Precise control of selective hydrogenation of α,β-unsaturated aldehydes in water mediated by ammonia borane

Hydrogenation of unsaturated biomass in a control manner is highly desirable but challenging, especially under mild conditions. We here report selective hydrogenation of α,β-unsaturated aldehydes (UALs), featuring a precise control of all potential products by adjustment of the role of ammonia boran...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2022-08, Vol.311, p.121348, Article 121348
Hauptverfasser: Zhou, Yangyang, Chen, Chen, Li, Qiling, Liu, Yanbo, Wei, Ting, Liu, Youzhen, Zeng, Zebing, Bradshaw, Darren, Zhang, Bing, Huo, Jia
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container_issue
container_start_page 121348
container_title Applied catalysis. B, Environmental
container_volume 311
creator Zhou, Yangyang
Chen, Chen
Li, Qiling
Liu, Yanbo
Wei, Ting
Liu, Youzhen
Zeng, Zebing
Bradshaw, Darren
Zhang, Bing
Huo, Jia
description Hydrogenation of unsaturated biomass in a control manner is highly desirable but challenging, especially under mild conditions. We here report selective hydrogenation of α,β-unsaturated aldehydes (UALs), featuring a precise control of all potential products by adjustment of the role of ammonia borane (AB) in transfer and/or catalytic hydrogenation. The hydrogenation can be readily operated in neat water without using any external H2-source, because AB as the H2-source is favorable in aqueous solution. Impressively, unsaturated alcohols are prepared in 100% conversion by the room-temperature transfer hydrogenation of UALs with AB, while saturated aldehydes are obtained in 100% conversion and > 90% selectivity with high activity (i.e., turnover frequency = 0.98 s−1 for cinnamaldehyde), by the catalytic hydrogenation with H2 released from AB and Pd immobilized on two-dimensional metal organic layer. On the other hand, UALs can be completely converted into the saturated alcohols through a combination of transfer and catalytic hydrogenation in one pot. This strategy can be extended to more than 8 types of UALs, and provides a facile way to fine-control the selective hydrogenation of unsaturated compounds with competing bonds. Precise control of selective hydrogenation of α,β-unsaturated aldehydes (UALs) under environmentally benign conditions is achieved by simply switching the roles of ammonia borane (AB) in transfer and/or catalytic hydrogenation. Unsaturated alcohols are easily prepared by room-temperature transfer hydrogenation of UALs with 100% conversion by AB. Saturated aldehydes are selectively prepared through catalytic hydrogenation by Pd/MOL and in-situ released H2 from AB. UALs are completely hydrogenated to prepare saturated alcohols by transfer hydrogenation along with catalytic hydrogenation using Pd/MOL and AB together. [Display omitted] •A facile strategy is developed to precisely control of selective hydrogenation of α,β-unsaturated aldehydes.•The hydrogenation is controlled by switching the roles of ammonia borane in transfer and/or catalytic hydrogenation.•α,β-Unsaturated aldehydes are converted into three potential products with extremely high conversion and selectivity.•The hydrogenation is carried out in neat water without using additional H2 source.
