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The ability to predict supramolecular structure from molecular structure is, in general, an unsolved problem (Maddox, J. Nature 1988, 335, 201). Fortunately, useful supramolecular structures do not require complete control of supramolecular structure, just control of certain molecular functionalities.
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The interest in low dimensional solids, one dimensional rods and two dimensional layers is due primarily to the high degree of anisotropy of their solid state properties. Physics and Chemistry of Materials with Low-Dimensional Structures; D. Reidel: Dordrecht, The Netherlands.
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For other recent approaches to the preparation of layered structures see: (a) Hollingsworth, M. D.; Brown, M.E.; Santarsiero, B.D.; Huffman, J.C.; Goss, C.R. Chem. Mater. 1994, 6, 1227-1244.
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(c) Kiji, J.; Kaiser, J.; Wegner, G.; Schulz, R. C. Polymer 1973, 14, 433. For a recent report on some small oligomers possessing the polytriacetylene backbone see Anthony, J.; Boudon, C.; Diederkh, F.; Gisselbrechl, J.-P.; Gramlich, V.; Gross, M.; Hobi, M.; Seiler, P. Angew. Chem., Int. Ed. Eng. 1994, 33, 763.
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(c) Kiji, J.; Kaiser, J.; Wegner, G.; Schulz, R. C. Polymer 1973, 14, 433. For a recent report on some small oligomers possessing the polytriacetylene backbone see Anthony, J.; Boudon, C.; Diederkh, F.; Gisselbrechl, J.-P.; Gramlich, V.; Gross, M.; Hobi, M.; Seiler, P. Angew. Chem., Int. Ed. Eng. 1994, 33, 763.
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(d) Bernstein, J.; Etter, M. C.; Leiserowitz, L. in Structure Correlation, Bürgi, H.-B., Dunitz, J. D., Eds Vol. 2, VCH: Weinheim, FRG, 1994, pp. 490-507.
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85030196989
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note
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When two molecules of similar complexity are involved in a host-guest complex it can be difficult to identify the host and the guest. Because the of-network of the heterocycle is intact its supramolecular structure is the more complex component and it is more appropriate to call it the host and the dicarboxylic acid the guest. If the α-network is not present then it is more appropriate to call the complex simply a co-crystal.
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0000831957
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There are a few examples of this hydrogen bond motif reported in the literature. For example, see reference 6 and previous work cited. Also this motif has recently been observed in the crystal structure of a parallel-stranded duplex of a deoxycytidylyl-(3′-5′)-deoxycytidine analogue (Egli, M.; Lubini, P.; Bolli, M.; Dobler, M.; Leumann, C. J. Amer. Chem. Soc. 1993,115, 5855-5856).
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Egli, M.1
Lubini, P.2
Bolli, M.3
Dobler, M.4
Leumann, C.5
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0001325812
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Levene, P. A.; Bass, L. W.; Simms, H. S. J. Biol. Chem. 1926, 70, 229-241.
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Levene, P.A.1
Bass, L.W.2
Simms, H.S.3
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25
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85030197055
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note
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For example, a molecule with five different hydrogen bond donors and five different hydrogen bond acceptors can theoretically result in 120 different hydrogen bond motifs.
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