Incorporating Ester Functionality within a Solid-State [2 + 2] Cycloaddition Reaction Based Upon Halogen Bonding Interactions

• Published in: Crystal growth & design 2020-03, Vol.20 (3), p.1969-1974
• Main Authors: Kruse, Samantha J, Bosch, Eric, Brown, Fayeshun, Groeneman, Ryan H
• Format: Article
• Language: English
• ISSN: 1528-7483; 1528-7505
• DOI: 10.1021/acs.cgd.9b01624

The formation of cocrystals based upon 1,4-diiodoperchlorobenzene (C6I2Cl4) as a halogen bond donor along with a series of isomeric pyridine vinyl esters, namely, (E)-methyl-3-(pyridine-X-yl)­prop-2-enoate (where X = 4, 3, and 2) (4-PAMe), (3-PAMe), and (2-PAMe), has been achieved. In all cases, C6I2Cl4 halogen bonds to a combination of pyridine nitrogen atoms as well as ester oxygen atoms to yield an extended solid. The cocrystals (C6I2Cl4)·(4-PAMe) and (C6I2Cl4)·2­(3-PAMe) were observed to be photoreactive. X-ray structural analysis revealed that molecules of C6I2Cl4 are stacked in a homogeneous face-to-face π–π orientation which then positions a pair of carbon–carbon double bonds (CC) in the correct orientation to undergo a solid-state [2 + 2] cycloaddition reaction. Thus, upon exposure to ultraviolet light, both (C6I2Cl4)·(4-PAMe) and (C6I2Cl4)·2­(3-PAMe) undergo a regioselective and quantitative photoreaction to yield the head-to-head photoproduct, namely, (rctt)-dimethyl-3,4-bis­(pyridine-4-yl)­cyclobutane-1,2-dicarboxylate and (rctt)-dimethyl-3,4-bis­(pyridine-3-yl)­cyclobutane-1,2-dicarboxylate, respectively. X-ray analysis of (C6I2Cl4)·(2-PAMe) revealed the structural reason behind the observed photostability which is attributed to the large parallel displacement of the double bonds.