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Vol. 32 No. 5 (2020): Vol 32 Issue 5

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Synthesis and Characterization of [CrLCl2]Cl Complexes (where L = S4 Macrocyclic Ligands): A Photoelectron Spectroscopic Study

Krishna Kumar Yadav
Department of Chemistry, Bipin Bihari P.G. College, Jhansi-284002, India
Anil Kumar
Department of Chemistry, Bipin Bihari P.G. College, Jhansi-284002, India
Mohd Kashif Aziz
Department of Chemistry, University of Allahabad, Allahabad-211002, India
Rafat Saba
Department of Chemistry, University of Allahabad, Allahabad-211002, India
Ashish Rajak
Department of Chemistry, University of Allahabad, Allahabad-211002, India
Shekhar Srivastava
Department of Chemistry, University of Allahabad, Allahabad-211002, India

Corresponding Author(s) : Shekhar Srivastava

shekhsri@rediffmail.com

Asian Journal of Chemistry, Vol. 32 No. 5 (2020): Vol 32 Issue 5

Abstract

In this study, five complexes of the type [CrLCl2]Cl [where L = S4 macrocyclic ligands] were prepared and analyzed by elemental analysis, molar conductivity, infrared and X-ray photoelectron spectroscopy and their geometry was established as octahedral.

