2012
DOI: 10.1016/j.micromeso.2012.06.033
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Is their potential for post-synthetic brominating reactions on benzene bridged PMOs?

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Cited by 5 publications
(3 citation statements)
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“…Moreover, by performing NMR analysis of the final product one can provide an indepth view of the chemical stability before and after modification. As described by Smeulders et al [33], assessment of the chemical linkages between the organic bridging units is of pivotal importance. Figure 7 shows the 1 H- 29 Si CPMAS NMR spectra of benzene bridged and bromobenzene bridged PMO.…”
Section: Resultsmentioning
confidence: 99%
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“…Moreover, by performing NMR analysis of the final product one can provide an indepth view of the chemical stability before and after modification. As described by Smeulders et al [33], assessment of the chemical linkages between the organic bridging units is of pivotal importance. Figure 7 shows the 1 H- 29 Si CPMAS NMR spectra of benzene bridged and bromobenzene bridged PMO.…”
Section: Resultsmentioning
confidence: 99%
“…Organic synthesis on PMOs is, however, not so straight-forward. As described in literature by Smeulders et al [33], structural changes may occur due to unwanted side reactions. In this article, three different strategies for bromination of benzene bridged PMO are investigated: 1) Br 2 with AlCl 3 as catalyst, 2) Nbromosuccinimide (NBS) with azobisisobutyronitrile (AIBN) as radical initiator, and 3) NaBrO 3 in combination with H 2 SO 4 in order to create in situ generation of bromine.…”
Section: Introductionmentioning
confidence: 89%
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