首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Fluorescence investigations of the thermally induced conformational transition of poly(N-isopropylacrylamide)
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Fluorescence investigations of the thermally induced conformational transition of poly(N-isopropylacrylamide)

机译:聚(N-异丙基丙烯酰胺)热诱导构象转变的荧光研究

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critical solution temperature (LCST). Upon subsequent cooling, the dispersion rapidly clears again, at the LCST, to form a single, homogeneous phase. In this paper we report that fluorescence techniques, including quenching and time-resolved anisotropy measurements (TRAMS) on ultra-dilute (10(-3) wt%) aqueous solutions of an acenaphthylene labelled sample, provide conclusive evidence that a coil collapse mechanism is implicated in the thermoreversible behaviour: the polymer undergoes a conformational switch from an open coil below 32 degreesC to a compact, globular structure above the LCST. TRAMS reveal that a marked reduction in the segmental mobility of the polymer occurs at the onset of the LCST. In addition, a dramatic change in the accessibility of the label to aqueous-borne quenchers is also apparent at temperatures in excess of 32 degreesC. PNIPAM is capable of solubilising low molar mass species in its compact form: changes in the vibrational fine structure of the emission spectrum of pyrene have been used to monitor uptake and release of the probe. Excited state lifetime measurements have also proven to be sensitive monitors of the conformational switch of PNIPAM: at temperatures greater than 32 degreesC, tau increases to ca. 160 ns which is indicative of pyrene sequestered in a hydrophobic, protective environment. Release of the probe into the aqueous phase results in a dramatic reduction of tau to ca. 130 ns which is characteristic of pyrene dispersed in water. These data highlight the potential of NIPAM based polymers to act as carriers in controlled release applications. Fluorescence techniques have proved capable of monitoring changes in chain mobility, the degree of coil compaction and solubilization capacity (for organic guests) of PNIPAM as it is raised through its LCST. Information of this type is not readily obtained through other techniques and fluorescence approaches should prove invaluable in future investigations of the effects of chemical modification in attempts to manipulate the LCST of NIPAM-based systems. (C) 2001 Published by Elsevier Science Ltd. [References: 35]
机译:临界溶液温度(LCST)。在随后的冷却中,分散体在LCST处再次迅速清除,形成一个单一的均相。在本文中,我们报告了荧光技术,包括对ultra烯标记样品的超稀(10(-3)wt%)水溶液的猝灭和时间分辨各向异性测量(TRAMS),提供了确凿的证据表明线圈塌陷机理是与热可逆行为有关:聚合物经历构象转换,从低于32摄氏度的开放式线圈转变为高于LCST的致密球形结构。 TRAMS表明,在LCST开始时,聚合物的节段迁移率显着降低。此外,在超过32℃的温度下,标签对水性淬灭剂的可及性也发生了显着变化。 PNIPAM能够以紧凑的形式溶解低摩尔质量的物质:the发射光谱的振动精细结构的变化已用于监测探针的吸收和释放。激发态寿命测量也已被证明是PNIPAM构象转换的灵敏监测器:在高于32摄氏度的温度下,tau升高至约200摄氏度。 160 ns,这表明pyr被隔离在疏水的保护性环境中。探针释放到水相中导致tau显着降低至约。 130 ns是is分散在水中的特征。这些数据突出了基于NIPAM的聚合物在控释应用中作为载体的潜力。事实证明,荧光技术能够监测PNIPAM通过LCST升高时链迁移率,线圈压紧程度和增溶能力(对于有机客体)的变化。通过其他技术无法轻松获得此类信息,并且荧光方法应在未来对化学修饰效果的研究中发挥重要作用,以尝试操纵基于NIPAM的系统的LCST。 (C)2001年由Elsevier Science Ltd.发布。[参考:35]

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