Keywords

Chromium S4 macrocyclic ligands X-ray photoelectron spectroscopy
Yadav, K. K., Kumar, A., Aziz, M. K., Saba, R., Rajak, A., & Srivastava, S. (2020). Synthesis and Characterization of [CrLCl2]Cl Complexes (where L = S4 Macrocyclic Ligands): A Photoelectron Spectroscopic Study. Asian Journal of Chemistry, 32(5), 1097–1100. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/2432
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References
  1. E.K. Barefield, Coord. Chem. Rev., 254, 1607 (2010); https://doi.org/10.1016/j.ccr.2010.03.007
  2. J.C. Timmons and T.J. Hubin, Coord. Chem. Rev., 254, 1661 (2010); https://doi.org/10.1016/j.ccr.2009.09.018
  3. R.E. Mewis and S.J. Archibald, Coord. Chem. Rev., 254, 1686 (2010); https://doi.org/10.1016/j.ccr.2010.02.025
  4. B. Korybut-Daszkiewicz, R. Bilewicz and K. Wozniak, Coord. Chem. Rev., 254, 1637 (2010); https://doi.org/10.1016/j.ccr.2009.12.004
  5. L.F. Lindoy, G.V. Meehan, I.M. Vasilescu, H.J. Kim, J.-E. Lee and S.S. Lee, Coord. Chem. Rev., 254, 1713 (2010); https://doi.org/10.1016/j.ccr.2009.11.012
  6. L. Tusek-Bozic, E. Marotta and P. Traldi, Polyhedron, 26, 1663 (2007); https://doi.org/10.1016/j.poly.2006.12.012
  7. R. Chakrabarty, P.S. Mukherjee and P.J. Stang, Chem Rev., 111, 6810 (2011); https://doi.org/10.1021/cr200077m
  8. A. Kilic, E. Tas, B. Deveci and I. Yilmaz, Polyhedron, 26, 4009 (2007); https://doi.org/10.1016/j.poly.2007.05.013
  9. D.E. Fenton and H. Okawa, Chem. Ber., 130, 433 (1997); https://doi.org/10.1002/cber.19971300402
  10. S. Di Bella and I. Fragala, Synth. Matals, 115, 191 (2000); https://doi.org/10.1016/S0379-6779(00)00354-4
  11. P.G. Lacroix, Eur. J. Inorg. Chem., 2001, 339 (2001); https://doi.org/10.1002/1099-0682(200102)2001:2<339::AIDEJIC339>3.0.CO;2-Z
  12. N.E. Borisova, M.D. Reshetova and Y.A. Ustynyuk, Chem. Rev., 107, 46 (2007); https://doi.org/10.1021/cr0683616
  13. N.A. Rey, A. Neves, A. Bortoluzzi, C.T. Pich and H. Terenzi, Inorg. Chem., 46, 348 (2007); https://doi.org/10.1021/ic0613107
  14. J. Gao, F.R. Woolley and R.A. Zingaro, Org. Biomol. Chem., 3, 2126 (2005); https://doi.org/10.1039/b503971a
  15. C. Edder, C. Piguet, J.-C.G. Bünzli and G. Hopfgartner, Chem. Eur. J., 7, 3014 (2001); https://doi.org/10.1002/1521-3765(20010716)7:14<3014::AIDCHEM3014>3.0.CO;2-D
  16. W.K. Wong, H. Liang, W.Y. Wong, Z. Cai, K.F. Li and K.W. Cheah, New J. Chem., 26, 275 (2002); https://doi.org/10.1039/b104175b
  17. A. Bianchi, E. Garcia-Espana and K. Bownman-James, Supramolecular Chemistry of Anions, Wiley-VCH: New York (1997).
  18. A. Bianchi, M. Micheloni and P. Paoletti, Coord. Chem. Rev., 130, 17 (1991); https://doi.org/10.1016/0010-8545(91)80023-7
  19. D.L. Grisenti, M.B. Smith, L. Fang, N. Bishop and P.S. Wagenknecht, Inorg. Chim. Acta, 363, 157 (2010); https://doi.org/10.1016/j.ica.2009.09.020
  20. S.R. Cooper, Crown Compounds Towards Future Applications, WileyVCH: New York (1992).
  21. R.D. Hancock and A.E. Martell, Chem. Rev., 89, 1875 (1989); https://doi.org/10.1021/cr00098a011
  22. S. Rani, S. Kumar and S. Chandra, Spectrochim. Acta A Mol. Biomol. Spectrosc., 78, 1507 (2011); https://doi.org/10.1016/j.saa.2011.01.041
  23. M. Shokeen and C. Anderson, Acc. Chem. Res., 42, 832 (2009); https://doi.org/10.1021/ar800255q
  24. R. Delgado, V. Felix, L.M.P. Lima and D.W. Price, J. Chem. Soc., Dalton Trans., 2734 (2007); https://doi.org/10.1039/B704360K
  25. H. Keypour, M. Rezaeivala, L. Valencia, P. Perez-Lourido and A.H. Mahmoud Khani, Polyhedron, 28, 3415 (2009); https://doi.org/10.1016/j.poly.2009.07.012
  26. H. Keypour, H. Goudarziafshar, A.K. Brisdon and R.G. Pritchard, Inorg. Chim. Acta, 360, 2298 (2007); https://doi.org/10.1016/j.ica.2006.11.023
  27. C. Núñez, R. Bastida, A. Macías, A. Aldrey and L. Valencia, Polyhedron, 29, 126 (2010); https://doi.org/10.1016/j.poly.2009.06.093
  28. F. Firdaus, K. Fatma, M. Azam, S.N. Khan, A.U. Khan and M. Shakir, Spectrochim. Acta A, 72, 591 (2009); https://doi.org/10.1016/j.saa.2008.10.054
