메뉴 건너뛰기




Volumn 122, Issue 18, 2000, Pages 4394-4402

Three-dimensional hexagonal structures from a novel self-complementary molecular building block

Author keywords

[No Author keywords available]

Indexed keywords

1,10 PHENANTHROLINE; NITRILOTRI(METHYLPHOSPHONIC ACID); PHOSPHONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0034630852     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9935512     Document Type: Article
Times cited : (125)

References (57)
  • 1
    • 0003943828 scopus 로고    scopus 로고
    • NATO ASI series; Kluwer: Dordecht, The Netherlands
    • For a very good overview of recent developments in crystal engineering see the following multiauthored volumes and review articles: (a) Crystal Engineering: From Molecules and Crystals To Materials; Braga, D., Orpen, A. G., Eds.; NATO ASI series; Kluwer: Dordecht, The Netherlands, 1999. (b) Weber, E., Ed. Design of Organic Solids; Topics in Current Chemistry; Springer-Verlag, Heidelberg, 1998; Vol. 198. (c) Comprehensive Supramolecular Chemistry: Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford, 1996; Vol. 6. (d) Desiraju, G. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2311-2327. (e) Aakeroy, C. B. Acta Crystallogr. 1997, B53, 569-583. (f) Braga, D.; Grepioni, F.; Desiraju, G. R. Chem. Rev. 1998, 98, 1375-1405. (g) Bernstein, J.; Davis, R. E.; Shimoni, L.; Chang, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 1555-1573. (h) MacDonald, J. C.; Whitesides, G. M. Chem. Rev. 1994, 94, 2383-2420. (i) Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. Engl. 1998, 37, 1460-1494. (j) Zaworotko, M. J. Coordination Polymers. In Crystal Engineering: The Design and Applications of Functional Solids; Seddon, K. R., Zaworotko, M. J., Eds.; NATO ASI series; Kluwer; Dordecht, The Netherlands, 1998. (k) Hagrman, P. J.; Hagrman, D.; Zubieta, J. Angew. Chem., Int. Ed. Engl. 1999, 38, 2639- 2684. (l) Alivisatos, A. P.; Barbara, P. F.; Castelman, A. W.; Chang, J.; Dixon, D. A.; Klein, M. L.; McLendon, G. L.; Miller, J. S.; Ratner, M. A.; Rossky, P. J.; Stupp, S. I.; Thompson, M. E. Adv. Mater. 1998, 10, 1297- 1336.
    • (1999) Crystal Engineering: From Molecules and Crystals to Materials
    • Braga, D.1    Orpen, A.G.2
  • 2
    • 0002285424 scopus 로고    scopus 로고
    • Design of Organic Solids
    • Springer-Verlag, Heidelberg
    • For a very good overview of recent developments in crystal engineering see the following multiauthored volumes and review articles: (a) Crystal Engineering: From Molecules and Crystals To Materials; Braga, D., Orpen, A. G., Eds.; NATO ASI series; Kluwer: Dordecht, The Netherlands, 1999. (b) Weber, E., Ed. Design of Organic Solids; Topics in Current Chemistry; Springer-Verlag, Heidelberg, 1998; Vol. 198. (c) Comprehensive Supramolecular Chemistry: Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford, 1996; Vol. 6. (d) Desiraju, G. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2311-2327. (e) Aakeroy, C. B. Acta Crystallogr. 1997, B53, 569-583. (f) Braga, D.; Grepioni, F.; Desiraju, G. R. Chem. Rev. 1998, 98, 1375-1405. (g) Bernstein, J.; Davis, R. E.; Shimoni, L.; Chang, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 1555-1573. (h) MacDonald, J. C.; Whitesides, G. M. Chem. Rev. 1994, 94, 2383-2420. (i) Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. Engl. 1998, 37, 1460-1494. (j) Zaworotko, M. J. Coordination Polymers. In Crystal Engineering: The Design and Applications of Functional Solids; Seddon, K. R., Zaworotko, M. J., Eds.; NATO ASI series; Kluwer; Dordecht, The Netherlands, 1998. (k) Hagrman, P. J.; Hagrman, D.; Zubieta, J. Angew. Chem., Int. Ed. Engl. 1999, 38, 2639- 2684. (l) Alivisatos, A. P.; Barbara, P. F.; Castelman, A. W.; Chang, J.; Dixon, D. A.; Klein, M. L.; McLendon, G. L.; Miller, J. S.; Ratner, M. A.; Rossky, P. J.; Stupp, S. I.; Thompson, M. E. Adv. Mater. 1998, 10, 1297- 1336.
    • (1998) Topics in Current Chemistry , vol.198
    • Weber, E.1
  • 3
    • 0003461218 scopus 로고    scopus 로고
    • Pergamon: Oxford
    • For a very good overview of recent developments in crystal engineering see the following multiauthored volumes and review articles: (a) Crystal Engineering: From Molecules and Crystals To Materials; Braga, D., Orpen, A. G., Eds.; NATO ASI series; Kluwer: Dordecht, The Netherlands, 1999. (b) Weber, E., Ed. Design of Organic Solids; Topics in Current Chemistry; Springer-Verlag, Heidelberg, 1998; Vol. 198. (c) Comprehensive Supramolecular Chemistry: Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford, 1996; Vol. 6. (d) Desiraju, G. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2311-2327. (e) Aakeroy, C. B. Acta Crystallogr. 1997, B53, 569-583. (f) Braga, D.; Grepioni, F.; Desiraju, G. R. Chem. Rev. 1998, 98, 1375-1405. (g) Bernstein, J.; Davis, R. E.; Shimoni, L.; Chang, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 1555-1573. (h) MacDonald, J. C.; Whitesides, G. M. Chem. Rev. 1994, 94, 2383-2420. (i) Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. Engl. 1998, 37, 1460-1494. (j) Zaworotko, M. J. Coordination Polymers. In Crystal Engineering: The Design and Applications of Functional Solids; Seddon, K. R., Zaworotko, M. J., Eds.; NATO ASI series; Kluwer; Dordecht, The Netherlands, 1998. (k) Hagrman, P. J.; Hagrman, D.; Zubieta, J. Angew. Chem., Int. Ed. Engl. 1999, 38, 2639- 2684. (l) Alivisatos, A. P.; Barbara, P. F.; Castelman, A. W.; Chang, J.; Dixon, D. A.; Klein, M. L.; McLendon, G. L.; Miller, J. S.; Ratner, M. A.; Rossky, P. J.; Stupp, S. I.; Thompson, M. E. Adv. Mater. 1998, 10, 1297- 1336.
