Role of charge transfer interaction and the chemical physics behind effective fulleropyrrolidine/porphyrin non-covalent interaction in solution

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy

Volumn 121, Issue , 2014, Pages 559-568

  Mondal, Ashis ^a   Santhosh, Kotni ^b   Bauri, Ajoy ^c   Bhattacharya, S ^a  

^a UNIVERSITY OF BURDWAN   (India)

^b UNIVERSITY OF HYDERABAD   (India)

^c BHABHA ATOMIC RESEARCH CENTRE   (India)

Author keywords

DFT and hybrid DFT calculations; Monoporphyrin; Transient absorption study; UV Vis, steady state and time resolved fluorescence measurements

Indexed keywords

CHARGE TRANSFER; DENSITY FUNCTIONAL THEORY; TOLUENE;

CHARGE TRANSFER INTERACTION; GROUND-STATE INTERACTIONS; MONOPORPHYRIN; STEADY-STATE MEASUREMENTS; SUPRAMOLECULAR INTERACTIONS; TIME-RESOLVED FLUORESCENCE MEASUREMENTS; TRANSIENT ABSORPTION;

AROMATIC COMPOUNDS;

FULLERENE DERIVATIVE; METALLOPORPHYRIN; PORPHYRIN; PYRROLIDINE DERIVATIVE; SOLVENT;

ABSORPTION; ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; DFT AND HYBRID-DFT CALCULATIONS; ELECTRON; KINETICS; MONOPORPHYRIN; PHYSICAL CHEMISTRY; PYC(60); QUANTUM THEORY; SOLUTION AND SOLUBILITY; SPECTROFLUOROMETRY; STATIC ELECTRICITY; TIME; TITRIMETRY; TRANSIENT ABSORPTION STUDY; ULTRAVIOLET SPECTROPHOTOMETRY; UV-VIS, STEADY STATE AND TIME RESOLVED FLUORESCENCE MEASUREMENTS;

DFT AND HYBRID-DFT CALCULATIONS; MONOPORPHYRIN; PYC(60); TRANSIENT ABSORPTION STUDY; UV-VIS, STEADY STATE AND TIME RESOLVED FLUORESCENCE MEASUREMENTS;

ABSORPTION; ELECTRONS; FULLERENES; KINETICS; METALLOPORPHYRINS; MODELS, MOLECULAR; MOLECULAR CONFORMATION; PHYSICOCHEMICAL PHENOMENA; PORPHYRINS; PYRROLIDINES; QUANTUM THEORY; SOLUTIONS; SOLVENTS; SPECTROMETRY, FLUORESCENCE; SPECTROPHOTOMETRY, ULTRAVIOLET; STATIC ELECTRICITY; TIME FACTORS; TITRIMETRY;

EID: 84888247169     PISSN: 13861425     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.saa.2013.07.054     Document Type: Article

References (35)

