Phospha[3]radialenes. Syntheses, structures, strain energies, and reactions

C. M.D. Komen, C. J. Horan, S. Krill, G. M. Gray, M. Lutz, A. L. Spek, A. W. Ehlers, K. Lammertsma

Research output: Contribution to journalArticlepeer-review

25 Citations (Scopus)

Abstract

In situ-generated terminal phosphinidene complex PhPW(CO) 5 adds in a 1,2-fashion to the terminal double bond of tetramethylcumulene and cyclic 1,2,3-cyclodecatriene. The resulting alkenylidenephosphiranes 19A and 20A, which are three-membered phosphiranes containing an exocyclic allenic group, subsequently rearrange to the corresponding phospha[3]radiales 19B and 20B, which are phosphiranes having two exocyclic double bonds. All four organophosphorus compounds were characterized by single-crystal X-ray structure determinations. Bicyclic 20A contains a significantly bent (171.5(7)°) and twisted (14.2(8)°) allenic unit in contrast to 19A. The rearrangement to the thermodynamically favored radialenes is considered to occur by a phosphirane ring opening/closure sequence. On using a second equivalent of PhPW(CO)5, insertion takes place into a PC bond of 20B, but not of 19B, to give two new phospha[4]radialene isomers, viz. cis-20C and trans-20C, both of which were characterized by crystal structure determinations. The PPCC ring in these systems is significantly puckered (∼150°), causing the olefinic bonds of the butadiene unit to be much twisted from planarity. Both phospha[3]radialenes undergo Diels - Alder reactions with methyl-1,2,4-triazole-3,5-dione (MTAD), resulting in the case of the acyclic cumulene in the expected addition product 19D of which the phosphirane ring easily hydrolyzes. Cycloaddition of MTAD to 20B does not occur at the radialene's diene unit but rather invokes one of its PC bonds, possibly in a concerted [(σ2 + π2) + π2] mechanism, to give the unexpected adduct 20F. Ab initio theoretical studies on the parent systems, using the G3(MP2) method, show phospha[3]radialene to be 3.6 kcal/mol more stable than ethenylidenephosphirane. Their strain energies (SE) are calculated to be 32.3 and 29.7 kcal/mol, respectively. The 22.2 kcal/mol SE of phosphirane increases by 5.9 kcal/mol on introducing one exocyclic double bond and by another 4.2 kcal/mol on introducing the second one. Still, the SE of phospha[3]radialene is less than the 39.0 kcal/mol of the more condensed-phosphirene.

Original languageEnglish
Pages (from-to)12507-12516
Number of pages10
JournalJournal of the American Chemical Society
Volume122
Issue number50
DOIs
Publication statusPublished - 20 Dec 2000
Externally publishedYes

ASJC Scopus subject areas

  • Catalysis
  • General Chemistry
  • Biochemistry
  • Colloid and Surface Chemistry

Fingerprint

Dive into the research topics of 'Phospha[3]radialenes. Syntheses, structures, strain energies, and reactions'. Together they form a unique fingerprint.

Cite this