    • (1996) Comprehensive Supramolecular Chemistry , vol.6
    • Atwood, J.L.1    Davies, J.E.D.2    MacNicol, D.D.3    Vogtle, F.4    Lehn, J.-M.5
  • 4
    • 33745394944 scopus 로고
    • For a very good overview of recent developments in crystal engineering see the following multiauthored volumes and review articles: (a) Crystal Engineering: From Molecules and Crystals To Materials; Braga, D., Orpen, A. G., Eds.; NATO ASI series; Kluwer: Dordecht, The Netherlands, 1999. (b) Weber, E., Ed. Design of Organic Solids; Topics in Current Chemistry; Springer-Verlag, Heidelberg, 1998; Vol. 198. (c) Comprehensive Supramolecular Chemistry: Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford, 1996; Vol. 6. (d) Desiraju, G. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2311-2327. (e) Aakeroy, C. B. Acta Crystallogr. 1997, B53, 569-583. (f) Braga, D.; Grepioni, F.; Desiraju, G. R. Chem. Rev. 1998, 98, 1375-1405. (g) Bernstein, J.; Davis, R. E.; Shimoni, L.; Chang, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 1555-1573. (h) MacDonald, J. C.; Whitesides, G. M. Chem. Rev. 1994, 94, 2383-2420. (i) Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. Engl. 1998, 37, 1460-1494. (j) Zaworotko, M. J. Coordination Polymers. In Crystal Engineering: The Design and Applications of Functional Solids; Seddon, K. R., Zaworotko, M. J., Eds.; NATO ASI series; Kluwer; Dordecht, The Netherlands, 1998. (k) Hagrman, P. J.; Hagrman, D.; Zubieta, J. Angew. Chem., Int. Ed. Engl. 1999, 38, 2639- 2684. (l) Alivisatos, A. P.; Barbara, P. F.; Castelman, A. W.; Chang, J.; Dixon, D. A.; Klein, M. L.; McLendon, G. L.; Miller, J. S.; Ratner, M. A.; Rossky, P. J.; Stupp, S. I.; Thompson, M. E. Adv. Mater. 1998, 10, 1297- 1336.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 2311-2327
    • Desiraju, G.R.1
  • 5
    • 0346613495 scopus 로고    scopus 로고
    • For a very good overview of recent developments in crystal engineering see the following multiauthored volumes and review articles: (a) Crystal Engineering: From Molecules and Crystals To Materials; Braga, D., Orpen, A. G., Eds.; NATO ASI series; Kluwer: Dordecht, The Netherlands, 1999. (b) Weber, E., Ed. Design of Organic Solids; Topics in Current Chemistry; Springer-Verlag, Heidelberg, 1998; Vol. 198. (c) Comprehensive Supramolecular Chemistry: Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford, 1996; Vol. 6. (d) Desiraju, G. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2311-2327. (e) Aakeroy, C. B. Acta Crystallogr. 1997, B53, 569-583. (f) Braga, D.; Grepioni, F.; Desiraju, G. R. Chem. Rev. 1998, 98, 1375-1405. (g) Bernstein, J.; Davis, R. E.; Shimoni, L.; Chang, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 1555-1573. (h) MacDonald, J. C.; Whitesides, G. M. Chem. Rev. 1994, 94, 2383-2420. (i) Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. Engl. 1998, 37, 1460-1494. (j) Zaworotko, M. J. Coordination Polymers. In Crystal Engineering: The Design and Applications of Functional Solids; Seddon, K. R., Zaworotko, M. J., Eds.; NATO ASI series; Kluwer; Dordecht, The Netherlands, 1998. (k) Hagrman, P. J.; Hagrman, D.; Zubieta, J. Angew. Chem., Int. Ed. Engl. 1999, 38, 2639- 2684. (l) Alivisatos, A. P.; Barbara, P. F.; Castelman, A. W.; Chang, J.; Dixon, D. A.; Klein, M. L.; McLendon, G. L.; Miller, J. S.; Ratner, M. A.; Rossky, P. J.; Stupp, S. I.; Thompson, M. E. Adv. Mater. 1998, 10, 1297- 1336.
