A [4+2] mixed ligand approach to ruthenium DNA metallointercalators [Ru(tpa)(N-N)](PF6)2 using a tris(2-pyridylmethyl)amine (tpa) capping ligand

Journal of Inorganic Biochemistry

Volumn 103, Issue 8, 2009, Pages 1126-1134

  Kraft, Sabine Seeberg née ^a   Bischof, Caroline ^b   Loos, Annette ^a   Braun, Sebastian ^b   Jafarova, Nigar ^a,b   Schatzschneider, Ulrich ^a,b  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b RUHR UNIVERSITY BOCHUM   (Germany)

Author keywords

Bioinorganic chemistry; Density functional calculations; DNA intercalation; N ligands; Ruthenium

Indexed keywords

[TRIS(2,2' BIPYRIDINE)RUTHENIUM] 1,10 PHENANTHROLINE; [TRIS(2,2' BIPYRIDINE)RUTHENIUM] 4,5,9,16 TETRAAZADIBENZO[A,C]NAPHTHACENE; [TRIS(2,2' BIPYRIDINE)RUTHENIUM]DIPYRIDO[3,2 A:2',3' F]PHENAZINE; [TRIS(2,2' BIPYRIDINE)RUTHENIUM]DIPYRIDO[3,2 D:2',3' F]QUINOXALINE; [TRIS(2,2' BIPYRIDINE)RUTHENIUM]HEXAFLUOROPHOSPHATE; DNA; LIGAND; RUTHENIUM COMPLEX; TRIS(2 PYRIDYLMETHYL)AMINE; UNCLASSIFIED DRUG;

ARTICLE; CALCULATION; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; CYCLIC POTENTIOMETRY; DNA BINDING; ENERGY; FLUORESCENCE SPECTROSCOPY; HYDRODYNAMICS; INTERCALATION COMPLEX; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS; ULTRAVIOLET SPECTROSCOPY; VISCOMETRY;

CIRCULAR DICHROISM; DNA; ELECTROCHEMICAL TECHNIQUES; ETHIDIUM; LIGANDS; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; ORGANOMETALLIC COMPOUNDS; PYRIDINES; RUTHENIUM COMPOUNDS; SPECTROPHOTOMETRY; VISCOSITY;

EID: 67651100629     PISSN: 01620134     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jinorgbio.2009.05.013     Document Type: Article

References (55)

