Bertrand Donnio

Phosphorescent, Terdentate, Liquid‐Crystalline Complexes of Platinum(II): Stimulus‐Dependent Emission

Liquid crystals shining bright. A highly efficient platinum(II) luminophore is rendered liquid crystalline using a simple and flexible synthetic approach. Ordering in the liquid-crystalline state allows monomer emission when the characteristic for the material is exciplex-like emission. More than that, emission characteristics are subject to tribological control, with the initial state re-obtained by thermal cycling.

Liquid crystalline dendrimers

In recent years, there has been an increasing interest in the field of liquid crystalline dendrimers. Such a fast development is, among other things, driven by the multiple possibilities offered by combining the mesomorphic properties of single mesogenic subunits with the supermolecular and versatile architectures of dendrimers to yield a new class of highly functional materials. The induction and the control of the mesomorphic properties (phase type and stability) in dendrimers can be achieved by a dedicated molecular design which depends on the chemical nature and structure of both the functional groups and the dendritic matrix. In particular, the intrinsic connectivity of the dendrimer such as the multivalency of the focal core and the multiplicity of the branches, both controlling the geometrical rate of growth, or the dendritic generation, plays a crucial role and influences at various stages the subtle relationships between the supermolecular structure and the mesophase structure and stability. In this critical review article, an account of the various types of dendritic systems that form liquid-crystalline mesophases along with a description of the self-organization of representative case-study supermolecules into liquid crystalline mesophases will be discussed. Some basics of thermotropic liquid crystals and dendrimers will be given in the introduction. Then, in the following sections, selected examples including side-chain, main-chain, fullerodendrimers, shape-persistent dendrimers, supramolecular dendromesogens and metallodendrimers, as representative families of LC dendrimers, will be described. In the conclusion some further developments will be highlighted. This review will not cover liquid crystalline hyperbranched and dendronized polymers that might be considered as being somehow less structurally “perfect”. (147 references.)

Luminescent Ethynyl−Pyrene Liquid Crystals and Gels for Optoelectronic Devices

Two functional ethynyl-pyrene derivatives have been designed and synthesized by di- and tetra-substitutions of bromo pyrene derivatives with N-(4-ethynylphenyl)-3,4,5-tris(hexadecyloxy)benzamide fragments. The photoluminescence wavelength of the pyrene core can be tuned by the substitution pattern and the state of matter (solid, solution, gel, or liquid crystal). The disubstituted pyrene derivative 1 is not mesomorphic but produces robust and highly fluorescent gels in DMF, toluene, and cyclohexane. The well-defined fibers and ropes of the gel states were characterized by SEM and laser scanning confocal microscopy, and extended over several micrometers. The gels were integrated as active layers in field-effect transistors, which provided good bulk electron and hole charge mobilities as well as light emission generation. The tetra-substituted pyrene derivative is not a gelator but displays a stable liquid crystalline phase with 2D hexagonal symmetry between 20 and 200 degrees C. The pronounced luminescence properties of the mesophase allow one to observe original mesophase textures with flower-like patterns directly by fluorescence microscopy without crossed-polarizers.

Liquid-crystalline fullerodendrimers

Addition of liquid-crystalline dendrimers onto [60]fullerene led to thermotropic liquid crystals which displayed various types of mesophases, including chiral nematic, smectic B, smectic A and columnar phases. This approach represents an interesting way for the design of self-organized structures based on [60]fullerene, and opens the way to optoelectronic applications for this carbon allotrope, such as for the development of photovoltaic devices and molecular switches.

Liquid Crystalline Dendrimers and Polypedes

The purpose of this review article is to give an account of the various types of dendritic systems that form liquid-crystalline mesophases and to describe the way they are organized within supramolecular organizations. It is shown that tuning of the mesophase structure can be achieved by an appropriate molecular design depending upon the chemical nature of the terminal mesogenic groups, dendritic core and dendrimer generation. The division of the subject in this review is made by the nature of the dendritic scaffold. After a general introduction on dendrimers, supramolecular liquid-crystalline dendrimers are first discussed. Then, a large part of the review is devoted to side-chain liquid-crystalline dendrimers with different chemical skeletons. The section concerning main-chain liquid-crystalline dendrimers is divided into two parts, the willow-like and the octopus dendrimers. Liquid crystals based on other types of dendritic matrices are finally discussed, including shape-persistent dendrimers, metallodendrimers, fullerodendrimers, polypedes and rod-coil block co-dendrimers.

