Transition metal derivatives of 1,10-phenanthroline-5,6-dione: Controlled growth of coordination polynuclear derivatives

Inorganica Chimica Acta

Volumn 359, Issue 12, 2006, Pages 3911-3920

  Calucci, Lucia ^a   Pampaloni, Guido ^b   Pinzino, Calogero ^a   Prescimone, Alessandro ^b  

^a AREA DELLA RICERCA   (Italy)

^b UNIVERSITY OF PISA   (Italy)

Author keywords

1,10 Phenanthroline 5,6 dione; Chromium; EPR; Molybdenum; Polynuclear compounds

Indexed keywords

CHROMIUM; DECOMPOSITION; ELECTRON SPIN RESONANCE SPECTROSCOPY; IRON COMPOUNDS; MOLYBDENUM; PARAMAGNETIC RESONANCE; TRANSITION METALS;

1 ,10-PHENANTHROLINE-5 ,6-DIONE; CONTROLLED GROWTH; EPR SPECTROSCOPY; GENERAL FORMULAS; METAL DERIVATIVES; POLYMETALLIC; POLYNUCLEAR COMPOUNDS; POLYNUCLEAR DERIVATIVES;

MOLYBDENUM COMPOUNDS;

EID: 33746720208     PISSN: 00201693     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ica.2006.04.040     Document Type: Article

References (90)

