Synthesis, reactivity, electrochemical and crystallographic studies of diferrocenoyl diselenide and ferrocenoyl selenides
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Title |
Synthesis, reactivity, electrochemical and crystallographic studies of diferrocenoyl diselenide and ferrocenoyl selenides
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Creator |
KUMAR, S
TRIPATHI, SK SINGH, HB WOLMERSHAUSER, G |
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Subject |
glutathione-peroxidase
stereoselective-synthesis antioxidant activity radical cyclization diacyl diselenides facile synthesis selenol esters cyclic ethers se-77 nmr derivatives selenol esters ferrocene thiol peroxidase x-ray crystal structures |
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Description |
Diacyl diselenide (8), diacyl selenide (9) and acyl selenol esters (10-12) incorporating the ferrocenoyl substituent have been synthesized from ferrocene carboxylic acid (13). The new compounds (8-10) have been characterized by multinuclear NMR (H-1, C-13, Se-77), IR spectroscopy and electrospray mass spectrometry. All compounds (8-13) undergo a one electron reversible oxidation at significantly more positive potential than ferrocene. The structures of the diselenide and selenide (8 and 10) have been confirmed by single crystal X-ray diffraction. The absolute structure parameter of 8 indicates that it crystallizes in an enan-tiomerically pure form. The peroxidase-like activities of the diselenide (8) and selenides (9-12) have been determined by the thiol assay. (C) 2004
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Publisher |
ELSEVIER SCIENCE SA
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Date |
2011-07-29T00:20:06Z
2011-12-26T12:47:40Z 2011-12-27T05:38:19Z 2011-07-29T00:20:06Z 2011-12-26T12:47:40Z 2011-12-27T05:38:19Z 2004 |
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Type |
Article
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Identifier |
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 689(19), 3046-3055
0022-328X http://dx.doi.org/10.1016/j.jorganchem.2004.06.054 http://dspace.library.iitb.ac.in/xmlui/handle/10054/7531 http://hdl.handle.net/10054/7531 |
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Language |
en
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