    • (1997) Acta Crystallogr. , vol.B53 , pp. 569-583
    • Aakeroy, C.B.1
  • 6
    • 1542337460 scopus 로고    scopus 로고
    • For a very good overview of recent developments in crystal engineering see the following multiauthored volumes and review articles: (a) Crystal Engineering: From Molecules and Crystals To Materials; Braga, D., Orpen, A. G., Eds.; NATO ASI series; Kluwer: Dordecht, The Netherlands, 1999. (b) Weber, E., Ed. Design of Organic Solids; Topics in Current Chemistry; Springer-Verlag, Heidelberg, 1998; Vol. 198. (c) Comprehensive Supramolecular Chemistry: Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford, 1996; Vol. 6. (d) Desiraju, G. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2311-2327. (e) Aakeroy, C. B. Acta Crystallogr. 1997, B53, 569-583. (f) Braga, D.; Grepioni, F.; Desiraju, G. R. Chem. Rev. 1998, 98, 1375-1405. (g) Bernstein, J.; Davis, R. E.; Shimoni, L.; Chang, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 1555-1573. (h) MacDonald, J. C.; Whitesides, G. M. Chem. Rev. 1994, 94, 2383-2420. (i) Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. Engl. 1998, 37, 1460-1494. (j) Zaworotko, M. J. Coordination Polymers. In Crystal Engineering: The Design and Applications of Functional Solids; Seddon, K. R., Zaworotko, M. J., Eds.; NATO ASI series; Kluwer; Dordecht, The Netherlands, 1998. (k) Hagrman, P. J.; Hagrman, D.; Zubieta, J. Angew. Chem., Int. Ed. Engl. 1999, 38, 2639- 2684. (l) Alivisatos, A. P.; Barbara, P. F.; Castelman, A. W.; Chang, J.; Dixon, D. A.; Klein, M. L.; McLendon, G. L.; Miller, J. S.; Ratner, M. A.; Rossky, P. J.; Stupp, S. I.; Thompson, M. E. Adv. Mater. 1998, 10, 1297- 1336.
    • (1998) Chem. Rev. , vol.98 , pp. 1375-1405
    • Braga, D.1    Grepioni, F.2    Desiraju, G.R.3
  • 7
    • 33748502022 scopus 로고
    • For a very good overview of recent developments in crystal engineering see the following multiauthored volumes and review articles: (a) Crystal Engineering: From Molecules and Crystals To Materials; Braga, D., Orpen, A. G., Eds.; NATO ASI series; Kluwer: Dordecht, The Netherlands, 1999. (b) Weber, E., Ed. Design of Organic Solids; Topics in Current Chemistry; Springer-Verlag, Heidelberg, 1998; Vol. 198. (c) Comprehensive Supramolecular Chemistry: Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford, 1996; Vol. 6. (d) Desiraju, G. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2311-2327. (e) Aakeroy, C. B. Acta Crystallogr. 1997, B53, 569-583. (f) Braga, D.; Grepioni, F.; Desiraju, G. R. Chem. Rev. 1998, 98, 1375-1405. (g) Bernstein, J.; Davis, R. E.; Shimoni, L.; Chang, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 1555-1573. (h) MacDonald, J. C.; Whitesides, G. M. Chem. Rev. 1994, 94, 2383-2420. (i) Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. Engl. 1998, 37, 1460-1494. (j) Zaworotko, M. J. Coordination Polymers. In Crystal Engineering: The Design and Applications of Functional Solids; Seddon, K. R., Zaworotko, M. J., Eds.; NATO ASI series; Kluwer; Dordecht, The Netherlands, 1998. (k) Hagrman, P. J.; Hagrman, D.; Zubieta, J. Angew. Chem., Int. Ed. Engl. 1999, 38, 2639- 2684. (l) Alivisatos, A. P.; Barbara, P. F.; Castelman, A. W.; Chang, J.; Dixon, D. A.; Klein, M. L.; McLendon, G. L.; Miller, J. S.; Ratner, M. A.; Rossky, P. J.; Stupp, S. I.; Thompson, M. E. Adv. Mater. 1998, 10, 1297- 1336.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 1555-1573
    • Bernstein, J.1    Davis, R.E.2    Shimoni, L.3    Chang, N.4
  • 8
    • 4244071593 scopus 로고
    • For a very good overview of recent developments in crystal engineering see the following multiauthored volumes and review articles: (a) Crystal Engineering: From Molecules and Crystals To Materials; Braga, D., Orpen, A. G., Eds.; NATO ASI series; Kluwer: Dordecht, The Netherlands, 1999. (b) Weber, E., Ed. Design of Organic Solids; Topics in Current Chemistry; Springer-Verlag, Heidelberg, 1998; Vol. 198. (c) Comprehensive Supramolecular Chemistry: Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford, 1996; Vol. 6. (d) Desiraju, G. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2311-2327. (e) Aakeroy, C. B. Acta Crystallogr. 1997, B53, 569-583. (f) Braga, D.; Grepioni, F.; Desiraju, G. R. Chem. Rev. 1998, 98, 1375-1405. (g) Bernstein, J.; Davis, R. E.; Shimoni, L.; Chang, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 1555-1573. (h) MacDonald, J. C.; Whitesides, G. M. Chem. Rev. 1994, 94, 2383-2420. (i) Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. Engl. 1998, 37, 1460-1494. (j) Zaworotko, M. J. Coordination Polymers. In Crystal Engineering: The Design and Applications of Functional Solids; Seddon, K. R., Zaworotko, M. J., Eds.; NATO ASI series; Kluwer; Dordecht, The Netherlands, 1998. (k) Hagrman, P. J.; Hagrman, D.; Zubieta, J. Angew. Chem., Int. Ed. Engl. 1999, 38, 2639- 2684. (l) Alivisatos, A. P.; Barbara, P. F.; Castelman, A. W.; Chang, J.; Dixon, D. A.; Klein, M. L.; McLendon, G. L.; Miller, J. S.; Ratner, M. A.; Rossky, P. J.; Stupp, S. I.; Thompson, M. E. Adv. Mater. 1998, 10, 1297- 1336.
