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Newkome GR, Moorefield CN, Vögtle F. Dendritic Molecules: Concepts, Syntheses, Perspectives. 1996;VCH, Weinheim.
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Dendritic Molecules: Concepts, Syntheses, Perspectives
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Newkome, G.R.1
Moorefield, C.N.2
Vögtle, F.3
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Interlocked and intertwined structures and superstructures
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Amabilino DB, Stoddart JF. Interlocked and intertwined structures and superstructures. Chem Rev. 95:1995;2725-2828.
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Amabilino, D.B.1
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Semlyen J.A. New York: J Wiley and Sons
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Gibson HW. Rotaxanes. Semlyen JA. Large Ring Molecules. 1995;191-262 J Wiley and Sons, New York.
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Large Ring Molecules
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Gibson, H.W.1
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Molecular and supramolecular synthesis with dibenzofuran-containing systems
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of special interest. Regiochemistry of disubstituted benzofuran crown ethers greatly influences the yield and properties of the resulting catenanes because of the variation in the separation of the bipyridinium units in a tetracationic cyclophane.
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Asakawa M, Ashton PR, Brown CL, Fyfe MCT, Menzer S, Pasini D, Scheuer C, Spencer N, Stoddart JF, White AJP, Williams DJ. Molecular and supramolecular synthesis with dibenzofuran-containing systems. of special interest Chem Euro J. 3:1997;1136-1150 Regiochemistry of disubstituted benzofuran crown ethers greatly influences the yield and properties of the resulting catenanes because of the variation in the separation of the bipyridinium units in a tetracationic cyclophane.
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Chem Euro J
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Asakawa, M.1
Ashton, P.R.2
Brown, C.L.3
Fyfe, M.C.T.4
Menzer, S.5
Pasini, D.6
Scheuer, C.7
Spencer, N.8
Stoddart, J.F.9
White, A.J.P.10
Williams, D.J.11
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6
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18844478093
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Self-assembly of novel [2]catenanes and [2]pseudorotaxanes incorporating thiacrown ethers or their acyclic analogues
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of special interest. Thioethers have low association constants with the Stoddart tetracationic cyclophane but the analogous thiacrown ethers still produce catenanes in excellent yields. These catenanes exhibit novel thermal responses.
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Asakawa M, Ashton PR, Dehaen W, L'abbé G, Menzer S, Nouwen J, Raymo FM, Stoddart JF, Tolley MS, Toppet S, et al. Self-assembly of novel [2]catenanes and [2]pseudorotaxanes incorporating thiacrown ethers or their acyclic analogues. of special interest Chem Euro J. 3:1997;772-787 Thioethers have low association constants with the Stoddart tetracationic cyclophane but the analogous thiacrown ethers still produce catenanes in excellent yields. These catenanes exhibit novel thermal responses.
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(1997)
Chem Euro J
, vol.3
, pp. 772-787
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Asakawa, M.1
Ashton, P.R.2
Dehaen, W.3
L'Abbé, G.4
Menzer, S.5
Nouwen, J.6
Raymo, F.M.7
Stoddart, J.F.8
Tolley, M.S.9
Toppet, S.10
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7
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0032536465
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A chemically and electrochemically switchable[2]catenane incorporating a tetrathiafulvalene unit
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of special interest. Int Ed Engl. Oxidation/reduction of a TTF unit in a 1,5-dioxynapthalene crown ether-based catenane controls the movement of the tetracationic cyclophane between the two units.
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Asakawa M, Ashton PR, Balzani V, Credi A, Hamers C, Mattersteig G, Montalti M, Shipway AN, Spencer N, Stoddart JF, et al. A chemically and electrochemically switchable[2]catenane incorporating a tetrathiafulvalene unit. of special interest Int Ed Engl Angew Chem. 37:1998;333-337 Oxidation/reduction of a TTF unit in a 1,5-dioxynapthalene crown ether-based catenane controls the movement of the tetracationic cyclophane between the two units.
