1379653-83-4Relevant academic research and scientific papers
Tuning methyl 4,6-O-benzylidene α-D-glucopyranosides' gelation ability by minor group modifications
Abreu, Marlon F.,Salvador, Vítor T.,Vitorazi, Letícia,Gatts, Carlos E.N.,Dos Santos, Denise R.,Giacomini, Rosana,Cardoso, Sergio L.,Miranda, Paulo C.M.L.
, p. 69 - 78 (2012/07/02)
Ten methyl 4,6-O-benzylidene α-d-glucopyranosides were synthesized for the purpose of studying systematically the effect of small group changes at position 4 of the aromatic ring on the ability to gelate organic solvents. The gelation properties are discussed on the basis of small angle X-ray scattering (SAXS), Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC) measurements, and scanning electron microscopy (SEM) observations. Sol-gel transition temperatures were determined simultaneously by DSC and temperature-dependent FTIR measurements. The current study emphasizes that carbohydrates furnish not only valuable information about structural requirements for organogelator design, but also for molecular assembly systems in general.
