Hydroboration as an Efficient Tool for the Preparation of Electronically and Structurally Diverse N→B‐Heterocycles |
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| Authors: | Markus Grandl Thomas Kaese Anke Krautsieder Dr Yu Sun Dr Frank Pammer |
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| Institution: | 1. Institute of Organic Chemistry II and Advanced Materials, University of Ulm, Albert-Einstein-Allee 11, Ulm, Germany;2. Institut für Anorganische und Analytische Chemie, Goethe-Universit?t Frankfurt, Frankfurt am Main, Germany;3. Fachbereich Chemie, Technische Universit?t Kaiserslautern, Kaiserslautern, Germany |
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| Abstract: | Ladder‐type organoboranes featuring intramolecular N→B coordination have been prepared through hydroboration of a 2‐(ortho‐styryl)pyridine ( PhPy ) with a series of hydroboranes, including 9H‐9‐borabicyclo3.3.1]nonyl (9H‐BBN), BH3 ? THF, HBCl2 ? SMe2, HB(C6F5)2, and a 9H‐9‐borafluorene derivative. The hydroboration reaction results in highly regioselective borylation under mild conditions and gives the products in good to excellent yields. The molecular structure and electronic properties of the obtained boranes have been experimentally investigated in detail, and complemented with DFT calculations to further elucidate the origin of differences in optical and electronic properties. The electron affinity of the conjugated system can be controlled through variation of the borane, while the optical properties are likewise directly linked to the type and molecular structure of the substituents on boron. The broad substrate range shows that this preparative approach is widely applicable to introduce chemically diverse boryl groups into conjugated systems. |
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| Keywords: | boranes density functional calculations hydroboration Lewis pairs n-Type Materials |
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