    • (1994) Chem. Rev. , vol.94 , pp. 2383-2420
    • MacDonald, J.C.1    Whitesides, G.M.2
  • 9
    • 0032546766 scopus 로고    scopus 로고
    • For a very good overview of recent developments in crystal engineering see the following multiauthored volumes and review articles: (a) Crystal Engineering: From Molecules and Crystals To Materials; Braga, D., Orpen, A. G., Eds.; NATO ASI series; Kluwer: Dordecht, The Netherlands, 1999. (b) Weber, E., Ed. Design of Organic Solids; Topics in Current Chemistry; Springer-Verlag, Heidelberg, 1998; Vol. 198. (c) Comprehensive Supramolecular Chemistry: Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford, 1996; Vol. 6. (d) Desiraju, G. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2311-2327. (e) Aakeroy, C. B. Acta Crystallogr. 1997, B53, 569-583. (f) Braga, D.; Grepioni, F.; Desiraju, G. R. Chem. Rev. 1998, 98, 1375-1405. (g) Bernstein, J.; Davis, R. E.; Shimoni, L.; Chang, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 1555-1573. (h) MacDonald, J. C.; Whitesides, G. M. Chem. Rev. 1994, 94, 2383-2420. (i) Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. Engl. 1998, 37, 1460-1494. (j) Zaworotko, M. J. Coordination Polymers. In Crystal Engineering: The Design and Applications of Functional Solids; Seddon, K. R., Zaworotko, M. J., Eds.; NATO ASI series; Kluwer; Dordecht, The Netherlands, 1998. (k) Hagrman, P. J.; Hagrman, D.; Zubieta, J. Angew. Chem., Int. Ed. Engl. 1999, 38, 2639- 2684. (l) Alivisatos, A. P.; Barbara, P. F.; Castelman, A. W.; Chang, J.; Dixon, D. A.; Klein, M. L.; McLendon, G. L.; Miller, J. S.; Ratner, M. A.; Rossky, P. J.; Stupp, S. I.; Thompson, M. E. Adv. Mater. 1998, 10, 1297- 1336.
    • (1998) Angew. Chem., Int. Ed. Engl. , vol.37 , pp. 1460-1494
    • Batten, S.R.1    Robson, R.2
  • 10
    • 0003364716 scopus 로고    scopus 로고
    • Coordination Polymers
    • Seddon, K. R., Zaworotko, M. J., Eds.; NATO ASI series; Kluwer; Dordecht, The Netherlands
    • For a very good overview of recent developments in crystal engineering see the following multiauthored volumes and review articles: (a) Crystal Engineering: From Molecules and Crystals To Materials; Braga, D., Orpen, A. G., Eds.; NATO ASI series; Kluwer: Dordecht, The Netherlands, 1999. (b) Weber, E., Ed. Design of Organic Solids; Topics in Current Chemistry; Springer-Verlag, Heidelberg, 1998; Vol. 198. (c) Comprehensive Supramolecular Chemistry: Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford, 1996; Vol. 6. (d) Desiraju, G. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2311-2327. (e) Aakeroy, C. B. Acta Crystallogr. 1997, B53, 569-583. (f) Braga, D.; Grepioni, F.; Desiraju, G. R. Chem. Rev. 1998, 98, 1375-1405. (g) Bernstein, J.; Davis, R. E.; Shimoni, L.; Chang, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 1555-1573. (h) MacDonald, J. C.; Whitesides, G. M. Chem. Rev. 1994, 94, 2383-2420. (i) Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. Engl. 1998, 37, 1460-1494. (j) Zaworotko, M. J. Coordination Polymers. In Crystal Engineering: The Design and Applications of Functional Solids; Seddon, K. R., Zaworotko, M. J., Eds.; NATO ASI series; Kluwer; Dordecht, The Netherlands, 1998. (k) Hagrman, P. J.; Hagrman, D.; Zubieta, J. Angew. Chem., Int. Ed. Engl. 1999, 38, 2639- 2684. (l) Alivisatos, A. P.; Barbara, P. F.; Castelman, A. W.; Chang, J.; Dixon, D. A.; Klein, M. L.; McLendon, G. L.; Miller, J. S.; Ratner, M. A.; Rossky, P. J.; Stupp, S. I.; Thompson, M. E. Adv. Mater. 1998, 10, 1297- 1336.
    • (1998) Crystal Engineering: The Design and Applications of Functional Solids
    • Zaworotko, M.J.1
  • 11
    • 0000687581 scopus 로고    scopus 로고
    • For a very good overview of recent developments in crystal engineering see the following multiauthored volumes and review articles: (a) Crystal Engineering: From Molecules and Crystals To Materials; Braga, D., Orpen, A. G., Eds.; NATO ASI series; Kluwer: Dordecht, The Netherlands, 1999. (b) Weber, E., Ed. Design of Organic Solids; Topics in Current Chemistry; Springer-Verlag, Heidelberg, 1998; Vol. 198. (c) Comprehensive Supramolecular Chemistry: Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford, 1996; Vol. 6. (d) Desiraju, G. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2311-2327. (e) Aakeroy, C. B. Acta Crystallogr. 1997, B53, 569-583. (f) Braga, D.; Grepioni, F.; Desiraju, G. R. Chem. Rev. 1998, 98, 1375-1405. (g) Bernstein, J.; Davis, R. E.; Shimoni, L.; Chang, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 1555-1573. (h) MacDonald, J. C.; Whitesides, G. M. Chem. Rev. 1994, 94, 2383-2420. (i) Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. Engl. 1998, 37, 1460-1494. (j) Zaworotko, M. J. Coordination Polymers. In Crystal Engineering: The Design and Applications of Functional Solids; Seddon, K. R., Zaworotko, M. J., Eds.; NATO ASI series; Kluwer; Dordecht, The Netherlands, 1998. (k) Hagrman, P. J.; Hagrman, D.; Zubieta, J. Angew. Chem., Int. Ed. Engl. 1999, 38, 2639-2684. (l) Alivisatos, A. P.; Barbara, P. F.; Castelman, A. W.; Chang, J.; Dixon, D. A.; Klein, M. L.; McLendon, G. L.; Miller, J. S.; Ratner, M. A.; Rossky, P. J.; Stupp, S. I.; Thompson, M. E. Adv. Mater. 1998, 10, 1297- 1336.
