首页 | 本学科首页   官方微博 | 高级检索  
     检索      

苯氧乙酰基四羰基钴催化亚胺与一氧化碳交替共聚反应合成多肽类聚合物
引用本文:张永坡,孙怀林.苯氧乙酰基四羰基钴催化亚胺与一氧化碳交替共聚反应合成多肽类聚合物[J].高等学校化学学报,2014,35(1):54-57.
作者姓名:张永坡  孙怀林
作者单位:南开大学化学系, 天津 300071
基金项目:国家自然科学基金(批准号:20834002);天津市自然科学基金(批准号:08JCZDJC21600)和高等学校博士学科点专项科研基金(批准号:20090031110012)资助.
摘    要:报道了一种新的苯氧乙酰基四羰基钴催化剂,并将其用于催化亚胺与一氧化碳的交替共聚反应. 1H NMR分析结果表明,该催化剂在1个大气压的CO气氛下以烷基钴和酰基钴平衡的形式存在. 催化反应结果表明,该催化剂具有良好的催化性能,可以得到具有较高分子量、N端为苯氧乙酰基的多肽类聚合物,且具有较窄的分子量分布. 利用核磁共振\,红外光谱和质谱等对多肽聚合物的结构进行了表征,结果表明,聚合物链终止端除了具有慕尼黑酮类结构的端基以外,还存在酰胺类的端基,并对后者的生成机制进行了解释.

关 键 词:酰基钴  烷基钴  催化剂  亚胺  多肽
收稿时间:2013-05-09

Phenoxyacetylcobalt Tetracarbonyl as Catalyst for Copolymerization of Imines and CO to Produce Polypeptides
ZHANG Yongpo,SUN Huailin.Phenoxyacetylcobalt Tetracarbonyl as Catalyst for Copolymerization of Imines and CO to Produce Polypeptides[J].Chemical Research In Chinese Universities,2014,35(1):54-57.
Authors:ZHANG Yongpo  SUN Huailin
Institution:Department of Chemistry, Nankai Univeristy, Tianjin 300071, China
Abstract:A new phenoxyacetylcobalt tetracarbonyl catalyst was synthesis and used to catalyze alternating copolymerization of imines and CO. 1H NMR study indicated that this catalyst existed in the form of an equilebium between the aklycobalt and acylcobalt complexes under 1×105 Pa of CO atmosphere. The results obtained using the catalyst in imines and CO copolymerization demonstrates that this catalyst had good performance, producing polypeptides of high molecular weights, with phenoxyacetyl groups at the starting ends of the polymer chains, and of narrow molecular weight distributions. The structures of polypeptide obtained were characterized by 1H NMR and 13C NMR, IR as well as MALDI-TOF MS methods. It is revealed that at the terminal ends of the polymer chains there exist end groups of amide structures in addition to those observed previously. Possible mechanism for the formation of the amide end groups was provided.
Keywords:Acylcobalt  Alkylcobalt  Catalyst  Imine  Polypeptide
本文献已被 CNKI 等数据库收录!
点击此处可从《高等学校化学学报》浏览原始摘要信息
点击此处可从《高等学校化学学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号