-
2
-
-
33748853938
-
-
b) G. Seeber, B. E. F. Tiedemann, K. N. Raymond, Top. Curr. Chem. 2006, 265, 147;
-
(2006)
Top. Curr. Chem
, vol.265
, pp. 147
-
-
Seeber, G.1
Tiedemann, B.E.F.2
Raymond, K.N.3
-
3
-
-
38749099876
-
-
c) G. A. Hembury, V. V. Borovkov, Y. Inoue, Chem. Rev. 2008, 108, 1.
-
(2008)
Chem. Rev
, vol.108
, pp. 1
-
-
Hembury, G.A.1
Borovkov, V.V.2
Inoue, Y.3
-
4
-
-
0001412882
-
-
a) J. S. Seo, D. Whang, H. Lee, S. I. Jun, J. Oh, Y. J. Jeon, K. Kim, Nature 2000, 404, 982;
-
(2000)
Nature
, vol.404
, pp. 982
-
-
Seo, J.S.1
Whang, D.2
Lee, H.3
Jun, S.I.4
Oh, J.5
Jeon, Y.J.6
Kim, K.7
-
5
-
-
0035874999
-
-
b) J. M. Ribó, J. Crusats, F. Sagués, J. Claret, R. Rubires, Science 2001, 292, 2063;
-
(2001)
Science
, vol.292
, pp. 2063
-
-
Ribó, J.M.1
Crusats, J.2
Sagués, F.3
Claret, J.4
Rubires, R.5
-
6
-
-
31444440235
-
-
c) R. Fasel, M. Parschau, K.-H. Ernst, Nature 2006, 439, 449;
-
(2006)
Nature
, vol.439
, pp. 449
-
-
Fasel, R.1
Parschau, M.2
Ernst, K.-H.3
-
7
-
-
34548637582
-
-
d) M. D. Ward, Nature 2007, 449, 149.
-
(2007)
Nature
, vol.449
, pp. 149
-
-
Ward, M.D.1
-
11
-
-
53349122475
-
-
Enantiophobic molecules would aggregate leading to a conglomerate, while enantiophilic molecules would give a racemic compound.[3b
-
[3b]
-
-
-
-
13
-
-
34548153336
-
-
b) W. Lin, MRS Bull. 2007, 32, 544.
-
(2007)
MRS Bull
, vol.32
, pp. 544
-
-
Lin, W.1
-
14
-
-
0033553103
-
-
T. Ezuhara, K. Endo, Y. Aoyama, J. Am. Chem. Soc. 1999, 121, 3279.
-
(1999)
J. Am. Chem. Soc
, vol.121
, pp. 3279
-
-
Ezuhara, T.1
Endo, K.2
Aoyama, Y.3
-
15
-
-
0242668325
-
-
a) E.-Q. Gao, S.-Q. Bai, Z.-M. Wang, C.-H. Yan, J. Am. Chem. Soc. 2003, 125, 4984;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 4984
-
-
Gao, E.-Q.1
Bai, S.-Q.2
Wang, Z.-M.3
Yan, C.-H.4
-
16
-
-
1042263363
-
-
b) E.-Q. Gao, Y.-F. Yue, S.-Q. Bai, Z. He, C.-H. Yan, J. Am. Chem. Soc. 2004, 126, 1419.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 1419
-
-
Gao, E.-Q.1
Yue, Y.-F.2
Bai, S.-Q.3
He, Z.4
Yan, C.-H.5
-
18
-
-
6044263674
-
-
b) X.-C. Huang, J.-P. Zhang, X.-M. Chen, J. Am. Chem. Soc. 2004, 126, 13218;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 13218
-
-
Huang, X.-C.1
Zhang, J.-P.2
Chen, X.-M.3
-
19
-
-
18844462468
-
-
c) X.-C. Huang, J.-P. Zhang, Y.-Y. Lin, X.-M. Chen, Chem. Commun. 2005, 2232.
-
(2005)
Chem. Commun
, pp. 2232
-
-
Huang, X.-C.1
Zhang, J.-P.2
Lin, Y.-Y.3
Chen, X.-M.4
-
20
-
-
0040995579
-
-
a) C. Piguet, G. Bernardinelli, G. Hopfgartner, Chem. Rev. 1997, 97, 2005;
-
(2005)
Chem. Rev
, vol.1997
, pp. 97
-
-
Piguet, C.1
Bernardinelli, G.2
Hopfgartner, G.3
-
23
-
-
34547749878
-
-
d) C. He, Y. Zhao, D. Guo, Z. Lin, C. Duan, Eur. J. Inorg. Chem. 2007, 3451.
