2015
DOI: 10.1016/j.dyepig.2015.05.024
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Synthesis and properties of broad-band absorption POSS-based hybrids

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Cited by 7 publications
(2 citation statements)
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“…The preparation of POSS-based fluorescent materials can be divided into chemical synthesis and physical blending. Recently, a variety of the traditional and the burgeoning chemical synthesis methods have been widely used in the design and synthesis of POSS-based fluorescent materials, such as hydrolytic condensation [ 46 ], hydrosilylation [ 47 , 48 , 49 , 50 ], Heck reaction [ 51 , 52 , 53 , 54 ], atom transfer radical polymerization (ATRP) [ 55 , 56 , 57 ], reversible addition-fragmentation chain transfer polymerization [ 58 ], ring-opening metathesis polymerization [ 59 ], as well as “click” chemistry reaction [ 60 , 61 , 62 , 63 ]. The method of physical blending is mainly used in the quantum dots (QDs) coated and lanthanide-doped POSS-based fluorescent materials [ 64 , 65 , 66 , 67 ].…”
Section: Synthesis and Design Of Poss-based Fluorescent Materialsmentioning
confidence: 99%
“…The preparation of POSS-based fluorescent materials can be divided into chemical synthesis and physical blending. Recently, a variety of the traditional and the burgeoning chemical synthesis methods have been widely used in the design and synthesis of POSS-based fluorescent materials, such as hydrolytic condensation [ 46 ], hydrosilylation [ 47 , 48 , 49 , 50 ], Heck reaction [ 51 , 52 , 53 , 54 ], atom transfer radical polymerization (ATRP) [ 55 , 56 , 57 ], reversible addition-fragmentation chain transfer polymerization [ 58 ], ring-opening metathesis polymerization [ 59 ], as well as “click” chemistry reaction [ 60 , 61 , 62 , 63 ]. The method of physical blending is mainly used in the quantum dots (QDs) coated and lanthanide-doped POSS-based fluorescent materials [ 64 , 65 , 66 , 67 ].…”
Section: Synthesis and Design Of Poss-based Fluorescent Materialsmentioning
confidence: 99%
“…The emission spectra were recorded in toluene, showing emission maxima wavelengths λ em = 440 (H1), 461 (H3) and 458 (H2) nm, which were compared to the spectra for solids that disclosed red-shifts Δλ = 42–51 nm, suggesting known phenomena of possible anthracene unit aggregation (the smallest effect for H1). The same authors reported on the further modification of dianthracene(hexavinyl)octasilsesquioxane (H2), and using Heck coupling to introduce one diazophenylnaphtalenediamine moiety followed by an amidation process to introduce a complex structure of a chromophore that possess broad-band absorbing properties [49]. The presence of different chromophores allows the absorbing bands of the dyes to be combined, reduces the possibility of their aggregation and possesses a broad red-emission band at λ em = 638 nm.…”
Section: Catalytic Reactions Leading To Functionalized Silsesquioxmentioning
confidence: 99%