1. Erkkila K.E., Odom D.T., and Barton J.K. Chem. Rev. 99 (1999) 2777-2795
2. Metcalfe C., and Thomas J.A. Chem. Soc. Rev. 32 (2003) 215-224
3. Zeglis B.M., Pierre V.C., and Barton J.K. Chem. Commun. (2007) 4565-4579
4. Holmlin R.E., Dandliker P.J., and Barton J.K. Angew. Chem. Int. Ed. 36 (1997) 2714-2730
5. Holmlin R.E., Dandliker P.J., and Barton J.K. Angew. Chem. 109 (1997) 2830-2848
6. Nunez M.E., and Barton J.K. Curr. Opin. Chem. Biol. 4 (2000) 199-206
7. Treadway C.R., Hill M.G., and Barton J.K. Chem. Phys. 281 (2002) 409-428
8. Delaney S., and Barton J.K. J. Org. Chem. 68 (2003) 6475.-6483
9. P. Lincoln, B. Norden, Int. Pat., WO 99/15535 (1999).
10. Liu J., Zou X.-H., Zhang Q.-L., Mei W.-J., Liu J.-Z., and Ji L.-N. Met.-Based Drugs 7 (2000) 343-348
11. Ma D.-L., Che C.-M., Siu F.-M., Yang M., and Wong K.-Y. Inorg. Chem. 46 (2007) 740-749
12. Pascu G.I., Hotze A.C.G., Sanchez-Cano C., Kariuki B.M., and Hannon M.J. Angew. Chem. Int. Ed. 46 (2007) 4374-4378
13. Pascu G.I., Hotze A.C.G., Sanchez-Cano C., Kariuki B.M., and Hannon M.J. Angew. Chem. 119 (2007) 4452-4456
14. Puckett C.A., and Barton J.K. J. Am. Chem. Soc. 129 (2007) 46-47
15. Schatzschneider U., Niesel J., Ott I., Gust R., Alborzinia H., and Wölfl S. Chem. MedChem. 3 (2008) 1104-1109
16. Strouse G.F., Anderson P.A., Schoonover J.R., Meyer T.J., and Keene F.R. Inorg. Chem. 31 (1992) 3004-3006
17. Anderson P.A., Deacon G.B., Haarmann K.H., Keene F.R., Meyer T.J., Reitsma D.A., Skelton B.W., Strouse G.F., Thomas N.C., Treadway J.A., and White A.H. Inorg. Chem. 34 (1995) 6145-6157
18. Treadway J.A., and Meyer T.J. Inorg. Chem. 38 (1999) 2267-2278
19. Freedman D.A., Evju J.K., Omije M.K., and Mann K.R. Inorg. Chem. 40 (2001) 5711-5715
20. Spiccia L., Deacon G.B., and Kepert C.M. Coord. Chem. Rev. 248 (2004) 1329-1341
21. Maxwell K.A., Sykora M., DeSimone J.M., and Meyer T.J. Inorg. Chem. 39 (2000) 71-75
22. Aldrich-Wright J.R., Fenton R.F., Greguric I.D., Hambley T.W., and Williams P.A. Dalton Trans. (2002) 4666-4671
23. Rajendiran V., Murali M., Suresh E., Sinha S., Somasundaram K., and Palaniandavar M. Dalton Trans. (2008) 148-163
24. Blackman A.G. Polyhedron 24 (2005) 1-39
25. Blackman A.G. Eur. J. Inorg. Chem. (2008) 2633-2647
26. Bjernemose J., Hazell A., McKenzie C.J., Mahon M.F., Nielsen L.P., Raithby P.R., Simonsen O., Toftlund H., and Wolny J.A. Polyhedron 22 (2003) 875-885
27. Kojima T., Morimoto T., Sakamoto T., Miyazaki S., and Fukuzumi S. Chem. Eur. J. 14 (2008) 8904-8915
28. Kojima T., Sakamoto T., and Matsuda Y. Inorg. Chem. 43 (2004) 2243-2245
29. Friedman A.E., Chambron J.-C., Sauvage J.-P., Turro N.J., and Barton J.K. J. Am. Chem. Soc. 112 (1990) 4960-4962
30. Fees J., Ketterle M., Klein A., Fiedler J., and Kaim W. Dalton Trans. (1999) 2595-2599
31. Foxon S.P., Metcalfe C., Adams H., Webb M., and Thomas J.A. Inorg. Chem. 46 (2007) 409-416
32. Nickita N., Belousoff M.J., Bhatt A.I., Bond A.M., Deacon G.B., Gasser G., and Spiccia L. Inorg. Chem. 46 (2007) 8638-8651
33. Batista E.R., and Martin R.L. J. Phys. Chem. A 109 (2005) 3128-3133
34. Li J., Chen J.-C., Xu L.-C., Zheng K.-C., and Ji L.-N. J. Organomet. Chem. 692 (2007) 831-838
35. Schmechel D.E.V., and Crothers D.M. Biopolymers 10 (1971) 463-480
36. Wolfe A., Shimer G.H., and Meehan T. Biochemistry 26 (1987) 6392-6396
37. Metcalfe C., Rajput C., and Thomas J.A. J. Inorg. Biochem. 100 (2006) 1314-1319
38. Liu J.-G., Zhang Q.-L., Shi X.-F., and Ji L.-N. Inorg. Chem. 40 (2001) 5045-5050
39. Frodl A., Herebian D., and Sheldrick W.S. Dalton Trans. (2002) 3664-3673
40. Fasman G. Circular Dichroism and Conformational Analysis of Biomolecules (1996), Plenum Press, New York
41. Rajendiran V., Murali M., Suresh E., Palaniandavar M., Periasamy V.S., and Akbarsha M.A. Dalton Trans. (2008) 2157-2170
42. Suh D., Oh Y.-K., and Chaires J.B. Process Biochem. 37 (2001) 521-525
43. Chouai A., Wicke S.E., Turro C., Bacsa J., Dunbar K.R., Wang D., and Thummel R.P. Inorg. Chem. 44 (2005) 5996-6003
44. Gottlieb H.E., Kotlyar V., and Nudelman A. J. Org. Chem. 62 (1997) 7512-7515
45. Canary J.W., Wang Y., and Roy R. Inorg. Synth. 32 (1998) 71-72
46. van der Tol E.B., van Ramesdonk H.J., Verhoeven J.W., Steemers F.J., Kerver E.G., Verboom W., and Reinhoudt D.N. Chem. Eur. J. 4 (1998) 2315-2323
47. Yamada M., Tanaka Y., Yoshimoto Y., Kuroda S., and Shimao I. Bull. Chem. Soc. Jpn. 65 (1992) 1006-1011
48. Yam V.W.W., Lo K.K.-W., Cheung K.-K., and Kong R.Y.-C. Chem. Commun. (1995) 1191-1193
49. Evans I.P., Spencer A., and Wilkinson G. Dalton Trans. (1973) 204-209
50. Holmlin R.E., Yao J.A., and Barton J.K. Inorg. Chem. 38 (1999) 174-189
51. Morgan J.L., Buck D.P., Turley A.G., Collins J.G., and Keene F.R. J. Biol. Inorg. Chem. 11 (2006) 824-834
52. Schaftenaar G., and Noordik J.H. J. Comput.-Aid. Mol. Des. 14 (2000) 123-134
53. F. Neese, ORCA Version 2.6.35.
54. Schäfer A., Horn H., and Ahlrichs R. J. Chem. Phys. 97 (1992) 2571-2577
55. The Ahlrichs DZ basis set was obtained from the TurboMole basis set library under .