33082-06-3Relevant articles and documents
Studies on iodination reactions of phosphiniminocyclotrithiazenes
Sivaramakrishna, Akella,Swarnalatha,Sudheendra Rao
, p. 1349 - 1354 (2013)
Iodination reactions of various phosphiniminocyclotrithiazenes [R 3PNS3N3; R = (i) phenyl-, (ii) morpholino-, and (iii) p-chlorophenyl-] have been studied under different experimental conditions. Iodination of Ph3PNS3N3 yields interesting products such as [(Ph3PN)2S3N 3]I3, ((Ph3PN)3S)2I 4, (Ph3PNH2)I3, ((Ph 3PSI2)2I2, and [(Ph 3PN)3SO]2I6 depending on the experimental conditions. All the products have been isolated and characterized by the spectroscopic and analytical techniques. Copyright Taylor & Francis Group, LLC.
The cycloaddition of norbornadiene to (triphenylphosphoranediyl)aminocyclotrithiatriazene; the crystal and molecular structure of Ph3PN-S3N3*C7H8
Liblong, Stephen W.,Oakley, Richard T.,Cordes, A. Wallace,Noble, Mark C.
, p. 2062 - 2067 (2007/10/02)
The reaction of norbornadiene with (triphenylphosphoranediyl)aminocyclotrithiatriazene produces the cycloadduct Ph3PN-S3N3*C7H8.The crystal and molecular structure of this compound has been determined by X-ray crystallography.Crystals of Ph3PN-S3N3*C7H8 are monoclinic, space group P21/c, a=9.757(1), b=15.114(1), c=16.535(2) Angstroem, β=100.73(1) deg, V=2395.7(9) Angstroem3, and Z=4.The structure was solved by direct methods and refined by Furier and full-matrix least-squares procedures to give a final R of 0.040 and Rw of 0.058 for 2620 observed reflections.The structure reveals that the S3N3 ring adds to norbornadiene in an exo fashion via two sulphur atoms.The S3N3 ring adopts a chair conformation with the three ligands occupying axial positions an the same side of the ring.The relative rates of this and other cycloadditions involving SN substrates and olefins are discussed in terms of the energies of the interacting frontier orbitals.The results suggest that HOMO(olefin)-LUMO(SN substrate) interactions control the kinetics of these reactions.
