Abstract
We report on B←N coordination to support a single-crystal-to-single-crystal reaction in the solid state. A [2 + 2] photodimerization is achieved with face-to-face π-stacks of monotopic B←N adducts composed of a phenylboronic acid catechol ester and an alkene with a terminal thiophene group. The photoreaction generates a ditopic B-adduct involving a head-to-tail cyclobutane regio- and stereoselectively. The photodimerization is accompanied by an increase in the tetrahedral character of the B atom. The resulting boron enables channel confinement of chloroform upon recrystallization.
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CITATION STYLE
Campillo-Alvarado, G., Li, C., Feng, Z., Hutchins, K. M., Swenson, D. C., Höpfl, H., … Macgillivray, L. R. (2020). Single-Crystal-to-Single-Crystal [2 + 2] Photodimerization Involving B←N Coordination with Generation of a Thiophene Host. Organometallics, 39(12), 2197–2201. https://doi.org/10.1021/acs.organomet.0c00258
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