Practical polymerization of functionalized lactones and carbonates with Sn(OTf)2 in metal catalysed ring-opening polymerization methods
文献信息
David M. Stevens, Harry A. Watson, Marc-Andre LeBlanc, Ray Y. Wang, Joanne Chou, Westley S. Bauer, Eva Harth
We report the synthesis of functionalized polycarbonates and polyesters employing stannous(II) trifluoromethane sulfonate [Sn(OTf)2] in homo and copolymerizations with monomers of the valerolactone family such as valerolactone and α-allyl-valerolactone using ring-opening polymerization (ROP) techniques and 5-methyl-5-allyloxycarbonyl-1,3-dioxane-2-one (MAC) and 5-methyl-5-ethyloxycarbonyl-1,3-dioxane-2-one (MEC). Practical reaction and work up conditions were established which circumvented the typically high polydispersities associated with Sn catalysts. Monomer concentration was found to be critical to incorporate challenging monomers such as α-allyl-valerolactone in the desired monomer ratios. Moreover, carbonate polymerizations were well controlled and facilitated products with narrow polydispersities. Bulk conditions for the polycarbonate polymerization were found to be preferential compared to traditional solution conditions. Additionally, the incorporation of α-allyl-valerolactone into polyester copolymers varied with monomer concentration, and highest incorporation was achieved using more dilute conditions.
相关文献
Solvent structural relaxation dynamics in dipolar solvation studied by resonant pump polarizability response spectroscopy
Sungnam Park, Jeongho Kim, Andrew M. Moran, Norbert F. Scherer
DOI: 10.1039/C0CP01252A
Multilayered Pt/Runanorods with controllable bimetallic sites as methanol oxidationcatalysts
Sung Jong Yoo, Tae-Yeol Jeon, Kyoung Sik Kim, Tae-Hoon Lim, Yung-Eun Sung
DOI: 10.1039/C0CP00737D
Measuring the three-phase contact angle of nanoparticles at fluid interfaces
Olivier J. Cayre, Martien A. Cohen Stuart, Simeon D. Stoyanov, Vesselin N. Paunov
DOI: 10.1039/B917353F
Quantification of surface species present on a nickel/alumina methane reformingcatalyst
Ian P. Silverwood, Neil G. Hamilton, Christian J. Laycock, John Z. Staniforth, R. Mark Ormerod, Christopher D. Frost, Stewart F. Parker, David Lennon
DOI: 10.1039/B919977B
The role of molecular modeling in confined systems: impact and prospects
Keith E. Gubbins, Joshua D. Moore, Jeremy C. Palmer
DOI: 10.1039/C0CP01475C
Solvent polarity effect on intramolecular electron transfer in a corrole–naphthalene bisimide dyad
Lucia Flamigni, Dagmara Wyrostek, Roman Voloshchuk, Daniel T. Gryko
DOI: 10.1039/B916525H
Ionic liquid silver salt complexes for propene/propane separation
Friederike Agel, Fee Pitsch, Florian Felix Krull, Peter Schulz, Matthias Wessling, Thomas Melin, Peter Wasserscheid
DOI: 10.1039/C0CP01104E
Molecular dynamics simulations of atomically flat and nanoporous electrodes with a molten salt electrolyte
Jenel Vatamanu, Oleg Borodin, Grant D. Smith
DOI: 10.1039/B917592J
您可能还喜欢
如何储存1,2-环己二酮环乙缩醛(CAS号:4746-96-7)?
1,2-环己二酮环乙缩醛应储存在阴凉、干燥、通风良好的地方,避免阳光直射。建议使用密封容器保存,并保持环境温度在室温范围内,远离火源和热源。
Ecopladib(CAS号:381683-92-7)的市场或研究趋势如何?
Ecopladib作为一种新型的药物,主要应用于治疗高胆固醇等疾病。目前,市场和研究趋势显示,Ecopladib因其独特的药理作用而受到关注。随着对心血管疾病治...
2,3-Dimethyl-3H-imidazo[4,5-c]pyridine(CAS号:52538-09-7)通常如何合成?
2,3-二甲基-3H-咪唑[4,5-c]吡啶通常通过咪唑和2,3-二甲基吡啶的缩合反应合成。具体来说,将咪唑和2,3-二甲基吡啶在适当的溶剂中进行加热或加压反应...
2,3,4,5-tetrahydro-1H-3-苯并氮杂环;盐酸盐(CAS号:17379-01-0)的市场或研究趋势如何?
该化合物在药物化学和有机合成中有一定的应用。近年来,随着对新型药物化合物的需求增加,该化合物的研究趋势主要集中在探索其生物活性,尤其是其在神经系统疾病治疗中的潜...
如何储存盐酸甘氨酸丁酯(CAS号:13048-99-2)?
盐酸甘氨酸丁酯应储存在阴凉、干燥、通风良好的地方,避免阳光直射和高温环境,温度应控制在25℃以下。储存容器应密封,避免与空气中的水分和酸性物质接触,以防发生水解...
什么是2-Iodo-N,N-dimethylbenzamide(CAS号:54616-46-5)?
2-碘-N,N-二甲基苯胺是一种有机化合物,化学名为2-Iodo-N,N-dimethylbenzamide。其分子式为C<sub>9</sub>H<sub>1...
5-溴-2-(4H-1,2,4-三唑-4-基)吡啶(CAS号:959240-99-4)的市场或研究趋势如何?
随着医药、农药和新材料领域的发展,该化合物作为关键中间体的应用日益增多。特别是在药物合成中,由于其独特的化学性质,可以用于合成多种药物分子。未来的研究趋势可能集...
2,4-二溴-6-三氟甲基嘧啶(CAS号:785778-00-9)通常如何合成?
2,4-二溴-6-三氟甲基嘧啶通常通过溴化反应合成。首先,将6-三氟甲基嘧啶与溴化剂(如液溴)在适当的溶剂(如二氯甲烷、四氢呋喃)中反应,加入适当的催化剂(如四...
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.














