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Layered copper bromide coordination polymers from bis(pyridyl)piperazine-type precursors: Ligand dependent valence tuning and in situ hydrothermal reaction chemistry
被引:10
作者:
Banisafar, Arash
LaDuca, Robert L.
[1
]
机构:
[1] Michigan State Univ, Lyman Briggs Coll, E Lansing, MI 48825 USA
关键词:
Copper;
Bromide;
Coordination polymer;
In situ reaction;
Chirality;
METAL-ORGANIC FRAMEWORKS;
CRYSTAL-STRUCTURE;
FLUORESCENCE;
COMPLEXES;
NLO;
ZEOLITE;
ACID;
D O I:
10.1016/j.ica.2011.03.068
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
Hydrothermal reaction of copper(II) bromide with either bis(4-pyridylmethyl)piperazine (bpmp) or bis(4-pyridylformyl)piperazine (bpfp) afforded layered coordination polymer solids. The racemic S,S and R, R stereochemistry dped ligands in [Cu2Br2(dped)](n) (1, dped = 1,2-di(4-pyridyl)ethanediol) were formed by the in situ transformation of bpmp via putative 4-pyridylmethanol intermediates, along with concomitant reduction to monovalent copper. The structure of 1 contains [Cu2Br2](n) chains comprising edge-shared [Cu3Br3] boat-conformation six-membered rings, linked into layer motifs by dped tethers with alternating stereochemistry. Lack of benzylic hydrogen atoms in bpfp causes that ligand to stay intact under the reaction conditions, generating the 2-D layered divalent copper phase [CuBr2(bpfp)](n) (2). (C) 2011 Elsevier B. V. All rights reserved.
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页码:295 / 300
页数:6
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