Liquid-crystalline nanoparticles: Hybrid design and mesophase structures

Summary Liquid-crystalline nanoparticles represent an exciting class of new materials for a variety of potential applications. By combining supramolecular ordering with the fluid properties of the liquid-crystalline state, these materials offer the possibility to organise nanoparticles into addressable 2-D and 3-D arrangements exhibiting high processability and self-healing properties. Herein, we review the developments in the field of discrete thermotropic liquid-crystalline nanoparticle hybrids, with special emphasis on the relationship between the nanoparticle morphology and the nature of the organic ligand coating and their resulting phase behaviour. Mechanisms proposed to explain the supramolecular organisation of the mesogens within the liquid-crystalline phases are discussed.

Dendromesogens: liquid crystal organizations of poly(amidoamine) dendrimers versus starburst structures.

A new series of liquid crystalline poly(amidoamine) (PAMAM) dendrimers is described. These dendrimers are made by attaching to the 0-, 1-, 2-, 3-, and 4-generation of PAMAM-terminal promesogenic units that carry two decyloxy chains in the 3- and 4-positions of their peripheral aromatic ring. X-ray diffraction studies show that all the compounds display a hexagonal columnar mesophase. A high density of aliphatic chains imposes a curved interface with the promesogenic units that forces the molecules to adopt a radial conformation, and therefore, the columnar structure. A model for the supramolecular organization of the different generations within the columnar mesophase is proposed based on the variation of some of the structural parameters.

Bending and shaping: cubics, calamitics and columnars

The mesomorphism of a series of complexes of Pd(II), Pt(II) and Ag(I) is discussed and systematic structural variations are highlighted which lead to an appreciation of important factors determining the liquid-crystalline polymorphism of these complexes. Models are proposed for cubic phase formation and the occurrence of an unusual lamellar phase in-between a SmC and a columnar phase is discussed.

Mesomorphic imidazolium salts: new vectors for efficient siRNA transfection.

The preparation of chloride (1(n)) and bromide (2(n)) derivatives of 1-methyl-3-[3,4-bis(alkoxy)benzyl]-4H-imidazolium with n = 6, 12, 16, 18 is described. The two series of salts possess a rich thermotropic mesomorphism, chain-length dependent. Thus, a lamellar smectic A phase, a bicontinuous cubic Ia3d phase, and a columnar hexagonal liquid crystalline mesophase are induced as a function of increasing chain length. The mesomorphic properties were studied by polarizing optical microscopy, differential scanning calorimetry, and X-ray diffraction, and with the support of dilatometry and molecular dynamics, models for the various supramolecular arrangements of the salts are proposed. Such cationic amphiphiles were expected to be candidate molecules to design a new delivery reagent for nucleic acid transfection, particularly for short interfering RNA (siRNA). The use of an RNA interference mechanism, by introduction into cells by transfection of chemically synthesized siRNAs, is a powerful method for gene silencing studies. To exploit the potential of these amphilic imidazolium salts, these molecules were formulated with cohelper lipids and tested for their efficacy to deliver active siRNAs. Our results show high transfection efficacy of our formulated compounds and high silencing efficiency with more than 80% inhibition of the targeted gene at 10 nM siRNA concentration. Taken together our results show the potency of amphiphilic imidazolium salts as a new generation of transfection reagents for RNA interference.

The Quest for Nanoscale Magnets: The example of [Mn12] Single Molecule Magnets

Recent advances on the organization and characterization of [Mn12] single molecule magnets (SMMs) on a surface or in 3D are reviewed. By using nonconventional techniques such as X-ray magnetic circular dichroism (XMCD) and scanning tunneling microscopy (STM), it is shown that [Mn12]-based SMMs deposited on a surface lose their SMM behavior, even though the molecules seem to be structurally undamaged. A new approach is reported to get high-density information-storage devices, based on the 3D assembling of SMMs in a liquid crystalline phase. The 3D nanostructure exhibits the anisotropic character of the SMMs, thus opening the way to address micrometric volumes by two photon absorption using the pump-probe technique. We present recent developments such as µ-SQUID, magneto-optical Kerr effect (MOKE), or magneto-optical circular dichroism (MOCD), which enable the characterization of SMM nanostructures with exceptional sensitivity. Further, the spin-polarized version of the STM under ultrahigh vacuum is shown to be the key tool for addressing not only single molecule magnets, but also magnetic nano-objects.