Metallacyclobuta‐(2,3)‐diene: A Bidentate Ligand for Stream‐line Synthesis of First Row Transition Metal Catalysts for Cyclic Polymerization of Phenylacetylene
John B. Russell, Debabrata Konar, Taylor M. Keller, Michael R. Gau, Patrick J. Carroll, Joshua Telser, Daniel W. Lester, Adam S. Veige, Brent S. Sumerlin, Daniel J. Mindiola
Abstract
Abstract Described here is a direct entry to two examples of 3d transition metal catalysts that are active for the cyclic polymerization of phenylacetylene, namely, [(BDI)M{κ 2 ‐ C , C ‐(Me 3 SiC 3 SiMe 3 )}] ( 2‐M ) (BDI=[ArNC(CH 3 )] 2 CH − , Ar=2,6‐ i Pr 2 C 6 H 3 ; M = Ti, V ). Catalysts are prepared in one step by the treatment of [(BDI)MCl 2 ] ( 1‐M , M = Ti , V ) with 1,3‐dilithioallene [Li 2 (Me 3 SiC 3 SiMe 3 )]. Complexes 2‐M have been spectroscopically and structurally characterized and the polymers that are catalytically formed from phenylacetylene were verified to have a cyclic topology based on a combination of size‐exclusion chromatography (SEC) and intrinsic viscosity studies. Two‐electron oxidation of 2‐V with nitrous oxide (N 2 O) cleanly yields a [V V ] alkylidene‐alkynyl oxo complex [(BDI)V(=O){κ 1 ‐ C ‐(=C(SiMe 3 )CC(SiMe 3 ))}] ( 3 ), which lends support for how this scaffold in 2‐M might be operating in the polymerization of the terminal alkyne. This work demonstrates how alkylidynes can be circumvented using 1,3‐dianionic allene as a segue into M−C multiple bonds.