1991
DOI: 10.1016/0032-3950(91)90333-l
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Soluble polyimides based on 4,4′-diaminotriphenylamine. Synthesis, molecular mass characteristics and solution properties

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Cited by 9 publications
(7 citation statements)
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“…To the best of our knowledge, the first PI containing TPA was prepared by Vasilenko et al [18] in 1991, followed by Nishikata et al [19], who prepared PIs containing TPA derivatives with a methoxy substituent in the para position. The methoxy substituent in the para position is important because TPA derivatives could be dimerised during the anodic oxidation pathway [20], which can be prevented by incorporating electron donating groups at the para position, which also creates stable cationic radicals with lower potential [21].…”
Section: Triphenylaminementioning
confidence: 99%
“…To the best of our knowledge, the first PI containing TPA was prepared by Vasilenko et al [18] in 1991, followed by Nishikata et al [19], who prepared PIs containing TPA derivatives with a methoxy substituent in the para position. The methoxy substituent in the para position is important because TPA derivatives could be dimerised during the anodic oxidation pathway [20], which can be prevented by incorporating electron donating groups at the para position, which also creates stable cationic radicals with lower potential [21].…”
Section: Triphenylaminementioning
confidence: 99%
“…It should be noted that no solubility data has been reported for poly (triphenylaminepyromellitimide ) . 4 So, PM-TPM seems to be one of the very few poly-( pyromellitimides ) that are soluble in organic solvents.…”
Section: Solubilitymentioning
confidence: 99%
“…In order to overcome this problem, the derivatives of 4,4' diaminodiphenylmethane, such as 4,4'-diaminotetraphenylmethane * or 1,l-bis (4-aminophenyl) -1-(4-ethynylphenyl) -2,2,2-trifluoroethane,2 as well as 4,4'-diaminotriphenylamine, [3][4][5] have been used as monomers in several previous studies for the synthesis of aromatic polyamides and polyimides.…”
Section: Introductionmentioning
confidence: 99%
“…[23] Earlier research carried out for the structurally similar N,N-diamine triphenylamine (DA-TPA) showed that the incorporation of a pendant phenyl group into the polymer backbone is a successful approach to increase solubility and processability of PIs. [15,20,[25][26] The synthesis of DA-TPM developed in our group is simple and highly efficient using commercially available and cheap starting materials such as aniline and benzaldehyde. This is a big advantage in comparison to N,N-diamine triphenylamine, whose synthesis is much more complicated and required expensive reagents.…”
Section: Introductionmentioning
confidence: 99%