化学
卡宾
反应性(心理学)
亚胺离子
亲核细胞
环加成
烷基
阳离子聚合
烯酮
异氰
亲核加成
加合物
分子
药物化学
光化学
有机化学
催化作用
医学
替代医学
病理
作者
Xiaofeng Mao,Shuang Qiu,Rui Guo,Yuyang Dai,Jie Zhang,Lingbing Kong,Zuowei Xie
摘要
BN/CC isosterism is an effective strategy to build hybrid functional molecules with unique properties. In contrast to the alkynyl iminium salts derived from cyclic (alkyl)(amino)carbenes (CAACs) that feature only one reversible reduction wave, the isoelectronic cationic CAAC-iminoboryl adducts could be singly and doubly reduced smoothly. Both the resultant neutral radical and anionic azaborataallenes bear NBC-mixed allenic structures. The former radical has a high spin-density of 0.55e at CCAAC carbon, yet exhibits formal boron-centered radical reactivity. The latter azaborataallenes feature the nucleophilic CCAAC center and polar N(δ–)═B(δ+)═C(δ–) unit, and readily undergo nucleophilic substitution, isocyanide insertion, dipolar addition and cycloaddition reactions etc. The N-substituents have been shown to have a significant influence on the solid-state structure, thermal stability, and reactivity of azaborataallenes. This work showcases the allenic BN-unsaturated species as versatile building blocks in organic synthesis.
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