Fronczyk Tomasz, Mielańczyk Anna, Klymenko Olesya, Erfurt Karol, Neugebauer Dorota
Department of Physical Chemistry and Technology of Polymers, Faculty of Chemistry, Silesian University of Technology, M. Strzody 9 Street, 44-100 Gliwice, Poland.
Department of Histology and Cell Pathology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland.
Molecules. 2023 Dec 21;29(1):55. doi: 10.3390/molecules29010055.
This study explores the synthesis, characterization, and application of a heterofunctional initiator derived from 2-hydroxypropyl cyclodextrin (HP-β-CD), having eight bromoester groups and thirteen hydroxyl groups allowing the synthesis of mikto-arm star-shaped polymers. The bromoesterification of HP-β-CD was achieved using α-bromoisobutyryl bromide as the acylation reagent, modifying the cyclodextrin (CD) molecule as confirmed by electrospray ionization mass spectrometry (ESI-MS), nuclear magnetic resonance (NMR), attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectroscopy analysis, and differential scanning calorimetry (DSC) thermograms. The initiator's effectiveness was further demonstrated by obtaining star-comb and mikto-arm polymers via an enzymatically assisted atom transfer radical polymerization (ATRP) method and subsequent ring-opening polymerization (ROP). The ATR polymerization quality and control depended on the type of monomer and was optimized by the way of introducing the initiator into the reaction mixture. In the case of ATRP, high conversion rates for poly(ethylene oxide) methyl ether methacrylate (OEOMA), with molecular weights (Mn) of 500 g/mol and 300 g/mol, were achieved. The molecular weight distribution of the obtained polymers remained in the range of 1.23-1.75. The obtained star-comb polymers were characterized by different arm lengths. Unreacted hydroxyl groups in the core of exemplary star-comb polymers were utilized in the ROP of ε-caprolactone (CL) to obtain a hydrophilic mikto-arm polymer. Cloud point temperature (T) values of the synthesized polymers increased with arm length, indicating the polymers' reduced hydrophobicity and enhanced solvation by water. Atomic force microscopy (AFM) analysis revealed the ability of the star-comb polymers to create fractals. The study elucidates advancements in the synthesis and utilization of hydrophilic sugar-based initiators for enzymatically assisted ATRP in an aqueous solution for obtaining complex star-comb polymers in a controlled manner.
本研究探索了一种源自2-羟丙基环糊精(HP-β-CD)的杂功能引发剂的合成、表征及应用,该引发剂具有八个溴酯基团和十三个羟基,可用于合成多臂星形聚合物。使用α-溴异丁酰溴作为酰化试剂实现了HP-β-CD的溴酯化反应,通过电喷雾电离质谱(ESI-MS)、核磁共振(NMR)、衰减全反射傅里叶变换红外(ATR-FTIR)光谱分析以及差示扫描量热法(DSC)热分析图谱证实了环糊精(CD)分子的改性。通过酶促原子转移自由基聚合(ATRP)方法及随后的开环聚合(ROP)获得星型梳状和多臂聚合物,进一步证明了该引发剂的有效性。ATRP的聚合质量和可控性取决于单体类型,并通过将引发剂引入反应混合物的方式进行了优化。在ATRP的情况下,实现了聚(环氧乙烷)甲基醚甲基丙烯酸酯(OEOMA)的高转化率,其分子量(Mn)分别为500 g/mol和300 g/mol。所得聚合物的分子量分布保持在1.23 - 1.75范围内。所获得的星型梳状聚合物具有不同的臂长。示例性星型梳状聚合物核心中未反应的羟基用于ε-己内酯(CL)的ROP反应,以获得亲水性多臂聚合物。合成聚合物的浊点温度(T)值随臂长增加而升高,表明聚合物疏水性降低且水合作用增强。原子力显微镜(AFM)分析揭示了星型梳状聚合物形成分形的能力。该研究阐明了在水溶液中用于酶促ATRP的亲水性糖基引发剂的合成及应用进展,以便以可控方式获得复杂的星型梳状聚合物。