Exchange of boryl ligand substituents in Os[B(OEt) 2]Cl(CO)(PPh 3) 2

Abstract

Reaction between Os[B(OEt) 2]Cl(CO)(PPh 3) 2 and 1,2-ethanediol in the presence of Me 3SiCl (1 equivalent) leads to the tethered boryl complex, ▪Cl(CO)(PPh 3) 2 ( 1), in which one ethoxy substituent on the boryl ligand is exchanged with one hydroxy group of the 1,2-ethanediol leaving the other OH group available to coordinate to osmium, so giving a six coordinate complex. This formulation is confirmed by crystal structure determination. The same reactants, but with 2 equivalents of Me 3SiCl, lead to the yellow, coordinatively unsaturated complex, Os ▪Cl(CO)(PPh 3) 2 ( 2). Complex ( 2) adds CO to give Os ▪Cl(CO) 2 (PPh 3) 2 ( 3). Crystal structure determinations of 2 and 3 reveal a very marked difference in the Os–B distances found in the five coordinate complex 2 (2.043(4) Å) and the six coordinate complex 3 (2.179(7) Å). In a reaction similar to that used for forming 2 but with 1,3-propanediol replacing 1,2-ethanediol, the product is Os ▪Cl(CO)(PPh 3) 2 ( 4). The crystal structure for 4 is also reported.