2012
DOI: 10.1016/j.reactfunctpolym.2011.03.002
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On the nature of “functional groups” in non-functionalized hypercrosslinked polystyrenes

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Cited by 51 publications
(26 citation statements)
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“…This works also suggests the existence of peaks that occur in the carbonyl region of the IR spectra are not due to the presence of carbonyl groups, but are likely the CvC stretching from substituted aromatic rings, which grow in intensity as a higher degree of substituted aromatic rings are formed with increasing amounts of FDA. These findings support recent work upon the assignment of these peaks in HCP networks, 62,63 and explains why the position of these peaks are dependent upon the monomer used to form the HCP. The small amount of mass lost from the polymers and the minimal levels of iron residues in the polymers as measured by TGA and XPS, respectively, indicate the discrepancies in the microanalysis data and greater than 100% yields are more a consequence of non-ideal network formation rather than the presence of contaminants in the polymer.…”
Section: Discussionsupporting
confidence: 89%
“…This works also suggests the existence of peaks that occur in the carbonyl region of the IR spectra are not due to the presence of carbonyl groups, but are likely the CvC stretching from substituted aromatic rings, which grow in intensity as a higher degree of substituted aromatic rings are formed with increasing amounts of FDA. These findings support recent work upon the assignment of these peaks in HCP networks, 62,63 and explains why the position of these peaks are dependent upon the monomer used to form the HCP. The small amount of mass lost from the polymers and the minimal levels of iron residues in the polymers as measured by TGA and XPS, respectively, indicate the discrepancies in the microanalysis data and greater than 100% yields are more a consequence of non-ideal network formation rather than the presence of contaminants in the polymer.…”
Section: Discussionsupporting
confidence: 89%
“…In our case, we used DCE as a swelling medium for the HCL reaction, and therefore the presence of large amounts of carboxyl groups was unexpected. A detailed explanation of the presence of absorption bands in the range 1600-1740 cm À1 for HCL Davankov-type resins was reported by Tsyrupa et al, 57 that denied the presence of C]O functionalities in the HCL polystyrenes, attributing these bands to hindered vibrations of carbon-carbon bonds and valence angles in aromatic rings. In our case, the hypothesis denying the dependence of these bands on C]O groups is conrmed by EDX results on the HCL systems that have evidenced comparable oxygen contents, 3.72 AE 0.13 mol% and 3.55 AE 0.23 mol%, for X_DVB-VBC and for X_DVB-ST-VBC, respectively, with no signicant differences recorded for the corresponding nanocomposites.…”
Section: Hcl Resins and Nanocomposites Characterizationmentioning
confidence: 87%
“…After accomplishing the reaction, the beads of the product were filtered and washed with dry acetone, 0.5 M pure HCl and excess distilled water that was additionally purified by passing through a column with hypercross‐linked Macronet MN‐200. The beads were dried in an oven at 80°C .…”
Section: Methodsmentioning
confidence: 99%