Self-Assembly of 1-D Chains of Different Topologies Using the Hydrogen-Bonded Inorganic Supramolecular Synthons N-H⋯Cl3M or N-H⋯Cl3M

Inorganic Chemistry

Volumn 37, Issue 19, 1998, Pages 4756-4757

  Mareque Rivas, Juan C ^a   Brammer, Lee ^a  

^a UNIVERSITY OF MISSOURI ST LOUIS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000682124     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic9805269     Document Type: Article

References (26)

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3. For an emphasis on crystal engineering using hydrogen bonds, see: (a) Aakeröy, C. B. ACM Crystallogr. 1997, B53, 569. (b) Subramanian, S.; Zawarotko, M. J. Coord. Chem. Rev. 1994, 137, 357.
4. Desiraju, G. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2311.
5. For example, see: (a) Eller, M. C.; Adsmond, D. A. J. Chem. Soc. Chem. Commun. 1990, 589. (b) Lehn, J.-M.; Mascal, M.; DeCian A.; Fischer, J. J. Chem. Soc., Chem. Commun. 1990, 479. (c) Zerkowski, J. A.; MacDonald J. C.; Whiiesides, G. M. Chem. Mater. 1994, 6, 1250. (d) Aakeröy, C. B.; Hughes, D. P.; Nieuwenhuyzen, M. J. Am. Chem. Soc. 1996, 118, 10983.
6. For example, see: (a) Eller, M. C.; Adsmond, D. A. J. Chem. Soc. Chem. Commun. 1990, 589. (b) Lehn, J.-M.; Mascal, M.; DeCian A.; Fischer, J. J. Chem. Soc., Chem. Commun. 1990, 479. (c) Zerkowski, J. A.; MacDonald J. C.; Whiiesides, G. M. Chem. Mater. 1994, 6, 1250. (d) Aakeröy, C. B.; Hughes, D. P.; Nieuwenhuyzen, M. J. Am. Chem. Soc. 1996, 118, 10983.
7. For example, see: (a) Eller, M. C.; Adsmond, D. A. J. Chem. Soc. Chem. Commun. 1990, 589. (b) Lehn, J.-M.; Mascal, M.; DeCian A.; Fischer, J. J. Chem. Soc., Chem. Commun. 1990, 479. (c) Zerkowski, J. A.; MacDonald J. C.; Whiiesides, G. M. Chem. Mater. 1994, 6, 1250. (d) Aakeröy, C. B.; Hughes, D. P.; Nieuwenhuyzen, M. J. Am. Chem. Soc. 1996, 118, 10983.
8. For example, see: (a) Eller, M. C.; Adsmond, D. A. J. Chem. Soc. Chem. Commun. 1990, 589. (b) Lehn, J.-M.; Mascal, M.; DeCian A.; Fischer, J. J. Chem. Soc., Chem. Commun. 1990, 479. (c) Zerkowski, J. A.; MacDonald J. C.; Whiiesides, G. M. Chem. Mater. 1994, 6, 1250. (d) Aakeröy, C. B.; Hughes, D. P.; Nieuwenhuyzen, M. J. Am. Chem. Soc. 1996, 118, 10983.
9. For example, see: (a) Burrows, A. D.; Chan, C-W.; Chowdry, M. M.; McGrudy, J. E.; Mingos, D. M. P. Chem. Soc. Rev. 1995, 24, 329. (b) Copp, S. B.; Subramanian, S.; Zawarotko, M. J. J. Chem. Soc., Chem. Commun. 1993, 1078. Braga, D.; Grepioni, F.; Byrne, J. J.; Wolf, A. J. Chem. Soc., Chem. Commun. 1995, 1023.
10. For example, see: (a) Burrows, A. D.; Chan, C-W.; Chowdry, M. M.; McGrudy, J. E.; Mingos, D. M. P. Chem. Soc. Rev. 1995, 24, 329. (b) Copp, S. B.; Subramanian, S.; Zawarotko, M. J. J. Chem. Soc., Chem. Commun. 1993, 1078. Braga, D.; Grepioni, F.; Byrne, J. J.; Wolf, A. J. Chem. Soc., Chem. Commun. 1995, 1023.
