Polyphosphinoborane Block Copolymer Synthesis Using Catalytic Reversible Chain‐Transfer Dehydropolymerization

Abstract

An amphiphilic block copolymer of polyphosphinoborane has been prepared by a mechanism-led strategy of the sequential catalytic dehydropolymerization of precursor monomers, H₃ B ⋅ PRH₂ (R=Ph, n-hexyl), using the simple pre-catalyst [Rh(Ph₂ PCH₂ CH₂ PPh₂ )₂ ]Cl. Speciation, mechanism and polymer chain growth studies support a step-growth process where reversible chain transfer occurs, i.e. H₃ B ⋅ PRH₂ /oligomer/polymer can all coordinate with, and be activated by, the catalyst. Block copolymer [H₂ BPPhH]₁₁₀ -b-[H₂ BP(n-hexyl)H]₁₁ can be synthesized and self-assembles in solution to form either rod-like micelles or vesicles depending on solvent polarity.