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Synthesis of new pyrrole-pyridine-based ligands using an in situ Suzuki coupling method.


ABSTRACT: The compounds 6-(pyrrol-2-yl)-2,2'-bipyridine, 2-(pyrrol-2-yl)-1,10-phenanthroline and 2-(2-(N-methylbenz[d,e]imidazole)-6-(pyrrol-2-yl)-pyridine were synthesized by using an in situ generated boronic acid for the Suzuki coupling. Crystals of the products could be grown and exhibited interesting structures by X-ray analysis, one of them showing a chain-like network with the adjacent molecules linked to each other via intermolecular N-H(…)N hydrogen bonds.

SUBMITTER: Bottger M 

PROVIDER: S-EPMC3458721 | biostudies-literature | 2012

REPOSITORIES: biostudies-literature

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Synthesis of new pyrrole-pyridine-based ligands using an in situ Suzuki coupling method.

Böttger Matthias M   Wiegmann Björn B   Schaumburg Steffen S   Jones Peter G PG   Kowalsky Wolfgang W   Johannes Hans-Hermann HH  

Beilstein journal of organic chemistry 20120709


The compounds 6-(pyrrol-2-yl)-2,2'-bipyridine, 2-(pyrrol-2-yl)-1,10-phenanthroline and 2-(2-(N-methylbenz[d,e]imidazole)-6-(pyrrol-2-yl)-pyridine were synthesized by using an in situ generated boronic acid for the Suzuki coupling. Crystals of the products could be grown and exhibited interesting structures by X-ray analysis, one of them showing a chain-like network with the adjacent molecules linked to each other via intermolecular N-H(…)N hydrogen bonds. ...[more]

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