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Molecular assembly and photoluminescence of novel rare earth/inorganic/polymeric hybrid materials with functional covalent linkages
Affiliation:1. IBM Research at Albany Nano-Technology Center, 257 Fuller Road, Albany, NY 12203, USA;2. GLOBALFOUNDRIES USA, 257 Fuller Road, Albany, NY 12203, USA;3. IBM T.J. Watson Research Center, Yorktown Heights, NY 10598, USA;4. Lam Research Corporation, 255 Fuller Road, Albany, NY 12203, USA;5. STMicroelectronics, 257 Fuller Road, Albany, NY 12203, USA;1. School of Materials Science and Engineering, Northeastern University, Shenyang 110004, China;2. College of Sciences, Northeastern University, Shenyang 110004, China
Abstract:In the context, organic polymeric precursor, polyethylene glycol (PEG) was firstly modified by inorganic component of 3-(triethoxysilyl)-propyl isocyanate (TEPIC) to form the inorganic/organic polymeric functional bridge precursor. Subsequently, the corresponding organic/inorganic molecular-based hybrids were assembled to behave the structural polymeric ligands with the two components equipped with covalent bonds. The coupling reagent part is a functional ureasils –NHC(=O)–O–group which is applied to coordinate to RE3+ and further formed Si–O backbones after hydrolysis and polycondensation processes. Furthermore, aromatic carboxylic acids (picolinic acid (HPIC), 2-chlorobenzoic acid (HCBA) and salicylic acid (HSAL)) were used as functional sensitized ligands to coordinate with RE3+(Eu3+, Tb3+ and Dy3+) and resulting in the quaternary rare earth/inorganic/organic polymeric hybrid materials with chemical bond (covalent bonds of –CO–NH– and Si–O, coordination bond of RE–O–C). Luminescence spectra were utilized to characterize the photophysical properties of the obtained hybrid material and the intramolecular energy transfer process took place within these molecular-based hybrids and characteristic emissions of RE3+ have been achieved.
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