Doubly Bridged Anthracenes: Blue Emitters for OLEDs.

The photooxidative stability of a series of doubly bridged anthracenes was evaluated after their preparation via twofold macrocyclization of a bis(resorcinyl)anthracene. Lightfastness correlates with the energy levels of the highest occupied molecular orbital (HOMO), resulting in superior stability of the tetraesters compared to the tetraethers. The lengths and steric demand of the linker only plays a minor role for the ester-based compounds, which can be prepared in reasonable yields and thus tested in proof-of-concept organic light-emitting diodes. Double ester-bridging allows deep blue electro-luminescence, highlighting the importance of the choice of the functional groups used for macrocyclization.

Efficient Intramolecular Singlet Fission in Spiro-Linked Heterodimers.

We investigate intramolecular singlet fission (iSF) of spiro-linked azaacene heterodimers by time-resolved spectroscopy and quantum chemical calculations. Combining two different azaacenes through a nonconjugated linker using condensation chemistry furnishes azaacene heterodimers. Compared to their homodimers, iSF quantum yields are improved at an extended absorption range. The driving force of iSF, the energy difference ΔEiSF between the S1 state and the correlated triplet pair 1(TT), is tuned by the nature of the heterodimers. iSF is exothermic in all of the herein studied molecules. The overall quantum yield for triplet exciton formation reaches approximately 174%. This novel concept exploits large energy differences between singlet electronic states in combination with spatially fixed chromophores, which achieves efficient heterogeneous iSF, if the through-space interaction between the chromophores is minimal.

Etheno-bridged Azaacene Spiro Dimers.

We present the synthesis of two sets of spiro-connected azaacene dimers. Their geometry and electronic coupling are critically determined by a secondary linker, i. e., an etheno- and an ethano-bridge. The core fragment of the etheno-bridged dimer corresponds to a conformationally locked cis-stilbene. Optoelectronic properties, single crystal X-ray structures and stability with respect to oxidation of the conjugated and non-conjugated dimers are reported and compared. The conjugated dimers exhibit smaller optical gaps and bathochromically shifted absorption maxima, but are prone to unexpected oxygen addition, dearomatizing one of the azaacene substituents.

Diazapentacenes from Quinacridones.

Bis(silylethynylated) 5,7- and 5,12-diazapentacenes were synthesized from cis- and trans-quinacridone using protection, alkynylation and deoxygenation. The solid-state packing of the targets is determined by choice and position of the silylethynyl substituents. The position of the substituents and nitrogen atoms influence the optical properties of the targets.

TIPS-Ethynylated Naphthodiquinoline and Naphthodiacridine: Novel Diazabisacenes.

The synthesis of two diazabisacenes is reported. A bisboronated naphthalene was Suzuki-coupled to substituted ethyl nicotinates, then cyclized by intramolecular Friedel-Crafts acylation. The resulting diketones were alkynylated and reduced to give the title compounds, bis(TIPS-ethynyl)-substituted naphtha[1,8-gh:5,4-g'h']diquinoline and naphtho[1,8-bc:5,4-b'c']diacridine. Nitrogen incorporation stabilizes the bisacenes with respect to oxidation compared to their consanguine nonaza analogs.

Cata-Annulated Azaacene Bisimides.

Ultra-electron-deficient azaacenes were synthesized via Buchwald-Hartwig coupling of ortho-diaminoarenes with chlorinated mellophanic diimide followed by oxidation of the intermediate N,N'-dihydro compounds with MnO2 or PbO2 . The resulting cata-annulated bisimide azaacenes have ultrahigh electron affinities with first reduction potentials as low as -0.35 V recorded for a tetraazapentacene. Attempts to prepare a tetrakis(dicarboximide)tetraazaheptacene resulted in the formation of a symmetric butterfly dimer.

(Aza)Pentacenes Clipped into a Ring: Stabilization of Large (Aza)Acenes.

A doubly alkylene bridged 6,13-diphenylpentacene and analogously bridged azapentacenes were prepared; they are persistent. The doubly bridged azapentacenes display superior photochemical, oxidative and thermal stabilities compared to azapentacenes protected by bis(TIPS-ethynyl)-substituents-clipping an azaacene into a large ring is a viable complement in stabilization.

Azaacene Dimers: Acceptor Materials with a Twist.

The synthesis of five spiro-linked azaacene dimers is reported and their properties are compared to that of their monomers. Dimerization quenches emission of the longer (≥(hetero)tetracenes) derivatives and furnishes amorphous thin-films, the absorption is not affected. The larger derivatives were tested as acceptors in bulk-heterojunction photovoltaic devices with a maximum power conversion efficiency of up to 1.6 %.

5,7,12,14-Tetrafunctionalized 6,13-Diazapentacenes.

The synthesis, property evaluation, and single crystal X-ray structures of four 5,7,12,14-tetrafunctionalized diazapentacenes are presented. The synthesis of these compounds either starts from tetrabromo-N,N-dihydrodiazapentacene or from a diazapentacene tetraketone. Pd-catalyzed coupling or addition of a lithium acetylide gave the precursors that furnish, after further redox reactions, the diazapentacenes as stable crystalline materials. The performance of the tetraphenyl-substituted compound as n-channel semiconductor was evaluated in organic field effect transistors.

N-Acenoacenes.

The syntheses of new, fourfold alkynylated tetraazaacenoacenes (tetraazaanthracenoanthracene, tetraazatetracenotetracene and tetraazapentacenopentacene) are reported. This novel heteroacenoacene motif exhibits surprisingly strong electronic coupling between its constituting diazaacene units.

Different Selectivities in the Insertions into C(sp2 )-H Bonds: Benzofulvenes by Dual Gold Catalysis Competition Experiments.

An unprecedented, often almost quantitative access to tricyclic aromatic compounds by dual gold catalysis was developed. This synthetic route expands the scope of benzofulvene derivatives through a C(sp2 )-H bond insertion in easily available starting materials. The insertion takes place with an exclusive chemoselectivity with respect to the competing aromatic C-H positions. A bidirectional synthesis with two competing ortho-aryl C-H bonds in the selectivity-determining step also shows perfect selectivity; this result is explained by a computational investigation of the two conceivable intermediates. The intramolecular competition of two non-equivalent aryl C-H bonds with a benzylic methyl group also showed perfect selectivity.

Structure Set in Stone: Designing Rigid Linkers to Control the Efficiency of Intramolecular Singlet Fission.

Research on materials facilitating efficient singlet fission (SF) is driven by a possible reduction of thermalization losses in organic photovoltaic devices. Intramolecular SF (iSF) is in this context of special interest, as the targeted modification of either chromophores or linkers enables gradual variations of molecular properties. In this combined synthetic, spectroscopic, and computational work, we present and investigate nine novel spiro-linked azaarene dimers, which undergo efficient iSF with triplet yields up to 199%. Additional molecular braces enhance the rigidity of these tailor-made dimers (TMDs), resulting in great agreement between crystal structures and predicted optimal geometries for iSF in solution. Regardless of the employed chromophores and linkages, the dynamics of all nine TMDs are perfectly described by a unified kinetic model. Most notably, an increase in the orbital overlap of the π-systems by decreasing the twist angle between the two chromophores does not only increase the rate of formation of the correlated triplet pair but also further promotes its decorrelation. This new structure-function relationship represents a promising strategy toward TMDs with high triplet lifetimes to be utilized in optoelectronic devices.