r-1,t-3-Bis[4-(di-methyl-amino)-phen-yl]-c-2,t-4-bis-(pyridin-4-yl)cyclo-butane.

Acta Crystallogr Sect E Struct Rep Online

Department of Organic Chemistry, Faculty of Science, Beijing University of Chemical Technology, Beijing 100029, People's Republic of China.

Published: March 2014

AI Article Synopsis

  • The compound C30H32N4 was created through photodimerization using UV light to irradiate a specific precursor in benzene.
  • The resulting structure features a cyclo-butane ring that has a unique puckered shape with distinctive angles, making it the largest known among similar compounds.
  • In its solid state, the molecules arrange themselves into a hollow, one-dimensional formation along the c axis, facilitated by interactions between carbon-hydrogen groups and aromatic rings.

Article Abstract

The title compound, C30H32N4, was synthesized by the photodimerization of trans-4-{2-[4-(di-methyl-amino)-phen-yl]ethen-yl}pyridine in benzene upon irradiation with UV light. This photodimer has a puckered cyclo-butane ring with the four aryl substituents in an r-1,t-2,c-3,t conformation. The puckering angle of the cyclo-butane ring is 32.22 (7)°, which is the largest among reported tetra-aryl-substituted cyclo-butanes. In the crystal, the mol-ecules form a hollow, one-dimensional structure extending parallel to the c axis via two different pairs of C-H⋯π inter-actions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998431PMC
http://dx.doi.org/10.1107/S1600536814002311DOI Listing

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