3,3′-Di(pyrazinamoyl)-2,2′-bipyridine: rational ligand design for the self-assembly of a 1-D coordination polymer

2015 ◽  
Vol 44 (4) ◽  
pp. 1866-1874 ◽  
Author(s):  
Nicholas J. Hurley ◽  
Jeremy M. Rawson ◽  
Melanie Pilkington

A new pyrazine functionalized polydentate ligand with distinct binding domains facilitates the self-assembly of a unique paddlewheel bridged 1D coordination polymer of formula {[Cu3(L3)2(Cl)2(OAc)6]·2H2O·2MeOH}n that has been structurally and magnetically characterized.

Soft Matter ◽  
2021 ◽  
Vol 17 (13) ◽  
pp. 3654-3663
Author(s):  
Botian Li ◽  
Da Xiao ◽  
Xiaodong Gai ◽  
Bo Yan ◽  
Haimu Ye ◽  
...  

A multi-responsive self-healable organogel and colloid were fabricated by the assembly of a coordination polymer derived from Ag(i) and azopyridine ligands.


2021 ◽  
Author(s):  
Heyi Zhang ◽  
Fangyuan He ◽  
Xiaonan Li ◽  
Zhi-Hui Wang ◽  
Hong Zhang

Through the self-assembly of 1,1'-bis(3-cyanobenzyl)-[4,4'-bipyridine] dichloride ligand, m-H2BDC and Zn(NO3)2·6H2O, a novel one-dimensional chain structure multifunctional coordination polymer was successfully synthesized. Due to electron transfer during irradiation and heating to...


CrystEngComm ◽  
2002 ◽  
Vol 4 (35) ◽  
pp. 199-201 ◽  
Author(s):  
Janusz Szklarzewicz ◽  
Robert Podgajny ◽  
Krzysztof Lewiński ◽  
Barbara Sieklucka

CrystEngComm ◽  
2020 ◽  
Vol 22 (34) ◽  
pp. 5601-5605 ◽  
Author(s):  
Seulgi Kim ◽  
In-Hyeok Park ◽  
Shim Sung Lee ◽  
Wonbo Sim ◽  
Jai Young Lee

The self-assembly reactions of bis-o-xylyl-(17-crown-5) with alkali metal salts afforded binding mode (good fit, perching and sandwich)-dependent supramolecular complexes, including a sandwich-type cesium(i) coordination polymer.


2008 ◽  
pp. 1027-1036 ◽  
Author(s):  
Thomas B. Jensen ◽  
Rosario Scopelliti ◽  
Jean-Claude G. Bünzli
Keyword(s):  

Crystals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 823
Author(s):  
Saied M. Soliman ◽  
Raghdaa A. Massoud ◽  
Hessa H. Al-Rasheed ◽  
Ayman El-Faham

Molecular and supramolecular structures of two polymeric and one trinuclear Cd(II) complex with hydralazine-type ligands were presented. Self-assembly of E-1-(2-(thiophen-2-ylmethylene)hydrazinyl)phthalazine (HL) and CdCl2 gave the 1D coordination polymer [Cd(H2L)Cl3]n*H2O, 1, in which the Cd(II) ion is hexa-coordinated with one cationic monodentate ligand (H2L+) and five chloride ions, two of them acting as connectors between Cd(II) centers, leading to the formation of a 1D coordination polymer along the a-direction. Using DFT calculations, the cationic ligand (H2L+) could be described as a protonated HL with an extra proton at the hydrazone moiety. Repeating the same reaction by heating under reflux conditions in the presence of 1 mL saturated aqueous KSCN solution, the ligand HL underwent cyclization to the corresponding [1,2,4]triazolo[3,4-a]phthalazine-3(2H)-thione (TPT) followed by the formation of [Cd(TPT)(SCN)2]n*H2O, 2, a 1D coordination polymer. In this complex, the Cd(II) is coordinated with one NS-donor TPT bidentate chelate and two bridged μ(1,3)-thiocyanate ions connecting the Cd(II) centers forming the 1D polymer array along the b-direction. Heating E-2-(1-(2-(phthalazin-1-yl)hydrazono)ethyl)phenol HLOH with CdCl2 under reflux condition gave the trinuclear complex [Cd3(Hydralazine)2(H2O)2Cl6], 3, indicating the hydrolysis of the hydrazonophthalazine ligand HLOH during the course of the reaction. Due to symmetry considerations, there are only two different Cd(II) centers having CdN2Cl3O and CdN2Cl4 coordination environments. Hirshfeld topology analysis was used to analyze the solid-state supramolecular structure of the studied complexes.


2018 ◽  
Vol 74 (12) ◽  
pp. 1774-1780
Author(s):  
Allison M. Rabon ◽  
Kayla L. Goolsby ◽  
Michael C. Young

Self-assembly of metal–organic coordination polymers occurs because of enthalpically favorable interactions. In the case of the bulky 4,4′-(anthracene-9,10-diyl)dibenzoic acid ligand (abdH2), we demonstrate that the presence of numerous π–π and C—H...π interactions outweigh the formation of saturated coordination complexes with zinc, leading to the formation of a dimethylformamide (DMF) solvate, namely 4,4′-(anthracene-9,10-diyl)dibenzoic acid dimethylformamide disolvate, C28H18O4·2C3H7NO or [(abdH2)(DMF)2], at low concentrations of zinc. Meanwhile, at higher zinc concentrations, the abdH2 ligand gives rise to the nonporous one-dimensional coordination polymer catena-poly[[bis(dimethylformamide-κO)zinc(II)]-μ-4,4′-(anthracene-9,10-diyl)dibenzoato-κ2 O:O′], [Zn(C28H16O4)(C3H7NO)2] n or [Zn(abd)(DMF)2] n , when assembled in dimethylformamide, while a related compound is observed when N,N-dimethylacetamide (DMA) is used as the solvent, namely catena-poly[[[bis(N,N-dimethylacetamide-κO)zinc(II)]-μ-4,4′-(anthracene-9,10-diyl)dibenzoato-κ2 O:O′] N,N-dimethylacetamide monosolvate], {[Zn(C28H16O4)(C4H9NO)2]·C4H9NO} n or {[Zn(abd)(DMA)2]·DMA} n . Attempts to use other amide-based solvents did not give rise to any other assembled structures.


2019 ◽  
Vol 48 (12) ◽  
pp. 3815-3818 ◽  
Author(s):  
Marco Villa ◽  
Myriam Roy ◽  
Giacomo Bergamini ◽  
Marc Gingras ◽  
Paola Ceroni

Persulfurated asterisks functionalized with six carboxylic groups form a strongly green phosphorescent coordination polymer upon addition of Pb2+ ions in aqueous solution. The self-assembly process is selective and reversible, enabling Pb2+ sensing with a detection limit of 6.0 × 10−7 M.


2008 ◽  
pp. 3582 ◽  
Author(s):  
Xue-Qin Song ◽  
Wei-Sheng Liu ◽  
Wei Dou ◽  
Jiang-Rong Zheng ◽  
Xiao-Liang Tang ◽  
...  

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