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利用“二聚体”二吡咯合成的纳米级金属配位大环化合物。

Nanoscale metal coordination macrocycles fabricated by using "dimeric" dipyrrins.

作者信息

Maeda Hiromitsu, Hashimoto Takashi

机构信息

Department of Bioscience and Biotechnology, Faculty of Science and Engineering, Ritsumeikan University, Kusatsu 525-8577, Japan.

出版信息

Chemistry. 2007;13(28):7900-7. doi: 10.1002/chem.200700444.

Abstract

Covalently linked dipyrrin (dipyrromethene) dimers have afforded nanoscale [2+2]-type neutral coordination macrocycles with a diagonal of about 1.6 nm. Two moieties of the achiral dipyrrin-Zn(II) complex yield the chiral coordination macrocycles as minor species, as well as major meso stereoisomers by the covalent linkages. Tetrahedral Zn(II) coordination by using acyclic ligands enables the dipyrrin-metal complex units to readily rotate and pass through the cavity of the nanorings in order to reveal the transitions between the chiral and achiral isomers.

摘要

共价连接的二吡咯(二吡咯亚甲基)二聚体形成了对角线约为1.6 nm的纳米级[2+2]型中性配位大环。非手性二吡咯-Zn(II)配合物的两个部分通过共价键产生手性配位大环作为次要物种,以及主要的内消旋立体异构体。使用无环配体的四面体Zn(II)配位使二吡咯-金属配合物单元能够轻松旋转并穿过纳米环的空腔,以揭示手性和非手性异构体之间的转变。

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