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基于动态共价亚胺缩合和金属配位化学的非对映选择性多组分组装:机理与自识别立体化学自分类

Diasteroselective multi-component assemblies from dynamic covalent imine condensation and metal-coordination chemistry: mechanism and narcissistic stereochemistry self-sorting.

作者信息

Badetti Elena, Carmo Dos Santos Nadia Alessandra, Scaramuzzo Francesca A, Bravin Carlo, Wurst Klaus, Licini Giulia, Zonta Cristiano

机构信息

Department of Chemical Sciences, University of Padova, Via Marzolo 1 35131 Padova (PD) Italy

Institute of General, Inorganic and Theoretical Chemistry, University of Innsbruck Innrain 80/82 6020 Innsbruck Austria.

出版信息

RSC Adv. 2018 May 29;8(35):19494-19498. doi: 10.1039/c8ra03989e. eCollection 2018 May 25.

Abstract

Self-assembly of a modified tris(2-pyridylmethyl)amine TPMA ligand, zinc(ii) or cobalt(ii) ions, and amino acids have been used effectively as stereo dynamic optical probes for the determination of the enantiomeric excess of free amino acids either using Electronic or Vibrational Circular Dichroism (CD and VCD). Herein, we report the mechanistic and stereochemical study of the self-assembly process which reveals a complex equilibrium in solution where even small variations in the experimental conditions can profoundly affect the final products of the reaction. In particular, variation on the metal stoichiometry switch give rises to an entirely enantio narcissistic self-assembly of the structure.

摘要

一种修饰的三(2-吡啶甲基)胺(TPMA)配体、锌(II)或钴(II)离子与氨基酸的自组装已被有效地用作立体动态光学探针,通过电子圆二色光谱(CD)或振动圆二色光谱(VCD)来测定游离氨基酸的对映体过量。在此,我们报道了自组装过程的机理和立体化学研究,该研究揭示了溶液中的复杂平衡,其中即使实验条件的微小变化也会深刻影响反应的最终产物。特别是,金属化学计量比的变化会导致结构完全对映自恋的自组装。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bce/9080712/41b1884e7b6e/c8ra03989e-f1.jpg

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