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We here report selective hydrogenation of α,β-unsaturated aldehydes (UALs), featuring a precise control of all potential products by adjustment of the role of ammonia borane (AB) in transfer and/or catalytic hydrogenation. The hydrogenation can be readily operated in neat water without using any external H2-source, because AB as the H2-source is favorable in aqueous solution. Impressively, unsaturated alcohols are prepared in 100% conversion by the room-temperature transfer hydrogenation of UALs with AB, while saturated aldehydes are obtained in 100% conversion and &gt; 90% selectivity with high activity (i.e., turnover frequency = 0.98 s−1 for cinnamaldehyde), by the catalytic hydrogenation with H2 released from AB and Pd immobilized on two-dimensional metal organic layer. On the other hand, UALs can be completely converted into the saturated alcohols through a combination of transfer and catalytic hydrogenation in one pot. This strategy can be extended to more than 8 types of UALs, and provides a facile way to fine-control the selective hydrogenation of unsaturated compounds with competing bonds. Precise control of selective hydrogenation of α,β-unsaturated aldehydes (UALs) under environmentally benign conditions is achieved by simply switching the roles of ammonia borane (AB) in transfer and/or catalytic hydrogenation. Unsaturated alcohols are easily prepared by room-temperature transfer hydrogenation of UALs with 100% conversion by AB. Saturated aldehydes are selectively prepared through catalytic hydrogenation by Pd/MOL and in-situ released H2 from AB. UALs are completely hydrogenated to prepare saturated alcohols by transfer hydrogenation along with catalytic hydrogenation using Pd/MOL and AB together. [Display omitted] •A facile strategy is developed to precisely control of selective hydrogenation of α,β-unsaturated aldehydes.•The hydrogenation is controlled by switching the roles of ammonia borane in transfer and/or catalytic hydrogenation.•α,β-Unsaturated aldehydes are converted into three potential products with extremely high conversion and selectivity.•The hydrogenation is carried out in neat water without using additional H2 source.</description><identifier>ISSN: 0926-3373</identifier><identifier>EISSN: 1873-3883</identifier><identifier>DOI: 10.1016/j.apcatb.2022.121348</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Alcohols ; Aldehydes ; Ammonia ; Ammonia borane ; Aqueous solutions ; Boranes ; Chemical bonds ; Cinnamaldehyde ; Conversion ; Hydrogenation ; Hydrogenation selectivity ; Metal organic layer ; Palladium ; Pd based catalyst ; Room temperature ; Selectivity ; β-unsaturated aldehydes</subject><ispartof>Applied catalysis. 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[Display omitted] •A facile strategy is developed to precisely control of selective hydrogenation of α,β-unsaturated aldehydes.•The hydrogenation is controlled by switching the roles of ammonia borane in transfer and/or catalytic hydrogenation.•α,β-Unsaturated aldehydes are converted into three potential products with extremely high conversion and selectivity.•The hydrogenation is carried out in neat water without using additional H2 source.</description><subject>Alcohols</subject><subject>Aldehydes</subject><subject>Ammonia</subject><subject>Ammonia borane</subject><subject>Aqueous solutions</subject><subject>Boranes</subject><subject>Chemical bonds</subject><subject>Cinnamaldehyde</subject><subject>Conversion</subject><subject>Hydrogenation</subject><subject>Hydrogenation selectivity</subject><subject>Metal organic layer</subject><subject>Palladium</subject><subject>Pd based catalyst</subject><subject>Room temperature</subject><subject>Selectivity</subject><subject>β-unsaturated aldehydes</subject><issn>0926-3373</issn><issn>1873-3883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kMFOGzEQhi0EUkPgDThY6rUbbI_Z3VwqVYhCpUjlAGfLa4-po6yd2g4oj0UfJM9Up8u5h9FIM_P_o_8j5IqzBWe8vV4v9NboMiwEE2LBBQfZn5AZ7ztooO_hlMzYUrQNQAefyHnOa8aYANHPyPiY0PiM1MRQUtzQ6GjGDZriX5H-2tsUXzDo4mM4rg7vXw5_ml3IuuySLmip3lisZ5ipD_StjhId0fp_u2FP9TjG4DUdYtIBL8iZ05uMlx99Tp6_3z3dPjSrn_c_br-tGgMgS-Ns33OweMOA3ziBUiPTw9JpaWtCxmQt7TpuhJCwBCk5B67d4MAtTYsW5uTz5LtN8fcOc1HruEuhvlSi7VjbdqKimBM5XZkUc07o1Db5Uae94kwdwaq1msCqI1g1ga2yr5MMa4JXj0ll4zGYmrqyLMpG_3-Dv9UmhZg</recordid><startdate>20220815</startdate><enddate>20220815</enddate><creator>Zhou, Yangyang</creator><creator>Chen, Chen</creator><creator>Li, Qiling</creator><creator>Liu, Yanbo</creator><creator>Wei, Ting</creator><creator>Liu, Youzhen</creator><creator>Zeng, Zebing</creator><creator>Bradshaw, Darren</creator><creator>Zhang, Bing</creator><creator>Huo, Jia</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7ST</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>JG9</scope><scope>KR7</scope><scope>L7M</scope><scope>SOI</scope></search><sort><creationdate>20220815</creationdate><title>Precise