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Diiron azadithiolat...
Diiron azadithiolates with hydrophilic phosphatriazaadamantane ligand as iron-only hydrogenase active site models : Synthesis, structure, and electrochemical study
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Wang, Zhen (author)
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Liu, Jianhui (author)
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He, Chengjiang (author)
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Jiang, Shi (author)
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- Åkermark, Björn (author)
- Stockholms universitet,Institutionen för organisk kemi
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- Sun, Licheng (author)
- KTH,Organisk kemi
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(creator_code:org_t)
- Elsevier BV, 2007
- 2007
- English.
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In: Inorganica Chimica Acta. - : Elsevier BV. - 0020-1693 .- 1873-3255. ; 360:7, s. 2411-2419
- Related links:
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https://urn.kb.se/re...
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https://doi.org/10.1...
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https://urn.kb.se/re...
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Abstract
Subject headings
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- Three novel complexes (mu-adt)[Fe-2(CO)(5)PTA] (2-PTA), (mu-adt)[Fe-2(CO)(4)PTA(2)](2-PTA(2)) and (mu-adt)[Fe-2(CO)(5)DAPTA] (2-DAPTA), where adt is SCH2N(CH2CH2CH3)CH2S, PTA stands for 1,3,5-triaza-7-phosphaadamantane and DAPTA is 3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane, were prepared as the models of the iron hydrogenase active site through controlled CO displacement of (mu-adt)[Fe-2(CO)(6)] with PTA and DAPTA. The coordination configurations of 2-PTA and 2-PTA(2) were characterized by X-ray crystallography. The disubstituted diiron complex 2-PTA(2) features a basal/apical coordination mode, instead of the typical transoid basal/basal configuration. Protonation of three complexes only occurred at the bridging-N atom, rather than at the tertiary nitrogen atom on the PTA or DAPTA ligands. Electrochemical properties of the complexes were studied in acetonitrile or a mixture of acetonitrile and water in the presence of acetic acid, by cyclic voltammetry. The current sensitivity of the reduced species to acid concentration in the presence of H2O is greater than in the pure CH3CN solution.
Subject headings
- NATURVETENSKAP -- Kemi -- Organisk kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Organic Chemistry (hsv//eng)
Keyword
- Fe-only hydrogenases
- water solubility
- electrochemistry
- 1,3,5-triaza-7-phosphaadamantane pta
- desulfovibrio-desulfuricans
- chemistry
- complexes
- coordination
- reduction
- evolution
- h-2
- Organic chemistry
Publication and Content Type
- ref (subject category)
- art (subject category)
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