Supramolecular interaction of keto-substituted pyrroles

Tatsuki Morimoto, Hiroyuki Furuta

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Several types of pyrrole derivatives bearing carbonyl groups were synthesized and their structures in the solid states were elucidated by single crystal X-ray analysis. In the case of -ketopyrroles, the molecules exist as hydrogen bonding dimers between the pyrrole NH and carbonyl groups, while in the case of -ketopyrrole derivatives, hydrogen bonding networks are formed. Both the ,'-diketo-substituted pyrroles and their derivatives are suggested to be suitable for the construction of 1-D chain networks. Overall, the effects of substituents on the supramolecular interactions are discussed in detail.

Original languageEnglish
Pages (from-to)493-500
Number of pages8
JournalSupramolecular Chemistry
Volume19
Issue number7
DOIs
Publication statusPublished - Oct 1 2007

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Pyrroles
Derivatives
Hydrogen bonds
Bearings (structural)
X ray analysis
Dimers
Single crystals
Molecules

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

Cite this

Supramolecular interaction of keto-substituted pyrroles. / Morimoto, Tatsuki; Furuta, Hiroyuki.

In: Supramolecular Chemistry, Vol. 19, No. 7, 01.10.2007, p. 493-500.

Research output: Contribution to journalArticle

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