57666-61-2Relevant academic research and scientific papers
High-Density Noncovalent Functionalization of DNA by Electrostatic Interactions
Chen, Wei,Gerasimov, Jennifer Y.,Zhao, Pei,Liu, Kai,Herrmann, Andreas
, p. 12884 - 12889 (2015)
Preserving DNA hybridization in organic solvents could someday serve to significantly extend the applicability of DNA-based technologies. Here, we present a method that can be used to solubilize double-stranded DNA at high concentrations in organic media.
Synthesis, mesomorphic and dielectric properties of 4-(cyanomethoxy)phenyl 4-alkoxybenzoates, 4-(cyanomethoxy)-4′-alkoxyazo- and -azoxybenzenes
Kuvshinova,Burmistrov,Novikov,Litov,Aleksandriiskii,Koifman
, p. 615 - 620 (2014/07/08)
Preparation methods were developed for homologs of 4-(cyanomethoxy)phenyl 4-alkoxybenzoates (C7, C8, C9), 4-(cyanomethoxy)-4′-alkoxyazo (C2, C3, C 6), -azoxybenzenes (C3, C6) whose composition and structure were proved by elemental analysis and 1H NMR spectra. 4-(Cyanomethoxy) group destabilizes the mesophase, consequently, only four among the compounds obtained exhibit the thermotropic nematic mesomorphism.
Effect of Molecular Structure on Mesomorphism. 22. Liquid Crystalline 1-Alkanol Derivatives
Griffin, A. C.,Vaidya, S. R.
, p. 85 - 88 (2007/10/02)
Several 1-alkanols having a mesogenic unit attached to the omega-carbon have been prepared.Many of these are liquid crystalline.The nematic mesophase is predominant for these materials.This is presumably due to intermolecular hydrogen-bonding between polar terminal groups such as cyano or nitro and the primary hydroxyl functionality of a proximal molecule.The resulting end-to-end association favors a nematic mesophase.
