Self-Assembly of Silver(I) and Ditopic Heteroscorpionate Ligands. Spontaneous Chiral Resolution in Helices and Sequence Isomerism in Coordination Polymers

被引:34
作者
Dura, Gema [1 ]
Carmen Carrion, M. [1 ,2 ]
Jalon, Felix A. [1 ]
Rodriguez, Ana M. [3 ]
Manzano, Blanca R. [1 ]
机构
[1] Univ Castilla La Mancha, Dept Quim Inorgan Organ & Bioquim, Fac Ciencias & Tecnol Quim IRICA, E-13071 Ciudad Real, Spain
[2] Fdn PCYTA, Albacete 02006, Spain
[3] Univ Castilla La Mancha, Escuela Tecn Super Ingenieros Ind, Dept Quim Inorgan Organ & Bioquim, E-13071 Ciudad Real, Spain
关键词
METAL-ORGANIC FRAMEWORKS; ANION-PI INTERACTIONS; BOX-LIKE DINUCLEAR; CRYSTAL-STRUCTURE; HALOGEN INTERACTIONS; HYDROGEN STORAGE; SOLID-STATE; SUPRAMOLECULAR ISOMERISM; MOLECULAR-STRUCTURES; PALLADIUM COMPLEXES;
D O I
10.1021/cg400636a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The self-assembly of the ligands bis(pyrazol-1-yl) (pyridine-4-yl)methane (L-1) and bis(3,S-dimethylpyrazol-1-yl) (pyridine-4-yl)methane (L-2) with AgBF4 leads to three types of species: L-1 gives rise to the formation of a boxlike cyclic dimer (1) while L-2 leads to two different coordination polymers that are sequence isomers. With dependence on the crystallization conditions, either a homochiral helix (2) with spontaneous resolution or a zigzag polymer is formed (3). By means of solid-state circular dichroism studies, the presence of both enantiomers in 2 is observed, enriched locally in colonies of crystals. The homochiral motif is stable, even upon removal of guest solvent molecules. The noncovalent interactions in the crystalline structure are clearly affected by the presence of the methyl groups on the pyrazolyl rings. The behavior of the compounds in solution is discussed.
引用
收藏
页码:3275 / 3282
页数:8
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