    • (1999) Angew. Chem., Int. Ed. Engl. , vol.38 , pp. 2639-2684
    • Hagrman, P.J.1    Hagrman, D.2    Zubieta, J.3
  • 12
    • 0032206869 scopus 로고    scopus 로고
    • For a very good overview of recent developments in crystal engineering see the following multiauthored volumes and review articles: (a) Crystal Engineering: From Molecules and Crystals To Materials; Braga, D., Orpen, A. G., Eds.; NATO ASI series; Kluwer: Dordecht, The Netherlands, 1999. (b) Weber, E., Ed. Design of Organic Solids; Topics in Current Chemistry; Springer-Verlag, Heidelberg, 1998; Vol. 198. (c) Comprehensive Supramolecular Chemistry: Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford, 1996; Vol. 6. (d) Desiraju, G. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2311-2327. (e) Aakeroy, C. B. Acta Crystallogr. 1997, B53, 569-583. (f) Braga, D.; Grepioni, F.; Desiraju, G. R. Chem. Rev. 1998, 98, 1375-1405. (g) Bernstein, J.; Davis, R. E.; Shimoni, L.; Chang, N. Angew. Chem., Int. Ed. Engl. 1995, 34, 1555-1573. (h) MacDonald, J. C.; Whitesides, G. M. Chem. Rev. 1994, 94, 2383-2420. (i) Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. Engl. 1998, 37, 1460-1494. (j) Zaworotko, M. J. Coordination Polymers. In Crystal Engineering: The Design and Applications of Functional Solids; Seddon, K. R., Zaworotko, M. J., Eds.; NATO ASI series; Kluwer; Dordecht, The Netherlands, 1998. (k) Hagrman, P. J.; Hagrman, D.; Zubieta, J. Angew. Chem., Int. Ed. Engl. 1999, 38, 2639- 2684. (l) Alivisatos, A. P.; Barbara, P. F.; Castelman, A. W.; Chang, J.; Dixon, D. A.; Klein, M. L.; McLendon, G. L.; Miller, J. S.; Ratner, M. A.; Rossky, P. J.; Stupp, S. I.; Thompson, M. E. Adv. Mater. 1998, 10, 1297-1336.
    • (1998) Adv. Mater. , vol.10 , pp. 1297-1336
    • Alivisatos, A.P.1    Barbara, P.F.2    Castelman, A.W.3    Chang, J.4    Dixon, D.A.5    Klein, M.L.6    McLendon, G.L.7    Miller, J.S.8    Ratner, M.A.9    Rossky, P.J.10    Stupp, S.I.11    Thompson, M.E.12
  • 30
    • 0030888675 scopus 로고    scopus 로고
    • d symmetry and complementary intermolecular interactions. In this article, we tried to devise a new strategy of constructing generic 3D hexagonal open networks using a novel self-complementary molecular building block. However, see the following references and ref 6 for some very interesting 3D networks and open networks based on hydrogen bonding: (a) Brunet, P.; Simard, M.; Wuest, J. D. J. Am. Chem. Soc. 1997, 119, 2737-2738. (b) Bhyrappa, P.; Wilson, S. R.; Suslick, K. S. J. Am. Chem. Soc. 1997, 119, 8492-8502. (c) Ung, A. T.; Gizachew, D.; Bishop, R.; Scudder, M. L.; Dance, I. G.; Craig, D. C. J. Am. Chem. Soc. 1995, 117, 8745-8756. (d) Endo, K.; Sawaki, T.; Koyanagi, M.; Kobayashi, K.; Masuda, H.; Aoyama, Y. J. Am. Chem. Soc. 1995, 117, 8341-8352. (e) Martin, J. D.; Leafblad, B. Angew. Chem., Int. Ed. Engl. 1998, 37, 3318- 3320. (f) Aakeroy, C. B.; Beatty, A. M.; Leinen, D. S. Angew. Chem., Int. Ed. Engl. 1999, 38, 1815-1819. (g) Kumar, R. K.; Balasubramanian, S.; Goldberg, I. Chem. Commun. 1998, 1435-1436. (h) Kepert, C. J.; Hesek, D.; Beer, P. D.; Rosseinsky, M. J. Angew. Chem., Int. Ed. Engl. 1998, 37, 3158-3160. (i) Ranford, J. D.; Vittal, J. J.; Wu, D.; Yang, X. Angew. Chem., Int. Ed. Engl. 1999, 38, 3498-3501.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 2737-2738
    • Brunet, P.1    Simard, M.2    Wuest, J.D.3
  • 31
    • 0030833305 scopus 로고    scopus 로고
    • d symmetry and complementary intermolecular interactions. In this article, we tried to devise a new strategy of constructing generic 3D hexagonal open networks using a novel self-complementary molecular building block. However, see the following references and ref 6 for some very interesting 3D networks and open networks based on hydrogen bonding: (a) Brunet, P.; Simard, M.; Wuest, J. D. J. Am. Chem. Soc. 1997, 119, 2737-2738. (b) Bhyrappa, P.; Wilson, S. R.; Suslick, K. S. J. Am. Chem. Soc. 1997, 119, 8492-8502. (c) Ung, A. T.; Gizachew, D.; Bishop, R.; Scudder, M. L.; Dance, I. G.; Craig, D. C. J. Am. Chem. Soc. 1995, 117, 8745-8756. (d) Endo, K.; Sawaki, T.; Koyanagi, M.; Kobayashi, K.; Masuda, H.; Aoyama, Y. J. Am. Chem. Soc. 1995, 117, 8341-8352. (e) Martin, J. D.; Leafblad, B. Angew. Chem., Int. Ed. Engl. 1998, 37, 3318- 3320. (f) Aakeroy, C. B.; Beatty, A. M.; Leinen, D. S. Angew. Chem., Int. Ed. Engl. 1999, 38, 1815-1819. (g) Kumar, R. K.; Balasubramanian, S.; Goldberg, I. Chem. Commun. 1998, 1435-1436. (h) Kepert, C. J.; Hesek, D.; Beer, P. D.; Rosseinsky, M. J. Angew. Chem., Int. Ed. Engl. 1998, 37, 3158-3160. (i) Ranford, J. D.; Vittal, J. J.; Wu, D.; Yang, X. Angew. Chem., Int. Ed. Engl. 1999, 38, 3498-3501.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 8492-8502
