Crystal engineering of a 3-D coordination polymer from 2-D building blocks

2001 ◽  
pp. 495-496 ◽  
Author(s):  
Timothy J. Prior ◽  
Matthew J. Rosseinsky
2016 ◽  
Vol 72 (2) ◽  
pp. 166-169 ◽  
Author(s):  
Jiajia Guo ◽  
Wenli Cao ◽  
Shuailei Li ◽  
Kanghua Miao ◽  
Jirong Song ◽  
...  

The crystal engineering of coordination polymers has aroused interest due to their structural versatility, unique properties and applications in different areas of science. The selection of appropriate ligands as building blocks is critical in order to afford a range of topologies. Alkali metal cations are known for their mainly ionic chemistry in aqueous media. Their coordination number varies depending on the size of the binding partners, and on the electrostatic interaction between the ligands and the metal ions. The two-dimensional coordination polymer poly[tetra-μ-aqua-[μ4-4,4′-(diazenediyl)bis(5-oxo-1H-1,2,4-triazolido)]disodium(I)], [Na2(C4H2N8O2)(H2O)4]n, (I), was synthesized from 4-amino-1H-1,2,4-triazol-5(4H)-one (ATO) and its single-crystal structure determined. The mid-point of the imino N=N bond of the 4,4′-(diazenediyl)bis(5-oxo-1H-1,2,4-triazolide) (ZTO2−) ligand is located on an inversion centre. The asymmetric unit consists of one Na+cation, half a bridging ZTO2−ligand and two bridging water ligands. Each Na+cation is coordinated in a trigonal antiprismatic fashion by six O atoms,i.e.two from two ZTO2−ligands and the remaining four from bridging water ligands. The Na+cation is located near a glide plane, thus the two bridging O atoms from the two coordinating ZTO2−ligands are on adjacent apices of the trigonal antiprism, rather than being in ananticonfiguration. All water and ZTO2−ligands act as bridging ligands between metal centres. Each Na+metal centre is bridged to a neigbouring Na+cation by two water molecules to give a one-dimensional [Na(H2O)2]nchain. The organic ZTO2−ligand, an O atom of which also bridges the same pair of Na+cations, then crosslinks these [Na(H2O)2]nchains to form two-dimensional sheets. The two-dimensional sheets are further connected by intermolecular hydrogen bonds, giving rise to a stabile hydrogen-bonded network.


2021 ◽  
Vol 50 (12) ◽  
pp. 4152-4158
Author(s):  
Kai-Ping Xie ◽  
Si-Guo Wu ◽  
Long-Fei Wang ◽  
Guo-Zhang Huang ◽  
Zhao-Ping Ni ◽  
...  

The first spin-crossover example of a two-dimensional coordination polymer containing [Pd(SCN)4]2− building blocks was explored.


2017 ◽  
Vol 56 (6) ◽  
pp. 3512-3516 ◽  
Author(s):  
Stefano Canossa ◽  
Alessia Bacchi ◽  
Claudia Graiff ◽  
Paolo Pelagatti ◽  
Giovanni Predieri ◽  
...  

2003 ◽  
Vol 22 (22) ◽  
pp. 4396-4398 ◽  
Author(s):  
Yong-Rong Xie ◽  
Xi-Sen Wang ◽  
Hong Zhao ◽  
Jing Zhang ◽  
Ling-Hong Weng ◽  
...  

2018 ◽  
Vol 4 (4) ◽  
pp. 43 ◽  
Author(s):  
Luca Rigamonti ◽  
Manuela Vaccari ◽  
Fabrizio Roncaglia ◽  
Carlo Baschieri ◽  
Alessandra Forni

In continuation of our work on supramolecular architectures of single-molecule magnets (SMMs) as a promising strategy in developing their magnetic performance, in this paper we report the synthesis and single crystal X-ray structure of the centered triangular tetrairon(III) SMM, [Fe4(PhpPy)2(dpm)6], Fe4 (Hdpm = dipivaloylmethane, H3PhpPy = 2-(hydroxymethyl)-2-(4-(pyridine-4-yl)phenyl)propane-1,3-diol), and its assembly in the coordination polymer {[Fe4(PhpPy)2(dpm)6Ag](ClO4)}n, Fe4Ag, upon reaction with silver(I) perchlorate. Thanks to the presence of the pyridyl rings on the two tripodal ligands, Fe4 behaves as divergent ditopic linker, and due to the Fe4:AgClO4 1:1 ratio, Fe4Ag probably possesses a linear arrangement in which silver(I) ions are linearly coordinated by two nitrogen atoms, forming 1D chains whose positive charge is balanced by the perchlorate anions. The stabilization of such a polymeric structure can be ascribed to the long distance between the two donor nitrogen atoms (23.4 Å) and their donor power. Fe4Ag shows slow relaxation of the magnetization which follows a thermally activated process with Ueff/kB = 11.17(18) K, τ0 = 2.24(17) 10−7 s in zero field, and Ueff/kB = 14.49(5) K, τ0 = 3.88(8) 10−7 s in 1-kOe applied field, in line with what reported for tetrairon(III) SMMs acting as building blocks in polymeric structures.