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(1998)
Angew Chem
, vol.37
, pp. 333-337
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Asakawa, M.1
Ashton, P.R.2
Balzani, V.3
Credi, A.4
Hamers, C.5
Mattersteig, G.6
Montalti, M.7
Shipway, A.N.8
Spencer, N.9
Stoddart, J.F.10
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8
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0031804329
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Cyclophanes and [2]catenanes as ligands for transition metal complexes: Synthesis, structure, absorption spectra, and excited state and electrochemical properties
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Ashton PR, Balzani V, Credi A, Kocian O, Pasini D, Prodi L, Spencer N, Stoddart JF, Tolley MS, Venturi M, et al. Cyclophanes and [2]catenanes as ligands for transition metal complexes: synthesis, structure, absorption spectra, and excited state and electrochemical properties. Chem Eur J. 4:1998;590-607.
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Chem Eur J
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Ashton, P.R.1
Balzani, V.2
Credi, A.3
Kocian, O.4
Pasini, D.5
Prodi, L.6
Spencer, N.7
Stoddart, J.F.8
Tolley, M.S.9
Venturi, M.10
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9
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0002871221
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Neutral [2]catenanes from oxidative coupling of π-stacked components
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of special interest. Catenanes can be formed through π-π interactions using a neutral di-imide motif as the electron deficient template.
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Hamilton DG, Sanders JKM, Davies JE, Clegg W, Teat SJ. Neutral [2]catenanes from oxidative coupling of π-stacked components. of special interest J Chem Soc Chem Commun. 1997;897-898 Catenanes can be formed through π-π interactions using a neutral di-imide motif as the electron deficient template.
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(1997)
J Chem Soc Chem Commun
, pp. 897-898
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Hamilton, D.G.1
Sanders, J.K.M.2
Davies, J.E.3
Clegg, W.4
Teat, S.J.5
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10
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0031804095
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Synthesis, structure and photophysics of neutral π-associated [2]catenanes
-
of outstanding interest. A combination of solid state packing and dynamic processes discerned from NMR are used to explain the photophysics of new neutral catenanes.
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Hamilton DG, Davies JE, Prodi L, Sanders JKM. Synthesis, structure and photophysics of neutral π-associated [2]catenanes. of outstanding interest Chem Euro J. 4:1998;608-620 A combination of solid state packing and dynamic processes discerned from NMR are used to explain the photophysics of new neutral catenanes.
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(1998)
Chem Euro J
, vol.4
, pp. 608-620
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Hamilton, D.G.1
Davies, J.E.2
Prodi, L.3
Sanders, J.K.M.4
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11
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0032506983
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Tandem hetero-catenation: Templating and self-assembly in the mutual closure of two different interlocking rings
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of special interest. Oxidative coupling is used to form both of the rings of a heterocircuit catenane in one-pot. The importance of hydrogen-bonding in the formation of these catenanes is investigated.
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Hamilton DG, Feeder N, Prodi L, Teat SJ, Clegg W, Sanders JKM. Tandem hetero-catenation: templating and self-assembly in the mutual closure of two different interlocking rings. of special interest J Am Chem Soc. 120:1998;1096-1097 Oxidative coupling is used to form both of the rings of a heterocircuit catenane in one-pot. The importance of hydrogen-bonding in the formation of these catenanes is investigated.
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(1998)
J Am Chem Soc
, vol.120
, pp. 1096-1097
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-
Hamilton, D.G.1
Feeder, N.2
Prodi, L.3
Teat, S.J.4
Clegg, W.5
Sanders, J.K.M.6
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12
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0030738752
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High yield synthesis of [2]catenanes by intramolecular ring-closing metathesis
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of outstanding interest. Int Ed Engl. A high yielding catenane synthesis is developed using ring closing metathesis and preorganisation around metal ions.
