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  Tetralithio Metalla‐aromatics with Two Independent Perpendicular Dilithio Aromatic Rings Spiro‐fused by One Manganese Atom

Zhang, Y., Wei, J., Zhu, M., Chi, Y., Zhang, W.-X., Ye, S., et al. (2019). Tetralithio Metalla‐aromatics with Two Independent Perpendicular Dilithio Aromatic Rings Spiro‐fused by One Manganese Atom. Angewandte Chemie International Edition, 58(28), 9625-9631. doi:10.1002/anie.201904681.

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 Creators:
Zhang, Yongliang1, Author
Wei, Junnian1, Author
Zhu, Miaomiao1, Author
Chi, Yue1, Author
Zhang, Wen-Xiong1, Author
Ye, Shengfa2, Author           
Xi, Zhenfeng1, 3, Author
Affiliations:
1Beijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing, 100871 P. R. China, ou_persistent22              
2Research Group Ye, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_2541708              
3State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Shanghai, 200032 P. R. China, ou_persistent22              

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Free keywords: lithium; metalla-aromatics;metallacycles; non-innocent ligands; spiro aromatics
 Abstract: Herein, we present the realization of a class of unprecedented aromatic structures 2: metalla‐aromatics with two independent and perpendicular aromatic rings spiro‐fused by a transition‐metal spiro atom, of which their corresponding organic analogues are impossible. Tetralithio spiro manganacycles 2 are readily synthesized from 1,4‐dilithio‐1,3‐butadienes 1 and MnCl2 in the presence of lithium. The aromaticity of 2 is supported by experimental measurements (X‐ray structural analysis, NMR) and theoretical analyses (NICS, ACID, MOs). The spiro atom Mn in 2 uses its 3dxz and 3dxy orbitals to form the two perpendicular manganacycles, which are two independent 6π aromatic systems. Theoretical analyses reveal that the Li cations play an indispensable role in governing their geometric and electronic structures and hence their aromaticity. Therefore, this work contributes not only to enrich the concept of aromaticity, but also to deepen the understanding of the fundamental chemical bonding.

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Language(s): eng - English
 Dates: 2019-04-152019-05-182019-07-08
 Publication Status: Issued
 Pages: 7
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/anie.201904681
 Degree: -

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Title: Angewandte Chemie International Edition
  Other : Angewandte Chemie, International Edition
  Other : Angew. Chem. Int. Ed.
Source Genre: Journal
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Publ. Info: Weinheim : Wiley-VCH
Pages: - Volume / Issue: 58 (28) Sequence Number: - Start / End Page: 9625 - 9631 Identifier: ISSN: 1433-7851
CoNE: https://pure.mpg.de/cone/journals/resource/1433-7851