首页> 外文期刊>Chirality: The pharmacological, biological, and chemical consequences of molecular asymmetry >Circular Dichroism of Host-Guest Complexes of Achiral Pyridino- and Phenazino-18-crown-6 Ligands with the Enantiomers of Chiral Aralkyl Ammonium Salts
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Circular Dichroism of Host-Guest Complexes of Achiral Pyridino- and Phenazino-18-crown-6 Ligands with the Enantiomers of Chiral Aralkyl Ammonium Salts

机译:非手性吡啶并-和苯并--18-冠-6配体的客体-客体配合物与手性芳烷基铵盐的对映体的圆二色性

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Circular dichroism (CD) spectroscopy was used for distinguishing different types of chiral interactions in host-guest complexes of achiral pyridino- and phenazino-18-crown-6 ligands with chiral aralkyl ammonium salts. The general feature of the CD spectra of many homochiral (e.g., (R,R)-host and (R)-guest) and heterochiral (e.g., (R,R)-host and (S)-guest) α-(1-naphthyl)ethylamine hydrogenperchlorate salt (NEA) complexes with chiral pyridino- and phenazino-18-crown-6 hosts is exciton interaction. The most interesting example is the coupling of the transitions of the chiral guest NEA with the energetically close transitions of the achiral phenazino-18-crown-6 host 6. The CD spectrum of the complex is predominated by exciton coupling between the ~1B_b transition of the chiral guest and the ~1B_b transition of the achiral host. The redshifted intense spectra of the complexes of (R)- or (S)-1-phenylethylamine hydrogenperchlorate salt (PEA) with the achiral diester-pyridino-18-crown-6 host 4 are indicative of merging the π electron systems into one joint charge transfer chromophore. The appearance of weak bands with alternating sign in the spectrum of PEA complexes of the achiral "parent" pyridino-18-crown-6 host (1) indicates the presence of two or more conformers. The CD spectra of the complexes of achiral phenazino-18-crown-6 host 6 with PEA are also determined by π-π interaction. In addition to charge transfer bands, CD bands are also induced in the long-wavelength spectral region of the achiral host. The weak π-π interaction between the achiral phenazino-18-crown-6 host and methyl phenylglycinate hydrogenperchlorate (PGMA) or methyl phenylalaninate hydrogenperchlorate (PAMA) does not result in a definite spectral effect in the ~1L_a region of the spectrum of the chiral guest, but its existence is proven by the weak CD bands induced in the long-wavelength spectral region of the achiral host.
机译:圆二色性(CD)光谱用于区分手性芳烷基铵盐的非手性吡啶基和吩并基18冠6配体的客体-客体复合物中的不同类型的手性相互作用。许多同手性(例如,(R,R)-宿主和(R)-来宾)和异手性(例如,(R,R)-宿主和(S)-来宾)的CD光谱的一般特征α-(1 -萘基)乙胺高氯酸氢盐(NEA)与手性吡啶基和苯并基18冠6主体的复合物是激子相互作用。最有趣的例子是手性客体NEA的跃迁与非手性phenazino-18-crown-6主体6的能量上接近的跃迁的耦合。络合物的CD谱主要由的〜1B_b跃迁之间的激子耦合所决定。手性客人和非手性宿主的〜1B_b过渡。 (R)-或(S)-1-苯基乙胺高氯酸氢盐(PEA)与非手性二酯-吡啶基-18-皇冠-6主体4的配合物的红移强光谱表明π电子系统合并为一个接头电荷转移生色团。在非手性“亲代” pyridino-18-crown-6宿主的PEA配合物谱中出现带交替符号的弱带(1),表明存在两个或更多个构象体。还通过π-π相互作用来确定非手性吩嗪诺-18-冠-6主体6与PEA的复合物的CD光谱。除电荷转移带外,在非手性宿主的长波长光谱区中还诱导出CD带。非手性吩嗪诺-18-crown-6主体与苯基甘氨酸甲酯高氯酸氢盐(PGMA)或苯丙氨酸甲酯高氯酸氢盐(PAMA)之间的弱π-π相互作用不会在手性光谱的〜1L_a区域产生确定的光谱效应客体,但它的存在被非手性宿主的长波长光谱区域中诱导的弱CD波段所证明。

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