Synthesis of a Novel Potential Tridentate Anthracene Ligand, 1,8-Bis(dimethylamino)-9-bromoanthracene, and Its Application as Chelate Ligand for Synthesis of the Corresponding Boron and Palladium Compounds

Chemistry - A European Journal Volume 8 Issue 13 Page 2976-2979 published_at 2002
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Title ( eng )
Synthesis of a Novel Potential Tridentate Anthracene Ligand, 1,8-Bis(dimethylamino)-9-bromoanthracene, and Its Application as Chelate Ligand for Synthesis of the Corresponding Boron and Palladium Compounds
Creator
Yamashita Makoto
Kamura Kumiko
Akiba Kin-ya
Source Title
Chemistry - A European Journal
Volume 8
Issue 13
Start Page 2976
End Page 2979
Abstract
A novel potential tridentate ligand, 1,8-bis(dimethylamino)-9-bromoanthracene, was synthesized. The key steps are as follows: 1) dimethylamination of 1,8-dibromo-9-methoxyanthracene by a modified Buchwald's method to afford 1,8-bis(dimethylamino)-9-methoxyanthracene, and 2) reduction of the methoxy group by LDBB (lithium di-tert-butylbiphenylide) followed by treatment with BrCF2CF2Br. The corresponding 1,8-bis(dimethylamino)-9-lithioanthracene, which should be a useful versatile tridentate ligand, could be generated by treatment of the bromide with one equivalent of nBuLi. The lithioanthracene reacted with B-chloroborane derivatives to give three 9-boryl derivatives. Although we recently reported that the crystal structure of 1,8-dimethoxy-9-B-catecholateborylanthracene was a symmetrical compound with the almost identical two OB distances (2.379(2) and 2.441(2) Å), the newly prepared 1,8-bis(dimethylamino)-9-borylanthracene derivatives clearly have unsymmetrical structures with coordination of only one NMe2 group toward the central boron atom. However, the energy difference between the unsymmetrical and symmeterical structures was found to be very small based on 1H NMR measurements, in which symmetrical anthracene patterns in the aromatic region (two kinds of doublets and a triplet) and a sharp singlet signal of the two NMe2 groups were observed even at -80 ーC. 1,8-Bis(dimethylamino)-9-bromoanthracene itself can be a versatile ligand for transition metal compounds. In fact, direct palladation of the bromide took place by the reaction with [Pd2(dba)3]CHCl3 in THF to give the 9-palladated product. X-ray crystallographic analysis of the Pd compound showed that the square planar palladium atom was coordinated in a symmetrical fashion by both NMe2 groups (PdN bonds are 2.138(5) and 2.146(5) Å).
Keywords
anthracene
boron
N ligands
palladium
NDC
Chemistry [ 430 ]
Language
eng
Resource Type journal article
Publisher
Wiley-VCH Verlag GmbH
Date of Issued 2002
Rights
Copyright (c) 2002 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany
Publish Type Author’s Original
Access Rights open access
Source Identifier
[ISSN] 0947-6539
[DOI] 10.1002/1521-3765(20020703)8:13<2976::AID-CHEM2976>3.0.CO;2-G
[NCID] AA11076269
[DOI] http://dx.doi.org/10.1002/1521-3765(20020703)8:13<2976::AID-CHEM2976>3.0.CO;2-G