Issue 5, 2006

Structurally diverse penta- and hexacoordinate phosphorus compounds from the reaction of diethyl or diisopropyl azodicarboxylates with phosphorus(iii) compounds

Abstract

The reaction of diethyl azodicarboxylate (DEAD) or diisopropyl azodicarboxylate (DIAD) with cyclic phosphites/phosphoramidites has been examined in an effort to delineate the structural preferences in spirocyclic penta- and tricyclic hexacoordinate (amino)oxyphosphoranes. It is shown that the familiar Bent’s or apicophilicity rules referred to in standard books give an oversimplified picture. Thus the reaction of CH2(6-t-Bu-4-Me–C6H2O)2PCl (19) with DEAD/DIAD leads to the chlorophosphoranes CH2(6-t-Bu-4-Me–C6H2O)2PCl[N(COOR)–N[double bond, length as m-dash]C(OR)O–] [R = Et (21a), i-Pr (21b)]. Treatment of 21a–b with pyrazole or imidazole leads to CH2(6-t-Bu-4-Me–C6H2O)2P(NRR′)[N(COOR)–N[double bond, length as m-dash]C(OR)O–] [NRR′ = pyrazolyl (12a–b), imidazolyl (13a–b)] that have trigonal bipyramidal phosphorus with ‘reversed apicophilicity’. Compound S(6-t-Bu-4-Me–C6H2O)2P(NH–i-Pr) (20b) affords the pentacoordinate derivative S(6-t-Bu-4-Me–C6H2O)2P(NH–i-Pr)[N(COOR)–N[double bond, length as m-dash]C(OR)O–] (15), but S(6-t-Bu-4-Me–C6H2O)2PCl (20a) gives the hexacoordinate phosphorane S(6-t-Bu-4-Me–C6H2O)2PCl[N(COOR)–N[double bond, length as m-dash]C(OR)O–] (16) with the shortest known S→P coordinate bond. Compound 15 also exhibits the ‘reversed apicophilicity’ phenomenon, but the disposition of substituents is different from that in 12–13. The compound S(6-t-Bu-4-Me–C6H2O)2PPh[N(COOR)–N[double bond, length as m-dash]C(OR)O–] (17) is prepared similarly. Reaction of 16 with imidazole gives S(6-t-Bu-4-Me–C6H2O)2P(imidazolyl)[N(COOR)–N[double bond, length as m-dash]C(OR)O–] (18). Both 17 and 18 show distorted octahedral geometry with S→P coordination, but the sulfur is trans to the phenyl/imidazolyl group (while it is cis to –Cl in 16). The variable temperature 31P NMR spectra of 15 exhibit four totally distinct signals showing a dynamic behaviour with isomeric pentacoordinate species present. Theoretical calculations suggest that the compound as isolated is the favoured one for S(6-t-Bu-4-Me–C6H2O)2P{(N-t-Bu)[N(CO2Et)NH(CO2Et)]} (2, previously reported) as well as 15 and 16.

Graphical abstract: Structurally diverse penta- and hexacoordinate phosphorus compounds from the reaction of diethyl or diisopropyl azodicarboxylates with phosphorus(iii) compounds

Supplementary files

Article information

Article type
Paper
Submitted
19 Oct 2005
Accepted
27 Jan 2006
First published
07 Mar 2006

New J. Chem., 2006,30, 717-728

Structurally diverse penta- and hexacoordinate phosphorus compounds from the reaction of diethyl or diisopropyl azodicarboxylates with phosphorus(III) compounds

K. V. P. P. Kumar, N. S. Kumar and K. C. Kumara Swamy, New J. Chem., 2006, 30, 717 DOI: 10.1039/B514839A

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