Philippe Leclère

White-Light Emitting Hydrogen-Bonded Supramolecular Copolymers Based on π-Conjugated Oligomers

Three different pi-conjugated oligomers (a blue-emitting oligofluorene, a green-emitting oligo(phenylene vinylene), and a red-emitting perylene bisimide) have been functionalized with self-complementary quadruple hydrogen bonding ureidopyrimidinone (UPy) units at both ends. The molecules self-assemble in solution and in the bulk, forming supramolecular polymers. When mixed together in solution, random noncovalent copolymers are formed that contain all three types of chromophores, resulting in energy transfer upon excitation of the oligofluorene energy donor. At a certain mixing ratio, a white emissive supramolecular polymer can be created in solution. In contrast to their unfunctionalized counterparts, bis-UPy-chromophores can easily be deposited as smooth thin films on surfaces by spin coating. No phase separation is observed in these films, and energy transfer is much more efficient than in solution, giving rise to white fluorescence at much lower ratios of energy acceptor to donor. Light emitting diodes based on these supramolecular polymers have been prepared from all three types of pure materials, yielding blue, green, and red devices, respectively. At appropriate mixing ratios of these three compounds, white electroluminescence is observed. This approach yields a toolbox of molecules that can be easily used to construct pi-conjugated supramolecular polymers with a variety of compositions, high solution viscosities, and tuneable emission colors.

Supramolecular organization in block copolymers containing a conjugated segment: a joint AFM/molecular modeling study

Abstract The solid-state supramolecular organization of block copolymers containing one π-conjugated block and one non-conjugated block is elucidated with a joint experimental and theoretical approach. This approach combines atomic force microscopy (AFM) measurements on thin polymer deposits, which reveal the typical microscopic morphologies, and molecular modeling, which allows one to derive the models for chain packing that are most likely to explain the AFM observations. The conjugated systems considered in this study are based on aromatic building blocks (i.e. phenylene, phenylene ethylene, fluorene, or indenofluorene), substituted with alkyl groups to provide solubility; they are attached to non-conjugated blocks such as polydimethylsiloxane, polyethylene oxide, or polystyrene. Films are prepared from solutions in solvents which are good for both blocks, in order to prevent aggregation processes in solution. Therefore, the morphology observed in the solid state is expected to result mostly from the intrinsic self-assembly of the chains, with little specific influence of the solvent. In such conditions, the vast majority of compounds show deposits made of fibrilar objects. Closer examination of single fibrils on the substrate surface indicates that the objects are ribbon-like, i.e. their width is significantly larger than their height, with typical dimensions of a few tens of nanometers and a few nanometers, respectively. These results suggest that a single type of packing process, governed by the π-stacking of the conjugated chains, is at work in those block copolymers. This prevalence of such a type of packing is supported by the theoretical simulations. Molecular mechanics/dynamics calculations show that the conjugated segments tend to form stable π-stacks. In these assemblies, the block copolymer molecules can organize in either a head-to-tail or head-to-head configuration. The former case appears to be most likely because it allows for significant coiling of the non-conjugated blocks while maintaining the conjugated blocks in a compact, regular assembly. Such supramolecular organization is likely responsible for the formation of the thin, ‘elementary’ ribbons, which can further assemble into larger bundles. The issue of chain packing in fluorene-based systems has been modeled separately, since in these compounds, the alkyl groups attached to sp 3 -hybridized sites inherently accommodate out of the plane of the conjugated backbone, which can disturb the chain packing. Various possibilities of chain packing have been explored, starting from short alkyl substituents and extending the size of the side groups to n -octyl. The calculations indicate that, when in zig-zag planar conformation, linear alkyl side groups can orient in such a way that close π-stacking of the conjugated chains is preserved. In contrast, branched alkyl groups are too bulky to allow close packing of the conjugated backbones to take place. This difference is consistent with the presence or absence of fibrilar structures observed in thin deposits of the corresponding polymers; it can also account for the differences observed in the optical properties.

Oligo(p-phenylenevinylene) peptide conjugates: Synthesis and self-assembly in solution and at the solid-liquid interface

Two oligo(p-phenylenevinylene)-peptide hybrid amphiphiles have been synthesized using solid- and liquid-phase strategies. The amphiliphiles are composed of a pi-conjugated oligo(p-phenylenevinylene) trimer (OPV) which is coupled at either a glycinyl-alanyl-glycinyl-alanyl-glycine (GAGAG) silk-inspired beta-sheet or a glycinyl-alanyl-asparagyl-prolyl-asparagy-alanyl-alanyl-glycine (GANPNAAG) beta-turn forming oligopeptide sequence. The solid-phase strategy enables one to use longer peptides if strong acidic conditions are avoided, whereas the solution-phase coupling gives better yields. The study of the two-dimensional (2D) self-assembly of OPV-GAGAG by scanning tunneling microscopy (STM) at the submolecular level demonstrated the formation of bilayers in which the molecules are lying antiparallel in a beta-sheet conformation. In the case of OPV-GANPNAAG self-assembled monolayers could not be observed. Absorption, fluorescence, and circular dichroism studies showed that OPV-GAGAG and OPV-GANPNAAG are aggregated in a variety of organic solvents. In water cryogenic temperature transmission electron microscopy (cryo-TEM), atomic force microscopy (AFM), light scattering, and optical studies reveal that self-assembled nanofibers are formed in which the helical organization of the OPV segments is dictated by the peptide sequence.

