连锁
化学
硼
分子
质子化
三键
计算化学
光化学
离子
高分子化学
有机化学
双键
生物化学
DNA
作者
Marc‐André Légaré,Maximilian Rang,Guillaume Bélanger‐Chabot,Julia I. Schweizer,Ivo Krummenacher,Rüdiger Bertermann,Merle Arrowsmith,Max C. Holthausen,Holger Braunschweig
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2019-03-21
卷期号:363 (6433): 1329-1332
被引量:227
标识
DOI:10.1126/science.aav9593
摘要
The coupling of two or more molecules of dinitrogen (N2) occurs naturally under the radiative conditions present in the ionosphere and may be achieved synthetically under ultrahigh pressure or plasma conditions. However, the comparatively low N-N single-bond enthalpy generally renders the catenation of the strongly triple-bonded N2 diatomic unfavorable and the decomposition of nitrogen chains a common reaction motif. Here, we report the surprising organoboron-mediated catenation of two N2 molecules under near-ambient conditions to form a complex in which a [N4]2- chain bridges two boron centers. The reaction entails reductive coupling of two hypovalent-boron-bound N2 units in a single step. Both this complex and a derivative protonated at both ends of the chain were characterized crystallographically.
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