Application of a tetrapyrimidyl cyclobutane synthesized in the organic solid state: A halogen-bonded supramolecular ladder
Abstract
A halogen-bonded supramolecular ladder comprised of a novel pyrimidine-based cyclobutane photoproduct synthesized in the organic solid state via a [2 + 2] photoreaction is reported. The photoproduct rctt-tetrakis(5′-pyrimidyl)cyclobutane functions as rungs while the linear divergent halogen-bond donor 1,4-diiodoperchlorobenzene acts as the rails. Our report also confirms the structure and stereochemistry of the tetrapyrimidyl cyclobutane ring system.
Department(s)
Chemistry and Biochemistry
Document Type
Article
DOI
https://doi.org/10.1039/d0ce01280g
Publication Date
11-7-2020
Recommended Citation
Sinnwell, Michael A., Carlos L. Santana, Eric Bosch, Leonard R. MacGillivray, and Ryan H. Groeneman. "Application of a tetrapyrimidyl cyclobutane synthesized in the organic solid state: a halogen-bonded supramolecular ladder." CrystEngComm 22, no. 41 (2020): 6780-6782.
Journal Title
CrystEngComm