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One-dimensional C—H...N hydrogen-bonded polymers in flexible tetra­pyridyl systems

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dc.contributor.authorMambanda, A.
dc.contributor.authorJaganyi, D.
dc.contributor.authorMunro, O. Q.
dc.date.accessioned2024-07-04T07:39:40Z
dc.date.available2024-07-04T07:39:40Z
dc.date.issued2007
dc.description.abstractIn N,N,N′,N′-tetra­kis(2-pyridyl­methyl)­propane-1,3-diamine, C27H30N6, (I), and N,N,N′,N′-tetra­kis(2-pyridyl­methyl)­butane-1,4-diamine, C28H32N6, (II), the twofold rotational symmetry of (I) favours the formation of a one-dimensional hydrogen-bonded polymer with two columns of C—H...N hydrogen bonds, while the inversion symmetry of (II) allows the formation of a one-dimensional hydrogen-bonded polymer stabilized by four columns of C—H...N hydrogen bonds. The possible role played by the chain length of the linking alkanediamine in determining the type of supra­molecular architecture in this series of compounds is discussed.
dc.identifier.urihttps://doi.org/10.1107/S0108270107049293
dc.identifier.urihttps://erepository.mku.ac.ke/handle/123456789/5982
dc.language.isoen
dc.publisherStructural Chemistry
dc.titleOne-dimensional C—H...N hydrogen-bonded polymers in flexible tetra­pyridyl systems
dc.typeArticle
dspace.entity.typePublication
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