1. K. Lee, H. Song, and J.T. Park Acc. Chem. Res. 36 2003 78 86
2. D. Kim, and A. Osuka Acc. Chem. Res. 37 2004 735 826
3. F. Diederich, and M. Gomez-Lopez Chem. Soc. Rev. 28 1999 263 277
4. D. Sun, F.S. Tham, C.A. Reed, and P.D.W. Boyd Proc. Natl. Acad. Sci. USA 99 2002 5088-592
5. P.D.W. Boyd, and C.A. Reed Acc. Chem. Res. 38 2005 235 242
6. D. Gust, T.A. Moore, and A.L. Moore Acc. Chem. Res. 34 2001 40 48
7. M.R. Wasielewski J. Org. Chem. 71 2006 5051 5066
8. D.M. Guldi Chem. Commun. 2000 321 327
9. F. D'Souza, G.M. Venukadasula, K. Yamanaka, N.K. Subbaiyan, M.E. Zandler, and O. Ito Org. Biomol. Chem. 7 2009 1076 1080
10. E.M. Perez, and N. Martin Pure Appl. Chem. 82 2010 523 533
11. M.E. El-Khouly, O. Ito, P.M. Smith, and F. D'Souza J. Photochem. Photobiol. C: Photochem. Rev. 5 2004 79 104
12. G. Bottari, O. Trukhina, M. Ince, and T. Torres Coord. Chem. Rev. 256 2012 2453 2477
13. M. Prato, and M. Maggini Acc. Chem. Res. 31 1998 519 526
14. J.L. Sessler, J. Jayawickramarajah, A. Gouloumis, G.D. Pantos, T. Torres, and D.M. Guldi Tetrahedron 62 2006 2123 2131
15. A. Ray, K. Santhosh, and S. Bhattacharya J. Phys. Chem. A 115 2011 9929 9940
16. A. Mishra, M.K.R. Fischer, and P. Buerle Angew. Chem. Int. Ed. 48 2009 2474 2499
17. K. Hara, T. Sato, R. Katoh, A. Furube, Y. Ohga, A. Shinpo, S. Suga, K. Sayama, H. Sugihara, and H. Arakawa J. Phys. Chem. B 107 2003 597 606
18. H. Imahori, N.V. Tkachenko, V. Vehmanen, K. Tamaki, H. Lemmetyinen, Y. Sakata, and S. Fukuzumi J. Phys. Chem. A 105 2001 1750 1756
19. V. Chukharev, N.V. Tkachenko, A. Efimov, D.M. Guldi, A. Hirsch, M. Scheloske, and H. Lemmetyinen J. Phys. Chem. B. 108 2004 16377 16385
20. V. Chukharev, N.V. Tkachenko, A. Efimov, and H. Lemmetyinen Chem. Phys. Lett. 411 2005 501 505
21. A.H. Al-Subi, M. Niemi, J. Ranta, N.V. Tkachenko, and H. Lemmetyinen Chem. Phys. Lett. 531 2012 164 168
22. H.A. Benesi, and J.H. Hildebrand J. Am. Chem. Soc. 71 1949 2703 2707
23. D.M. Guldi, I. Zilbermann, A. Gouloumis, P. Vazquez, and T. Torres J. Phys. Chem. B 108 2004 18485 18494
24. D.I. Schuster, K. Li, D.M. Guldi, A. Palkar, L. Echegoyen, C. Stanisky, R.J. Cross, M. Niemi, N.V. Tkachenko, and H. Lemmetyinen J. Am. Chem. Soc. 129 2007 15973 15982
25. D. Sun, F.S. Tham, C.A. Reed, L. Chaker, M. Burgess, and P.D.W. Boyd J Am. Chem. Soc. 122 2000 10704 10705
26. M. Dudic, P. Lothak, I. Stibor, H. Petrickova, and K. Lang New. J. Chem. 28 2004 85 90
27. Y. Kubo, A. Sugasaki, M.Ikeda K. Sugiyasu, K. Sonoda, A. Ikeda, M. Takeuchi, and S. Shinkai Org. Lett. 4 2002 925 928
28. J.Y. Zheng, K. Tashiro, Y. Hirabayashi, K. Kinbara, K. Saigo, T. Aida, S. Sakamoto, and K. Yamaguchi Angew. Chem. Int. Ed. 40 2001 1858 1861
29. M. Ayabe, A. Ikeda, S. Shinkai, S. Sakamoto, and K. Yamaguchi Chem. Commun. 2002 1032 1033
30. H. Imahori, and Y. Sakata Eur. J. Org. Chem. 1999 2445 2457
31. D. Balbinot, S. Atalick, D.M. Guldi, M. Hatzimarinaki, A. Hirsch, and N. Jux J. Phys. Chem. B 107 2003 13273 13279
32. R.A. Marcus Angew. Chem. Int. Ed. 32 1993 1111 1222
33. F. Hauke, A. Hirsch, S.G. Liu, L. Echegoyen, A. Swartz, C. Luo, and D.M. Guldi Chem. Phys. Chem. 3 2002 195 205
34. D.A. Williamson, and E.B. Bruce Inorg. Chim. Acta 297 2000 47 55
35. A. Rosspeintner, D.R. Kattnig, G. Angulo, S. Landgraf, and G. Grampp Chem. Eur. J. 14 2008 6213 6221