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Pasteur's tartaramide/malamide quasiracemates: new entries and departures from near inversion symmetry

机译:巴斯德尔的鞑靼酰胺/ malamide quasiracemates:来自近代对称的新条目和偏离

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摘要

This investigation explores Pasteur's 1853 (+)-tartaramide/(?)-malamide quasiracemate, extends this system to the crystallization behavior of methyl and butyl derivatives, and challenges the well-known notion that pairs of quasienantiomers assemble without exception to give near centrosymmetric crystal packing motifs. Each of the structures included in this study exhibits an extensive set of N/O–H?O contacts with component alignment in the quasiracemates defined by inversion and/or glide symmetry. Solid-state density functional theory calculations were applied to quantify the crystal stabilization and rationalize the observed packing tendencies.
机译:该调查探讨巴斯德的1853(+) - 酒石酰胺/(?) - 丙酰氨酸喹啉酸酯,将该系统延伸到甲基和丁基衍生物的结晶行为,并挑战众所周知的Quasienantiomers组装的众所周知的观念,而无一例外地给予靠近CentroSmmetric晶体 包装图案。 本研究中包括的每个结构具有广泛的N / O-H·O触点,其与通过反转和/或滑动对称限定的QuasiRaceMate中的组分对准。 固态密度功能理论计算用于量化晶体稳定化并合理化观察到的包装趋势。

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