Composition processing property relationship of vitrimers Based on polyethyleneimine
文献情報
Natanel Jarach, Daniel Golani, Ofer Asaf, Hanna Dodiuk, Yoav Shamir, Amir Goldbourt, Samuel Kenig, Naum Naveh
The composition–processing–property relationship of imine containing reversible covalent bond containing polymers (RCBPs) was studied using an innovative (regarding this type of polymer) combination of characterization methods. This combination led, for the first time, to a classification of the various chemical reactions occurring during the processing of imine based RCBP, affecting their final chemical structure and properties. RCBPs, based on PIs (polyimines), were synthesized from polyethyleneimine (PEI) and terephthalaldehyde (TPA) in the presence of ethanol. The chemical composition and derived thermal and mechanical properties were investigated. Material characterization using ATR-IR, 13C-solid state NMR, swell tests, and a novel illustrative model based on the Flory–Rehner equation led to the conclusion that at least 80% of the secondary amine groups reacted to form a cross-linking network, along with 100% of the primary amines, and that during 20 min compression molding at 220 °C under 2.7 MPa, a post-curing reaction occurs. 13C-SSNMR and ATR-IR indicated that the chemical structure is determined not only by the reactants but also by the elevated temperature processing conditions. During heating, three mechanisms affect the final composition–transimination, reduction (back into amine groups) and oxidation (to oxaziridine and amide groups which are almost negligible). The reduction/oxidation processes were found to dominate the mechanical properties. The vitrification temperature (Tv), which is characteristic of RCBPs, is dependent on the thermal history, with a higher Tv resulting from longer compression molding times. The mechanical properties are affected by the processing temperatures, changing from high-performance to very low strength. Under specific processing conditions, the imine cross-linking bonds are reduced/oxidized, which causes the formation of more polar but lower energy bond cross-linking, resulting in lower tensile strength and a change in the hydrophobicity of the polymer, which may be used in future applications.
おすすめジャーナル

