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2
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0011362257
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General methods for the construction of complex molecules
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and refers to a sub-structural unit
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E. J. Corey, Pure Appl. Chem., "General methods for the construction of complex molecules", 1967, 14, 19-37), and refers to a sub-structural unit.
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Corey, E.J.1
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3
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0001367546
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Supramolecular synthons in crystal engineering-a new organic synthesis
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G. R. Desiraju, "Supramolecular synthons in crystal engineering-a new organic synthesis", Angew. Chem. 1995, 107, 2541-2557.
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Desiraju, G.R.1
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0001601505
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Retrosynthetic thinking-essentials and examples
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E. J. Corey, "Retrosynthetic thinking-essentials and examples", Chem. Soc. Rev. 1988, 17, 111-133.
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Corey, E.J.1
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0001544275
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Supramolecular structures-reason and imagination
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A. Nangia, G. R. Desiraju, "Supramolecular structures-reason and imagination", Acta Crystallogr., Section A 1998, 54, 934-944.
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Acta Crystallogr., Section A
, vol.54
, pp. 934-944
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Nangia, A.1
Desiraju, G.R.2
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6
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1842479637
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Supramolecular synthons in crystal engineering. Structure simplification, synthon robustness and supramolecular retrosynthesis
-
V. R. Thalladi, B. S. Goud, V. J. Hoy, F. H. Allen, J. A. K. Howard, G. R. Desiraju, "Supramolecular synthons in crystal engineering. Structure simplification, synthon robustness and supramolecular retrosynthesis", Chem.Commun., 1996, 401-402.
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Chem.Commun.
, pp. 401-402
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Thalladi, V.R.1
Goud, B.S.2
Hoy, V.J.3
Allen, F.H.4
Howard, J.A.K.5
Desiraju, G.R.6
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7
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84949969744
-
-
No special significance need be ascribed to the use of the word ribbon, as opposed to say, tape. By ribbon is meant a generally flat one-dimensional motif
-
No special significance need be ascribed to the use of the word ribbon, as opposed to say, tape. By ribbon is meant a generally flat one-dimensional motif.
-
-
-
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8
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37049074649
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Molecular recognition via iodo5 5 5 nitro and iodo 5 5 5 cyano interactions: crystal structures of the 1:1 complexes of 1,4-diiodobenzene with 1,4-dinitrobenzene and 7,7,8,8-tetracyanoquinodimethane (TCNQ)
-
F. H. Allen, B. S. Goud, V. J. Hoy, J. A. K. Howard, G. R. Desiraju, "Molecular recognition via iodo5 5 5 nitro and iodo 5 5 5 cyano interactions: crystal structures of the 1:1 complexes of 1,4-diiodobenzene with 1,4-dinitrobenzene and 7,7,8,8-tetracyanoquinodimethane (TCNQ)", J. Chem. Soc., Chem. Commun., 1994, 2729-2730.
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J. Chem. Soc., Chem. Commun.
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-
Allen, F.H.1
Goud, B.S.2
Hoy, V.J.3
Howard, J.A.K.4
Desiraju, G.R.5
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9
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0001385822
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Design of a SHG-active crystal, 4-iodo-4'-nitrobiphenyl. The role of supramolecular synthons
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J. A. R. P. Sarma, F. H. Allen, V. J. Hoy, J. A. K. Howard, R. Thaimattam, K. Biradha, G. R. Desiraju, "Design of a SHG-active crystal, 4-iodo-4'-nitrobiphenyl. The role of supramolecular synthons", Chem. Commun., 1997, 101-102.
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Chem. Commun.
, pp. 101-102
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-
Sarma, J.A.R.P.1
Allen, F.H.2
Hoy, V.J.3
Howard, J.A.K.4
Thaimattam, R.5
Biradha, K.6
Desiraju, G.R.7
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10
-
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0002140018
-
Comments on the elusive crystal structure of 4-iodo-4'-nitrobiphenyl
-
N. Masciocchi, M. Bergamo, A. Sironi, "Comments on the elusive crystal structure of 4-iodo-4'-nitrobiphenyl" Chem. Comm., 1998, 1347-1348
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(1998)
Chem. Comm.
