构化。胂硼烯FB-As═BF的这一发现进一步扩展了重主族元素与硼之间的多重键合体系系列。