2019
DOI: 10.3390/app9071497
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Nanoplasmonic Sensor Based on Surface Plasmon-Coupled Emission: Review

Abstract: The surface plasmon resonance (SPR) technique is a powerful method to detect chemical molecules. Fluorescent spectroscopy is a subject of great interest in the field of material science and biology. Recently, some optical sensors, based on plasmonic properties of nanomaterial, were introduced to enhance the investigation of the interaction of molecular while detecting the low concentration of molecular. The surface plasmon-coupled emission (SPCE) technique is a merit and accurate method to evaluate the interac… Show more

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Cited by 14 publications
(16 citation statements)
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References 51 publications
(58 reference statements)
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“…7 (see vertical distance). It can also be mentioned the obtained thickness is nearer to the most typical configuration in the SPR system with a 50 nm gold film, which is responsive to the local gold-dielectric interface [85][86][87] .…”
Section: Resultsmentioning
confidence: 99%
“…7 (see vertical distance). It can also be mentioned the obtained thickness is nearer to the most typical configuration in the SPR system with a 50 nm gold film, which is responsive to the local gold-dielectric interface [85][86][87] .…”
Section: Resultsmentioning
confidence: 99%
“…We focused on the conversion of the vinyl function and the grafting position of the thiol on this function (in α or β position relative to the silicon atom). For the 2-phenylethane-1thiol (5) and for the fluorinated thiol 6, the reaction occurred at 100 % on the carbon in β of the silicon atom, but in the case of N-methyl-2-sulfanylacetamide (4), 14 % of the thiol-ene reaction occurred on the carbon in α of the silicon, which can be quantified by 1 H-NMR ( Figure 2 and Supporting Information, SI-2). The results are reported in Table 1.…”
Section: Synthesis Of Functionalized Polydimethylsiloxanesmentioning
confidence: 99%
“…Yield: 71 %. 1 29 Si-NMR (CDCl 3 + 0.03 M Cr(acac) 3 ): À 20 to À 23 (m, Si (CH 3 ) 2 , 2 Si); À 23 to À 26 (m, SiCH 3 (CH 2 À CH 2 À SÀ ), 1 Si). 13 C-NMR (CDCl 3 ): 170 (CO); 36.3 (SÀ CH 2 À CO); 28.5-27.5 (SiÀ CH 2 À CH 2 À S); 26.9 (CH 3 À NH); 18.2 (SiÀ CH 2 À CH 2 À S); 2.1, 1.6 -1.2, 0.4 to À 0.2 (H 3 CÀ Si).…”
Section: Preparation Of Poly(methyl-n-methylaminocarbonylmethylthioetunclassified
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