2003
DOI: 10.1021/ma0215767
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Amination of Poly(vinylbenzyl chloride) with N,N-Dimethylformamide

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Cited by 17 publications
(16 citation statements)
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“…As predicted, the resin 1D synthesized in DMF reveal sharp peak at 1660 cm -1 (1D, Fig. 2) responsible for the -C=N-bonds, created due to the dimethyl formamide [8]. The effect, as described in our previous work [7] will affect final sorption capacity of the resin 1D.…”
Section: Evaluation Of the Ft-ir Spectrasupporting
confidence: 69%
See 1 more Smart Citation
“…As predicted, the resin 1D synthesized in DMF reveal sharp peak at 1660 cm -1 (1D, Fig. 2) responsible for the -C=N-bonds, created due to the dimethyl formamide [8]. The effect, as described in our previous work [7] will affect final sorption capacity of the resin 1D.…”
Section: Evaluation Of the Ft-ir Spectrasupporting
confidence: 69%
“…As a result, synthesis was proceeded in N,N-dimethylformamide (DMF) using amines as functionalizing agents. Executed analyzes revealed that the microwaves facilitate creation, instead of amino functional groups, the -C=N-bonds, derived from DMF, resulting with smaller sorption capacity of the received anion exchangers [7,8].…”
Section: Introductionmentioning
confidence: 99%
“…3) or significantly lower (resins D2-D4MV, Fig. 3) sorption capacity support the conclusion that microwaves could promote the nucleophilic attack of oxygen derived from DMF on the chloromethyl groups located in the polymer matrices [49] creating the -C=N-bonds (Fig. 2).…”
Section: Sorption Studiessupporting
confidence: 63%
“…In contrast, organic solvents (such as N,N, ‐dimethylformamide) are less expected to form emulsions with polymers due to their higher miscibility 56. Indeed, poly(vinylbenzyl chloride) has been reported to dissolve in N , N ,‐dimethylformamide,57 which helps to account for why the pulsed plasma deposited poly(vinylbenzyl chloride) layers are not templated by N,N, ‐dimethylformamide solutions.…”
Section: Discussionmentioning
confidence: 99%