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Redox Active Mesoporous Hybrid Materials by In situ Syntheses with Urea‐linked Triethoxysilylated Phenothiazines
Author(s) -
Zhou Zhou,
Franz Adam W.,
Bay Sarah,
Sarkar Biprajit,
Seifert Andreas,
Yang Piaoping,
Wagener Alex,
Ernst Stefan,
Pagels Markus,
Müller Thomas J. J.,
Thiel Werner R.
Publication year - 2010
Publication title -
chemistry – an asian journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 106
eISSN - 1861-471X
pISSN - 1861-4728
DOI - 10.1002/asia.201000098
Subject(s) - mesoporous material , phenothiazine , hybrid material , electron paramagnetic resonance , molecule , intermolecular force , redox , spectroscopy , adsorption , in situ , infrared spectroscopy , ultraviolet visible spectroscopy , chemistry , materials science , urea , combinatorial chemistry , polymer chemistry , inorganic chemistry , organic chemistry , catalysis , medicine , nuclear magnetic resonance , quantum mechanics , pharmacology , physics
Triethoxysilyl functionalized phenothiazinyl ureas were synthesized and immobilized by in situ synthesis into mesoporous hybrid materials . The designed precursor molecules influence the structure of the final materials and the intermolecular distance of the phenothiazines. XRD and N 2 adsorption measurements indicate the presence of highly ordered two‐dimensional hexagonally structured functional materials , while the incorporation of the organic compounds in the solid materials was proved by means of 13 C and 29 Si solid state NMR spectroscopy as well as by FT‐IR spectroscopy. Upon oxidation with (NO)BF 4 or SbCl 5 , stable phenothiazine radical cations were generated in the pores of the materials, which was detected by means of UV/Vis, emission, and EPR spectroscopies.