15088-70-7Relevant articles and documents
Enantiomeric Recognition of d - And l -Lactate by CEST with the Aid of a Paramagnetic Shift Reagent
Zhang, Lei,Martins, André F.,Zhao, Piyu,Tieu, Michael,Esteban-Gómez, David,McCandless, Gregory T.,Platas-Iglesias, Carlos,Sherry, A. Dean
, p. 17431 - 17437 (2017)
A previous report demonstrated that EuDO3A could be used as an NMR shift reagent for imaging extracellular lactate produced by cancer cells using CEST imaging. In this work, a series of heptadentate macrocyclic YbDO3A-trisamide complexes with δ-chiral car
Synthesis and organogelating behaviour of amino acid-functionalised triphenylenes
Meegan, Jonathan E.,Yang, Xiaofei,Rungsirisakun, Ratana,Cosgrove, Sebastian C.,Bushby, Richard J.,Sadeghpour, Amin,Rappolt, Michael,Brydson, Rik,Ansell, Richard J.
, p. 5922 - 5932 (2017)
Four novel amino acid-functionalised triphenylenes have been prepared with glycine, l-alanine, l-phenylalanine and l-tryptophan ethyl ester side-chains. The glycine derivative is a good gelator of chloroform, the alanine derivative gels ethanol and toluene, and the phenylalanine derivative gels benzene and toluene. The tryptophan derivative does not gel any of the solvents tested, most probably due to its more bulky structure, but forms microspheres by evaporation-induced self-assembly. The self-assembly properties of the π-gelators have been investigated using infrared, UV-absorption and fluorescence spectroscopy, concentration- and temperature-dependent NMR, and X-ray scattering experiments on dried xerogel as well as the wet organogel. The latter experiments suggest the glycine gel in chloroform includes columnar aggregates, with an overall disordered columnar oblique mesophase. These compounds are of interest because of the well-known hole-transporting properties of triphenylene liquid crystals: 1-D columnar assemblies of these compounds may find applications in organic electronic devices.
A 4 - phenyl quinoline compound, preparation method and application thereof (by machine translation)
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Paragraph 0073, (2017/08/31)
The invention discloses a 4 - phenyl quinoline compound, its preparation method and application, the invention of the 4 - phenyl quinoline compound to, its structure (I) shown in the diimmonium: Wherein R1 Is - OH, - Cl, - OCH3 Or -