Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Aoba, Sendai, Japan.
Chemistry. 2012 Oct 1;18(40):12644-54. doi: 10.1002/chem.201201929. Epub 2012 Sep 11.
An (amido-ethynyl)helicene bidomain compound and an (amido-ethynyl-amido)helicene tridomain compound were synthesized. The multidomain compounds were designed on the basis of previous findings that amido and ethynyl oligomers form dimeric aggregates with properties orthogonal to each other. Four aggregate states of multidomain compounds, namely, all-dimer, amido-dimer, ethynyl-dimer, and random-coil states, were obtained in different solvents, which were analyzed by circular dichroism (CD), UV/Vis, (1)H NMR, and IR spectroscopy; vapor pressure osmometry (VPO); dynamic light scattering (DLS); and atomic force microscopy (AFM). The amido and ethynyl domains independently aggregated and disaggregated in a two-state manner. Reversible structural changes occurred for a tridomain compound between the ethynyl-dimer/random-coil state and the all-dimer/amido-dimer state with heating and cooling. Two structural change processes with different properties were obtained using a single compound.
合成了一种(酰胺-乙炔基)螺旋双域化合物和一种(酰胺-乙炔基-酰胺)螺旋三域化合物。多域化合物是基于以前的发现设计的,即酰胺和乙炔基低聚物形成具有相互正交性质的二聚体聚集体。在不同溶剂中获得了多域化合物的四种聚集态,即全二聚体、酰胺二聚体、乙炔基二聚体和无规线团态,通过圆二色性(CD)、紫外/可见(1)H NMR 和红外光谱、蒸气压渗透法(VPO)、动态光散射(DLS)和原子力显微镜(AFM)进行了分析。酰胺和乙炔基域以二态方式独立聚集和解聚。三域化合物在乙炔基二聚体/无规线团态和全二聚体/酰胺二聚体态之间随加热和冷却发生可逆结构变化。使用单个化合物获得了两种具有不同性质的结构变化过程。