The increased mechanical flexibility, solution processability, ease of fabrication, and high Verdet constants have made organic Faraday rotators a promising alternative to conventional inorganic magneto-optical (MO) materials. Despite this, organic Faraday rotators have not been developed to address near-infrared (NIR) MO applications, limiting their device applications. Here, we describe a three-step synthesis and MO characterization of a fused octapyrrolyl cyclooctatetraene (FOPCOT) which exhibits a record high Verdet constant of a small molecule in the NIR-II region. Notably, the cyclooctatetraene core is constructed in a three-step one-pot reaction whereby a N,N′-dipyrrolyl acetylene is generated and immediately reacted with Rosenthal’s complex to produce the corresponding zirconacycle intermediate in situ. The cascade is completed with a copper-mediated transmetalation that reductively eliminates to yield the octapyrrolyl cyclooctatetraene. This transformation offers a distinct alternative to conventional methods for pyrrole incorporation into polycyclic aromatic hydrocarbons. Stoichiometric oxidation with AgPF6 affords the oxidized analogues FOPCOT•+ and FOPCOT2+, which display strong optical absorptions at 1743 and 1198 nm, respectively. Magnetic circular dichroism study on spin-coated thin films of FOPCOT2+ yielded a maximum Verdet constant of −2.5 × 105 deg T–1 m–1 at 1224 nm.

The first crystalline diradical dication [9]CPP2•2+ was successfully synthesized via an oxidation reaction under the support of weakly coordinating anion. Both experimental and theoretical analyses c...

Photoswitching molecules like the azoarenes have myriad potential applications, ranging from energy storage to targeted drug delivery. Upon irradiation, azoarenes convert from an E-form to a Z-form. T...

This review presents recent advances in the chemistry of expanded helicenes, defined as helicenes containing linearly fused benzene rings, as novel aromatic compounds. This review begins with a summa...

Cyclo[N]carbons, molecular rings consisting solely of N carbon atoms, have previously been studied in the gas phase and on surfaces at cryogenic temperatures, but they are generally considered too rea...

Two distorted nanographenes combining helicenes and a fluoranthene unit within their polycyclic scaffolds were synthesized. Their structural and electronic properties were elucidated by various spectr...

This study presents a molecular design strategy for bright NIR-II fluorophores by addressing fluorescence quenching and low absorption in aggregates. Through structural optimization of donor-acceptor...

A new class of curved, chiral polycyclic aromatic hydrocarbon emerges from the fusion of indeno[2,1-c]fluorene and quasi[8]circulene motifs. These redox-active, antiaromatic scaffolds offer great syn...

The synthesis and properties of a fused Koelsch radical derivative incorporating a seven-membered ring are described. The strategic incorporation of a heptagon into the extended π-system was hypothesi...

We synthesized a series of carbon nanohoops, [n]CPP-BODIPY (n = 6, 7, and 9), by embedding boron dipyrromethene (BODIPY) dye into cycloparaphenylene scaffolds. Due to the unique size effect and intra...

Silver-mediated phosphacyclic ring expansion with strategic placement of phosphorus and dimethyl acetylenedicarboxylate (DMAD) on Vat Orange 3 was carried out. The target compounds possess narrow HOMO...

Celebrating the molecule that changed the world

Chiral π-conjugated molecules hold great potential for applications in spin-selective organic semiconductors and chiroptical electronic devices that respond to circularly polarized light. Their perfor...

High quantum yields and dissymmetry factors are key to enhancing the chiroptical properties of [n]helicene-functionalized polycyclic aromatic hydrocarbons for the development of circularly polarized materials. In a two-step synthesis, a C2-symmetric perylene-embedded double [5]helicene was obtained through Suzuki–Miyaura cross-coupling and base-catalyzed condensation. With a configurational stability of 23 kcal mol–1, the short-lived enantiomers were separated using chiral HPLC. Compared to pristine [5]helicene, the compound shows enhanced (chir)optical properties with a quantum yield of 0.7, a gabs of up to 8.8 × 10–3, and a glum of 0.7 × 10–3.