2009
DOI: 10.1002/app.29106
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New polymer syntheses, Part 44: Synthesis, characterization, and corrosion inhibition behavior of new polyurea derivatives based on diaryl ether in the polymers backbone

Abstract: A new interesting class of polyurea derivatives 5 a-c was synthesized using solution polycondensation technique by the interaction of 1 mol of 4,4 0 -bis(2 00 -aminothiazol-4 00 -yl)diphenyl ether monomer 3 with 1 mol of diisocyanate compounds in pyridine. The model compound 4 was synthesized by the interaction of 1 mol of monomers 3 with 2 mol of phenylisocyanate in pyridine, and the structure was confirmed by correct elemental and spectral analyses. The resulting polymers were characterized by elemental and … Show more

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Cited by 23 publications
(10 citation statements)
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“…On the other hand, some of the polymers are partially soluble in n-hexane, benzene and chloroform, while the majority are partially or completely soluble in acetonitrile except polymers 2 c,d which are completely insoluble in the same solvent. Furthermore, polymers based on flexible polymethylene spacers (CH 2 ) 4 and (CH 2 ) 8 have slightly more solubility than other polymers containing aromatic moieties, like the same observation in analogues polymers described in our previous work (36,37). The results presented in Table 2 are clearly indicate that Friedel-Crafts polyketones based cyclohexanone moiety in the polymers backbone have slightly more solubility than Friedel-Crafts polyketones based cyclopentanone moiety, which appeared clearly in most of tested solvents.…”
supporting
confidence: 74%
“…On the other hand, some of the polymers are partially soluble in n-hexane, benzene and chloroform, while the majority are partially or completely soluble in acetonitrile except polymers 2 c,d which are completely insoluble in the same solvent. Furthermore, polymers based on flexible polymethylene spacers (CH 2 ) 4 and (CH 2 ) 8 have slightly more solubility than other polymers containing aromatic moieties, like the same observation in analogues polymers described in our previous work (36,37). The results presented in Table 2 are clearly indicate that Friedel-Crafts polyketones based cyclohexanone moiety in the polymers backbone have slightly more solubility than Friedel-Crafts polyketones based cyclopentanone moiety, which appeared clearly in most of tested solvents.…”
supporting
confidence: 74%
“…This observation was also more pronounced for the shorter aliphatic methylene spacers [(CH 2 ) 2 ] and appeared clearly in both the n ‐hexane and acetonitrile solvents. The resulting PAKA hybrid polymers acting as analogue polymers were described in our previous study . The higher flexibility of the cyclohexanone moiety gave better solubility for most of the polymers in most of the tested solvents compared to the other moieties described elsewhere .…”
Section: Resultsmentioning
confidence: 91%
“…The initial decomposition temperature (IDT)59 corresponded to the temperature at which the initial degradation could occur. The IDTs of all of the prepared polymers appeared at the temperatures for 10% weight loss percentages ( T 10 ), which was considered at the same time the polymers decomposition temperatures;60, 61 it occurred in the range 212–330°C. Therefore, the data in Table II indicate that the thermal stabilities of polyazomethines 7 a –7 c and 7 e (at 10%) were in the order: 7 b > 7 a and 7 c > 7 e .…”
Section: Resultsmentioning
confidence: 99%