Morphology-driven absorption and emission colour changes in liquid-crystalline, cyclometallated platinum(ii) complexes

Platinum(II) complexes of 1,3-bis(2-pyridyl)benzene containing two alkyl chains are unexpectedly mesomorphic and capable of changing absorption and emission colour depending on the phase obtained after thermal treatment

Slit/Robo Signaling Regulates Cell Fate Decisions in the Intestinal Stem Cell Lineage of Drosophila

SummaryIn order to maintain tissue homeostasis, cell fate decisions within stem cell lineages have to respond to the needs of the tissue. This coordination of lineage choices with regenerative demand remains poorly characterized. Here, we identify a signal from enteroendocrine cells (EEs) that controls lineage specification in the Drosophila intestine. We find that EEs secrete Slit, a ligand for the Robo2 receptor in intestinal stem cells (ISCs) that limits ISC commitment to the endocrine lineage, establishing negative feedback control of EE regeneration. Furthermore, we show that this lineage decision is made within ISCs and requires induction of the transcription factor Prospero in ISCs. Our work identifies a function for the conserved Slit/Robo pathway in the regulation of adult stem cells, establishing negative feedback control of ISC lineage specification as a critical strategy to preserve tissue homeostasis. Our results further amend the current understanding of cell fate commitment within the Drosophila ISC lineage

Luminescence modulation in liquid crystalline phases containing a dispiro[fluorene-9,11′-indeno[1,2-b]fluorene-12′,9′′-fluorene] core

International audienceA luminescent liquid crystalline compound containing a bulky dispiro[fluorene-9,11′-indeno[1,2-b]fluorene-12′,9′′-fluorene] has been designed and synthesized by di-substitution of a bromo derivative with N-(4-ethynylphenyl)-3,4,5-tris(hexadecyloxy)benzamide fragments. This di-substituted 3π-2spiro derivative forms stable and well-organized mesophases over large temperature ranges. Combination of DSC, POM and SAXS analyses has revealed the formation of a lamellar mesophase between 60 and 150 °C followed by another mesophase with a 2-dimensional lattice of rectangular symmetry that remains up to the isotropization point near 225 °C. In the original molecular packing model deduced from SAXS, the tert-butyl terminal groups fill the centre of hollow columns constituted by both the dihydro(1,2-b)indenofluorene and benzamide fragments and separated from each other by the surrounding aliphatic tails. The merging of the columns yielding the lamellar phase turned out to be governed by the dynamics of both, the micro-phase segregation process and the network of hydrogen bonds. In the various mesomorphic states and in solution, a strong luminescence was observed. The emission spectrum however depends on temperature and drastically changes between both mesophases and the isotropic liquid. In particular, a strong modulation of the emission wavelength occurs at the isotropic to 2D phase transition. This luminescence modulation results from an enhanced contribution of the vibronic peaks at higher energies in the emission profile. The compound was also found to be soluble in 5CB and was integrated in a guest-host LC cell, allowing efficient modulation of the photoluminescence polarization, in the presence or absence of an electrical field

Synthesis of alternating metallocopolymers by chiral recognition

International audienceWe report the synthesis of chiral enantiopure polytopic bridging ligands, which may lead to the formation of metallosupramolecular polymers with zinc (II) as metal linker. We show that chiral C2‐symmetric bisoxazoline ligands are useful moieties to efficiently generate heterochiral complexes and thus polymeric entities. The corresponding metallopolymers were further characterized by powder X‐ray diffraction (PXRD) to obtain information on the level of crystallinity of our different metallopolymers

Room‐Temperature Columnar Mesophases in Triazine–Gold Thiolate Metal–Organic Supramolecular Aggregates

