Suppr超能文献

作为苯胺酶促聚合软模板的囊泡

Vesicles as soft templates for the enzymatic polymerization of aniline.

作者信息

Guo Zengwei, Rüegger Heinz, Kissner Reinhard, Ishikawa Takashi, Willeke Martin, Walde Peter

机构信息

Department of Materials, ETH Zürich, Wolfgang-Pauli-Str. 10, CH-8093 Zürich, Switzerland.

出版信息

Langmuir. 2009 Oct 6;25(19):11390-405. doi: 10.1021/la901510m.

Abstract

The feasibility of using surfactant vesicles as soft templates for the peroxidase-triggered polymerization of aniline was investigated. It was found that mixed anionic vesicles (diameter approximately 80 nm) composed of sodium dodecylbenzenesulfonate (SDBS) and decanoic acid (1:1, molar ratio) are promising templates. In the presence of the vesicles and horseradish peroxidase/hydrogen peroxide (H2O2) as initiator system, aniline polymerizes under optimized conditions at pH=4.3 to the desired conductive emeraldine form of polyaniline (PANI). The optimal polymerization conditions were elaborated, and some of the chemical and physicochemical aspects of the reaction system were investigated. After addition of aniline and peroxidase to the vesicles, aniline is only loosely associated with the vesicles, as shown by NOESY-NMR and zeta potential measurements. In contrast, the peroxidase strongly binds to the vesicle surface, as shown by fluorescence measurements using TNS (2-(p-toluidino)naphthalene-6-sulfonate) as vesicle membrane probe. This binding of the enzyme to the vesicle surface indicates that the polymerization reaction is initiated predominantly on the surface of the vesicles. Cryo-transmission electron microscopy indicates that the polymerization product remains associated with the vesicles on their surface. For short reaction times (30 s<t<60 s), it is shown that oligoanilines containing an excess of oxidized units are obtained, as shown by VIS/NIR spectroscopy and MALDI-TOF mass spectrometry. For longer reaction times (1 min<t<30 min), the relative amount of over oxidized units in PANI decreases until polymers are obtained which have a VIS/NIR spectrum that is typical for the emeraldine salt form of PANI (lambdamax approximately 1000 nm). The appearance of stable unpaired electrons during the reaction was demonstrated by EPR measurements, in full support of the in situ formation of the conductive emeraldine salt form of PANI. At the end of the reaction (after 1 h), the PANI formed remains homogenously dispersed in the aqueous solution thanks to the presence of the vesicles. No precipitation occurs on a time scale of at least several weeks. FTIR and 13C NMR measurements of the product isolated from the reaction mixture confirm the formation of the emeraldine form of PANI. If the polymerization reaction is carried out in the absence of vesicles but under otherwise identical reaction conditions, the outcome of the reaction is very different, i.e., no indication at all for the formation of the conductive form of PANI.

摘要

研究了使用表面活性剂囊泡作为软模板用于过氧化物酶引发的苯胺聚合反应的可行性。发现由十二烷基苯磺酸钠(SDBS)和癸酸(摩尔比1:1)组成的混合阴离子囊泡(直径约80nm)是有前景的模板。在囊泡以及辣根过氧化物酶/过氧化氢(H₂O₂)作为引发剂体系存在的情况下,苯胺在pH = 4.3的优化条件下聚合为所需的导电聚苯胺(PANI)的翠绿亚胺形式。阐述了最佳聚合条件,并研究了反应体系的一些化学和物理化学方面。将苯胺和过氧化物酶加入囊泡后,如通过NOESY-NMR和zeta电位测量所示,苯胺仅与囊泡松散结合。相比之下,如使用TNS(2 - (对甲苯胺基)萘 - 6 - 磺酸盐)作为囊泡膜探针的荧光测量所示,过氧化物酶强烈结合到囊泡表面。酶与囊泡表面的这种结合表明聚合反应主要在囊泡表面引发。冷冻透射电子显微镜表明聚合产物在其表面仍与囊泡相关联。对于短反应时间(30s < t < 60s),如通过VIS/NIR光谱和MALDI-TOF质谱所示,得到含有过量氧化单元的低聚苯胺。对于较长反应时间(1min < t < 30min),PANI中过度氧化单元的相对量减少,直到获得具有PANI翠绿亚胺盐形式典型VIS/NIR光谱(λmax约1000nm)的聚合物。通过EPR测量证明了反应过程中稳定未成对电子的出现,充分支持了导电翠绿亚胺盐形式PANI的原位形成。在反应结束时(1小时后),由于囊泡的存在,形成的PANI仍均匀分散在水溶液中。在至少几周的时间尺度上没有沉淀发生。从反应混合物中分离出的产物的FTIR和¹³C NMR测量证实了PANI翠绿亚胺形式的形成。如果在没有囊泡的情况下但在其他相同反应条件下进行聚合反应,反应结果则大不相同,即根本没有迹象表明形成了导电形式的PANI。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验