, pp. 1347-1348
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Masciocchi, N.1
Bergamo, M.2
Sironi, A.3
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11
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0032494969
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On intrinsic and extrinsic defect-forming mechanisms determining the disordered structure of 4-iodo-4'-nitrobiphenyl
-
J. Hulliger, P. J. Langley, "On intrinsic and extrinsic defect-forming mechanisms determining the disordered structure of 4-iodo-4'-nitrobiphenyl" Chem. Comm., 1998, 2557-2558.
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Chem. Comm.
, pp. 2557-2558
-
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Hulliger, J.1
Langley, P.J.2
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13
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84949990665
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This author has always distinguished between the terms synthon and building block and has rarely used the latter, because it implies modularity and a chemical insensitivity that is scarcely known in molecular crystals
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This author has always distinguished between the terms synthon and building block and has rarely used the latter, because it implies modularity and a chemical insensitivity that is scarcely known in molecular crystals.
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14
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0001695572
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The halogen 5 5 5 O(nitro) supramolecular synthon in crystal engineering: a combined crystallographic database and ab initio molecular orbital study
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F. H. Allen, J. P. M. Lommerse, V. J. Hoy, J. A. K. Howard, G. R. Desiraju, "The halogen 5 5 5 O(nitro) supramolecular synthon in crystal engineering: a combined crystallographic database and ab initio molecular orbital study", Acta Crystallogr., Section B 1997, 53, 1469-149.
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Acta Crystallogr., Section B
, vol.53
, pp. 1469-2149
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Allen, F.H.1
Lommerse, J.P.M.2
Hoy, V.J.3
Howard, J.A.K.4
Desiraju, G.R.5
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15
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0032546766
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Interpenetrating nets: ordered, periodic entanglement
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S. R. Batten, R. Robson, "Interpenetrating nets: ordered, periodic entanglement", Angew. Chem. Int. Ed. Engl., 1998, 37, 1469-1494.
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Angew. Chem. Int. Ed. Engl.
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, pp. 1469-1494
-
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Batten, S.R.1
Robson, R.2
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16
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0001971367
-
Nature of the intermolecular forces operative in biological processes
-
L. Pauling, M. Delbrück, "Nature of the intermolecular forces operative in biological processes", Science 1940, 92, 77-79.
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(1940)
Science
, vol.92
, pp. 77-79
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Pauling, L.1
Delbrück, M.2
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17
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84892166712
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Einfluss der Configuration auf die Wirkung der Enzyme
-
E. Fischer, "Einfluss der Configuration auf die Wirkung der Enzyme", Ber. Dtsch. Chem. Ges., 1894, 27, 2985-2993
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(1894)
Ber. Dtsch. Chem. Ges.
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, pp. 2985-2993
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Fischer, E.1
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18
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84949939119
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An important distinction between molecular and supramolecular chemistry is that, in the latter, hydrocarbon residues are functionalities
-
An important distinction between molecular and supramolecular chemistry is that, in the latter, hydrocarbon residues are functionalities.
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-
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19
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0032790258
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Systematic analysis of the probabilities of formation of bimolecular hydrogen-bonded ring motifs in organic crystal structures
-
F. H. Allen, W. D. S. Motherwell, P. R. Raithby, G. P. Shields, R. Taylor, "Systematic analysis of the probabilities of formation of bimolecular hydrogen-bonded ring motifs in organic crystal structures", New. J. Chem., 1999, 25-34.
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New. J. Chem.
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Allen, F.H.1
Motherwell, W.D.S.2
Raithby, P.R.3
Shields, G.P.4
Taylor, R.5
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20
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0346156221
-
Interplay of strong and weak hydrogen bonding in molecular complexes of some 4,4'-disubstituted biphenyls with urea, thiourea and water
-
R. Thaimattam, D. S. Reddy, F. Xue, T. C.W. Mak, A. Nangia, G. R. Desiraju, "Interplay of strong and weak hydrogen bonding in molecular complexes of some 4,4'-disubstituted biphenyls with urea, thiourea and water", J. Chem. Soc., Perkin Trans. 2, 1998,1783-1789.
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J. Chem. Soc., Perkin Trans.