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Mohr B, Weck M, Sauvage J-P, Grubbs RH. High yield synthesis of [2]catenanes by intramolecular ring-closing metathesis. of outstanding interest Int Ed Engl Angew Chem. 36:1997;1308-1310 A high yielding catenane synthesis is developed using ring closing metathesis and preorganisation around metal ions.
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(1997)
Angew Chem
, vol.36
, pp. 1308-1310
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Mohr, B.1
Weck, M.2
Sauvage J-P3
Grubbs, R.H.4
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13
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0032580376
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Recent advances in olefin metathesis and its application in organic synthesis
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Grubbs RH, Chang S. Recent advances in olefin metathesis and its application in organic synthesis. Tetrahedron. 54:1998;4413-4450.
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(1998)
Tetrahedron
, vol.54
, pp. 4413-4450
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Grubbs, R.H.1
Chang, S.2
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14
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0032573870
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Made-to-order assembling of [2]catenanes from palladium(II)-linked rectangular molecular boxes
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of outstanding interest. Labile metal - ligand coordination and hydrophobic forces are used in a quantitative catenane synthesis.
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Fujita M, Aoyagi M, Ibukuro F, Ogura K, Yamaguchi K. Made-to-order assembling of [2]catenanes from palladium(II)-linked rectangular molecular boxes. of outstanding interest J Am Chem Soc. 120:1998;611-612 Labile metal - ligand coordination and hydrophobic forces are used in a quantitative catenane synthesis.
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(1998)
J Am Chem Soc
, vol.120
, pp. 611-612
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Fujita, M.1
Aoyagi, M.2
Ibukuro, F.3
Ogura, K.4
Yamaguchi, K.5
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15
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0002900071
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Reversible five component assembly of a [2]catenane from an achiral metallomacrocycle and a dinaphtho-crown ether
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of special interest. The lability of a zinc porphyrin coordination complex and π-π interactions are used to give catenanes under thermodynamic control.
-
Try AC, Harding MM, Hamilton DG, Sanders JKM. Reversible five component assembly of a [2]catenane from an achiral metallomacrocycle and a dinaphtho-crown ether. of special interest J Chem Soc Chem Commun. 1998;723-724 The lability of a zinc porphyrin coordination complex and π-π interactions are used to give catenanes under thermodynamic control.
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(1998)
J Chem Soc Chem Commun
, pp. 723-724
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-
Try, A.C.1
Harding, M.M.2
Hamilton, D.G.3
Sanders, J.K.M.4
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16
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33748720064
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Facile synthesis and solid-state structure of a benzylic amide [2]catenane
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Int Ed Engl
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Johnston AG, Leigh DA, Pritchard RJ, Deegan MD. Facile synthesis and solid-state structure of a benzylic amide [2]catenane. Int Ed Engl Angew Chem. 34:1995;1209-1216.
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Angew Chem
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, pp. 1209-1216
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Johnston, A.G.1
Leigh, D.A.2
Pritchard, R.J.3
Deegan, M.D.4
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17
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0029849783
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The synthesis and solubilization of amide macrocycles via rotaxane formation
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Johnston AG, Leigh DA, Murphy A, Smart JP, Deegan MD. The synthesis and solubilization of amide macrocycles via rotaxane formation. J Am Chem Soc. 118:1996;10662-10663.
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(1996)
J Am Chem Soc
, vol.118
, pp. 10662-10663
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Johnston, A.G.1
Leigh, D.A.2
Murphy, A.3
Smart, J.P.4
Deegan, M.D.5
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18
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0030802575
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Glycylglycine rotaxanes - The hydrogen bond directed assembly of synthetic peptide rotaxanes
-
of outstanding interest. Int Ed Engl. Lessons learnt from templating of catenanes are used to design and synthesis the first synthetic peptide rotaxanes.