control of selective hydrogenation of α,β-unsaturated aldehydes in water mediated by ammonia borane</title><author>Zhou, Yangyang ; Chen, Chen ; Li, Qiling ; Liu, Yanbo ; Wei, Ting ; Liu, Youzhen ; Zeng, Zebing ; Bradshaw, Darren ; Zhang, Bing ; Huo, Jia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c334t-fd8813de50315f2e4ae0ab9fa4d202004200af71c224393441131afbf3f9c6ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Alcohols</topic><topic>Aldehydes</topic><topic>Ammonia</topic><topic>Ammonia borane</topic><topic>Aqueous solutions</topic><topic>Boranes</topic><topic>Chemical bonds</topic><topic>Cinnamaldehyde</topic><topic>Conversion</topic><topic>Hydrogenation</topic><topic>Hydrogenation selectivity</topic><topic>Metal organic layer</topic><topic>Palladium</topic><topic>Pd based catalyst</topic><topic>Room temperature</topic><topic>Selectivity</topic><topic>β-unsaturated aldehydes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Yangyang</creatorcontrib><creatorcontrib>Chen, Chen</creatorcontrib><creatorcontrib>Li, Qiling</creatorcontrib><creatorcontrib>Liu, Yanbo</creatorcontrib><creatorcontrib>Wei, Ting</creatorcontrib><creatorcontrib>Liu, Youzhen</creatorcontrib><creatorcontrib>Zeng, Zebing</creatorcontrib><creatorcontrib>Bradshaw, Darren</creatorcontrib><creatorcontrib>Zhang, Bing</creatorcontrib><creatorcontrib>Huo, Jia</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Environment Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Environment Abstracts</collection><jtitle>Applied catalysis. 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We here report selective hydrogenation of α,β-unsaturated aldehydes (UALs), featuring a precise control of all potential products by adjustment of the role of ammonia borane (AB) in transfer and/or catalytic hydrogenation. The hydrogenation can be readily operated in neat water without using any external H2-source, because AB as the H2-source is favorable in aqueous solution. Impressively, unsaturated alcohols are prepared in 100% conversion by the room-temperature transfer hydrogenation of UALs with AB, while saturated aldehydes are obtained in 100% conversion and &gt; 90% selectivity with high activity (i.e., turnover frequency = 0.98 s−1 for cinnamaldehyde), by the catalytic hydrogenation with H2 released from AB and Pd immobilized on two-dimensional metal organic layer. On the other hand, UALs can be completely converted into the saturated alcohols through a combination of transfer and catalytic hydrogenation in one pot. This strategy can be extended to more than 8 types of UALs, and provides a facile way to fine-control the selective hydrogenation of unsaturated compounds with competing bonds. Precise control of selective hydrogenation of α,β-unsaturated aldehydes (UALs) under environmentally benign conditions is achieved by simply switching the roles of ammonia borane (AB) in transfer and/or catalytic hydrogenation. Unsaturated alcohols are easily prepared by room-temperature transfer hydrogenation of UALs with 100% conversion by AB. Saturated aldehydes are selectively prepared through catalytic hydrogenation by Pd/MOL and in-situ released H2 from AB. UALs are completely hydrogenated to prepare saturated alcohols by transfer hydrogenation along with catalytic hydrogenation using Pd/MOL and AB together. [Display omitted] •A facile strategy is developed to precisely control of selective hydrogenation of α,β-unsaturated aldehydes.•The hydrogenation is controlled by switching the roles of ammonia borane in transfer and/or catalytic hydrogenation.•α,β-Unsaturated aldehydes are converted into three potential products with extremely high conversion and selectivity.•The hydrogenation is carried out in neat water without using additional H2 source.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.apcatb.2022.121348</doi></addata></record>
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subjects Alcohols
Aldehydes
Ammonia
Ammonia borane
Aqueous solutions
Boranes
Chemical bonds
Cinnamaldehyde
Conversion
Hydrogenation
Hydrogenation selectivity
Metal organic layer
Palladium
Pd based catalyst
Room temperature
Selectivity
β-unsaturated aldehydes
title Precise control of selective hydrogenation of α,β-unsaturated aldehydes in water mediated by ammonia borane
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