Effect of guest molecules, metal ions and linker length on the assembly of chiral [2+2] metallomacrocycles: solution studies and crystal structures

被引:63
作者
Houghton, MA [1 ]
Bilyk, A [1 ]
Harding, MM [1 ]
Turner, P [1 ]
Hambley, TW [1 ]
机构
[1] UNIV SYDNEY,SCH CHEM,SYDNEY,NSW 2006,AUSTRALIA
来源
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 1997年 / 15期
关键词
D O I
10.1039/a702378b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Eight new 2,2'-bipyridines, containing functionalised acetylenes at the 6 position, have been prepared. The azido derivatives were used to prepare three compounds L-1, L-2 and L-3, which contain pyromellitimide spacers connected to 6,6'-disubstituted 2,2'-bipyridines with propynyl, butynyl and propynyloxy linkers respectively, via iminophosphoranes. In the presence of an equimolar amount of zinc(Ir) triflate (trifluoromethanesulfonate), L-1 was assembled exclusively into the chiral [2 + 2] metallomacrocycle [Zn2L21](4+) at low concentrations (<10 mmol dm(-3)) or in the presence of an aromatic guest molecule S, which stabilises the complex through binding in the cavity of the metallomacrocycle. The crystal structures of diquabis{N,N'-bis[3-(6'-methyl-2,2'-bipyridine-6-yl)prop-2-ynyl]naphthalene-1,8:4,5-tetracarboximide}dizinc tetrakis(triflate) [Zn2L21][CF3SO3](4) . 2H(2)O, containing either p- or o-dimethoxybenzene bound in the cavity, were determined by X-ray diffraction methods. In both cases the crystals were extremely fragile and there was extensive disorder of substrate and solvate molecules and the triflate counter ions in channels in the lattice. These structures, while of limited quality, confirm the identity of the complexes, and reveal several substrate-dependent differences. Comparison of the two structures provided clear evidence for the metallomacrocycle adjusting its shape and dimensions to accommodate optimum binding of the substrate th rough pi-stacking/electrostatic interact io ns, and provides the first example of a metallosupramolecular complex in which the cavity size is determined by the bound substrate. The assembly of the chiral [2 + 2] metallomacrocycle was also achieved with L-1 and cadmium(II) and L-1 and copper(I) in the presence of >20 equivalents of m-dimethoxybenzene. In contrast, L-2 and L-3 formed zinc(II) complexes which gave only broadened NMR spectra consistent with equilibrating mixtures of oligomers. The different results obtained with L-1, L-2 and L-3 highlight the importance of the rigid propargyl(prop-2-ynyl) linker in directing the outcome of the assembly process.
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页码:2725 / 2733
页数:9
相关论文
共 40 条
[1]   FORMATION OF A MESO-HELICATE BY SELF-ASSEMBLY OF 3 BIS(CATECHOLATE) LIGANDS AND 2 TITANIUM(IV) IONS [J].
ALBRECHT, M ;
KOTILA, S .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1995, 34 (19) :2134-2137
[2]   Counter-ion induced self-assembly of a meso-helicate type molecular box [J].
Albrecht, M ;
Kotila, S .
CHEMICAL COMMUNICATIONS, 1996, (20) :2309-2310
[3]  
ALBRECHT M, 1996, ANGEW CHEM INT EDIT, V35, P1038
[4]   GUEST-INDUCED ASSEMBLY OF A CHIRAL [2+2] METALLOMACROCYCLE [J].
BILYK, A ;
HARDING, MM .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1995, (16) :1697-1698
[5]   ASSEMBLY OF [2+2] BIMETALLIC MACROCYCLIC COMPLEXES FROM BIS(BIPYRIDYL) LIGANDS AND METAL-IONS [J].
BILYK, A ;
HARDING, MM .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1994, (01) :77-82
[6]  
BILYK A, 1995, J CHEM SOC DA, P395
[7]  
BILYK A, 1995, J CHEM SOC DA, P3905
[8]  
DIETZ TM, 1996, CHEM COMMUN, P379
[9]   GUEST-INDUCED ORGANIZATION OF A 3-DIMENSIONAL PALLADIUM(II) CAGE-LIKE COMPLEX - A PROTOTYPE FOR INDUCED-FIT MOLECULAR RECOGNITION [J].
FUJITA, M ;
NAGAO, S ;
OGURA, K .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (05) :1649-1650
[10]   SPECTROSCOPIC OBSERVATION OF SELF-ASSEMBLY OF A MACROCYCLIC TETRANUCLEAR COMPLEX COMPOSED OF PT2+ AND 4,4'-BIPYRIDINE [J].
FUJITA, M ;
YAZAKI, J ;
OGURA, K .
CHEMISTRY LETTERS, 1991, (06) :1031-1032