Highly Stereoselective Heterogeneous Diene Polymerization by Co-MFU‑4<i>l</i>: A Single-Site Catalyst Prepared by Cation Exchange

Molecular catalysts offer tremendous advantages for stereoselective polymerization because their activity and selectivity can be optimized and understood mechanistically using the familiar tools of organometallic chemistry. Yet, this exquisite control over selectivity comes at an operational price that is generally not justifiable for the large-scale manufacture of polyfolefins. In this report, we identify Co-MFU-4<i>l</i>, prepared by cation exchange in a metal–organic framework, as a solid catalyst for the polymerization of 1,3-butadiene with high stereoselectivity (>99% 1,4-<i>cis</i>). To our knowledge, this is the highest stereoselectivity achieved with a heterogeneous catalyst for this transformation. The polymer’s low polydispersity (PDI ≈ 2) and the catalyst’s ready recovery and low leaching indicate that our material is a structurally resilient single-site heterogeneous catalyst. Further characterization of Co-MFU-4<i>l</i> by X-ray absorption spectroscopy provided evidence for discrete, tris-pyrazolylborate-like coordination of Co­(II). With this information, we identify a soluble cobalt complex that mimics the structure and reactivity of Co-MFU-4<i>l</i>, thus providing a well-defined platform for studying the catalytic mechanism in the solution phase. This work underscores the capacity for small molecule-like tunability and mechanistic tractability available to transition metal catalysis in metal–organic frameworks