1. Inglett G.E., and Smith G.F. J. Am. Chem. Soc. 72 (1950) 842
2. Druey J., and Schmidt P. Helv. Chim. Acta 33 (1950) 1080
3. Dickeson J.E., and Summers L.A. Aust. J. Chem. 23 (1970) 1023
4. Evans D.H., and Griffith D.A. J. Electroanal. Chem. 134 (1982) 301
5. Lei Y., Shi C., and Anson F.C. Inorg. Chem. 35 (1996) 3044
6. López R.B., Loeb B.L., Boussie T., and Meyer T.J. Tetrahedron Lett. 37 (1996) 5437
7. Kradolfer F., and Neipp L. Antibiot. Chemother. 8 (1958) 297
8. Eckert T.S., and Bruice T.C. J. Am. Chem. Soc. 105 (1983) 4431
9. Hilt G., and Steckhan E. J. Chem. Soc., Chem. Commun. (1993) 1706
10. Moody C.J., Rees C.W., and Thomas R. Tetrahedron 48 (1992) 3589
11. Shabir G.A., and Forrow N.J. J. Pharm. Biomed. Anal. 33 (2003) 219
12. Hilt G., Jarbawi T., Heinemann W.R., and Steckhan E. Chem. Eur. J. 3 (1997) 79
13. Shavaleev N.M., Moorcraft L.P., Pope S.J.A., Bell Z.R., Faulkner S., and Ward M.D. Chem. Eur. J. 9 (2003) 5283
14. Tobalina F., Pariente F., Hernández L., Abruña H.D., and Lorenzo E. Anal. Chim. Acta 395 (1999) 17
15. Wu Q., Maskus M., Pariente F., Tobalina F., Fernández V.M., Lorenzo E., and Abruña H.D. Anal. Chem. 68 (1996) 3688
16. Shi M., and Anson F.C. Anal. Chem. 70 (1998) 1489
17. Gillard R.D., Hill R.E.E., and Maskill R. J. Chem. Soc. (A) (1970) 1447
18. Gillard R.D., and Hill R.E.E. J. Chem. Soc., Dalton Trans. (1974) 1217
19. Goss C.A., and Abruña H.D. Inorg. Chem. 24 (1985) 4263
20. Ernst S., Hänel P., Jordanov J., Kaim W., Kosack V., and Roth E. J. Am. Chem. Soc. 111 (1989) 1733
21. Calderazzo F., Marchetti F., Pampaloni G., and Passarelli V. J. Chem. Soc., Dalton Trans. (1999) 4389
22. Liu H., Du M., Leng X.-B., Bu X.-H., and Zhang R.-H. Chin. J. Struct. Chem. 19 (2000) 427
23. Calderazzo F., Pampaloni G., and Passarelli V. Inorg. Chim. Acta 330 (2002) 136
24. Larsson K., and Öhström L. Inorg. Chim. Acta 357 (2004) 657
25. Fujihara T., Okamura R., Wada T., and Tanaka K. Dalton Trans. (2003) 3221
26. Fujihara T., Wada T., and Tanaka K. Dalton Trans. (2004) 645
27. Margiotta N., Bertolasi V., Capitelli F., Maresca L., Moliterni A.G.G., Vizza F., and Natile G. Inorg. Chim. Acta 357 (2004) 149
28. Ghumaan S., Sarkar B., Patra S., Van Slageren J., Fiedler J., Kaim W., and Lahiri G.K. Inorg. Chem. 44 (2005) 3210
29. Fox G.A., Bhattacharya S., and Pierpont C.G. Inorg. Chem. 30 (1991) 2895
30. Paw W., and Eisenberg R. Inorg. Chem. 36 (1997) 2287
31. Hill P.L., Lee L.Y., Younkin T.R., Orth S.D., and McElwee-White L. Inorg. Chem. 36 (1997) 5655
32. Yamada M., Tanaka Y., Yashimoto Y., Kuroda S., and Shimano I. Bull. Chem. Soc. Jpn. 65 (1992) 1006
33. From homoleptic metal-carbonyl derivatives. Hieber W., Mühlbauer F., and Ehmann E.A. Chem. Ber. 65 (1932) 1090
34. Dewar J., and Jones H.O. Proc. R. Soc. Lond. 76 (1905) 558
35. Fitch J.W., and Lagowski J.J. Inorg. Chem. 4 (1965) 910
36. Calderazzo F., Floriani C., Henzi R., and L'Eplattenier F. J. Chem. Soc. (A) (1969) 1378
37. Bannister E., and Wilkinson G. Chem. Ind. (London) (1960) 319
38. Stephenson T.A., Bannister E., and Wilkinson G. J. Chem. Soc. (1964) 2538
39. Larson M.L., and Moore F.W. Inorg. Chem. 1 (1962) 856
40. Dunne T.G., and Cotton F.A. Inorg. Chem. 2 (1963) 263
41. Calderazzo F., and Pampaloni G. J. Organomet. Chem. 330 (1987) 47
42. Cass M.E., Gordon N.R., and Pierpont C.G. Inorg. Chem. 25 (1986) 3962
43. Calderazzo F., Pampaloni G., Pelizzi G., and Vitali D. Polyhedron 7 (1988) 2039
44. Calderazzo F., Englert U., Pampaloni G., Passarelli V., Serni G., and Wang R.M. Can. J. Chem. 79 (2001) 495
45. From metal-arene derivatives:. Natta G., Ercoli R., and Calderazzo F. Chim. Ind. (Milan) 40 (1958) 1003
