Nitroxide mediated controlled synthesis of glycidyl methacrylate-rich copolymers enabled by SG1-based alkoxyamines bearing succinimidyl ester groups
文献信息
Ali Moayeri, Benoit Lessard, Milan Maric
The controlled nitroxide-mediated copolymerization of glycidyl methacrylate (GMA) and styrene (S) with varying GMA molar feed fractions (fGMA,0 = 0.12–0.94) was accomplished by using a SG1-based alkoxyamine initiator bearing a N-succinimidyl ester group (NHS-BlocBuilder) in 50 wt% 1,4-dioxane solution at 90 °C. Copolymerizations indicated linear evolution of number average molecular weight Mn with respect to conversion up to approximately 50% and narrow molecular weight distributions with Mw/Mn = 1.22–1.44 and GMA incorporation into copolymer (FGMA) as high as 0.92. No additional SG1 free nitroxide was required to control polymerizations, even at high fGMA,0. Chain extensions of poly(GMA-ran-S) macroinitiators with S at 110 °C yielded a high fraction of block copolymer in most cases (except at the highest FGMA), as clear, monomodal shifts in Mn using gel permeation chromatography (GPC) were observed, thereby suggesting the poly(GMA-ran-S) macroinitiators were substantially “living”.
相关文献
Beyond the formation: unveiling the atmospheric transformation of organosulfates via heterogeneous OH oxidation
Sze In Madeleine Ng
DOI: 10.1039/D3CC03700B
Simply accessible platinum(ii) complexes enabling alkene hydrosilylation at ppm catalyst loadings
Benon P. Maliszewski, Eleonora Casillo, Perrine Lambert, Catherine S. J. Cazin, Steven P. Nolan
DOI: 10.1039/D3CC05033E
Site-selective template-directed synthesis of antibody Fc conjugates with concomitant ligand release
Viktoriia Postupalenko, Léo Marx, Mathilde Pantin, Nadège Gsponer, Gaëlle Giudice, Natalia Gasilova, Frédéric Lévy, Patrick Garrouste, Jean-Manuel Segura, Origène Nyanguile
DOI: 10.1039/D3SC04324J
Hierarchical assembly of foldable polymers and applications in organic optoelectronics and antibacterial or antiviral materials
Ranajit Barman, Anurag Mukherjee, Atish Nag, Priya Rajdev, Suhrit Ghosh
DOI: 10.1039/D3CC04855A
CO2 switchable adhesion of ionic polydimethylsiloxane elastomers
Masatoshi Tsunoda, Shoei Shimozaki, Rina Sawada, Shoichi Kutsumizu
DOI: 10.1039/D3CC04575G
Chemical pressure-induced PtIII–I Mott–Hubbard nanowire, [Pt(en)2I](Asp-Cn)2·H2O (13 ≤ n), detected via polarized infrared spectroscopy
Shohei Kumagai, Takefumi Yoshida, Hiroaki Iguchi, Masanori Wakizaka, Nobuto Funakoshi, Shinya Takaishi
DOI: 10.1039/D3CC04285E
What is the nature of the uranium(iii)–arene bond?
Sabyasachi Roy Chowdhury, Bess Vlaisavljevich
DOI: 10.1039/D3SC04715F
Significant hydrogen generation via photo-mechanical coupling in flexible methylammonium lead iodide nanowires
Yucheng Zhang, Jiawei Huang, Mengya Zhu, Zhouyang Zhang, Kaiqi Nie, Zhiguo Wang, Xiaxia Liao, Longlong Shu, Tingfang Tian, Zhao Wang, Yang Lu, Linfeng Fei
DOI: 10.1039/D3SC05434A
Visible-light-induced iron-catalyzed reduction of nitroarenes to anilines
Shilei Yang, Min He, Yi Wang, Ming Bao, Xiaoqiang Yu
DOI: 10.1039/D3CC04324J
Recent advancements in the use of Bobbitt's salt and 4-acetamidoTEMPO
Jean M. Bray, Shannon M. Stephens, Shayne M. Weierbach, Karen Vargas, Kyle M. Lambert
DOI: 10.1039/D3CC04709A
您可能还喜欢
2-(甲基磺酰基)嘧啶-5-胺(CAS号:56621-92-2)适用哪些法规指南?
