2015
DOI: 10.3389/fmats.2015.00005
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Smart Synthesis of High-Performance Thermosets Based on ortho-Amide–Imide Functional Benzoxazines

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Cited by 28 publications
(32 citation statements)
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“…In this study, the hydrogen bonding behavior of two isomeric amide‐containing benzoxazines, substituted at the para and ortho position, are studied by FT‐IR. These results complement not only the long hypothesized existence of an intramolecular five‐membered‐ring hydrogen bond in o HBA‐a proposed in previous papers but also those more recently reported using NMR techniques . It must be highlighted that to make this spectroscopic study fully reliable much emphasis has been paid on obtaining highly purified benzoxazine resins.…”
Section: Introductionsupporting
confidence: 87%
See 1 more Smart Citation
“…In this study, the hydrogen bonding behavior of two isomeric amide‐containing benzoxazines, substituted at the para and ortho position, are studied by FT‐IR. These results complement not only the long hypothesized existence of an intramolecular five‐membered‐ring hydrogen bond in o HBA‐a proposed in previous papers but also those more recently reported using NMR techniques . It must be highlighted that to make this spectroscopic study fully reliable much emphasis has been paid on obtaining highly purified benzoxazine resins.…”
Section: Introductionsupporting
confidence: 87%
“…Later, Zhang and co‐workers found that the ortho ‐amide‐imide functional benzoxazine and ortho ‐norbornene functional benzoxazine monomers showed milder synthesis condition (shorter reaction time with high yield) as compared to para counterpart. Furthermore, the corresponding ortho ‐functionalized polymer showed higher T g …”
Section: Introductionmentioning
confidence: 99%
“…Robust mechanical performance, especially high T g values, low flammability, high hydophobicity, rich hydrogen bondings etc . were obtained using phenolphthalein, aromatic ketone, imide, amide, and nitrile group containing phenols or amines . Likewise, benzoxazines from renewable reagents were synthesized, successfully .…”
Section: The Journey Of Phenolicsmentioning
confidence: 99%
“…In fact, it is now well known that the introduction of electron-withdrawing or electron-donating groups on the structural skeleton of benzoxazine monomers can greatly affect their reactivity by activating the ring-opening or stabilizing the intermediates [27]. Indeed, the catalyst effect of neighboring groups accelerating benzoxazine polymerization has been clearly shown in the case of carboxylic acid- [28], hydroxyl- [29], and amide [30] containing benzoxazine monomers. Moreover, the substitution on the ortho-position was found to further stimulate and activate the ring-opening polymerization when compared to its para-substituted counterpart as well in the case of a methylol functional benzoxazine [23,31] as in the case of an ortho-amide-imide functional benzoxazine [30].…”
Section: Introductionmentioning
confidence: 99%