All-Photochemical Rotation of Molecular Motors with a Phosphorus Stereoelement
Author(s) -
Gregory B. Boursalian,
Eise Nijboer,
Ruth Dorel,
Lukas Pfeifer,
Omer Markovitch,
Alex Blokhuis,
Ben L. Feringa
Publication year - 2020
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.0c08249
Subject(s) - chemistry , diastereomer , molecular motor , chirality (physics) , rotation (mathematics) , isomerization , axial chirality , epimer , phosphine , molecular machine , photochemistry , stereochemistry , nanotechnology , organic chemistry , catalysis , enantioselective synthesis , chiral symmetry , quark , nambu–jona lasinio model , materials science , physics , geometry , mathematics , quantum mechanics
Unidirectional molecular rotation based on alternating photochemical and thermal isomerizations of overcrowded alkenes is well established, but rotary cycles based purely on photochemical isomerizations are rare. Herein we report three new second-generation molecular motors featuring a phosphorus center in the lower half, which engenders a unique element of axial chirality. These motors exhibit unusual behavior, in that all four diastereomeric states can interconvert solely photochemically. Kinetic analysis and modeling reveal that the behavior of the new motors is consistent with all-photochemical unidirectional rotation. Furthermore, X-ray crystal structures of all four diastereomeric states of two of these new motors were obtained, which constitute the first achievements of crystallographic characterization of the full 360° rotational cycle of overcrowded-alkene-based molecular motors. Finally, the axial phosphorus stereoelement in the phosphine motor can be thermally inverted, and this epimerization enables a "shortcut" of the traditional rotational cycle of these compounds.
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