Luminescent mesoporous molecular materials based on neutral tetrametallic rectangles

Angewandte Chemie - International Edition

Volumn 39, Issue 16, 2000, Pages 2891-2893

  Benkstein, Kurt D ^a   Hupp, Joseph T ^a   Stern, Charlotte L ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

Author keywords

Host guest chemistry; Luminescence; Mesoporosity; Metallacycles; Sensors

Indexed keywords

GLYCOLIPID; MACROCYCLIC COMPOUND; METAL; VOLATILE ORGANIC COMPOUND;

ARTICLE; BINDING AFFINITY; FILM; LUMINESCENCE; MASS SPECTROMETRY; MOLECULE; POROSITY; PROTON NUCLEAR MAGNETIC RESONANCE; SENSOR; SOLID STATE; STOICHIOMETRY; X RAY DIFFRACTION;

EID: 0034682924     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3773(20000818)39:16<2891::AID-ANIE2891>3.0.CO;2-Q     Document Type: Article

References (22)

1. M. Fujita, K. Ogura, Bull. Chem. Soc. Jpn. 1996, 69, 1471, and references therein.
2. P. J. Stang, B. Olenyuk, Acc. Chem. Res. 1997, 30, 502, and references therein.
3. W.-H. Leung, J. Y. K. Cheng, T. S. M. Hun, C-M. Che, W.-T. Wong, K.-K. Cheung, Organometallics 1996, 15, 1497.
4. H. A. Cruse, N. E. Leadbeater, Inorg. Chem. 1999, 38, 4149.
5. S.-S. Sun, A. J. Lees, Inorg. Chem. 1999, 38, 4181.
6. S. M. Woessner, J. B. Helms, J. F. Houlis, B. P. Sullivan, Inorg. Chem. 1999, 38, 4380.
7. R. V. Slone, K. D. Benkstein, S. Bélanger, J. T. Hupp, I. A. Guzei, A. L. Rheingold, Coord. Chem. Rev. 1998, 171, 221, and references therein.
8. R. V. Slone, D. I. Yoon, R. M. Calhoun, J. T. Hupp, J. Am. Chem. Soc. 1995, 117, 11 813.
9. For the experimental setup, see: M. H. Keefe, R. V. Slone, J. T. Hupp, K. F. Czaplewski, R. Q. Snurr, Langmuir 2000, in press.
10. a) K. D. Benkstein, J. T. Hupp, C. L. Stern, Inorg. Chem. 1998, 37, 5404;
11. b) K. D. Benkstein, J. T. Hupp, C. L. Stern, J. Am. Chem. Soc. 1998, 120, 12 982.
12. See also: S. M. Woessner, J. B. Helms, Y. Shen, B. P. Sullivan, Inorg. Chem. 1998, 37, 5406.
13. Charged, fluxionally rectangular organic cyclophanes are known, see: B. Odell, M. V. Reddington, A. M. Z. Slawin, N. Spencer, J. F. Stoddart, D. J. Williams, Angew. Chem. 1988, 100, 1605; Angew. Chem. Int. Ed. Engl. 1988, 27, 1547.
14. Charged, fluxionally rectangular organic cyclophanes are known, see: B. Odell, M. V. Reddington, A. M. Z. Slawin, N. Spencer, J. F. Stoddart, D. J. Williams, Angew. Chem. 1988, 100, 1605; Angew. Chem. Int. Ed. Engl. 1988, 27, 1547.
15. w |F| = 0.090.
16. G. Z. Sauerbrey, Physica 1959, 155, 206.
17. R. Uson, J. Gimeno, J. Organomet. Chem. 1981, 220, 173.
18. M. C. Rezende, C. A. Marques, E. L. Dall'Oglio, C Zucco, Liebigs Ann. 1997, 925.
19. M. P. Gamasa, E. Garcia, J. Gimeno, C. J. Ballesteros, Organomet. Chem. 1986, 307, 39.
20. 1. LR-MS: 1b · 2CO: calcd: m/z = 772.7; found: 773.0. Elemental analysis: calcd: C 31.88, H 0.92, N 6.76; found: C 31.66, H 0.97, N 6.50.
21. -/0), -2.42 V (multielectron wave).
22. /0), -2.28 V, -2.43 V.