2016 ◽  
Vol 72 (2) ◽  
pp. 128-132 ◽  
Author(s):  
Long Tang ◽  
Ji-Jiang Wang ◽  
Feng Fu ◽  
Sheng-Wen Wang ◽  
Qi-Rui Liu

With regard to crystal engineering, building block or modular assembly methodologies have shown great success in the design and construction of metal–organic coordination polymers. The critical factor for the construction of coordination polymers is the rational choice of the organic building blocks and the metal centre. The reaction of Zn(OAc)2·2H2O (OAc is acetate) with 3-nitrobenzoic acid (HNBA) and 4,4′-bipyridine (4,4′-bipy) under hydrothermal conditions produced a two-dimensional zinc(II) supramolecular architecture,catena-poly[[bis(3-nitrobenzoato-κ2O,O′)zinc(II)]-μ-4,4′-bipyridine-κ2N:N′], [Zn(C7H4NO4)2(C10H8N2)]nor [Zn(NBA)2(4,4′-bipy)]n, which was characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis and single-crystal X-ray diffraction analysis. The ZnIIions are connected by the 4,4′-bipy ligands to form a one-dimensional zigzag chain and the chains are decorated with anionic NBA ligands which interact further through aromatic π–π stacking interactions, expanding the structure into a threefold interpenetrated two-dimensional supramolecular architecture. The solid-state fluorescence analysis indicates a slight blue shift compared with pure 4,4′-bipyridine and HNBA.


2018 ◽  
Vol 49 (1) ◽  
pp. 21-28
Author(s):  
Gui Chen ◽  
Hai-Hang Lan ◽  
Si-Yuan Cheng ◽  
Wei-Qing Chen ◽  
Song-Liang Cai ◽  
...  

Author(s):  
Dan Zhao ◽  
Yanyan An ◽  
Tingting Guo ◽  
Juanzhi Yan ◽  
Danmei Song

Hydrothermal reaction of Mn2+ with the ditopic ligand 2,5-bis(1H-1,2,4-triazol-1-yl)benzoic acid (Hdtba) resulted in the complex poly[aqua[μ3-2,5-bis(1H-1,2,4-triazol-1-yl)benzoato-κ3 N 4:N 4′:O]chloridomanganese(II)] monohydrate], {[Mn(C11H7N6O2)Cl(H2O)]·H2O} n , (I). Coordination polymer I has been characterized by X-ray diffraction, IR spectroscopy, elemental analysis, thermogravimetry and susceptibility measurements. The topology of I corresponds to a three-dimensional (3,6)-conn net linked by {Mn2Cl2(COO)2} building blocks and dtba− anions. Significant antiferromagnetic exchange is observed within the dinuclear {Mn2Cl2(COO)2} subunits. A fit of the susceptibility data resulted in the magnetic parameters g = 1.93 and J = −1.52. Studies of the photoluminescence properties revealed that I represents a promising luminescence sensor for sensitively detecting dichromate ions in aqueous solution. The associated photochemical detection mechanism was studied in detail.


Crystals ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 45 ◽  
Author(s):  
Aleksandra Pacanowska ◽  
Mateusz Reczyński ◽  
Beata Nowicka

The 1D {[CuII(cyclam)]3[WV(CN)8]2.5H2O}n (1·5H2O) (cyclam = 1,4,8,11-tetraazacyclotetradecane) coordination polymer of ladder topology can be obtained in water-alcohol solution from [Cu(cyclam)]2+ and [W(CN)8]3− building blocks. Upon dehydration, 1·5H2O undergoes a single-crystal-to-single-crystal structural transformation to the anhydrous {[CuII(cyclam)]3[WV(CN)8]2}n (1) form, which retains the same topology, but is characterized by shorter Cu-W distances and significantly more bent CN-bridges. The deformation of the coordination skeleton is reflected in magnetic properties: the predominant intra-chain interactions change from ferromagnetic in 1·5H2O to antiferromagnetic in 1. The reaction between the same building blocks in water solution under slow diffusion conditions leads to the formation of a 0D {[CuII(cyclam)(H2O)]2[CuII(cyclam)][WV(CN)8]2}.3H2O pentanuclear assembly (2·3H2O).


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