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H-2 NMR reveals liquid state-like dynamics of arene guests inside hexameric pyrogallol[4]arene capsules in the solid state

机译:H-2 NMR在固态中揭示了内部六聚吡吡唑啉[4]芳烯胶囊内的芳ene客人的液体状动态

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The dynamics of guests in molecular encapsulation complexes have been studied extensively in solution, but the corresponding behavior of those guests when the capsules are present in the solid state is not as well understood. Here we report on comparative solution H-1 and solid-state H-2 NMR measurements of encapsulation complexes of fluorene(-d(2)), fluoranthene(-d(10)), and pyrene(-d(10)) in pyrogallol[4] arene hexamers assembled in the solid state by ball milling. In solution, the H-1 spectra show that these rigid guests tumble and exchange positions quickly within the capsules' interiors, with the exception of pyrene, which has slower tumbling and positional exchange. Static solid-state H-2 NMR using the deuterated guests shows that, when the capsules are in the solid state, their guests retain the liquid state-like dynamics observed for the capsules in solution. When the pyrogallol[4]arene hexamers' pendant decyl groups were substituted with propyl groups, guest dynamics in the solid state were slowed. We propose that these pendant alkyl groups form an interdigitated and dynamic waxy domain surrounding the capsules in the solid state, and that the greater mobility of the decyl groups is translated across the walls of the host, resulting in more rapid guest dynamics in the capsules' interiors.
机译:在溶液中广泛研究了分子包封复合物的客人的动态,但是当胶囊以固态存在时,这些客人的相应行为不太了解。在这里,我们报告芴(-D(2)),氟(-D(-D(10))和芘(-D(10))中的氟化烯(-D(2)),氟化络合物的封装复合物的H-1和固态H-2 NMR测量。吡羟吡咯[4]通过球磨用固态组装的芳樟醇六烷烃。在解决方案中,H-1光谱表明,这些刚性客人在胶囊内的内部速度快速翻滚和交换位置,除芘外,具有较慢的翻滚和位置交换。使用氘代客人的静态固态H-2 NMR表明,当胶囊处于固态时,其客人将在溶液中保留在胶囊中观察到的液体样动态。当吡羟基醇[4]芳烃六聚体的悬浮液被丙基取代时,速度较慢的客体动态。我们提出这些侧链烷基形成固态中胶囊的间隙和动态蜡状结构域,并且癸基的较大迁移率在宿主的壁上翻译,导致胶囊中的更快速的客体动态'室内设计。

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