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1,1'-联异喹啉——杂环二亚胺家族中被忽视的配体,引发立体化学思考。

1,1'-Biisoquinolines-Neglected Ligands in the Heterocyclic Diimine Family That Provoke Stereochemical Reflections.

机构信息

Department of Chemistry, University of Basel, BPR 1096, Mattenstrasse 24a, CH-4058 Basel, Switzerland.

School of Physical and Chemical Sciences, University of Canterbury, CT1 1PL Christchurch, New Zealand.

出版信息

Molecules. 2021 Mar 13;26(6):1584. doi: 10.3390/molecules26061584.

DOI:10.3390/molecules26061584
PMID:33805632
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7998815/
Abstract

1,1'-Biisoquinolines are a class of bidentate nitrogen donor ligands in the heterocyclic diimine family. This review briefly discusses their properties and the key synthetic pathways available and then concentrates upon their coordination behaviour. The ligands are of interest as they exhibit the phenomenon of atropisomerism (hindered rotation about the C1-C1' bond). A notation for depicting the stereochemistry in coordination compounds containing multiple stereogenic centers is developed. The consequences of the chirality within the ligand on the coordination behaviour is discussed in detail.

摘要

1,1'-联异喹啉是杂环二亚胺家族中一类双齿氮供体配体。本文简要讨论了它们的性质和现有的关键合成途径,然后集中讨论了它们的配位行为。这些配体很有趣,因为它们表现出阻转异构现象(C1-C1' 键的旋转受阻)。开发了一种用于描述含有多个手性中心的配位化合物立体化学的符号表示法。详细讨论了配体内部手性对配位行为的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/e886eb6824db/molecules-26-01584-g017.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/7d721297b4aa/molecules-26-01584-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/24e98835b65e/molecules-26-01584-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/48d5d4006a23/molecules-26-01584-sch002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/e886eb6824db/molecules-26-01584-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/f1628fb3c513/molecules-26-01584-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/b6b6712c7e54/molecules-26-01584-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/51df124211df/molecules-26-01584-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/afab5d27d4af/molecules-26-01584-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/7d721297b4aa/molecules-26-01584-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/24e98835b65e/molecules-26-01584-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/48d5d4006a23/molecules-26-01584-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/d3e64d44d9a0/molecules-26-01584-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/f5b28f472337/molecules-26-01584-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/8120b314bc8a/molecules-26-01584-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/2a5d3b68607d/molecules-26-01584-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/2073c2ed99c5/molecules-26-01584-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/821c4c040ccf/molecules-26-01584-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/993a71ba2fc2/molecules-26-01584-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/f279460771ec/molecules-26-01584-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/c33c1740423d/molecules-26-01584-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/a33176f661ca/molecules-26-01584-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6941/7998815/6157b43fdc70/molecules-26-01584-g014.jpg
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本文引用的文献

1
Synthesis of Pyridylsulfonium Salts and Their Application in the Formation of Functionalized Bipyridines.吡啶𬭩盐的合成及其在功能化联吡啶形成中的应用。
Org Lett. 2020 Nov 6;22(21):8451-8457. doi: 10.1021/acs.orglett.0c03048. Epub 2020 Oct 22.
2
The C-H Activation/Bidirecting Group Strategy for Selective Direct Synthesis of Diverse 1,1'-Biisoquinolines.用于选择性直接合成多种1,1'-联异喹啉的C-H活化/导向基团策略
Org Lett. 2020 Jun 5;22(11):4207-4212. doi: 10.1021/acs.orglett.0c01260. Epub 2020 May 19.
3
Exploiting racemism enhanced organic room-temperature phosphorescence to demonstrate Wallach's rule in the lighting chiral chromophores.
利用外消旋体增强的有机室温磷光来展示手性发色团中的瓦拉赫规则。
Nat Commun. 2020 May 1;11(1):2145. doi: 10.1038/s41467-020-15976-5.
4
: from visualization to analysis, design and prediction.从可视化到分析、设计与预测。
J Appl Crystallogr. 2020 Feb 1;53(Pt 1):226-235. doi: 10.1107/S1600576719014092.
5
The Early Years of 2,2'-Bipyridine-A Ligand in Its Own Lifetime.2,2'-联吡啶配体的早年生涯。
Molecules. 2019 Oct 31;24(21):3951. doi: 10.3390/molecules24213951.
6
Aerobic and Ligand-Free Manganese-Catalyzed Homocoupling of Arenes or Aryl Halides via in Situ Formation of Aryllithiums.通过原位生成芳基锂实现的需氧且无配体的锰催化芳烃或芳基卤化物的均偶联反应
J Org Chem. 2019 Apr 5;84(7):4413-4420. doi: 10.1021/acs.joc.8b02834. Epub 2019 Mar 13.
7
An Unprecedented, Lewis Acid-Mediated, Metal-Free Iodoannulation Strategy to Aromatic Iodides.一种前所未有的、路易斯酸介导的、无金属碘环化策略,用于芳基碘化物。
Chem Asian J. 2018 Dec 4;13(23):3676-3680. doi: 10.1002/asia.201801454. Epub 2018 Oct 23.
8
Axial-Chiral Biisoquinoline N, N'-Dioxides Bearing Polar Aromatic C-H Bonds as Catalysts in Sakurai-Hosomi-Denmark Allylation.轴手性双异喹啉 N,N'-二氧化物作为 Sakurai-Hosomi-Denmark 烯丙基化反应中带极性芳香 C-H 键的催化剂。
Org Lett. 2018 Sep 21;20(18):5757-5761. doi: 10.1021/acs.orglett.8b02457. Epub 2018 Sep 10.
9
Electrospray mass spectrometry and molecular modeling study of formation and stability of silver complexes with diazaperylene and bisisoquinoline.电喷雾质谱法及分子模拟研究二氮杂苝和双异喹啉与银配合物的形成及稳定性
J Mass Spectrom. 2018 May;53(5):408-418. doi: 10.1002/jms.4071.
10
Ruthenium water oxidation catalysts containing the non-planar tetradentate ligand, biisoquinoline dicarboxylic acid (biqaH).
Dalton Trans. 2016 Dec 6;45(48):19361-19367. doi: 10.1039/c6dt03880h.