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Polarity Control at Interfaces: Quantifying Pseudo‐solvent Effects in Nano‐confined Systems
Author(s) -
SingappuliArachchige Dilini,
Manzano J. Sebastian,
Sherman Lindy M.,
Slowing Igor I.
Publication year - 2016
Publication title -
chemphyschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.201600740
Subject(s) - solvatochromism , polarity (international relations) , nile red , mesoporous silica , mesoporous material , chemistry , solvent , nanoparticle , chemical physics , photochemistry , chemical engineering , pyrene , adsorption , fluorescence , materials science , catalysis , nanotechnology , organic chemistry , biochemistry , physics , quantum mechanics , engineering , cell
Surface functionalization controls local environments and induces solvent‐like effects at liquid–solid interfaces. We explored structure–property relationships between organic groups bound to pore surfaces of mesoporous silica nanoparticles and Stokes shifts of the adsorbed solvatochromic dye Prodan. Correlating shifts of the dye on the surfaces with its shifts in solvents resulted in a local polarity scale for functionalized pores. The scale was validated by studying the effects of pore polarity on quenching of Nile Red fluorescence and on the vibronic band structure of pyrene. Measurements were done in aqueous suspensions of porous particles, proving that the dielectric properties in the pores are different from the bulk solvent. The precise control of pore polarity was used to enhance the catalytic activity of TEMPO in the aerobic oxidation of furfuryl alcohol in water. An inverse relationship was found between pore polarity and activity of TEMPO in the pores, demonstrating that controlling the local polarity around an active site allows modulating the activity of nanoconfined catalysts.