Halina Zhylitskaya

Conductive π-conjugated polymers were electrochemically generated from a variety of donor–acceptor pyrroles containing fused perimidine subunits. Alternating oxidative and reductive polarization of these precursors induces multidirectional coupling involving both perimidine and acenaphtho[1,2-c]pyrrole moieties, producing cross-linked polymeric structures. Chemical oxidation experiments and computational analyses of spin densities in the charged pyrrole intermediates indicate that the formation of inter-perimidine linkages occurs prior to pyrrole–pyrrole couplings. In the resulting polymers, a very stable dication state is achievable with the positive charge located on the bis-perimidine linker. These polymers do not show any stable neutral state and can be easily reduced. Cationic and anionic states of these electrogenerated films were investigated in the solid state by UV–vis–NIR and EPR spectroelectrochemistry, assisted by DFT calculations.

Free base, zinc and palladium π-extended porphyrins containing fused naphthalenediamide units were employed as photosensitizers in antimicrobial photodynamic therapy (aPDT). Their efficacy, assessed by photophysical and in vitro photobiological studies on Gram-positive bacteria, was found to depend on metal coordination, showing a dramatic enhancement of photosensitizing activity for the palladium complex.

Oxidative transformation of hexapyrrolylbenzenes into azacoronenes using bromine electrophiles as alternative coupling agents is shown to occur according to a distinct mechanism, different from those proposed for typical high-potential oxidants. It is shown that consecutive cyclizations do not involve brominated intermediates and can be rationalized by assuming a relayed arenium cation attack followed by deprotonation and conjugate elimination. The final cyclization is incompatible with this mechanism and is found to involve double-electrophilic bromination followed by thermal elimination of dibromine. These findings provide insight into the reactivity of sterically congested aromatic systems and may help in designing new methods of C–C bond formation.

Chiral heteroaromatic propellers based on radially π-extended hexapyrrolohexaazacoronenes were obtained in a concise synthesis from suitably functionalized donor–acceptor monopyrroles. To overcome steric hindrance, a new cyclodehydrogenation method was developed, and it uses bromine electrophiles as oxidative coupling agents instead of the commonly employed high-potential oxidants. The new reaction offers high yields of propeller-shaped targets, even for electron-deficient precursors, and shows electrophile-dependent stereoselectivity, with N-bromosuccinimide and dibromine yielding, respectively D₆- and C₂-symmetric products. The propeller azacoronenes are chiral and can be separated into configurationally stable enantiomers. In addition to providing steric bulk, peripheral functionalization considerably affects the electronic properties of the propellers, which exhibit reduced optical and electrochemical band gaps, and a more clearly defined electroreduction behavior.

Versatile π-aromatic building blocks and selective coupling transformations enable rapid assembly of complex electron-deficient molecules, useful as n-type organic semiconductors.,

Recent advances in the chemistry of electron-poor polycyclic aromatic molecules are reviewed with a focus on new structural designs and emerging synthetic methods. We review various classes of building blocks, notably those based on rylene imides, and highlight the application of the most successful C–C bond-forming reactions, e.g., tandem Pd-catalyzed couplings, photocyclizations, and the glyoxylic Perkin condensation. These advances are presented in the context of the electronic properties of the resulting materials, which are of high current interest as n-type organic semiconductors.

1,n-Dipyrrolylalkanes can be efficiently converted into extensively π-conjugated bipyrroles by Pd^II-mediated annulative double C–H activation, and this approach might be further developed into tandem processes involving further cyclization of substituents or oxygenation of pyrrolic α-positions. Herein, the mechanism of these transformations is explored using NMR spectroscopy and DFT calculations. The kinetics of the annulation are found to depend on the conjugation extent and donor–acceptor character of the pyrroles, as well as on substitution and the linker length. Combined experimental and theoretical evidence indicates that a change of the rate-determining step occurs for the most electron-deficient substrates. The unprecedented double α-oxygenation of bipyrroles is found to be a stepwise process, involving α-acetoxylated intermediates.

Pd^II-mediated annulative double C−H activation is shown to efficiently convert 1,n-dipyrrolylalkanes into extensively π-conjugated bipyrroles not accessible by conventional oxidative coupling protocols. This approach is applicable to both electron-rich and electron-deficient systems, and has been further developed into tandem processes involving further cyclization of substituents or oxygenation of pyrrolic α-positions. The new bipyrrole intermediates show enhanced fluorescence as well as tunable optical properties controlled by the alignment of chromophore subunits. Photophysical data, including femtosecond transient absorptions, reveal solvent-induced intramolecular charge transfer in their excited states, dependent on the polarity of the medium.

A hexapyrrolohexaazacoronene derivative containing 37 fused rings, the largest such system to date, was obtained from a naphthalenomonoimide–pyrrole hybrid in a concise and efficient synthesis. This large heterocycle is electron-deficient and shows extended redox activity, spanning at least 13 oxidation levels, but is otherwise chemically stable. Radial expansion of the π system creates a chromophore characterized by strong fluorescence and solvatochromism in the neutral state, and strong near‐infrared absorption in the charged states. Additionally, the enlarged and ruffled aromatic surface supports a unique self‐assembly mode in the crystal, leading to the formation of highly solvated organic clathrates.