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新型大环手性(salen)配体及其铀和锰配合物的合成与构象研究。

Synthesis and conformational study of a novel macrocyclic chiral(salen) ligand and its uranyl and Mn complexes.

机构信息

Dipartimento di Scienze Chimiche, Università di Catania, Viale Andrea Doria 6, Catania 95125, Italy.

出版信息

Molecules. 2010 Mar 9;15(3):1442-52. doi: 10.3390/molecules15031442.

DOI:10.3390/molecules15031442
PMID:20335992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6257184/
Abstract

A novel chiral macrocyclic ligand incorporating a chiral salen moiety into a framework containing two biphenyl units was synthesized. Structural properties and conformational aspects of the free ligand and an UO2 complex were studied by using NMR spectroscopy in solution and MM calculations. The Mn(III) complex was tested as catalyst in enantioselective oxidation of prochiral unfunctionalized olefins to the corresponding optically active epoxides under very mild conditions.

摘要

合成了一种新型手性大环配体,该配体将手性席夫碱部分引入到含有两个联苯单元的骨架中。通过溶液中的 NMR 光谱和 MM 计算研究了游离配体和 UO2 配合物的结构性质和构象方面。在非常温和的条件下,Mn(III)配合物被测试为手性非官能化烯烃对映选择性氧化为相应的光学活性环氧化物的催化剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6228/6257184/72b180c0bc56/molecules-15-01442-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6228/6257184/ab9563a35095/molecules-15-01442-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6228/6257184/638bb494a2de/molecules-15-01442-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6228/6257184/9ba6a254c229/molecules-15-01442-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6228/6257184/81e2c5e17b60/molecules-15-01442-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6228/6257184/72b180c0bc56/molecules-15-01442-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6228/6257184/ab9563a35095/molecules-15-01442-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6228/6257184/638bb494a2de/molecules-15-01442-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6228/6257184/9ba6a254c229/molecules-15-01442-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6228/6257184/81e2c5e17b60/molecules-15-01442-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6228/6257184/72b180c0bc56/molecules-15-01442-g004.jpg

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本文引用的文献

1
Synthesis of metal-(pentadentate-salen) complexes: asymmetric epoxidation with aqueous hydrogen peroxide and asymmetric cyclopropanation (salenH2: N,N'-bis(salicylidene)ethylene-1,2-diamine).金属 -(五齿 - 水杨醛缩邻苯二胺)配合物的合成:用过氧化氢水溶液进行不对称环氧化反应和不对称环丙烷化反应(salenH2:N,N'-双(水杨基亚甲基)乙二胺)。
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Stereomutations of atropisomers of sterically hindered salophen ligands.位阻型双水杨醛缩邻苯二胺配体的阻转异构体的立体突变
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均相和多相催化不对称环氧化反应的进展
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Unprecedented detection of inherent chirality in uranyl-salophen complexes.首次检测到铀酰-沙罗酚配合物中的固有手性
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