Chiral molecular tapes from novel tetra(thiafulvalene-crown-ether)- substituted phthalocyanine building blocks

Chemical Communications

Volumn , Issue 10, 2005, Pages 1255-1257

  Sly, Joseph ^a   Kasák, Peter ^a   Gomar Nadal, Elba ^b   Rovira, Concepció ^b   Górriz, Lucía ^a   Thordarson, Pall ^a   Amabilino, David B ^b   Rowan, Alan E ^a   Nolte, Roeland J M ^a  

^a RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

^b INSTITUT DE CIÈNCIA DE MATERIALS DE BARCELONA ICMAB CSIC   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CROWN ETHER DERIVATIVE; NANOPARTICLE; PHTHALOCYANINE; TETRATHIAFULVALENE CROWN ETHER; TETRATHIAFULVALENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CONDUCTOR; CYCLIC POTENTIOMETRY; DEPROTECTION REACTION; ELECTRONICS; MOLECULAR MODEL; TRANSMISSION ELECTRON MICROSCOPY; ULTRAVIOLET SPECTROSCOPY;

EID: 16244392465     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b416034g     Document Type: Article

References (16)

1. A. G. MacDiarmid, Angew. Chem. Int. Ed., 2001, 40, 2581.
2. Phthalocyanines, Properties and Applications, ed. C. C. Leznoff and A. B. P. Lever, VCH, New York, 1989-1993.
3. M. Hanack and M. Lang, Adv. Mater., 1994, 6, 819.
4. M. J. Cook, J. Mater. Chem, 1996, 6, 677.
5. M. R. Bryce, Adv. Mater., 1999, 11, 11.
6. J. L. Segura and N. Martin, Angew. Chem. Int. Ed., 2001, 40, 1372.
7. J. Becher, J. O. Jeppesen and K. Nielen, Synth. Met., 2003, 133-134, 309.
8. C. F. van Nostrum, S. J. Picken, A.-J. Schouten and R. J. M. Nolte, J. Am. Chem. Soc., 1995, 117, 9957.
9. C. F. Van Nostrum, Adv. Mater., 1996, 8, 1027.
10. H. Engelkamp, S. Middelbeek and R. J. M. Nolte, Science, 1999, 284, 785.
11. P. Samori, H. Engelkamp, P. de Witte, A. E. Rowan, R. J. M. Nolte and J. P. Rabe, Angew. Chem. Int. Ed., 2001, 40, 2348.
12. 3 at reflux for 3 h. See also: N. Svenstrup, K. M. Rasmussen, T. Kruse and J. Becher, Synthesis, 1994, 809; P. Wu, G. Saito, K. Imeda, Z. Shi, T. Mori, T. Enoki and H. Inokuchi, Chem. Lett., 1986, 441; K. B. Simonsen and J. Becher, Synlett, 1997, 1213.
13. 3 at reflux for 3 h. See also: N. Svenstrup, K. M. Rasmussen, T. Kruse and J. Becher, Synthesis, 1994, 809; P. Wu, G. Saito, K. Imeda, Z. Shi, T. Mori, T. Enoki and H. Inokuchi, Chem. Lett., 1986, 441; K. B. Simonsen and J. Becher, Synlett, 1997, 1213.
14. 3 at reflux for 3 h. See also: N. Svenstrup, K. M. Rasmussen, T. Kruse and J. Becher, Synthesis, 1994, 809; P. Wu, G. Saito, K. Imeda, Z. Shi, T. Mori, T. Enoki and H. Inokuchi, Chem. Lett., 1986, 441; K. B. Simonsen and J. Becher, Synlett, 1997, 1213.
15. C. Wang, M. R. Bryce, A. S. Batsanov, C. F. Stanely, A. Beeby and J. A. K. Howard, J. Chem. Soc., Perkin Trans. 2, 1997, 1671.
16. Molecular modeling was conducted using Spartan 04 for windows ('Wavefunctions Inc.' California, 2004) using the MMFF force field.