11. For example, see: (a) Burrows, A. D.; Chan, C-W.; Chowdry, M. M.; McGrudy, J. E.; Mingos, D. M. P. Chem. Soc. Rev. 1995, 24, 329. (b) Copp, S. B.; Subramanian, S.; Zawarotko, M. J. J. Chem. Soc., Chem. Commun. 1993, 1078. Braga, D.; Grepioni, F.; Byrne, J. J.; Wolf, A. J. Chem. Soc., Chem. Commun. 1995, 1023.
12. Braga, D.; Grepioni, F.; Desiraju. G. R. J. Organomet. Chem. 1997, 548, 33.
13. The terms donor arid acceptor- are used in the sense of hydrogen bond donor and hydrogen bond acceptor throughout the paper.
14. (a) Aullón, G.; Bellamy, D.; Brammer, L.; Bruton, E. A.; Orpen, A. G. Chem. Commun. 1998, 653.
15. (a) Davies, P. J.; Veldman, N.; Grove, D. M.; Spek, A. L.; Lutz, B. T. G.; van Koten. G. Angew. Chem., Int. Ed. Engl. 1996, 35, 1959.
16. (b) Yap, G. A. P.; Rheingold, A. L.; Das, P.; Crabtree, R. H. Inorg. Chem. 1995, 34, 3474.
17. (c) Dadon, H.; Bernstein. J. Inorg. Chem. 1997, 36, 2898.
18. (d) Allen, F. H.; Kennard, O. Chem. Design Automation News 1993, 8, 1, 31-37.
19. 2- with loss of HCl. This conversion can be accelerated by heating the suspension of 2, to remove HCl from solution. Yellow crystals of 3, with crystalline 2 as ;i minor product. were obtained by evaporation of water from such a heated (80 °C) solution, Elemental analyses concur with expected values.
20. 2). Distances and angles involving hydrogen atoms are calculated assuming N-H and C-H bond lengths normalized to neutron values of 1.01 and 1.08 A. respectively.
21. 4 plane.
22. 9d search (April 1998 version) identified 41 C-H⋯Pt contacts with H⋯Pt ≤ 2.8 Å and C-H⋯Pt ≥ 120⋯. For discussion of C-H⋯ Pt hydrogen bonds see refs 13b-d. (b) Brammer, L.; Charnock, J. M.; Goggin, P. L.; Goodteliow, R. J.; Koetzle, T. F.; Orpen, A. G. J. Chem. Soc., Dalton Trans. 1991, 1789. (c) Gao, Y.; Eisenstein O.; Crabtree, R. H. Inorg. Chim. Acta 1997, 254, 105. (d) Braga, D.; Grepioni, F.; Tedesco, E.; Biradha K.; Desiraju, G. R. Organometallics 1997, 16, 1846.
23. 9d search (April 1998 version) identified 41 C-H⋯Pt contacts with H⋯Pt ≤ 2.8 Å and C-H⋯Pt ≥ 120⋯. For discussion of C-H⋯ Pt hydrogen bonds see refs 13b-d. (b) Brammer, L.; Charnock, J. M.; Goggin, P. L.; Goodteliow, R. J.; Koetzle, T. F.; Orpen, A. G. J. Chem. Soc., Dalton Trans. 1991, 1789. (c) Gao, Y.; Eisenstein O.; Crabtree, R. H. Inorg. Chim. Acta 1997, 254, 105. (d) Braga, D.; Grepioni, F.; Tedesco, E.; Biradha K.; Desiraju, G. R. Organometallics 1997, 16, 1846.
24. 9d search (April 1998 version) identified 41 C-H⋯Pt contacts with H⋯Pt ≤ 2.8 Å and C-H⋯Pt ≥ 120⋯. For discussion of C-H⋯ Pt hydrogen bonds see refs 13b-d. (b) Brammer, L.; Charnock, J. M.; Goggin, P. L.; Goodteliow, R. J.; Koetzle, T. F.; Orpen, A. G. J. Chem. Soc., Dalton Trans. 1991, 1789. (c) Gao, Y.; Eisenstein O.; Crabtree, R. H. Inorg. Chim. Acta 1997, 254, 105. (d) Braga, D.; Grepioni, F.; Tedesco, E.; Biradha K.; Desiraju, G. R. Organometallics 1997, 16, 1846.
25. 14b
26. (b) Kazarian, S. G.; Hamley, P. A.; Poliakoff, M. J. Am. Chem. Soc. 1993, 115, 9069.