<i>N</i>,<i>N′</i>-Bis([1,1′-biphenyl]-2-yl)-<i>N</i>-hydroxymethanimidamide

The title compound, C<sub>25</sub>H<sub>20</sub>N<sub>2</sub>O, crystallizes in the monoclinic <i>C</i>2/c space group, as the <i>N</i>-hy-droxy-formamidine isomer, in the <i>E</i> conformation (when referring to the C=N bond). Inversion dimers formed through pairwise O-H⋯N hydrogen bonds are present in the structure. C-H⋯π and π-π stacking inter-actions complete the crystal packing.

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Journal
IUCrData
Published
2025-09-28
DOI
https://doi.org/10.1107/s2414314625008314
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.00

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article

N,N′-Bis([1,1′-biphenyl]-2-yl)-N-hydroxymethanimidamide

Garry S. Hanan, Mihaela Cibian, Arindam Saha, Elizabeth Lamothe
IUCrData
Synthesis and biological activity
article

N,N′-Bis([1,1′-biphenyl]-2-yl)-N-hydroxymethanimidamide

Garry S. Hanan, Mihaela Cibian, Arindam Saha, Elizabeth Lamothe
article en

Abstract

The title compound, C<sub>25</sub>H<sub>20</sub>N<sub>2</sub>O, crystallizes in the monoclinic <i>C</i>2/c space group, as the <i>N</i>-hy-droxy-formamidine isomer, in the <i>E</i> conformation (when referring to the C=N bond). Inversion dimers formed through pairwise O-H⋯N hydrogen bonds are present in the structure. C-H⋯π and π-π stacking inter-actions complete the crystal packing.

IUCrDataVol. 10(9)
Université du Québec à Montréal (CA), Université du Québec à Trois-Rivières (CA)
Centre in Green Chemistry and Catalysis, Centre québécois sur les matériaux fonctionnels, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 80%
Synthesis and biological activity
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<i>N</i>,<i>N′</i>-Bis([1,1′-biphenyl]-2-yl)-<i>N</i>-hydroxymethanimidamide — Garry S. Hanan, Mihaela Cibian, et al. · IUCrData (2025) | TGRS Research Map | TGRS