Polymers that exhibit aggregation‐induced emission (AIE) find use, for example, as cell‐imaging agents and as fluorometric sensors due to their unique optical properties. However, the structural diversity of AIE‐active polymers has not necessarily advanced at the same rate as their applications. In this work, ring‐opening metathesis polymerization is used to synthesize the first example of a polymer (Mn = 61,600 g mol−1, Đ = 1.32) containing boron difluoride hydrazone (BODIHY) heterocycles in its repeating unit. The BODIHY monomer and polymer described absorb and emit in the visible region in solution (λabs = 428 and 429 nm, λem = 528 and 526 nm) and as thin films (λabs = 443 and 440 nm, λem = 535 and 534 nm). Monomer (ΦFilm = 10%) and polymer (ΦFilm = 6%) exhibit enhanced emission as thin films compared to solution (ΦSoln ≤ 1%) as well as AIE upon the addition of water to DMF solutions as a result of restriction of intramolecular motion. Enhancement factors for the monomer and polymer are determined to be 58 and 15, respectively. The title BODIHY polymer exhibited an earlier onset of AIE and enhanced sensitivity to solution viscosity when compared to the parent monomer.

While they are often encountered as reaction intermediates, phosphenium cations are not commonly incorporated into π-conjugated systems. We report the synthesis and characterization of donor-stabilized phosphenium cations supported by pyridylhydrazonide ligands. The preparation of these cations relies on precise control of ligand E-Z isomerism. The heterocycles were treated with a variety of transition metals, with [Rh(COD)Cl] 2 yielding the only well-defined organometallic products. The optoelectronic properties of the phosphenium heterocycles and their transition-metal complexes were examined using UV−vis absorption spectroscopy, cyclic voltammetry, and modeling by density functional theory (DFT). Computations support the description of these compounds as phosphenium cations and corroborate our observation of a weak P−N pyridine bond, which was manifested experimentally as the Rh adducts undergo selective insertion of Rh into the P−N pyridine bond, depending on the substituent at phosphorus. The reported compounds provide a framework for further study of π-conjugated, N,N′-chelated phosphenium cations and their transition-metal adducts.