-
Leigh DA, Murphy A, Smart JP, Slawin AMZ. Glycylglycine rotaxanes - the hydrogen bond directed assembly of synthetic peptide rotaxanes. of outstanding interest Int Ed Engl Angew Chem. 36:1997;728-732 Lessons learnt from templating of catenanes are used to design and synthesis the first synthetic peptide rotaxanes.
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(1997)
Angew Chem
, vol.36
, pp. 728-732
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Leigh, D.A.1
Murphy, A.2
Smart, J.P.3
Slawin, A.M.Z.4
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19
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0032496950
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Controlling the frequency of macrocyclic ring rotation in benzylic amide [2]catenanes
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of outstanding interest. The processes involved in the circumvolution of benzylic amide [2]catenanes are elucidated and used to control interring dynamics through variations in structure and solvent polarity.
-
Leigh DA, Murphy A, Smart JP, Deleuze MS, Zerbetto F. Controlling the frequency of macrocyclic ring rotation in benzylic amide [2]catenanes. of outstanding interest J Am Chem Soc. 120:1998;6458-6467 The processes involved in the circumvolution of benzylic amide [2]catenanes are elucidated and used to control interring dynamics through variations in structure and solvent polarity.
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(1998)
J Am Chem Soc
, vol.120
, pp. 6458-6467
-
-
Leigh, D.A.1
Murphy, A.2
Smart, J.P.3
Deleuze, M.S.4
Zerbetto, F.5
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20
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0000944977
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High-frequency vibrations of the simplest benzylic amide [2]catenane
-
of special interest. The first comprehensive characterisation of the vibrational signature of an interlocked ring system is described.
-
Fanti M, Fustin C-A, Leigh DA, Murphy A, Rudolf P, Caudano R, Zamboni R, Zerbetto F. High-frequency vibrations of the simplest benzylic amide [2]catenane. of special interest J Phys Chem A. 102:1998;5782-5788 The first comprehensive characterisation of the vibrational signature of an interlocked ring system is described.
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(1998)
J Phys Chem a
, vol.102
, pp. 5782-5788
-
-
Fanti, M.1
Fustin C-A2
Leigh, D.A.3
Murphy, A.4
Rudolf, P.5
Caudano, R.6
Zamboni, R.7
Zerbetto, F.8
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21
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0039124341
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Thin films of a benzylic amide [2]catenane as a novel versatile photonic material
-
of special interest. Films of benzylic amide catenanes are found to have unusually high refractive indices by virtue of their interlocked architectures.
-
Gase T, Grando D, Chollet PA, Kajzar F, Lorin A, Tetard D, Leigh DA. Thin films of a benzylic amide [2]catenane as a novel versatile photonic material. of special interest Photonics Sci News. 3:1998;16-21 Films of benzylic amide catenanes are found to have unusually high refractive indices by virtue of their interlocked architectures.
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(1998)
Photonics Sci News
, vol.3
, pp. 16-21
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-
Gase, T.1
Grando, D.2
Chollet, P.A.3
Kajzar, F.4
Lorin, A.5
Tetard, D.6
Leigh, D.A.7
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22
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0000253651
-
Kinetic and thermodynamic effects in the self-assembly of [3]catenanes in the solution and solid states
-
of outstanding interest. A change in the constitution of the classic Stoddart tetracationic cyclophane effects both the efficiencies and selectivities of [2]- and [3]catenane formation.
-
Amabilino DB, Ashton PR, Stoddart JF, White AJP, Williams DJ. Kinetic and thermodynamic effects in the self-assembly of [3]catenanes in the solution and solid states. of outstanding interest Chem Eur J. 4:1998;460-468 A change in the constitution of the classic Stoddart tetracationic cyclophane effects both the efficiencies and selectivities of [2]- and [3]catenane formation.
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(1998)
Chem Eur J
, vol.4
, pp. 460-468
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-
Amabilino, D.B.1
Ashton, P.R.2
Stoddart, J.F.3
White, A.J.P.4
Williams, D.J.5
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23
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0032513696
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Oligocatenanes made to order
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of outstanding interest. The synthesis of interlocked rings up to a [7]catenane are made by judicious choice of components and experimental conditions.