    • Bhyrappa, P.1    Wilson, S.R.2    Suslick, K.S.3
  • 32
    • 0001390844 scopus 로고
    • d symmetry and complementary intermolecular interactions. In this article, we tried to devise a new strategy of constructing generic 3D hexagonal open networks using a novel self-complementary molecular building block. However, see the following references and ref 6 for some very interesting 3D networks and open networks based on hydrogen bonding: (a) Brunet, P.; Simard, M.; Wuest, J. D. J. Am. Chem. Soc. 1997, 119, 2737-2738. (b) Bhyrappa, P.; Wilson, S. R.; Suslick, K. S. J. Am. Chem. Soc. 1997, 119, 8492-8502. (c) Ung, A. T.; Gizachew, D.; Bishop, R.; Scudder, M. L.; Dance, I. G.; Craig, D. C. J. Am. Chem. Soc. 1995, 117, 8745-8756. (d) Endo, K.; Sawaki, T.; Koyanagi, M.; Kobayashi, K.; Masuda, H.; Aoyama, Y. J. Am. Chem. Soc. 1995, 117, 8341-8352. (e) Martin, J. D.; Leafblad, B. Angew. Chem., Int. Ed. Engl. 1998, 37, 3318- 3320. (f) Aakeroy, C. B.; Beatty, A. M.; Leinen, D. S. Angew. Chem., Int. Ed. Engl. 1999, 38, 1815-1819. (g) Kumar, R. K.; Balasubramanian, S.; Goldberg, I. Chem. Commun. 1998, 1435-1436. (h) Kepert, C. J.; Hesek, D.; Beer, P. D.; Rosseinsky, M. J. Angew. Chem., Int. Ed. Engl. 1998, 37, 3158-3160. (i) Ranford, J. D.; Vittal, J. J.; Wu, D.; Yang, X. Angew. Chem., Int. Ed. Engl. 1999, 38, 3498-3501.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 8745-8756
    • Ung, A.T.1    Gizachew, D.2    Bishop, R.3    Scudder, M.L.4    Dance, I.G.5    Craig, D.C.6
  • 33
    • 0001653953 scopus 로고
    • d symmetry and complementary intermolecular interactions. In this article, we tried to devise a new strategy of constructing generic 3D hexagonal open networks using a novel self-complementary molecular building block. However, see the following references and ref 6 for some very interesting 3D networks and open networks based on hydrogen bonding: (a) Brunet, P.; Simard, M.; Wuest, J. D. J. Am. Chem. Soc. 1997, 119, 2737-2738. (b) Bhyrappa, P.; Wilson, S. R.; Suslick, K. S. J. Am. Chem. Soc. 1997, 119, 8492-8502. (c) Ung, A. T.; Gizachew, D.; Bishop, R.; Scudder, M. L.; Dance, I. G.; Craig, D. C. J. Am. Chem. Soc. 1995, 117, 8745-8756. (d) Endo, K.; Sawaki, T.; Koyanagi, M.; Kobayashi, K.; Masuda, H.; Aoyama, Y. J. Am. Chem. Soc. 1995, 117, 8341-8352. (e) Martin, J. D.; Leafblad, B. Angew. Chem., Int. Ed. Engl. 1998, 37, 3318- 3320. (f) Aakeroy, C. B.; Beatty, A. M.; Leinen, D. S. Angew. Chem., Int. Ed. Engl. 1999, 38, 1815-1819. (g) Kumar, R. K.; Balasubramanian, S.; Goldberg, I. Chem. Commun. 1998, 1435-1436. (h) Kepert, C. J.; Hesek, D.; Beer, P. D.; Rosseinsky, M. J. Angew. Chem., Int. Ed. Engl. 1998, 37, 3158-3160. (i) Ranford, J. D.; Vittal, J. J.; Wu, D.; Yang, X. Angew. Chem., Int. Ed. Engl. 1999, 38, 3498-3501.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 8341-8352
    • Endo, K.1    Sawaki, T.2    Koyanagi, M.3    Kobayashi, K.4    Masuda, H.5    Aoyama, Y.6
  • 34
    • 0032542384 scopus 로고    scopus 로고
    • d symmetry and complementary intermolecular interactions. In this article, we tried to devise a new strategy of constructing generic 3D hexagonal open networks using a novel self-complementary molecular building block. However, see the following references and ref 6 for some very interesting 3D networks and open networks based on hydrogen bonding: (a) Brunet, P.; Simard, M.; Wuest, J. D. J. Am. Chem. Soc. 1997, 119, 2737-2738. (b) Bhyrappa, P.; Wilson, S. R.; Suslick, K. S. J. Am. Chem. Soc. 1997, 119, 8492-8502. (c) Ung, A. T.; Gizachew, D.; Bishop, R.; Scudder, M. L.; Dance, I. G.; Craig, D. C. J. Am. Chem. Soc. 1995, 117, 8745-8756. (d) Endo, K.; Sawaki, T.; Koyanagi, M.; Kobayashi, K.; Masuda, H.; Aoyama, Y. J. Am. Chem. Soc. 1995, 117, 8341-8352. (e) Martin, J. D.; Leafblad, B. Angew. Chem., Int. Ed. Engl. 1998, 37, 3318-3320. (f) Aakeroy, C. B.; Beatty, A. M.; Leinen, D. S. Angew. Chem., Int. Ed. Engl. 1999, 38, 1815-1819. (g) Kumar, R. K.; Balasubramanian, S.; Goldberg, I. Chem. Commun. 1998, 1435-1436. (h) Kepert, C. J.; Hesek, D.; Beer, P. D.; Rosseinsky, M. J. Angew. Chem., Int. Ed. Engl. 1998, 37, 3158-3160. (i) Ranford, J. D.; Vittal, J. J.; Wu, D.; Yang, X. Angew. Chem., Int. Ed. Engl. 1999, 38, 3498-3501.
