Hanna Tracy A, Liu Lihua, Angeles-Boza Alfredo M, Kou Xiaodi, Gutsche C David, Ejsmont Krzysztof, Watson William H, Zakharov Lev N, Incarvito Christopher D, Rheingold Arnold L
Department of Chemistry, Texas Christian University, Box 298860, Fort Worth 76129, USA.
J Am Chem Soc. 2003 May 21;125(20):6228-38. doi: 10.1021/ja0289797.
The synthesis, complete characterization, and solid state structural and solution conformation determination of calix[n]arenes (n = 4, 6, 8) is reported. A complete series of X-ray structures of the alkali metal salts of calix[4]arene (HC4) illustrate the great influence of the alkali metal ion on the solid state structure of calixanions (e.g., the Li salt of monoanionic HC4 is a monomer; the Na salt of monoanionic HC4 forms a dimer; and the K, Rb, and Cs salts exist in polymeric forms). Solution NMR spectra of alkali metal salts of monoanionic calix[4]arenes indicate that they have the cone conformation in solution. Variable-temperature NMR spectra of salts HC4.M (M = Li, Na, K, Rb, Cs) show that they possess similar coalescence temperatures, all higher than that of HC4. Due to steric hindrance from tert-butyl groups in the para position of p-tert-butylcalix[4]arene (Bu(t)C4), the alkali metal salts of monoanionic Bu(t)C4 exist in monomeric or dimeric form in the solid state. Calix[6]arene (HC6) and p-tert-butylcalix[6]arene (Bu(t)C6) were treated with a 2:1 molar ratio of M(2)CO(3) (M = K, Rb, Cs) or a 1:1 molar ratio of MOC(CH(3))(3) (M = Li, Na) to give calix[6]arene monoanions, but calix[6]arenes react in a 1:1 molar ratio with M(2)CO(3) (M = K, Rb, Cs) to afford calix[6]arene dianions. Calix[8]arene (HC8) and p-tert-butylcalix[8]arene (Bu(t)()C8) have similar reactivity. The alkali metal salts of monoanionic calix[6]arenes are more conformationally flexible than the alkali metal salts of dianionic calix[6]arenes, which has been shown by their solution NMR spectra. X-ray crystal structures of HC6.Li and HC6.Cs indicate that the size of the alkali metal has some influence on the conformation of calixanions; for example, HC6.Li has a cone-like conformation, and HC6.Cs has a 1,2,3-alternate conformation. The calix[6]arene dianions show roughly the same structural architecture, and the salts tend to form polymeric chains. For most calixarene salts cation-pi arene interactions were observed.
本文报道了杯[n]芳烃(n = 4, 6, 8)的合成、完整表征以及固态结构和溶液构象的测定。一系列杯[4]芳烃(HC4)碱金属盐的X射线结构表明,碱金属离子对杯芳烃阴离子的固态结构有很大影响(例如,单阴离子HC4的锂盐是单体;单阴离子HC4的钠盐形成二聚体;而钾、铷和铯盐以聚合形式存在)。单阴离子杯[4]芳烃碱金属盐的溶液核磁共振谱表明它们在溶液中具有锥式构象。盐HC4.M(M = Li、Na、K、Rb、Cs)的变温核磁共振谱表明它们具有相似的聚结温度,均高于HC4的聚结温度。由于对叔丁基杯[4]芳烃(Bu(t)C4)对位叔丁基的空间位阻,单阴离子Bu(t)C4的碱金属盐在固态中以单体或二聚体形式存在。杯[6]芳烃(HC6)和对叔丁基杯[6]芳烃(Bu(t)C6)用碳酸M(2)(M = K、Rb、Cs)的2:1摩尔比或MOC(CH(3))(3)(M = Li、Na)的1:1摩尔比处理,得到杯[6]芳烃单阴离子,但杯[6]芳烃与碳酸M(2)(M = K、Rb、Cs)以1:1摩尔比反应生成杯[6]芳烃二阴离子。杯[8]芳烃(HC8)和对叔丁基杯[8]芳烃(Bu(t)()C8)具有相似的反应活性。单阴离子杯[6]芳烃的碱金属盐在构象上比二阴离子杯[6]芳烃的碱金属盐更具柔性,这已通过它们的溶液核磁共振谱得到证明。HC6.Li和HC6.Cs的X射线晶体结构表明,碱金属的大小对杯芳烃阴离子的构象有一定影响;例如,HC6.Li具有锥状构象,而HC6.Cs具有1,2,3 - 交替构象。杯[6]芳烃二阴离子显示出大致相同的结构架构,并且这些盐倾向于形成聚合物链。对于大多数杯芳烃盐,观察到了阳离子 - π芳烃相互作用。