Highly Regular Organization of Conjugated Polymer Chains via Block Copolymer Self-Assembly

The microscopic organization in thin films of block copolymers containing either polyparaphenylene, or polyphenyleneethynylene rigid segments covalently bound to a flexible polydimethylsiloxane or polystyrene sequence was investigated. Atomic force microscopy and theoretical modeling based on molecular mechanics/molecular dynamics calculations were combined. The typical morphology obtained revealed the presence of bright elongated structures.

Characterization of an acrylamide-based dry photopolymer holographic recording material

Recent work on an acrylamide-based photopolymer holographic recording medium is presented. The lifetime of recorded gratings is improved by the addition of cross-linking monomers. Shelf life is also improved. The effects of various constituents of the photosensitive material are studied to determine an optimum composition, and five xanthene dyes are compared as possible sensitizers for the system. With the most sensitive dye and optimum concentrations of the other constituents an improved formulation is presented with high sensitivity and very high diffraction efficiency. The new formulation also works well in reflection mode.

Supramolecular Materials from Benzene-1,3,5-tricarboxamide-Based Nanorods

Telechelic polymers end-capped or copolymerized with the benzene-1,3,5-tricarboxamide (BTA) moiety lead to supramolecular materials. The intrinsic phase segregation of BTA nanorods with an amorphous polymer such as poly(ethylene butylene) results in thermoplastic elastomeric behavior.

Dilution-induced self-assembly of porphyrin aggregates: A consequence of coupled equilibria

The self-assembly of organic molecules has attracted sub-stantialinterest asa bottom-upapproachto createnano-sizedobjects. Their properties depend strongly on the design,arrangement, and number of molecules in the aggregate. Forsupramolecular polymers, the monomers are entirely heldtogether by non-covalent interactions; these interactions aretypically weak, reversible, and highly sensitive to variablessuch as temperature, concentration, and solvent polarity.

Study of ZrN layers deposited by reactive magnetron sputtering

Zirconium nitride films are deposited onto borosilicate wafers by reactive magnetron sputtering. The films are analysed in situ by X-ray photoelectron spectroscopy (XPS). We have studied by XPS the effects of the nitrogen partial pressure (1–100%), the subtract temperature (ambient to 450 °C), and biasing (0–80 W) on the stoichiometry of ZrN films. The N1s peak is composed of three components at 397.2, 396.4 and 395.8 eV in binding energy. These components are correlated with the three existing phases of zirconium nitride (ZrN, Zr3N4 and ZrN2). With an increase of the nitrogen partial pressure, a shift of the Zr3d line to the high binding energy and the increase of the N1s component at 395.8 eV are observed. These observations are explained by the charge transfer between Zr to N which increases with P(N2) as previously described for the Ti–N2 system [1]. The bulk stoichiometry is calculated by Rutherford backscattering and nuclear reaction measurements. The resistivity of the films is measured by the four-point probes technique. The reflectivity of the films are recorded by a spectrophotometer in the IR–Vis range. A correlation between the reflectivity and the resistivity is observed. The roughness of the films is measured by atomic force microscopy. The bias voltage has a great influence on the surface roughness and on the reflectivity of the films. The dependence of the ZrNx films structure and morphology with the discharge parameters is established.

Surface-controlled self-assembly of chiral sexithiophenes

We report on the self-assembly of two enantiomeric sexithiophenes in solution and on surfaces. Circular dichromism of aggregated sexithiophenes and drop-cast films reveals, as expected, mirror image spectra for both enantiomers. The aggregation in thin deposits from sexithiophenes molecularly dispersed in a solution on different types of substrates was investigated by atomic force microscopy (AFM). On graphite, one-dimensional objects (nanowires) are formed while on mica platelets are generated. Remarkably, we found that both enantiomers form left-handed helices on silicon. This observation depends on the hydrophilicity of the silicon. Furthermore, the achiral sexithiophene did not form helical aggregates suggesting that the stereocenter is required to obtain chirality in the fibers.

XPS/AFM study of the PET surface modified by oxygen and carbon dioxide plasmas: Al/PET adhesion

The formation of the interface between aluminium and O2 or CO2 plasma-modified poly(ethylene terephthalate) (PET) has been investigated by X-ray photoelectron spectroscopy (XPS). As demonstrated by the changes in the C 1s, O 1s, and A1 2p core level spectra upon A1 deposition, the metal was found to react preferentially with the original ester, with the plasma-induced carboxyl and carbonyl groups to form interfacial complexes. The phenyl ring at the modified PET surface was seen to be involved in the formation of the interface, but to a lesser extent. This confirms the high reactivity of the oxygen-containing groups towards the deposited A1 atoms. The adhesion between A1 and the plasma-modified PET films was evaluated by means of a 180° peel test. A considerable (up to ten times) improvement in adhesion was achieved by plasma treatment of the PET substrate, but for either plasma gas the adhesion strength was found to depend strongly on the plasma power and treatment time. The results are discussed in term...