该化合物适用的法规指南包括GHS(全球化学品统一分类和标签制度)分类为特定目标器官毒性-单次接触类别3;根据欧盟REACH法规,该化合物需要进行注册和评估;在美...
在合成中是否有4-(4-氯苯基)-1H-咪唑(CAS号:35512-29-9)的替代品?
在合成中,可以考虑使用一些类似的化合物作为4-(4-氯苯基)-1H-咪唑的替代品,如4-(4-溴苯基)-1H-咪唑或4-(4-甲氧基苯基)-1H-咪唑。这些化合...
什么是N~2~-甲基丙氨酸酰胺(CAS号:32012-16-1)?
N~2~-甲基丙氨酸酰胺是一种有机化合物,其化学名为2-(Methylamino)propanamide。它是一种酰胺类化合物,分子式为C4H10N2O,相对分...
如何处理含有N-苄基-3-氨基氧杂环丁烷草酸盐(CAS号:1956341-96-0)的废料?
处理含有N-苄基-3-氨基氧杂环丁烷草酸盐(CAS号:1956341-96-0)的废料时,应首先确保遵循相关法规要求,如GHS和REACH等。通常,废液应先进行...
4-bromo-2-chloro-6-methylbenzoic acid(CAS号:877149-07-0)的物理化学性质是什么?
4-溴-2-氯-6-甲基苯甲酸是一种固体化合物,具有较高的熔点和较低的沸点。它的分子量为261.03 g/mol。该化合物在水中几乎不溶,在有机溶剂中溶解度适中...
2-[(2,5-二氯-4-嘧啶)氨基]-N-甲基苯甲酰胺(CAS号:761440-08-8)通常如何合成?
该化合物通常通过缩合反应合成,典型的方法是将2,5-二氯嘧啶与N-甲基苯甲酰胺在碱性条件下进行偶联反应。常用的碱包括NaH、LDA等强碱。该合成路线具有较高的选...
在合成中是否有3,5-二溴-4-甲基苯胺(CAS号:13194-73-5)的替代品?
3,5-二溴-4-甲基苯胺在某些合成路线中可能没有直接替代品。然而,在某些应用场景下,可以考虑使用其他类似结构的化合物如3,5-二溴-4-硝基苯胺或3,5-二碘...
2-氯喹啉-4-羧酸甲酯(CAS号:62482-26-2)的主要用途是什么?
2-氯喹啉-4-羧酸甲酯主要用于有机合成和药物合成领域,作为中间体或原料。它在合成某些药物和染料时具有重要作用。此外,该化合物还可能用于某些特定的化学研究中。
i>]吡啶(CAS号:474708-88-8)安全吗?
6-溴-8-氯咪唑[1,2-a]吡啶在操作过程中需要谨慎以确保安全。该化合物具有一定的毒性,吸入其蒸气或粉尘可能导致呼吸道刺激。处理时应佩戴适当的防护装备,如手...
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.











![5-Methoxy-1H-pyrrolo[3,2-b]pyridine structure 5-Methoxy-1H-pyrrolo[3,2-b]pyridine structure](https://cnstatic.chemtradehub.com/structs/172/17288-40-3-a8d1.webp)

![(1R,3S,5R)-2-{[(2-Methyl-2-propanyl)oxy]carbonyl}-2-azabicyclo[3.1.0]hexane-3-carboxylic acid structure (1R,3S,5R)-2-{[(2-Methyl-2-propanyl)oxy]carbonyl}-2-azabicyclo[3.1.0]hexane-3-carboxylic acid structure](https://cnstatic.chemtradehub.com/structs/197/197142-34-0-6a44.webp)
![5-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-2H-pyrazolo[3,4-c]pyridazin-3-amine structure 5-(2-Phenylpyrazolo[1,5-a]pyridin-3-yl)-2H-pyrazolo[3,4-c]pyridazin-3-amine structure](https://cnstatic.chemtradehub.com/structs/865/865362-74-9-0091.webp)