ISOLATION OF THE OPEN FORM OF CYCLENPHOSPHORANE BY DEPROTONATION AND REACTION WITH ELECTROPHILIC REAGENTS

Citation
Dv. Khasnis et al., ISOLATION OF THE OPEN FORM OF CYCLENPHOSPHORANE BY DEPROTONATION AND REACTION WITH ELECTROPHILIC REAGENTS, Inorganic chemistry, 34(7), 1995, pp. 1638-1641
Citations number
24
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00201669
Volume
34
Issue
7
Year of publication
1995
Pages
1638 - 1641
Database
ISI
SICI code
0020-1669(1995)34:7<1638:IOTOFO>2.0.ZU;2-S
Abstract
Depending on the electrophilic reagent RX, the substitution reactions of Li(cyclen)P afford both the ''open'' N-R bonded species R(cyclen)P as well as the ''closed'' P-R bonded species (cyclen)PR. With Mes(2)BF or Ph(2)PCl, the open products Mes(2)B(cyclen)P and Ph(2)P(cyclen)P a re formed. With MeCl, a mixture of both (cyclen)PMe and Me(cyclen)P ar e produced, with the former being the primary product. The X-ray cryst al structure of Mes(2)B(cyclen)P was obtained and reveals that there i s no interaction between the (boron-bound) nitrogen and the phosphorus , while the B-N bond length of 1.407(5) Angstrom indicates significant pi-bonding. These data suggest that larger substituents capable of pi -bonding favor the open isomer. Crystal data: Pbca, orthorhombic, a 12 .083 (3) Angstrom, b = 13.447 (3) Angstrom, 30.533 (7) Angstrom, Z = 8 .