Crystal engineering based on nitro derivatives of 10-hydroxy-10,9-borazarophenanthrene

James M.A. Robinson; Benson M. Kariuki; Douglas Philp; Kenneth D.M. Harris

doi:10.1016/S0040-4039(97)01408-1

Crystal engineering based on nitro derivatives of 10-hydroxy-10,9-borazarophenanthrene

James M.A. Robinson, Benson M. Kariuki, Douglas Philp, Kenneth D.M. Harris^*

^*Corresponding author for this work

Chemistry

Research output: Contribution to journal › Article › peer-review

11 Scopus citations

Abstract

The steric and molecular recognition properties of the nitro group control the molecular packing of 10-hydroxy-10,9-borazaophenanthrene derivatives facilitating the formation of stepped hydrogen bonded molecular tapes of 8-nitro-10-hydroxy-10,9-borazarophenanthrene and cyclic homodimers of 6-nitro-10-hydroxy-10,9-borazarophenanthrene.

Original language	English (US)
Pages (from-to)	6281-6284
Number of pages	4
Journal	Tetrahedron Letters
Volume	38
Issue number	35
DOIs	https://doi.org/10.1016/S0040-4039(97)01408-1
State	Published - Sep 1 1997

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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abstract = "The steric and molecular recognition properties of the nitro group control the molecular packing of 10-hydroxy-10,9-borazaophenanthrene derivatives facilitating the formation of stepped hydrogen bonded molecular tapes of 8-nitro-10-hydroxy-10,9-borazarophenanthrene and cyclic homodimers of 6-nitro-10-hydroxy-10,9-borazarophenanthrene.",

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AU - Harris, Kenneth D.M.

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