Holerca Marian N, Sahoo Dipankar, Partridge Benjamin E, Peterca Mihai, Zeng Xiangbing, Ungar Goran, Percec Virgil
Roy & Diana Vagelos Laboratories, Department of Chemistry , University of Pennsylvania , Philadelphia , Pennsylvania 19104-6323 , United States.
Department of Physics and Astronomy , University of Pennsylvania , Philadelphia , Pennsylvania 19104-6396 , United States.
J Am Chem Soc. 2018 Dec 12;140(49):16941-16947. doi: 10.1021/jacs.8b11103. Epub 2018 Nov 28.
Liquid quasicrystals (LQC) have been discovered in self-assembling benzyl ether, biphenylmethyl ether, phenylpropyl ether, biphenylpropyl ether and some of their hybrid dendrons and subsequently in block copolymers, surfactants and other assemblies. These quasiperiodic arrays, which lack long-range translational periodicity, are approximated by two Frank-Kasper periodic arrays, Pm3̅ n cubic (Frank-Kasper A15) and P4/ mnm tetragonal (Frank-Kasper σ), which have been discovered in complex soft matter in the same order and compounds. Poly(2-oxazoline)s dendronized with (3,4) nG1 minidendrons (where n denotes an alkyl chain, C H) self-organize into the Pm3̅ n cubic phase ( n = 14 and 15) and, as reported recently, the P4/ mnm tetragonal phase ( n = 16). However, no LQC of a poly(2-oxazoline) is yet known. Here we report the synthesis, structural and retrostructural analysis of a dendronized poly(2-oxazoline) with n = 17 which self-organizes not only into the LQC but also in the above two Frank-Kasper approximants. All three phases are observed from the same polymer within a very narrow range of degree of polymerization that corresponds to only five monomer repeat units (5 ≤ DP ≤ 10). The formation of the Pm3̅ n cubic, P4/ mnm tetragonal and LQC phases from a single polymer chain within such a narrow range of DP raises the questions of how and why each of these phases is self-organized. This system may provide a model for theoretical investigations into the self-organization of soft matter into Frank-Kasper and related periodic and quasiperiodic arrays.
液态准晶体(LQC)已在自组装的苄基醚、联苯甲基醚、苯丙基醚、联苯丙基醚及其一些混合树枝状分子中被发现,随后在嵌段共聚物、表面活性剂及其他聚集体中也有发现。这些缺乏长程平移周期性的准周期阵列,可由两种弗兰克 - 卡斯帕周期阵列近似表示,即立方晶系的Pm3̅ n(弗兰克 - 卡斯帕A15)和四方晶系的P4/ mnm(弗兰克 - 卡斯帕σ),它们已在相同顺序的复杂软物质和化合物中被发现。用(3,4)nG1 微型树枝状分子(其中n表示烷基链,C H)枝化的聚(2 - 恶唑啉)自组装成Pm3̅ n立方相(n = 14和15),并且如最近报道的那样,还能形成P4/ mnm四方相(n = 16)。然而,聚(2 - 恶唑啉)的液态准晶体尚未为人所知。在此,我们报告了一种n = 17的枝化聚(2 - 恶唑啉)的合成、结构及逆向结构分析,该聚(2 - 恶唑啉)不仅能自组装成液态准晶体,还能形成上述两种弗兰克 - 卡斯帕近似相。在非常窄的聚合度范围内,从同一聚合物中观察到了所有这三个相,该范围仅对应于五个单体重复单元(5≤DP≤10)。在如此窄的DP范围内,单个聚合物链形成Pm3̅ n立方相、P4/ mnm四方相和液态准晶体相,这引发了关于这些相如何以及为何自组装的问题。该体系可能为软物质自组装成弗兰克 - 卡斯帕及相关的周期和准周期阵列的理论研究提供一个模型。