-
1
-
-
33745817572
-
-
ed. by G. Schill, Academic Press, New York
-
a) Catenanes, Rotaxanes, and Knots, Organic Chemistry, ed. by G. Schill, Academic Press, New York, 1971, Vol. 22.
-
(1971)
Catenanes, Rotaxanes, and Knots, Organic Chemistry
, vol.22
-
-
-
2
-
-
0003542983
-
-
ed. by J.-P. Sauvage, C. Dietrich-Buchecker, Wiley-VCH, Weinheim
-
b) Molecular Catenanes, Rotaxanes and Knots, ed. by J.-P. Sauvage, C. Dietrich-Buchecker, Wiley-VCH, Weinheim, 1999.
-
(1999)
Molecular Catenanes, Rotaxanes and Knots
-
-
-
3
-
-
0034596923
-
-
a) V. Balzani, A. Credi, F. M. Raymo, J. F. Stoddart, Angew. Chem. Int. Ed. 2000, 39, 3348.
-
(2000)
Angew. Chem. Int. Ed
, vol.39
, pp. 3348
-
-
Balzani, V.1
Credi, A.2
Raymo, F.M.3
Stoddart, J.F.4
-
4
-
-
0012317549
-
-
ed. by V. Balzani, M. Venturi, A. Credi, Wiley-VCH, Weinheim
-
b) Molecular Devices and Machines, A Journey into the Nanoworld, ed. by V. Balzani, M. Venturi, A. Credi, Wiley-VCH, Weinheim, 2003.
-
(2003)
Molecular Devices and Machines, A Journey into the Nanoworld
-
-
-
5
-
-
33646380845
-
-
c) K. Osakada, T. Sakano, M. Horie, Y. Suzaki, Coord. Chem. Rev. 2006, 250, 1012.
-
(2006)
Coord. Chem. Rev
, vol.250
, pp. 1012
-
-
Osakada, K.1
Sakano, T.2
Horie, M.3
Suzaki, Y.4
-
8
-
-
0032210211
-
-
d) N. Nakashima, A. Kawabuchi, H. Murakami, J. Inclusion Phenom. Mol. Recognit. Chem. 1998, 32, 363.
-
(1998)
J. Inclusion Phenom. Mol. Recognit. Chem
, vol.32
, pp. 363
-
-
Nakashima, N.1
Kawabuchi, A.2
Murakami, H.3
-
10
-
-
33645331847
-
-
e) G. Wenz, B.-H. Han, A. Müller, Chem. Rev. 2006, 106, 782.
-
(2006)
Chem. Rev
, vol.106
, pp. 782
-
-
Wenz, G.1
Han, B.-H.2
Müller, A.3
-
11
-
-
33748623526
-
-
f) A. Harada, A. Hashidzume, Y. Takashima, Advances in Polymer Science, 2006, Vol. 201, p. 1.
-
(2006)
Advances in Polymer Science
, vol.201
, pp. 1
-
-
Harada, A.1
Hashidzume, A.2
Takashima, Y.3
-
12
-
-
34547810955
-
-
g) S. Loethen, J.-M. Kim, D. H. Thompson, Polym. Rev. 2007, 47, 383.
-
(2007)
Polym. Rev
, vol.47
, pp. 383
-
-
Loethen, S.1
Kim, J.-M.2
Thompson, D.H.3
-
13
-
-
0000827460
-
-
A. Harada, J. Li, M. Kamachi, Nature 1992, 356, 325.
-
(1992)
Nature
, vol.356
, pp. 325
-
-
Harada, A.1
Li, J.2
Kamachi, M.3
-
14
-
-
33746924101
-
-
Examples of [3]rotaxanes: a H. Yamaguchi, T. Oshikiri, A. Harada, J. Phys.: Condens. Matter 2006, 18, S1809.
-
Examples of [3]rotaxanes: a) H. Yamaguchi, T. Oshikiri, A. Harada, J. Phys.: Condens. Matter 2006, 18, S1809.
-
-
-
-
15
-
-
33846250896
-
-
b) K. Sakamoto, Y. Takashima, H. Yamaguchi, A. Harada, J. Org. Chem. 2007, 72, 459.
-
(2007)
J. Org. Chem
, vol.72
, pp. 459
-
-
Sakamoto, K.1
Takashima, Y.2
Yamaguchi, H.3
Harada, A.4
-
16
-
-
34548800799
-
-
c) H. W. Daniell, E. J. F. Klotz, B. Odell, T. D. W. Claridge, H. L. Anderson, Angew. Chem., Int. Ed. 2007, 46, 6845.
-
(2007)
Angew. Chem., Int. Ed
, vol.46
, pp. 6845
-
-
Daniell, H.W.1
Klotz, E.J.F.2
Odell, B.3
Claridge, T.D.W.4
Anderson, H.L.5
-
17
-
-
0031447883
-
-
A. Harada, J. Li, M. Kamachi, Y. Kitagawa, Y. Katsube, Carbohydr. Res. 1998, 305, 127.
-
(1998)
Carbohydr. Res
, vol.305
, pp. 127
-
-
Harada, A.1
Li, J.2
Kamachi, M.3
Kitagawa, Y.4
Katsube, Y.5
-
18
-
-
33748725372
-
-
a) N. Solladié, J.-C. Chambron, C. O. Dietrich-Buchecker, J.-P. Sauvage, Angew. Chem., Int. Ed. Engt. 1996, 35, 906.
-
(1996)
Angew. Chem., Int. Ed. Engt
, vol.35
, pp. 906
-
-
Solladié, N.1
Chambron, J.-C.2
Dietrich-Buchecker, C.O.3
Sauvage, J.-P.4
-
19
-
-
0033594517
-
-
b) N. Solladié, J.-C. Chambron, J.-P. Sauvage, J. Am. Chem. Soc. 1999, 121, 3684.
