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This study explores the dynamic self-assembly and disassembly of hypervalent iodine-based macrocycles (HIMs) guided by secondary bonding interactions. The reversible disassembly and reassembly of HIMs are facilitated through anion binding via the addition of tetrabutylammonium (TBA) salts or removal of the anion by the addition of silver nitrate. The association constants for HIM monomers with TBA(Cl) and TBA(Br) are calculated and show a correlation with the strength of the iodine–anion bond. A unique tetracoordinate hypervalent iodine-based compound was identified as the disassembled monomer. Last, the study reveals the dynamic bonding nature of these macrocycles in solution, allowing for rearrangement and participation in dynamic bonding chemistry. 

Novel boron dipyrromethene (BODIPY) photocages release a strong organobase, tetramethylguanidine, with record efficiency upon green light exposure to enable rapid anionic step-growth polymerizations. 

Novel coumarinylmethyl photobase generators (PBGs) that induce polymerization upon exposure to visible light are described. PBG composition governs anionic vs. radical mechanisms, which will lead to disparate polymer topologies and properties. 

Isomerically pure 5,11-dibromo-2,8-dihexylanthra[2,3- b :76- b ′]dithiophene, a brominated analog of anthracenedithiophene (ADT), was prepared and utilized for a palladium catalyzed cyclopentannulation reaction with 3,3′-dimethoxy-phenylacetylene to give cyclopentannulated ADT (CP-ADTs). A further Scholl cyclodehydrogenation reaction gave contorted aromatics with large splay angles, low optical gaps, and low LUMOs. 

Abstract The use of visible light to drive polymerizations with spatiotemporal control offers a mild alternative to contemporary UV‐light‐based production of soft materials. In this spectral region, photoredox catalysis represents the most efficient polymerization method, yet it relies on the use of heavy‐atoms, such as precious metals or toxic halogens. Herein, spin‐orbit charge transfer intersystem crossing from boron dipyrromethene (BODIPY) dyads bearing twisted aromatic groups is shown to enable efficient visible light polymerizations in the absence of heavy‐atoms. A ≈5–15× increase in polymerization rate and improved photostability was achieved for twisted BODIPYs relative to controls. Furthermore, monomer polarity had a distinct effect on polymerization rate, which was attributed to charge transfer stabilization based on ultrafast transient absorption and phosphorescence spectroscopies. Finally, rapid and high‐resolution 3D printing with a green LED was demonstrated using the present photosystem.