Hydroboration as an Efficient Tool for the Preparation of Electronically and Structurally Diverse N→B‐Heterocycles. Issue 40 (18th August 2016)

• Record Type: Journal Article
• Authors: Grandl, Markus; Kaese, Thomas; Krautsieder, Anke; Sun, Yu; Pammer, Frank
• Is Part Of: Chemistry. Volume 22:Issue 40(2016)
• Page Start: 14373
• Page End: 14382
• Publication Date: 2016-08-18
• Subjects: boranes -- density functional calculations -- hydroboration -- Lewis pairs -- n-Type Materials; Chemistry -- Periodicals; 540
• DOI: 10.1002/chem.201602458
• Languages: English
• ISSNs: 0947-6539

Abstract

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 9 H ‐9‐borabicyclo[3.3.1]nonyl (9 H ‐BBN), BH3 ⋅ THF, HBCl2 ⋅ SMe2, HB(C6 F5 )2, and a 9 H ‐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. Abstract : Climb the ladder : Regioselective hydroboration of a 2‐( ortho ‐styryl)pyridine gives access to N→B ladder boranes in high yield. This preparative approach allows the introduction of boryl groups with a wide range of structural motifs and electronic properties.