13205-49-7Relevant articles and documents
Mirror Symmetry Breaking and Network Formation in Achiral Polycatenars with Thioether Tail
Alaasar, Mohamed,Darweesh, Ahmed F.,Cai, Xiaoqian,Liu, Feng,Tschierske, Carsten
, p. 14921 - 14930 (2021/10/14)
Mirror symmetry breaking in systems composed of achiral molecules is of importance for the design of functional materials for technological applications as well as for the understanding of the mechanisms of spontaneous emergence of chirality. Herein, we report the design and molecular self-assembly of two series of rod-like achiral polycatenar molecules derived from a π-conjugated 5,5’-diphenyl-2,2’-bithiophene core with a fork-like triple alkoxylated end and a variable single alkylthio chain at the other end. In both series of liquid crystalline materials, differing in the chain length at the trialkoxylated end, helical self-assembly of the π-conjugated rods in networks occurs, leading to wide temperature ranges (>200 K) of bicontinuous cubic network phases, in some cases being stable even around ambient temperatures. The achiral bicontinuous cubic Ia (Formula presented.) d phase (gyroid) is replaced upon alkylthio chain elongation by a spontaneous mirror symmetry broken bicontinuous cubic phase (I23) and a chiral isotropic liquid phase (Iso1[*]). Further chain elongation results in removing the I23 phase and the re-appearance of the Ia (Formula presented.) d phase with different pitch lengths. In the second series an additional tetragonal phase separates the two cubic phase types.
Hydrogen bonding liquid crystalline benzoic acids with alkylthio groups: Phase transition behavior and insights into the cybotactic nematic phase
Arakawa, Yuki,Sasaki, Yukito,Igawa, Kazunobu,Tsuji, Hideto
, p. 6514 - 6522 (2017/07/17)
A simple but novel class of hydrogen bonding liquid crystalline benzoic acids with alkylthio (or alkylsulfanyl; SR) groups was established. In general, although it is difficult for laterally non-substituted rod-like molecules with an alkylthio group to form some mesophases, the present molecules exclusively form a nematic (N) regime, owing to spontaneous carboxylic dimerization. It was found that the number of carbons in the alkylthio groups strongly correlated with transition temperatures as well as nematogenic stability: odd-even effects. Even-members displayed wider monotropic and enantiotropic N phases, despite the fact that almost all odd-members showed either none or only monotropic-narrower ones. Interestingly, their thermal transition temperatures were lower compared to those for alkoxy (OR) analogues, on account of the small angle (or large bend) of the C-S-C bond as well as the low electron density on their aromatic ring due to the weak electron donor properties of alkylthio groups. Additionally, in-depth wide-angle X-ray diffraction measurements revealed that an alkylthio analogue exhibited significantly enhanced smectic clusters formed in the N regime (or Ncyb phase) as well as the cluster type close to smectic (Sm) A, in comparison with an alkoxy analogue exhibiting a clear SmC-type cluster. The results indicate that a robust S?S intermolecular interaction for an alkylthio group into a mesogen affects the kind of smectic cluster in the Ncyb phase.
Second-Generation Non-Covalent NAAA Inhibitors are Protective in a Model of Multiple Sclerosis
Migliore, Marco,Pontis, Silvia,Fuentes de Arriba, Angel Luis,Realini, Natalia,Torrente, Esther,Armirotti, Andrea,Romeo, Elisa,Di Martino, Simona,Russo, Debora,Pizzirani, Daniela,Summa, Maria,Lanfranco, Massimiliano,Ottonello, Giuliana,Busquet, Perrine,Jung, Kwang -Mook,Garcia-Guzman, Miguel,Heim, Roger,Scarpelli, Rita,Piomelli, Daniele
supporting information, p. 11193 - 11197 (2016/10/13)
Palmitoylethanolamide (PEA) and oleoylethanolamide (OEA) are endogenous lipid mediators that suppress inflammation. Their actions are terminated by the intracellular cysteine amidase, N-acylethanolamine acid amidase (NAAA). Even though NAAA may offer a new target for anti-inflammatory therapy, the lipid-like structures and reactive warheads of current NAAA inhibitors limit the use of these agents as oral drugs. A series of novel benzothiazole–piperazine derivatives that inhibit NAAA in a potent and selective manner by a non-covalent mechanism are described. A prototype member of this class (8) displays high oral bioavailability, access to the central nervous system (CNS), and strong activity in a mouse model of multiple sclerosis (MS). This compound exemplifies a second generation of non-covalent NAAA inhibitors that may be useful in the treatment of MS and other chronic CNS disorders.