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Amabilino DB, Ashton PR, Balzani V, Boyd SE, Credi A, Lee JY, Menzer S, Stoddart JF, Venturi M, Williams DJ. Oligocatenanes made to order. of outstanding interest J Am Chem Soc. 120:1998;4295-4307 The synthesis of interlocked rings up to a [7]catenane are made by judicious choice of components and experimental conditions.
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(1998)
J Am Chem Soc
, vol.120
, pp. 4295-4307
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-
Amabilino, D.B.1
Ashton, P.R.2
Balzani, V.3
Boyd, S.E.4
Credi, A.5
Lee, J.Y.6
Menzer, S.7
Stoddart, J.F.8
Venturi, M.9
Williams, D.J.10
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24
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0031011963
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A novel type of isomerism in [3]catenanes
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Ashton PR, Boyd SE, Claessens CG, Gillard RE, Menzer S, Stoddart JF, Tolley MS, White AJP, Williams DJ. A novel type of isomerism in [3]catenanes. Chem Eur J. 3:1997;788-798.
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(1997)
Chem Eur J
, vol.3
, pp. 788-798
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Ashton, P.R.1
Boyd, S.E.2
Claessens, C.G.3
Gillard, R.E.4
Menzer, S.5
Stoddart, J.F.6
Tolley, M.S.7
White, A.J.P.8
Williams, D.J.9
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25
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33748621704
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Clympiadane
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Int Ed Engl
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Amabilino DB, Ashton PR, Reder AS, Spencer N, Stoddart JF. Clympiadane. Int Ed Engl Angew Chem. 33:1994;1286-1290.
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(1994)
Angew Chem
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Amabilino, D.B.1
Ashton, P.R.2
Reder, A.S.3
Spencer, N.4
Stoddart, J.F.5
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26
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0030962426
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Towards a molecular anchor chain. Synthesis and catenations of spiro crown ethers
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of special interest. [3]Catenane models of a novel type of poly[2]catenane are prepared and the effect on yield of coulombic repulsions between the tetracationic macrocyclic components are discussed.
-
Ashton PR, Horn T, Menzer S, Preece JA, Spencer N, Stoddart JF, Williams DJ. Towards a molecular anchor chain. Synthesis and catenations of spiro crown ethers. of special interest Synthesis. 4:1997;480-488 [3]Catenane models of a novel type of poly[2]catenane are prepared and the effect on yield of coulombic repulsions between the tetracationic macrocyclic components are discussed.
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(1997)
Synthesis
, vol.4
, pp. 480-488
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Ashton, P.R.1
Horn, T.2
Menzer, S.3
Preece, J.A.4
Spencer, N.5
Stoddart, J.F.6
Williams, D.J.7
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27
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0347397243
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Tetrathiafulvalenophanes and their catenanes
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Nielsen MB, Li ZT, Becher J. Tetrathiafulvalenophanes and their catenanes. J Mater Chem. 7:1997;1175-1187.
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(1997)
J Mater Chem
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, pp. 1175-1187
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Nielsen, M.B.1
Li, Z.T.2
Becher, J.3
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28
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0002259505
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Bis[2]catenanes and a bis[2]rotaxane-model compounds for polymers with mechanically interlocked components
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Ashton PR, Huff J, Menzer S, Parsons IW, Preece JA, Stoddart JF, Tolley MS, White AJP, Williams DJ. Bis[2]catenanes and a bis[2]rotaxane-model compounds for polymers with mechanically interlocked components. Chem Eur J. 2:1996;31-44.