    • (1998) Angew. Chem., Int. Ed. Engl. , vol.37 , pp. 3318-3320
    • Martin, J.D.1    Leafblad, B.2
  • 35
    • 0033553833 scopus 로고    scopus 로고
    • d symmetry and complementary intermolecular interactions. In this article, we tried to devise a new strategy of constructing generic 3D hexagonal open networks using a novel self-complementary molecular building block. However, see the following references and ref 6 for some very interesting 3D networks and open networks based on hydrogen bonding: (a) Brunet, P.; Simard, M.; Wuest, J. D. J. Am. Chem. Soc. 1997, 119, 2737-2738. (b) Bhyrappa, P.; Wilson, S. R.; Suslick, K. S. J. Am. Chem. Soc. 1997, 119, 8492-8502. (c) Ung, A. T.; Gizachew, D.; Bishop, R.; Scudder, M. L.; Dance, I. G.; Craig, D. C. J. Am. Chem. Soc. 1995, 117, 8745-8756. (d) Endo, K.; Sawaki, T.; Koyanagi, M.; Kobayashi, K.; Masuda, H.; Aoyama, Y. J. Am. Chem. Soc. 1995, 117, 8341-8352. (e) Martin, J. D.; Leafblad, B. Angew. Chem., Int. Ed. Engl. 1998, 37, 3318- 3320. (f) Aakeroy, C. B.; Beatty, A. M.; Leinen, D. S. Angew. Chem., Int. Ed. Engl. 1999, 38, 1815-1819. (g) Kumar, R. K.; Balasubramanian, S.; Goldberg, I. Chem. Commun. 1998, 1435-1436. (h) Kepert, C. J.; Hesek, D.; Beer, P. D.; Rosseinsky, M. J. Angew. Chem., Int. Ed. Engl. 1998, 37, 3158-3160. (i) Ranford, J. D.; Vittal, J. J.; Wu, D.; Yang, X. Angew. Chem., Int. Ed. Engl. 1999, 38, 3498-3501.
    • (1999) Angew. Chem., Int. Ed. Engl. , vol.38 , pp. 1815-1819
    • Aakeroy, C.B.1    Beatty, A.M.2    Leinen, D.S.3
  • 36
    • 0002270364 scopus 로고    scopus 로고
    • d symmetry and complementary intermolecular interactions. In this article, we tried to devise a new strategy of constructing generic 3D hexagonal open networks using a novel self-complementary molecular building block. However, see the following references and ref 6 for some very interesting 3D networks and open networks based on hydrogen bonding: (a) Brunet, P.; Simard, M.; Wuest, J. D. J. Am. Chem. Soc. 1997, 119, 2737-2738. (b) Bhyrappa, P.; Wilson, S. R.; Suslick, K. S. J. Am. Chem. Soc. 1997, 119, 8492-8502. (c) Ung, A. T.; Gizachew, D.; Bishop, R.; Scudder, M. L.; Dance, I. G.; Craig, D. C. J. Am. Chem. Soc. 1995, 117, 8745-8756. (d) Endo, K.; Sawaki, T.; Koyanagi, M.; Kobayashi, K.; Masuda, H.; Aoyama, Y. J. Am. Chem. Soc. 1995, 117, 8341-8352. (e) Martin, J. D.; Leafblad, B. Angew. Chem., Int. Ed. Engl. 1998, 37, 3318- 3320. (f) Aakeroy, C. B.; Beatty, A. M.; Leinen, D. S. Angew. Chem., Int. Ed. Engl. 1999, 38, 1815-1819. (g) Kumar, R. K.; Balasubramanian, S.; Goldberg, I. Chem. Commun. 1998, 1435-1436. (h) Kepert, C. J.; Hesek, D.; Beer, P. D.; Rosseinsky, M. J. Angew. Chem., Int. Ed. Engl. 1998, 37, 3158-3160. (i) Ranford, J. D.; Vittal, J. J.; Wu, D.; Yang, X. Angew. Chem., Int. Ed. Engl. 1999, 38, 3498-3501.
