These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Search MEDLINE/PubMed
Title: Triazolate-based 3D frameworks and a 2D layer with centrosymmetric Cu(II)7, Cu(II)5, Cu(II)4 clusters and tunable interlayer/interchain compactness: hydrothermal syntheses, crystal structures and magnetic properties. Author: Zhang YY, Zhao H, Yang EC, Liu ZY, Shang Q, Zhao XJ. Journal: Dalton Trans; 2015 Mar 28; 44(12):5826-36. PubMed ID: 25716907. Abstract: Four 1,2,3-triazolate-based coordination polymers (CPs) with varied dimensionality, different nuclearity numbers and core topologies, [Cu4(μ-OH)(μ3-OH)(ta)2(btec)]n (1), {[Cu6(μ3-OH)2(ta)8(tp)]·2.5H2O}n (2), {[Cu5(μ3-OH)2(ta)4(ip)2]·2H2O}n (3) and {[Cu5(μ-OH)2(μ3-OH)2(ta)2(pa)2]·2H2O}n (4) (ta = 1,2,3-triazolate, btec = 1,2,4,5-benzenetetracarboxylate, tp = terephthalate, ip = isophthalate and pa = phthalate), were hydrothermally synthesized by varying the numbers and positions of the carboxylate group appended on the phenyl tether, and structurally and magnetically characterized. The former three entities are three-dimensional (3D) robust frameworks with a (4(4)·6(2))(4(11)·6(5))2(4(13)·6(10)·8(5)) topological net containing centrosymmetric Cu(II)7 clusters, square-planar Cu(II)1 cores and tetratopic btec(4-) linkers for 1, a pillared-layered structure consisting of Cu(II)5 + Cu(II)1-based coplanar layers and ditopic tp(2-) pillars for 2 as well as a microporous architecture derived from Cu(II)5 clusters and directional ip(2-) connectors for 3. In contrast, complex exhibits an undulated two-dimensional (2D) layer with alternating Cu(II)4 + Cu(II)1 chains interconnected by anionic pa(2-) connectors. Crystallographically, the increment of the local nuclearity from Cu(II)4 up to Cu(II)7 in 1-4 benefits greatly from the synergistic co-coordination of the hydroxyl group and the coplanar ta(-) ligand towards the metal ion, and the interlayer/interchain compactness is significantly tuned by the position isomerism of the dicarboxylate moieties. Due to the antiferromagnetic coupling in the local clusters and the asymmetric superexchange by μ3-ta(-) mediator, these complexes 4 exhibit different spin ground states (paramagnetic S = 1 and 1/2, ferrimagnetic S = 1/2 as well as spin canting) at low temperatures, which are informative for polynuclear-based magnetic materials.[Abstract] [Full Text] [Related] [New Search]