2009
DOI: 10.1002/app.30725
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Synthesis, characterization, and coordination behavior of copoly(styrene‐maleimide) functionalized with terpyridine

Abstract: A maleimide functionalized terpyridine, 4 0 (4-maleimidophenyl)-2, 2 0 : 6 0 , 2 00 -terpyridine, was synthesized and copolymerized with styrene via radical polymerization. The synthesized monomer was characterized by CHN elemental analysis, FT-IR, 1 H NMR, and Mass spectrometry. The structure of polymer was also confirmed by FT-IR and UV-Vis spectroscopy. The resulting polymer was soluble in chloroform and polar aprotic solvents, and showed an inherent viscosity of 1.5 dL/g in N,N-dimethyl formamide at 25 C. … Show more

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Cited by 9 publications
(8 citation statements)
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“…Chemical shifts are reported in ppm (d) with residual solvent used as the internal reference. 4-(4'phenyl-2,2':6',2"-terpyridyl)benzoic acid [40] (1), 3-(4-nitrophenyl)-1-(pyridin-2-yl)prop-2-en-1-one [41] (2), and 4-(2-hydroxy-4-oxopent-2en-3-yl)benzoic acid [42] (3) were synthesized according to literature procedures. Copper(I) iodide was purified using potassium iodide and activated carbon.…”
Section: Discussionmentioning
confidence: 99%
“…Chemical shifts are reported in ppm (d) with residual solvent used as the internal reference. 4-(4'phenyl-2,2':6',2"-terpyridyl)benzoic acid [40] (1), 3-(4-nitrophenyl)-1-(pyridin-2-yl)prop-2-en-1-one [41] (2), and 4-(2-hydroxy-4-oxopent-2en-3-yl)benzoic acid [42] (3) were synthesized according to literature procedures. Copper(I) iodide was purified using potassium iodide and activated carbon.…”
Section: Discussionmentioning
confidence: 99%
“…[RuT1B0(NO 2 )](PF 6 ) (form B) was prepared chemically as an intermediate towards the synthesis of [RuT1B0(NO)](PF 6 ) 3 [ 23 ]. Bromophenylterpyridine [ 49 ] and nitrophenylterppyridine [ 50 ] were prepared as previously described.…”
Section: Methodsmentioning
confidence: 99%
“…4 -(4-hydroxyphenyl)-2,2 :6 ,2 -terpyridine was synthesized according to the literature with a modified synthesis to higher yield (57%) [24]. 4 -(4-aminophenyl)-2,2 :6 ,2 -terpyridine, was prepared as described elsewhere [25].…”
Section: Methodsmentioning
confidence: 99%