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Thaimattam, R.1
Reddy, D.S.2
Xue, F.3
Mak, T.C.W.4
Nangia, A.5
Desiraju, G.R.6
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21
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84949942870
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The novel feature of these inclusion compounds is that the species which is linked with weak hydrogen bonds completely surrounds the species which employs strong hydrogen bonding in crystal assembly. Using topological conventions, the former is the host, and the latter the guest. All this discussion shows is that the terms host and guest are somewhat subjective, and that their definition is partly chemical and partly linguistic
-
The novel feature of these inclusion compounds is that the species which is linked with weak hydrogen bonds completely surrounds the species which employs strong hydrogen bonding in crystal assembly. Using topological conventions, the former is the host, and the latter the guest. All this discussion shows is that the terms host and guest are somewhat subjective, and that their definition is partly chemical and partly linguistic.
-
-
-
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22
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0001475723
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Molecular packing modes. Carboxylic acids
-
L. Leiserowitz, "Molecular packing modes. Carboxylic acids", Acta Crystallogr. Section B. 1976, 32, 775-802.
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(1976)
Acta Crystallogr. Section B.
, vol.32
, pp. 775-802
-
-
Leiserowitz, L.1
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23
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84949964592
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Shortened C-C bonds and antiplanar O=C-O-H torsion angles in 1,4-cubanecarboxylic acid
-
O. Ermer, J. Lex, "Shortened C-C bonds and antiplanar O=C-O-H torsion angles in 1,4-cubanecarboxylic acid", Angew. Chem. Int. Ed. Engl. 1987, 1987, 26.
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Angew. Chem. Int. Ed. Engl.
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, pp. 26
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Ermer, O.1
Lex, J.2
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24
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0031482542
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Network hydrogen bonding: the crystal and molecular structure of cubane-1,3,5,7-tetracarboxylic acid dihydrate
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R. J. Butcher, A. Bashir-Hashemi, R. Gilardi, "Network hydrogen bonding: the crystal and molecular structure of cubane-1,3,5,7-tetracarboxylic acid dihydrate", J. Chem. Cryst., 1997, 27, 455-457..
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J. Chem. Cryst.
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Butcher, R.J.1
Bashir-Hashemi, A.2
Gilardi, R.3
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25
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0033541118
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Cubane carboxylic acids. Crystal engineering considerations and the role of C-H5 5 5O hydrogen bonds in determining O-H5 5 5O networks
-
S. S. Kuduva, D. C. Craig, A. Nangia, G. R. Desiraju, "Cubane carboxylic acids. Crystal engineering considerations and the role of C-H5 5 5O hydrogen bonds in determining O-H5 5 5O networks", J. Am. Chem. Soc. 1999, 121, 1936-1944.
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J. Am. Chem. Soc.
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Kuduva, S.S.1
Craig, D.C.2
Nangia, A.3
Desiraju, G.R.4
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26
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0030703631
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Synthesis and chemistry of 1,3,5,7- tetranitrocubane including measurement of its acidity, formation of o-nitro anions, and the first preparations of pentanitrocubane and hexanitrocubane
-
6 times more acidic than vinyl and phenyl hydrogens (K. A. Lukin, J. Li, P. E. Eaton, N. Kanomata, J. Hain, E. Punzalan, R. Gilardi, "Synthesis and chemistry of 1,3,5,7- tetranitrocubane including measurement of its acidity, formation of o-nitro anions, and the first preparations of pentanitrocubane and hexanitrocubane", J. Am. Chem. Soc. 1997, 119, 9591-9602.
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J. Am. Chem. Soc.
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Lukin, K.A.1
Li, J.2
Eaton, P.E.3
Kanomata, N.4
Hain, J.5
Punzalan, E.6
Gilardi, R.7
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28
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0033973635
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Establishing structural repeti- tivity in systems with interaction interference: crystal engineering in the gem-alkynol family
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N.N. L. Madhavi, C. Bilton, J.A. K.Howard, F. H. Allen,A. Nangia, G. R. Desiraju, "Establishing structural repeti- tivity in systems with interaction interference: crystal engineering in the gem-alkynol family", New J. Chem. 2000, 24, 1-4.
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New J. Chem.
