2017
DOI: 10.1016/j.carbpol.2017.07.040
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Chiroplasmonic magnetic gold nanocomposites produced by one-step aqueous method using κ-carrageenan

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Cited by 29 publications
(9 citation statements)
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“…The obtained similar FTIR spectra of all synthesized NCs and their polysaccharides, largely coinciding with each other, can be explained by the common polysaccharide nature of biopolymer matrices in these NCs ( Figure 1 and Figure S1 ). Thus, the prevailing broad absorption in the range of 3000–3800 cm −1 , as well as 1636 cm −1 , refers to hydroxyl groups in macromolecules of polysaccharides, the IR absorption region of 2850–3000 cm −1 refers to the CH bonds, and the group of signals in the region 1000–1200 cm −1 refer to ether C–O–C bonds ( Figure 1 , depicted by a continuous oval) [ 50 ]. In addition to these IR absorption bands common to all NC bands, there was also a region from 1230–1260 cm −1 for Se/CAR NC, which belongs to the sulfoether groups of carrageenan, a band with a maximum of 928 cm −1 , which belongs to the C–O–C ester bond of the anhydrogalactose carrageenan cycle, as well as the 845 cm −1 band, which belongs to the sulfo groups of galactose-4-sulfate carrageenan units [ 50 ].…”
Section: Discussionmentioning
confidence: 99%
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“…The obtained similar FTIR spectra of all synthesized NCs and their polysaccharides, largely coinciding with each other, can be explained by the common polysaccharide nature of biopolymer matrices in these NCs ( Figure 1 and Figure S1 ). Thus, the prevailing broad absorption in the range of 3000–3800 cm −1 , as well as 1636 cm −1 , refers to hydroxyl groups in macromolecules of polysaccharides, the IR absorption region of 2850–3000 cm −1 refers to the CH bonds, and the group of signals in the region 1000–1200 cm −1 refer to ether C–O–C bonds ( Figure 1 , depicted by a continuous oval) [ 50 ]. In addition to these IR absorption bands common to all NC bands, there was also a region from 1230–1260 cm −1 for Se/CAR NC, which belongs to the sulfoether groups of carrageenan, a band with a maximum of 928 cm −1 , which belongs to the C–O–C ester bond of the anhydrogalactose carrageenan cycle, as well as the 845 cm −1 band, which belongs to the sulfo groups of galactose-4-sulfate carrageenan units [ 50 ].…”
Section: Discussionmentioning
confidence: 99%
“…Thus, the prevailing broad absorption in the range of 3000–3800 cm −1 , as well as 1636 cm −1 , refers to hydroxyl groups in macromolecules of polysaccharides, the IR absorption region of 2850–3000 cm −1 refers to the CH bonds, and the group of signals in the region 1000–1200 cm −1 refer to ether C–O–C bonds ( Figure 1 , depicted by a continuous oval) [ 50 ]. In addition to these IR absorption bands common to all NC bands, there was also a region from 1230–1260 cm −1 for Se/CAR NC, which belongs to the sulfoether groups of carrageenan, a band with a maximum of 928 cm −1 , which belongs to the C–O–C ester bond of the anhydrogalactose carrageenan cycle, as well as the 845 cm −1 band, which belongs to the sulfo groups of galactose-4-sulfate carrageenan units [ 50 ]. The absence of pronounced changes in the FTIR absorption bands between polysaccharides and their corresponding Se NCs indicates that polysaccharide matrices are not involved in the redox processes of the synthesis of Se NCs.…”
Section: Discussionmentioning
confidence: 99%
“…This problem could be addressed by the synthesis of Se 0 NPs directly from the elemental bulk selenium, which is an inexpensive and available chemical precursor, and also using natural water-soluble sulphated polysaccharide κ-carrageenan (κ-CG). Previously, κ-CG has shown itself as an effective stabiliser of the inorganic nanoparticles (Ag, Au, CdSe, and NH 4 MgPO 4 ) [19][20][21][22]. At the same time, κ-CG is a renewable natural raw material widely employed in the food and pharmaceutical industries [23].…”
Section: Introductionmentioning
confidence: 99%
“…The κ‐carrageenan's family includes gelling κ‐, ι‐carrageenans widely used in food technology, cosmetics, and medicine . κ‐carrageenan was also applied as a template and reducing agent in the synthesis of different inorganic nanoparticles …”
Section: Introductionmentioning
confidence: 99%
“…The alkaline treatment is accompanied by peeling, for example, progressive decreasing of molecular mass . Intensive alkaline peeling of κ‐carrageenan during the synthesis of Au nanoparticles (NP) where κ‐carrageenan is used both as reducing and capping agent is indicated by increasing amount of reducing aldehyde groups . Therefore, the aim of the current work was to study independently deep alkaline hydrolysis of the virgin κ‐carrageenan in order to get better insight into the structure of colloids formed by its nanocomposites.…”
Section: Introductionmentioning
confidence: 99%