Title: Radical Reactivity of Frustrated Lewis Pairs with Diaryl Esters - data

Citation
Soltani Y, Dasgupta A, Gazis TA, et al. (2019). Radical Reactivity of Frustrated Lewis Pairs with Diaryl Esters - data. Cardiff University. http://doi.org/10.17035/d.2020.0091287984


This data is not currently available because: Intent to publish project results
Access Method: Click to email a request for this data to opendata@cardiff.ac.uk

Dataset Details
Publisher: Cardiff University
Date (year) of data becoming publicly available: 2019
Coverage start date: 01/01/2017
Coverage end date: 22/12/2019
Data format: .pdf, .cif
Software Required: MNova
Mercury

Estimated total storage size of dataset: Less than 100 megabytes
DOI: 10.17035/d.2020.0091287984

Description

Here we report the reaction of diaryl substituted esters with frustrated Lewis pairs. Interestingly this results in divergent pathways, one whereby the diaryl moiety is stabilized by the Lewis basic phosphine or the alternative pathway, wherein a single-electron transfer process occurs generating the [Mes3P]/[C(H)Ar2]· radical ion pair. The latter species undergoes a homocoupling reaction to yield tetraphenylethane derivatives. In the presence of olefins, this reactivity can be harnessed through an sp2-sp3 C–C heterocoupling reaction to generate α,β-substituted olefins. Notably, this work showcases a frustrated Lewis pair approach to metal-free radical C–H bond activation with subsequent C–C bond formation which also displays complementary reactivity to other approaches. Data includes description of experimental procedures, NMR data and X-ray data.

Research results based upon these data can be found at https://doi.org/10.1016/j.xcrp.2020.100016



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Last updated on 2020-24-02 at 10:27