Reactions of ferrocene-derived bis(hydroxymethyl) phosphine sulfides FcCH(R)P(S)(CH2OH)(2) (R = H, CH3)with cyclic thionylphosphazenes: crystal structures of FcCH(2)P(S)(CH2O)(2)PN(NPCl2)[NS(O)Ph] and FcCH(2)P(S)(CH2O)(2)PN2P[N(Me)CH2](2)[NS(O)Ph] (Fc = ferrocenyl)

Citation
Tvv. Ramakrishna et Aj. Elias, Reactions of ferrocene-derived bis(hydroxymethyl) phosphine sulfides FcCH(R)P(S)(CH2OH)(2) (R = H, CH3)with cyclic thionylphosphazenes: crystal structures of FcCH(2)P(S)(CH2O)(2)PN(NPCl2)[NS(O)Ph] and FcCH(2)P(S)(CH2O)(2)PN2P[N(Me)CH2](2)[NS(O)Ph] (Fc = ferrocenyl), J ORGMET CH, 637, 2001, pp. 382-389
Citations number
35
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF ORGANOMETALLIC CHEMISTRY
ISSN journal
0022328X → ACNP
Volume
637
Year of publication
2001
Pages
382 - 389
Database
ISI
SICI code
0022-328X(200112)637:<382:ROFBPS>2.0.ZU;2-I
Abstract
The cyclic six-membered thionylphosphazenes, (NPCl2)(2)[NS(O)X] X = Cl (1), Ph (2) and 4-Cl-C6H4 (3) as well as the monospirocyclic derivatives (NPCl2 )NP[N(Me)CH2](2)[NS(O)Ph] (4) and (NPCl2)NP[N(Me)CH2](2)[NS(O)4-Cl-C6H4] (5 ) were synthesized. Reactions of these compounds were carried out with dili thiated ferrocene-derived hydroxymethyl phosphine sulfides, FcCH(2)P(S)(CH2 OH)(2) (6) and FcCH(CH3)P(S)(CH2OH)(2) (7) under different conditions. Reac tions of 1 with 6 and 7 did not yield any desired products. In contrast, 1: 1 reactions of 2 with 6 and 7 readily yielded air stable monospirocyclic co mpounds FcCH(2)P(S)(CH2O)(2)PN(NPCl2)[NS(O)Ph] (8) and FcCH(CH3)P(S)(CH2O)( 2)PN(NPCl2)[NS(O)Ph] (9), respectively. Controlled reactions of 4 and 5 wit h 6 were performed in which dispirocyclic compounds FcCH(2)P(S)(CH2O)(2)PN2 P[N(Me)CH2](2)[NS(O)Ph] (10) and FcCH(2)P(S)(CH2O)(2)PN2P[N(Me)CH2](2)[NS(O )4-Cl-C6H4] (11) were isolated. The product obtained in the 1:1 reaction of HOCH2(CF2)(2)CH2OH with (NPCl2)(2)[NS(O)4-Cl-C6H4] (3) when reacted with 6 resulted in the dispirocyclic compound FcCH(2)P(S)[(CH2O)(2)PN2P (OCH2CF2) (2)][NS(O)4-Cl-C6H4] (12). Compound 12 was found to exist as isomers. To co nfirm the formation of isomers, {[CH2N(Me)](2)PN2P(OCH2CF2)(2)}[NS(O)Ph] (1 3) was synthesized by the reaction of 4 with HOCH2(CF2)(2)CH2OH which was a lso found to exist as isomers. Attempts to synthesize intermolecular bridge d compounds of 2 with 6 and 7 resulted in compounds 8 and 9 exclusively. Th e crystal structures of compounds 8 and 10 were determined. (C) 2001 Elsevi er Science B.V. All rights reserved.