Literature DB >> 34324230

Surprising Condensation Reactions of the Azadithiolate Cofactor.

Fanjun Zhang1, Casseday P Richers1, Toby J Woods1, Thomas B Rauchfuss1.   

Abstract

Azadithiolate, a cofactor found in all [FeFe]-hydrogenases, is shown to undergo acid-catalyzed rearrangement. Fe2 [(SCH2 )2 NH](CO)6 self-condenses to give Fe6 [(SCH2 )3 N]2 (CO)17 . The reaction, which is driven by loss of NH4+ , illustrates the exchange of the amine group. X-ray crystallography reveals that three Fe2 (SR)2 (CO)x butterfly subunits interconnected by the aminotrithiolate [N(CH2 S)3 ]3- . Mechanistic studies reveal that Fe2 [(SCH2 )2 NR](CO)6 participate in a range of amine exchange reactions, enabling new methodologies for modifying the adt cofactor. Ru2 [(SCH2 )2 NH](CO)6 also rearranges, but proceeds further to give derivatives with Ru-alkyl bonds Ru6 [(SCH2 )3 N][(SCH2 )2 NCH2 ]S(CO)17 and [Ru2 [(SCH2 )2 NCH2 ](CO)5 ]2 S.
© 2021 Wiley-VCH GmbH.

Entities:  

Keywords:  carbonyls; cofactors; hydrogenase; iron; thiolate

Mesh:

Substances:

Year:  2021        PMID: 34324230      PMCID: PMC8429227          DOI: 10.1002/anie.202108135

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   16.823


  14 in total

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Authors:  Iain D G Watson; Andrei K Yudin
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Authors:  Constanze Sommer; Casseday P Richers; Wolfgang Lubitz; Thomas B Rauchfuss; Edward J Reijerse
Journal:  Angew Chem Int Ed Engl       Date:  2018-03-26       Impact factor: 15.336

4.  Diiron azadithiolates as models for the [FeFe]-hydrogenase active site and paradigm for the role of the second coordination sphere.

Authors:  Thomas B Rauchfuss
Journal:  Acc Chem Res       Date:  2015-06-16       Impact factor: 22.384

5.  Ligand versus metal protonation of an iron hydrogenase active site mimic.

Authors:  Gerriet Eilers; Lennart Schwartz; Matthias Stein; Giuseppe Zampella; Luca de Gioia; Sascha Ott; Reiner Lomoth
Journal:  Chemistry       Date:  2007       Impact factor: 5.236

6.  Synthetic models for the active site of the [FeFe]-hydrogenase: catalytic proton reduction and the structure of the doubly protonated intermediate.

Authors:  Maria E Carroll; Bryan E Barton; Thomas B Rauchfuss; Patrick J Carroll
Journal:  J Am Chem Soc       Date:  2012-11-05       Impact factor: 15.419

7.  Oxygen-Tolerant H2 Production by [FeFe]-H2ase Active Site Mimics Aided by Second Sphere Proton Shuttle.

Authors:  Md Estak Ahmed; Subal Dey; Marcetta Y Darensbourg; Abhishek Dey
Journal:  J Am Chem Soc       Date:  2018-09-18       Impact factor: 15.419

8.  Bioassembly of complex iron-sulfur enzymes: hydrogenases and nitrogenases.

Authors:  R David Britt; Guodong Rao; Lizhi Tao
Journal:  Nat Rev Chem       Date:  2020-07-22       Impact factor: 34.571

9.  Spectroscopic and Computational Evidence that [FeFe] Hydrogenases Operate Exclusively with CO-Bridged Intermediates.

Authors:  James A Birrell; Vladimir Pelmenschikov; Nakul Mishra; Hongxin Wang; Yoshitaka Yoda; Kenji Tamasaku; Thomas B Rauchfuss; Stephen P Cramer; Wolfgang Lubitz; Serena DeBeer
Journal:  J Am Chem Soc       Date:  2019-12-30       Impact factor: 15.419

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  1 in total

1.  Lewis acid protection turns cyanide containing [FeFe]-hydrogenase mimics into proton reduction catalysts.

Authors:  Holly J Redman; Ping Huang; Michael Haumann; Mun Hon Cheah; Gustav Berggren
Journal:  Dalton Trans       Date:  2022-03-22       Impact factor: 4.390

  1 in total

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