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, pp. 1-4
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-
Madhavi, N.N.L.1
Bilton, C.2
Howard, J.A.K.3
Allen, F.H.4
Nangia, A.5
Desiraju, G.R.6
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29
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5544220334
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Generation of crystal structures of acetic acid and its halogenated analogs
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R. S. Payne, R. J. Roberts, R. C. Rowe, R. Docherty, "Generation of crystal structures of acetic acid and its halogenated analogs", J. Comput. Chem., 1998, 19, 1-20
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, pp. 1-20
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Payne, R.S.1
Roberts, R.J.2
Rowe, R.C.3
Docherty, R.4
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30
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0000036732
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Crystal structure predictions for acetic acid
-
W. T. M. Mooij, B. P. van Eijck, S. L. Price, P. Verwer, J. Kroon, "Crystal structure predictions for acetic acid", J. Comput. Chem., 1998, 19, 459-474
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J. Comput. Chem.
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, pp. 459-474
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Mooij, W.T.M.1
van Eijck, B.P.2
Price, S.L.3
Verwer, P.4
Kroon, J.5
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31
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0030696761
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Crystal gazing: structure prediction and polymorphism
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G. R. Desiraju, "Crystal gazing: structure prediction and polymorphism", Science 1997, 278, 404-405.
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(1997)
Science
, vol.278
, pp. 404-405
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Desiraju, G.R.1
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32
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84949999619
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The correction of mistakes is an important aspect of crystal nucleation and is achieved by the inherent weakness of most interactions in the typical molecular crystal. Such correction could be facile because only around 15 % of all crystal structures in the CSD are disordered
-
The correction of mistakes is an important aspect of crystal nucleation and is achieved by the inherent weakness of most interactions in the typical molecular crystal. Such correction could be facile because only around 15 % of all crystal structures in the CSD are disordered.
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33
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0033521188
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Concomitant polymorphs
-
J. Bernstein, R. J. Davey, J.-O. Henck, "Concomitant polymorphs", Angew. Chem. Int. Ed., 1999, 38, 3440-3461.
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(1999)
Angew. Chem. Int. Ed.
, vol.38
, pp. 3440-3461
-
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Bernstein, J.1
Davey, R.J.2
Henck, J.-O.3
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34
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84949984773
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In general, polymorphism can be enthalpically and entropically driven and, in general, is susceptible to both thermodynamic and kinetic factors
-
In general, polymorphism can be enthalpically and entropically driven and, in general, is susceptible to both thermodynamic and kinetic factors.
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35
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0002957649
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Crystal engineering: some further strategies
-
A. Anthony, G. R. Desiraju, R. K. R. Jetti, S. S. Kuduva, N. N. L.Madhavi, A. Nangia, R. Thaimattam, V. R. Thalladi, "Crystal engineering: some further strategies", Crystal Engineering 1998, 1, 1-18.
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(1998)
Crystal Engineering
, vol.1
, pp. 1-18
-
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Anthony, A.1
Desiraju, G.R.2
Jetti, R.K.R.3
Kuduva, S.S.4
Madhavi, N.N.L.5
Nangia, A.6
Thaimattam, R.7
Thalladi, V.R.8
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36
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84949953428
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-
2 suite of programs from Molecular Simulations.We thank MSI (Cambridge and San Diego) for their continuing cooperation and assistance
-
2 suite of programs from Molecular Simulations.We thank MSI (Cambridge and San Diego) for their continuing cooperation and assistance.
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2
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37
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0343239746
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Isoquinoline
-
K. Hensen, R. Mayr-Stein, M. Bolte, "Isoquinoline", Acta Crystallogr., Section C, 55, 1565-1567.
-
Acta Crystallogr., Section C
, vol.55
, pp. 1565-1567
-
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Hensen, K.1
Mayr-Stein, R.2
Bolte, M.3
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38
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84949940272
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Solvent, in general, can affect crystallization during any of three stages-nucleation, growth and transformation. Here, we are concerned only with the first of these stages
-
Solvent, in general, can affect crystallization during any of three stages-nucleation, growth and transformation. Here, we are concerned only with the first of these stages.
-
-
-
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39
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0346085179
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α-and g -Guttiferins
-
K. V. N. Rao, P. L. N. Rao, " α-and g -Guttiferins", Experientia 1961, 17, 213-214.
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(1961)
Experientia
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, pp. 213-214
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Rao, K.V.N.1
Rao, P.L.N.2
|