Self-assembly of silver(I) polymers with single strand double-helical structures containing the ligand O,O′-bis(8-quinolyl)-1,8-dioxaoctane

被引:75
作者
Cai, YP
Zhang, HX
Xu, AW
Su, CY [1 ]
Chen, CL
Liu, HQ
Zhang, L
Kang, BS
机构
[1] Zhongshan Univ, Sch Chem & Chem Engn, Guangzhou 510275, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organomet Chem, Shanghai 200032, Peoples R China
来源
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 2001年 / 16期
关键词
D O I
10.1039/b102525m
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The flexible multidentate ligand O,O'-bis(8-quinolyl)-1,8-dioxaoctane (ODOQ) reacted with AgX (X = ClO4-, BF4-, CF3SO3-, or CF3CO2-) to give four new complexes [Ag(ODOQ)](n)X-n: X = ClO4- 1; X = BF4- 2; X = CF3SO3- 3, and [Ag(ODOQ)(CF3CO2)](n) 4. All four complexes have been characterized by elemental analyses, IR and H-1 NMR spectroscopy. Single crystal X-ray analyses showed that they have similar 1-D extended architectures with each ligand in "similar to" shape, while the chains are alternately and parallelly arranged with the silver(I) atoms as the backbone to form double helical mesomeric strands. The structures are controlled more by the spacer (CH2)(6) than by the anions: the versatile coordination geometry of the silver(I) atom is trigonally bonded but changes to distorted tetrahedral or trigonal bipyrimidal via weak Ag...O interactions. In addition, face-to-face pi...pi (in 1-4) and edge-to-face C-H... ic (in 3) interactions as well as hydrogen bonds C-H...O and C-H... F between adjacent strands assemble the cations in 1-3 or neutral molecules in 4 into an extended network.
引用
收藏
页码:2429 / 2434
页数:6
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