Institute of Inorganic Chemistry, University of Regensburg , 93040 Regensburg , Germany.
ICSM, CEA, CNRS, ENSCM, Univ Montpellier , 34199 Marcoule , France.
J Am Chem Soc. 2019 May 1;141(17):6890-6899. doi: 10.1021/jacs.8b12181. Epub 2019 Apr 18.
We show here for the first time that short chain poly( N-isopropylacrylamide) (PNIPAM), one of the most famous thermoresponsive polymers, self-assembles in water to form (i) discrete nanometer-globules and (ii) micrometric sheets with nm-thickness upon addition of the well-known Keggin-type polyoxometalate (POM) HPWO (PW). The type of self-assembly is controlled by PW concentration: at low PW concentrations, PW adsorbs on PNIPAM chains to form globules consisting of homogeneously distributed PWs in PNIPAM droplets of several nm in size. Upon further addition of PW, a phase transition from globules to micrometric sheets is observed for PNIPAMs above a polymer critical chain length, between 18 and 44 repeating units. The thickness of the sheets is controlled by the PNIPAM chain length, here from 44 to 88 repeating units. The PNIPAM sheets are electrostatically stabilized PWs accumulated on each side of the sheets. The shortest PNIPAM chain with 18 repeating units produces PNIPAM/PW globules with 5-20 nm size but no sheets. The PW/PNIPAM self-assembly arises from a solvent mediated mechanism associated with the partial dehydration of PW and of the PNIPAM, which is related to the general propensity of POMs to adsorb on neutral hydrated surfaces. This effect, known as superchaotropy, is further highlighted by the significant increase in the lower critical solubilization temperature (LCST) of PNIPAM observed upon the addition of PW in the mM range. The influence of the POM nature on the self-assembly of PNIPAM was also investigated by using HSiWO (SiW) and HPMoO (PMo), i.e. changing the POM's charge density or polarizability in order to get deeper understanding on the role of electrostatics and polarizability in the PNIPAM self-assembly process. We show here that the superchaotropic behavior of POMs with PNIPAM polymers enables the formation and the shape control of supramolecular organic-inorganic hybrids.
我们首次表明,短链聚(N-异丙基丙烯酰胺)(PNIPAM)是最著名的温敏聚合物之一,在水中自组装形成(i)离散的纳米球和(ii)具有纳米厚度的微米片,加入众所周知的 Keggin 型多金属氧酸盐(POM)HPWO(PW)后。自组装的类型由 PW 浓度控制:在低 PW 浓度下,PW 吸附在 PNIPAM 链上,形成由均匀分布的 PW 组成的纳米球,PNIPAM 液滴的大小为数纳米。当 PNIPAM 超过聚合物临界链长(18 至 44 个重复单元)时,进一步加入 PW 会观察到从纳米球到微米片的相转变。片的厚度由 PNIPAM 链长控制,这里从 44 到 88 个重复单元。PNIPAM 片是在片的每一侧积累的静电稳定的 PW。具有 18 个重复单元的最短 PNIPAM 链产生 5-20nm 大小的 PNIPAM/PW 纳米球,但没有片。PW/PNIPAM 自组装源于与 PW 和 PNIPAM 的部分脱水相关的溶剂介导机制,这与 POM 吸附在中性水合表面的一般倾向有关。这种效应,称为超亲液性,在 PW 在 mM 范围内加入时观察到 PNIPAM 的下临界溶解温度(LCST)显著增加时进一步得到强调。通过使用 HSiWO(SiW)和 HPMoO(PMo)即改变 POM 的电荷密度或极化率来研究 POM 性质对 PNIPAM 自组装的影响,以更深入地了解静电和极化率在 PNIPAM 自组装过程中的作用。我们首次表明,具有 PNIPAM 聚合物的 POM 的超亲液性行为能够形成和控制超分子有机-无机杂化。