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The reactions of alkylamino substituted phosphines with I2 and (Ph2Se2I2)2: structural features of alkylamino phosphonium cations

Barnes, Nicholas A; Godfrey, Stephen M; Halton, Ruth T A; Mushtaq, Imrana; Pritchard, Robin G

Dalton Transactions. 2008;(10):1346-1354.

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Abstract

The reactions of the tris-dialkylamino phosphines (Et2N)(3)P and ((Pr2N)-Pr-n)(3)P, and the pyrrolidinyl substituted phosphines (C4H8N)(3)P and tBuP(NC4H8)(2), with I-2 and (Ph2Se2I2)(2), have been reported. The reactions with diiodine lead to the formation of [R3PI]I adducts, which are essentially ionic, but show a tendency to display long, soft-soft, I center dot center dot center dot I interactions in the solid state. The crystal structures of [(Et2N)(3)PI]I, (1), [((Pr2N)-Pr-n)(3)PI]I, (2), and [(C4H8N)(3)PI]I, (3), have all been determined, and display I center dot center dot center dot I interactions varying between 3.5170(6) and 3.6389(14) angstrom. The analogous reactions with (Ph2Se2I2)(2) lead to the formation of phenylseleno-phosphonium salts, [R3PSePh]I. The structures of [(C4H8N)(3)PSePh]I, (6) and [(C4H8N)(2) tBuPSePh]I, (7), have been determined and do not display any soft-soft interactions between the selenium and iodine atoms. All of the phosphonium salts represent examples of structures containing tris-dialkylamino phosphine fragments which show no "special" nitrogen atom, i.e. all three nitrogen atoms are planar. This type of arrangement is usually observed when a C-3 symmetric conformation is observed, (which is the case for 1 and 2), but not for the (C4H8N)(3)P adducts 3 and 6, where the conformation is closer to C-s, although the nitrogen atoms are still essentially planar. The P-N bonds in all the compounds reported herein are short, ranging between 1.599(12) angstrom and 1.643(12) angstrom, and are consistent with the previously reported short P-N bonds in phosphonium salts featuring tris-dialkylamino substituted phosphines.

Bibliographic metadata

Content type:
Publication type:
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Published date:
Language:
english
Journal title:
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ISSN:
Issue:
10
Start page:
1346
End page:
1354
Total:
9
Pagination:
1346-1354
Digital Object Identifier:
10.1039/b713640d
ISI Accession Number:
ISI:000253643900013
General notes:
  • Barnes, Nicholas A. Godfrey, Stephen M. Halton, Ruth T. A. Mushtaq, Imrana Pritchard, Robin G. 49 ROYAL SOC CHEMISTRY CAMBRIDGE 269IY
Access state:
Active

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Manchester eScholar ID:
uk-ac-man-scw:1f476
Created:
7th September, 2009, 15:04:24
Last modified by:
Godfrey, Stephen
Last modified:
1st November, 2011, 19:20:29

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