Mann Sarah K, Devgan Mohit K, Franks W Trent, Huband Steven, Chan Chi Long, Griffith Jeraime, Pugh David, Brooks Nicholas J, Welton Tom, Pham Tran N, McQueen Lisa L, Lewandowski Józef R, Brown Steven P
Department of Physics, University of Warwick, Coventry CV4 7AL, U.K.
Department of Chemistry, Imperial College London, London SW7 2AZ, U.K.
J Phys Chem B. 2020 Jun 18;124(24):4975-4988. doi: 10.1021/acs.jpcb.0c02328. Epub 2020 Jun 4.
The structure and molecular order in the thermotropic ionic liquid crystal (ILC), [choline][geranate(H)octanoate], an analogue of Choline And GEranate (CAGE), which has potential for use as a broad-spectrum antimicrobial and transdermal and oral delivery agent, were investigated by magic-angle spinning (MAS) nuclear magnetic resonance (NMR), polarizing optical microscopy, small-angle X-ray scattering (SAXS), and mass spectrometry. Mass spectrometry and the H NMR chemical shift reveal that CAGE-oct is a dynamic system, with metathesis (the exchange of interacting ions) and hydrogen exchange occurring between hydrogen-bonded/ionic complexes such as [(choline)(geranate)(H)(octanoate)], [(choline)(octanoate)(H)], and [(choline)(geranate)(H)]. These clusters, which are shown by mass spectrometry to be significantly more stable than expected for typical electrostatic ion clusters, involve hydrogen bonding between the carboxylic acid, carboxylate, and hydroxyl groups, with rapid hydrogen bond breaking and re-formation observed to average the H chemical shifts. The formation of a partial bilayer liquid crystal (LC) phase was identified by SAXS and polarizing optical microscopy at temperatures below ∼293 K. The occurrence of this transition close to room temperature could be utilized as a potential temperature-induced "switch" of the anisotropic properties for particular applications. The presence of an isotropic component of approximately 23% was observed to coexist with the LC phase, as detected by polarizing optical microscopy and quantified by both H-C dipolar-chemical shift correlation (DIPSHIFT) and H double-quantum (DQ) MAS NMR experiments. At temperatures above the LC-to-isotropic transition, intermediate-range order (clustering of polar and nonpolar domains), a feature of many ILs, persists. Site-specific order parameters for the LC phase of CAGE-oct were obtained from the MAS NMR measurement of the partially averaged C-H dipolar couplings () by cross-polarization (CP) build-up curves and DIPSHIFT experiments, and H-H dipolar couplings () by double-quantum (DQ) build-up curves. The corresponding order parameters, and , are in the range 0-0.2 and are lower compared to those for smectic (i.e., layered) phases of conventional nonionic liquid crystals, resembling those of lamellar phases formed by lyotropic surfactant-solvent systems.
热致离子液晶(ILC)[胆碱][香叶酸(H)辛酸酯]是胆碱与香叶酸(CAGE)的类似物,具有作为广谱抗菌剂以及透皮和口服给药剂的潜力,通过魔角旋转(MAS)核磁共振(NMR)、偏光显微镜、小角X射线散射(SAXS)和质谱对其结构和分子有序性进行了研究。质谱和氢核磁共振化学位移表明,CAGE - oct是一个动态系统;在诸如[(胆碱)(香叶酸)(H)(辛酸酯)]、[(胆碱)(辛酸酯)(H)]和[(胆碱)(香叶酸)(H)]等氢键/离子络合物之间发生复分解反应(相互作用离子的交换)和氢交换。质谱显示这些簇比典型的静电离子簇预期的要稳定得多,涉及羧酸、羧酸盐和羟基之间的氢键,观察到氢键快速断裂和重新形成以使氢化学位移平均化。通过SAXS和偏光显微镜在温度低于约293 K时确定形成了部分双层液晶(LC)相。接近室温时这种转变的出现可被用作特定应用中各向异性性质的潜在温度诱导“开关”。通过偏光显微镜观察到约23%的各向同性成分与LC相共存,并通过氢 - 碳偶极 - 化学位移相关(DIPSHIFT)和氢双量子(DQ)MAS NMR实验进行了量化。在高于LC - 各向同性转变的温度下,许多离子液体所具有的中程有序(极性和非极性域的聚集)仍然存在。通过交叉极化(CP)累积曲线和DIPSHIFT实验对部分平均的碳 - 氢偶极耦合()进行MAS NMR测量,以及通过双量子(DQ)累积曲线对氢 - 氢偶极耦合()进行测量,从而获得了CAGE - oct的LC相的位点特异性序参量。相应的序参量和在0 - 0.2范围内,与传统非离子液晶的近晶(即层状)相相比更低,类似于溶致表面活性剂 - 溶剂体系形成的层状相。