83789-92-8Relevant academic research and scientific papers
Liquid crystal dimers having vary oxyethylene flexible spacers
Park, Joo Hoon,Singu, Bal Sydulu,Choi, Ok Byung,Lee, Hwan Myung,Lee, Jin Young,Kim, Sung Jo,Cha, Eun Hee,Park, Seon Nam,Kwak, Myeong Heon,So, Bong Keun,Kim, Ran Hee,Lee, Soo Min,Yoon, Kuk Ro
, p. 1 - 6 (2017)
In this article, we are prepared that the liquid crystal dimers have aromatic-ester type mesogenic units or aromatic-Schiff base type mesogonic units and confirmed by 1H-NMR spectrometry. The mesomorphic and optical properties of the resultant dimers were studied by differential scanning calorimetry and polarizing optical microscopy.
Anion, cation and ion-pair recognition by bis-urea based receptors containing a polyether bridge
Gómez-Vega, Jancarlo,Moreno-Corral, Ramón Alfonso,Santacruz Ortega, Hisila,Corona-Martínez, David Octavio,H?pfl, Herbert,Sotelo-Mundo, Rogerio R.,Ochoa-Terán, Adrián,Escobar-Picos, Raymundo Enrique,Ramírez-Ramírez, José Zeferino,Juárez-Sánchez, Octavio,Lara, Karen Ochoa
, p. 322 - 335 (2019)
Two bis-urea type receptors were synthesized containing a polyether bridge and two 4-nitrophenyl groups as chromogenic units, R1 and R2. Molecular recognition studies of receptors towards different tetraalkylammonium and alkali metal salts were carried out in DMSO by UV-Vis and 1H-NMR spectroscopy. The receptors were found to have high affinity for diverse anions and ion-pairs, showing the highest affinities towards the tetramethylammonium and sodium salts. The cation binding ability of the receptors was evidenced by means 1H NMR, mass spectrometric ESI+ studies and the crystal structures of some precursors. Additionally, the molecular modelling at the DFT level of the tetramethylammonium acetate complexes illustrates the potential ion-pair binding ability of the receptors: the anion is recognized through strong hydrogen bonds from the NH─ groups from the two urea sites, while the cation is bound by a combination of cation─π, C-H···O and C-H···π interactions.
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Ji, Liguo,Yang, Zaiwen,Zhao, Yanxia,Sun, Meng,Cao, Liping,Yang, Xiao-Juan,Wang, Yao-Yu,Wu, Biao
, p. 7310 - 7313 (2016/06/09)
Four heteroditopic macrocyclic ligands incorporating both anion coordination sites (tris-urea units) and a cation binding fragment (polyether) were designed for possible application in molecular devices. Sandwich-type phosphate complexes were formed, which display a reversible rotation around the anion upon protonation/deprotonation of phosphate and binding of the cation (Emim+).
ISOCYANATE TERMINATED MACROMER AND FORMULATION THEREOF FOR USE AS AN INTERNAL ADHESIVE OR SEALANT
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Page/Page column 8-9, (2010/07/04)
A novel macromer or mixture thereof is described herein, comprising isocyanatophenyl ether terminal moieties and at least two residues of a water-soluble polymer having a molecular weight ranging from 80 to 10,000 adjacent to the ether group of the isocya
Synthesis and Properties of a New Series of Troegerophanes
Ibrahim, Alhussein A.,Matsumoto, Mutsumi,Miyahara, Yuji,Izumi, Kenji,Suenaga, Masahiko,Shimizu, Nobujiro,Inazu, Takahiko
, p. 209 - 215 (2007/10/03)
A new series of macrocyclic compounds with one or two Troeger base skeletons has been synthesized by condensing mono-, di-, tri-, and teraethyleneglycol bis(p-aminophenoxy) ethers with formalin in the presence of concentrated hydrochloric acid in ethanol at room temperature for 13 days. This simple one-step cyclization provided 19 in remarkably high yield (46%) and 17, 18, and 20 in yields reflecting the strain of the rings and statistical factors. Complexation with lithium thiocyanate was observed for 20, the structure of which was elucidated by X-ray crystallography.
New supramolecular hosts: Synthesis and cation binding studies of novel Troger's base-crown ether composites
Manjula, Alla,Nagarajan, Madhavarao
, p. 11859 - 11868 (2007/10/03)
A simple and straightforward synthesis of a novel class of supramolecular hosts containing the Troger's base moiety is reported. The cation binding properties of these macrocycles were investigated using Cram's picrate extraction method.
