Synthesis, excited state dynamics, and optical characteristics of oligophenyl-based swivel cruciforms in solution and solid state.

Oligophenyl-based swivel cruciforms are an amorphous class of materials for potential use in display applications. In this work, we describe the design, synthesis, and structural and optical properties of a group of chromophores with varying degrees of π-conjugation that produce blue emission and high photoluminescence quantum yields (PLQYs). The swivel cruciforms are branched complexes consisting of two arms, and the relative rotation of these arms is an important factor that determines the optical properties of these systems. The studies reveal that the physical size of the system, that is, the arms, and the presence and position of functional groups results in different degrees of sterical effects. This has a dramatic impact on the interplay between nonradiative and radiative decay of the excited state. For the least π-extended system, control of the excited state decay can be achieved by modifying the properties of the medium through an increase in the viscosity, which is demonstrated accordingly. The data shows that an intramolecular excited state is responsible for the swivel cruciform emission in solution. The character of this "aggregate" and its emission is not dissimilar to an excimer, and we therefore attribute it to an intramolecular excimer. In the solid state, a combination of intra- and intermolecular excimers are the most likely source of the emission. The data also shows that intra molecular excimers can produce a surprisingly high PLQY, when either properties of the medium facilitate this or when functional groups introduce steric hindrance, which subsequently prevents the nonraditive decay through conformational change.

Decoupling 2D inter- and intrachain energy transfer in conjugated polymers.

The dimensionality of conjugated polymer systems plays an important role in energy-transfer processes, and 1D and 2D energy transfer of excitations are typically much slower than that between pi-stacked chains within a 3D polymeric solid. However, whether 2D energy transfer in conjugated polymers occurs mainly along polymer chains (intrachain), or between in-plain-adjacent polymer chains (interchain), has yet to be determined due to the difficulty of experimentally decoupling inter- and intrachain interaction in a 2D polymer system. This can be achieved by incorporating conjugated polymer chains into the planar galleries of layered matrices which sterically hinder polymer aggregation and pi-pi interchain interactions. Here, pristine blue-emitting polyfluorene chains and polyfluorene chains with known concentrations of green-emitting on-chain fluorenone defects are either separately or collectively incorporated into layered SnS(2). X-ray powder diffraction of the composite films confirms incorporation of the polymer chains into the layered galleries. Monitoring the fluorene-to-fluorenone energy transfer as a function of fluorenone concentration and distribution in the layered galleries allows differentiation between inter- and intrachain fluorene-fluorenone energy transfer. It is found that, 2D energy transfer in conjugated polymers follows mainly an interchain process, despite the absence of pi-pi interchain interactions.

Preferential oxidative addition in Suzuki cross-coupling reactions across one fluorene unit.

The Suzuki-type cross-coupling reaction of 2,7-dihalofluorenes with 1 equiv of arylboronic acid and Pd2(dba)3/P(t-Bu3) as a catalyst system is investigated. The exclusive formation of the diarylated coupling product demonstrates that "preferential oxidative addition" is also applicable to fluorene monomers due to a controlled intramolecular motion of the regenerated Pd(0) catalyst across the "large" distance between the 2- and the 7-position of one fluorene monomer.

Solution processable organic field-effect transistors utilizing an alpha,alpha'-dihexylpentathiophene-based swivel cruciform.

A pentathiophene-based swivel cruciform, which allows rotation between the cruciform arms, was synthesized. Homogeneous microcrystalline films were processed from solution, and field-effect transistors utilizing this dimer gave hole mobilities up to 0.012 cm2/V.s.

Synthesis and spectroscopy of an oligophenyl based cruciform with remarkable pi-pi assisted folding.

A facile route has been developed for the preparation of a new family of oligophenyls based on a 2,5,2',5'-tetra-aryl substituted biphenyl structural motif. The cruciform terphenyl dimer 2,5,2',5'-tetra(4-tert-butylphenyl)-1,1'-biphenyl () has been prepared in a two step protocol as a representative of this interesting class of materials. The thermal behaviour of the cruciform was analysed by DSC and shows that forms an amorphous glass when cooled from the isotropic melt. Subsequent heating reveals a glass transition temperature at 130 degrees C. X-Ray single crystal structure analysis of 2,2'-bis(4-tert-butylphenyl)-1,1'-biphenyl () and shows that both these molecules with a quater-phenyl substructure adopt a folded solid-state structure. Examining the (1)H NMR spectra of and reveals that the interactions that induce this folding in the solid-state are sufficiently strong to bias foldamer formation also in solution. Consequently, it is reasonable to assume that the folded conformation within the lattice is due to intramolecular pi-pi interaction rather than being imposed by crystal packing. The optical properties of the cruciform terphenyl dimer are discussed relative to the linear analogue 1,4-bis(4-tert-butylterphenyl)benzene ().

Semiconducting polyfluorenes with electrophosphorescent on-chain platinum-salen chromophores.

The synthesis of statistical fluorene-type copolymers with on-chain Pt-salen phosphorescent units and their use in electrophosphorescent OLEDs is reported.