One-pot synthesis of PLA-b-PHEA via sequential ROP and RAFT polymerizations
文献信息
Diana Kalden, Matthias Westerhausen
A block copolymer library of polylactide (PLA) and poly(2-hydroxyethyl acrylate) (PHEA) was prepared via sequential ring opening polymerization (ROP) and reversible addition fragmentation chain transfer (RAFT) polymerization in a one-pot approach. The whole process was conducted at room temperature in THF without employing any protection chemistry or intermediate purification steps. The ROP of L-lactide was performed via in situ calcium alkoxide formation by using 4-cyano-4-[(dodecylsulfanylthiocarbonyl)sulfanyl]pentanol (CDP) and [(THF)2Ca{N(SiMe3)2}2]. The PLA based macro chain transfer agent (CTA) (Mn = 2550 g mol−1, Đ = 1.18) was characterized in-depth by (tandem) mass spectrometry and proved to be suitable to obtain PHEA blocks with Mn values up to 10 000 g mol−1 (Đ ≤ 1.28). Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) measurements indicated an increased miscibility between both blocks in bulk as the length of the PHEA unit increases. The amphiphilic block copolymers self-assembled into micellar structures in aqueous media, which were studied by dynamic light scattering (DLS) and cryo-transmission electron microscopy (cryo-TEM).
相关文献
Organocatalytic regio-, diastereo- and enantioselective γ-additions of isoxazol-5(4H)-ones to β,γ-alkynyl-α-imino esters for the synthesis of axially chiral tetrasubstituted α-amino allenoates
Fushuai Li, Shuai Liang, Yepeng Luan, Xuling Chen, Hanhui Zhao, Anqi Huang, Pengfei Li, Wenjun Li
DOI: 10.1039/D0QO01505A
Self-recognition and hydrogen bonding by polycyclic bridgehead monoalcohols
Amelia García Fraile, David G. Morris, Antonio García Martínez, Santiago de la Moya Cerero, Kenneth W. Muir, Karl S. Ryder, Enrique Teso Vilar
DOI: 10.1039/B209427D
Stereoselective synthesis and applications of spirocyclic oxindoles
Alexander J. Boddy, James A. Bull
DOI: 10.1039/D0QO01085E
Theoretical study of rhodium- and cobalt-catalyzed decarboxylative transformations of isoxazolones: origin of product selectivity
Wei Rong, Tian Zhang, Ting Li, Juan Li
DOI: 10.1039/D0QO01498B
Dioxygenase-catalysed oxidation of monosubstituted thiophenes: sulfoxidation versus dihydrodiol formation
Derek R. Boyd, Narain D. Sharma, Nimal Gunaratne, Simon A. Haughey, Martina A. Kennedy, John F. Malone, Christopher C. R. Allen, Howard Dalton
DOI: 10.1039/B300867N
Fluorescence visualization of cucurbit[8]uril-triggered dynamic host–guest assemblies
Xiaodong Zhang, Tao Sun, Xin-Long Ni
DOI: 10.1039/D0QO00649A
Recent advances in quinazolinones as an emerging molecular platform for luminescent materials and bioimaging
Zhiming Xing, Wanhui Wu, Yongxiang Miao, Yingqun Tang, Youkang Zhou, Lifang Zheng, Yang Fu, Zhibin Song, Yiyuan Peng
DOI: 10.1039/D0QO01425G
Recent advances in cascade radical cyclization of radical acceptors for the synthesis of carbo- and heterocycles
Jianhua Liao, Xiao Yang, Lu Ouyang, Yinlong Lai, Jiuzhong Huang, Renshi Luo
DOI: 10.1039/D0QO01453B
Trends in alkyl substituent effects on nucleophilic reactions of carbonyl compounds: Gas phase reactions between ammonia and R1R2COCH3+ oxonium ions
Lihn Bache-Andreassen, Einar Uggerud
DOI: 10.1039/B209955C
您可能还喜欢
4-[4-三氟甲基苯基]恶唑(CAS号:1126636-40-5)通常如何合成?
4-[4-三氟甲基苯基]恶唑通常通过将4-三氟甲基苯酚与异硫氰酸苯酯在有机溶剂中进行酯化反应合成。该反应可在无水条件下,使用适当的催化剂,如四丁基氢氧化铵,以提...
RockPhos Pd G3(CAS号:2009020-38-4)通常如何合成?
RockPhos Pd G3 通常通过钯催化偶联反应合成,使用配体 (2'-Amino-2-biphenylyl)(methanesulfonato-kappa...
1-哌啶甲酰胺(CAS号:2158-03-4)的市场或研究趋势如何?
1-哌啶甲酰胺作为有机合成中的重要中间体,其市场需求主要受医药、农药、染料等行业推动。近年来,随着新药开发和绿色化学的发展,该化合物的研究趋势集中在开发更高效、...
2-(二苯基膦基)乙胺(CAS号:4848-43-5)适用哪些法规指南?
2-(二苯基膦基)乙胺适用于多种法规指南,包括但不限于《全球化学品统一分类和标签制度》(GHS),欧盟《化学品注册、评估、授权和限制》法规(REACH),以及美...
如何储存间苯二甲酸二烯丙酯(CAS号:1087-21-4)?
间苯二甲酸二烯丙酯应储存在阴凉、干燥、通风良好的地方,远离火源和热源。储存容器应密封,避免光照和高温。储存温度应控制在25℃以下,相对湿度应低于80%。避免与其...
什么是间甲苯异硫代异氰酸酯(CAS号:621-30-7)?
间甲苯异硫代异氰酸酯是一种有机化合物,分子式为C7H7NO2S,具有刺激性气味。它是一种重要的有机合成中间体,在合成其他化合物时广泛应用。
在合成中是否有N-Boc-D-苯丙氨醇(CAS号:106454-69-7)的替代品?
在合成中,可以考虑使用N-Cbz-D-苯丙氨醇或N-Fmoc-D-苯丙氨醇作为替代品。这些化合物同样具有保护氨基的功能,且在合成过程中表现出良好的反应性能。
3-羟甲基-2-氧异丙基吡啶(CAS号:954240-50-7)的主要用途是什么?
3-羟甲基-2-氧异丙基吡啶主要用于有机合成领域,可以作为合成其他药物、农药或精细化学品的中间体。此外,它还可能在实验室研究中作为特定反应的前体或溶剂。
6-氨基-9-甲基嘌呤(CAS号:700-00-5)应用于哪些行业?
6-氨基-9-甲基嘌呤目前主要应用于医药行业,作为某些药物的中间体。此外,它还可能用于聚合物、传感器和半导体的某些领域,作为功能性单体或掺杂剂。
来源期刊
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.













![4-Chloro-1-[(4-methylphenyl)sulfonyl]-1H-pyrrolo[2,3-b]pyridine structure 4-Chloro-1-[(4-methylphenyl)sulfonyl]-1H-pyrrolo[2,3-b]pyridine structure](https://cnstatic.chemtradehub.com/structs/348/348640-05-1-7db8.webp)
![4-{(2R,3R)-3-Methyl-5-[(1E)-1-propen-1-yl]-2,3-dihydro-1-benzofuran-2-yl}phenol structure 4-{(2R,3R)-3-Methyl-5-[(1E)-1-propen-1-yl]-2,3-dihydro-1-benzofuran-2-yl}phenol structure](https://cnstatic.chemtradehub.com/structs/221/221666-27-9-20a9.webp)