期刊文献+

基于聚磷腈可降解电活性材料的合成及其降解行为研究 被引量:4

Synthesis and degradation behavior study of biodegradable electroactive materials based on polyphosphazene
下载PDF
导出
摘要 以六氯环三磷腈为原料,加热开环聚合制备了聚二氯磷腈,再分别以苯胺五聚体为功能单元、甘氨酸乙酯和赖氨酸为调节基团,通过两步亲核取代反应,合成了两种可用于神经支架工程材料的可降解电活性高分子聚[(甘氨酸乙酯/苯胺五聚体)磷腈](PGAP)和聚[(赖氨酸/苯胺五聚体)磷腈](PLAP)。通过红外、热重、核磁、循环伏安、紫外等对聚合物进行了全面的表征。在此基础上,重点研究了氨基酸类侧链取代基对聚磷腈降解行为的影响。研究结果表明,侧链氨基酸类取代基的类型和比例对此高分子材料的降解行为有着关键性影响。其降解速率随着取代基比例的增加而加快,此外,随着氨基酸侧链基团极性的增加,降解速率增加。 Using hexachlorocyclohexane three phosphazene as raw material,polydichlorophosphazene was pre-pared by ring-opening polymerization.Then using aniline pentamer as functional unit,lysine and glycine ethyl ester as adj usting units,two electro-active biodegradable polymers of poly [(glycine ethyl ester/aniline pen-tamer)phosphazene](PGAP)and poly [(lysine/aniline pentamer)phosphazene](PLAP)were synthesized. Structure and electro-active property of the polymers were characterized by IR,TG,1 H NMR,UV and cyclic voltammetry.On this basis,influences of mass ratio and polarity of substituted side group on degradation of the polymers were studied.The experimental results show that,the side adj usting units had a critical impact on the degradation behavior of these polymers.The degradation rate will augment with increasing the proportion and polarity of amino acid derivative group.
出处 《功能材料》 EI CAS CSCD 北大核心 2015年第2期2013-2018,共6页 Journal of Functional Materials
基金 中国博士后基金资助项目(20100481084)
关键词 聚磷腈 电活性 PGAP PLAP 降解 PGAP PLAP polyphosphazene electroactive PGAP PLAP biodegradable
  • 相关文献

参考文献5

二级参考文献63

共引文献19

同被引文献46

  • 1鲍志素.磷腈化合物的合成及其对聚丙烯阻燃的应用[J].阻燃材料与技术,2006(2):13-14. 被引量:7
  • 2甘雪萍,仵亚婷,刘磊,沈彬,胡文彬.以次磷酸钠为还原剂涤纶织物化学镀铜研究[J].功能材料,2007,38(5):782-786. 被引量:39
  • 3Allcock H R. Chemistry and applications of polyphosphazenes [M]. New YorkJohn Wiley g Sons Inc,2003,1-100.
  • 4Carriedo G A, Garcia Alonso F J, G6mez-Elipe P, et al. A sim- plified and convenient laboratory-scMe preparation of 14N or tSN high molecular weight poly(dichlorophosphazene) directly from PCI [J]. Cheminform, 2003,9 (16) : 3833-3836.
  • 5Allcock H R, Nelson J M, Rohby P. Synthesis of teche[ic polyphosphazenes via the ambient temperature living cationic polymerization of amino phophoranimines[J]. Macromolecules, 1999,32(18) :5736 5743.
  • 6Blackstone V,Pfirrmann S, Helten H, et al. A cooperative role for the counteranion in the PCls-initiated living, cationic chain growth polycondensation of the phosphoranimine CI3P NSiMea[J]. J Am Chem Soc,2012,134(37):15293-15296.
  • 7Liu X,Breon J P, Chen C, et al. Suhstituent exchange reactions of linear oligomeric aryloxyphosphazenes with sodium 2,2,2- trifluoroethoxide[J]. Inorg Chem,2012,51(21) :11910-11916.
  • 8Wilfert S, Henke H, Schoefberger W, et al. Chain-end-function alized polyphosphazenes via a one-pot phosphine-mediated living polymerization[J]. Maeromol Rapid Commun, 2014, 35 (12) : 1135-1141.
  • 9Tian Z C,Chen C,Allcock H R. New mixed-substituent fluoro- phosphazene high polymers and small molecule cyclophosp- hazene models: synthesis, characterization, and structure prop- erty correlations[J]. Maeromolecule.,2015,48(5):1483-1492.
  • 10Wang S G,Jiang X,Chen P C,et al. Preparation of coaxial-elec trospun poly E bis( p-methylphenoxy)l phosphazene nanofiber membrane for enzyme immohi[ization[J]. Int J Mol Sci, 2012,13 (11) : 14136-14148.

引证文献4

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部