Institut de Chimie des Substances Naturelles, CNRS UPR2301, Université Paris-Sud, Université Paris-Saclay, Avenue de la Terrasse, 91198, Gif-sur-Yvette, France.
Aix Marseille Univ, CNRS, ICR, UMR7273, 13397, Marseille, France / Institut Universitaire de France, 75000, Paris, France.
Nat Commun. 2019 Jan 10;10(1):113. doi: 10.1038/s41467-018-07751-4.
Calixarenes are cyclic oligomers obtained by condensation of suitable p-functionalised phenols with formaldehyde, usually allowing for the synthesis of the well known small calixarenes (including up to eight phenolic subunits). We report here the discovery of much larger members of this family, exhibiting sizes up to 90 phenolic subunits: the giant calixarenes. These macrocycles are obtained according to simple, easily scalable processes, in yields up to 65%. We show that the formation of these giant macrocycles is favored by an oxygen-containing-group at the para-position of the starting phenol, high concentrations of heavy alkaline bases (rubidium or cesium hydroxides) and long reaction times. A mechanism is proposed to rationalize these observations. These giant macrocycles can also be obtained in the quasi-solid state, opening interesting perspectives in the field of calixarenes chemistry. Along with their intrinsic fundamental interest, these objects are also opening interesting applicative potentialities.
杯芳烃是通过合适的对位官能化苯酚与甲醛缩合得到的环状低聚物,通常可用于合成众所周知的小分子杯芳烃(包括多达 8 个酚基单元)。我们在这里报告了该家族更大成员的发现,其尺寸可达 90 个酚基单元:巨型杯芳烃。这些大环通过简单、易于扩展的工艺获得,产率高达 65%。我们表明,起始苯酚对位上含氧基团、高浓度重堿(如氢氧化铷或氢氧化铯)和长反应时间有利于这些巨型大环的形成。提出了一种机制来合理化这些观察结果。这些巨型大环也可以在准固态中获得,为杯芳烃化学领域开辟了有趣的前景。除了内在的基础研究意义外,这些物质还具有有趣的应用潜力。