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Mono- and polynuclear Cu(II) coordination compounds that contain diazine ligands
Cu(OTf) 2(2-mepyz) 2(H 2O) 2 ( 1) and Cu(OTf) 2(H 2O) 2(pyz) ( 2) are two new Cu(II) coordination compounds comprised of diazine synthons organized into quasi-2D and 1D structures, respectively. While long-range magnetic ordering was not observed for either compound, significant Cu-pyz-Cu exchange i...
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Published in: | Polyhedron 2008-08, Vol.27 (12), p.2650-2654 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Cu(OTf)
2(2-mepyz)
2(H
2O)
2 (
1) and Cu(OTf)
2(H
2O)
2(pyz) (
2) are two new Cu(II) coordination compounds comprised of diazine synthons organized into quasi-2D and 1D structures, respectively. While long-range magnetic ordering was not observed for either compound, significant Cu-pyz-Cu exchange interactions were found in
2.
Cu(OTf)
2(2-mepyz)
2(H
2O)
2 (2-mepyz
=
2-methylpyrazine; OTf
−
=
CF
3
SO
3
-
=
triflate),
1, and Cu(OTf)
2(H
2O)
2(pyz) (pyz
=
pyrazine),
2, consist of monomeric and polymeric structures, respectively. Both compounds contain octahedral Cu(II) metal centers surrounded by
trans-coordinated OTf
−, H
2O, and diazines, either 2-mepyz in the case of
1 or pyz in
2. In
1, O–H⋯O(triflate) hydrogen bonds link CuO
4N
2 monomers into quasi-1D chains which are joined via O–H⋯N interactions to afford a three-dimensional (3D) network. Pyz ligands in
2 link CuO
4N
2 octahedra into linear chains similar to Cu(NO
3)
2(pyz). Magnetically, neither
1 or
2 show indications for long-range magnetic ordering (LRO) above 2
K. Least-squares fits of the magnetic susceptibility data,
χ(
T), to a Bonner–Fisher uniform chain model gave 2
J/
k
B
=
−0.005(1) and −6.0(1)
K for compounds
1 and
2, respectively, indicative of negligible and moderate antiferromagnetic coupling between spin-1/2 Cu(II) ions. Inter-chain magnetic interactions seem to be negligible for both systems. |
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ISSN: | 0277-5387 |
DOI: | 10.1016/j.poly.2008.05.007 |