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Chiral-discriminative amino acid films prepared by vacuum vaporization and/or plasma processing

机译:通过真空汽化和/或等离子体处理制备的手性区分氨基酸膜

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摘要

D-Phenylalanine (D-Phe) films capable of discriminating optical isomers were prepared by dry processing: radiofrequency sputtering or vacuum vaporization with and without the assistance of an inductively coupled plasma (ICP). Chemical and spectroscopic analyses revealed that the majority of the constituents of the vaporized film are D-Phe molecules. However, the film prepared by ICP-assisted vaporization contains scarcely any D-Phe. The chiral-sensing properties of these D-Phe films were confirmed by sorption measurements on cyclic monoterpenes. Quartz crystal resonators coated with these films respond to the (-)-forms of limonene and alpha-pinene preferentially to their (+)-forms at the ppm level. This chiral preference was not observed for carvone, which induced comparable frequency shifts to limonene and alpha-pinene even at sub-ppm levels. The strong electrostatic interactions of the carbonyl group in carvone probably overcome the weak interactions of the discriminative optical isomers. [References: 31]
机译:通过干式工艺制备能够区分光学异构体的D-苯丙氨酸(D-Phe)膜:在有或没有感应耦合等离子体(ICP)的情况下进行射频溅射或真空蒸发。化学和光谱分析表明,汽化膜的大部分成分是D-Phe分子。然而,通过ICP辅助汽化制备的膜几乎不含任何D-Phe。这些D-Phe膜的手性传感特性通过在环状单萜上的吸附测量得到证实。涂有这些薄膜的石英晶体谐振器对柠檬烯和α-pine烯的(-)形式响应优先于其ppm级的(+)形式。香芹酮没有观察到这种手性偏好,香芹酮甚至在低于ppm的水平下也引起相当的频移至柠檬烯和α-pine烯。香芹酮中羰基的强静电相互作用可能克服了区分性旋光异构体的弱相互作用。 [参考:31]

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