Photophysics of manisyl-substituted 2-pyridin-2-yl-1,10-phenanthrolines. Dual emission dependent on structure and solvent

Physical Chemistry Chemical Physics

Volumn 11, Issue 26, 2009, Pages 5408-5415

  Klosterman, Jeremy K ^a   Baldridge, Kim K ^a   Siegel, Jay S ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

PHENANTHROLINE DERIVATIVE; PYRIDINE DERIVATIVE; SOLVENT;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; COMPUTER SIMULATION; PHOTOCHEMISTRY; PHYSICS; SPECTROFLUOROMETRY;

COMPUTER SIMULATION; MODELS, MOLECULAR; MOLECULAR STRUCTURE; PHENANTHROLINES; PHOTOCHEMISTRY; PHYSICS; PYRIDINES; SOLVENTS; SPECTROMETRY, FLUORESCENCE;

EID: 70349255955     PISSN: 14639076     EISSN: None     Source Type: Journal    
DOI: 10.1039/b818533f     Document Type: Article

References (45)

1. C. Kaes A. Katz M. W. Hosseini Chem. Rev. 2000 100 3553 3590
2. P. G. Sammes G. Yahioglu Chem. Soc. Rev. 1994 23 327 334
3. A. M. W. C. Thompson Coord. Chem. Rev. 1997 160 1 52
4. G. A. Crosby Acc. Chem. Res. 1975 8 231 238
5. J. H. Alstrum-Acevedo M. K. Brennaman T. J. Meyer Inorg. Chem. 2005 44 6802 6827
6. D. Gust T. A. Moore A. L. Moore Acc. Chem. Res. 2001 34 40 48
7. T. J. Meyer Pure Appl. Chem. 1986 58 1193 1206
8. V. Balzani A. Juris M. Venturi S. Campagna S. Serroni Chem. Rev. 1996 96 759 833
9. A. Juris V. Balzani F. Barigelletti S. Campagna P. Belser A. Von Zelewsky Coord. Chem. Rev. 1988 84 85 277
10. F. Barigelletti L. Flamigni Chem. Soc. Rev. 2000 29 1 12
11. J. Jortner and M. Ratner, Molecular Electronics, Blackwell Science, London, 1997
12. J. C. Loren J. S. Siegel Angew. Chem., Int. Ed. 2001 40 754 757
13. J. K. Klosterman A. Linden J. S. Siegel Org. Biomol. Chem. 2008 6 2655 2764
14. H. S. Joshi R. Jamshidi Y. Tor Angew. Chem., Int. Ed. 1999 38 2721 2725
15. G. A. Crosby J. N. Demas J. Phys. Chem. 1971 75 991 1024
16. M. W. Schmidt K. K. Baldridge J. A. Boatz S. T. Elbert M. S. Gordon J. H. Jensen S. Koseki N. Matsunaga K. A. Nguyen S. Su T. L. Windus S. T. Elbert J. Comput. Chem. 1993 14 1347 1395
17. C. Lee W. Yang R. G. Parr Phys. Rev. 1988 B37 785 789
18. C. Møller M. S. Plesset Phys. Rev. 1934 46 618 622
19. T. H. Dunning and P. J. Hay, in Methods of Electronic Structure Theory, ed., H. F. Schaeffer, Plenum, New York, 1977, ch. 1, pp. 1-27
20. K. K. Baldridge J. P. Greenberg J. Mol. Graphics 1995 13 63 66
21. N. Armaroli L. De Cola V. Balzani J.-P. Sauvage C. O. Dietrich-Buchecker J.-M. Kern J. Chem. Soc., Faraday Trans. 1992 88 553 556
22. E. Birckner U.-W. Grummt A. H. Göller T. Pautzsch D. A. M. Egbe M. Al-Higari E. Klemm J. Phys. Chem. A 2001 105 10307 10315
23. G. M. Badger I. S. Walker J. Chem. Soc. 1956 122
24. The artifact at 450 nm results from the fluorimeter switching between monochromators
25. B. N. Bandyopadhyay A. Harriman J. Chem. Soc., Faraday Trans. 1 1977 73 663 674
26. M. S. Henry M. Z. Hoffman J. Phys. Chem. 1979 83 618 625
27. Z. R. Grabowksi K. Rotkiewicz W. Rettig Chem. Rev. 2003 103 3899 4031
28. N. J. Turro, Modern Molecular Photochemistry, University Science Books, Sausalito, 1991
29. J. R. Lakowicz, Principles of Fluorescence Spectroscopy, Springer, New York, 3rd edn, 2006
30. C. Reichardt, Solvents and Solvent Effects in Organic Chemistry, VCH, Weinheim, 2nd edn, 1990
31. C. Reichardt Chem. Rev. 1994 94 2319 2358
32. The assignment of the LE* emission to a singlet state is further supported by the insensitivity to molecular oxygen
33. U.-W. Grummt E. Birckner M. Al-Higari D. A. M. Egbe E. Klemm J. Fluoresc. 2001 11 41 51
34. J. G. Calvert and J. N. Pitts Jr., Photochemistry, John Wiley and Sons, Inc., New York, 1966
35. Pyridyl-phenanthroline 6 was specifically chosen as it exhibits dual emission in polar solvents
36. J. J. Moore J. J. Nash P. E. Fanwick D. R. McMillin Inorg. Chem. 2002 41 6387 6396
37. M. Maestri N. Armaroli V. Balzani E. C. Constable A. M. W. C. Thompson Inorg. Chem. 1995 34 2759 2767
38. A. Ceulemans L. G. Vanquickenborne J. Am. Chem. Soc. 1981 103 2238 2241
39. P. Day N. Sanders J. Chem. Soc. A 1967 1536 1541
40. S. Ernst C. Vogler A. Klein W. Kaim S. Zalis Inorg. Chem. 1996 35 1295 1300
41. J. C. Loren P. Gantzel A. Linden J. S. Siegel Org. Biomol. Chem. 2005 3 3105 3116
42. K. Arias, T. Barder, J. C. Loren, E. Zysman-Coleman, K. K. Baldridge and J. S. Siegel, in preparation
43. Z. R. Grabowksi K. Rotkiewicz A. Siemiarczuk D. J. Cowley W. Baumann Nouv. J. Chim. 1979 3 443 454
44. K. A. Al-Hassan T. Azumi W. Rettig Chem. Phys. Lett. 1993 206 25 29
45. E. Kosower Acc. Chem. Res. 1982 15 259 266