Donor Strength Determination of Buchwald-Type Phosphines

The electronic properties of eight Buchwald-type phosphines were determined and ranked by <sup>13</sup>C NMR spectroscopy, highlighting the sensitivity of the Huynh electronic parameter (HEP). Furthermore, the <sup>13</sup>C<sub>carbene</sub> NMR signals of 19 known and new P-donor complexes in CDCl<sub>3</sub> (HEP values) are found to be highly correlated to those in C<sub>6</sub>D<sub>6</sub>. This enables the donor strength determination of P-donors even where the complexes are unstable or undergo rapid isomerization due to transphobia in CDCl<sub>3</sub>.

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Publication Details

Journal
Inorganic Chemistry
Published
2024-09-17
DOI
https://doi.org/10.1021/acs.inorgchem.4c03104
Citations
1
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.25

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article

Donor Strength Determination of Buchwald-Type Phosphines

Han Vinh Huynh, Jia Nuo Leung
1 citations
Inorganic Chemistry
Catalytic Cross-Coupling Reactions
0.25
article

Donor Strength Determination of Buchwald-Type Phosphines

Han Vinh Huynh, Jia Nuo Leung
article en
1 citations

Abstract

The electronic properties of eight Buchwald-type phosphines were determined and ranked by <sup>13</sup>C NMR spectroscopy, highlighting the sensitivity of the Huynh electronic parameter (HEP). Furthermore, the <sup>13</sup>C<sub>carbene</sub> NMR signals of 19 known and new P-donor complexes in CDCl<sub>3</sub> (HEP values) are found to be highly correlated to those in C<sub>6</sub>D<sub>6</sub>. This enables the donor strength determination of P-donors even where the complexes are unstable or undergo rapid isomerization due to transphobia in CDCl<sub>3</sub>.

Inorganic ChemistryVol. 63(39)
National University of Singapore (SG)
National University of Singapore, Ministry of Education - Singapore
Openalex Percentile: Top 48%
Catalytic Cross-Coupling Reactions
0.25
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