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Chem Eur J
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, pp. 31-44
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Ashton, P.R.1
Huff, J.2
Menzer, S.3
Parsons, I.W.4
Preece, J.A.5
Stoddart, J.F.6
Tolley, M.S.7
White, A.J.P.8
Williams, D.J.9
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29
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0031647060
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Self-assembly of functionalised [2]catenanes bearing a reactive functional group on either one or both macrocyclic components-from monomeric [2]catenanes to polycatenanes
-
of outstanding interest. The incorporation of tetracationic cyclophane-based catenanes into main chain polyisocyanates is described.
-
Menzer S, White AJP, Williams DJ. Self-assembly of functionalised [2]catenanes bearing a reactive functional group on either one or both macrocyclic components-from monomeric [2]catenanes to polycatenanes. of outstanding interest Macromolecules. 31:1998;295-307 The incorporation of tetracationic cyclophane-based catenanes into main chain polyisocyanates is described.
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(1998)
Macromolecules
, vol.31
, pp. 295-307
-
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Menzer, S.1
White, A.J.P.2
Williams, D.J.3
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30
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0000977648
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Synthesis and switchable condensation reaction of bifunctional [2]catenane
-
of special interest. The reactivity of a catenane monomer can be controlled to give either intramolecular cyclisation or polymerisation products.
-
Shimada S, Ishikawa K, Tamaoki N. Synthesis and switchable condensation reaction of bifunctional [2]catenane. of special interest Acta Chem Scand. 52:1998;374-376 The reactivity of a catenane monomer can be controlled to give either intramolecular cyclisation or polymerisation products.
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(1998)
Acta Chem Scand
, vol.52
, pp. 374-376
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Shimada, S.1
Ishikawa, K.2
Tamaoki, N.3
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31
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0031515677
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Synthesis of a novel poly[2]-catenane containing rigid catenanes
-
of special interest. Seven out of the eight amides of a catenane are N-methylated to greatly enhance solubility but give a catenane where the rings cannot rotate.
-
Muscat D, Witte A, Köhler W, Müllen K, Geerts Y. Synthesis of a novel poly[2]-catenane containing rigid catenanes. of special interest Macromol Rapid Commun. 18:1997;233-241 Seven out of the eight amides of a catenane are N-methylated to greatly enhance solubility but give a catenane where the rings cannot rotate.
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(1997)
Macromol Rapid Commun
, vol.18
, pp. 233-241
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-
Muscat, D.1
Witte, A.2
Köhler, W.3
Müllen, K.4
Geerts, Y.5
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32
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0000955163
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Poly[2]-catenanes containing alternating topological and covalent bonds
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Weidmann JL, Kern JM, Sauvage JP, Geerts Y, Muscat D, Müllen K. Poly[2]-catenanes containing alternating topological and covalent bonds. Chem Commun. 1996;1243-1244.
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Chem Commun
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Weidmann, J.L.1
Kern, J.M.2
Sauvage, J.P.3
Geerts, Y.4
Muscat, D.5
Müllen, K.6
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33
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0031328558
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A catenated cyclic octamine: A noncovalently bonded molecular system without attractive interaction between the two units
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of special interest. Reduction of amide roups in a catenane removes the H-bonding interactions responsible for interlocking and leaves the rings free to rotate.
-
Takata T, Shoji J, Furusho Y. A catenated cyclic octamine: a noncovalently bonded molecular system without attractive interaction between the two units. of special interest Chem Lett. 9:1997;881-882 Reduction of amide roups in a catenane removes the H-bonding interactions responsible for interlocking and leaves the rings free to rotate.
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(1997)
Chem Lett
, vol.9
, pp. 881-882
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Takata, T.1
Shoji, J.2
Furusho, Y.3
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34
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0002951936
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Catenands built on poly(ethylenimine). Attachment of two phenanthrolines in close proximity on the polymer backbone
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Suh J, Lee SH. Catenands built on poly(ethylenimine). Attachment of two phenanthrolines in close proximity on the polymer backbone. J Org Chem. 63:1998;1519-1526.
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J Org Chem
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Suh, J.1
Lee, S.H.2
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