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  Synthesis, characterization, X-ray structural analysis, and iodination ability of benzyl(triphenyl)phosphonium dichloroiodate.

Imanieh, H., Ghammamy, S., Nikje, M. M. A., Khavasi, H. R., & Kia, R. (2011). Synthesis, characterization, X-ray structural analysis, and iodination ability of benzyl(triphenyl)phosphonium dichloroiodate. Helvetica Chimica Acta, 94(12), 2248-2255. doi:10.1002/hlca.201100198.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-002C-1789-E Version Permalink: http://hdl.handle.net/11858/00-001M-0000-002C-178F-2
Genre: Journal Article

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2368717.pdf (Publisher version), 422KB
 
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Imanieh, H., Author
Ghammamy, S., Author
Nikje, M. M. A., Author
Khavasi, H. R., Author
Kia, R.1, Author              
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1Research Group of Structural Dynamics of (Bio)Chemical Systems, MPI for Biophysical Chemistry, Max Planck Society, ou_578564              

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 Abstract: Benzyl(triphenyl)phosphonium dichloroiodate (BTPPICl2), BnPh3P+(ICl2)−, is easily synthesized in a nearly quantitative yield by the addition of BnPh3P+Cl− to a CH2Cl2 solution of iodine monochloride (ICl). BnPh3P+Cl− can be prepared by the reaction of Ph3P and BnCl. The compound was characterized by physicochemical and spectroscopic methods (elemental analysis, FT-IR, and 1H-NMR). The use of phosphonium counterion improves the quality of the BTPPICl2 crystals. BTPPICl2 crystallizes in the monoclinic system, and its crystal and molecular structure has been determined at 100(1) K by X-ray diffraction. The structure was solved by the direct method and had refined R value of 0.0637 for 699 reflections (I>2σ(I)), space group P21/n with a=12.4700(3), b=13.2196(3), c=14.4580(3) Å, β=102.6340(10)°, V=2325.67(9) Å3, and Z=4. The I-atom is coordinated by two Cl-atoms as ligands in a linear geometry. This compound is a versatile reagent for the efficient and selective iodination of organic substrates, in particular of aromatic phenols to the corresponding iodo compounds, under mild conditions. To assess the generality of method, a wide variety of phenols with electron-donating and electron-withdrawing substituents were studied. BTPPICl2 is a mild iodination reagent, which offers a new avenue for an expeditious iodination of phenols. The inexpensive, relatively non-toxic reagent, and mild conditions are the positive features of the procedure and reagent.

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Language(s): eng - English
 Dates: 2011-12-082011-12
 Publication Status: Published in print
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 Rev. Method: Peer
 Identifiers: DOI: 10.1002/hlca.201100198
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Title: Helvetica Chimica Acta
Source Genre: Journal
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Pages: 8 Volume / Issue: 94 (12) Sequence Number: - Start / End Page: 2248 - 2255 Identifier: -