2016
DOI: 10.1134/s199507801604008x
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Preparation of chemosensor materials based on silica nanoparticles with covalently anchored fluorophores by inkjet printing

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Cited by 15 publications
(4 citation statements)
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“…Functional cyclic stereoregular cis -tetracyclosiloxanes 1 a,b were prepared by the hydrolytic condensation reaction of trifunctional alkoxysilanes in the presence of alkali metal ions followed by the reaction of the obtained siloxanolate salt with dimethylchlorosilane by the method described earlier . The functional allyl-DBMBF 2 precursors 2 a,b were synthesized by the reaction of the corresponding β-diketones with boron trifluoride diethyl etherate earlier by us. , The organosilicon model compounds 3 a,b and dyads 4 a–d (Figure ), which were used for comparing optical properties, were prepared from allyl-DBMBF 2 2 a,b by the hydrosilylation reaction with mono- or difunctional hydridesiloxanes using the method described earlier by us …”
Section: Results and Discussionmentioning
confidence: 99%
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“…Functional cyclic stereoregular cis -tetracyclosiloxanes 1 a,b were prepared by the hydrolytic condensation reaction of trifunctional alkoxysilanes in the presence of alkali metal ions followed by the reaction of the obtained siloxanolate salt with dimethylchlorosilane by the method described earlier . The functional allyl-DBMBF 2 precursors 2 a,b were synthesized by the reaction of the corresponding β-diketones with boron trifluoride diethyl etherate earlier by us. , The organosilicon model compounds 3 a,b and dyads 4 a–d (Figure ), which were used for comparing optical properties, were prepared from allyl-DBMBF 2 2 a,b by the hydrosilylation reaction with mono- or difunctional hydridesiloxanes using the method described earlier by us …”
Section: Results and Discussionmentioning
confidence: 99%
“…89 The functional allyl-DBMBF 2 precursors 2 a,b were synthesized by the reaction of the corresponding β-diketones with boron trifluoride diethyl etherate earlier by us. 88,90 The organosilicon model compounds 3 a,b and dyads 4 a−d (Figure 1), which were used for comparing optical properties, were prepared from allyl-DBMBF 2 2 a,b by the hydrosilylation reaction with mono-or difunctional hydridesiloxanes using the method described earlier by us. 88 Tetrachromophoric dyes 5 a−d were obtained from the corresponding functional stereoregular cis-tetracyclosiloxanes 1 a,b and allyl-DBMBF 2 derivatives 2 a,b by the hydrosilylation reaction in the presence of Karstedt's catalyst in toluene at 25 °C according to Scheme 1.…”
Section: ■ Introductionmentioning
confidence: 99%
“…61 One of the most promising applications of DBMBF 2 derivatives is the detection of trace amounts of vapours of benzene, toluene, and xylenes (BTX). [61][62][63][64][65][66][67][68][69][70][71][72] Despite the fact that DBMBF 2 derivatives have been well studied to date, there is almost no data on the use of these chromophores in RET systems, with the exception of a few ref. 73.…”
Section: Introductionmentioning
confidence: 99%
“…61 One of the most promising applications of DBMBF 2 derivatives is the detection of trace amounts of vapours of benzene, toluene, and xylenes (BTX). 61–72…”
Section: Introductionmentioning
confidence: 99%