Tethered Boryl and Base-Stabilized Borylene Osmium Complexes from the Reaction of Os(BCl2)Cl(CO)(PPh3)2 with 2-Aminopyridine

• Published in: Organometallics 2002-10, Vol.21 (22), p.4862-4872
• Main Authors: Rickard, Clifton E. F, Roper, Warren R, Williamson, Alex, Wright, L. James
• Format: Article
• Language: English
• ISSN: 0276-7333; 1520-6041
• DOI: 10.1021/om0203431

Reaction between Os(BCl2)Cl(CO)(PPh3)2 and 2-aminopyridine in the presence of ethanol leads to a mixture of two products. In the first, replacement of one chloride on the dichloroboryl ligand through condensation with the amino function and coordination of the pyridine nitrogen atom to osmium leads to the tethered, six-coordinate boryl complex (1). In the second, the direction of addition of the aminopyridine is reversed, leading to the tethered, pyridine-stabilized borylene complex (2). The five-membered chelate ring formed in 1 is stable and persists through reactions involving replacement of chloride both at osmium and at boron. When 1 is treated with NaBr or with NaBH4, replacement of chloride at osmium occurs exclusively, leaving the B−Cl bond intact and giving (3) or (4), respectively. Replacement of chloride at boron requires the assistance of AgSbF6, and the following derivatives of 1 have been characterized:  (5) (with 1 equiv of AgSbF6), (6) (with 2 equiv of AgSbF6 in MeCN), and (7) (with 2 equiv of AgSbF6 and CO in the presence of EtOH). Reaction between Os(BCl2)Cl(CO)(PPh3)2 and 2-(methylamino)pyridine leads to only one product, the tethered, pyridine-stabilized borylene complex (8). Four further pyridine-stabilized borylene complexes have been derived from 8. Reaction of 8 with NaBH4 gives (9), and 9 is hydrolyzed by water to (10). Ethanol converts 8 to (11), and 2 equiv of AgSbF6 in acetonitrile converts 8 to (12). Crystal structures of complexes 2−6 and 9 are reported.