-
(1999)
J. Am. Chem. Soc
, vol.121
, pp. 3684
-
-
Solladié, N.1
Chambron, J.-C.2
Sauvage, J.-P.3
-
20
-
-
33746397549
-
-
D. Tuncel, N. Cindir, Ü. Koldemir, J. Incl. Phenom. Macro. Chem. 2006, 55, 373.
-
(2006)
J. Incl. Phenom. Macro. Chem
, vol.55
, pp. 373
-
-
Tuncel, D.1
Cindir, N.2
Koldemir, U.3
-
21
-
-
0033104834
-
-
S.-G. Roh, K.-M. Park, G.-J. Park, S. Sakamoto, K. Yamaguchi, K. Kim, Angew. Chem., Int. Ed. 1999, 38, 637.
-
(1999)
Angew. Chem., Int. Ed
, vol.38
, pp. 637
-
-
Roh, S.-G.1
Park, K.-M.2
Park, G.-J.3
Sakamoto, S.4
Yamaguchi, K.5
Kim, K.6
-
22
-
-
0036432940
-
-
N. Watanabe, T. Yagi, N. Kihara, T. Takata, Chem. Commun. 2002, 2720.
-
(2002)
Chem. Commun
, pp. 2720
-
-
Watanabe, N.1
Yagi, T.2
Kihara, N.3
Takata, T.4
-
24
-
-
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-
-
b) Y. Suzaki, T. Taira, D. Takeuchi, K. Osakada, Org. Lett. 2007, 9, 887.
-
(2007)
Org. Lett
, vol.9
, pp. 887
-
-
Suzaki, Y.1
Taira, T.2
Takeuchi, D.3
Osakada, K.4
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25
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40449141036
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Data of 2: 1HNMR (300MHz, D2O, rt, δ 1.02-1.59 (14H, CH2-axle, 1.70-2.04 (br, 2H, NCH2CH 2, 3.29-3.82 (80H, CH-α-CD, CH2-α-CD, OCH2-axle, OMe, 4.86 (br, 12H, CH-α-CD, 5.94 (s, 2H, ortho-C6H3, 6.04 (s, 1H, para-C 6H3, 7.73 (br, 2H, C10H8N 2, 8.22 (d, 2H, J, 5 Hz, 8.58 (br, 2H, C10H 8N2, 8.80 (d, 2H, C10H8N 2, J, 5Hz, The signal of NCH2 hydrogens was overlapped with the signal of HDO (δ 4.63, IR (KBr, rt, v 3000-3700 (O-H, 1206 (C-O-C) cm-1. Anal. Calcd for C100H 157N2O63Cl·OH2O, C, 47.31; H, 6.71; N, 1.10; Cl, 1.40, Found: C, 47.25; H, 6.59; N, 1.23; Cl, 1.31
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2O): C, 47.31; H, 6.71; N, 1.10; Cl, 1.40%. Found: C, 47.25; H, 6.59; N, 1.23; Cl, 1.31%.
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26
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40449102816
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Data of 3: 1HNMR (400MHz, D2O, rt, δ 1.07-1.53 (28H, CH2-axle, 1.96 (br, 4H, NCH2CH 2, 2.77 (s, 4H, CH2NH2, 3.34-3.85 (160H, CH-α-CD, CH2-α-CD, OCH2-Axle, OCH 3, 4.52 (br, NCH2, 4H, 4.88 (br, 24H, CH-α-CD, 5.98 (s, 4H, ortho-C6H3, 6.08 (s, 2H, para-C6H3, 7.91 (br, 4H, C10H 8N2, 8.21 (br, 4H, C10H8N 2, 8.85 (8H, C10H8N2, Signals of OH and NH2 hydrogens were not observed. 13C{1H} NMR (100 MHz, D2O, rt, δ 28.1 (CH2, 29.0 (CH 2, 31.2 (CH2, 31.7 (CH2, 32.0 (CH 2, 32.8 (2C, CH2, 33.0 (CH2, 48.7 (en, 57.4 (OCH3, 61.4 CH2
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2O): C, 44.17; H, 6.50; N, 2.55%. Found: C, 44.17; H, 6.30; N, 2.19%.
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27
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40449088321
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Data of 4: 1HNMR (300MHz, D2O, rt, δ 1.22-1.41 (24H, CH2-axle, 1.49 (br, 4H, OCH2CH 2, 1.95 (br, 4H, NCH2CH2, 2.69 (s, 4H, CH2NH2, 3.28-3.86 (160H, CH-α-CD, CH 2-α-CD, OCH2-axle, OCH3, 4.88 (d, 24H, CH-α-CD, J, 5Hz, 5.98 (s, 4H, ortho-C6H 3, 6.10 (s, 2H, para-C6H3, 7.90 (d, 4H, C10H8N2, J, 5Hz, 8.24 (d, 4H, C10H8N2, J, 7Hz, 8.87 (8H, C 10H8N2, The signal of NCH2 hydrogens was overlapped with the signal of HDO (δ 4.63, Signals of OH and NH2 hydrogens were not observed. 13C{1H}NMR (100 MHz, D2O, rt, δ 28.1 (CH2, 29.1 (CH 2, 31.2 CH2
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3). 3-(Trimethylsilyl)-1- propanesulfonic acid, sodium salt was used as external standard.
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28
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40449090480
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NOESY measurement of rotaxane 3 and 4 did not provide any further information to discuss head-to-head (or head-to-tail) arrangement of two CDs in a ligand.
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NOESY measurement of rotaxane 3 and 4 did not provide any further information to discuss head-to-head (or head-to-tail) arrangement of two CDs in a ligand.
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