Synthesis and Photochemical Uncaging of Alkene-Protected, Polymer-Bound Vicinal Frustrated Lewis Pairs

Polymeric materials bearing Frustrated Lewis Pair (FLP) functionality are promising candidates for use as heterogeneous catalysts and adaptive materials, but synthetic access to FLP-functional polymers remains limited due to the incompatibility of FLPs with standard polymerization chemistries. Herein, we describe a synthetic approach that "cages" highly reactive vicinal phosphine-borane FLPs as covalent alkene adducts, which are stable to Ni-mediated vinyl addition polymerization. We discovered that the caged FLP adducts can be photochemically activated to liberate vicinal FLPs, enabling spatiotemporally controlled release of FLPs from polymeric precursors.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-08-26
DOI
https://doi.org/10.1021/jacs.4c09012
Citations
14
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
3.50

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article

Synthesis and Photochemical Uncaging of Alkene-Protected, Polymer-Bound Vicinal Frustrated Lewis Pairs

Nathan A. Romero, Emily A. Latif, Jeremy D. Hilgar
14 citations
Journal of the American Chemical Society
Organoboron and organosilicon chemistry
3.50
article

Synthesis and Photochemical Uncaging of Alkene-Protected, Polymer-Bound Vicinal Frustrated Lewis Pairs

Nathan A. Romero, Emily A. Latif, Jeremy D. Hilgar
article en
14 citations

Abstract

Polymeric materials bearing Frustrated Lewis Pair (FLP) functionality are promising candidates for use as heterogeneous catalysts and adaptive materials, but synthetic access to FLP-functional polymers remains limited due to the incompatibility of FLPs with standard polymerization chemistries. Herein, we describe a synthetic approach that "cages" highly reactive vicinal phosphine-borane FLPs as covalent alkene adducts, which are stable to Ni-mediated vinyl addition polymerization. We discovered that the caged FLP adducts can be photochemically activated to liberate vicinal FLPs, enabling spatiotemporally controlled release of FLPs from polymeric precursors.

Journal of the American Chemical SocietyVol. 146(36)
University of California San Diego (US)
National Science Foundation, University of California, San Diego, Air Force Office of Scientific Research
Zero hunger
Openalex Percentile: Top 7%
Organoboron and organosilicon chemistry
3.50
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Synthesis and Photochemical Uncaging of Alkene-Protected, Polymer-Bound Vicinal Frustrated Lewis Pairs — Nathan A. Romero, Emily A. Latif, et al. · Journal of the American Chemical Society (2024) | TGRS Research Map | TGRS