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Amidine Dications: Isolation and [Fe]-Hydrogenase-Related Hydrogenation
This commmunication demonstrates the preparation, isolation, and full characterization of superelectrophilic salts based on amidine dications in organic solvent, as their triflate salts. These dications are highly activated toward regiospecific reaction with hydrogen gas under mild conditions in the...
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Published in: | Journal of the American Chemical Society 2009-07, Vol.131 (26), p.9174-9175 |
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cited_by | cdi_FETCH-LOGICAL-a469t-d2c2e47183bf9c225efc8c7d547b6d454081875012bb136f369a80942d060bf43 |
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cites | cdi_FETCH-LOGICAL-a469t-d2c2e47183bf9c225efc8c7d547b6d454081875012bb136f369a80942d060bf43 |
container_end_page | 9175 |
container_issue | 26 |
container_start_page | 9174 |
container_title | Journal of the American Chemical Society |
container_volume | 131 |
creator | Corr, Michael J Gibson, Kirsty F Kennedy, Alan R Murphy, John A |
description | This commmunication demonstrates the preparation, isolation, and full characterization of superelectrophilic salts based on amidine dications in organic solvent, as their triflate salts. These dications are highly activated toward regiospecific reaction with hydrogen gas under mild conditions in the presence of a metal catalyst (Pd/C), mimicking the behavior of the natural substrate, N 5,N 10-methenyltetrahydromethanopterin, in the iron−sulfur cluster-free [Fe]-hydrogenase. |
doi_str_mv | 10.1021/ja9035847 |
format | article |
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Am. Chem. Soc</addtitle><date>2009-07-08</date><risdate>2009</risdate><volume>131</volume><issue>26</issue><spage>9174</spage><epage>9175</epage><pages>9174-9175</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>This commmunication demonstrates the preparation, isolation, and full characterization of superelectrophilic salts based on amidine dications in organic solvent, as their triflate salts. These dications are highly activated toward regiospecific reaction with hydrogen gas under mild conditions in the presence of a metal catalyst (Pd/C), mimicking the behavior of the natural substrate, N 5,N 10-methenyltetrahydromethanopterin, in the iron−sulfur cluster-free [Fe]-hydrogenase.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>19534467</pmid><doi>10.1021/ja9035847</doi><tpages>2</tpages><oa>free_for_read</oa></addata></record> |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Alkylation Amidines - chemical synthesis Amidines - chemistry Bacteria - chemistry Bacterial Proteins - chemistry Biomimetics Catalysis Cations - chemical synthesis Cations - chemistry Communication Crystallography, X-Ray Hydrogen - chemistry Hydrogenase - chemistry Hydrogenation Iron-Sulfur Proteins - chemistry Molecular Structure |
title | Amidine Dications: Isolation and [Fe]-Hydrogenase-Related Hydrogenation |
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