  29. M.C. Fernández-Fernández, R. Bastida, A. Macías, P.P. Lourido and L. Valencia, Polyhedron, 28, 2371 (2009); https://doi.org/10.1016/j.poly.2009.04.042
  30. M. Shakir, P. Chingsubam, H.T.N. Chishti, Y. Azim and N. Begum, Indian Chem., 43A, 556 (2004).
  31. M. Shakir, N. Begum, S. Parveen, P. Chingsubam and S. Tabassum, Synth. React. Inorg. Met.-Org. Chem., 34, 1135 (2004); https://doi.org/10.1081/SIM-120039262
  32. S.E. Livingstone, Quart. Rev., 19, 386 (1965); https://doi.org/10.1039/qr9651900386
  33. R.L. Carlin and E. Weissberger, Inorg. Chem., 3, 611 (1964); https://doi.org/10.1021/ic50014a044
  34. F.A. Cotton and D.L. Weaver, J. Am. Chem. Soc., 87, 4189 (1965); https://doi.org/10.1021/ja01096a034
  35. Z.J. Zhong, N. Matsumoto, H. Okawa and S. Kida, Inorg. Chem., 30, 436 (1991); https://doi.org/10.1021/ic00003a015
  36. H. Tamaki, Z.J. Zhong, N. Matsumoto, S. Kida, M. Koikawa, N. Achiwa, Y. Hashimoto and H. Okawa, J. Am. Chem. Soc., 114, 6974 (1992); https://doi.org/10.1021/ja00044a004
  37. H. Tsubuke, T. Yoden, T. Iwachido and M. Zenki, J. Chem. Soc. Chem. Commun., 1069 (1991); https://doi.org/10.1039/C39910001069
  38. S. Wherland and H.B. Gray, Biological Aspects of Inorganic Chemistry, Wiley Eastern: New York, p. 289 (1977).
  39. D. Cummins and H.B. Gray, J. Am. Chem. Soc., 99, 5158 (1977); https://doi.org/10.1021/ja00457a042
  40. N.C. Patra, A.K. Rout, A.K. Bhattacharya, U. Pujapanda and P.K. Sahoo, Indian J. Chem., 30A, 225 (1991).
  41. M.B.H. Howlader, M.S. Islam and M.R. Karim, Indian J. Chem., 39A, 407 (2000).
  42. R.V. Chaudhary and A. Singh, Indian J. Chem., 41A, 3536 (2002).
  43. Z. Shourong, L. Huakuan, X. Jingchun and C. Yun-ti, Polyhedron, 13, 759 (1994); https://doi.org/10.1016/S0277-5387(00)81681-2
  44. D. Christodoulou, M.G. Kanatzidis and D. Coucouvanis, Inorg. Chem., 29, 191 (1990); https://doi.org/10.1021/ic00327a010
  45. Z.A. Siddiqi and V.J. Mathew, Polyhedron, 13, 799 (1994); https://doi.org/10.1016/S0277-5387(00)81687-3
  46. W.E. Keyes, J.B.R. Dunn and T.M. Loehr, J. Am. Chem. Soc., 99, 4527 (1977); https://doi.org/10.1021/ja00455a065
  47. T.M. Barclay, A. McAuley and S. Subramanian, Chem. Commun., 170 (2002); https://doi.org/10.1039/b109793h
  48. J.C. Previdi and R.A. Krause, Inorg. Chem., 15, 462 (1976); https://doi.org/10.1021/ic50156a044
  49. R.W. Hay, G.A. Lawrance and U.R. Shone, J. Chem. Soc., Dalton Trans., 1976, 942 (1976); https://doi.org/10.1039/DT9760000942
  50. A. Dei and F. Mani, Inorg. Chim. Acta, 19, L39 (1976); https://doi.org/10.1016/S0020-1693(00)91126-5
  51. R.W. Hay and D.P. Piplani, J. Chem. Soc., Dalton Trans., 1977, 1956 (1977); https://doi.org/10.1039/dt9770001956
  52. G. Irwin, A.D. Kirk, I. Mackay and J. Nera, Inorg. Chem., 41, 874 (2002); https://doi.org/10.1021/ic010236j
  53. S. Chandra, L. Gupta and K. Gupta, J. Indian Chem. Soc., 81, 833 (2004).
  54. J.C. Byun, C.H. Han and Y.C. Park, Bull. Korean Chem. Soc., 26, 1044 (2005); https://doi.org/10.5012/bkcs.2005.26.7.1044
  55. T.J. Collins, C. Slebodnick and E.S. Uffelman, Inorg. Chem., 29, 3433 (1990); https://doi.org/10.1021/ic00343a030
  56. P.K. Baker, M.C. Durrant, S.D. Harris, D.L. Hughes and R.L. Richards, J. Chem. Soc., Dalton Trans., 509 (1997); https://doi.org/10.1039/a606193a
  57. P. Comba, A. Fath, A. Kühner and B. Nuber, J. Chem. Soc., Dalton Trans., 1889 (1997); https://doi.org/10.1039/a607859a
  58. W.J. Geary, Coord. Chem. Rev., 7, 81 (1971); https://doi.org/10.1016/S0010-8545(00)80009-0
  59. S.A.A. Nami and K.S. Siddiqi, Synth. React. Inorg. Met.-Org. Chem., 34, 1581 (2004); https://doi.org/10.1081/SIM-200026593
  60. W. Levason, G. Reid and W. Zhang, Z. Anorg. Allg. Chem., 640, 35 (2013); https://doi.org/10.1002/zaac.201300482
  61. S. Srivastava, Appl. Spectrosc. Rev., 22, 401 (1986); https://doi.org/10.1080/05704928608060441
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