Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Jan;68(Pt 1):o158-9.
doi: 10.1107/S1600536811053220. Epub 2011 Dec 17.

3,3'-Bis(quinolin-8-yl)-1,1'-[4,4'-methyl-enebis(4,1-phenyl-ene)]diurea

3,3'-Bis(quinolin-8-yl)-1,1'-[4,4'-methyl-enebis(4,1-phenyl-ene)]diurea

Avijit Pramanik et al. Acta Crystallogr Sect E Struct Rep Online. 2012 Jan.

Abstract

The title compound, C(33)H(26)N(6)O(2), contains two 3-(quinolin-8-yl)urea groups linked to a diphenyl-methane. The asymmetric unit contains two mol-ecules, A and B. Each quinoline plane is essentially parallel to the attached urea unit [dihedral angles = 8.97 (18) and 8.81 (19) in molecule A and 18.47 (18) and 4.09 (19)° in molecule B]. The two benzene rings are twisted, making dihedral angles of 81.36 (8)° in A and 87.20 (9)° in B. The molecular structures are stabilized by intramolecular N-H⋯N hydrogen bonds. In the crystal, each urea O atom is involved in two N-H⋯O hydrogen bonds, generating two inter-penetrating three-dimensional sets of mol-ecules.

PubMed Disclaimer

Figures

Fig. 1.
Fig. 1.
The molecular structure of the title compound showing two molecules (A and B) with the atom-numbering scheme. The hydrogen atoms have been omitted clarity. Displacement ellipsoids are drawn at the 50% probability level.
Fig. 2.
Fig. 2.
Packing structure of title compound viewed along c axis.

References

    1. Bruker (2007). SMART and SAINT Bruker AXS Inc., Madison, Wisconsin, USA.
    1. Caltagirone, C., Hiscock, J. R., Hursthouse, M. B., Light, M. E. & Gale, P. A. (2008). Chem. Eur. J. 14, 10236–10243. - PubMed
    1. Custelcean, R., Moyer, B. A. & Hay, B. P. (2005). Chem. Commun. pp. 5971–5973. - PubMed
    1. Fan, E., Van Arman, S. A., Kincaid, S. & Hamilton, A. D. (1993). J. Am. Chem. Soc. 115, 369–370.
    1. Pramanik, A., Thompson, B., Hayes, T., Tucker, K., Powell, D. R., Bonnesen, P. V., Ellis, E. D., Lee, K. S., Yu, H. & Hossain, M. A. (2011). Org. Biomol. Chem. 9, 4444–4447. - PMC - PubMed