Metal cation induced modulation of the photophysical properties of a platinum(II) complex featuring a dipicolylanilino-acetylide ligand

European Journal of Inorganic Chemistry

Volumn , Issue 8, 2011, Pages 1255-1259

  Lanoë, Pierre Henri ^a   Fillaut, Jean Luc ^a   Guerchais, Véronique ^a   Le Bozec, Hubert ^a   Williams, J A Gareth ^b  

^a UNIVERSITÉ DE RENNES 1   (France)

^b DURHAM UNIVERSITY   (United Kingdom)

Author keywords

Alkyne ligands; Cations; Luminescence; Platinum

Indexed keywords

CHELATION; EXCITED STATES; GROUND STATE; LIGANDS; METAL IONS; PLATINUM COMPOUNDS; POSITIVE IONS;

ABSORPTION STATE; ACETYLIDE LIGANDS; ALKYNE LIGANDS; COMPLEX 1; DIVALENT METAL ION; EXCITED-STATES; GROUND STATE ABSORPTION; METAL CATION; PHOTOPHYSICAL PROPERTIES; ZN 2+;

LUMINESCENCE;

EID: 79952122951     PISSN: 14341948     EISSN: 10990682     Source Type: Journal    
DOI: 10.1002/ejic.201001164     Document Type: Article

References (44)