-
(2007)
Eur. J. Inorg. Chem
, pp. 3451
-
-
He, C.1
Zhao, Y.2
Guo, D.3
Lin, Z.4
Duan, C.5
-
24
-
-
0142254736
-
-
For examples, see: a
-
For examples, see: a) Y. Wang, J. Yu, M. Guo, R. Xu, Angew. Chem. 2003, 115, 4223;
-
(2003)
Angew. Chem
, vol.115
, pp. 4223
-
-
Wang, Y.1
Yu, J.2
Guo, M.3
Xu, R.4
-
26
-
-
33847267419
-
-
b) Y.-Q. Sun, J. Zhang, Y.-M. Chen, G.-Y. Yang, Angew. Chem. 2005, 117, 5964;
-
(2005)
Angew. Chem
, vol.117
, pp. 5964
-
-
Sun, Y.-Q.1
Zhang, J.2
Chen, Y.-M.3
Yang, G.-Y.4
-
28
-
-
33748477765
-
-
c) H.-Y. An, E.-B. Wang, D.-R. Xiao, Y.-G. Li, Z.-M. Su, L. Xu, Angew. Chem. 2006, 118, 918;
-
(2006)
Angew. Chem
, vol.118
, pp. 918
-
-
An, H.-Y.1
Wang, E.-B.2
Xiao, D.-R.3
Li, Y.-G.4
Su, Z.-M.5
Xu, L.6
-
30
-
-
53349114567
-
-
d) J.-Z. Hou, M. Li, Z. Li, S.-Z. Zhan, X.-C. Huang, D. Li, Angew. Chem. 2008, 120, 1735;
-
(2008)
Angew. Chem
, vol.120
, pp. 1735
-
-
Hou, J.-Z.1
Li, M.2
Li, Z.3
Zhan, S.-Z.4
Huang, X.-C.5
Li, D.6
-
33
-
-
27744485848
-
-
b) L. Hou, D. Li, W.-J. Shi, Y.-G. Yin, S. W. Ng, Inorg. Chem. 2005, 44, 7825;
-
(2005)
Inorg. Chem
, vol.44
, pp. 7825
-
-
Hou, L.1
Li, D.2
Shi, W.-J.3
Yin, Y.-G.4
Ng, S.W.5
-
34
-
-
33646559216
-
-
c) X.-J. Zhang, D. Li, X.-P. Zhou, New J. Chem. 2006, 30, 706;
-
(2006)
New J. Chem
, vol.30
, pp. 706
-
-
Zhang, X.-J.1
Li, D.2
Zhou, X.-P.3
-
35
-
-
34250692084
-
-
d) S.-S. Zhang, S.-Z. Zhan, M. Li, R. Peng, D. Li, Inorg. Chem. 2007, 46, 4365.
-
(2007)
Inorg. Chem
, vol.46
, pp. 4365
-
-
Zhang, S.-S.1
Zhan, S.-Z.2
Li, M.3
Peng, R.4
Li, D.5
-
36
-
-
53349088120
-
-
Crystal data for 2a: C22H17ZnN 3Cl2, Mr, 459.66, trigonal, space group P3121 (no. 152, a, 13.3238(10, b, 13.3238(10, c, 32.414(5) Å, γ, 120.00°, V, 4983.3(9) Å3, Z, 9, ρcalcd, 1.379 g cm-3, μ, 1.361 mm-1, F(000, 2106, T, 296(2) K, 12 990 reflections collected, 5142 unique (Rint, 0.0420, R1, 0.0516, final R1, 0.0731, wR2, 0.1314, GOF, 1.023 for all data. Crystal data for 2b: C22H17ZnN3Cl2, Mr, 459.68, monoclinic, space group P2 1/n (no. 14, a, 10.4621(11, b, 16.9501(18, c, 14.9931(17) Å, β, 52.498(2)°, V, 2109.3(4) Å3, Z
-
3, the largest peak is 0.65. Therefore, compound 2a is considered to contain no solvent in the lattice. The asymmetric unit of 3 contains both solvent water molecules and EtOH molecules. The solvent EtOH molecules are disordered by translation over three sites, with site occupancy factors of 0.5, 0.25, and 0.25, respectively. CCDC 682963 (2a), 682964 (2b), and 682965 (3) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/ data_request/cif
-
-
-
-
37
-
-
8544284818
-
-
For examples, see: a
-
For examples, see: a) V. V. Borovkov, G. A. Hembury, Y. Inoue, Angew. Chem. 2003, 115, 5468;
-
(2003)
Angew. Chem
, vol.115
, pp. 5468
-
-
Borovkov, V.V.1
Hembury, G.A.2
Inoue, Y.3
-
40
-
-
34247128650
-
-
c) L. Jiang, X.-L. Feng, C.-Y. Su, X.-M. Chen, T.-B. Lu, Inorg. Chem. 2007, 46, 2637;
-
(2007)
Inorg. Chem
, vol.46
, pp. 2637
-
-
Jiang, L.1
Feng, X.-L.2
Su, C.-Y.3
Chen, X.-M.4
Lu, T.-B.5
-
41
-
-
34547167040
-
-
d) C.-Y. Chen, P.-Y. Cheng, H.-H. Wu, H. M. Lee, Inorg. Chem. 2007, 46, 5691.
-
(2007)
Inorg. Chem
, vol.46
, pp. 5691
-
-
Chen, C.-Y.1
Cheng, P.-Y.2
Wu, H.-H.3
Lee, H.M.4
-
42
-
-
85045721751
-
-
a) J. Rasburn, D. A. Foucher, W. F. Reynolds, I. Manners, G. J. Vancso, Chem. Commun. 1998, 843;
-
(1998)
Chem. Commun
, pp. 843
-
-
Rasburn, J.1
Foucher, D.A.2
Reynolds, W.F.3
Manners, I.4
Vancso, G.J.5
-
45
-
-
53349112954
-
-
[14b] invoked this set of concepts in the description of chiral coordination polymers, because in the usual nomenclature, the term heterochiral does not distinguish between the R,S,R,S and R,R,S,S sequences. Herein, we feel comfortable following this nomenclature in describing supramolecular chirality, because of the similar dilemma encountered and the novelty of the structure of 3.
-
[14b] invoked this set of concepts in the description of chiral coordination polymers, because in the usual nomenclature, the term heterochiral does not distinguish between the R,S,R,S and R,R,S,S sequences. Herein, we feel comfortable following this nomenclature in describing supramolecular chirality, because of the similar dilemma encountered and the novelty of the structure of 3.
-
-
-
|