Producción CientíficaSupramolecular mono‐ and dinuclear liquid‐crystalline gold(I) aggregates have been synthesized by means of hydrogen bond interactions of 2,4,6‐triarylamino‐1,3,5‐triazine with thiolate moities of gold metalloacids [Au(PR3)(SC6H4COOH)] or [μ‐(binap){Au(SC6H4COOH)}2], in 1:1 and 2:1 molar ratio, respectively. All of the supramolecular aggregates display a stable columnar hexagonal mesophase (Colh) at room‐temperature. The supramolecular arrangement within the columns consists of the one‐dimensional stacking of triazine units, with the core of the attached metallic thioacid fragments acting as the fourth branch. The phosphine‐containing moieties of the metallic thioacid protrude out in the aliphatic continuum. These complexes do not show metallophilic interactions, but this strategy appears very promising for the future design of room‐temperature LC mesophases containing interacting metallic fragments.Ministerio de Ciencia e Innovación (Proyect CTQ2011–25137)Junta de Castilla y León (programa de apoyo a proyectos de investigación – Ref. VA248 A11‐2

Diphenylphosphinobenzoic Acids as Linkers in [2,4,6– {(C10H21O)3C6H2NH}3C3N3] Triazine Adducts with Metal Complex, which Self–Organize into Room Temperature Hexagonal Columnar Mesophases

Producción CientíficaDisplacement of a labile ligand from appropriate precursor complexes by 2- or 4-PPh2C6H4COOH yields neutral gold(I) and gold(III) [AuXn(PPh2C6H4COOH)] (n = 1, X = Cl; n = 3, X = C6F5), cationic gold(I) [Au(PPh2C6H4COOH)2](CF3SO3), and neutral chromium(0) [Cr(CO)5(PPh2C6H4COOH)] metallo-organic acids. [AuCl(4-PPh2C6H4COOH)], [Au(C6F5)3(4-PPh2C6H4COOH)], and [Cr(CO)5(2-PPh2C6H4COOH)] have dimeric structures with typical carboxylic H-bond bridges, whereas [Au(C6F5)3(2-PPh2C6H4COOH)] gives a monomeric species with the carboxylic acid H bonded to cocrystallized solvent molecules. All gold-containing acids are emissive at 77 K in the range 404-520 nm and some of them also at 298 K with emission maxima from 441 to 485 nm. Reaction of these acid metal complexes with the triazine mesogen 2,4,6-{(C10H21O)3C6H2NH}3C3N3 affords some new hydrogen-bonded gold(I) and chromium(0) supramolecular adducts, but the related gold(III) complexes do not form adducts. The 4-diphenylphosphinobenzoic adducts display a columnar hexagonal mesophase (Colhex) at room temperature, with a random one-dimensional stacking of the pseudo-discoid triazine-metallo-organic adducts into columns, where the metallo-phosphinoacid fragments act as the fourth branch of the trifold triazine core. The 2-diphenylphosphinobenzoic mixtures do not display mesophases, as they appear in the X-ray studies as mixtures of the triazine and the metallo-phosphinoacid complex. The aggregates are luminescent at 77 K, with emission maxima in the range 419-455 nm.Ministerio de Economía, Industria y Competitividad (CTQ2011–25137)Junta de Castilla y León (programa de apoyo a proyectos de investigación – Ref. VA302U13

Functionalization of biphenylcarbazole (CBP) with siloxane-hybrid chains for solvent-free liquid materials

Funding: This research was funded by the French National Research Agency (ANR) through the Programme d’Investissement d’Avenir under contract ANR-11-LABX-0058-NIE within the Investissement d’Avenir program ANR-10-IDEX-0002-02 and was supported by Khalifa University through the grant RC2-2018-024.We report herein the synthesis of siloxane-functionalized CBP molecules (4,4′-bis(carbazole)-1,1′-biphenyl) for liquid optoelectronic applications. The room-temperature liquid state is obtained through a convenient functionalization of the molecules with heptamethyltrisiloxane chains via hydrosilylation of alkenyl spacers. The synthesis comprises screening of metal-catalyzed methodologies to introduce alkenyl linkers into carbazoles (Stille and Suzuki Miyaura cross-couplings), incorporate the alkenylcarbazoles to dihalobiphenyls (Ullmann coupling), and finally introduce the siloxane chains. The used conditions allowed the synthesis of the target compounds, despite the high reactivity of the alkenyl moieties bound to π-conjugated systems toward undesired side reactions such as polymerization, isomerization, and hydrogenation. The features of these solvent-free liquid CBP derivatives make them potentially interesting for fluidic optoelectronic applications.Peer reviewe