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Spectroscopic investigations of poly(propyleneimine)dendrimers using the solvatochromic probe phenol blue and comparisons to poly(Amidoamine) dendrimers

机译:使用溶剂化变色探针酚蓝的聚(丙烯亚胺)树状聚合物的光谱研究以及与聚(酰胺基胺)树状聚合物的比较

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The physical and chemical properties of PPI dendrimers' interior were investigated using the fluorescent, solvatochromic probe phenol blue. In aqueous solutions of each generation studied, two discrete dye populations were clearly observed. PPI dendrimers were shown to form a tight, nonpolar association with the vast majority of available dye, within the dendrimer interior, near the core. In the steady-state fluorescence emission spectra, a microenvironment of decreasing polarity in increasingly larger-generation PPI dendrimers (up to G3) was seen for the associated probe. Each of the remaining larger-generation dendrimers provided a microenvironment of essentially equal polarity. Fluorescence anisotropy values for phenol blue in the PPI dendrimers demonstrated the dye's sensitivity to the changing molecular volumes of the dendrimer generations. Model compounds that mimicked PPI's surface groups and branching moieties were used to better define the associated dye's location. The mimics further confirmed that phenol blue was associated inside the dendrimer, where it did not interact with the dendrimer surface groups. The comparison of amine-terminated PPI and PAMAM dendrimers clearly demonstrated the effects of their structural differences and the ability of phenol blue to have sensed those differences, including the initiator core length, branching unit length, and branching unit chemical composition.
机译:使用荧光,溶剂变色探针酚蓝研究了PPI树状聚合物内部的物理和化学性质。在研究的每一代水溶液中,清楚地观察到两个离散的染料群体。已显示,PPI树状聚合物与树状聚合物内部核心附近的绝大多数可用染料形成紧密的非极性缔合。在稳态荧光发射光谱中,相关探针观察到越来越大的PPI树状聚合物(直至G3)中极性降低的微环境。其余每个较大的树枝状大分子都提供了极性基本相同的微环境。 PPI树状聚合物中酚蓝的荧光各向异性值证明了染料对树状聚合物世代不断变化的分子体积的敏感性。模仿PPI表面基团和分支部分的模型化合物用于更好地定义相关染料的位置。该模拟物进一步证实酚蓝与树枝状聚合物内部缔合,在酚醛蓝中它不与树枝状聚合物表面基团相互作用。胺封端的PPI和PAMAM树枝状大分子的比较清楚地表明了它们的结构差异的影响以及酚蓝感测这些差异的能力,包括引发剂核心长度,分支单元长度和分支单元化学组成。

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