1. A. F. Rausch, H. H. H. Homeier, H. Yersin in Photophysics of Organometallics, Springer, Berlin, 2010, vol. 29, pp. 193-235.
2. J. A. G. Williams, Top. Curr. Chem. 2007, 281, 205-268.
3. J. A. G. Williams, S. Develay, D. L. Rochester, L. Murphy, Coord. Chem. Rev. 2008, 252, 2596-2611.
4. R. C. Evans, P. Douglas, C. J. Winscom, Coord. Chem. Rev. 2006, 250, 2093-2126.
5. M. Hissler, J. E. McGarrah, W. B. Connick, D. K. Geiger, S. D. Cummings, R. Eisenberg, Coord. Chem. Rev. 2000, 208, 115-137.
6. C.-M. Che, J.-L. Zhang, L.-R. Lin, Chem. Commun. 2002, 2556-2557.
7. N. C. Fletcher, M. C. Lagunas, Top. Organomet. Chem. 2010, 28, 143-170.
8. R. McGuire Jr., M. H. Wilson, J. J. Nash, P. E. Fanwick, D. R. McMillin, Inorg. Chem. 2008, 47, 2946-2948.
9. K. M. C. Wong, V. W. W. Yam, Coord. Chem. Rev. 2007, 251, 2477-2488.
10. Q. A. Zhao, F. Y. Li, C. H. Huang, Chem. Soc. Rev. 2010, 39, 3007-3030.
11. K.-H. Wong, M. C.-W. Chan, C.-M. Che, Chem. Eur. J. 1999, 5, 2845-2849.
12. F. N. Castellano, I. E. Pomestchenko, E. Shikhova, F. Hua, M. L. Muro, N. Rajapakse, Coord. Chem. Rev. 2006, 250, 1819-1828.
13. W. Lu, B.-X. Mi, M. C. W. Chan, Z. Hui, C.-M. Che, N. Zhu, S.-T. Lee, J. Am. Chem. Soc. 2004, 126, 4958-4971.
14. W. Lu, B.-X. Mi, M. C. W. Chan, Z. Hui, N. Zhu, S.-T. Lee, C.-M. Che, Chem. Commun. 2002, 206-207.
15. G. S. M. Tong, Y. C. Law, S. C. F. Kui, N. Y. Zhu, K. H. Leung, D. L. Phillips, C. M. Che, Chem. Eur. J. 2010, 16, 6540-6554.
16. T. J. Wadas, R. J. Lachicotte, R. Eisenberg, Inorg. Chem. 2003, 42, 3772-3778.
17. R. Ziessel, J. B. Seneclauze, B. Ventura, A. Barbieri, F. Barigelletti, Dalton Trans. 2008, 1686-1688.
18. M. L. Clark, S. Diring, P. Retailleau, D. R. McMillin, R. Ziessel, Chem. Eur. J. 2008, 14, 7168-7179.
19. J. Schneider, P. Du, P. Jarosz, T. Lazarides, X. Wang, W. W. Brennessel, R. Eisenberg, Inorg. Chem. 2009, 48, 4306-4316.
20. H. S. Lo, S. K. Yip, K. M. C. Wong, N. Zhu, V. W.-W. Yam, Organometallics 2006, 25, 3537-3540.
21. P. K. M. Siu, S.-W. Lai, W. Lu, N. Zhu, C.-M. Che, Eur. J. Inorg. Chem. 2003, 2749-2752.
22. V. W.-W. Yam, K. M.-C. Wong, N. Zhu, J. Am. Chem. Soc. 2002, 124, 6506-6507.
23. Q. Z. Yang, L. Z. Wu, H. Zhang, B. Chen, Z. X. Wu, L. P. Zhang, C. H. Tung, Inorg. Chem. 2004, 43, 5195-5197.
24. Y. Fan, Y.-M. Zhu, F.-R. Dai, L.-Y. Zhang, Z.-N. Chen, Dalton Trans. 2007, 3885-3892.
25. K. M.-C. Wong, W.-S. Tang, X.-X. Lu, N. Zhu, V. W.-W. Yam, Inorg. Chem. 2005, 44, 1492-1498.
26. K. Huang, H. Yang, Z. Zhou, H. Chen, F. Li, T. Yi, C. Huang, Inorg. Chim. Acta 2009, 362, 2577-2580.
27. Q. Z. Yang, Q. X. Tong, L. Z. Wu, Z. X. Wu, L. P. Zhang, C. H. Tung, Eur. J. Inorg. Chem. 2004, 1948-1954.
28. P.-H. Lanoë, J.-L. Fillaut, L. Toupet, J. A. G. Williams, H. Le Bozec, V. Guerchais, Chem. Commun. 2008, 4333-4335.
29. P.-H. Lanoë, H. Le Bozec, J. A. G. Williams, J.-L. Fillaut, V. Guerchais, Dalton Trans. 2010, 39, 707-710.
30. X. Huang, Z. Guo, W. Zhu, Y. Xie, H. Tian, Chem. Commun. 2008, 5143-5145.
31. X. Peng, J. Du, J. Fan, J. Wang, W. Y. J. Zhao, S. Sun, T. Xu, J. Am. Chem. Soc. 2007, 129, 1500-1501.
32. T. Sakamoto, A. Ojida, I. Hamachi, Chem. Commun. 2009, 141-152.
33. S. Takebayashi, S. Shinkai, M. Ikeda, M. Takeuchi, Org. Biomol. Chem. 2008, 6, 493-499.
34. L. Zhang, R. J. Clark, L. Zhu, Chem. Eur. J. 2008, 14, 2894-2903.
35. N. C. Lim, C. Bruckner, Chem. Commun. 2004, 1094-1095.
36. H.-H. Wang, L. Xue, Z.-J. Fang, G.-P. Li, H. Jiang, New J. Chem. 2010, 34, 1239-1242.
37. M.-W. Louie, H.-W. Liu, M. H.-C. Lam, T.-C. Lau, K. K.-W. Lo, Organometallics 2009, 28, 4297-4307.
38. N. Zhao, Y.-H. Wu, H.-M. Wen, X. Zhang, Z.-N. Chen, Organometallics 2009, 28, 5603-5611.
39. J. C. Araya, J. Gajardo, S. A. Moya, P. Aguirre, L. Toupet, J. A. G. Williams, M. Escadeillas, H. Le Bozec, V. Guerchais, New J. Chem. 2010, 34, 21-24.
40. 2+, which involves the lone pair and thus inhibits the PET process.
41. W.-S. Tang, X.-X. Lu, K. M.-C. Wong, V. W.-W. Yam, J. Mater. Chem. 2005, 15, 2714-2720.
42. D. B. MacQueen, K. S. Schanze, J. Am. Chem. Soc. 1991, 113, 6108-6110.
43. L. Murphy, A. Congreve, L.-O. Palsson, J. A. G. Williams, Chem. Commun. 2010, 46, 8743.
44. R. A. Binstead, SPECFIT, Spectrum Software Associates, Chapell Hill, NC, 1996.