2006
DOI: 10.1021/cm060664t
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A Novel Approach to Monodisperse, Luminescent Silica Spheres

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Cited by 75 publications
(63 citation statements)
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“…Chen et al [50] also demonstrated that at basic pH, the terminal protonated amine (-NH 3 þ ) group is prone to hydrogen bonding to the Si-O À group of a second APTES molecule. This bond might be strong enough to avoid condensation with other APTES molecules, which was confirmed by a previous study [51].…”
Section: Influence Of the Silica/spions Ratios On Morphologysupporting
confidence: 83%
“…Chen et al [50] also demonstrated that at basic pH, the terminal protonated amine (-NH 3 þ ) group is prone to hydrogen bonding to the Si-O À group of a second APTES molecule. This bond might be strong enough to avoid condensation with other APTES molecules, which was confirmed by a previous study [51].…”
Section: Influence Of the Silica/spions Ratios On Morphologysupporting
confidence: 83%
“…The above-mentioned methods provided a simple and convenient process for luminescent silica spheres without addition of inorganic or organic fluorophores. The submicrometer size was in the range of 150-250 nm in Schmedake's report [20], and 50-250 nm spheres in Tan's report under their operating conditions, respectively [21]. As we see, the control of size and the fundamental understanding of the emission mechanism are important to the phosphor materials.…”
Section: Introductionmentioning
confidence: 78%
“…Inorganic emission centers can be doped into silica spheres with lanthanides [16] and quantum dots [17], or inorganic phosphor layers can be coated on spherical silica by a sol-gel method [18,19]. Besides, monodisperse and luminescent silica spheres produced by calcinations of hybrid aminopropyl-silica spheres have been reported [20,21]. The above-mentioned methods provided a simple and convenient process for luminescent silica spheres without addition of inorganic or organic fluorophores.…”
Section: Introductionmentioning
confidence: 99%
“…The resulting mixture was stirred under nitrogen until the starting material was consumed (monitored by TLC). Then the mixture was diluted with anhydrous ether (100 mL), the product was precipitated out as a sticky semisolid material, which was further purified by silica-gel chromatography using (10:1) (m,2H,NCH 2 ), 3.90 (m, 2H, NCH 2 ), 3.77 (q, J 6.0, 6H, OCH 2 CH 3 ), 3.20 (m, 2H, NHCH 2 ), 2.74 (m, 2H, OCCH 2 CH 2 ), 1.81(m, 2H, CH 2 CH 2 CH 3 ), 1.64 (s, 12H, CH 3 ), 1.19(t, J 6.0, 9H, SiOCH 2 CH 3 ), 1.05 (t, J 6.0, 3H, NCH 2 CH 2 CH 3 ), 0.61 (m, 2H, SiCH 2 CH 2 ).…”
Section: Synthesis Of 1 (Scheme 1)mentioning
confidence: 99%