scholarly journals One-Dimensional Mercury Halide Coordination Polymers Based on A Semi-Rigid N-Donor Ligand: Reversible Structural Transformation

Polymers ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 436 ◽  
Author(s):  
Pradhumna Mahat Chhetri ◽  
Xiang-Kai Yang ◽  
Chih-Tung Yang ◽  
Jhy-Der Chen

Four one-dimensional (1D) mercury(II) halide coordination polymers have been synthesized by using a semi-rigid N-donor ligand, 2,2′-(1,4-phenylene)-bis(N-(pyridin-3-yl)acetamide) (1,4-pbpa). While [Hg(1,4-pbpa)Cl2·CH3OH]n, 1, forms a sinusoidal chain, the complexes [Hg(1,4-pbpa)X2]n (X = Cl, 2; Br, 3; I, 4) are helical. The sinusoidal 1 undergoes reversible structural transformation with helical 2 upon removal and uptake of CH3OH, which was accompanied with the conformation adjustment of the 1,4-pbpa ligand from trans anti-anti to trans syn-anti. Pyridyl ring rotation of the 1,4-pbpa ligand that results in the change of the ligand conformation is proposed for the initiation of the structural transformation.

CrystEngComm ◽  
2018 ◽  
Vol 20 (15) ◽  
pp. 2126-2134 ◽  
Author(s):  
Pradhumna Mahat Chhetri ◽  
Xiang-Kai Yang ◽  
Jhy-Der Chen

The structural transformation in 1D helical and mesohelical Hg(ii) chains which demonstrate elastic stretching during the process is investigated.


CrystEngComm ◽  
2020 ◽  
Vol 22 (44) ◽  
pp. 7565-7574
Author(s):  
Chia-Jou Chen ◽  
Wei-Te Lee ◽  
Ji-Hong Hu ◽  
Pradhumna Mahat Chhetri ◽  
Jhy-Der Chen

The coordination of 5-tert-IPA2− ligands, the relaxation of the interdigitated 2D net and the breaking and connecting of the bis-pyridyl-bis-amide ligand demonstrate the peculiar reversible structural transformation between a 1D ladder and 2D layer.


2020 ◽  
Vol 76 (5) ◽  
pp. 500-506
Author(s):  
Kamil Twaróg ◽  
Małgorzata Hołyńska ◽  
Andrzej Kochel

Employment of the organic 2-(pyridin-4-yl)quinoline-4-carboxylic acid ligand with extended coordination capabilities leads to the formation of the one-dimensional copper(II) coordination polymer catena-poly[[diaquacopper(II)]-bis[μ-2-(pyridin-4-yl)quinoline-4-carboxylato]-κ2 N 2:O;κ2 O:N], {[Cu(C15H9N2O2)2(H2O)2]·2H2O} n , under hydrothermal conditions. The ligand, isolated as its hydrochloride salt, namely, 4-(4-carboxyquinolin-2-yl)pyridinium chloride monohydrate, C15H11N2O2 +·Cl−·H2O, reveals a pseudosymmetry element (translation a/2) in its crystal structure. The additional pyridyl N atom, in comparison with the previously reported analogues with an arene ring instead of the pyridyl ring in the present ligand molecule, promotes the formation of a one-dimensional coordination polymer, rather than discrete molecules. This polymer shows photoluminescent properties with bathochromic/hypsochromic shifts of the ligand absorption bands, leading to a single band at 479 nm. The CuII ions are involved in weak antiferromagnetic interactions within dimeric units, as evidenced by SQUID magnetometry.


CrystEngComm ◽  
2021 ◽  
Author(s):  
Ji-Hong Hu ◽  
Yuan-Chin Liu ◽  
Jhy-Der Chen

Hydrothermal reactions of cobalt(II) salts and bis(N-pyrid-3-ylmethyl)adipoamide (L) with various polycarboxylic acids in water and NaOH solutions afforded {[Co(L)0.5(1,3,5-HBTC)(H2O)]·H2O}n (1,3,5-H3BTC = benzene-1,3,5-tricarboxylic acid), 1, {[Co1.5(L)1.5(1,3,5-BTC)(H2O)4]·4H2O}n, 2, [Co(L)(5-tert-IPA)(H2O)2]n (5-tert-H2IPA = 5-tert-butylbenzene-1,3-dicarboxylic...


CrystEngComm ◽  
2020 ◽  
Vol 22 (19) ◽  
pp. 3322-3328 ◽  
Author(s):  
Chih-Tung Yang ◽  
Xiang-Kai Yang ◽  
Ji-Hong Hu ◽  
Wei-Te Lee ◽  
Tsun-Ren Chen ◽  
...  

Two extended metal chains based on linear tetracopper units are reported, in which the bromide complex undergoes reversible structural transformation and luminescence change.


2018 ◽  
Vol 42 (18) ◽  
pp. 15014-15021 ◽  
Author(s):  
Behrouz Notash ◽  
Bahareh Rezaei Kheirkhah

We transformed one one-dimensional coordination polymer directly to another by carrying out a dissolution–recrystallization structural transformation (DRST).


2000 ◽  
Vol 39 (9) ◽  
pp. 1990-1993 ◽  
Author(s):  
Zhan Shi ◽  
Lirong Zhang ◽  
Shan Gao ◽  
Guoyu Yang ◽  
Jia Hua ◽  
...  

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