79
Views
1
CrossRef citations to date
0
Altmetric
Original Articles

Synthesis, Characterization and Applications of Novel Iminophosphinites

, , &
Pages 652-656 | Published online: 21 Jun 2008

REFERENCES

  • Slone , C. S. , Weinberger , D. A. and Mirkin , C. A. 1999 . Prog. Inorg. Chem. , 48 : 233 Hemilabile reviews
  • Bader , A. and Lindner , E. 1991 . Coord. Chem. Rev. , 108 : 27 and references therein
  • Ramirez , A. , Sun , S. and Collum , D. B. 2006 . J. Am. Chem. Soc. , 128 : 10326 Recent hemilabile applications
  • Kohl , G. , Rudolph , R. , Pritzkow , H. and Enders , M. 2005 . Organometallics , 24 : 4774
  • Whelligan , D. K. and Bolm , C. 2006 . J. Org. Chem. , 71 : 4609 Recent examples of novel P,N type ligands
  • Phillips , A. D. , Bolano , S. , Bosquain , S. S. , Daran , J.-C. , Malacea , R. , Peruzzini , M. , Poli , R. and Gonsalvi , L. 2006 . Organometallics , 25 : 2189
  • Sun , X.-M. , Koizumi , M. , Manabe , K. and Kobayashi , S. 2005 . Adv. Synth, Catal. , 347 : 1893
  • Knopfel , T. F. , Zarotti , P. , Ichikawa , T. and Carreira , E. M. 2005 . J. Am. Chem. Soc. , 127 : 9682
  • Caballero , A. , Jalon , F. A. , Manzano , B. R. , Espino , G. , Perez-Manrique , M. , Mucientes , A. , Poblete , F. J. and Maestro , M. 2004 . Organometallics , 23 : 5694
  • Chang , S. , Jones , L. II , Wang , C. , Lawrence , M. and Grubbs , R. H. 1998 . Organometallics , 17 : 3460
  • Tauer , E. and Grellmann , K. H. 1981 . J. Org. Chem. , 46 : 4252
  • Characterization of 1: m.p. 109–111°C. IR (KBr, cm− 1): 2957, 1627, 1596, 1457, 1436, 1222, 1096, 885, 760, 696. 1H NMR (CD2Cl2): δ 8.62 (1H, s, CH = N), 7.13–7.59 (17H, m, phenyl), 2.97 (2H, sept, CH(CH3)2), 1.13 (12H, d, CH(CH 3)2). 13C NMR (CD2Cl2): δ 158.20 (C = N), 123.36–138.07 (phenyl), 28.34 (CH(CH3)2), 23.76 (CH(CH3)2). 31P1H NMR (CD2Cl2): δ 107.85
  • Characterization of 2: m.p. 75–76°C. IR (KBr, cm− 1): 3055, 1638, 1578, 1480, 1442, 1432, 1293, 1238, 1198, 891, 747, 740, 693. 1H NMR (CD2Cl2): δ 6.62–7.73 (22H, m, phenyl). 13C NMR (CD2Cl2): δ 145.78 (C = N), 121.80–131.21 (phenyl). 31P1H NMR (CD2Cl2, ppm): δ 111.93
  • Characterization of 3: m.p. 222°C (dec.). IR (KBr, cm− 1): 3053, 1596, 1580, 1565, 1477, 1437, 1238, 1110, 1096, 906, 771, 748, 735, 702. 1H NMR (CD2Cl2): δ 6.82–8.12 (22H, m, phenyl). 13C NMR (CD2Cl2): δ 149.96 (C = N), 120.99–137.76 (phenyl). 31P1H NMR (CD2Cl2): δ 131.55
  • Jibril , I. , El-Khateeb , M. , Barakat , H. , Rheinwald , G. and Lang , H. 2002 . Inorg. Chim. Acta. , 333 : 1
  • Romeo , R. , Scolaro , L. M. , Plutino , M. R. and Del Zotto , A. 1998 . Trans. Met. Chem. , 23 : 789
  • Diaz , C. and Araya , E. 1997 . Polyhedron , 16 : 1775
  • Suzuki , A. 2005 . Chem. Commun. , : 4759
  • Amatore , C. , Bahsoun , K. A. A. , Jutand , M. , Meyer , G. , Ntepe , A. N. and Ricard , L. 2003 . J. Am. Chem. Soc. , 125 : 4212
  • Tang , H. , Menzel , K. and Fu , G. C. 2003 . Angew. Chem. Int. Ed. , 42 : 5079
  • Gasperini , M. , Ragaini , F. , Gazzola , E. , Caselli , A. and Macchi , P. 2004 . Dalton Trans , : 3376 – 3382 .
  • Faller , J. W. , Stokes-Huby , H. L. and Albrizzio , M. A. 2001 . Helv. Chim. Acta , 84 : 3031 – 3042 .

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.