    • (1998) Chem. Commun. , pp. 1435-1436
    • Kumar, R.K.1    Balasubramanian, S.2    Goldberg, I.3
  • 37
    • 0032484053 scopus 로고    scopus 로고
    • d symmetry and complementary intermolecular interactions. In this article, we tried to devise a new strategy of constructing generic 3D hexagonal open networks using a novel self-complementary molecular building block. However, see the following references and ref 6 for some very interesting 3D networks and open networks based on hydrogen bonding: (a) Brunet, P.; Simard, M.; Wuest, J. D. J. Am. Chem. Soc. 1997, 119, 2737-2738. (b) Bhyrappa, P.; Wilson, S. R.; Suslick, K. S. J. Am. Chem. Soc. 1997, 119, 8492-8502. (c) Ung, A. T.; Gizachew, D.; Bishop, R.; Scudder, M. L.; Dance, I. G.; Craig, D. C. J. Am. Chem. Soc. 1995, 117, 8745-8756. (d) Endo, K.; Sawaki, T.; Koyanagi, M.; Kobayashi, K.; Masuda, H.; Aoyama, Y. J. Am. Chem. Soc. 1995, 117, 8341-8352. (e) Martin, J. D.; Leafblad, B. Angew. Chem., Int. Ed. Engl. 1998, 37, 3318- 3320. (f) Aakeroy, C. B.; Beatty, A. M.; Leinen, D. S. Angew. Chem., Int. Ed. Engl. 1999, 38, 1815-1819. (g) Kumar, R. K.; Balasubramanian, S.; Goldberg, I. Chem. Commun. 1998, 1435-1436. (h) Kepert, C. J.; Hesek, D.; Beer, P. D.; Rosseinsky, M. J. Angew. Chem., Int. Ed. Engl. 1998, 37, 3158-3160. (i) Ranford, J. D.; Vittal, J. J.; Wu, D.; Yang, X. Angew. Chem., Int. Ed. Engl. 1999, 38, 3498-3501.
    • (1998) Angew. Chem., Int. Ed. Engl. , vol.37 , pp. 3158-3160
    • Kepert, C.J.1    Hesek, D.2    Beer, P.D.3    Rosseinsky, M.J.4
  • 38
    • 0033521212 scopus 로고    scopus 로고
    • d symmetry and complementary intermolecular interactions. In this article, we tried to devise a new strategy of constructing generic 3D hexagonal open networks using a novel self-complementary molecular building block. However, see the following references and ref 6 for some very interesting 3D networks and open networks based on hydrogen bonding: (a) Brunet, P.; Simard, M.; Wuest, J. D. J. Am. Chem. Soc. 1997, 119, 2737-2738. (b) Bhyrappa, P.; Wilson, S. R.; Suslick, K. S. J. Am. Chem. Soc. 1997, 119, 8492-8502. (c) Ung, A. T.; Gizachew, D.; Bishop, R.; Scudder, M. L.; Dance, I. G.; Craig, D. C. J. Am. Chem. Soc. 1995, 117, 8745-8756. (d) Endo, K.; Sawaki, T.; Koyanagi, M.; Kobayashi, K.; Masuda, H.; Aoyama, Y. J. Am. Chem. Soc. 1995, 117, 8341-8352. (e) Martin, J. D.; Leafblad, B. Angew. Chem., Int. Ed. Engl. 1998, 37, 3318- 3320. (f) Aakeroy, C. B.; Beatty, A. M.; Leinen, D. S. Angew. Chem., Int. Ed. Engl. 1999, 38, 1815-1819. (g) Kumar, R. K.; Balasubramanian, S.; Goldberg, I. Chem. Commun. 1998, 1435-1436. (h) Kepert, C. J.; Hesek, D.; Beer, P. D.; Rosseinsky, M. J. Angew. Chem., Int. Ed. Engl. 1998, 37, 3158-3160. (i) Ranford, J. D.; Vittal, J. J.; Wu, D.; Yang, X. Angew. Chem., Int. Ed. Engl. 1999, 38, 3498-3501.
    • (1999) Angew. Chem., Int. Ed. Engl. , vol.38 , pp. 3498-3501
    • Ranford, J.D.1    Vittal, J.J.2    Wu, D.3    Yang, X.4
  • 40
    • 0002464446 scopus 로고    scopus 로고
    • Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford
    • Herbstein, F. H. In Comprehensive Supramolecular Chemistry; Atwood, J. L., Davies, J. E. D., MacNicol, D. D., Vogtle, F., Lehn, J.-M., Eds.; Pergamon: Oxford, 1996; Vol. 6, pp 61-82.
    • (1996) Comprehensive Supramolecular Chemistry , vol.6 , pp. 61-82
    • Herbstein, F.H.1
  • 50
    • 0342510941 scopus 로고    scopus 로고
    • note
    • The UV/vis spectra of neutral and protonated forms of 2 in MeOH: 326 (s), 356 (m), 366 nm (m), 2; 320 (s), 345 (m), 400-500 nm (broad), 2H. The protonation of 3 (324 (s), 384 nm (w)) and 4 (302 (s), 336 (s), 388 nm (w)) has no effect on their absorption spectra.
  • 54
    • 54649083741 scopus 로고    scopus 로고
    • Metal phosphonate chemistry
    • Karlin, K. D., Ed.; John Wiley & Sons: New York
    • Indeed, organophosphonic acids are widely used in the design of advanced inorganic solids and thin films, but their potential in the context of organic solids design has not been exploited. For example, see: (a) Clearfield, A. Metal phosphonate chemistry. In Progress in Inorganic Chemistry; Karlin, K. D., Ed.; John Wiley & Sons: New York, 1998; Vol. 47, pp 371-510. (b) Mallouk, T. E.; Gavin, J. A. Acc. Chem. Res. 1998, 31, 219-227.
    • (1998) Progress in Inorganic Chemistry , vol.47 , pp. 371-510
    • Clearfield, A.1
  • 55
    • 54649083741 scopus 로고    scopus 로고
    • Indeed, organophosphonic acids are widely used in the design of advanced inorganic solids and thin films, but their potential in the context of organic solids design has not been exploited. For example, see: (a) Clearfield, A. Metal phosphonate chemistry. In Progress in Inorganic Chemistry; Karlin, K. D., Ed.; John Wiley & Sons: New York, 1998; Vol. 47, pp 371-510. (b) Mallouk, T. E.; Gavin, J. A. Acc. Chem. Res. 1998, 31, 219-227.
    • (1998) Acc. Chem. Res. , vol.31 , pp. 219-227
    • Mallouk, T.E.1    Gavin, J.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.