2417-69-8Relevant articles and documents
1-(4-Alkyloxybenzyl)-3-methyl-1H-imidazol-3-ium organic backbone: A versatile smectogenic moiety
Dobbs, William,Douce, Laurent,Heinrich, Benoit
experimental part, (2010/04/22)
The merger of ionic liquid and liquid crystal fields, obtained by using the imidazolium ring as a common element, has allowed us to tailor a new set of materials which associate specific functionalities. These functionalities are consequences of the origi
Positional and charged effects of heterocyclic N atoms on mesogenic properties of stilbazoles and analogous N-oxides
Lin, Hong-Cheu,Lai, Long-Li,Lin, Yu-Sheng,Tsai, Chiitang,Chen, Rong-Chi
, p. 55 - 71 (2007/10/03)
The synthesis and the phase behavior of stilbazoles and corresponding N-oxides containing different positions of heterocyclic N atoms, i.e. trans-2′-, 3′-, 4′- stilbazoles and their N-oxides, are reported. Their phase transition temperatures and the mesog
Alkoxylated p-phenylenevinylene oligomers: Synthesis and spectroscopic and electrochemical properties
Ndayikengurukiye, Henri,Jacobs, Sven,Tachelet, Wim,Van Der Looy, Johan,Pollaris, Anne,Geise, Herman J.,Claeys, Magda,Kauffmann, Jean M.,Janietz, Silvia
, p. 13811 - 13828 (2007/10/03)
Twenty-one n-alkoxy substituted phenylenevinylene oligomers were synthesized, varying in size, number and position of the OR groups. IR,MS and solubility data are presented. NMR measurements provided the molecular structure as well as information about conformations and molecular dynamics. UV and of cyclic voltammetric data give correlations of chemical structure (number and position of OR substituents) with separate HOMO and LUMO energies.
