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Sökning: onr:"swepub:oai:DiVA.org:kth-16892" > Protonation, electr...

Protonation, electrochemical properties and molecular structures of halogen-functionalized diiron azadithiolate complexes related to the active site of iron-only hydrogenases

Wang, Fujun (författare)
Wang, Mei (författare)
Liu, Xiaoyang (författare)
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Jin, Kun (författare)
Donga, Weibing (författare)
Sun, Licheng (författare)
KTH,Organisk kemi
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 (creator_code:org_t)
Royal Society of Chemistry (RSC), 2007
2007
Engelska.
Ingår i: Dalton Transactions. - : Royal Society of Chemistry (RSC). - 1477-9226 .- 1477-9234. ; :34, s. 3812-3819
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Diiron complexes [{( mu-SCH2) 2NCH(2)C(6)H(4)X}{Fe( CO)(2)L}(2)] ( L = CO, X = 2-Br, 1; 2-F, 2; 3-Br, 3; L = PMe3, X = 2-Br, 4) were prepared as biomimetic models of the iron-only hydrogenase active site. The N-protonated species [ 1( NH)]+ClO4-, [ 2( NH)]+ClO4- and the mu-hydride diiron complex [ 4( FeHFe)]+PF6- were obtained in the presence of proton acids and well characterized. The protonation process of 4 was studied by in-situ IR and NMR spectroscopy, which suggests the formation of the diprotonated species [ 4( NH)( FeHFe)](2+) in the presence of an excess of proton acid. The molecular structures of 1, [ 1( NH)]+ClO4-, 4 and [ 4( FeHFe)]+PF6- were determined by X-ray crystallography. The single-crystal X-ray analysis reveals that an intramolecular H center dot center dot center dot Br contact ( 2.82 angstrom) in the crystalline state of [ 1( NH)]+ClO4-. In the presence of 1-6 equiv of the stronger acid HOTf, complex 1 is readily protonated on the bridged-N atom and can electrochemically catalyze the proton reduction at a relatively mild potential ( ca. -1.0 V). Complex 4 is also electrocatalytic active at -1.4 V in the presence of HOTf with formation of the mu-hydride diiron species.

Nyckelord

desulfovibrio-desulfuricans
bridging ligand
model complexes
h-2 evolution
coordination
reduction
catalysis
relevant
hydride
cluster

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