46. Calderazzo F., De Benedetto G.E., Pampaloni G., Maichle-Mössmer C., Strähle J., and Wurst K. J. Organomet. Chem. 451 (1993) 73
47. Calderazzo F., De Benedetto G.E., Detti S., and Pampaloni G. J. Chem. Soc., Dalton Trans. (1997) 3319
48. Calderazzo F., De Benedetto G.E., Englert U., Ferri I., Pampaloni G., and Wagner T. Z. Naturforsch. B 51 (1996) 506
49. Calderazzo F., Englert U., Pampaloni G., and Volpe M. J. Organomet. Chem. 690 (2005) 3321
50. Pierpont C.G., and Buchanan R.M. Coord. Chem. Rev. 38 (1981) 45
51. Pierpont C.G., and Lange C.W. Progr. Inorg. Chem. 41 (1994) 331
52. Pierpont C.G. Coord. Chem. Rev. 219-221 (2001) 415 and references therein
53. Calderazzo F., Englert U., Pampaloni G., Kölle U., and Tripepi G. J. Organomet. Chem. 543 (1997) 201
54. Burch R.R. Chem. Mater. 2 (1990) 633
55. For a general review on the IR spectra of quinines, see. Sahini V.E., and Ciurea L. Rev. Roum. Chim. 17 (1972) 273
56. See also. Berger St., and Rieker A. In: Patai S. (Ed). The Chemistry of Quinonoid Compounds vol. 1 (1974), Wiley, New York 163
57. Pierpont C.G., and Buchanan R.M. J. Am. Chem. Soc. 97 (1975) 4912
58. Buchanan R.M., Kessel S.L., Downs H.H., Pierpont C.G., and Hendrickson D.N. J. Am. Chem. Soc. 100 (1978) 7894
59. Buchanan R.M., Downs H.H., Shorthill W.B., Pierpont C.G., Kessel S.L., and Hendrickson D.N. J. Am. Chem. Soc. 100 (1978) 4318
60. Passarelli V. Tesi di Laurea in Chimica (1997), Università di Pisa
61. Konno M., Ishii T., and Saito Y. Acta Crystallogr., Sect. B 33 (1977) 763
62. Hausser K.H. Naturwissenschaften 48 (1961) 666
63. Henrici-Olivé G., and Olivé S. Z. Phys. Chem. Neue Folge 56 (1967) 223
64. Prins R. J. Chem. Phys. 50 (1969) 4804
65. Prins R., and Reinders F. J. Chem. Phys. Lett. 3 (1969) 45
66. Gribov B.G., Kozyrkin B.I., Krivospitskii A.D., and Chirkin G.K. Proc. Acad. Sci. USSR 193 (1970) 457
67. Karthe W., and Kleinwächter W. Z. Phys. Chem., Leipzig 247 (1971) 241
68. Elschenbroich C., and Zenneck U. J. Organomet. Chem. 160 (1978) 125
69. Elschenbroich C., Möckel R., Zenneck U., and Clack D.W. Ber. Bunsenges. Phys. Chem. 83 (1979) 1008
70. Li T.T.-T., Kung W.J., Ward D.L., McCulloch B., and Brubaker Jr. C.H. Organometallics 1 (1982) 1229
71. Reiger P.H. Coord. Chem. Rev. 135/136 (1996) 203
72. Madeja K., and König E. J. Inorg. Nucl. Chem. 25 (1963) 377
73. Basolo F., and Dwyer F.P. J. Am. Chem. Soc. 76 (1954) 1454
74. Fu X.-C., Li M.-T., and Wang C.-G. Acta Crystallogr., Sect. E 61 (2005) m1221
75. n; see. Hawker P.N., and Twig M.V. In: Wilkinson G., Gillard R.D., and McCleverty J.A. (Eds). Comprehensive Coordination Chemistry (1987), Pergamon Press, Oxford 1216
76. Lee T.S., Kolthoff I.M., and Leussing D.L. J. Am. Chem. Soc. 70 (1948) 2348
77. Lee T.S., Kolthoff I.M., and Leussing D.L. J. Am. Chem. Soc. 70 (1948) 3596
78. Kolthoff I.M., Leussing D.L., and Lee T.S. J. Am. Chem. Soc. 72 (1950) 2173
79. Broomhead J.A., and Dwyer F.P. Aust. J. Chem. 14 (1961) 250
80. Ambrosetti R., and Ricci D. Rev. Sci. Instrum. 62 (1991) 2281
81. C. Pinzino, C. Forte, EPR-ENDOR, ICQEM-CNR Rome, Italy, 1992.
82. Duling D.R. J. Magn. Res. B 104 (1994) 105
83. Spartan'02, Wavefunction, Inc., 18401 Von Karman Avenue, Suite 370 Irvine, CA 92612, USA.
84. Becke A.D. Phys. Rev. A 38 (1988) 3098
85. Perdew J.P. Phys. Rev. B 33 (1986) 8822
86. Calderazzo F., Invernizzi R., Marchetti F., Masi F., Moalli A., Pampaloni G., and Rocchi L. Gazz. Chim. Ital. 123 (1993) 53
87. Kern R.J. J. Inorg. Nucl. Chem. 24 (1962) 1105
88. Cotton F.A., Duraj S.A., Powell G.L., and Roth W.J. Inorg. Chim. Acta 113 (1986) 81
89. Clark R.J.H., and Errington W. Inorg. Chem. 5 (1966) 650
90. Borden R.S., Loeffler P.A., and Dyer D.S. Inorg. Chem. 11 (1972) 2481