Enable biomass-derived alcohols mediated alkylation and transfer hydrogenation

A single-atom catalyst with generally regarded inert Zn-N<sub>4</sub> motifs derived from ZIF-8 is unexpectedly efficient for the activation of alcohols, enabling alcohol-mediated alkylation and transfer hydrogenation. C-alkylation of nitriles, ketones, alcohols, N-heterocycles, amides, keto acids, and esters, and N-alkylation of amines and amides all go smoothly with the developed method. Taking the α-alkylation of nitriles with alcohols as an example, the α-alkylation starts from the (1) nitrogen-doped carbon support catalyzed dehydrogenation of alcohols into aldehydes, which further condensed with nitriles to give vinyl nitriles, followed by (2) transfer hydrogenation of C=C bonds in vinyl nitriles on Zn-N<sub>4</sub> sites. The experimental results and DFT calculations reveal that the Lewis acidic Zn-N<sub>4</sub> sites promote step (2) by activating the alcohols. This is the first example of highly efficient single-atom catalysts for various organic transformations with biomass-derived alcohols as the alkylating reagents and hydrogen donors.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2024-08-15
DOI
https://doi.org/10.1038/s41467-024-51307-8
Citations
28
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
4.44

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Enable biomass-derived alcohols mediated alkylation and transfer hydrogenation

Liangfang Zhu, Yuandie Ma, Liang Wei Huang, Yanyan Zhu et al.
28 citations
Nature Communications
Asymmetric Hydrogenation and Catalysis
4.44
article

Enable biomass-derived alcohols mediated alkylation and transfer hydrogenation

Liangfang Zhu, Yuandie Ma, Liang Wei Huang, Yanyan Zhu, Guoqiang She, Zehui Zhang, Xixi Liu
article en
28 citations

Abstract

A single-atom catalyst with generally regarded inert Zn-N<sub>4</sub> motifs derived from ZIF-8 is unexpectedly efficient for the activation of alcohols, enabling alcohol-mediated alkylation and transfer hydrogenation. C-alkylation of nitriles, ketones, alcohols, N-heterocycles, amides, keto acids, and esters, and N-alkylation of amines and amides all go smoothly with the developed method. Taking the α-alkylation of nitriles with alcohols as an example, the α-alkylation starts from the (1) nitrogen-doped carbon support catalyzed dehydrogenation of alcohols into aldehydes, which further condensed with nitriles to give vinyl nitriles, followed by (2) transfer hydrogenation of C=C bonds in vinyl nitriles on Zn-N<sub>4</sub> sites. The experimental results and DFT calculations reveal that the Lewis acidic Zn-N<sub>4</sub> sites promote step (2) by activating the alcohols. This is the first example of highly efficient single-atom catalysts for various organic transformations with biomass-derived alcohols as the alkylating reagents and hydrogen donors.

Nature CommunicationsVol. 15(1)
Minzu University of China (CN), Sichuan University (CN), Ministry of Education (PT), Wuhan University of Science and Technology (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hubei Province
Openalex Percentile: Top 4%
Asymmetric Hydrogenation and Catalysis
4.44
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.