Chemical Communications

Current Opinion in Solid State & Materials Science

Nature Medicine

Russian Journal of Coordination Chemistry

Russian Journal of Organic Chemistry

Journal of Saudi Chemical Society

Russian Journal of Applied Chemistry

Organic Process Research & Development

Russian Chemical Bulletin

Journal of Peptide Science
関連文献
Effect of polymer chemistry on globular protein–polymer block copolymer self-assembly
Dongsook Chang, Christopher N. Lam, Shengchang Tang, Bradley D. Olsen
DOI: 10.1039/C4PY00448E
How does a tiny terminal alkynyl end group drive fully hydrophilic homopolymers to self-assemble into multicompartment vesicles and flower-like complex particles?
Tingting Liu, Wei Tian, Yunqing Zhu, Yang Bai, Hongxia Yan, Jianzhong Du
DOI: 10.1039/C4PY00501E
Co-delivery of 5-fluorocytosine and cytosine deaminase into glioma cells mediated by an intracellular environment-responsive nanovesicle
Yuanyuan Yuan, Shudong Lin, Du Cheng, Xiaoying Wang, Qing Jiang, Xintao Shuai
DOI: 10.1039/C4PY00291A
Injectable enzymatically crosslinked hydrogels based on a poly(l-glutamic acid) graft copolymer
Chaoliang He, Yilong Cheng, Gao Li, Xuesi Chen
DOI: 10.1039/C4PY00420E
Engineering the band gap and energy level of conjugated polymers using a second acceptor unit
Khalid Mahmood, Heng Lu, Zheng-Ping Liu, Cuihong Li, Zhen Lu, Xiao Liu, Tao Fang, Qiaohong Peng, Guangwu Li, Lin Li, Zhishan Bo
DOI: 10.1039/C4PY00004H
The first amphiphilic graft copolymer bearing a hydrophilic poly(2-hydroxylethyl acrylate) backbone synthesized by successive RAFT and ATRP
Xiuyu Jiang, Xue Jiang, Guolin Lu, Chun Feng, Xiaoyu Huang
DOI: 10.1039/C4PY00415A
Synthesis of triphenylamine based polysiloxane as a blue phosphorescent host
Dianming Sun, Zhaomin Yang, Xiaoli Sun, Huihui Li, Zhongjie Ren, Junteng Liu, Dongge Ma, Shouke Yan
DOI: 10.1039/C4PY00450G
Nano-building block based-hybrid organic–inorganic copolymers with self-healing properties
A. Guinault, S. Delalande
DOI: 10.1039/C4PY00172A
こちらもおすすめ
2,3-スチオエポキシマドルを取り扱う際の実験室安全事項は何ですか?
取り扱いにはPPE(プロテクティブ・パーソナル・エイド)が必要で、防ぐ手袋と保護眼鏡を着用してください。ドラフトチャンバーの使用を推奨します。漏洩した場合は、適...
BOC-S-3-アミニ-4-(4-メチオキシベンチル)-ブタン酸の代替品はありますか?
この化合物の代替品としては、BOC保護基を有さないアミノ酸やその他の保護基化合物が考えられます。また、メチオキシ基を有しない他の芳香族アミノ酸も代替品として挙げ...
Methyl 2-(chloromethyl)-3-nitrobenzoate(1218910-61-2)の代替品はありますか?
Methyl 2-(chloromethyl)-3-nitrobenzoate(1218910-61-2)の代替品としては、化学組成を変えることで効果を達成する...
(2R)-2-アミノ-N-ベンジル-3-ヒドロキシプロパナミドを含む廃棄物はどのように処理すべきですか?
(2R)-2-アミノ-N-ベンジル-3-ヒドロキシプロパナミドを含む廃棄物は、適切な廃棄物管理ガイドラインに基づき処理する必要があります。まず、廃棄物を適切に収...
6,7-二氢-咪唑並[1,2-a]ピリドイン-8(5h)-酮はどのように合成されますか?
6,7-二氢-咪唑並[1,2-a]ピリドイン-8(5h)-酮は、2-ブロモフェニルアセトインとリン酸ハロゲン化物を反応させることで合成できます。この反応は高温で...
エチル(3R)-3-ピロリジニル酢酸水和塩とは何ですか?
エチル(3R)-3-ピロリジニル酢酸水和塩は、CAS番号1332459-32-1の化合物で、(R)-乙基2-(ピロリジン-3-基)酢酸塩水和塩と呼ばれます。この...
(2S)-{[(2-メチルエチルオキシ]カルボニル}アミノ)[2-(トリアフルオロメチルフェニル]エチカシック酸の物理化学的性質は何ですか?
(2S)-{[(2-メチルエチルオキシ]カルボニル}アミノ)[2-(トリアフルオロメチルフェニル]エチカシック酸のCAS番号は1203454-45-8です。この...
2-ブロモ-1-(2-メチル-2-プロパニル)-4-ニトロベンゼンはどのように保存すればよいですか?
2-ブロモ-1-(2-メチル-2-プロパニル)-4-ニトロベンゼンは、直射日光を避けて暗所で、室温(約15℃〜25℃)、乾燥した場所に保存する必要があります。ま...
1-[(4-硝基フェニル)スルホニル]-1H-1,2,4-三唑の市場動向や研究トレンドはどうですか?
市場動向としては、1-[(4-硝基フェニル)スルホニル]-1H-1,2,4-三唑は主に農業用除草剤や合成化学製品の原料として利用されています。研究トレンドとして...
掲載誌
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.




![Ethyl 4-[8-chloro(5,5,6,6,7-~2~H_5_)-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene]-1-piperidinecarboxylate structure Ethyl 4-[8-chloro(5,5,6,6,7-~2~H_5_)-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene]-1-piperidinecarboxylate structure](https://static.chemtradehub.com/structs/102/1020719-57-6-37e2.webp)